{"id":418,"date":"2019-11-15T19:13:58","date_gmt":"2019-11-15T19:13:58","guid":{"rendered":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/chapter\/9-4-antidiabetics\/"},"modified":"2021-12-07T11:27:40","modified_gmt":"2021-12-07T11:27:40","slug":"9-4-antidiabetics","status":"publish","type":"chapter","link":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/chapter\/9-4-antidiabetics\/","title":{"raw":"9.4 Antidiabetics","rendered":"9.4 Antidiabetics"},"content":{"raw":"<div class=\"pancreas-\">\n<h2>Pancreatic Basics: A&amp;P Review<\/h2>\n<strong>Pancreas<\/strong>\n\nThe pancreas is a long, slender organ located near the stomach (see Figure 9.7).<sup>[footnote]\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:1820_The_Pancreas.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">1820 The Pancreas.jpg<\/a>\"\" by <a href=\"https:\/\/openstax.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">OpenStax<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0.<\/a> Access for free at <a href=\"https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas<\/a>[\/footnote]<\/sup>\u00a0Although it is primarily an <strong>[pb_glossary id=\"1740\"]exocrine gland[\/pb_glossary]<\/strong>, secreting a variety of digestive enzymes, the pancreas also has an endocrine function. Pancreatic islets, clusters of cells formerly known as the islets of Langerhans, secrete glucagon and insulin. Glucagon plays an important role in blood glucose regulation because low blood glucose levels stimulate its release. On the other hand, elevated blood glucose levels stimulate the release of insulin.\n\n[caption id=\"\" align=\"aligncenter\" width=\"1092\"]<img title=\"&quot;1820 The Pancreas.jpg&quot; by OpenStax is licensed under CC BY 4.0 Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2019\/11\/image1-9.png\" alt=\"Illustration and micrograph showing pancreas and surrounding structures, with labels.\" width=\"1092\" height=\"551\"> Figure 9.7 Pancreas[\/caption]\n<h3>Regulation of Blood Glucose Levels by Insulin and Glucagon<\/h3>\nGlucose is the preferred fuel for all body cells. The body derives glucose from the breakdown of the carbohydrate-containing foods and drinks we consume. Glucose not immediately taken up by cells for fuel can be stored by the liver and muscles as glycogen or converted to triglycerides and stored in the adipose tissue. Hormones regulate both the storage and the utilization of glucose as required. Receptors located in the pancreas sense blood glucose levels, and subsequently, the pancreatic cells secrete glucagon or insulin to maintain normal levels.\n<h4>Glucagon<\/h4>\nReceptors in the pancreas can sense the decline in blood glucose levels, such as during periods of fasting or during prolonged labor or exercise. In response, the alpha cells of the pancreas secrete the hormone glucagon, which has several effects:\n<ul>\n \t<li>It stimulates the liver to convert stores of glycogen back into glucose. This response is known as glycogenolysis. The glucose is then released into the circulation for use by body cells.<\/li>\n \t<li>It stimulates the liver to take up amino acids from the blood and convert them into glucose. This response is known as gluconeogenesis.<\/li>\n \t<li>It stimulates lipolysis, the breakdown of stored triglycerides into free fatty acids and glycerol. Some of the free glycerol released into the bloodstream travels to the liver, which converts it into glucose. This is also a form of gluconeogenesis.<\/li>\n<\/ul>\nTaken together, these actions increase blood glucose levels. The activity of glucagon is regulated through a negative feedback mechanism; rising blood glucose levels inhibit further glucagon production and secretion. (See Figure 9.8 for an illustration of homeostatic regulation of blood glucose levels.)<sup>[footnote]\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:1822_The_Homostatic_Regulation_of_Blood_Glucose_Levels.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">1822 The Homostatic Regulation of Blood Glucose Levels.jpg<\/a>\" by <a href=\"https:\/\/openstax.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">OpenStax<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0.<\/a> Access for free at <a href=\"https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"alignnone\" width=\"1054\"]<img title=\"&quot;1822 The Homostatic Regulation of Blood Glucose Levels.jpg&quot; by OpenStax is licensed under CC BY 4.0 Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image2-9.png\" alt=\"Illustration showing homeostatic regulation of blook glucose levels, with labels.\" width=\"1054\" height=\"1478\"> Figure 9.8 Homeostatic Regulation of Blood Glucose Levels. Blood glucose concentration is tightly maintained between 70 mg\/dL and 110 mg\/dL. If blood glucose concentration rises above this range, insulin is released, which stimulates body cells to remove glucose from the blood. If blood glucose concentration drops below this range, glucagon is released, which stimulates body cells to release glucose into the blood.[\/caption]\n<h4>Insulin<\/h4>\n<strong>[pb_glossary id=\"1746\"]Insulin[\/pb_glossary]<\/strong> facilitates the uptake of glucose into skeletal and adipose body cells. The presence of food in the intestine triggers the release of gastrointestinal tract hormones. This, in turn, triggers insulin production and secretion by the beta cells of the pancreas. Once nutrient absorption occurs, the resulting surge in blood glucose levels further stimulates insulin secretion.\n\nInsulin triggers the rapid movement of glucose transporter vesicles to the cell membrane, where they are exposed to the extracellular fluid. The transporters then move glucose by facilitated diffusion into the cell interior.\n\nInsulin also reduces blood glucose levels by stimulating <strong>[pb_glossary id=\"1745\"]glycolysis[\/pb_glossary]<\/strong>, the metabolism of glucose for generation of ATP. It further stimulates the liver to convert excess glucose into glycogen for storage, and it inhibits enzymes involved in glycogenolysis and gluconeogenesis. Finally, insulin promotes triglyceride and protein synthesis. The secretion of insulin is regulated through a negative feedback mechanism. As blood glucose levels decrease, further insulin release is inhibited.\n<h3>Disorders of the Endocrine System: Diabetes Mellitus<\/h3>\nDysfunction of insulin production and secretion, as well as the target cells\u2019 responsiveness to insulin, can lead to a condition called diabetes mellitus, a common disease that affects the ability of the body to produce and\/or utilize insulin. There are two main forms of diabetes mellitus. <strong>[pb_glossary id=\"1748\"]Type 1 diabetes [\/pb_glossary]<\/strong> is an autoimmune disease affecting the beta cells of the pancreas. The beta cells of people with type 1 diabetes do not produce insulin; thus, synthetic insulin must be administered by injection or infusion. <strong>[pb_glossary id=\"1749\"]Type 2 diabetes[\/pb_glossary]<\/strong> accounts for approximately 95 percent of all cases. It is acquired, and lifestyle factors such as poor diet and inactivity greatly increase a person\u2019s risk. In type 2 diabetes, the body\u2019s cells become resistant to the effects of insulin. In response, the pancreas increases its insulin secretion, but over time, the beta cells become exhausted. In many cases, type 2 diabetes can be reversed by moderate weight loss, regular physical activity, and consumption of a healthy diet. However, if blood glucose levels cannot be controlled, oral diabetic medication is implemented and eventually the type 2 diabetic may require insulin.\n\nDiabetes is diagnosed when lab tests reveal that blood glucose levels are higher than normal, a condition called <strong>[pb_glossary id=\"2190\"]hyperglycemia[\/pb_glossary]<\/strong>.<sup>[footnote]This work is a derivative of <a href=\"https:\/\/openstax.org\/details\/books\/anatomy-and-physiology\" target=\"_blank\" rel=\"noopener noreferrer\">Anatomy and Physiology<\/a> by <a href=\"https:\/\/openstax.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">OpenStax<\/a> licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0<\/a>. Access for free at <a href=\"https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/1-introduction\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/1-introduction<\/a>[\/footnote]<\/sup> According to the American Diabetes Association (ADA), normal fasting blood glucose levels are 80-130 mg\/dL. Glycosylated hemoglobin, also called A1C, is used to assess long-term blood glucose levels over 3 months. The ADA states that A1C target levels vary according to age and health, but the generalized A1C target is less than 7%.<sup>[footnote]American Diabetes Association. (2019). The Big Picture: Checking your Blood Glucose. <a href=\"https:\/\/www.diabetes.org\/diabetes\/medication-management\/blood-glucose-testing-and-control\/checking-your-blood-glucose\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.diabetes.org\/diabetes\/medication-management\/blood-glucose-testing-and-control\/checking-your-blood-glucose<\/a>[\/footnote]<\/sup>\n<h2>Nursing Considerations<\/h2>\n<h3><strong>Assessment<\/strong><\/h3>\nDiabetic patients should be continuously monitored for signs of hypoglycemia and hyperglycemia. When a diabetic patient is experiencing stress or an infection, the nurse should plan to assess the blood glucose levels more frequently.\n<h3><strong>Implementation <\/strong><\/h3>\nThe nurse should follow agency policy and ISMP guidelines for safe insulin administration. See the \"Legal Ethical\" chapter for more information about ISMP guidelines. Onset and peak times of insulin and sulfonylureas, in association with anticipated meal times, should always be considered to avoid hypoglycemia episodes. If a hypoglycemia episode occurs, the nurse should intervene quickly using the agency\u2019s established hypoglycemia protocol, and the event should be reported to the provider and in the shift-to-shift report. Symptomatic hyperglycemia should be immediately reported to the provider. Patient education should be provided to patients, family members, and\/or caregivers according to ADA and ISMP guidelines.\n<h3><strong>Evaluation<\/strong><\/h3>\nThe nurse should evaluate A1C levels to determine effectiveness (and compliance with) the treatment regimen.\n<h2>Diabetic Medication Classes: Insulins<\/h2>\nBecause the hallmark of type 1 diabetes is absent or near-absent \u03b2-cell function, insulin treatment is essential for individuals with type 1 diabetes. Current evidence-based recommendations regarding pharmacological treatment of type 1 diabetes from the American Diabetes Association (ADA) include:\n<ul>\n \t<li>Most people with type 1 diabetes should be treated with multiple daily injections of prandial and basal insulin or continuous subcutaneous insulin infusion.<\/li>\n \t<li>Most individuals with type 1 diabetes should use rapid-acting insulin analogs to reduce hypoglycemia risk.<\/li>\n \t<li>Individuals with type 1 diabetes on prandial insulin doses should be educated on carbohydrate intake, premeal blood glucose levels, and anticipated physical activity.<\/li>\n \t<li>Individuals with type 1 diabetes who have been successfully using continuous subcutaneous insulin infusion should have continued access to this therapy after they turn 65 years of age.<\/li>\n<\/ul>\n<strong>[pb_glossary id=\"1751\"]Basal insulin[\/pb_glossary]<\/strong> can be long-acting (insulin glargine or insulin detemir) or intermediate-acting (insulin isophane suspension [NPH]). <strong>[pb_glossary id=\"1752\"]Prandial insulins [\/pb_glossary] <\/strong>are used with meals and may be rapid acting (insulin lispro, insulin aspart, or insulin glulisine) or short acting (regular insulin).\n\nAccording to the ADA, insulin requirements can be estimated based on weight, with typical doses ranging from 0.4 to 1.0 units\/kg\/day. Higher amounts are required during puberty, pregnancy, and medical illness. Physiologic insulin secretion varies with glycemia, meal size, and tissue demands for glucose. To approach this variability in people using insulin treatment, strategies have evolved to adjust meal-time doses based on predicted needs. Thus, education of patients on how to adjust insulin to account for carbohydrate intake, premeal glucose levels, and anticipated activity is important. Ensuring that patients and\/or caregivers understand correct insulin injection technique is also important to optimize glucose control and insulin use safety.<sup>[footnote]American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S009\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S009<\/a>[\/footnote]<\/sup>\n\nPatients on insulin therapy are at risk for <strong>[pb_glossary id=\"1754\"]hypoglycemia[\/pb_glossary]<\/strong>. It is essential for the nurse to monitor for signs of hypoglycemia and to intervene appropriately. See Figure 9.9 for symptoms of hypoglycemia. Hypoglycemia is defined as a blood glucose level below 70 mg\/dL; severe hypoglycemia refers to a blood glucose level below 40 mg\/dL.\n<h3 style=\"text-align: left\">Hypoglycemia Symptoms<\/h3>\n<table class=\"grid\" style=\"width: 691px;height: 249px\" border=\"0\">\n<tbody>\n<tr style=\"height: 14px\">\n<th style=\"width: 326.063px;height: 14px;text-align: left\" scope=\"col\"><strong>Mild-to-Moderate<\/strong><\/th>\n<th style=\"width: 336.063px;height: 14px\" scope=\"col\"><strong>Severe<\/strong><\/th>\n<\/tr>\n<tr style=\"height: 235px\">\n<td style=\"width: 326.063px;height: 235px\">\n<ul>\n \t<li>Shaky or jittery<\/li>\n \t<li>Sweaty<\/li>\n \t<li>Hungry<\/li>\n \t<li>Headache<\/li>\n \t<li>Blurred vision<\/li>\n \t<li>Sleepy or tired<\/li>\n \t<li>Dizzy or lightheaded<\/li>\n \t<li>Confused or disoriented<\/li>\n \t<li>Pale<\/li>\n \t<li>Uncoordinated<\/li>\n \t<li>Irritable or nervous<\/li>\n \t<li>Argumentative or combative<\/li>\n \t<li>Changed behavior or personality<\/li>\n \t<li>Trouble concentrating<\/li>\n \t<li>Weak<\/li>\n \t<li>Fast or irregular heart beat<\/li>\n<\/ul>\n<\/td>\n<td style=\"width: 336.063px;height: 235px\">\n<ul>\n \t<li>Unable to eat or drink<\/li>\n \t<li>Seizures or convulsions (jerky movements)<\/li>\n \t<li>Unconsciousness<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<em>Figure 9.9 Hypoglycemia Symptoms<\/em>\n\nIf a patient with diabetes shows a sudden change in mood or mental status or other symptoms of hypoglycemia, the nurse should immediately check the blood glucose level. Healthcare agencies use hypoglycemia protocols so that the nurse can react quickly to episodes of hypoglycemia before they become severe. Hypoglycemia protocols contain orders for immediate treatment by the nurse. For instance, in patients who can tolerate oral intake, 15 grams of rapidly digested carbohydrates (such as 4 ounces of fruit juice) are recommended. In patients who are NPO or can\u2019t take oral treatment, dextrose 50% IV or glucagon IM or subcutaneously are administered. Patients who have had a hypoglycemic episode should be monitored closely for the following 24 hours because they are at increased risk for another episode. The provider and the oncoming nurse should be notified of hypoglycemia episodes to discuss the possible cause of the hypoglycemic event and make insulin adjustments, if needed, to avoid additional hypoglycemia. Tracking hypoglycemia episodes and analyzing causes are important performance improvement activities.<sup>[footnote]Seggelke, S., Everhart, B. (2012, September 11) Managing glucose levels in hospital patients. <em>American Nurse Today.<\/em> <a href=\"https:\/\/www.americannursetoday.com\/managing-glucose-levels-in-hospital-patients\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.americannursetoday.com\/managing-glucose-levels-in-hospital-patients\/<\/a>.[\/footnote]<\/sup>\n\n<\/div>\n<div class=\"pancreas-\">\n\n&nbsp;\n\nThe arrival of continuous glucose monitors to clinical practice has been proven to reduce nocturnal hypoglycemia in people using insulin pumps with glucose sensors due to automatic suspension of insulin delivery at a preset glucose level. The U.S. Food and Drug Administration has also approved the first hybrid closed-loop pump system.<sup>[footnote]American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S009\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S009<\/a>[\/footnote]<\/sup> A hybrid closed-loop pump system automatically adjusts basal insulin delivery every 5 minutes based on sensor glucose to maintain blood glucose levels as close to a specific target as possible.<sup>[footnote]Weaver, H., Hirsch, I (2018, June 6). The Hybrid Closed Loop System: Evolution and Practical Applications. <em>Diabetes Technology &amp; Therapeutics 20<\/em>(S2). <a href=\"https:\/\/www.liebertpub.com\/doi\/10.1089\/dia.2018.0091\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.liebertpub.com\/doi\/10.1089\/dia.2018.0091<\/a>.[\/footnote]<\/sup>\n\nAccording to the ADA, lifestyle modifications that improve health should be emphasized, along with any pharmacologic therapy. Lifestyle modifications include healthy food choices to stabilize blood glucose levels, as well as daily exercise.\n<h3><strong>Hypokalemia<\/strong><\/h3>\nAll insulin products cause a shift in potassium from the extracellular to intracellular space, which can possibly lead to hypokalemia. Untreated hypokalemia may cause respiratory paralysis, ventricular arrhythmia, and death. Monitor potassium levels in patients at risk for hypokalemia due to other medications such as diuretics.\n<h3><strong>Insulin Pens<\/strong><\/h3>\nInsulin pens are often used in inpatient settings, as well as for self-administration, to facilitate safe and accurate self-administration of insulin. See Figure 9.10 for an image of an insulin pen.<sup>[footnote]\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Human_insulin_100_IU-1ml_pen_yellow_background_(02).jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Human insulin 100 IU-1ml pen yellow background (02).jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/wiki\/User:Wesalius\" target=\"_blank\" rel=\"noopener noreferrer\">Wesalius<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0<\/a>[\/footnote]<\/sup> According to the ISMP, insulin pens offer several advantages over vials beyond dosing accuracy, convenience, and ease of use:\n<ul>\n \t<li>Each pen is already labeled by the manufacturer with the product name and product barcode (whereas syringes of insulin prepared on the patient care unit from vials run the risk of being unlabeled).<\/li>\n \t<li>Each pen can be individually labeled with the patient\u2019s name (and ideally with a patient-specific barcode).<\/li>\n \t<li>The pen provides the patient\u2019s insulin in a form ready for administration.<\/li>\n \t<li>The pen lessens nursing time needed to prepare and administer insulin.<\/li>\n \t<li>Insulin pens reduce medication waste that can occur when dispensing 10 mL-sized insulin vials for each patient.<\/li>\n<\/ul>\nHowever, improper sharing of insulin pens among multiple patients has exposed patients to bloodborne pathogens. Insulin pens should never be reused for multiple patients; even if the needle is changed between patients, there can still be body fluid exposure.<sup>[footnote]Institute for Safe Medication Practices. (2017). ISMP Guidelines for Optimizing Safe Subcutaneous Insulin Use in Adults.\u00a0 <a href=\"https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"aligncenter\" width=\"682\"]<img title=\"&quot;Human insulin 100 IU-1ml pen yellow background (02).jpg&quot; by Wesalius is licensed under CC BY 4.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image3-10.png\" alt=\"Photo showing Humulin KwikPen\" width=\"682\" height=\"196\"> Figure 9.10 Insulin Pens[\/caption]\n<h3><strong>High-Alert Medication and Prevention of Errors<\/strong><\/h3>\nInsulin is a high-alert medication that can be associated with significant patient harm when used in error. A variety of error types have been associated with insulin therapy, including administration of the wrong insulin product, improper dosing (underdosing and overdosing), dose omissions, incorrect use of insulin delivery devices, wrong route (intramuscular versus subcutaneous), and improper patient monitoring. Many errors result in serious hypoglycemia or hyperglycemia. Hypoglycemia is often caused by a failure to adjust insulin therapy in response to a reduction in nutritional intake or an excessive insulin dose stemming from a prescribing or dose measurement error. Other factors that contribute to serious hypoglycemia include inappropriate timing of insulin doses with food intake, creatinine clearance, body weight, changes in medications that affect blood glucose levels, poor communication during patient transfer to different care teams, and poor coordination of blood glucose testing with insulin administration at meal time.\n\nIn an inpatient setting, manifestations of poor glycemic control, including severe hypoglycemia and hyperglycemia, are deemed hospital-acquired conditions by the Centers for Medicare and Medicaid Services (CMS). CMS notes that poor glycemic control can be reasonably prevented with implementation of evidence-based guidelines; thus, the CMS denies payment for diabetic ketoacidosis, hypoglycemic coma, and other serious conditions related to poor glycemic control. Agency policies and procedures should be closely followed to avoid these errors and manifestations of poor glycemic control.\n\nOne strategy for look-alike medications such as Humalog and Humalin is tall man lettering on the label. Tall man lettering describes a method for differentiating the unique letter characters of similar drug names known to be confused with one another, such as HumaLOG and HumaLIN.\n\nISMP recommends the following safe practice guidelines for the administration of insulin by the nurse:\n<ul>\n \t<li>Patient-specific insulin pens are stored on clinical units in a manner that prevents their inadvertent use on more than one patient.<\/li>\n \t<li>A coordinated process is developed to ensure timely blood glucose checks and administration of prandial insulin in conjunction with meal delivery.<\/li>\n \t<li>Verbal communication of point-of-care blood glucose value results are avoided as much as possible and are NEVER routinely used as the only source of information when determining insulin doses.<\/li>\n \t<li>Appropriately label all clinician-prepared syringes of subcutaneous insulin, unless the medication is prepared at the patient\u2019s bedside and is immediately administered to the patient without any break in the process.<\/li>\n \t<li>Prior to subcutaneous insulin administration, the practitioner:\n<ul>\n \t<li>Confirms that there is an appropriate indication<\/li>\n \t<li>Assesses the patient\u2019s most current blood glucose value<\/li>\n \t<li>Assesses the patient for symptoms of hypoglycemia<\/li>\n \t<li>Informs the patient of their most current blood glucose level<\/li>\n \t<li>Informs the patient of their dose, the full name of the product, and the insulin\u2019s intended action<\/li>\n<\/ul>\n<\/li>\n \t<li>An individual insulin pen is never used for more than one patient.<\/li>\n \t<li>Barcode scanning is used to verify that a patient-specific pen is used to administer the correct insulin to the correct patient.<\/li>\n \t<li>Prior to transitions of care, a process is in place to ensure that patients will have the necessary prescriptions, supplies, a follow-up care plan, and printed instructions for all prescribed insulin and blood glucose monitoring.<\/li>\n \t<li>Patients discharged on insulin are assessed for understanding of their self-management, including:\n<ul>\n \t<li>Demonstration of proper dose measurement and self-administration using the same administration device that will be used at home (e.g., vial and syringe, pen, pump)<\/li>\n \t<li>Correct monitoring of blood glucose values<\/li>\n \t<li>The signs and symptoms of hyper- and hypoglycemia and how to respond if these symptoms occur<\/li>\n \t<li>Common types of errors possible with their insulin therapy and how to prevent or detect these errors<\/li>\n \t<li>The importance of regular follow-up with their primary care provider\/specialist, including the date of their next appointment<\/li>\n \t<li>Patients who self-administer concentrated U-500 insulin using a vial and syringe are taught to use only a U-500 syringe and communicate their doses in terms of the name and concentration of the insulin and the actual dose in units using only the U-500 syringe<sup>[footnote]Institute for Safe Medication Practices. (2017). ISMP Guidelines for Optimizing Safe Subcutaneous Insulin Use in Adults.\u00a0 <a href=\"https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf<\/a>[\/footnote]<\/sup><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3>Lifespan Considerations<\/h3>\n<h4><strong>Elderly<\/strong><\/h4>\nThe elderly are at higher risk for hypoglycemia episodes. The ADA has the following recommendations for elderly patients with diabetes:\n<ul>\n \t<li>In older adults at increased risk of hypoglycemia, medication classes with low risk of hypoglycemia are preferred.<\/li>\n \t<li>Overtreatment of diabetes is common in older adults and should be avoided.<\/li>\n \t<li>Deintensification (or simplification) of complex regimens is recommended to reduce the risk of hypoglycemia, if it can be achieved within the individualized A1C target.<sup>[footnote]American Diabetes Association (2019) 12. Older adults: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S012\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S012<\/a>[\/footnote]<\/sup><\/li>\n<\/ul>\n<h4><strong>Children and Adolescents<\/strong><\/h4>\nType 1 diabetes is the most common form of diabetes in youth. Unique aspects of care and management of children and adolescents with type 1 diabetes must be considered, such as changes in insulin sensitivity related to physical growth and sexual maturation, ability to provide self-care, supervision in the child care and school environment, neurological vulnerability to hypoglycemia and hyperglycemia in young children, as well as possible adverse neurocognitive effects of diabetic ketoacidosis (DKA). Evidence-based ADA recommendations for glycemic control for children and adolescents include:\n<ul>\n \t<li>The majority of children and adolescents with type 1 diabetes should be treated with intensive insulin regimens, either via multiple daily injections or continuous subcutaneous insulin infusion.<\/li>\n \t<li>All children and adolescents with type 1 diabetes should self-monitor glucose levels multiple times daily (up to 6\u201310 times\/day), including pre-meal, pre-bedtime, and as needed for safety in specific situations such as exercise, driving, or the presence of symptoms of hypoglycemia.<\/li>\n \t<li>Continuous glucose monitoring should be considered in all children and adolescents with type 1 diabetes, whether using injections or continuous subcutaneous insulin infusion, as an additional tool to help improve glucose control. Benefits of continuous glucose monitoring correlate with adherence to ongoing use of the device.<\/li>\n \t<li>Automated insulin delivery systems appear to improve glycemic control and reduce hypoglycemia in children and should be considered in children with type 1 diabetes.<\/li>\n \t<li>An A1C target of &lt;7.5% should be considered in children and adolescents with type 1 diabetes but should be individualized based on the needs and situation of the patient and family. <sup>[footnote]American Diabetes Association. (2019). 13. Children and adolescents: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S013\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S013<\/a>[\/footnote]<\/sup><\/li>\n<\/ul>\nThere are several different types of insulins that vary in terms of onset, peak, and duration. It is critical for the nurse to be knowledgeable of these differences to help prevent episodes of hypoglycemia due to mismatched administration of insulin with food intake.\n<h3>Rapid-Acting Insulin<\/h3>\nRapid-acting insulins include insulin lispro (Humalog) and insulin aspart (Novolog) and are also available via inhalation (Afrezza). See Figure 9.11 for an image of Novolog insulin.<sup>[footnote]\"<a href=\"https:\/\/pxhere.com\/de\/photo\/1209814\" target=\"_blank\" rel=\"noopener noreferrer\">Untitled<\/a>\" from <a href=\"https:\/\/pxhere.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">Pxhere<\/a> website is licensed under <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/cc0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC0<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"aligncenter\" width=\"411\"]<img title=\"&quot;Untitled&quot; by Pxhere is licensed under CC0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image4-9.png\" alt=\"Photo showing package of Novalog with vial next to it.\" width=\"411\" height=\"368\"> Figure 9.11 Novolog insulin[\/caption]\n\n<strong>Indications<\/strong>\n\nRapid-acting insulins are also called prandial insulins because they are administered with meals to mimic the effects of endogenous insulin release when food is eaten. Dosages of rapid-acting insulin are individualized based on carbohydrate intake, premeal glucose levels, and anticipated activity.\n\n<strong>Mechanism of Action<\/strong>\n\nInsulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat and by inhibiting hepatic glucose production.\n\n<strong>Specific Administration Considerations<\/strong>\n\nHumalog-100 (100 units per ml) and Humalog-200 (200 units per ml) are administered subcutaneously; however, only Humalog-100 is administered via continuous subcutaneous injection or intravenously. Humalog-100 can only be mixed with NPH insulin, but Humalog-200 should not be mixed with other insulin. Inspect insulin visually before use. It should appear clear and colorless; do not use if particulate matter or coloration is seen. Humalog-100 is available in vials, KwikPens, and cartridges; Humalog-200 is only available in KwikPens. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy. Lipodystrophy can be a lump or small dent in the skin that forms when a person performs injections repeatedly in the same spot.\n\nBecause of the rapid onset of insulin lispro and insulin aspart and the potential for hypoglycemia, these insulins should be administered within 15 minutes before or right after eating a meal. Peak serum levels are seen 30 to 90 minutes after dosing. Inhaled insulin enters the bloodstream within 1 minute and peaks in 30-60 minutes. Inhaled insulin is contraindicated in patients with chronic lung disease such as asthma or COPD.\n\nAdverse effects of all insulins include hypoglycemia and hypokalemia. Inhaled insulin has a Black Box Warning for potentially causing acute bronchoconstriction.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nSee ISMP guidelines for patient teaching in the previous section titled \u201cHigh Risk Medications and Prevention of Errors.\u201d\n<h3>Short-Acting Insulin<\/h3>\nShort-acting insulins include regular insulin with a brand name of Humulin R or Novolin R. A concentrated formulation of Humulin R u-500 is also available. See Figure 9.12 for an image of Humulin R insulin.<sup>[footnote]\"<a href=\"https:\/\/americanhistory.si.edu\/collections\/search\/object\/nmah_1000969\" target=\"_blank\" rel=\"noopener noreferrer\">Humulin R, Insulin, 1987<\/a>\" by National Museum of American History Smithsonian Institution is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/2.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-NC-ND 2.0<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"aligncenter\" width=\"489\"]<img class=\"\" title=\"&quot;Humulin R, Insulin, 1987&quot; by National Museum of American History Smithsonian Institution is licensed under CC BY-NC-ND 2.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image5-8.png\" alt=\"Photo showing package of Humulin R with vial next to it.\" width=\"489\" height=\"322\"> Figure 9.12 Humulin R insulin[\/caption]\n\n<strong>Indications<\/strong>\n\nShort-acting insulins are given with meals to mimic the effects of endogenous insulin release when food is eaten. Dosages of short-acting insulin are individualized based on carbohydrate intake, premeal glucose levels, and anticipated activity levels.\n\n<strong>Mechanism of Action<\/strong>\n\nThe primary activity of insulin is the regulation of glucose metabolism. Insulin lowers blood glucose by stimulating peripheral glucose uptake, especially by skeletal muscle and fat, and by inhibiting hepatic glucose production.\n\n<strong>Specific Administration Considerations<\/strong>\n\nRegular insulin is generally administered subcutaneously.\u00a0 It is the only insulin that can be administered intravenously under close supervision of blood glucose and potassium levels. It is available in vials and insulin pens. Inspect insulin visually before use. It should appear clear and colorless; do not use if particulate matter or coloration is seen. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy. Subcutaneous doses should be administered approximately 30 minutes before meals because this is the typical onset of action. Peak effects occur in 3 hours with a duration of 8 hours. Do not mix with insulin preparations other than NPH.\n\nHumulin R u-500 should only be administered in u-500 insulin syringes to avoid dosage calculation errors.\n\nAdverse effects of insulin include hypoglycemia and hypokalemia.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nSee IMSP guidelines for patient teaching in the previous section entitled \u201cHigh Risk Medications and Prevention of Errors.\u201d\n<h3>Intermediate-Acting Insulin<\/h3>\nNPH insulin, also known as isophane insulin, is an intermediate\u2013acting insulin. Brand names include Humulin-N or Novolin-N. Mixtures of short- and intermediate-acting insulin include Humulin 70\/30 or Novolin 70\/30.\n\n<strong>Indications<\/strong>\n\nIntermediate insulins are administered once or twice daily to mimic endogenous basal insulin levels.\n\n<strong>Mechanism of Action<\/strong>\n\nInsulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat and by inhibiting hepatic glucose production.\n\n<strong>Specific Administration Considerations<\/strong>\n\nNPH insulin is a white and cloudy suspension. Gently roll or invert vial\/pen several times to re-suspend the insulin before administration. It should only be administered subcutaneously. It may be mixed with rapid-acting or short-acting insulins, but those insulins should be drawn into the syringe before the NPH is added. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy. The onset of action and peak are affected by the site of injection, physical activity level, and other variables but the median peak level occurs in 4 hours. See Figure 9.13 for an image of Novolin-N (a cloudy insulin) that can be mixed with Novolin R (a clear insulin).<sup>[footnote]\"<a href=\"https:\/\/www.flickr.com\/photos\/ladytaz\/1836553797\" target=\"_blank\" rel=\"noopener noreferrer\">The Gift of Life<\/a>\" by <a href=\"https:\/\/www.flickr.com\/photos\/ladytaz\/\" target=\"_blank\" rel=\"noopener noreferrer\">Melissa Johnson<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/2.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 2.0<\/a>[\/footnote]<\/sup>\n\n&nbsp;\n\n[caption id=\"\" align=\"aligncenter\" width=\"447\"]<img class=\"\" title=\"&quot;The Gift of Life&quot; by Melissa Johnson is licensed under CC BY 2.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image6-9.png\" alt=\"Photo showing two vials. One is Novolin N and the other is Novolin R.\" width=\"447\" height=\"323\"> Figure 9.13 Comparison of Novolin-N (a cloudy insulin) that can be mixed with Novolin-R (a clear insulin)[\/caption]\n\nMixed medications such as Humulin 70\/30 should be administered subcutaneously approximately 30 minutes before a meal. They are typically dosed twice daily (with each dose intended to cover 2 meals or a meal and a snack).\n\nUnopened vials should be stored in the refrigerator until the expiration date. Opened vials should be labelled with the open date and stored in the refrigerator for up to 28-42 days (depending on the formulation\/insulin type) and then discarded. Unopened pens should be stored in the refrigerator until the expiration date. Used pens should be stored at room temperature, but kept away from heat and light, for up to 10-28 days (depending on the formulation\/insulin type) and then discarded.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nSee IMSP guidelines for patient teaching in the previous section titled \u201cHigh Risk Medications and Prevention of Errors.\u201d\n<h3>Long-Acting Insulin<\/h3>\nInsulin glargine (Lantus) and insulin devemir (Levemir) are long-acting insulins given once or twice daily. See Figure 9.14 for an image of a levemir insulin pen.<sup>[footnote]\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Insulin analog 100 IU-1ml penfill levemir yellow background.jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/wiki\/User:Wesalius\" target=\"_blank\" rel=\"noopener noreferrer\">Wesalius<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0<\/a>[\/footnote]<\/sup>\n\n[caption id=\"attachment_417\" align=\"aligncenter\" width=\"716\"]<img class=\"wp-image-414 \" title=\"&quot;Insulin analog 100 IU-1ml penfill levemir yellow background.jpg&quot; by Wesalius is licensed under CC BY 4.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-1024x330.jpg\" alt=\"Photo showing vial used in Levemir insulin pen.\" width=\"716\" height=\"231\"> Figure 9.14 Vial used for Levemir insulin pen[\/caption]\n\n&nbsp;\n\n<strong>Indications<\/strong>\n\nLong-acting insulins are given once or twice daily. In type 1 diabetics, long-acting insulin should be used concomitantly with rapid- or short-acting insulin at mealtimes.\n\n<strong>Mechanism of Action<\/strong>\n\nInsulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat and by inhibiting hepatic glucose production.\n\n<strong>Specific Administration Considerations<\/strong>\n\nLong-acting insulin has a relatively constant concentration\/time profile over 24 hours with no pronounced peak in comparison to NPH insulin. It should only be administered subcutaneously and is available in vials and insulin pens . Inspect insulin visually before use. It should appear clear and colorless; do not use if particulate matter or coloration is seen. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nSee ISMP guidelines for patient teaching in the previous section titled \u201cHigh Risk Medications and Prevention of Errors.\u201d\n<h3>Glucagon<\/h3>\n<strong>Indications<\/strong>\n\nGlucagon is indicated as a treatment for severe hypoglycemia (low blood sugar), which may occur in patients with diabetes mellitus. Glucagon injection is used for patients who are unable to safely swallow carbohydrates to treat hypoglycemia due to the effects of hypoglycemia or other medical conditions.\n\n<strong>Mechanism of Action<\/strong>\n\nGlucagon increases blood glucose concentration during an episode of hypoglycemia. See Figure 9.15 for an image of an emergency glucagon kit.<sup>[footnote]\"<a href=\"https:\/\/en.wikipedia.org\/wiki\/File:Glucagon_emergency_rescue_kit.JPG\" target=\"_blank\" rel=\"noopener noreferrer\">Glucagon emergency rescue kit.JPG<\/a>\" by <a href=\"https:\/\/en.wikipedia.org\/wiki\/User:Mbbradford\" target=\"_blank\" rel=\"noopener noreferrer\">mbbradford<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/cc0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC0<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"aligncenter\" width=\"662\"]<img class=\"\" title=\"&quot;Glucagon emergency rescue kit.JPG&quot; by mbbradford is licensed under CC0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image8-9.png\" alt=\"Photo showing emergency glucagon kit.\" width=\"662\" height=\"496\"> Figure 9.15 Emergency glucagon kit[\/caption]\n\n<strong>Specific Administration Considerations<\/strong>\n\nGlucagon may be administered subcutaneously, intramuscularly, or intravenously. Peak glucose levels occur within 13-20 minutes of subcutaneous or IM injection.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nPatients with type 1 diabetes may have less of an increase in blood glucose levels compared with a stable type 2 patient, so a supplementary carbohydrate should be given as soon as possible, especially to a pediatric patient. <sup>[footnote]This work is a derivative of <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a> by <a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a> in the <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>. \u00a0[\/footnote]<\/sup>\n\nNow let\u2019s take a closer look at the medication grid comparing insulins in Table 9.4a.<sup>[footnote]This work is a derivative of <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a> by <a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a> in the <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>. \u00a0[\/footnote]<\/sup>\n<h5>Table 9.4a Insulins Medication Grid<\/h5>\n<table class=\"grid\" style=\"border-collapse: collapse;width: 100%;height: 112px\" border=\"0\">\n<tbody>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Class\/Subclass<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Prototypes\/Generics<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Onset\/Peak\/Duration<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Administration Considerations<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Therapeutic Effects<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Adverse\/Side Effects<\/th>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Rapid-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f\" target=\"_blank\" rel=\"noopener noreferrer\">insulin lispro<\/a> (Humalog)\n\n<a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=bee5b358-c863-420b-be73-ced2e920c499\" target=\"_blank\" rel=\"noopener noreferrer\">insulin aspart <\/a>(Novolog)\n\n<a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=29f4637b-e204-425b-b89c-7238008d8c10\">inhaled insulin<\/a> (Afreeza)\n\n&nbsp;<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 15-30 minutes\n\nPeak effect: 1-3 hours\n\nDuration: 3 - 5 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer within 15 minutes before a meal or immediately after a meal\n\nAfrezza is contraindicated in patients with asthma or COPD<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia\n\nHypokalemia\n\nAfrezza can cause acute bronchospasm<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Short-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=b519bd83-038c-4ec5-a231-a51ec5cc291f\" target=\"_blank\" rel=\"noopener noreferrer\">Humulin R<\/a>\n\nNovolin R<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 30 minutes\n\nPeak effect: 3 hours\n\nDuration: 8\u00a0 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer 30 minutes before a meal<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia\n\nHypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Intermediate-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f6edd793-440b-40c2-96b5-c16133b7a921\" target=\"_blank\" rel=\"noopener noreferrer\">Humulin N<\/a>\n\nNovolin N<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 1-2 hours\n\nPeak effect: 6 hours (range 2.8-13 hours)\n\nDuration: up to 24 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer once or twice daily\n\nOnly administer subcutaneously\n\nGently roll or invert vial\/pen several times to re-suspend the insulin before administration\n\nDo not mix with other insulin<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia\n\nHypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Combination: Intermediate-Acting\/Rapid-Acting<\/th>\n<td style=\"width: 16.6667%;height: 14px\">Humalog Mix 50\/50\n\nHumalog Mix 75\/25\n\nNovolog Mix 70\/30\n\n*First number is % intermediate-acting insulin, second number is % rapid-acting<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 15-30 minutes\n\nPeak effect:\n\n50\/50: 1-5 hours\n\nDuration: 11-22 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer twice daily, 15 minutes before a meal or immediately after a meal\n\nOnly administer subcutaneously\n\nGently roll or invert vial\/pen several times to re-suspend the insulin before administration<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia\n\nHypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Combination: Intermediate-Acting\/Short-Acting<\/th>\n<td style=\"width: 16.6667%;height: 14px\">Humulin 70\/30\n\nNovolin 70\/30<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 30-90 minutes\n\nPeak effect: 1.5-6.5 hours\n\nDuration: 18-24 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer twice daily, 30-45 minutes before a meal\n\nOnly administer subcutaneously\n\nGently roll or invert vial\/pen several times to re-suspend the insulin before administration\n\nDo not mix with other insulin\n\n&nbsp;<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia\n\nHypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Long-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=d5e07a0c-7e14-4756-9152-9fea485d654a\" target=\"_blank\" rel=\"noopener noreferrer\">insulin glargine<\/a> (Lantus)\n\ninsulin detemir (Levemir)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 3-4 hours\n\nPeak effect: none\n\nDuration: &gt;24 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer once daily (sometimes dose is split and administered twice daily)\n\nOnly administer subcutaneously\n\nDo not mix with other insulin<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia\n\nHypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Hyperglycemic<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f143db10-e889-41c3-84ed-603a0ab02f61\" target=\"_blank\" rel=\"noopener noreferrer\">glucagon<\/a><\/td>\n<td style=\"width: 16.6667%;height: 14px\"><\/td>\n<td style=\"width: 16.6667%;height: 14px\">May be administered subcutaneously, IM, or IV\n\nSupplementary carbohydrate should be given as soon as possible, especially to a pediatric patient\n\nUsed to reverse hypoglycemic episode if NPO administration is not appropriate<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Used to reverse hypoglycemic episode if NPO administration is not appropriate<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hyperglycemia<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n&nbsp;\n\n<strong>General adminstration considerations<\/strong>:\n<ul>\n \t<li>Review orders closely because they may include a standard meal dose, a \u201csliding scale\u201d dose, and a carb-related dose.<\/li>\n \t<li>Always read drug labelling closely as there are several types of dosages and formulations.<\/li>\n \t<li>See agency policies and ISMP guidelines for safe administration of insulin.<\/li>\n \t<li>When administering with an insulin pen, after inserting the pen count to 5 before removing the needle.<\/li>\n<\/ul>\n<strong>General therapeutic effects:<\/strong>\n<ul>\n \t<li>Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/li>\n<\/ul>\n<strong>General side effects:<\/strong>\n<ul>\n \t<li>Hypoglycemia and hypokalemia<\/li>\n<\/ul>\n<h2>Diabetic Medication: Oral Antihyperglycemics<\/h2>\nThere are several different classes of oral antihyperglycemic drugs used in conjunction with a healthy diet and exercise for the management of type 2 diabetes. According to the American Diabetes Association, metformin is the preferred initial pharmacologic agent for the treatment of type 2 diabetes.<sup>[footnote]American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S009\">https:\/\/doi.org\/10.2337\/dc19-S009<\/a><\/sup><span style=\"text-align: initial;font-size: 1em\"><sup>[\/footnote]<\/sup>Three of the most commonly used antihyperglycemic classes and prototypes are sulfonylureas (glipizide), biguanide (metformin), and DPP-IV (sitagliptin). The mechanism of action and administration considerations for each of these prototypes are described below.<\/span>\n<h3>Glipizide<\/h3>\n<strong>Mechanism of Action<\/strong>\n\nGlipizide is in the sulfonylurea class of antihyperglycemic medication. The mechanism of action is the stimulation of insulin secretion from the beta cells of pancreatic islet tissue and is thus dependent on functioning beta cells in the pancreatic islets. Peak plasma concentrations occur 1 to 3 hours after a single oral dose.\n\n<strong>Specific Administration Considerations<\/strong>\n\nAll sulfonylurea drugs are capable of producing severe hypoglycemia. Hypoglycemia may be difficult to recognize in the elderly and in people who are taking beta-adrenergic blocking drugs. Sulfonylurea medications should be given 30 minutes before a meal due to hypoglycemic effects.\n\nGlipizide is contraindicated in type 1 diabetics or for use of diabetic ketoacidosis; insulin should be used to treat this condition. Treatment of patients with glucose 6-phosphate dehydrogenase (G6PD) deficiency with sulfonylurea agents can lead to hemolytic anemia.\n\nThe hypoglycemic action of sulfonylureas may be potentiated by certain drugs such as nonsteroidal anti-inflammatory agents and other drugs that are highly protein bound.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nPatients should take the medication at the same time each day.\u00a0 It is important that patients understand that the medication helps control episodes of hyperglycemia but does not cure diabetes.\u00a0 Patients should be instructed regarding the signs of hyperglycemia and hypoglycemia.\u00a0 The use of sulfonylureas and alcohol may cause a disulfiram-like reaction.\n<h3>Met\u200bformin<\/h3>\n<strong>Mechanism of Action<\/strong>\n\n<strong>Metformin<\/strong> is in the biguanide class of antihyperglycemics. It decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. Unlike sulfonylureas, metformin does not produce hypoglycemia. See Figure 9.16 for an image of a metformin tablet.<sup>[footnote]\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Metformin_500mg_Tablets.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Metformin 500mg Tablets.jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/w\/index.php?title=User:Ash&amp;action=edit&amp;redlink=1\" target=\"_blank\" rel=\"noopener noreferrer\">User:Ash<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/cc0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC0<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"aligncenter\" width=\"462\"]<img class=\"\" title=\"&quot;Metformin 500mg Tablets.jpg&quot; by User:Ash is licensed under CC0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image9-7.png\" alt=\"Photo showing closeup of Metformin package, blister pack, and pill.\" width=\"462\" height=\"409\"> Figure 9.16 Metformin[\/caption]\n\n<strong>Specific Administration Considerations<\/strong>\n\nMetformin hydrochloride should be given in divided doses with meals. The therapeutic goal should be to decrease both fasting plasma glucose and glycosylated hemoglobin levels to near normal by using the lowest effective dose of metformin, either when used as monotherapy or in combination with sulfonylurea or insulin.\n\nCommon adverse reactions include diarrhea, nausea\/vomiting, weakness, flatulence, indigestion, abdominal discomfort, and headache.\n\nMetformin is contraindicated in patients with kidney disease (e.g., serum creatinine levels \u22651.5 mg\/dL [males] or \u22651.4 mg\/dL [females]) and should be temporarily discontinued in patients undergoing radiologic studies involving intravascular administration of iodinated contrast materials because use of such products may result in acute alteration of renal function. It is also contraindicated in patients with metabolic acidosis.\n\nLactic acidosis is a rare, but serious, metabolic complication that can occur due to metformin accumulation during treatment with metformin; when it occurs, it is fatal in approximately 50% of cases. The risk of lactic acidosis increases with the degree of renal dysfunction and the patient\u2019s age. Metformin should be promptly withheld in the presence of any condition associated with hypoxemia, dehydration, or sepsis. Because impaired hepatic function may significantly limit the ability to clear lactate, metformin should be avoided in patients with hepatic disease. The onset of lactic acidosis often is subtle and accompanied only by nonspecific symptoms such as malaise, myalgias, respiratory distress, increasing somnolence, and nonspecific abdominal distress.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\n\u200b\u200bPatients should take the medication at the same time each day.\u00a0 It is important that patients understand that the medication helps control episodes of hyperglycemia but does not cure diabetes.\u00a0 Patients should be instructed regarding the signs of hyperglycemia and hypoglycemia.\u00a0 The patient may be at risk for lactic acidosis and should report chills, low blood pressure, muscle pain, or dyspnea immediately to the healthcare provider.\u00a0 The use of medications like metformin can cause a metallic taste in the mouth.\n<h3>\u200bSitagliptin<\/h3>\n<strong>Mechanism of Action<\/strong>\n\nSitagliptin is an orally-active inhibitor of dipeptidyl peptidase-4 (DPP-4) enzyme that slows the inactivation of incretin hormones involved in the regulation of glucose homeostasis and thus, increases insulin release and decreases glucagon levels in the circulation. See Figure 9.17 for an image of sitagliptin.<sup>[footnote]\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Januvia_sitagliptin.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Januvia sitagliptin.jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/w\/index.php?title=User:Kimivanil&amp;action=edit&amp;redlink=1\" target=\"_blank\" rel=\"noopener noreferrer\">Kimivanil<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-sa\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-SA 4.0<\/a>[\/footnote]<\/sup>\n\n[caption id=\"\" align=\"aligncenter\" width=\"535\"]<img class=\"\" title=\"&quot;Januvia sitagliptin.jpg&quot; by Kimivanil is licensed under CC BY-SA 4.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image10-6.png\" alt=\"Photo showing closeup of Januvia package.\" width=\"535\" height=\"336\"> Figure 9.17 Sitagliptin[\/caption]\n\n<strong>Specific Administration Considerations<\/strong>\n\nSitagliptin is taken once daily and can be taken with or without food. It can cause hypoglycemia. Dose adjustment should occur for patients with kidney disease depending on their glomerular filtration rate. Report hypersensitivity reactions, blisters\/erosions, headache, or symptoms of pancreatitis, heart failure, severe arthralgia, and upper respiratory infection.\n\n<strong>Patient Teaching &amp; Education<\/strong>\n\nPatients should take the medication at the same time each day.\u00a0 It is important that patients understand that the medication helps control episodes of hyperglycemia but does not cure diabetes.\u00a0 Patients should be instructed regarding the signs of hyperglycemia and hypoglycemia.\u00a0 Patients should stop taking the medication if symptoms of hypersensitivity occur and follow up immediately with their provider to determine the next course of treatment.\n\nNow let\u2019s take a closer look at the medication grid comparing oral antihyperglycemics in Table 9.4b. <sup>[footnote]This work is a derivative of <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a> by <a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a> in the <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>. \u00a0[\/footnote]<\/sup>\n\nTable 9.4b Medication Grid Comparing Oral Antihyperglycemics\n<table class=\"grid\">\n<tbody>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\"><strong>Class<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\" scope=\"col\"><strong>Prototype<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\" scope=\"col\"><strong>Administration <\/strong><strong>Considerations<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\" scope=\"col\"><strong>Therapeutic Effects<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\" scope=\"col\"><strong>Adverse\/Side Effects<\/strong><\/th>\n<\/tr>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\">Sulfonylureas<\/th>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\"><a class=\"rId40\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=5565ccec-8000-48ab-a6af-37eca2d8c993\" target=\"_blank\" rel=\"noopener noreferrer\">glipizide<\/a><\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\">Time with meals; peak plasma concentrations occur 1 to 3 hours after administration<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\">Reduce fasting blood sugar and glycosylated hemoglobin to near normal<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\">Hypoglycemia; may be potentiated by nonsteroidal anti-inflammatory agents and other drugs that are highly protein bound<\/td>\n<\/tr>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\">Biguanide<\/th>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\"><a class=\"rId41\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=2d98aea3-35ba-447a-b88f-a5a20b612b2f\" target=\"_blank\" rel=\"noopener noreferrer\">metformin<\/a><\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\">Contraindicated in renal and hepatic disease\n\nShould be temporarily discontinued in patients undergoing radiologic studies involving intravascular administration of iodinated contrast materials<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\">Reduce fasting blood sugar and glycosylated hemoglobin to near normal<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\">Stop immediately if signs of lactic acidosis or any condition associated with hypoxemia, dehydration, or sepsis occurs\n\nCommon adverse effects: diarrhea, nausea\/vomiting, weakness, flatulence, indigestion, abdominal discomfort, and headache<\/td>\n<\/tr>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\">DPP-IV inhibitor<\/th>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\"><a class=\"rId42\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f85a48d0-0407-4c50-b0fa-7673a160bf01\" target=\"_blank\" rel=\"noopener noreferrer\">sitagliptin<\/a><\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\">Can be given with or without food<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\">Reduce fasting blood sugar and glycosylated hemoglobin to near norm<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\">Hypoglycemia\n\nReport hypersensitivity reactions, blisters\/erosions, headache, or symptoms of pancreatitis, heart failure, severe arthralgia, or upper respiratory infection<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n&nbsp;\n\n<\/div>\n<div class=\"__UNKNOWN__\">\n<div class=\"textbox textbox--examples\"><header class=\"textbox__header\">\n<h2>Critical Thinking Activity 9.4\n<img class=\"alignright wp-image-197\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2019\/11\/ORN-Icons_lightbulb-300x300-1.png\" alt=\"Image of lightbulb in a circle\" width=\"200\" height=\"200\"><\/h2>\n<\/header>\n<div class=\"textbox__content\" style=\"text-align: left\">\n\nA patient with diabetes mellitus type 2 is admitted to the hospital for hip replacement surgery. The nurse reviews the following orders:\n\nDiabetic diet with carb counting\n\nBedside blood glucose testing before meals and at bedtime with sliding scale Humalog insulin\n\nSliding scale Humalog insulin based on preprandial glucose level:\n<ul>\n \t<li>0-150: No coverage<\/li>\n \t<li>151-175: 2 units<\/li>\n \t<li>176-200: 4 units<\/li>\n \t<li>201-225: 6 units<\/li>\n \t<li>226-250: 8 units<\/li>\n \t<li>Over 250: call the provider<\/li>\n<\/ul>\nInsulin coverage per carbohydrate intake at meals: Humalog 2 units\/carb\n\nMetformin 1000 mg twice daily\n\nHumulin-N 20 units at breakfast and at bedtime\n\nHypoglycemia protocol\n<ol>\n \t<li>Explain the difference between type 1 and type 2 diabetes.<\/li>\n \t<li>The patient states that he usually does not take insulin at home. What is the likely rationale for insulin therapy while hospitalized?<\/li>\n \t<li>The patient\u2019s blood sugar before breakfast is 223 and he eats 3 carbs at breakfast. What types and amounts of insulin will the nurse administer?<\/li>\n \t<li>The nurse reviews the patient's morning lab results and finds a creatinine of 1.8. She plans to call the provider to discuss the impact of the results on the medications ordered. Which medication may require a dosage adjustment based on these results?<\/li>\n \t<li>When the nurse enters the room around 4 p.m., she discovers that the patient has become irritable and is shaky. The nurse performs a bedside blood glucose and obtains a value of 60. What is the nurse\u2019s best response?<\/li>\n \t<li>What is the likely cause of the patient\u2019s condition? Explain using the onset and peak actions of the insulin orders.<\/li>\n \t<li>On admission, the patient\u2019s A1C level was 10%. What does this lab value indicate?<\/li>\n \t<li>The provider states the discharge plan is to initiate Lantus insulin therapy at home, based on the admitting A1C level. What patient teaching should the nurse plan to provide before discharge?<\/li>\n<\/ol>\nNote: Answers to the Critical Thinking activities can be found in the \"Answer Key\" sections at the end of the book.\n\n<\/div>\n<\/div>\n<\/div>","rendered":"<div class=\"pancreas-\">\n<h2>Pancreatic Basics: A&amp;P Review<\/h2>\n<p><strong>Pancreas<\/strong><\/p>\n<p>The pancreas is a long, slender organ located near the stomach (see Figure 9.7).<sup><a class=\"footnote\" title=\"&quot;1820 The Pancreas.jpg&quot;&quot; by OpenStax is licensed under CC BY 4.0. Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" id=\"return-footnote-418-1\" href=\"#footnote-418-1\" aria-label=\"Footnote 1\"><sup class=\"footnote\">[1]<\/sup><\/a><\/sup>\u00a0Although it is primarily an <strong>exocrine gland<\/strong>, secreting a variety of digestive enzymes, the pancreas also has an endocrine function. Pancreatic islets, clusters of cells formerly known as the islets of Langerhans, secrete glucagon and insulin. Glucagon plays an important role in blood glucose regulation because low blood glucose levels stimulate its release. On the other hand, elevated blood glucose levels stimulate the release of insulin.<\/p>\n<figure style=\"width: 1092px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" title=\"&quot;1820 The Pancreas.jpg&quot; by OpenStax is licensed under CC BY 4.0 Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2019\/11\/image1-9.png\" alt=\"Illustration and micrograph showing pancreas and surrounding structures, with labels.\" width=\"1092\" height=\"551\" \/><figcaption class=\"wp-caption-text\">Figure 9.7 Pancreas<\/figcaption><\/figure>\n<h3>Regulation of Blood Glucose Levels by Insulin and Glucagon<\/h3>\n<p>Glucose is the preferred fuel for all body cells. The body derives glucose from the breakdown of the carbohydrate-containing foods and drinks we consume. Glucose not immediately taken up by cells for fuel can be stored by the liver and muscles as glycogen or converted to triglycerides and stored in the adipose tissue. Hormones regulate both the storage and the utilization of glucose as required. Receptors located in the pancreas sense blood glucose levels, and subsequently, the pancreatic cells secrete glucagon or insulin to maintain normal levels.<\/p>\n<h4>Glucagon<\/h4>\n<p>Receptors in the pancreas can sense the decline in blood glucose levels, such as during periods of fasting or during prolonged labor or exercise. In response, the alpha cells of the pancreas secrete the hormone glucagon, which has several effects:<\/p>\n<ul>\n<li>It stimulates the liver to convert stores of glycogen back into glucose. This response is known as glycogenolysis. The glucose is then released into the circulation for use by body cells.<\/li>\n<li>It stimulates the liver to take up amino acids from the blood and convert them into glucose. This response is known as gluconeogenesis.<\/li>\n<li>It stimulates lipolysis, the breakdown of stored triglycerides into free fatty acids and glycerol. Some of the free glycerol released into the bloodstream travels to the liver, which converts it into glucose. This is also a form of gluconeogenesis.<\/li>\n<\/ul>\n<p>Taken together, these actions increase blood glucose levels. The activity of glucagon is regulated through a negative feedback mechanism; rising blood glucose levels inhibit further glucagon production and secretion. (See Figure 9.8 for an illustration of homeostatic regulation of blood glucose levels.)<sup><a class=\"footnote\" title=\"&quot;1822 The Homostatic Regulation of Blood Glucose Levels.jpg&quot; by OpenStax is licensed under CC BY 4.0. Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" id=\"return-footnote-418-2\" href=\"#footnote-418-2\" aria-label=\"Footnote 2\"><sup class=\"footnote\">[2]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 1054px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" decoding=\"async\" title=\"&quot;1822 The Homostatic Regulation of Blood Glucose Levels.jpg&quot; by OpenStax is licensed under CC BY 4.0 Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image2-9.png\" alt=\"Illustration showing homeostatic regulation of blook glucose levels, with labels.\" width=\"1054\" height=\"1478\" \/><figcaption class=\"wp-caption-text\">Figure 9.8 Homeostatic Regulation of Blood Glucose Levels. Blood glucose concentration is tightly maintained between 70 mg\/dL and 110 mg\/dL. If blood glucose concentration rises above this range, insulin is released, which stimulates body cells to remove glucose from the blood. If blood glucose concentration drops below this range, glucagon is released, which stimulates body cells to release glucose into the blood.<\/figcaption><\/figure>\n<h4>Insulin<\/h4>\n<p><strong>Insulin<\/strong> facilitates the uptake of glucose into skeletal and adipose body cells. The presence of food in the intestine triggers the release of gastrointestinal tract hormones. This, in turn, triggers insulin production and secretion by the beta cells of the pancreas. Once nutrient absorption occurs, the resulting surge in blood glucose levels further stimulates insulin secretion.<\/p>\n<p>Insulin triggers the rapid movement of glucose transporter vesicles to the cell membrane, where they are exposed to the extracellular fluid. The transporters then move glucose by facilitated diffusion into the cell interior.<\/p>\n<p>Insulin also reduces blood glucose levels by stimulating <strong>glycolysis<\/strong>, the metabolism of glucose for generation of ATP. It further stimulates the liver to convert excess glucose into glycogen for storage, and it inhibits enzymes involved in glycogenolysis and gluconeogenesis. Finally, insulin promotes triglyceride and protein synthesis. The secretion of insulin is regulated through a negative feedback mechanism. As blood glucose levels decrease, further insulin release is inhibited.<\/p>\n<h3>Disorders of the Endocrine System: Diabetes Mellitus<\/h3>\n<p>Dysfunction of insulin production and secretion, as well as the target cells\u2019 responsiveness to insulin, can lead to a condition called diabetes mellitus, a common disease that affects the ability of the body to produce and\/or utilize insulin. There are two main forms of diabetes mellitus. <strong>Type 1 diabetes <\/strong> is an autoimmune disease affecting the beta cells of the pancreas. The beta cells of people with type 1 diabetes do not produce insulin; thus, synthetic insulin must be administered by injection or infusion. <strong>Type 2 diabetes<\/strong> accounts for approximately 95 percent of all cases. It is acquired, and lifestyle factors such as poor diet and inactivity greatly increase a person\u2019s risk. In type 2 diabetes, the body\u2019s cells become resistant to the effects of insulin. In response, the pancreas increases its insulin secretion, but over time, the beta cells become exhausted. In many cases, type 2 diabetes can be reversed by moderate weight loss, regular physical activity, and consumption of a healthy diet. However, if blood glucose levels cannot be controlled, oral diabetic medication is implemented and eventually the type 2 diabetic may require insulin.<\/p>\n<p>Diabetes is diagnosed when lab tests reveal that blood glucose levels are higher than normal, a condition called <strong>hyperglycemia<\/strong>.<sup><a class=\"footnote\" title=\"This work is a derivative of Anatomy and Physiology by OpenStax licensed under CC BY 4.0. Access for free at https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/1-introduction\" id=\"return-footnote-418-3\" href=\"#footnote-418-3\" aria-label=\"Footnote 3\"><sup class=\"footnote\">[3]<\/sup><\/a><\/sup> According to the American Diabetes Association (ADA), normal fasting blood glucose levels are 80-130 mg\/dL. Glycosylated hemoglobin, also called A1C, is used to assess long-term blood glucose levels over 3 months. The ADA states that A1C target levels vary according to age and health, but the generalized A1C target is less than 7%.<sup><a class=\"footnote\" title=\"American Diabetes Association. (2019). The Big Picture: Checking your Blood Glucose. https:\/\/www.diabetes.org\/diabetes\/medication-management\/blood-glucose-testing-and-control\/checking-your-blood-glucose\" id=\"return-footnote-418-4\" href=\"#footnote-418-4\" aria-label=\"Footnote 4\"><sup class=\"footnote\">[4]<\/sup><\/a><\/sup><\/p>\n<h2>Nursing Considerations<\/h2>\n<h3><strong>Assessment<\/strong><\/h3>\n<p>Diabetic patients should be continuously monitored for signs of hypoglycemia and hyperglycemia. When a diabetic patient is experiencing stress or an infection, the nurse should plan to assess the blood glucose levels more frequently.<\/p>\n<h3><strong>Implementation <\/strong><\/h3>\n<p>The nurse should follow agency policy and ISMP guidelines for safe insulin administration. See the &#8220;Legal Ethical&#8221; chapter for more information about ISMP guidelines. Onset and peak times of insulin and sulfonylureas, in association with anticipated meal times, should always be considered to avoid hypoglycemia episodes. If a hypoglycemia episode occurs, the nurse should intervene quickly using the agency\u2019s established hypoglycemia protocol, and the event should be reported to the provider and in the shift-to-shift report. Symptomatic hyperglycemia should be immediately reported to the provider. Patient education should be provided to patients, family members, and\/or caregivers according to ADA and ISMP guidelines.<\/p>\n<h3><strong>Evaluation<\/strong><\/h3>\n<p>The nurse should evaluate A1C levels to determine effectiveness (and compliance with) the treatment regimen.<\/p>\n<h2>Diabetic Medication Classes: Insulins<\/h2>\n<p>Because the hallmark of type 1 diabetes is absent or near-absent \u03b2-cell function, insulin treatment is essential for individuals with type 1 diabetes. Current evidence-based recommendations regarding pharmacological treatment of type 1 diabetes from the American Diabetes Association (ADA) include:<\/p>\n<ul>\n<li>Most people with type 1 diabetes should be treated with multiple daily injections of prandial and basal insulin or continuous subcutaneous insulin infusion.<\/li>\n<li>Most individuals with type 1 diabetes should use rapid-acting insulin analogs to reduce hypoglycemia risk.<\/li>\n<li>Individuals with type 1 diabetes on prandial insulin doses should be educated on carbohydrate intake, premeal blood glucose levels, and anticipated physical activity.<\/li>\n<li>Individuals with type 1 diabetes who have been successfully using continuous subcutaneous insulin infusion should have continued access to this therapy after they turn 65 years of age.<\/li>\n<\/ul>\n<p><strong>Basal insulin<\/strong> can be long-acting (insulin glargine or insulin detemir) or intermediate-acting (insulin isophane suspension [NPH]). <strong>Prandial insulins  <\/strong>are used with meals and may be rapid acting (insulin lispro, insulin aspart, or insulin glulisine) or short acting (regular insulin).<\/p>\n<p>According to the ADA, insulin requirements can be estimated based on weight, with typical doses ranging from 0.4 to 1.0 units\/kg\/day. Higher amounts are required during puberty, pregnancy, and medical illness. Physiologic insulin secretion varies with glycemia, meal size, and tissue demands for glucose. To approach this variability in people using insulin treatment, strategies have evolved to adjust meal-time doses based on predicted needs. Thus, education of patients on how to adjust insulin to account for carbohydrate intake, premeal glucose levels, and anticipated activity is important. Ensuring that patients and\/or caregivers understand correct insulin injection technique is also important to optimize glucose control and insulin use safety.<sup><a class=\"footnote\" title=\"American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). https:\/\/doi.org\/10.2337\/dc19-S009\" id=\"return-footnote-418-5\" href=\"#footnote-418-5\" aria-label=\"Footnote 5\"><sup class=\"footnote\">[5]<\/sup><\/a><\/sup><\/p>\n<p>Patients on insulin therapy are at risk for <strong>hypoglycemia<\/strong>. It is essential for the nurse to monitor for signs of hypoglycemia and to intervene appropriately. See Figure 9.9 for symptoms of hypoglycemia. Hypoglycemia is defined as a blood glucose level below 70 mg\/dL; severe hypoglycemia refers to a blood glucose level below 40 mg\/dL.<\/p>\n<h3 style=\"text-align: left\">Hypoglycemia Symptoms<\/h3>\n<table class=\"grid\" style=\"width: 691px;height: 249px\">\n<tbody>\n<tr style=\"height: 14px\">\n<th style=\"width: 326.063px;height: 14px;text-align: left\" scope=\"col\"><strong>Mild-to-Moderate<\/strong><\/th>\n<th style=\"width: 336.063px;height: 14px\" scope=\"col\"><strong>Severe<\/strong><\/th>\n<\/tr>\n<tr style=\"height: 235px\">\n<td style=\"width: 326.063px;height: 235px\">\n<ul>\n<li>Shaky or jittery<\/li>\n<li>Sweaty<\/li>\n<li>Hungry<\/li>\n<li>Headache<\/li>\n<li>Blurred vision<\/li>\n<li>Sleepy or tired<\/li>\n<li>Dizzy or lightheaded<\/li>\n<li>Confused or disoriented<\/li>\n<li>Pale<\/li>\n<li>Uncoordinated<\/li>\n<li>Irritable or nervous<\/li>\n<li>Argumentative or combative<\/li>\n<li>Changed behavior or personality<\/li>\n<li>Trouble concentrating<\/li>\n<li>Weak<\/li>\n<li>Fast or irregular heart beat<\/li>\n<\/ul>\n<\/td>\n<td style=\"width: 336.063px;height: 235px\">\n<ul>\n<li>Unable to eat or drink<\/li>\n<li>Seizures or convulsions (jerky movements)<\/li>\n<li>Unconsciousness<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><em>Figure 9.9 Hypoglycemia Symptoms<\/em><\/p>\n<p>If a patient with diabetes shows a sudden change in mood or mental status or other symptoms of hypoglycemia, the nurse should immediately check the blood glucose level. Healthcare agencies use hypoglycemia protocols so that the nurse can react quickly to episodes of hypoglycemia before they become severe. Hypoglycemia protocols contain orders for immediate treatment by the nurse. For instance, in patients who can tolerate oral intake, 15 grams of rapidly digested carbohydrates (such as 4 ounces of fruit juice) are recommended. In patients who are NPO or can\u2019t take oral treatment, dextrose 50% IV or glucagon IM or subcutaneously are administered. Patients who have had a hypoglycemic episode should be monitored closely for the following 24 hours because they are at increased risk for another episode. The provider and the oncoming nurse should be notified of hypoglycemia episodes to discuss the possible cause of the hypoglycemic event and make insulin adjustments, if needed, to avoid additional hypoglycemia. Tracking hypoglycemia episodes and analyzing causes are important performance improvement activities.<sup><a class=\"footnote\" title=\"Seggelke, S., Everhart, B. (2012, September 11) Managing glucose levels in hospital patients. American Nurse Today. https:\/\/www.americannursetoday.com\/managing-glucose-levels-in-hospital-patients\/.\" id=\"return-footnote-418-6\" href=\"#footnote-418-6\" aria-label=\"Footnote 6\"><sup class=\"footnote\">[6]<\/sup><\/a><\/sup><\/p>\n<\/div>\n<div class=\"pancreas-\">\n<p>&nbsp;<\/p>\n<p>The arrival of continuous glucose monitors to clinical practice has been proven to reduce nocturnal hypoglycemia in people using insulin pumps with glucose sensors due to automatic suspension of insulin delivery at a preset glucose level. The U.S. Food and Drug Administration has also approved the first hybrid closed-loop pump system.<sup><a class=\"footnote\" title=\"American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). https:\/\/doi.org\/10.2337\/dc19-S009\" id=\"return-footnote-418-7\" href=\"#footnote-418-7\" aria-label=\"Footnote 7\"><sup class=\"footnote\">[7]<\/sup><\/a><\/sup> A hybrid closed-loop pump system automatically adjusts basal insulin delivery every 5 minutes based on sensor glucose to maintain blood glucose levels as close to a specific target as possible.<sup><a class=\"footnote\" title=\"Weaver, H., Hirsch, I (2018, June 6). The Hybrid Closed Loop System: Evolution and Practical Applications. Diabetes Technology &amp; Therapeutics 20(S2). https:\/\/www.liebertpub.com\/doi\/10.1089\/dia.2018.0091.\" id=\"return-footnote-418-8\" href=\"#footnote-418-8\" aria-label=\"Footnote 8\"><sup class=\"footnote\">[8]<\/sup><\/a><\/sup><\/p>\n<p>According to the ADA, lifestyle modifications that improve health should be emphasized, along with any pharmacologic therapy. Lifestyle modifications include healthy food choices to stabilize blood glucose levels, as well as daily exercise.<\/p>\n<h3><strong>Hypokalemia<\/strong><\/h3>\n<p>All insulin products cause a shift in potassium from the extracellular to intracellular space, which can possibly lead to hypokalemia. Untreated hypokalemia may cause respiratory paralysis, ventricular arrhythmia, and death. Monitor potassium levels in patients at risk for hypokalemia due to other medications such as diuretics.<\/p>\n<h3><strong>Insulin Pens<\/strong><\/h3>\n<p>Insulin pens are often used in inpatient settings, as well as for self-administration, to facilitate safe and accurate self-administration of insulin. See Figure 9.10 for an image of an insulin pen.<sup><a class=\"footnote\" title=\"&quot;Human insulin 100 IU-1ml pen yellow background (02).jpg&quot; by Wesalius is licensed under CC BY 4.0\" id=\"return-footnote-418-9\" href=\"#footnote-418-9\" aria-label=\"Footnote 9\"><sup class=\"footnote\">[9]<\/sup><\/a><\/sup> According to the ISMP, insulin pens offer several advantages over vials beyond dosing accuracy, convenience, and ease of use:<\/p>\n<ul>\n<li>Each pen is already labeled by the manufacturer with the product name and product barcode (whereas syringes of insulin prepared on the patient care unit from vials run the risk of being unlabeled).<\/li>\n<li>Each pen can be individually labeled with the patient\u2019s name (and ideally with a patient-specific barcode).<\/li>\n<li>The pen provides the patient\u2019s insulin in a form ready for administration.<\/li>\n<li>The pen lessens nursing time needed to prepare and administer insulin.<\/li>\n<li>Insulin pens reduce medication waste that can occur when dispensing 10 mL-sized insulin vials for each patient.<\/li>\n<\/ul>\n<p>However, improper sharing of insulin pens among multiple patients has exposed patients to bloodborne pathogens. Insulin pens should never be reused for multiple patients; even if the needle is changed between patients, there can still be body fluid exposure.<sup><a class=\"footnote\" title=\"Institute for Safe Medication Practices. (2017). ISMP Guidelines for Optimizing Safe Subcutaneous Insulin Use in Adults.\u00a0 https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf\" id=\"return-footnote-418-10\" href=\"#footnote-418-10\" aria-label=\"Footnote 10\"><sup class=\"footnote\">[10]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 682px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" title=\"&quot;Human insulin 100 IU-1ml pen yellow background (02).jpg&quot; by Wesalius is licensed under CC BY 4.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image3-10.png\" alt=\"Photo showing Humulin KwikPen\" width=\"682\" height=\"196\" \/><figcaption class=\"wp-caption-text\">Figure 9.10 Insulin Pens<\/figcaption><\/figure>\n<h3><strong>High-Alert Medication and Prevention of Errors<\/strong><\/h3>\n<p>Insulin is a high-alert medication that can be associated with significant patient harm when used in error. A variety of error types have been associated with insulin therapy, including administration of the wrong insulin product, improper dosing (underdosing and overdosing), dose omissions, incorrect use of insulin delivery devices, wrong route (intramuscular versus subcutaneous), and improper patient monitoring. Many errors result in serious hypoglycemia or hyperglycemia. Hypoglycemia is often caused by a failure to adjust insulin therapy in response to a reduction in nutritional intake or an excessive insulin dose stemming from a prescribing or dose measurement error. Other factors that contribute to serious hypoglycemia include inappropriate timing of insulin doses with food intake, creatinine clearance, body weight, changes in medications that affect blood glucose levels, poor communication during patient transfer to different care teams, and poor coordination of blood glucose testing with insulin administration at meal time.<\/p>\n<p>In an inpatient setting, manifestations of poor glycemic control, including severe hypoglycemia and hyperglycemia, are deemed hospital-acquired conditions by the Centers for Medicare and Medicaid Services (CMS). CMS notes that poor glycemic control can be reasonably prevented with implementation of evidence-based guidelines; thus, the CMS denies payment for diabetic ketoacidosis, hypoglycemic coma, and other serious conditions related to poor glycemic control. Agency policies and procedures should be closely followed to avoid these errors and manifestations of poor glycemic control.<\/p>\n<p>One strategy for look-alike medications such as Humalog and Humalin is tall man lettering on the label. Tall man lettering describes a method for differentiating the unique letter characters of similar drug names known to be confused with one another, such as HumaLOG and HumaLIN.<\/p>\n<p>ISMP recommends the following safe practice guidelines for the administration of insulin by the nurse:<\/p>\n<ul>\n<li>Patient-specific insulin pens are stored on clinical units in a manner that prevents their inadvertent use on more than one patient.<\/li>\n<li>A coordinated process is developed to ensure timely blood glucose checks and administration of prandial insulin in conjunction with meal delivery.<\/li>\n<li>Verbal communication of point-of-care blood glucose value results are avoided as much as possible and are NEVER routinely used as the only source of information when determining insulin doses.<\/li>\n<li>Appropriately label all clinician-prepared syringes of subcutaneous insulin, unless the medication is prepared at the patient\u2019s bedside and is immediately administered to the patient without any break in the process.<\/li>\n<li>Prior to subcutaneous insulin administration, the practitioner:\n<ul>\n<li>Confirms that there is an appropriate indication<\/li>\n<li>Assesses the patient\u2019s most current blood glucose value<\/li>\n<li>Assesses the patient for symptoms of hypoglycemia<\/li>\n<li>Informs the patient of their most current blood glucose level<\/li>\n<li>Informs the patient of their dose, the full name of the product, and the insulin\u2019s intended action<\/li>\n<\/ul>\n<\/li>\n<li>An individual insulin pen is never used for more than one patient.<\/li>\n<li>Barcode scanning is used to verify that a patient-specific pen is used to administer the correct insulin to the correct patient.<\/li>\n<li>Prior to transitions of care, a process is in place to ensure that patients will have the necessary prescriptions, supplies, a follow-up care plan, and printed instructions for all prescribed insulin and blood glucose monitoring.<\/li>\n<li>Patients discharged on insulin are assessed for understanding of their self-management, including:\n<ul>\n<li>Demonstration of proper dose measurement and self-administration using the same administration device that will be used at home (e.g., vial and syringe, pen, pump)<\/li>\n<li>Correct monitoring of blood glucose values<\/li>\n<li>The signs and symptoms of hyper- and hypoglycemia and how to respond if these symptoms occur<\/li>\n<li>Common types of errors possible with their insulin therapy and how to prevent or detect these errors<\/li>\n<li>The importance of regular follow-up with their primary care provider\/specialist, including the date of their next appointment<\/li>\n<li>Patients who self-administer concentrated U-500 insulin using a vial and syringe are taught to use only a U-500 syringe and communicate their doses in terms of the name and concentration of the insulin and the actual dose in units using only the U-500 syringe<sup><a class=\"footnote\" title=\"Institute for Safe Medication Practices. (2017). ISMP Guidelines for Optimizing Safe Subcutaneous Insulin Use in Adults.\u00a0 https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf\" id=\"return-footnote-418-11\" href=\"#footnote-418-11\" aria-label=\"Footnote 11\"><sup class=\"footnote\">[11]<\/sup><\/a><\/sup><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3>Lifespan Considerations<\/h3>\n<h4><strong>Elderly<\/strong><\/h4>\n<p>The elderly are at higher risk for hypoglycemia episodes. The ADA has the following recommendations for elderly patients with diabetes:<\/p>\n<ul>\n<li>In older adults at increased risk of hypoglycemia, medication classes with low risk of hypoglycemia are preferred.<\/li>\n<li>Overtreatment of diabetes is common in older adults and should be avoided.<\/li>\n<li>Deintensification (or simplification) of complex regimens is recommended to reduce the risk of hypoglycemia, if it can be achieved within the individualized A1C target.<sup><a class=\"footnote\" title=\"American Diabetes Association (2019) 12. Older adults: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). https:\/\/doi.org\/10.2337\/dc19-S012\" id=\"return-footnote-418-12\" href=\"#footnote-418-12\" aria-label=\"Footnote 12\"><sup class=\"footnote\">[12]<\/sup><\/a><\/sup><\/li>\n<\/ul>\n<h4><strong>Children and Adolescents<\/strong><\/h4>\n<p>Type 1 diabetes is the most common form of diabetes in youth. Unique aspects of care and management of children and adolescents with type 1 diabetes must be considered, such as changes in insulin sensitivity related to physical growth and sexual maturation, ability to provide self-care, supervision in the child care and school environment, neurological vulnerability to hypoglycemia and hyperglycemia in young children, as well as possible adverse neurocognitive effects of diabetic ketoacidosis (DKA). Evidence-based ADA recommendations for glycemic control for children and adolescents include:<\/p>\n<ul>\n<li>The majority of children and adolescents with type 1 diabetes should be treated with intensive insulin regimens, either via multiple daily injections or continuous subcutaneous insulin infusion.<\/li>\n<li>All children and adolescents with type 1 diabetes should self-monitor glucose levels multiple times daily (up to 6\u201310 times\/day), including pre-meal, pre-bedtime, and as needed for safety in specific situations such as exercise, driving, or the presence of symptoms of hypoglycemia.<\/li>\n<li>Continuous glucose monitoring should be considered in all children and adolescents with type 1 diabetes, whether using injections or continuous subcutaneous insulin infusion, as an additional tool to help improve glucose control. Benefits of continuous glucose monitoring correlate with adherence to ongoing use of the device.<\/li>\n<li>Automated insulin delivery systems appear to improve glycemic control and reduce hypoglycemia in children and should be considered in children with type 1 diabetes.<\/li>\n<li>An A1C target of &lt;7.5% should be considered in children and adolescents with type 1 diabetes but should be individualized based on the needs and situation of the patient and family. <sup><a class=\"footnote\" title=\"American Diabetes Association. (2019). 13. Children and adolescents: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). https:\/\/doi.org\/10.2337\/dc19-S013\" id=\"return-footnote-418-13\" href=\"#footnote-418-13\" aria-label=\"Footnote 13\"><sup class=\"footnote\">[13]<\/sup><\/a><\/sup><\/li>\n<\/ul>\n<p>There are several different types of insulins that vary in terms of onset, peak, and duration. It is critical for the nurse to be knowledgeable of these differences to help prevent episodes of hypoglycemia due to mismatched administration of insulin with food intake.<\/p>\n<h3>Rapid-Acting Insulin<\/h3>\n<p>Rapid-acting insulins include insulin lispro (Humalog) and insulin aspart (Novolog) and are also available via inhalation (Afrezza). See Figure 9.11 for an image of Novolog insulin.<sup><a class=\"footnote\" title=\"&quot;Untitled&quot; from Pxhere website is licensed under CC0\" id=\"return-footnote-418-14\" href=\"#footnote-418-14\" aria-label=\"Footnote 14\"><sup class=\"footnote\">[14]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 411px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" title=\"&quot;Untitled&quot; by Pxhere is licensed under CC0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image4-9.png\" alt=\"Photo showing package of Novalog with vial next to it.\" width=\"411\" height=\"368\" \/><figcaption class=\"wp-caption-text\">Figure 9.11 Novolog insulin<\/figcaption><\/figure>\n<p><strong>Indications<\/strong><\/p>\n<p>Rapid-acting insulins are also called prandial insulins because they are administered with meals to mimic the effects of endogenous insulin release when food is eaten. Dosages of rapid-acting insulin are individualized based on carbohydrate intake, premeal glucose levels, and anticipated activity.<\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Insulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat and by inhibiting hepatic glucose production.<\/p>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>Humalog-100 (100 units per ml) and Humalog-200 (200 units per ml) are administered subcutaneously; however, only Humalog-100 is administered via continuous subcutaneous injection or intravenously. Humalog-100 can only be mixed with NPH insulin, but Humalog-200 should not be mixed with other insulin. Inspect insulin visually before use. It should appear clear and colorless; do not use if particulate matter or coloration is seen. Humalog-100 is available in vials, KwikPens, and cartridges; Humalog-200 is only available in KwikPens. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy. Lipodystrophy can be a lump or small dent in the skin that forms when a person performs injections repeatedly in the same spot.<\/p>\n<p>Because of the rapid onset of insulin lispro and insulin aspart and the potential for hypoglycemia, these insulins should be administered within 15 minutes before or right after eating a meal. Peak serum levels are seen 30 to 90 minutes after dosing. Inhaled insulin enters the bloodstream within 1 minute and peaks in 30-60 minutes. Inhaled insulin is contraindicated in patients with chronic lung disease such as asthma or COPD.<\/p>\n<p>Adverse effects of all insulins include hypoglycemia and hypokalemia. Inhaled insulin has a Black Box Warning for potentially causing acute bronchoconstriction.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>See ISMP guidelines for patient teaching in the previous section titled \u201cHigh Risk Medications and Prevention of Errors.\u201d<\/p>\n<h3>Short-Acting Insulin<\/h3>\n<p>Short-acting insulins include regular insulin with a brand name of Humulin R or Novolin R. A concentrated formulation of Humulin R u-500 is also available. See Figure 9.12 for an image of Humulin R insulin.<sup><a class=\"footnote\" title=\"&quot;Humulin R, Insulin, 1987&quot; by National Museum of American History Smithsonian Institution is licensed under CC BY-NC-ND 2.0\" id=\"return-footnote-418-15\" href=\"#footnote-418-15\" aria-label=\"Footnote 15\"><sup class=\"footnote\">[15]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 489px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"\" title=\"&quot;Humulin R, Insulin, 1987&quot; by National Museum of American History Smithsonian Institution is licensed under CC BY-NC-ND 2.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image5-8.png\" alt=\"Photo showing package of Humulin R with vial next to it.\" width=\"489\" height=\"322\" \/><figcaption class=\"wp-caption-text\">Figure 9.12 Humulin R insulin<\/figcaption><\/figure>\n<p><strong>Indications<\/strong><\/p>\n<p>Short-acting insulins are given with meals to mimic the effects of endogenous insulin release when food is eaten. Dosages of short-acting insulin are individualized based on carbohydrate intake, premeal glucose levels, and anticipated activity levels.<\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>The primary activity of insulin is the regulation of glucose metabolism. Insulin lowers blood glucose by stimulating peripheral glucose uptake, especially by skeletal muscle and fat, and by inhibiting hepatic glucose production.<\/p>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>Regular insulin is generally administered subcutaneously.\u00a0 It is the only insulin that can be administered intravenously under close supervision of blood glucose and potassium levels. It is available in vials and insulin pens. Inspect insulin visually before use. It should appear clear and colorless; do not use if particulate matter or coloration is seen. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy. Subcutaneous doses should be administered approximately 30 minutes before meals because this is the typical onset of action. Peak effects occur in 3 hours with a duration of 8 hours. Do not mix with insulin preparations other than NPH.<\/p>\n<p>Humulin R u-500 should only be administered in u-500 insulin syringes to avoid dosage calculation errors.<\/p>\n<p>Adverse effects of insulin include hypoglycemia and hypokalemia.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>See IMSP guidelines for patient teaching in the previous section entitled \u201cHigh Risk Medications and Prevention of Errors.\u201d<\/p>\n<h3>Intermediate-Acting Insulin<\/h3>\n<p>NPH insulin, also known as isophane insulin, is an intermediate\u2013acting insulin. Brand names include Humulin-N or Novolin-N. Mixtures of short- and intermediate-acting insulin include Humulin 70\/30 or Novolin 70\/30.<\/p>\n<p><strong>Indications<\/strong><\/p>\n<p>Intermediate insulins are administered once or twice daily to mimic endogenous basal insulin levels.<\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Insulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat and by inhibiting hepatic glucose production.<\/p>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>NPH insulin is a white and cloudy suspension. Gently roll or invert vial\/pen several times to re-suspend the insulin before administration. It should only be administered subcutaneously. It may be mixed with rapid-acting or short-acting insulins, but those insulins should be drawn into the syringe before the NPH is added. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy. The onset of action and peak are affected by the site of injection, physical activity level, and other variables but the median peak level occurs in 4 hours. See Figure 9.13 for an image of Novolin-N (a cloudy insulin) that can be mixed with Novolin R (a clear insulin).<sup><a class=\"footnote\" title=\"&quot;The Gift of Life&quot; by Melissa Johnson is licensed under CC BY 2.0\" id=\"return-footnote-418-16\" href=\"#footnote-418-16\" aria-label=\"Footnote 16\"><sup class=\"footnote\">[16]<\/sup><\/a><\/sup><\/p>\n<p>&nbsp;<\/p>\n<figure style=\"width: 447px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"\" title=\"&quot;The Gift of Life&quot; by Melissa Johnson is licensed under CC BY 2.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image6-9.png\" alt=\"Photo showing two vials. One is Novolin N and the other is Novolin R.\" width=\"447\" height=\"323\" \/><figcaption class=\"wp-caption-text\">Figure 9.13 Comparison of Novolin-N (a cloudy insulin) that can be mixed with Novolin-R (a clear insulin)<\/figcaption><\/figure>\n<p>Mixed medications such as Humulin 70\/30 should be administered subcutaneously approximately 30 minutes before a meal. They are typically dosed twice daily (with each dose intended to cover 2 meals or a meal and a snack).<\/p>\n<p>Unopened vials should be stored in the refrigerator until the expiration date. Opened vials should be labelled with the open date and stored in the refrigerator for up to 28-42 days (depending on the formulation\/insulin type) and then discarded. Unopened pens should be stored in the refrigerator until the expiration date. Used pens should be stored at room temperature, but kept away from heat and light, for up to 10-28 days (depending on the formulation\/insulin type) and then discarded.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>See IMSP guidelines for patient teaching in the previous section titled \u201cHigh Risk Medications and Prevention of Errors.\u201d<\/p>\n<h3>Long-Acting Insulin<\/h3>\n<p>Insulin glargine (Lantus) and insulin devemir (Levemir) are long-acting insulins given once or twice daily. See Figure 9.14 for an image of a levemir insulin pen.<sup><a class=\"footnote\" title=\"&quot;Insulin analog 100 IU-1ml penfill levemir yellow background.jpg&quot; by Wesalius is licensed under CC BY 4.0\" id=\"return-footnote-418-17\" href=\"#footnote-418-17\" aria-label=\"Footnote 17\"><sup class=\"footnote\">[17]<\/sup><\/a><\/sup><\/p>\n<figure id=\"attachment_417\" aria-describedby=\"caption-attachment-417\" style=\"width: 716px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-414\" title=\"&quot;Insulin analog 100 IU-1ml penfill levemir yellow background.jpg&quot; by Wesalius is licensed under CC BY 4.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-1024x330.jpg\" alt=\"Photo showing vial used in Levemir insulin pen.\" width=\"716\" height=\"231\" srcset=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-1024x330.jpg 1024w, https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-300x97.jpg 300w, https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-768x247.jpg 768w, https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-65x21.jpg 65w, https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-225x72.jpg 225w, https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background-350x113.jpg 350w, https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background.jpg 1164w\" sizes=\"auto, (max-width: 716px) 100vw, 716px\" \/><figcaption id=\"caption-attachment-417\" class=\"wp-caption-text\">Figure 9.14 Vial used for Levemir insulin pen<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<p><strong>Indications<\/strong><\/p>\n<p>Long-acting insulins are given once or twice daily. In type 1 diabetics, long-acting insulin should be used concomitantly with rapid- or short-acting insulin at mealtimes.<\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Insulins lower blood glucose by stimulating peripheral glucose uptake by skeletal muscle and fat and by inhibiting hepatic glucose production.<\/p>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>Long-acting insulin has a relatively constant concentration\/time profile over 24 hours with no pronounced peak in comparison to NPH insulin. It should only be administered subcutaneously and is available in vials and insulin pens . Inspect insulin visually before use. It should appear clear and colorless; do not use if particulate matter or coloration is seen. Administer subcutaneously into the outer lateral aspect of the upper arm, the abdomen (from below the costal margin to the iliac crest and more than two inches from the umbilicus), the anterior upper thighs, or the buttocks. Rotate injection sites within the same region from one injection to the next to reduce the risk of lipodystrophy.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>See ISMP guidelines for patient teaching in the previous section titled \u201cHigh Risk Medications and Prevention of Errors.\u201d<\/p>\n<h3>Glucagon<\/h3>\n<p><strong>Indications<\/strong><\/p>\n<p>Glucagon is indicated as a treatment for severe hypoglycemia (low blood sugar), which may occur in patients with diabetes mellitus. Glucagon injection is used for patients who are unable to safely swallow carbohydrates to treat hypoglycemia due to the effects of hypoglycemia or other medical conditions.<\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Glucagon increases blood glucose concentration during an episode of hypoglycemia. See Figure 9.15 for an image of an emergency glucagon kit.<sup><a class=\"footnote\" title=\"&quot;Glucagon emergency rescue kit.JPG&quot; by mbbradford is licensed under CC0\" id=\"return-footnote-418-18\" href=\"#footnote-418-18\" aria-label=\"Footnote 18\"><sup class=\"footnote\">[18]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 662px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"\" title=\"&quot;Glucagon emergency rescue kit.JPG&quot; by mbbradford is licensed under CC0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image8-9.png\" alt=\"Photo showing emergency glucagon kit.\" width=\"662\" height=\"496\" \/><figcaption class=\"wp-caption-text\">Figure 9.15 Emergency glucagon kit<\/figcaption><\/figure>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>Glucagon may be administered subcutaneously, intramuscularly, or intravenously. Peak glucose levels occur within 13-20 minutes of subcutaneous or IM injection.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>Patients with type 1 diabetes may have less of an increase in blood glucose levels compared with a stable type 2 patient, so a supplementary carbohydrate should be given as soon as possible, especially to a pediatric patient. <sup><a class=\"footnote\" title=\"This work is a derivative of Daily Med by U.S. National Library of Medicine in the public domain. \u00a0\" id=\"return-footnote-418-19\" href=\"#footnote-418-19\" aria-label=\"Footnote 19\"><sup class=\"footnote\">[19]<\/sup><\/a><\/sup><\/p>\n<p>Now let\u2019s take a closer look at the medication grid comparing insulins in Table 9.4a.<sup><a class=\"footnote\" title=\"This work is a derivative of Daily Med by U.S. National Library of Medicine in the public domain. \u00a0\" id=\"return-footnote-418-20\" href=\"#footnote-418-20\" aria-label=\"Footnote 20\"><sup class=\"footnote\">[20]<\/sup><\/a><\/sup><\/p>\n<h5>Table 9.4a Insulins Medication Grid<\/h5>\n<table class=\"grid\" style=\"border-collapse: collapse;width: 100%;height: 112px\">\n<tbody>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Class\/Subclass<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Prototypes\/Generics<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Onset\/Peak\/Duration<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Administration Considerations<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Therapeutic Effects<\/th>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"col\">Adverse\/Side Effects<\/th>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Rapid-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f\" target=\"_blank\" rel=\"noopener noreferrer\">insulin lispro<\/a> (Humalog)<\/p>\n<p><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=bee5b358-c863-420b-be73-ced2e920c499\" target=\"_blank\" rel=\"noopener noreferrer\">insulin aspart <\/a>(Novolog)<\/p>\n<p><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=29f4637b-e204-425b-b89c-7238008d8c10\">inhaled insulin<\/a> (Afreeza)<\/p>\n<p>&nbsp;<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 15-30 minutes<\/p>\n<p>Peak effect: 1-3 hours<\/p>\n<p>Duration: 3 &#8211; 5 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer within 15 minutes before a meal or immediately after a meal<\/p>\n<p>Afrezza is contraindicated in patients with asthma or COPD<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia<\/p>\n<p>Hypokalemia<\/p>\n<p>Afrezza can cause acute bronchospasm<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Short-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=b519bd83-038c-4ec5-a231-a51ec5cc291f\" target=\"_blank\" rel=\"noopener noreferrer\">Humulin R<\/a><\/p>\n<p>Novolin R<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 30 minutes<\/p>\n<p>Peak effect: 3 hours<\/p>\n<p>Duration: 8\u00a0 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer 30 minutes before a meal<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia<\/p>\n<p>Hypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Intermediate-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f6edd793-440b-40c2-96b5-c16133b7a921\" target=\"_blank\" rel=\"noopener noreferrer\">Humulin N<\/a><\/p>\n<p>Novolin N<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 1-2 hours<\/p>\n<p>Peak effect: 6 hours (range 2.8-13 hours)<\/p>\n<p>Duration: up to 24 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer once or twice daily<\/p>\n<p>Only administer subcutaneously<\/p>\n<p>Gently roll or invert vial\/pen several times to re-suspend the insulin before administration<\/p>\n<p>Do not mix with other insulin<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia<\/p>\n<p>Hypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Combination: Intermediate-Acting\/Rapid-Acting<\/th>\n<td style=\"width: 16.6667%;height: 14px\">Humalog Mix 50\/50<\/p>\n<p>Humalog Mix 75\/25<\/p>\n<p>Novolog Mix 70\/30<\/p>\n<p>*First number is % intermediate-acting insulin, second number is % rapid-acting<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 15-30 minutes<\/p>\n<p>Peak effect:<\/p>\n<p>50\/50: 1-5 hours<\/p>\n<p>Duration: 11-22 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer twice daily, 15 minutes before a meal or immediately after a meal<\/p>\n<p>Only administer subcutaneously<\/p>\n<p>Gently roll or invert vial\/pen several times to re-suspend the insulin before administration<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia<\/p>\n<p>Hypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Combination: Intermediate-Acting\/Short-Acting<\/th>\n<td style=\"width: 16.6667%;height: 14px\">Humulin 70\/30<\/p>\n<p>Novolin 70\/30<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 30-90 minutes<\/p>\n<p>Peak effect: 1.5-6.5 hours<\/p>\n<p>Duration: 18-24 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer twice daily, 30-45 minutes before a meal<\/p>\n<p>Only administer subcutaneously<\/p>\n<p>Gently roll or invert vial\/pen several times to re-suspend the insulin before administration<\/p>\n<p>Do not mix with other insulin<\/p>\n<p>&nbsp;<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia<\/p>\n<p>Hypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Long-Acting Insulin<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=d5e07a0c-7e14-4756-9152-9fea485d654a\" target=\"_blank\" rel=\"noopener noreferrer\">insulin glargine<\/a> (Lantus)<\/p>\n<p>insulin detemir (Levemir)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Onset: 3-4 hours<\/p>\n<p>Peak effect: none<\/p>\n<p>Duration: &gt;24 hours<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Administer once daily (sometimes dose is split and administered twice daily)<\/p>\n<p>Only administer subcutaneously<\/p>\n<p>Do not mix with other insulin<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hypoglycemia<\/p>\n<p>Hypokalemia<\/td>\n<\/tr>\n<tr>\n<th style=\"width: 16.6667%;height: 14px\" scope=\"row\">Hyperglycemic<\/th>\n<td style=\"width: 16.6667%;height: 14px\"><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f143db10-e889-41c3-84ed-603a0ab02f61\" target=\"_blank\" rel=\"noopener noreferrer\">glucagon<\/a><\/td>\n<td style=\"width: 16.6667%;height: 14px\"><\/td>\n<td style=\"width: 16.6667%;height: 14px\">May be administered subcutaneously, IM, or IV<\/p>\n<p>Supplementary carbohydrate should be given as soon as possible, especially to a pediatric patient<\/p>\n<p>Used to reverse hypoglycemic episode if NPO administration is not appropriate<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Used to reverse hypoglycemic episode if NPO administration is not appropriate<\/td>\n<td style=\"width: 16.6667%;height: 14px\">Hyperglycemia<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong>General adminstration considerations<\/strong>:<\/p>\n<ul>\n<li>Review orders closely because they may include a standard meal dose, a \u201csliding scale\u201d dose, and a carb-related dose.<\/li>\n<li>Always read drug labelling closely as there are several types of dosages and formulations.<\/li>\n<li>See agency policies and ISMP guidelines for safe administration of insulin.<\/li>\n<li>When administering with an insulin pen, after inserting the pen count to 5 before removing the needle.<\/li>\n<\/ul>\n<p><strong>General therapeutic effects:<\/strong><\/p>\n<ul>\n<li>Maintain serum blood glucose in normal range and achieve individualized target level of A1C (often 7%)<\/li>\n<\/ul>\n<p><strong>General side effects:<\/strong><\/p>\n<ul>\n<li>Hypoglycemia and hypokalemia<\/li>\n<\/ul>\n<h2>Diabetic Medication: Oral Antihyperglycemics<\/h2>\n<p>There are several different classes of oral antihyperglycemic drugs used in conjunction with a healthy diet and exercise for the management of type 2 diabetes. According to the American Diabetes Association, metformin is the preferred initial pharmacologic agent for the treatment of type 2 diabetes.<sup><a class=\"footnote\" title=\"American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). https:\/\/doi.org\/10.2337\/dc19-S009\" id=\"return-footnote-418-21\" href=\"#footnote-418-21\" aria-label=\"Footnote 21\"><sup class=\"footnote\">[21]<\/sup><\/a><\/sup>Three of the most commonly used antihyperglycemic classes and prototypes are sulfonylureas (glipizide), biguanide (metformin), and DPP-IV (sitagliptin). The mechanism of action and administration considerations for each of these prototypes are described below.<\/span><\/p>\n<h3>Glipizide<\/h3>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Glipizide is in the sulfonylurea class of antihyperglycemic medication. The mechanism of action is the stimulation of insulin secretion from the beta cells of pancreatic islet tissue and is thus dependent on functioning beta cells in the pancreatic islets. Peak plasma concentrations occur 1 to 3 hours after a single oral dose.<\/p>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>All sulfonylurea drugs are capable of producing severe hypoglycemia. Hypoglycemia may be difficult to recognize in the elderly and in people who are taking beta-adrenergic blocking drugs. Sulfonylurea medications should be given 30 minutes before a meal due to hypoglycemic effects.<\/p>\n<p>Glipizide is contraindicated in type 1 diabetics or for use of diabetic ketoacidosis; insulin should be used to treat this condition. Treatment of patients with glucose 6-phosphate dehydrogenase (G6PD) deficiency with sulfonylurea agents can lead to hemolytic anemia.<\/p>\n<p>The hypoglycemic action of sulfonylureas may be potentiated by certain drugs such as nonsteroidal anti-inflammatory agents and other drugs that are highly protein bound.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>Patients should take the medication at the same time each day.\u00a0 It is important that patients understand that the medication helps control episodes of hyperglycemia but does not cure diabetes.\u00a0 Patients should be instructed regarding the signs of hyperglycemia and hypoglycemia.\u00a0 The use of sulfonylureas and alcohol may cause a disulfiram-like reaction.<\/p>\n<h3>Met\u200bformin<\/h3>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p><strong>Metformin<\/strong> is in the biguanide class of antihyperglycemics. It decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. Unlike sulfonylureas, metformin does not produce hypoglycemia. See Figure 9.16 for an image of a metformin tablet.<sup><a class=\"footnote\" title=\"&quot;Metformin 500mg Tablets.jpg&quot; by User:Ash is licensed under CC0\" id=\"return-footnote-418-22\" href=\"#footnote-418-22\" aria-label=\"Footnote 22\"><sup class=\"footnote\">[22]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 462px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"\" title=\"&quot;Metformin 500mg Tablets.jpg&quot; by User:Ash is licensed under CC0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image9-7.png\" alt=\"Photo showing closeup of Metformin package, blister pack, and pill.\" width=\"462\" height=\"409\" \/><figcaption class=\"wp-caption-text\">Figure 9.16 Metformin<\/figcaption><\/figure>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>Metformin hydrochloride should be given in divided doses with meals. The therapeutic goal should be to decrease both fasting plasma glucose and glycosylated hemoglobin levels to near normal by using the lowest effective dose of metformin, either when used as monotherapy or in combination with sulfonylurea or insulin.<\/p>\n<p>Common adverse reactions include diarrhea, nausea\/vomiting, weakness, flatulence, indigestion, abdominal discomfort, and headache.<\/p>\n<p>Metformin is contraindicated in patients with kidney disease (e.g., serum creatinine levels \u22651.5 mg\/dL [males] or \u22651.4 mg\/dL [females]) and should be temporarily discontinued in patients undergoing radiologic studies involving intravascular administration of iodinated contrast materials because use of such products may result in acute alteration of renal function. It is also contraindicated in patients with metabolic acidosis.<\/p>\n<p>Lactic acidosis is a rare, but serious, metabolic complication that can occur due to metformin accumulation during treatment with metformin; when it occurs, it is fatal in approximately 50% of cases. The risk of lactic acidosis increases with the degree of renal dysfunction and the patient\u2019s age. Metformin should be promptly withheld in the presence of any condition associated with hypoxemia, dehydration, or sepsis. Because impaired hepatic function may significantly limit the ability to clear lactate, metformin should be avoided in patients with hepatic disease. The onset of lactic acidosis often is subtle and accompanied only by nonspecific symptoms such as malaise, myalgias, respiratory distress, increasing somnolence, and nonspecific abdominal distress.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>\u200b\u200bPatients should take the medication at the same time each day.\u00a0 It is important that patients understand that the medication helps control episodes of hyperglycemia but does not cure diabetes.\u00a0 Patients should be instructed regarding the signs of hyperglycemia and hypoglycemia.\u00a0 The patient may be at risk for lactic acidosis and should report chills, low blood pressure, muscle pain, or dyspnea immediately to the healthcare provider.\u00a0 The use of medications like metformin can cause a metallic taste in the mouth.<\/p>\n<h3>\u200bSitagliptin<\/h3>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Sitagliptin is an orally-active inhibitor of dipeptidyl peptidase-4 (DPP-4) enzyme that slows the inactivation of incretin hormones involved in the regulation of glucose homeostasis and thus, increases insulin release and decreases glucagon levels in the circulation. See Figure 9.17 for an image of sitagliptin.<sup><a class=\"footnote\" title=\"&quot;Januvia sitagliptin.jpg&quot; by Kimivanil is licensed under CC BY-SA 4.0\" id=\"return-footnote-418-23\" href=\"#footnote-418-23\" aria-label=\"Footnote 23\"><sup class=\"footnote\">[23]<\/sup><\/a><\/sup><\/p>\n<figure style=\"width: 535px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"\" title=\"&quot;Januvia sitagliptin.jpg&quot; by Kimivanil is licensed under CC BY-SA 4.0\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2021\/12\/image10-6.png\" alt=\"Photo showing closeup of Januvia package.\" width=\"535\" height=\"336\" \/><figcaption class=\"wp-caption-text\">Figure 9.17 Sitagliptin<\/figcaption><\/figure>\n<p><strong>Specific Administration Considerations<\/strong><\/p>\n<p>Sitagliptin is taken once daily and can be taken with or without food. It can cause hypoglycemia. Dose adjustment should occur for patients with kidney disease depending on their glomerular filtration rate. Report hypersensitivity reactions, blisters\/erosions, headache, or symptoms of pancreatitis, heart failure, severe arthralgia, and upper respiratory infection.<\/p>\n<p><strong>Patient Teaching &amp; Education<\/strong><\/p>\n<p>Patients should take the medication at the same time each day.\u00a0 It is important that patients understand that the medication helps control episodes of hyperglycemia but does not cure diabetes.\u00a0 Patients should be instructed regarding the signs of hyperglycemia and hypoglycemia.\u00a0 Patients should stop taking the medication if symptoms of hypersensitivity occur and follow up immediately with their provider to determine the next course of treatment.<\/p>\n<p>Now let\u2019s take a closer look at the medication grid comparing oral antihyperglycemics in Table 9.4b. <sup><a class=\"footnote\" title=\"This work is a derivative of Daily Med by U.S. National Library of Medicine in the public domain. \u00a0\" id=\"return-footnote-418-24\" href=\"#footnote-418-24\" aria-label=\"Footnote 24\"><sup class=\"footnote\">[24]<\/sup><\/a><\/sup><\/p>\n<p>Table 9.4b Medication Grid Comparing Oral Antihyperglycemics<\/p>\n<table class=\"grid\">\n<tbody>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\"><strong>Class<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\" scope=\"col\"><strong>Prototype<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\" scope=\"col\"><strong>Administration <\/strong><strong>Considerations<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\" scope=\"col\"><strong>Therapeutic Effects<\/strong><\/th>\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\" scope=\"col\"><strong>Adverse\/Side Effects<\/strong><\/th>\n<\/tr>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\">Sulfonylureas<\/th>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\"><a class=\"rId40\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=5565ccec-8000-48ab-a6af-37eca2d8c993\" target=\"_blank\" rel=\"noopener noreferrer\">glipizide<\/a><\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\">Time with meals; peak plasma concentrations occur 1 to 3 hours after administration<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\">Reduce fasting blood sugar and glycosylated hemoglobin to near normal<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\">Hypoglycemia; may be potentiated by nonsteroidal anti-inflammatory agents and other drugs that are highly protein bound<\/td>\n<\/tr>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\">Biguanide<\/th>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\"><a class=\"rId41\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=2d98aea3-35ba-447a-b88f-a5a20b612b2f\" target=\"_blank\" rel=\"noopener noreferrer\">metformin<\/a><\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\">Contraindicated in renal and hepatic disease<\/p>\n<p>Should be temporarily discontinued in patients undergoing radiologic studies involving intravascular administration of iodinated contrast materials<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\">Reduce fasting blood sugar and glycosylated hemoglobin to near normal<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\">Stop immediately if signs of lactic acidosis or any condition associated with hypoxemia, dehydration, or sepsis occurs<\/p>\n<p>Common adverse effects: diarrhea, nausea\/vomiting, weakness, flatulence, indigestion, abdominal discomfort, and headache<\/td>\n<\/tr>\n<tr class=\"a3-R\">\n<th class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 106.667px\" scope=\"col\">DPP-IV inhibitor<\/th>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 88px\"><a class=\"rId42\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f85a48d0-0407-4c50-b0fa-7673a160bf01\" target=\"_blank\" rel=\"noopener noreferrer\">sitagliptin<\/a><\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 383.111px\">Can be given with or without food<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 236.444px\">Reduce fasting blood sugar and glycosylated hemoglobin to near norm<\/td>\n<td class=\"a3-C\" style=\"background-color: transparent;padding: 5pt;border: 1pt solid #000000;width: 250.667px\">Hypoglycemia<\/p>\n<p>Report hypersensitivity reactions, blisters\/erosions, headache, or symptoms of pancreatitis, heart failure, severe arthralgia, or upper respiratory infection<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<\/div>\n<div class=\"__UNKNOWN__\">\n<div class=\"textbox textbox--examples\">\n<header class=\"textbox__header\">\n<h2>Critical Thinking Activity 9.4<br \/>\n<img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-197\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2019\/11\/ORN-Icons_lightbulb-300x300-1.png\" alt=\"Image of lightbulb in a circle\" width=\"200\" height=\"200\" \/><\/h2>\n<\/header>\n<div class=\"textbox__content\" style=\"text-align: left\">\n<p>A patient with diabetes mellitus type 2 is admitted to the hospital for hip replacement surgery. The nurse reviews the following orders:<\/p>\n<p>Diabetic diet with carb counting<\/p>\n<p>Bedside blood glucose testing before meals and at bedtime with sliding scale Humalog insulin<\/p>\n<p>Sliding scale Humalog insulin based on preprandial glucose level:<\/p>\n<ul>\n<li>0-150: No coverage<\/li>\n<li>151-175: 2 units<\/li>\n<li>176-200: 4 units<\/li>\n<li>201-225: 6 units<\/li>\n<li>226-250: 8 units<\/li>\n<li>Over 250: call the provider<\/li>\n<\/ul>\n<p>Insulin coverage per carbohydrate intake at meals: Humalog 2 units\/carb<\/p>\n<p>Metformin 1000 mg twice daily<\/p>\n<p>Humulin-N 20 units at breakfast and at bedtime<\/p>\n<p>Hypoglycemia protocol<\/p>\n<ol>\n<li>Explain the difference between type 1 and type 2 diabetes.<\/li>\n<li>The patient states that he usually does not take insulin at home. What is the likely rationale for insulin therapy while hospitalized?<\/li>\n<li>The patient\u2019s blood sugar before breakfast is 223 and he eats 3 carbs at breakfast. What types and amounts of insulin will the nurse administer?<\/li>\n<li>The nurse reviews the patient&#8217;s morning lab results and finds a creatinine of 1.8. She plans to call the provider to discuss the impact of the results on the medications ordered. Which medication may require a dosage adjustment based on these results?<\/li>\n<li>When the nurse enters the room around 4 p.m., she discovers that the patient has become irritable and is shaky. The nurse performs a bedside blood glucose and obtains a value of 60. What is the nurse\u2019s best response?<\/li>\n<li>What is the likely cause of the patient\u2019s condition? Explain using the onset and peak actions of the insulin orders.<\/li>\n<li>On admission, the patient\u2019s A1C level was 10%. What does this lab value indicate?<\/li>\n<li>The provider states the discharge plan is to initiate Lantus insulin therapy at home, based on the admitting A1C level. What patient teaching should the nurse plan to provide before discharge?<\/li>\n<\/ol>\n<p>Note: Answers to the Critical Thinking activities can be found in the &#8220;Answer Key&#8221; sections at the end of the book.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<hr class=\"before-footnotes clear\" \/><div class=\"footnotes\"><ol><li id=\"footnote-418-1\">\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:1820_The_Pancreas.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">1820 The Pancreas.jpg<\/a>\"\" by <a href=\"https:\/\/openstax.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">OpenStax<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0.<\/a> Access for free at <a href=\"https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas<\/a> <a href=\"#return-footnote-418-1\" class=\"return-footnote\" aria-label=\"Return to footnote 1\">&crarr;<\/a><\/li><li id=\"footnote-418-2\">\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:1822_The_Homostatic_Regulation_of_Blood_Glucose_Levels.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">1822 The Homostatic Regulation of Blood Glucose Levels.jpg<\/a>\" by <a href=\"https:\/\/openstax.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">OpenStax<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0.<\/a> Access for free at <a href=\"https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/17-9-the-endocrine-pancreas<\/a> <a href=\"#return-footnote-418-2\" class=\"return-footnote\" aria-label=\"Return to footnote 2\">&crarr;<\/a><\/li><li id=\"footnote-418-3\">This work is a derivative of <a href=\"https:\/\/openstax.org\/details\/books\/anatomy-and-physiology\" target=\"_blank\" rel=\"noopener noreferrer\">Anatomy and Physiology<\/a> by <a href=\"https:\/\/openstax.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">OpenStax<\/a> licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0<\/a>. Access for free at <a href=\"https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/1-introduction\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/anatomy-and-physiology\/pages\/1-introduction<\/a> <a href=\"#return-footnote-418-3\" class=\"return-footnote\" aria-label=\"Return to footnote 3\">&crarr;<\/a><\/li><li id=\"footnote-418-4\">American Diabetes Association. (2019). The Big Picture: Checking your Blood Glucose. <a href=\"https:\/\/www.diabetes.org\/diabetes\/medication-management\/blood-glucose-testing-and-control\/checking-your-blood-glucose\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.diabetes.org\/diabetes\/medication-management\/blood-glucose-testing-and-control\/checking-your-blood-glucose<\/a> <a href=\"#return-footnote-418-4\" class=\"return-footnote\" aria-label=\"Return to footnote 4\">&crarr;<\/a><\/li><li id=\"footnote-418-5\">American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S009\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S009<\/a> <a href=\"#return-footnote-418-5\" class=\"return-footnote\" aria-label=\"Return to footnote 5\">&crarr;<\/a><\/li><li id=\"footnote-418-6\">Seggelke, S., Everhart, B. (2012, September 11) Managing glucose levels in hospital patients. <em>American Nurse Today.<\/em> <a href=\"https:\/\/www.americannursetoday.com\/managing-glucose-levels-in-hospital-patients\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.americannursetoday.com\/managing-glucose-levels-in-hospital-patients\/<\/a>. <a href=\"#return-footnote-418-6\" class=\"return-footnote\" aria-label=\"Return to footnote 6\">&crarr;<\/a><\/li><li id=\"footnote-418-7\">American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S009\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S009<\/a> <a href=\"#return-footnote-418-7\" class=\"return-footnote\" aria-label=\"Return to footnote 7\">&crarr;<\/a><\/li><li id=\"footnote-418-8\">Weaver, H., Hirsch, I (2018, June 6). The Hybrid Closed Loop System: Evolution and Practical Applications. <em>Diabetes Technology &amp; Therapeutics 20<\/em>(S2). <a href=\"https:\/\/www.liebertpub.com\/doi\/10.1089\/dia.2018.0091\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.liebertpub.com\/doi\/10.1089\/dia.2018.0091<\/a>. <a href=\"#return-footnote-418-8\" class=\"return-footnote\" aria-label=\"Return to footnote 8\">&crarr;<\/a><\/li><li id=\"footnote-418-9\">\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Human_insulin_100_IU-1ml_pen_yellow_background_(02).jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Human insulin 100 IU-1ml pen yellow background (02).jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/wiki\/User:Wesalius\" target=\"_blank\" rel=\"noopener noreferrer\">Wesalius<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0<\/a> <a href=\"#return-footnote-418-9\" class=\"return-footnote\" aria-label=\"Return to footnote 9\">&crarr;<\/a><\/li><li id=\"footnote-418-10\">Institute for Safe Medication Practices. (2017). ISMP Guidelines for Optimizing Safe Subcutaneous Insulin Use in Adults.\u00a0 <a href=\"https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf<\/a> <a href=\"#return-footnote-418-10\" class=\"return-footnote\" aria-label=\"Return to footnote 10\">&crarr;<\/a><\/li><li id=\"footnote-418-11\">Institute for Safe Medication Practices. (2017). ISMP Guidelines for Optimizing Safe Subcutaneous Insulin Use in Adults.\u00a0 <a href=\"https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.ismp.org\/sites\/default\/files\/attachments\/2017-11\/ISMP138-Insulin%20Guideline-051517-2-WEB.pdf<\/a> <a href=\"#return-footnote-418-11\" class=\"return-footnote\" aria-label=\"Return to footnote 11\">&crarr;<\/a><\/li><li id=\"footnote-418-12\">American Diabetes Association (2019) 12. Older adults: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S012\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S012<\/a> <a href=\"#return-footnote-418-12\" class=\"return-footnote\" aria-label=\"Return to footnote 12\">&crarr;<\/a><\/li><li id=\"footnote-418-13\">American Diabetes Association. (2019). 13. Children and adolescents: Standards of Medical Care in Diabetes\u20142019. Diabetes Care 42(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S013\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.2337\/dc19-S013<\/a> <a href=\"#return-footnote-418-13\" class=\"return-footnote\" aria-label=\"Return to footnote 13\">&crarr;<\/a><\/li><li id=\"footnote-418-14\">\"<a href=\"https:\/\/pxhere.com\/de\/photo\/1209814\" target=\"_blank\" rel=\"noopener noreferrer\">Untitled<\/a>\" from <a href=\"https:\/\/pxhere.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">Pxhere<\/a> website is licensed under <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/cc0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC0<\/a> <a href=\"#return-footnote-418-14\" class=\"return-footnote\" aria-label=\"Return to footnote 14\">&crarr;<\/a><\/li><li id=\"footnote-418-15\">\"<a href=\"https:\/\/americanhistory.si.edu\/collections\/search\/object\/nmah_1000969\" target=\"_blank\" rel=\"noopener noreferrer\">Humulin R, Insulin, 1987<\/a>\" by National Museum of American History Smithsonian Institution is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/2.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-NC-ND 2.0<\/a> <a href=\"#return-footnote-418-15\" class=\"return-footnote\" aria-label=\"Return to footnote 15\">&crarr;<\/a><\/li><li id=\"footnote-418-16\">\"<a href=\"https:\/\/www.flickr.com\/photos\/ladytaz\/1836553797\" target=\"_blank\" rel=\"noopener noreferrer\">The Gift of Life<\/a>\" by <a href=\"https:\/\/www.flickr.com\/photos\/ladytaz\/\" target=\"_blank\" rel=\"noopener noreferrer\">Melissa Johnson<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/2.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 2.0<\/a> <a href=\"#return-footnote-418-16\" class=\"return-footnote\" aria-label=\"Return to footnote 16\">&crarr;<\/a><\/li><li id=\"footnote-418-17\">\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Insulin_analog_100_IU-1ml_penfill_levemir_yellow_background.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Insulin analog 100 IU-1ml penfill levemir yellow background.jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/wiki\/User:Wesalius\" target=\"_blank\" rel=\"noopener noreferrer\">Wesalius<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY 4.0<\/a> <a href=\"#return-footnote-418-17\" class=\"return-footnote\" aria-label=\"Return to footnote 17\">&crarr;<\/a><\/li><li id=\"footnote-418-18\">\"<a href=\"https:\/\/en.wikipedia.org\/wiki\/File:Glucagon_emergency_rescue_kit.JPG\" target=\"_blank\" rel=\"noopener noreferrer\">Glucagon emergency rescue kit.JPG<\/a>\" by <a href=\"https:\/\/en.wikipedia.org\/wiki\/User:Mbbradford\" target=\"_blank\" rel=\"noopener noreferrer\">mbbradford<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/cc0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC0<\/a> <a href=\"#return-footnote-418-18\" class=\"return-footnote\" aria-label=\"Return to footnote 18\">&crarr;<\/a><\/li><li id=\"footnote-418-19\">This work is a derivative of <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a> by <a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a> in the <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>. \u00a0 <a href=\"#return-footnote-418-19\" class=\"return-footnote\" aria-label=\"Return to footnote 19\">&crarr;<\/a><\/li><li id=\"footnote-418-20\">This work is a derivative of <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a> by <a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a> in the <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>. \u00a0 <a href=\"#return-footnote-418-20\" class=\"return-footnote\" aria-label=\"Return to footnote 20\">&crarr;<\/a><\/li><li id=\"footnote-418-21\">American Diabetes Association. (2019).\u00a0 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes\u20142019. <em>Diabetes Care 42<\/em>(S1). <a href=\"https:\/\/doi.org\/10.2337\/dc19-S009\">https:\/\/doi.org\/10.2337\/dc19-S009<\/a><\/sup><span style=\"text-align: initial;font-size: 1em\"><sup> <a href=\"#return-footnote-418-21\" class=\"return-footnote\" aria-label=\"Return to footnote 21\">&crarr;<\/a><\/li><li id=\"footnote-418-22\">\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Metformin_500mg_Tablets.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Metformin 500mg Tablets.jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/w\/index.php?title=User:Ash&amp;action=edit&amp;redlink=1\" target=\"_blank\" rel=\"noopener noreferrer\">User:Ash<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/cc0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC0<\/a> <a href=\"#return-footnote-418-22\" class=\"return-footnote\" aria-label=\"Return to footnote 22\">&crarr;<\/a><\/li><li id=\"footnote-418-23\">\"<a href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Januvia_sitagliptin.jpg\" target=\"_blank\" rel=\"noopener noreferrer\">Januvia sitagliptin.jpg<\/a>\" by <a href=\"https:\/\/commons.wikimedia.org\/w\/index.php?title=User:Kimivanil&amp;action=edit&amp;redlink=1\" target=\"_blank\" rel=\"noopener noreferrer\">Kimivanil<\/a> is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-sa\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-SA 4.0<\/a> <a href=\"#return-footnote-418-23\" class=\"return-footnote\" aria-label=\"Return to footnote 23\">&crarr;<\/a><\/li><li id=\"footnote-418-24\">This work is a derivative of <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a> by <a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a> in the <a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>. \u00a0 <a href=\"#return-footnote-418-24\" class=\"return-footnote\" aria-label=\"Return to footnote 24\">&crarr;<\/a><\/li><\/ol><\/div><div class=\"glossary\"><span class=\"screen-reader-text\" id=\"definition\">definition<\/span><template id=\"term_418_1740\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1740\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1746\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1746\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1745\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1745\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1748\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1748\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1749\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1749\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_2190\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_2190\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1751\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1751\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1752\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1752\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><template id=\"term_418_1754\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_418_1754\"><div tabindex=\"-1\"><\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><\/div>","protected":false},"author":2,"menu_order":4,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":"cc-by"},"chapter-type":[49],"contributor":[],"license":[53],"class_list":["post-418","chapter","type-chapter","status-publish","hentry","chapter-type-numberless","license-cc-by"],"part":392,"_links":{"self":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/418","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/users\/2"}],"version-history":[{"count":1,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/418\/revisions"}],"predecessor-version":[{"id":419,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/418\/revisions\/419"}],"part":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/parts\/392"}],"metadata":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/418\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/media?parent=418"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapter-type?post=418"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/contributor?post=418"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/license?post=418"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}