{"id":105,"date":"2019-09-22T17:51:13","date_gmt":"2019-09-22T17:51:13","guid":{"rendered":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/chapter\/3-6-cephalosporins\/"},"modified":"2021-12-07T11:06:19","modified_gmt":"2021-12-07T11:06:19","slug":"3-6-cephalosporins","status":"publish","type":"chapter","link":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/chapter\/3-6-cephalosporins\/","title":{"raw":"3.6 Cephalosporins","rendered":"3.6 Cephalosporins"},"content":{"raw":"[caption id=\"\" align=\"alignnone\" width=\"1300\"]<img title=\"&quot;OSC Microbio 14 02 BetaLactam.jpg&quot; by CNX Openstax is licensed under CC BY 4.0 Access for free at https:\/\/openstax.org\/books\/microbiology\/pages\/14-3-mechanisms-of-antibacterial-drugs\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2019\/09\/image11-1.png\" alt=\"Illustration and chart detailing Beta-lactam ring structure \" width=\"1300\" height=\"908\"> Figure 3.8 Comparison of beta-lactam ring structure across different classes of medications, spectrum of activity and routes of administration<sup><span style=\"text-align: initial\">[footnote]\"<\/span><a style=\"text-align: initial\" href=\"https:\/\/openstax.org\/resources\/875df04f09b347eb5af989aec39c17218e95e976\" target=\"_blank\" rel=\"noopener noreferrer\">OSC Microbio 14 02 BetaLactam.jpg<\/a><span style=\"text-align: initial\">\" by <\/span><a style=\"text-align: initial\" href=\"https:\/\/cnx.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">CNX Openstax<\/a><span style=\"text-align: initial\"> is licensed under<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\"> CC BY 4.0<\/a><span style=\"text-align: initial\"> Access for free at <\/span><a style=\"text-align: initial\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/14-3-mechanisms-of-antibacterial-drugs\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/microbiology\/pages\/14-3-mechanisms-of-antibacterial-drugs<\/a><span style=\"text-align: initial\">[\/footnote]<\/span><\/sup>[\/caption]Cephalosporins are a slightly modified chemical \"twin\" to penicillins due to their beta lactam chemical structure. (See Figure 3.8 for a comparison of the beta-lactam ring structure, spectrum of activity, and route of administration across different classes of medications.) Because of these similarities, some patients who have allergies to penicillins <span style=\"text-align: initial;font-size: 1em\">may experience cross-sensitivity to cephalosporins.<\/span>\n\n<strong>Indications:<\/strong> Cephalosporins are used to treat skin and skin-structure infections, bone infections, genitourinary infections, otitis media, and community-acquired respiratory tract infections.\n\n<strong>Mechanism of Action:<\/strong> Cephalosporins are typically bactericidal and are similar to penicillin in their action within the cell wall. Cephalosporins are sometimes grouped into \"generations\" by their antimicrobial properties. The 1st-generation drugs are effective mainly against gram-positive organisms. Higher generations generally have expanded spectra against aerobic gram-negative bacilli. The 5th-generation cephalosporins are active against methicillin-resistant <a class=\"rId35\" href=\"https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/gram-positive-cocci\/staphylococcal-infections\" target=\"_blank\" rel=\"noopener noreferrer\">Staphylococcus aureus<\/a> (MRSA) or other complicated infections. <sup>[footnote]Werth, B.J. (2018, August). <em>Cephalosporins.<\/em> Merck Manual Professional Version. <a href=\"https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/bacteria-and-antibacterial-drugs\/cephalosporins\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/bacteria-and-antibacterial-drugs\/cephalosporins<\/a> [\/footnote]<\/sup>\n\n<strong>Specific Administration Considerations:<\/strong> Patients who are allergic to pencillins may also be allergic to cephalosporins. Patients who consume cephalosporins while drinking alcoholic beverages may experience disulfiram-like reactions including severe headache, flushing, nausea, vomiting, etc.<sup>[footnote]Ren, S., Cao, Y., Zhang, X., Jiao, S., Qian, S., &amp; Liu, P. (2014). Cephalosporin induced disulfiram-like reaction: a retrospective review of 78 cases. <em>International Surgery, 99<\/em>(2), 142\u2013146. <a href=\"https:\/\/www.internationalsurgery.org\/doi\/full\/10.9738\/INTSURG-D-13-00086.1\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.internationalsurgery.org\/doi\/full\/10.9738\/INTSURG-D-13-00086.1<\/a>[\/footnote]\u00a0<\/sup>Additionally, like penicillins, cephalosporins may interfere with coagulability and increase a patient's risk of bleeding. Cephalosporin dosing may require adjustment for patients experiencing renal impairment. Blood urea nitrogen (BUN) and creatinine should be monitored carefully to identify signs of nephrotoxicity.\n\n<strong>Patient Teaching &amp; Education:<\/strong> Patients who are prescribed cephalosporins should be specifically cautioned about a disulfiram reaction, which can occur when alcohol is ingested while taking the medication.\u00a0 Additionally, individuals should be instructed to monitor for rash and signs of superinfection (such as black, furry overgrowth on tongue; vaginal itching or discharge; loose or foul-smelling stool) and report to the prescribing provider.\n\nIt is also important to note that cephalosporin can enter breastmilk and may alter bowel flora of the infant. Thus, use during breastfeeding is often discouraged.<sup>[footnote]uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.unboundmedicine.com\/ucentral<\/a>[\/footnote]<\/sup>\n\nNow let's take a closer look at the cephalosporin medication grid in Table 3.6.<sup>[footnote]Daily Med, <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm<\/a>, used for hyperlinked medications in this module. Retrieved June 27, 2019.[\/footnote]<\/sup>\n\nTable 3.6 Cephalosporin Medication Grid\n<table class=\"grid\" border=\"0\">\n<tbody>\n<tr>\n<th scope=\"col\">\n<h5><strong>Class\/Subclass<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Prototype\/Generics<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Administration Considerations<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Therapeutic Effects<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Side\/Adverse Effects<\/strong><\/h5>\n<\/th>\n<\/tr>\n<tr>\n<th scope=\"row\">Cephalosporins<\/th>\n<td>1st generation:\n\n<a class=\"rId36\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=19307ff0-71de-477b-965d-ea243e5ede3a&amp;audience=consumer\" target=\"_blank\" rel=\"noopener noreferrer\">cephalexin<\/a>\n\n<a class=\"rId37\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=48656c70-206d-652c-204f-62692d57616e&amp;audience=consumer\" target=\"_blank\" rel=\"noopener noreferrer\">Cefazolin<\/a>\n\n2nd generation:\n\n<a class=\"rId38\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=97675251-70b8-43bc-93ea-f9ef6bb8cb68\" target=\"_blank\" rel=\"noopener noreferrer\">cefprozil<\/a>\n\n3rd generation:\n\n<a class=\"rId39\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=4d1ad77f-2c6b-4250-82e5-ab3574444e08\" target=\"_blank\" rel=\"noopener noreferrer\">ceftriaxone<\/a>\n\n4th generation:\n\n<a class=\"rId40\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=28f1c403-ab91-405e-bf52-ad81b1c66220\" target=\"_blank\" rel=\"noopener noreferrer\">cefepime<\/a>\n\n5th generation:\n\n<a class=\"rId41\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=70ac1d90-eff3-4f0b-9f46-5846c571b32f\" target=\"_blank\" rel=\"noopener noreferrer\">ceftolozane<\/a><\/td>\n<td>Check for allergies, including if allergic to penicillin\n\nDosage adjustment if renal impairment\n\nUse with caution with seizure disorder\n\nPO: Administer without regard to food; if GI distress, give with food\n\nIV: Reconstitute drug with sterile water or normal saline; shake well until dissolved. Inject into large vein or free-flowing IV solution over 3-5 minutes\n\nDrug interaction: anticoagulants<\/td>\n<td>Monitor for systemic signs of infection:\n\n-WBCs\n\n- Fever\n\nMonitor actual site of infection\n\nMonitor culture results, if obtained<\/td>\n<td>Common side effects:\n\n-Nausea\n\n-Vomiting\n\n-Epigastric distress\n\n-Diarrhea\n\nMonitor for:\n\n-Rash\n\n-C-diff\n\nNephrotoxicity if pre-existing renal disease\n\nElevated INR and bleeding risk\n\nDevelopment of hemolytic anemia<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2>Critical Thinking Activity 3.6a<\/h2>\n<strong>Using the above grid information, consider the following clinical scenario question:<\/strong>\n\nMrs. Jenkins is an 89-year-old patient admitted to the medical surgical floor for treatment of a skin infection. The admitting provider prescribes Cefazolin 1 gram every 8 hours IV.\n\nMrs. Jenkins' admission laboratory tests include renal laboratory studies reflecting:\n\n<a class=\"rId42\" href=\"https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" target=\"_blank\" rel=\"noopener noreferrer\">Creatinine<\/a>: 1.3 mg\/dL (Normal range: 1.2 mg\/dL<sup>[footnote]U.S. National Library of Medicine, Medline Plus. (2020, February 13). <em>Basic metabolic panel.<\/em>\u00a0<a href=\"https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/medlineplus.gov\/ency\/article\/003462.htm<\/a>[\/footnote]<\/sup>\n\n<a class=\"rId43\" href=\"https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" target=\"_blank\" rel=\"noopener noreferrer\">Blood urea nitrogen (BUN)<\/a>: 25 mg\/dL (Normal: 8-20 mg\/dL)\n\n<a class=\"rId44\" href=\"https:\/\/medlineplus.gov\/ency\/article\/007305.htm\">Glomerular Filtration Rate<\/a>: 55 ml\/min (Normal: 90-120 ml\/min)<sup>[footnote]U.S. National Library of Medicine, Medline Plus. (2020, February 13). <em>Glomerular filtration rate.<\/em> <a href=\"https:\/\/medlineplus.gov\/ency\/article\/007305.htm\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/medlineplus.gov\/ency\/article\/007305.htm<\/a>[\/footnote]<\/sup>\n\nOn Day 3 Mrs. Jenkins has renal laboratory studies performed again. The results are:\n\nCreatinine: 1.6 mg\/dL\n\nBlood urea nitrogen (BUN): 57 mg\/dL\n\nGlomerular Filtration Rate: 20 ml\/min\n\nAre Day 3 findings expected or not? What course of action should the nurse take?\n\nNote: Answers to the Critical Thinking activities can be found in the \"Answer Key\" sections at the end of the book.","rendered":"<figure style=\"width: 1300px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" decoding=\"async\" title=\"&quot;OSC Microbio 14 02 BetaLactam.jpg&quot; by CNX Openstax is licensed under CC BY 4.0 Access for free at https:\/\/openstax.org\/books\/microbiology\/pages\/14-3-mechanisms-of-antibacterial-drugs\" src=\"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-content\/uploads\/sites\/5\/2019\/09\/image11-1.png\" alt=\"Illustration and chart detailing Beta-lactam ring structure\" width=\"1300\" height=\"908\" \/><figcaption class=\"wp-caption-text\">Figure 3.8 Comparison of beta-lactam ring structure across different classes of medications, spectrum of activity and routes of administration<sup><span style=\"text-align: initial\">[footnote]\"<\/span><a style=\"text-align: initial\" href=\"https:\/\/openstax.org\/resources\/875df04f09b347eb5af989aec39c17218e95e976\" target=\"_blank\" rel=\"noopener noreferrer\">OSC Microbio 14 02 BetaLactam.jpg<\/a><span style=\"text-align: initial\">\" by <\/span><a style=\"text-align: initial\" href=\"https:\/\/cnx.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">CNX Openstax<\/a><span style=\"text-align: initial\"> is licensed under<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\"> CC BY 4.0<\/a><span style=\"text-align: initial\"> Access for free at <\/span><a style=\"text-align: initial\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/14-3-mechanisms-of-antibacterial-drugs\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/openstax.org\/books\/microbiology\/pages\/14-3-mechanisms-of-antibacterial-drugs<\/a><span style=\"text-align: initial\">[\/footnote]<\/span><\/sup><\/figcaption><\/figure>\n<p>Cephalosporins are a slightly modified chemical &#8220;twin&#8221; to penicillins due to their beta lactam chemical structure. (See Figure 3.8 for a comparison of the beta-lactam ring structure, spectrum of activity, and route of administration across different classes of medications.) Because of these similarities, some patients who have allergies to penicillins <span style=\"text-align: initial;font-size: 1em\">may experience cross-sensitivity to cephalosporins.<\/span><\/p>\n<p><strong>Indications:<\/strong> Cephalosporins are used to treat skin and skin-structure infections, bone infections, genitourinary infections, otitis media, and community-acquired respiratory tract infections.<\/p>\n<p><strong>Mechanism of Action:<\/strong> Cephalosporins are typically bactericidal and are similar to penicillin in their action within the cell wall. Cephalosporins are sometimes grouped into &#8220;generations&#8221; by their antimicrobial properties. The 1st-generation drugs are effective mainly against gram-positive organisms. Higher generations generally have expanded spectra against aerobic gram-negative bacilli. The 5th-generation cephalosporins are active against methicillin-resistant <a class=\"rId35\" href=\"https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/gram-positive-cocci\/staphylococcal-infections\" target=\"_blank\" rel=\"noopener noreferrer\">Staphylococcus aureus<\/a> (MRSA) or other complicated infections. <sup><a class=\"footnote\" title=\"Werth, B.J. (2018, August). Cephalosporins. Merck Manual Professional Version. https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/bacteria-and-antibacterial-drugs\/cephalosporins\" id=\"return-footnote-105-1\" href=\"#footnote-105-1\" aria-label=\"Footnote 1\"><sup class=\"footnote\">[1]<\/sup><\/a><\/sup><\/p>\n<p><strong>Specific Administration Considerations:<\/strong> Patients who are allergic to pencillins may also be allergic to cephalosporins. Patients who consume cephalosporins while drinking alcoholic beverages may experience disulfiram-like reactions including severe headache, flushing, nausea, vomiting, etc.<sup><a class=\"footnote\" title=\"Ren, S., Cao, Y., Zhang, X., Jiao, S., Qian, S., &amp; Liu, P. (2014). Cephalosporin induced disulfiram-like reaction: a retrospective review of 78 cases. International Surgery, 99(2), 142\u2013146. https:\/\/www.internationalsurgery.org\/doi\/full\/10.9738\/INTSURG-D-13-00086.1\" id=\"return-footnote-105-2\" href=\"#footnote-105-2\" aria-label=\"Footnote 2\"><sup class=\"footnote\">[2]<\/sup><\/a>\u00a0<\/sup>Additionally, like penicillins, cephalosporins may interfere with coagulability and increase a patient&#8217;s risk of bleeding. Cephalosporin dosing may require adjustment for patients experiencing renal impairment. Blood urea nitrogen (BUN) and creatinine should be monitored carefully to identify signs of nephrotoxicity.<\/p>\n<p><strong>Patient Teaching &amp; Education:<\/strong> Patients who are prescribed cephalosporins should be specifically cautioned about a disulfiram reaction, which can occur when alcohol is ingested while taking the medication.\u00a0 Additionally, individuals should be instructed to monitor for rash and signs of superinfection (such as black, furry overgrowth on tongue; vaginal itching or discharge; loose or foul-smelling stool) and report to the prescribing provider.<\/p>\n<p>It is also important to note that cephalosporin can enter breastmilk and may alter bowel flora of the infant. Thus, use during breastfeeding is often discouraged.<sup><a class=\"footnote\" title=\"uCentral from Unbound Medicine. https:\/\/www.unboundmedicine.com\/ucentral\" id=\"return-footnote-105-3\" href=\"#footnote-105-3\" aria-label=\"Footnote 3\"><sup class=\"footnote\">[3]<\/sup><\/a><\/sup><\/p>\n<p>Now let&#8217;s take a closer look at the cephalosporin medication grid in Table 3.6.<sup><a class=\"footnote\" title=\"Daily Med, https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm, used for hyperlinked medications in this module. Retrieved June 27, 2019.\" id=\"return-footnote-105-4\" href=\"#footnote-105-4\" aria-label=\"Footnote 4\"><sup class=\"footnote\">[4]<\/sup><\/a><\/sup><\/p>\n<p>Table 3.6 Cephalosporin Medication Grid<\/p>\n<table class=\"grid\">\n<tbody>\n<tr>\n<th scope=\"col\">\n<h5><strong>Class\/Subclass<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Prototype\/Generics<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Administration Considerations<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Therapeutic Effects<\/strong><\/h5>\n<\/th>\n<th scope=\"col\">\n<h5><strong>Side\/Adverse Effects<\/strong><\/h5>\n<\/th>\n<\/tr>\n<tr>\n<th scope=\"row\">Cephalosporins<\/th>\n<td>1st generation:<\/p>\n<p><a class=\"rId36\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=19307ff0-71de-477b-965d-ea243e5ede3a&amp;audience=consumer\" target=\"_blank\" rel=\"noopener noreferrer\">cephalexin<\/a><\/p>\n<p><a class=\"rId37\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=48656c70-206d-652c-204f-62692d57616e&amp;audience=consumer\" target=\"_blank\" rel=\"noopener noreferrer\">Cefazolin<\/a><\/p>\n<p>2nd generation:<\/p>\n<p><a class=\"rId38\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=97675251-70b8-43bc-93ea-f9ef6bb8cb68\" target=\"_blank\" rel=\"noopener noreferrer\">cefprozil<\/a><\/p>\n<p>3rd generation:<\/p>\n<p><a class=\"rId39\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=4d1ad77f-2c6b-4250-82e5-ab3574444e08\" target=\"_blank\" rel=\"noopener noreferrer\">ceftriaxone<\/a><\/p>\n<p>4th generation:<\/p>\n<p><a class=\"rId40\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=28f1c403-ab91-405e-bf52-ad81b1c66220\" target=\"_blank\" rel=\"noopener noreferrer\">cefepime<\/a><\/p>\n<p>5th generation:<\/p>\n<p><a class=\"rId41\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=70ac1d90-eff3-4f0b-9f46-5846c571b32f\" target=\"_blank\" rel=\"noopener noreferrer\">ceftolozane<\/a><\/td>\n<td>Check for allergies, including if allergic to penicillin<\/p>\n<p>Dosage adjustment if renal impairment<\/p>\n<p>Use with caution with seizure disorder<\/p>\n<p>PO: Administer without regard to food; if GI distress, give with food<\/p>\n<p>IV: Reconstitute drug with sterile water or normal saline; shake well until dissolved. Inject into large vein or free-flowing IV solution over 3-5 minutes<\/p>\n<p>Drug interaction: anticoagulants<\/td>\n<td>Monitor for systemic signs of infection:<\/p>\n<p>-WBCs<\/p>\n<p>&#8211; Fever<\/p>\n<p>Monitor actual site of infection<\/p>\n<p>Monitor culture results, if obtained<\/td>\n<td>Common side effects:<\/p>\n<p>-Nausea<\/p>\n<p>-Vomiting<\/p>\n<p>-Epigastric distress<\/p>\n<p>-Diarrhea<\/p>\n<p>Monitor for:<\/p>\n<p>-Rash<\/p>\n<p>-C-diff<\/p>\n<p>Nephrotoxicity if pre-existing renal disease<\/p>\n<p>Elevated INR and bleeding risk<\/p>\n<p>Development of hemolytic anemia<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2>Critical Thinking Activity 3.6a<\/h2>\n<p><strong>Using the above grid information, consider the following clinical scenario question:<\/strong><\/p>\n<p>Mrs. Jenkins is an 89-year-old patient admitted to the medical surgical floor for treatment of a skin infection. The admitting provider prescribes Cefazolin 1 gram every 8 hours IV.<\/p>\n<p>Mrs. Jenkins&#8217; admission laboratory tests include renal laboratory studies reflecting:<\/p>\n<p><a class=\"rId42\" href=\"https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" target=\"_blank\" rel=\"noopener noreferrer\">Creatinine<\/a>: 1.3 mg\/dL (Normal range: 1.2 mg\/dL<sup><a class=\"footnote\" title=\"U.S. National Library of Medicine, Medline Plus. (2020, February 13). Basic metabolic panel.\u00a0https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" id=\"return-footnote-105-5\" href=\"#footnote-105-5\" aria-label=\"Footnote 5\"><sup class=\"footnote\">[5]<\/sup><\/a><\/sup><\/p>\n<p><a class=\"rId43\" href=\"https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" target=\"_blank\" rel=\"noopener noreferrer\">Blood urea nitrogen (BUN)<\/a>: 25 mg\/dL (Normal: 8-20 mg\/dL)<\/p>\n<p><a class=\"rId44\" href=\"https:\/\/medlineplus.gov\/ency\/article\/007305.htm\">Glomerular Filtration Rate<\/a>: 55 ml\/min (Normal: 90-120 ml\/min)<sup><a class=\"footnote\" title=\"U.S. National Library of Medicine, Medline Plus. (2020, February 13). Glomerular filtration rate. https:\/\/medlineplus.gov\/ency\/article\/007305.htm\" id=\"return-footnote-105-6\" href=\"#footnote-105-6\" aria-label=\"Footnote 6\"><sup class=\"footnote\">[6]<\/sup><\/a><\/sup><\/p>\n<p>On Day 3 Mrs. Jenkins has renal laboratory studies performed again. The results are:<\/p>\n<p>Creatinine: 1.6 mg\/dL<\/p>\n<p>Blood urea nitrogen (BUN): 57 mg\/dL<\/p>\n<p>Glomerular Filtration Rate: 20 ml\/min<\/p>\n<p>Are Day 3 findings expected or not? What course of action should the nurse take?<\/p>\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<hr class=\"before-footnotes clear\" \/><div class=\"footnotes\"><ol><li id=\"footnote-105-1\">Werth, B.J. (2018, August). <em>Cephalosporins.<\/em> Merck Manual Professional Version. <a href=\"https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/bacteria-and-antibacterial-drugs\/cephalosporins\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.merckmanuals.com\/professional\/infectious-diseases\/bacteria-and-antibacterial-drugs\/cephalosporins<\/a>  <a href=\"#return-footnote-105-1\" class=\"return-footnote\" aria-label=\"Return to footnote 1\">&crarr;<\/a><\/li><li id=\"footnote-105-2\">Ren, S., Cao, Y., Zhang, X., Jiao, S., Qian, S., &amp; Liu, P. (2014). Cephalosporin induced disulfiram-like reaction: a retrospective review of 78 cases. <em>International Surgery, 99<\/em>(2), 142\u2013146. <a href=\"https:\/\/www.internationalsurgery.org\/doi\/full\/10.9738\/INTSURG-D-13-00086.1\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.internationalsurgery.org\/doi\/full\/10.9738\/INTSURG-D-13-00086.1<\/a> <a href=\"#return-footnote-105-2\" class=\"return-footnote\" aria-label=\"Return to footnote 2\">&crarr;<\/a><\/li><li id=\"footnote-105-3\">uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.unboundmedicine.com\/ucentral<\/a> <a href=\"#return-footnote-105-3\" class=\"return-footnote\" aria-label=\"Return to footnote 3\">&crarr;<\/a><\/li><li id=\"footnote-105-4\">Daily Med, <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm<\/a>, used for hyperlinked medications in this module. Retrieved June 27, 2019. <a href=\"#return-footnote-105-4\" class=\"return-footnote\" aria-label=\"Return to footnote 4\">&crarr;<\/a><\/li><li id=\"footnote-105-5\">U.S. National Library of Medicine, Medline Plus. (2020, February 13). <em>Basic metabolic panel.<\/em>\u00a0<a href=\"https:\/\/medlineplus.gov\/ency\/article\/003462.htm\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/medlineplus.gov\/ency\/article\/003462.htm<\/a> <a href=\"#return-footnote-105-5\" class=\"return-footnote\" aria-label=\"Return to footnote 5\">&crarr;<\/a><\/li><li id=\"footnote-105-6\">U.S. National Library of Medicine, Medline Plus. (2020, February 13). <em>Glomerular filtration rate.<\/em> <a href=\"https:\/\/medlineplus.gov\/ency\/article\/007305.htm\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/medlineplus.gov\/ency\/article\/007305.htm<\/a> <a href=\"#return-footnote-105-6\" class=\"return-footnote\" aria-label=\"Return to footnote 6\">&crarr;<\/a><\/li><\/ol><\/div>","protected":false},"author":2,"menu_order":6,"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-105","chapter","type-chapter","status-publish","hentry","chapter-type-numberless","license-cc-by"],"part":84,"_links":{"self":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/105","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\/105\/revisions"}],"predecessor-version":[{"id":106,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/105\/revisions\/106"}],"part":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/parts\/84"}],"metadata":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/105\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/media?parent=105"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapter-type?post=105"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/contributor?post=105"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.publishdot.com\/nursingpharmacology\/wp-json\/wp\/v2\/license?post=105"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}