{"id":40,"date":"2019-09-18T16:00:13","date_gmt":"2019-09-18T16:00:13","guid":{"rendered":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/chapter\/1-6-excretion\/"},"modified":"2025-01-16T22:29:16","modified_gmt":"2025-01-16T22:29:16","slug":"1-6-excretion","status":"publish","type":"chapter","link":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/chapter\/1-6-excretion\/","title":{"raw":"1.6 Excretion","rendered":"1.6 Excretion"},"content":{"raw":"<h2>Excretion<\/h2>\n<strong>[pb_glossary id=\"474\"]Excretion[\/pb_glossary] <\/strong>is the final stage of a medication interaction within the body. The body has absorbed, distributed, and metabolized the medication molecules - now what does it do with the leftovers? Remaining parent drugs and metabolites in the bloodstream are often filtered by the kidney, where a portion undergoes reabsorption back into the bloodstream, and the remainder is excreted in the urine. The liver also excretes byproducts and waste into the bile. Another potential route of excretion is the lungs. For example, drugs like alcohol and the anesthetic gases are often eliminated by the lungs.<sup>[footnote]This work is a derivative of <a href=\"https:\/\/med.libretexts.org\/Bookshelves\/Pharmacology_and_Medicine\/Book%3A_Principles_of_Pharmacology_(OCW)\" target=\"_blank\" rel=\"noopener noreferrer\">Principles of Pharmacology<\/a> by <a href=\"https:\/\/libretexts.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">LibreTexts<\/a> and is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-NC-SA 4.0<\/a>[\/footnote]<\/sup>\n<h2>Routes of Excretion<\/h2>\n<h3>Kidney<\/h3>\nThe most common route of excretion is through the kidneys. As the kidneys filter blood, the majority of drug byproducts and waste are excreted in the urine. The rate of excretion can be estimated by taking into consideration several client factors, including age, weight, biological sex, and kidney function. There are known sex differences in the three main renal functions of glomerular filtration, tubular secretion and tubular reabsorption. Renal clearance is generally higher in men than in women.<sup>[footnote]Soldin, O. P., &amp; Mattison, D. R. (2009). Sex differences in pharmacokinetics and pharmacodynamics. <em>Clinical Pharmacokinetics, 48<\/em>(3), 143\u2013157. <a href=\"https:\/\/doi.org\/10.2165\/00003088-200948030-00001\" target=\"_blank\" rel=\"noopener\">https:\/\/doi.org\/10.2165\/00003088-200948030-00001<\/a>[\/footnote]<\/sup>\n\nKidney function is measured by lab values such as serum creatinine, glomerular filtration rate (GFR), and creatinine clearance. If a client's kidney function is decreased, then their ability to excrete medication is affected, and drug dosages must be altered for safe administration.\n\nRenal disorders, such as chronic kidney disease, can reduce kidney function and hinder drug excretion. As kidney function decreases with age, drug excretion becomes less efficient, and dosing adjustments may be needed. Other medical conditions that impact blood flow to the kidneys can also affect drug elimination. For example, heart failure can affect systemic blood flow to the kidney, resulting in decreased filtration and elimination of drugs.\n<h3>Liver<\/h3>\nAs the liver filters blood, some drugs and their metabolites are actively transported by hepatocytes (liver cells) to bile. Bile moves through the bile ducts to the gallbladder and then on to the small intestine. During this process, some drugs may be partially absorbed by the intestine back into the bloodstream. Other drugs are biotransformed (metabolized) by intestinal bacteria and reabsorbed. Unabsorbed drugs and byproducts\/metabolites are excreted in the feces.\n\nIf a client has decreased liver function, their ability to excrete medication is affected, and drug dosages must be adjusted. Lab studies used to evaluate liver function are called liver function tests and include measurement of alanine transaminase (ALT) and aspartate aminotransferase (AST) enzymes that the body releases in response to damage to or disease of the liver.\n\nConditions that cause decreased blood flow to the liver can also affect the metabolism and excretion of drugs. For example, conditions such as shock, hypovolemia, or hypotension cause decreased liver perfusion and may require adjustment of dosages of medication.\n<h3>Other Routes to Consider<\/h3>\nSweat, tears, reproductive fluids (such as seminal fluid), and breast milk can also contain drugs and byproducts\/metabolites of drugs. This can pose a toxic threat, such as the exposure of an infant to breast milk containing drugs or byproducts of drugs ingested by the mother. Therefore, nurses must refer to a drug reference and contact a health care provider with any concerns before administering medications to a mother who is breastfeeding.<sup>[footnote]This work is a derivative of <a href=\"https:\/\/med.libretexts.org\/Bookshelves\/Pharmacology_and_Medicine\/Book%3A_Principles_of_Pharmacology_(OCW)\" target=\"_blank\" rel=\"noopener noreferrer\">Principles of Pharmacology<\/a> by <a href=\"https:\/\/libretexts.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">LibreTexts<\/a> and is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-NC-SA 4.0<\/a>[\/footnote]<\/sup>\n<h2>Life Span Considerations<\/h2>\n<h3>Neonate &amp; Pediatrics<\/h3>\nNeonates and children have immature kidneys with decreased glomerular filtration, resorption, and tubular secretion. As a result, they do not excrete medications as efficiently from the body. Dosing for most medications used to treat infants and pediatric clients is commonly based on weight in kilograms, and a smaller dose is usually prescribed. In addition, pediatric clients may have higher levels of free circulating medication than anticipated and may become toxic quickly. Therefore, it is vital for nurses to diligently recheck dosages before administering medications and closely monitor infants and children for early identification of adverse effects and drug toxicity.<sup>[footnote]Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M., &amp; Ramos, J. T. (2011). Factors and mechanisms for pharmacokinetic differences between pediatric population and adults. <em>Pharmaceutics, 3<\/em>(1), 53\u201372. <a href=\"https:\/\/doi.org\/10.3390\/pharmaceutics3010053\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.3390\/pharmaceutics3010053<\/a>[\/footnote]<\/sup>\n<h3>Older Adult<\/h3>\nKidney and liver function often decrease with age, which can lead to decreased metabolism and excretion of medications. Subsequently, medication may have a prolonged half-life with a greater potential for toxicity due to elevated circulating drug levels. Some medications may be avoided or smaller doses recommended for older clients due to these factors, which is commonly referred to as \"Start low and go slow.\"<sup>[footnote]Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M., &amp; Ramos, J. T. (2011). Factors and mechanisms for pharmacokinetic differences between pediatric population and adults. <em>Pharmaceutics, 3<\/em>(1), 53\u201372. <a href=\"https:\/\/doi.org\/10.3390\/pharmaceutics3010053\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.3390\/pharmaceutics3010053<\/a>[\/footnote]<\/sup>\n<h2>Putting It All Together<\/h2>\nSafely administering medications to clients is a significant concern and requires team effort by pharmacists, prescribing health care providers, and nurses. In addition to the factors described in this chapter, there are many other considerations for safe medication administration that are further explained in the \"<a href=\"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/chapter\/2-1-legal-ethical-introduction\/\" target=\"_blank\" rel=\"noopener\">Legal\/Ethical<\/a>\" chapter.\n<div class=\"__UNKNOWN__\">\n<div class=\"textbox textbox--examples\"><header class=\"textbox__header\">\n<h2>Critical Thinking Activity 1.6<img class=\"alignright wp-image-36\" style=\"font-size: 14.4px;font-family: 'Encode Sans', sans-serif\" src=\"https:\/\/pressbooks.ccconline.org\/accdigitalmarketing\/wp-content\/uploads\/sites\/219\/2025\/01\/ORN-Icons_internet-copy_internet-copy-300x300-1.png\" alt=\"Image of a circle containing a speech bubble with a question mark in it.\" width=\"200\" height=\"200\"><\/h2>\n<\/header>\n<div class=\"textbox__content\" style=\"text-align: left\">\n\nWhen providing care for a client who has chronic kidney disease, how does this condition impact medication excretion?\n\nNote: Answers to the Critical Thinking activities can be found in the \"<a href=\"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/chapter\/chapter-1\/\" target=\"_blank\" rel=\"noopener\">Answer Key<\/a>\" section at the end of the book.\n\n<\/div>\n<div class=\"textbox\">\n<h3 class=\"star\">\u00a0Interactive Activity<\/h3>\n[h5p id=\"1\"]\n\n<sup>\u201cPharmacokinetics Quiz\u201d by E. Christman for Open RN is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener\">CC BY 4.0<\/a><\/sup>\n\n<\/div>\n<\/div>\n<\/div>","rendered":"<h2>Excretion<\/h2>\n<p><strong><a class=\"glossary-term\" aria-haspopup=\"dialog\" aria-describedby=\"definition\" href=\"#term_40_474\">Excretion<\/a> <\/strong>is the final stage of a medication interaction within the body. The body has absorbed, distributed, and metabolized the medication molecules &#8211; now what does it do with the leftovers? Remaining parent drugs and metabolites in the bloodstream are often filtered by the kidney, where a portion undergoes reabsorption back into the bloodstream, and the remainder is excreted in the urine. The liver also excretes byproducts and waste into the bile. Another potential route of excretion is the lungs. For example, drugs like alcohol and the anesthetic gases are often eliminated by the lungs.<sup><a class=\"footnote\" title=\"This work is a derivative of Principles of Pharmacology by LibreTexts and is licensed under CC BY-NC-SA 4.0\" id=\"return-footnote-40-1\" href=\"#footnote-40-1\" aria-label=\"Footnote 1\"><sup class=\"footnote\">[1]<\/sup><\/a><\/sup><\/p>\n<h2>Routes of Excretion<\/h2>\n<h3>Kidney<\/h3>\n<p>The most common route of excretion is through the kidneys. As the kidneys filter blood, the majority of drug byproducts and waste are excreted in the urine. The rate of excretion can be estimated by taking into consideration several client factors, including age, weight, biological sex, and kidney function. There are known sex differences in the three main renal functions of glomerular filtration, tubular secretion and tubular reabsorption. Renal clearance is generally higher in men than in women.<sup><a class=\"footnote\" title=\"Soldin, O. P., &amp; Mattison, D. R. (2009). Sex differences in pharmacokinetics and pharmacodynamics. Clinical Pharmacokinetics, 48(3), 143\u2013157. https:\/\/doi.org\/10.2165\/00003088-200948030-00001\" id=\"return-footnote-40-2\" href=\"#footnote-40-2\" aria-label=\"Footnote 2\"><sup class=\"footnote\">[2]<\/sup><\/a><\/sup><\/p>\n<p>Kidney function is measured by lab values such as serum creatinine, glomerular filtration rate (GFR), and creatinine clearance. If a client&#8217;s kidney function is decreased, then their ability to excrete medication is affected, and drug dosages must be altered for safe administration.<\/p>\n<p>Renal disorders, such as chronic kidney disease, can reduce kidney function and hinder drug excretion. As kidney function decreases with age, drug excretion becomes less efficient, and dosing adjustments may be needed. Other medical conditions that impact blood flow to the kidneys can also affect drug elimination. For example, heart failure can affect systemic blood flow to the kidney, resulting in decreased filtration and elimination of drugs.<\/p>\n<h3>Liver<\/h3>\n<p>As the liver filters blood, some drugs and their metabolites are actively transported by hepatocytes (liver cells) to bile. Bile moves through the bile ducts to the gallbladder and then on to the small intestine. During this process, some drugs may be partially absorbed by the intestine back into the bloodstream. Other drugs are biotransformed (metabolized) by intestinal bacteria and reabsorbed. Unabsorbed drugs and byproducts\/metabolites are excreted in the feces.<\/p>\n<p>If a client has decreased liver function, their ability to excrete medication is affected, and drug dosages must be adjusted. Lab studies used to evaluate liver function are called liver function tests and include measurement of alanine transaminase (ALT) and aspartate aminotransferase (AST) enzymes that the body releases in response to damage to or disease of the liver.<\/p>\n<p>Conditions that cause decreased blood flow to the liver can also affect the metabolism and excretion of drugs. For example, conditions such as shock, hypovolemia, or hypotension cause decreased liver perfusion and may require adjustment of dosages of medication.<\/p>\n<h3>Other Routes to Consider<\/h3>\n<p>Sweat, tears, reproductive fluids (such as seminal fluid), and breast milk can also contain drugs and byproducts\/metabolites of drugs. This can pose a toxic threat, such as the exposure of an infant to breast milk containing drugs or byproducts of drugs ingested by the mother. Therefore, nurses must refer to a drug reference and contact a health care provider with any concerns before administering medications to a mother who is breastfeeding.<sup><a class=\"footnote\" title=\"This work is a derivative of Principles of Pharmacology by LibreTexts and is licensed under CC BY-NC-SA 4.0\" id=\"return-footnote-40-3\" href=\"#footnote-40-3\" aria-label=\"Footnote 3\"><sup class=\"footnote\">[3]<\/sup><\/a><\/sup><\/p>\n<h2>Life Span Considerations<\/h2>\n<h3>Neonate &amp; Pediatrics<\/h3>\n<p>Neonates and children have immature kidneys with decreased glomerular filtration, resorption, and tubular secretion. As a result, they do not excrete medications as efficiently from the body. Dosing for most medications used to treat infants and pediatric clients is commonly based on weight in kilograms, and a smaller dose is usually prescribed. In addition, pediatric clients may have higher levels of free circulating medication than anticipated and may become toxic quickly. Therefore, it is vital for nurses to diligently recheck dosages before administering medications and closely monitor infants and children for early identification of adverse effects and drug toxicity.<sup><a class=\"footnote\" title=\"Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M., &amp; Ramos, J. T. (2011). Factors and mechanisms for pharmacokinetic differences between pediatric population and adults. Pharmaceutics, 3(1), 53\u201372. https:\/\/doi.org\/10.3390\/pharmaceutics3010053\" id=\"return-footnote-40-4\" href=\"#footnote-40-4\" aria-label=\"Footnote 4\"><sup class=\"footnote\">[4]<\/sup><\/a><\/sup><\/p>\n<h3>Older Adult<\/h3>\n<p>Kidney and liver function often decrease with age, which can lead to decreased metabolism and excretion of medications. Subsequently, medication may have a prolonged half-life with a greater potential for toxicity due to elevated circulating drug levels. Some medications may be avoided or smaller doses recommended for older clients due to these factors, which is commonly referred to as &#8220;Start low and go slow.&#8221;<sup><a class=\"footnote\" title=\"Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M., &amp; Ramos, J. T. (2011). Factors and mechanisms for pharmacokinetic differences between pediatric population and adults. Pharmaceutics, 3(1), 53\u201372. https:\/\/doi.org\/10.3390\/pharmaceutics3010053\" id=\"return-footnote-40-5\" href=\"#footnote-40-5\" aria-label=\"Footnote 5\"><sup class=\"footnote\">[5]<\/sup><\/a><\/sup><\/p>\n<h2>Putting It All Together<\/h2>\n<p>Safely administering medications to clients is a significant concern and requires team effort by pharmacists, prescribing health care providers, and nurses. In addition to the factors described in this chapter, there are many other considerations for safe medication administration that are further explained in the &#8220;<a href=\"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/chapter\/2-1-legal-ethical-introduction\/\" target=\"_blank\" rel=\"noopener\">Legal\/Ethical<\/a>&#8221; chapter.<\/p>\n<div class=\"__UNKNOWN__\">\n<div class=\"textbox textbox--examples\">\n<header class=\"textbox__header\">\n<h2>Critical Thinking Activity 1.6<img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-36\" style=\"font-size: 14.4px;font-family: 'Encode Sans', sans-serif\" src=\"https:\/\/pressbooks.ccconline.org\/accdigitalmarketing\/wp-content\/uploads\/sites\/219\/2025\/01\/ORN-Icons_internet-copy_internet-copy-300x300-1.png\" alt=\"Image of a circle containing a speech bubble with a question mark in it.\" width=\"200\" height=\"200\" srcset=\"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-content\/uploads\/sites\/219\/2025\/01\/ORN-Icons_internet-copy_internet-copy-300x300-1.png 300w, https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-content\/uploads\/sites\/219\/2025\/01\/ORN-Icons_internet-copy_internet-copy-300x300-1-150x150.png 150w, https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-content\/uploads\/sites\/219\/2025\/01\/ORN-Icons_internet-copy_internet-copy-300x300-1-65x65.png 65w, https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-content\/uploads\/sites\/219\/2025\/01\/ORN-Icons_internet-copy_internet-copy-300x300-1-225x225.png 225w\" sizes=\"auto, (max-width: 200px) 100vw, 200px\" \/><\/h2>\n<\/header>\n<div class=\"textbox__content\" style=\"text-align: left\">\n<p>When providing care for a client who has chronic kidney disease, how does this condition impact medication excretion?<\/p>\n<p>Note: Answers to the Critical Thinking activities can be found in the &#8220;<a href=\"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/chapter\/chapter-1\/\" target=\"_blank\" rel=\"noopener\">Answer Key<\/a>&#8221; section at the end of the book.<\/p>\n<\/div>\n<div class=\"textbox\">\n<h3 class=\"star\">\u00a0Interactive Activity<\/h3>\n<div id=\"h5p-1\">\n<div class=\"h5p-iframe-wrapper\"><iframe id=\"h5p-iframe-1\" class=\"h5p-iframe\" data-content-id=\"1\" style=\"height:1px\" src=\"about:blank\" frameBorder=\"0\" scrolling=\"no\" title=\"Module 1: Pharmacokinetics Quiz\"><\/iframe><\/div>\n<\/div>\n<p><sup>\u201cPharmacokinetics Quiz\u201d by E. Christman for Open RN is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\" target=\"_blank\" rel=\"noopener\">CC BY 4.0<\/a><\/sup><\/p>\n<\/div>\n<\/div>\n<\/div>\n<hr class=\"before-footnotes clear\" \/><div class=\"footnotes\"><ol><li id=\"footnote-40-1\">This work is a derivative of <a href=\"https:\/\/med.libretexts.org\/Bookshelves\/Pharmacology_and_Medicine\/Book%3A_Principles_of_Pharmacology_(OCW)\" target=\"_blank\" rel=\"noopener noreferrer\">Principles of Pharmacology<\/a> by <a href=\"https:\/\/libretexts.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">LibreTexts<\/a> and is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-NC-SA 4.0<\/a> <a href=\"#return-footnote-40-1\" class=\"return-footnote\" aria-label=\"Return to footnote 1\">&crarr;<\/a><\/li><li id=\"footnote-40-2\">Soldin, O. P., &amp; Mattison, D. R. (2009). Sex differences in pharmacokinetics and pharmacodynamics. <em>Clinical Pharmacokinetics, 48<\/em>(3), 143\u2013157. <a href=\"https:\/\/doi.org\/10.2165\/00003088-200948030-00001\" target=\"_blank\" rel=\"noopener\">https:\/\/doi.org\/10.2165\/00003088-200948030-00001<\/a> <a href=\"#return-footnote-40-2\" class=\"return-footnote\" aria-label=\"Return to footnote 2\">&crarr;<\/a><\/li><li id=\"footnote-40-3\">This work is a derivative of <a href=\"https:\/\/med.libretexts.org\/Bookshelves\/Pharmacology_and_Medicine\/Book%3A_Principles_of_Pharmacology_(OCW)\" target=\"_blank\" rel=\"noopener noreferrer\">Principles of Pharmacology<\/a> by <a href=\"https:\/\/libretexts.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">LibreTexts<\/a> and is licensed under <a href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\" target=\"_blank\" rel=\"noopener noreferrer\">CC BY-NC-SA 4.0<\/a> <a href=\"#return-footnote-40-3\" class=\"return-footnote\" aria-label=\"Return to footnote 3\">&crarr;<\/a><\/li><li id=\"footnote-40-4\">Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M., &amp; Ramos, J. T. (2011). Factors and mechanisms for pharmacokinetic differences between pediatric population and adults. <em>Pharmaceutics, 3<\/em>(1), 53\u201372. <a href=\"https:\/\/doi.org\/10.3390\/pharmaceutics3010053\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.3390\/pharmaceutics3010053<\/a> <a href=\"#return-footnote-40-4\" class=\"return-footnote\" aria-label=\"Return to footnote 4\">&crarr;<\/a><\/li><li id=\"footnote-40-5\">Fernandez, E., Perez, R., Hernandez, A., Tejada, P., Arteta, M., &amp; Ramos, J. T. (2011). Factors and mechanisms for pharmacokinetic differences between pediatric population and adults. <em>Pharmaceutics, 3<\/em>(1), 53\u201372. <a href=\"https:\/\/doi.org\/10.3390\/pharmaceutics3010053\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/doi.org\/10.3390\/pharmaceutics3010053<\/a> <a href=\"#return-footnote-40-5\" class=\"return-footnote\" aria-label=\"Return to footnote 5\">&crarr;<\/a><\/li><\/ol><\/div><div class=\"glossary\"><span class=\"screen-reader-text\" id=\"definition\">definition<\/span><template id=\"term_40_474\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_40_474\"><div tabindex=\"-1\"><p>The final stage of pharmacokinetics; process by which the body eliminates waste or excess.<\/p>\n<\/div><button><span aria-hidden=\"true\">&times;<\/span><span class=\"screen-reader-text\">Close definition<\/span><\/button><\/div><\/template><\/div>","protected":false},"author":83,"menu_order":6,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[48],"contributor":[],"license":[],"class_list":["post-40","chapter","type-chapter","status-publish","hentry","chapter-type-numberless"],"part":21,"_links":{"self":[{"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/40","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/wp\/v2\/users\/83"}],"version-history":[{"count":3,"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/40\/revisions"}],"predecessor-version":[{"id":776,"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/40\/revisions\/776"}],"part":[{"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/parts\/21"}],"metadata":[{"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/40\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/wp\/v2\/media?parent=40"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/pressbooks\/v2\/chapter-type?post=40"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/wp\/v2\/contributor?post=40"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.ccconline.org\/accnursingpharmacology\/wp-json\/wp\/v2\/license?post=40"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}