{"id":357,"date":"2019-11-19T16:58:43","date_gmt":"2019-11-19T21:58:43","guid":{"rendered":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/chapter\/8-10-anticonvulsants\/"},"modified":"2022-01-17T18:43:07","modified_gmt":"2022-01-17T23:43:07","slug":"8-10-anticonvulsants","status":"publish","type":"chapter","link":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/chapter\/8-10-anticonvulsants\/","title":{"raw":"8.10 Anticonvulsants","rendered":"8.10 Anticonvulsants"},"content":{"raw":"<div class=\"1.10-anticonvulsants-\">\r\n\r\nMedications used for seizures are called anticonvulsants or antiseizure drugs. Antiseizure drugs stabilize cell membranes and suppress the abnormal electric impulses in the cerebral cortex. These drugs prevent seizures but do not provide a cure. Antiseizure drugs are classified as CNS depressants. There are many types of medications used to treat seizures such as phenytoin, phenobarbital, benzodiazepines, carbamazepine, valproate, and levetiracetam.<sup>[footnote]McCuistion, L., Vuljoin-DiMaggio, K., Winton, M, &amp; Yeager, J. (2018). <em>Pharmacology: A patient-centered nursing process approach.<\/em> pp. 227-305. Elsevier.[\/footnote]<\/sup>\r\n\r\nThere are three main pharmacological effects of antiseizure medications. First, they increase the threshold of activity in the motor cortex, thus making it more difficult for a nerve to become excited. Second, they limit the spread of a seizure discharge from its origin by suppressing the transmission of impulses from one nerve to the next. Third, they decrease the speed of the nerve impulse conduction within a given neuron.\r\n\r\nSome drugs work by enhancing the effects of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA), which plays a role in regulating neuron excitability in the brain.<sup>[footnote]Lilley, L., Collins, S., &amp; Snyder, J. (2020). <em>Pharmacology and the Nursing Process.<\/em> pp. 246-272. Elsevier.[\/footnote]<\/sup> Gabapentin, although structurally similar to GABA and classified as an anticonvulsant, is commonly used to control chronic neuropathic pain. Neuropathic pain is defined by the International Association for the Study of Pain as \u201cpain caused by a lesion or disease of the somatosensory nervous system.\u201d<sup>[footnote]Murnion B. P. (2018, June 1). Neuropathic pain: current definition and review of drug treatment. <em>Australian prescriber, 41<\/em>(3), 60\u201363. <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6003018\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6003018\/<\/a>[\/footnote]<\/sup> An example of neuropathic pain is tingling or burning in the lower extremities that often occurs in clients with diabetes.\r\n<h3>Phenytoin<\/h3>\r\nPhenytoin, which was discovered in 1938, was the first anti-seizure medication and is still being used to control seizures.<sup>[footnote]McCuistion, L., Vuljoin-DiMaggio, K., Winton, M, &amp; Yeager, J. (2018). <em>Pharmacology: A patient-centered nursing process approach.<\/em> pp. 227-305. Elsevier.[\/footnote]<\/sup>\r\n\r\n<strong>Mechanism of Action<\/strong>\r\n\r\nPhenytoin improves evidence of seizures by interfering with sodium channels in the brain, resulting in a reduction of sustained high-frequency neuronal discharges.\r\n\r\n<strong>Indications for Use<\/strong>\r\n\r\nPhenytoin is indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and for the prevention and treatment of seizures occurring during or following neurosurgery.\r\n\r\n<strong>Nursing Considerations Across the Lifespan<\/strong>\r\n\r\nPhenytoin should not be administered to pregnant women because it will cause harm to the fetus. When given intravenously, there is a Black Box Warning that the rate of administration should not exceed 50 mg per minute in adults and 1 to 3 mg\/kg\/min (or 50 mg per minute, whichever is slower) in pediatric clients because of the risk of severe hypotension and cardiac arrhythmias. Careful cardiac monitoring is needed during and after administering intravenous phenytoin.\r\n\r\nPhenytoin has a narrow therapeutic drug level, usually between 40 - 80 uM\/L, so serum drug monitoring is required.<sup>[footnote]London Health Science Center. (2021). Phenytoin.\u00a0<a href=\"https:\/\/www.lhsc.on.ca\/critical-care-trauma-centre\/phenytoin-dilantin\">https:\/\/www.lhsc.on.ca\/critical-care-trauma-centre\/phenytoin-dilantin<\/a><\/sup><sup>[\/footnote]<\/sup>Serum levels of phenytoin sustained above the therapeutic range may produce confusional states referred to as delirium, psychosis, or encephalopathy. Accordingly, at the first sign of acute toxicity, serum levels should be immediately checked.\r\n\r\nAbrupt discontinuation can cause status epilepticus, so in the event of an allergic or hypersensitivity reaction, rapid substitution of alternative therapy may be necessary.\r\n\r\nUse with caution in clients with renal or hepatic impairment. Elderly clients may require dosage adjustment.\r\n\r\nThere are many potential drug interactions with phenytoin. Read drug label information before administering. Phenytoin is extensively bound to plasma proteins and is prone to competitive displacement. Phenytoin is metabolized by hepatic cytochrome P450 enzymes, so it is susceptible to inhibitory drug interactions, which may produce significant increases in circulating phenytoin concentrations and enhance the risk of drug toxicity.\r\n\r\n<strong>Adverse\/Side Effects<\/strong>\r\n\r\nSerious and sometimes fatal dermatologic reactions, including toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS), have been reported with phenytoin treatment. The onset of symptoms is usually within 28 days but can occur later. Phenytoin should be discontinued at the first sign of a rash.\r\n\r\n<strong>[pb_glossary id=\"648\"]Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)[\/pb_glossary]<\/strong> has been reported in clients taking antiepileptic drugs, including phenytoin. Some of these events have been fatal or life-threatening. DRESS typically presents with fever, rash, lymphadenopathy, and\/or facial swelling, in association with other organ system involvement. These findings should be immediately reported to the provider. Acute hepatotoxicity has been reported with phenytoin. These events may be part of the spectrum of DRESS or may occur in isolation.\r\n\r\nHematopoietic complications, some fatal, have occasionally been reported in association with the administration of phenytoin. These have included thrombocytopenia, leukopenia, granulocytopenia, agranulocytosis, and pancytopenia with or without bone marrow suppression.\r\n\r\nThe most common adverse reactions encountered with phenytoin therapy are nervous system reactions and are usually dose-related. Reactions include nystagmus, ataxia, slurred speech, decreased coordination, somnolence, and mental confusion.<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>\r\n\r\n<strong>Client Teaching &amp; Education<\/strong>\r\n\r\nClients should be advised to take medications as directed and that doses should be evenly spaced throughout the day.\u00a0 It may take several weeks to obtain the desired medication effect.\u00a0 Abrupt withdrawal of medication may cause status epilepticus. Clients should avoid alcohol and other CNS depressants while taking anticonvulsant drug therapy.\u00a0 Additionally, diabetic clients should monitor their blood glucose levels carefully.\r\n\r\nNow let's take a closer look at the medication grid for phenytoin in Table 8.10a.<span style=\"font-size: 12.8px\">[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>. <\/span><span style=\"font-size: 12.8px\">[\/footnote]<\/span>\r\n\r\nMedication cards like this are intended to assist students to learn key points about each medication. Because information about medication is constantly changing, nurses should always consult evidence-based resources to review current recommendations before administering specific medication. Basic information related to each class of medication is outlined below.\u00a0 Prototype or generic medication examples are also hyperlinked to a free resource at <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm\">Daily Med<\/a>. On the home page, enter the drug name in the search bar to read more about the medication.\r\n\r\nTable 8.10a <strong>\u00a0<\/strong><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=5b17816d-5b7f-4e4b-9471-30c93822afe8\">Phenytoin<\/a> Medication Card<sup style=\"text-align: initial\"><span style=\"text-align: initial\">[footnote] <\/span><\/sup><sup style=\"text-align: initial\"><span style=\"text-align: initial\">This work is a derivative of\u00a0 <\/span><a style=\"text-align: initial\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener\">Daily Med <\/a><span style=\"text-align: initial\">by\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener\">U.S. National Library of Medicine<\/a><span style=\"text-align: initial\">\u00a0in the\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener\">public domain<\/a><span style=\"text-align: initial\">.[\/footnote][footnote]RNPedia. (2021). <a href=\"https:\/\/www.rnpedia.com\">https:\/\/www.rnpedia.com<\/a>[\/footnote][footnote]OpenMD.Com at <a href=\"http:\/\/www.openmd.com\">www.openmd.com<\/a>[\/footnote][footnote]uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\">https:\/\/www.unboundmedicine.com\/ucentral<\/a>[\/footnote]\u00a0<\/span><\/sup>\r\n\r\n<img class=\"alignnone size-full wp-image-2331\" src=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin.png\" alt=\"\" width=\"2094\" height=\"662\" \/>\r\n<h3 style=\"text-align: center\">Levetiracetam<\/h3>\r\nLevetiracetam is indicated as adjunctive therapy in the treatment of partial-onset seizures in clients 12 years of age and older with epilepsy. It is generally well-tolerated.\r\n\r\n<strong>Mechanism of Action<\/strong>\r\n\r\nThe exact mechanism of action is unknown. This medication may interfere with sodium, calcium, potassium, or GABA transmission.<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>\r\n\r\n<strong>Indications for Use<\/strong>\r\n\r\nLevetiracetam is used for partial-onset seizures in clients with epilepsy.\r\n\r\n<strong>Nursing Considerations Across the Lifespan<\/strong>\r\n\r\nPlasma levels can gradually decrease during pregnancy and should be monitored closely. Safety and effectiveness in pediatric clients 12 years of age and older have been established.\r\n\r\nLevetiracetam immediate release and solution can be used in clients as young as 1 month.\r\n\r\nLevetiracetam should not be stopped abruptly or withdrawal seizures may occur. Use with caution in clients with renal impairment.\r\n\r\n<strong>Adverse\/Side Effects<\/strong>\r\n\r\nBehavioral abnormalities including psychotic symptoms, suicidal ideation, irritability, and aggressive behavior have been observed; monitor clients for psychiatric signs and symptoms.\r\n\r\nThe most common adverse reactions are somnolence and irritability. Advise clients not to drive or operate machinery until they have gained sufficient experience on levetiracetam.\r\n\r\nThis drug can cause anaphylaxis or angioedema after the first dose or at any time during treatment. Serious dermatological reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), have been reported, as well as coordination difficulties and hematologic abnormalities.\r\n\r\n<strong>Client Teaching &amp; Education<\/strong>\r\n\r\nMedications should be taken as directed and may cause increased dizziness and somnolence. Clients, family, and caregivers should also monitor carefully for suicidality during medication therapy.\r\n\r\nNow let's take a closer look at the medication grid for levetiracetam in Table 8.10b.<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>\r\n\r\nTable 8.10b <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=c508a392-0603-477d-8a45-3ec550371111\">Levetiracetam<\/a> Medication Grid <sup style=\"text-align: initial\"><span style=\"text-align: initial\">[footnote] <\/span><\/sup><sup style=\"text-align: initial\"><span style=\"text-align: initial\">This work is a derivative of\u00a0 <\/span><a style=\"text-align: initial\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener\">Daily Med <\/a><span style=\"text-align: initial\">by\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener\">U.S. National Library of Medicine<\/a><span style=\"text-align: initial\">\u00a0in the\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener\">public domain<\/a><span style=\"text-align: initial\">.[\/footnote][footnote]RNPedia. (2021). <a href=\"https:\/\/www.rnpedia.com\">https:\/\/www.rnpedia.com<\/a>[\/footnote][footnote]OpenMD.Com at <a href=\"http:\/\/www.openmd.com\">www.openmd.com<\/a>[\/footnote][footnote]uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\">https:\/\/www.unboundmedicine.com\/ucentral<\/a>[\/footnote]\u00a0<\/span><\/sup>\r\n\r\n<img class=\"alignnone size-full wp-image-2326\" src=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam.png\" alt=\"\" width=\"2094\" height=\"554\" \/>\r\n<h3>Gabapentin<\/h3>\r\nGabapentin is indicated as an adjunct treatment for partial seizures, but is most commonly used to treat neuropathic pain.<sup>[footnote]Lilley, L., Collins, S., &amp; Snyder, J. (2020). <em>Pharmacology and the Nursing Process.<\/em> pp. 246-272. Elsevier.[\/footnote]<\/sup>\r\n\r\n<strong>Mechanism of Action<\/strong>\r\n\r\nThe exact mechanism of action is unknown. It is structurally similar to GABA, but does not act on GABA receptors or influence GABA.\r\n\r\n<strong>Indications for Use<\/strong>\r\n\r\nGabapentin is used for partial seizures and neuropathic pain.\r\n\r\n<strong>Nursing Considerations Across the Lifespan<\/strong>\r\n\r\nThis drug can cause harm to the fetus of pregnant women.\r\n\r\nGabapentin use in pediatric clients with epilepsy 3 to 12 years of age is associated with the occurrence of central nervous system-related adverse events. The most significant of these can be classified into the following categories: 1) emotional lability (primarily behavioral problems); 2) hostility, including aggressive behaviors; 3) thought disorder, including concentration problems and change in school performance; and 4) hyperkinesia (primarily restlessness and hyperactivity).\r\n\r\nIn elderly clients, peripheral edema and ataxia tends to increase in incidence with age. Fall precautions should be considered.\r\n\r\nAntiepileptic drugs should not be abruptly discontinued because of the possibility of increasing seizure frequency.\r\n\r\n<strong>Adverse\/Side Effects<\/strong>\r\n\r\nAntiepileptic drugs, including gabapentin, increase the risk of suicidal thoughts or behavior in clients taking these drugs for any indication. Clients should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and\/or any unusual changes in mood or behavior.\r\n\r\nDrug Reaction with Eosinophilia and Systemic Symptoms (DRESS), also known as multiorgan hypersensitivity, has been reported in clients taking antiepileptic drugs, including gabapentin. Some of these events have been fatal or life-threatening. DRESS typically, although not exclusively, presents with fever, rash, and\/or lymphadenopathy, in association with other organ system involvement. If these symptoms occur, they should be immediately reported to the provider.\r\n\r\nGabapentin may cause dizziness, somnolence, and other symptoms and signs of CNS depression. Clients should be advised neither to drive a car nor to operate other complex machinery until they have gained sufficient experience on gabapentin to gauge whether or not it affects their mental and\/or motor performance adversely.<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>\r\n\r\n<strong>Client Teaching &amp; Education<\/strong>\r\n\r\nClients receiving gabapentin therapy should take medication as directed and be careful not to exceed dosage recommendations. Clients should not take gabapentin within 2 hours of antacid medications. Additionally, gabapentin may cause increased drowsiness and dizziness. Clients, family, and caregivers should also monitor for suicidality.\r\n\r\nNow let's take a closer look at the medication grid for gabapentin in Table 8.10c.<sup>[footnote]This work is a derivative of\u00a0<a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a>\u00a0by\u00a0<a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a>\u00a0in the\u00a0<a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>.\u00a0\u00a0[\/footnote]<\/sup>\r\n\r\nTable 8.10c <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f2d9c3de-4749-4265-a26e-50026ab46ee4\">Gabapentin<\/a> Medication Card <sup style=\"text-align: initial\"><span style=\"text-align: initial\">[footnote] <\/span><\/sup><sup style=\"text-align: initial\"><span style=\"text-align: initial\">This work is a derivative of\u00a0 <\/span><a style=\"text-align: initial\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener\">Daily Med <\/a><span style=\"text-align: initial\">by\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener\">U.S. National Library of Medicine<\/a><span style=\"text-align: initial\">\u00a0in the\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener\">public domain<\/a><span style=\"text-align: initial\">.[\/footnote][footnote]RNPedia. (2021). <a href=\"https:\/\/www.rnpedia.com\">https:\/\/www.rnpedia.com<\/a>[\/footnote][footnote]OpenMD.Com at <a href=\"http:\/\/www.openmd.com\">www.openmd.com<\/a>[\/footnote][footnote]uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\">https:\/\/www.unboundmedicine.com\/ucentral<\/a>[\/footnote]\u00a0<\/span><\/sup>\r\n\r\n<img class=\"alignnone size-full wp-image-2325\" src=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin.png\" alt=\"\" width=\"2094\" height=\"740\" \/>\r\n\r\n<\/div>\r\n<div class=\"__UNKNOWN__\">\r\n<div class=\"textbox textbox--examples\"><header class=\"textbox__header\">\r\n<h2>Clinical Reasoning and Decision-Making Activity 8.10<img class=\"alignright wp-image-197\" title=\"&quot;Lightbulb&quot; by Saperaud-commonswiki is licensed under CC BY SA 3.0.\" src=\"https:\/\/pressbooks.bccampus.ca\/knowinghome\/wp-content\/uploads\/sites\/1167\/2019\/09\/ORN-Icons_lightbulb-300x300-1.png\" alt=\"Image of lightbulb in a circle\" width=\"200\" height=\"200\" \/><\/h2>\r\n<\/header>\r\n<div class=\"textbox__content\" style=\"text-align: left\">\r\n\r\nA 70-year-client in a long-term care center has diabetes and has been prescribed gabapentin for neuropathic pain.\r\n\r\n1. The client states, \u201cI have never had a seizure. Why has the doctor prescribed an antiseizure medication for me?\u201d What is the nurse\u2019s best response?\r\n\r\n2. The nurse plans to implement additional fall precautions for this client. Why are additional fall precautions needed?\r\n\r\n3. What potential adverse effects should the nurse plan to monitor? What adverse effects would require immediate notification of the provider?\r\n\r\nNote: Answers to the Critical Thinking activities can be found in the \"<a href=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/chapter\/chapter-8\/\">Answer Key<\/a>\" sections at the end of the book.\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>","rendered":"<div class=\"1.10-anticonvulsants-\">\n<p>Medications used for seizures are called anticonvulsants or antiseizure drugs. Antiseizure drugs stabilize cell membranes and suppress the abnormal electric impulses in the cerebral cortex. These drugs prevent seizures but do not provide a cure. Antiseizure drugs are classified as CNS depressants. There are many types of medications used to treat seizures such as phenytoin, phenobarbital, benzodiazepines, carbamazepine, valproate, and levetiracetam.<sup><a class=\"footnote\" title=\"McCuistion, L., Vuljoin-DiMaggio, K., Winton, M, &amp; Yeager, J. (2018). Pharmacology: A patient-centered nursing process approach. pp. 227-305. Elsevier.\" id=\"return-footnote-357-1\" href=\"#footnote-357-1\" aria-label=\"Footnote 1\"><sup class=\"footnote\">[1]<\/sup><\/a><\/sup><\/p>\n<p>There are three main pharmacological effects of antiseizure medications. First, they increase the threshold of activity in the motor cortex, thus making it more difficult for a nerve to become excited. Second, they limit the spread of a seizure discharge from its origin by suppressing the transmission of impulses from one nerve to the next. Third, they decrease the speed of the nerve impulse conduction within a given neuron.<\/p>\n<p>Some drugs work by enhancing the effects of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA), which plays a role in regulating neuron excitability in the brain.<sup><a class=\"footnote\" title=\"Lilley, L., Collins, S., &amp; Snyder, J. (2020). Pharmacology and the Nursing Process. pp. 246-272. Elsevier.\" id=\"return-footnote-357-2\" href=\"#footnote-357-2\" aria-label=\"Footnote 2\"><sup class=\"footnote\">[2]<\/sup><\/a><\/sup> Gabapentin, although structurally similar to GABA and classified as an anticonvulsant, is commonly used to control chronic neuropathic pain. Neuropathic pain is defined by the International Association for the Study of Pain as \u201cpain caused by a lesion or disease of the somatosensory nervous system.\u201d<sup><a class=\"footnote\" title=\"Murnion B. P. (2018, June 1). Neuropathic pain: current definition and review of drug treatment. Australian prescriber, 41(3), 60\u201363. https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6003018\/\" id=\"return-footnote-357-3\" href=\"#footnote-357-3\" aria-label=\"Footnote 3\"><sup class=\"footnote\">[3]<\/sup><\/a><\/sup> An example of neuropathic pain is tingling or burning in the lower extremities that often occurs in clients with diabetes.<\/p>\n<h3>Phenytoin<\/h3>\n<p>Phenytoin, which was discovered in 1938, was the first anti-seizure medication and is still being used to control seizures.<sup><a class=\"footnote\" title=\"McCuistion, L., Vuljoin-DiMaggio, K., Winton, M, &amp; Yeager, J. (2018). Pharmacology: A patient-centered nursing process approach. pp. 227-305. Elsevier.\" id=\"return-footnote-357-4\" href=\"#footnote-357-4\" aria-label=\"Footnote 4\"><sup class=\"footnote\">[4]<\/sup><\/a><\/sup><\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>Phenytoin improves evidence of seizures by interfering with sodium channels in the brain, resulting in a reduction of sustained high-frequency neuronal discharges.<\/p>\n<p><strong>Indications for Use<\/strong><\/p>\n<p>Phenytoin is indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and for the prevention and treatment of seizures occurring during or following neurosurgery.<\/p>\n<p><strong>Nursing Considerations Across the Lifespan<\/strong><\/p>\n<p>Phenytoin should not be administered to pregnant women because it will cause harm to the fetus. When given intravenously, there is a Black Box Warning that the rate of administration should not exceed 50 mg per minute in adults and 1 to 3 mg\/kg\/min (or 50 mg per minute, whichever is slower) in pediatric clients because of the risk of severe hypotension and cardiac arrhythmias. Careful cardiac monitoring is needed during and after administering intravenous phenytoin.<\/p>\n<p>Phenytoin has a narrow therapeutic drug level, usually between 40 &#8211; 80 uM\/L, so serum drug monitoring is required.<sup><a class=\"footnote\" title=\"London Health Science Center. (2021). Phenytoin.\u00a0https:\/\/www.lhsc.on.ca\/critical-care-trauma-centre\/phenytoin-dilantin\" id=\"return-footnote-357-5\" href=\"#footnote-357-5\" aria-label=\"Footnote 5\"><sup class=\"footnote\">[5]<\/sup><\/a><\/sup>Serum levels of phenytoin sustained above the therapeutic range may produce confusional states referred to as delirium, psychosis, or encephalopathy. Accordingly, at the first sign of acute toxicity, serum levels should be immediately checked.<\/p>\n<p>Abrupt discontinuation can cause status epilepticus, so in the event of an allergic or hypersensitivity reaction, rapid substitution of alternative therapy may be necessary.<\/p>\n<p>Use with caution in clients with renal or hepatic impairment. Elderly clients may require dosage adjustment.<\/p>\n<p>There are many potential drug interactions with phenytoin. Read drug label information before administering. Phenytoin is extensively bound to plasma proteins and is prone to competitive displacement. Phenytoin is metabolized by hepatic cytochrome P450 enzymes, so it is susceptible to inhibitory drug interactions, which may produce significant increases in circulating phenytoin concentrations and enhance the risk of drug toxicity.<\/p>\n<p><strong>Adverse\/Side Effects<\/strong><\/p>\n<p>Serious and sometimes fatal dermatologic reactions, including toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS), have been reported with phenytoin treatment. The onset of symptoms is usually within 28 days but can occur later. Phenytoin should be discontinued at the first sign of a rash.<\/p>\n<p><strong><a class=\"glossary-term\" aria-haspopup=\"dialog\" aria-describedby=\"definition\" href=\"#term_357_648\">Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)<\/a><\/strong> has been reported in clients taking antiepileptic drugs, including phenytoin. Some of these events have been fatal or life-threatening. DRESS typically presents with fever, rash, lymphadenopathy, and\/or facial swelling, in association with other organ system involvement. These findings should be immediately reported to the provider. Acute hepatotoxicity has been reported with phenytoin. These events may be part of the spectrum of DRESS or may occur in isolation.<\/p>\n<p>Hematopoietic complications, some fatal, have occasionally been reported in association with the administration of phenytoin. These have included thrombocytopenia, leukopenia, granulocytopenia, agranulocytosis, and pancytopenia with or without bone marrow suppression.<\/p>\n<p>The most common adverse reactions encountered with phenytoin therapy are nervous system reactions and are usually dose-related. Reactions include nystagmus, ataxia, slurred speech, decreased coordination, somnolence, and mental confusion.<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-357-6\" href=\"#footnote-357-6\" aria-label=\"Footnote 6\"><sup class=\"footnote\">[6]<\/sup><\/a><\/sup><\/p>\n<p><strong>Client Teaching &amp; Education<\/strong><\/p>\n<p>Clients should be advised to take medications as directed and that doses should be evenly spaced throughout the day.\u00a0 It may take several weeks to obtain the desired medication effect.\u00a0 Abrupt withdrawal of medication may cause status epilepticus. Clients should avoid alcohol and other CNS depressants while taking anticonvulsant drug therapy.\u00a0 Additionally, diabetic clients should monitor their blood glucose levels carefully.<\/p>\n<p>Now let&#8217;s take a closer look at the medication grid for phenytoin in Table 8.10a.<span style=\"font-size: 12.8px\"><a class=\"footnote\" title=\"This work is a derivative of Daily Med by U.S. National Library of Medicine in the public domain.\" id=\"return-footnote-357-7\" href=\"#footnote-357-7\" aria-label=\"Footnote 7\"><sup class=\"footnote\">[7]<\/sup><\/a><\/span><\/p>\n<p>Medication cards like this are intended to assist students to learn key points about each medication. Because information about medication is constantly changing, nurses should always consult evidence-based resources to review current recommendations before administering specific medication. Basic information related to each class of medication is outlined below.\u00a0 Prototype or generic medication examples are also hyperlinked to a free resource at <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/index.cfm\">Daily Med<\/a>. On the home page, enter the drug name in the search bar to read more about the medication.<\/p>\n<p>Table 8.10a <strong>\u00a0<\/strong><a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=5b17816d-5b7f-4e4b-9471-30c93822afe8\">Phenytoin<\/a> Medication Card<sup style=\"text-align: initial\"><span style=\"text-align: initial\"><a class=\"footnote\" title=\"This work is a derivative of\u00a0 Daily Med by\u00a0U.S. National Library of Medicine\u00a0in the\u00a0public domain.\" id=\"return-footnote-357-8\" href=\"#footnote-357-8\" aria-label=\"Footnote 8\"><sup class=\"footnote\">[8]<\/sup><\/a><a class=\"footnote\" title=\"RNPedia. (2021). https:\/\/www.rnpedia.com\" id=\"return-footnote-357-9\" href=\"#footnote-357-9\" aria-label=\"Footnote 9\"><sup class=\"footnote\">[9]<\/sup><\/a><a class=\"footnote\" title=\"OpenMD.Com at www.openmd.com\" id=\"return-footnote-357-10\" href=\"#footnote-357-10\" aria-label=\"Footnote 10\"><sup class=\"footnote\">[10]<\/sup><\/a><a class=\"footnote\" title=\"uCentral from Unbound Medicine. https:\/\/www.unboundmedicine.com\/ucentral\" id=\"return-footnote-357-11\" href=\"#footnote-357-11\" aria-label=\"Footnote 11\"><sup class=\"footnote\">[11]<\/sup><\/a>\u00a0<\/span><\/sup><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2331\" src=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin.png\" alt=\"\" width=\"2094\" height=\"662\" srcset=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin.png 2094w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-300x95.png 300w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-1024x324.png 1024w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-768x243.png 768w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-1536x486.png 1536w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-2048x647.png 2048w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-65x21.png 65w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-225x71.png 225w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/phenytoin-350x111.png 350w\" sizes=\"auto, (max-width: 2094px) 100vw, 2094px\" \/><\/p>\n<h3 style=\"text-align: center\">Levetiracetam<\/h3>\n<p>Levetiracetam is indicated as adjunctive therapy in the treatment of partial-onset seizures in clients 12 years of age and older with epilepsy. It is generally well-tolerated.<\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>The exact mechanism of action is unknown. This medication may interfere with sodium, calcium, potassium, or GABA transmission.<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-357-12\" href=\"#footnote-357-12\" aria-label=\"Footnote 12\"><sup class=\"footnote\">[12]<\/sup><\/a><\/sup><\/p>\n<p><strong>Indications for Use<\/strong><\/p>\n<p>Levetiracetam is used for partial-onset seizures in clients with epilepsy.<\/p>\n<p><strong>Nursing Considerations Across the Lifespan<\/strong><\/p>\n<p>Plasma levels can gradually decrease during pregnancy and should be monitored closely. Safety and effectiveness in pediatric clients 12 years of age and older have been established.<\/p>\n<p>Levetiracetam immediate release and solution can be used in clients as young as 1 month.<\/p>\n<p>Levetiracetam should not be stopped abruptly or withdrawal seizures may occur. Use with caution in clients with renal impairment.<\/p>\n<p><strong>Adverse\/Side Effects<\/strong><\/p>\n<p>Behavioral abnormalities including psychotic symptoms, suicidal ideation, irritability, and aggressive behavior have been observed; monitor clients for psychiatric signs and symptoms.<\/p>\n<p>The most common adverse reactions are somnolence and irritability. Advise clients not to drive or operate machinery until they have gained sufficient experience on levetiracetam.<\/p>\n<p>This drug can cause anaphylaxis or angioedema after the first dose or at any time during treatment. Serious dermatological reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), have been reported, as well as coordination difficulties and hematologic abnormalities.<\/p>\n<p><strong>Client Teaching &amp; Education<\/strong><\/p>\n<p>Medications should be taken as directed and may cause increased dizziness and somnolence. Clients, family, and caregivers should also monitor carefully for suicidality during medication therapy.<\/p>\n<p>Now let&#8217;s take a closer look at the medication grid for levetiracetam in Table 8.10b.<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-357-13\" href=\"#footnote-357-13\" aria-label=\"Footnote 13\"><sup class=\"footnote\">[13]<\/sup><\/a><\/sup><\/p>\n<p>Table 8.10b <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=c508a392-0603-477d-8a45-3ec550371111\">Levetiracetam<\/a> Medication Grid <sup style=\"text-align: initial\"><span style=\"text-align: initial\"><a class=\"footnote\" title=\"This work is a derivative of\u00a0 Daily Med by\u00a0U.S. National Library of Medicine\u00a0in the\u00a0public domain.\" id=\"return-footnote-357-14\" href=\"#footnote-357-14\" aria-label=\"Footnote 14\"><sup class=\"footnote\">[14]<\/sup><\/a><a class=\"footnote\" title=\"RNPedia. (2021). https:\/\/www.rnpedia.com\" id=\"return-footnote-357-15\" href=\"#footnote-357-15\" aria-label=\"Footnote 15\"><sup class=\"footnote\">[15]<\/sup><\/a><a class=\"footnote\" title=\"OpenMD.Com at www.openmd.com\" id=\"return-footnote-357-16\" href=\"#footnote-357-16\" aria-label=\"Footnote 16\"><sup class=\"footnote\">[16]<\/sup><\/a><a class=\"footnote\" title=\"uCentral from Unbound Medicine. https:\/\/www.unboundmedicine.com\/ucentral\" id=\"return-footnote-357-17\" href=\"#footnote-357-17\" aria-label=\"Footnote 17\"><sup class=\"footnote\">[17]<\/sup><\/a>\u00a0<\/span><\/sup><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2326\" src=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam.png\" alt=\"\" width=\"2094\" height=\"554\" srcset=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam.png 2094w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-300x79.png 300w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-1024x271.png 1024w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-768x203.png 768w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-1536x406.png 1536w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-2048x542.png 2048w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-65x17.png 65w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-225x60.png 225w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/levetiracetam-350x93.png 350w\" sizes=\"auto, (max-width: 2094px) 100vw, 2094px\" \/><\/p>\n<h3>Gabapentin<\/h3>\n<p>Gabapentin is indicated as an adjunct treatment for partial seizures, but is most commonly used to treat neuropathic pain.<sup><a class=\"footnote\" title=\"Lilley, L., Collins, S., &amp; Snyder, J. (2020). Pharmacology and the Nursing Process. pp. 246-272. Elsevier.\" id=\"return-footnote-357-18\" href=\"#footnote-357-18\" aria-label=\"Footnote 18\"><sup class=\"footnote\">[18]<\/sup><\/a><\/sup><\/p>\n<p><strong>Mechanism of Action<\/strong><\/p>\n<p>The exact mechanism of action is unknown. It is structurally similar to GABA, but does not act on GABA receptors or influence GABA.<\/p>\n<p><strong>Indications for Use<\/strong><\/p>\n<p>Gabapentin is used for partial seizures and neuropathic pain.<\/p>\n<p><strong>Nursing Considerations Across the Lifespan<\/strong><\/p>\n<p>This drug can cause harm to the fetus of pregnant women.<\/p>\n<p>Gabapentin use in pediatric clients with epilepsy 3 to 12 years of age is associated with the occurrence of central nervous system-related adverse events. The most significant of these can be classified into the following categories: 1) emotional lability (primarily behavioral problems); 2) hostility, including aggressive behaviors; 3) thought disorder, including concentration problems and change in school performance; and 4) hyperkinesia (primarily restlessness and hyperactivity).<\/p>\n<p>In elderly clients, peripheral edema and ataxia tends to increase in incidence with age. Fall precautions should be considered.<\/p>\n<p>Antiepileptic drugs should not be abruptly discontinued because of the possibility of increasing seizure frequency.<\/p>\n<p><strong>Adverse\/Side Effects<\/strong><\/p>\n<p>Antiepileptic drugs, including gabapentin, increase the risk of suicidal thoughts or behavior in clients taking these drugs for any indication. Clients should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and\/or any unusual changes in mood or behavior.<\/p>\n<p>Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS), also known as multiorgan hypersensitivity, has been reported in clients taking antiepileptic drugs, including gabapentin. Some of these events have been fatal or life-threatening. DRESS typically, although not exclusively, presents with fever, rash, and\/or lymphadenopathy, in association with other organ system involvement. If these symptoms occur, they should be immediately reported to the provider.<\/p>\n<p>Gabapentin may cause dizziness, somnolence, and other symptoms and signs of CNS depression. Clients should be advised neither to drive a car nor to operate other complex machinery until they have gained sufficient experience on gabapentin to gauge whether or not it affects their mental and\/or motor performance adversely.<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-357-19\" href=\"#footnote-357-19\" aria-label=\"Footnote 19\"><sup class=\"footnote\">[19]<\/sup><\/a><\/sup><\/p>\n<p><strong>Client Teaching &amp; Education<\/strong><\/p>\n<p>Clients receiving gabapentin therapy should take medication as directed and be careful not to exceed dosage recommendations. Clients should not take gabapentin within 2 hours of antacid medications. Additionally, gabapentin may cause increased drowsiness and dizziness. Clients, family, and caregivers should also monitor for suicidality.<\/p>\n<p>Now let&#8217;s take a closer look at the medication grid for gabapentin in Table 8.10c.<sup><a class=\"footnote\" title=\"This work is a derivative of\u00a0Daily Med\u00a0by\u00a0U.S. National Library of Medicine\u00a0in the\u00a0public domain.\u00a0\u00a0\" id=\"return-footnote-357-20\" href=\"#footnote-357-20\" aria-label=\"Footnote 20\"><sup class=\"footnote\">[20]<\/sup><\/a><\/sup><\/p>\n<p>Table 8.10c <a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/drugInfo.cfm?setid=f2d9c3de-4749-4265-a26e-50026ab46ee4\">Gabapentin<\/a> Medication Card <sup style=\"text-align: initial\"><span style=\"text-align: initial\"><a class=\"footnote\" title=\"This work is a derivative of\u00a0 Daily Med by\u00a0U.S. National Library of Medicine\u00a0in the\u00a0public domain.\" id=\"return-footnote-357-21\" href=\"#footnote-357-21\" aria-label=\"Footnote 21\"><sup class=\"footnote\">[21]<\/sup><\/a><a class=\"footnote\" title=\"RNPedia. (2021). https:\/\/www.rnpedia.com\" id=\"return-footnote-357-22\" href=\"#footnote-357-22\" aria-label=\"Footnote 22\"><sup class=\"footnote\">[22]<\/sup><\/a><a class=\"footnote\" title=\"OpenMD.Com at www.openmd.com\" id=\"return-footnote-357-23\" href=\"#footnote-357-23\" aria-label=\"Footnote 23\"><sup class=\"footnote\">[23]<\/sup><\/a><a class=\"footnote\" title=\"uCentral from Unbound Medicine. https:\/\/www.unboundmedicine.com\/ucentral\" id=\"return-footnote-357-24\" href=\"#footnote-357-24\" aria-label=\"Footnote 24\"><sup class=\"footnote\">[24]<\/sup><\/a>\u00a0<\/span><\/sup><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-2325\" src=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin.png\" alt=\"\" width=\"2094\" height=\"740\" srcset=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin.png 2094w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-300x106.png 300w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-1024x362.png 1024w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-768x271.png 768w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-1536x543.png 1536w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-2048x724.png 2048w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-65x23.png 65w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-225x80.png 225w, https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-content\/uploads\/sites\/1167\/2019\/11\/gabapentin-350x124.png 350w\" sizes=\"auto, (max-width: 2094px) 100vw, 2094px\" \/><\/p>\n<\/div>\n<div class=\"__UNKNOWN__\">\n<div class=\"textbox textbox--examples\">\n<header class=\"textbox__header\">\n<h2>Clinical Reasoning and Decision-Making Activity 8.10<img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-197\" title=\"&quot;Lightbulb&quot; by Saperaud-commonswiki is licensed under CC BY SA 3.0.\" src=\"https:\/\/pressbooks.bccampus.ca\/knowinghome\/wp-content\/uploads\/sites\/1167\/2019\/09\/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 70-year-client in a long-term care center has diabetes and has been prescribed gabapentin for neuropathic pain.<\/p>\n<p>1. The client states, \u201cI have never had a seizure. Why has the doctor prescribed an antiseizure medication for me?\u201d What is the nurse\u2019s best response?<\/p>\n<p>2. The nurse plans to implement additional fall precautions for this client. Why are additional fall precautions needed?<\/p>\n<p>3. What potential adverse effects should the nurse plan to monitor? What adverse effects would require immediate notification of the provider?<\/p>\n<p>Note: Answers to the Critical Thinking activities can be found in the &#8220;<a href=\"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/chapter\/chapter-8\/\">Answer Key<\/a>&#8221; sections at the end of the book.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"media-attributions clear\" prefix:cc=\"http:\/\/creativecommons.org\/ns#\" prefix:dc=\"http:\/\/purl.org\/dc\/terms\/\"><h2>Media Attributions<\/h2><ul><li >phenytoin       <\/li><li >levetiracetam       <\/li><li >gabapentin       <\/li><\/ul><\/div><hr class=\"before-footnotes clear\" \/><div class=\"footnotes\"><ol><li id=\"footnote-357-1\">McCuistion, L., Vuljoin-DiMaggio, K., Winton, M, &amp; Yeager, J. (2018). <em>Pharmacology: A patient-centered nursing process approach.<\/em> pp. 227-305. Elsevier. <a href=\"#return-footnote-357-1\" class=\"return-footnote\" aria-label=\"Return to footnote 1\">&crarr;<\/a><\/li><li id=\"footnote-357-2\">Lilley, L., Collins, S., &amp; Snyder, J. (2020). <em>Pharmacology and the Nursing Process.<\/em> pp. 246-272. Elsevier. <a href=\"#return-footnote-357-2\" class=\"return-footnote\" aria-label=\"Return to footnote 2\">&crarr;<\/a><\/li><li id=\"footnote-357-3\">Murnion B. P. (2018, June 1). Neuropathic pain: current definition and review of drug treatment. <em>Australian prescriber, 41<\/em>(3), 60\u201363. <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6003018\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC6003018\/<\/a> <a href=\"#return-footnote-357-3\" class=\"return-footnote\" aria-label=\"Return to footnote 3\">&crarr;<\/a><\/li><li id=\"footnote-357-4\">McCuistion, L., Vuljoin-DiMaggio, K., Winton, M, &amp; Yeager, J. (2018). <em>Pharmacology: A patient-centered nursing process approach.<\/em> pp. 227-305. Elsevier. <a href=\"#return-footnote-357-4\" class=\"return-footnote\" aria-label=\"Return to footnote 4\">&crarr;<\/a><\/li><li id=\"footnote-357-5\">London Health Science Center. (2021). Phenytoin.\u00a0<a href=\"https:\/\/www.lhsc.on.ca\/critical-care-trauma-centre\/phenytoin-dilantin\">https:\/\/www.lhsc.on.ca\/critical-care-trauma-centre\/phenytoin-dilantin<\/a><\/sup><sup> <a href=\"#return-footnote-357-5\" class=\"return-footnote\" aria-label=\"Return to footnote 5\">&crarr;<\/a><\/li><li id=\"footnote-357-6\">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-357-6\" class=\"return-footnote\" aria-label=\"Return to footnote 6\">&crarr;<\/a><\/li><li id=\"footnote-357-7\">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>. <\/span><span style=\"font-size: 12.8px\"> <a href=\"#return-footnote-357-7\" class=\"return-footnote\" aria-label=\"Return to footnote 7\">&crarr;<\/a><\/li><li id=\"footnote-357-8\"> <\/span><\/sup><sup style=\"text-align: initial\"><span style=\"text-align: initial\">This work is a derivative of\u00a0 <\/span><a style=\"text-align: initial\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener\">Daily Med <\/a><span style=\"text-align: initial\">by\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener\">U.S. National Library of Medicine<\/a><span style=\"text-align: initial\">\u00a0in the\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener\">public domain<\/a><span style=\"text-align: initial\">. <a href=\"#return-footnote-357-8\" class=\"return-footnote\" aria-label=\"Return to footnote 8\">&crarr;<\/a><\/li><li id=\"footnote-357-9\">RNPedia. (2021). <a href=\"https:\/\/www.rnpedia.com\">https:\/\/www.rnpedia.com<\/a> <a href=\"#return-footnote-357-9\" class=\"return-footnote\" aria-label=\"Return to footnote 9\">&crarr;<\/a><\/li><li id=\"footnote-357-10\">OpenMD.Com at <a href=\"http:\/\/www.openmd.com\">www.openmd.com<\/a> <a href=\"#return-footnote-357-10\" class=\"return-footnote\" aria-label=\"Return to footnote 10\">&crarr;<\/a><\/li><li id=\"footnote-357-11\">uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\">https:\/\/www.unboundmedicine.com\/ucentral<\/a> <a href=\"#return-footnote-357-11\" class=\"return-footnote\" aria-label=\"Return to footnote 11\">&crarr;<\/a><\/li><li id=\"footnote-357-12\">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-357-12\" class=\"return-footnote\" aria-label=\"Return to footnote 12\">&crarr;<\/a><\/li><li id=\"footnote-357-13\">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-357-13\" class=\"return-footnote\" aria-label=\"Return to footnote 13\">&crarr;<\/a><\/li><li id=\"footnote-357-14\"> <\/span><\/sup><sup style=\"text-align: initial\"><span style=\"text-align: initial\">This work is a derivative of\u00a0 <\/span><a style=\"text-align: initial\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener\">Daily Med <\/a><span style=\"text-align: initial\">by\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener\">U.S. National Library of Medicine<\/a><span style=\"text-align: initial\">\u00a0in the\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener\">public domain<\/a><span style=\"text-align: initial\">. <a href=\"#return-footnote-357-14\" class=\"return-footnote\" aria-label=\"Return to footnote 14\">&crarr;<\/a><\/li><li id=\"footnote-357-15\">RNPedia. (2021). <a href=\"https:\/\/www.rnpedia.com\">https:\/\/www.rnpedia.com<\/a> <a href=\"#return-footnote-357-15\" class=\"return-footnote\" aria-label=\"Return to footnote 15\">&crarr;<\/a><\/li><li id=\"footnote-357-16\">OpenMD.Com at <a href=\"http:\/\/www.openmd.com\">www.openmd.com<\/a> <a href=\"#return-footnote-357-16\" class=\"return-footnote\" aria-label=\"Return to footnote 16\">&crarr;<\/a><\/li><li id=\"footnote-357-17\">uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\">https:\/\/www.unboundmedicine.com\/ucentral<\/a> <a href=\"#return-footnote-357-17\" class=\"return-footnote\" aria-label=\"Return to footnote 17\">&crarr;<\/a><\/li><li id=\"footnote-357-18\">Lilley, L., Collins, S., &amp; Snyder, J. (2020). <em>Pharmacology and the Nursing Process.<\/em> pp. 246-272. Elsevier. <a href=\"#return-footnote-357-18\" class=\"return-footnote\" aria-label=\"Return to footnote 18\">&crarr;<\/a><\/li><li id=\"footnote-357-19\">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-357-19\" class=\"return-footnote\" aria-label=\"Return to footnote 19\">&crarr;<\/a><\/li><li id=\"footnote-357-20\">This work is a derivative of\u00a0<a href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener noreferrer\">Daily Med<\/a>\u00a0by\u00a0<a href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">U.S. National Library of Medicine<\/a>\u00a0in the\u00a0<a href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener noreferrer\">public domain<\/a>.\u00a0\u00a0 <a href=\"#return-footnote-357-20\" class=\"return-footnote\" aria-label=\"Return to footnote 20\">&crarr;<\/a><\/li><li id=\"footnote-357-21\"> <\/span><\/sup><sup style=\"text-align: initial\"><span style=\"text-align: initial\">This work is a derivative of\u00a0 <\/span><a style=\"text-align: initial\" href=\"https:\/\/dailymed.nlm.nih.gov\/dailymed\/\" target=\"_blank\" rel=\"noopener\">Daily Med <\/a><span style=\"text-align: initial\">by\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/www.nlm.nih.gov\/\" target=\"_blank\" rel=\"noopener\">U.S. National Library of Medicine<\/a><span style=\"text-align: initial\">\u00a0in the\u00a0<\/span><a style=\"text-align: initial\" href=\"https:\/\/creativecommons.org\/share-your-work\/public-domain\/\" target=\"_blank\" rel=\"noopener\">public domain<\/a><span style=\"text-align: initial\">. <a href=\"#return-footnote-357-21\" class=\"return-footnote\" aria-label=\"Return to footnote 21\">&crarr;<\/a><\/li><li id=\"footnote-357-22\">RNPedia. (2021). <a href=\"https:\/\/www.rnpedia.com\">https:\/\/www.rnpedia.com<\/a> <a href=\"#return-footnote-357-22\" class=\"return-footnote\" aria-label=\"Return to footnote 22\">&crarr;<\/a><\/li><li id=\"footnote-357-23\">OpenMD.Com at <a href=\"http:\/\/www.openmd.com\">www.openmd.com<\/a> <a href=\"#return-footnote-357-23\" class=\"return-footnote\" aria-label=\"Return to footnote 23\">&crarr;<\/a><\/li><li id=\"footnote-357-24\">uCentral from Unbound Medicine. <a href=\"https:\/\/www.unboundmedicine.com\/ucentral\">https:\/\/www.unboundmedicine.com\/ucentral<\/a> <a href=\"#return-footnote-357-24\" 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_357_648\"><div class=\"glossary__definition\" role=\"dialog\" data-id=\"term_357_648\"><div tabindex=\"-1\"><p><strong>Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS):<\/strong> A condition reported in patients taking antiepileptic drugs. Some of these events have been fatal or life-threatening. DRESS typically presents with fever, rash, lymphadenopathy, and\/or facial swelling.<\/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":103,"menu_order":10,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":["open-resources-for-nursing-open-rn"],"pb_section_license":""},"chapter-type":[48],"contributor":[68],"license":[],"class_list":["post-357","chapter","type-chapter","status-publish","hentry","chapter-type-numberless","contributor-open-resources-for-nursing-open-rn"],"part":331,"_links":{"self":[{"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/357","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/wp\/v2\/users\/103"}],"version-history":[{"count":10,"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/357\/revisions"}],"predecessor-version":[{"id":2388,"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/357\/revisions\/2388"}],"part":[{"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/parts\/331"}],"metadata":[{"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapters\/357\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/wp\/v2\/media?parent=357"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/pressbooks\/v2\/chapter-type?post=357"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/wp\/v2\/contributor?post=357"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/nursingpharmacology\/wp-json\/wp\/v2\/license?post=357"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}