Nursing Process Focus: Patients Receiving Phenobarbital (Luminal) Assessment Potential Nursing Diagnoses Prior to administration: Sensory perception, Disturbed related to effects of drug. Obtain complete health history, including allergies, neurological, pulmonary, cardiac, Injury, Risk for, related to seizure renal, biliary, and mental disorders activity including blood studies: CBC, BUN, Nutrition: less than body requirements, creatinine, electrolytes, PT, PTT, liver Imbalanced, related to vitamin enzymes, etc. deficiency Obtain patient’s drug history to determine Knowledge, Deficient related to newly possible drug interactions and allergies prescribed drug. Assess neurological status, including Sleep Pattern, Disturbed. related to identification of recent seizure activity. medication induced somnolence Planning: Patient Goals and Expected Outcomes Patient will Experience the absence of, or reduction in the number or severity of, seizures. Avoid physical injury related to seizure activity or medication induced somnolence Demonstrate understanding of the drug's action by accurately describing drug effects and precautions. Implementation Interventions and (Rationales) Monitor vital signs, especially blood pressure and depth and rate of respirations. (Because phenobarbital produces sedation, respiratory depression occurs.) Keep resuscitative equipment accessible (Phenobarbital may produce laryngospasm) Perform neuro-checks regularly, including level of consciousness (LOC), according to unit protocol. Excessive somnolence may occur. Observe for persistent seizures. Patient Education/Discharge Planning Instruct the patient to: monitor vital signs regularly, particularly blood pressure and respirations. withhold medication for any difficulty in breathing or respirations below 12 breaths per minute. Instruct the patient to: Report any significant change in sensorium: lethargy, stupor, or auras, visual changes and other effects that may indicate an impending seizure. Report dizziness which may indicate hypotension. Monitor response to and effectiveness of drug therapy Ensure patient safety by monitoring ambulation until response of the drug is known. Elevate bed rails; place call bell within patient's reach. Monitor for adverse reactions, especially due to CNS depression: confusion, agitation, nightmares, GI upset, lethargy, anxiety, cognitive changes, etc. (Changes in response to medication may indicate toxicity and requires evaluation.) Report immediately. Monitor for signs of vitamin deficiency. (Phenobarbital increases metabolism of the nutrients Vitamin D, Vitamin K, folate and other B vitamins. Vitamin D deficiency results in impaired bone synthesis, Vitamin K deficiency results in impaired blood coagulation, other deficiencies result in impaired cellular reproduction and repair, causing anemia.) Obtain consult with dietitian per health care provider's order as needed. Monitor for signs of hepatic or renal toxicity. (Phenobarbital is metabolized by the liver and excreted by the kidneys.) Monitor laboratory blood tests and urinalysis: CBC with differential, electrolytes, BUN, PT, PTT, liver enzymes, etc. (Impaired function results in increased serum drug levels.) Instruct the patient to: Be aware that drug will cause initial drowsiness; this effect may diminish with continued therapy Avoid potentially hazardous activities that require mental alertness (driving, operating equipment etc) Bear in mind that full therapeutic effect of oral phenobarbital may take 2-3 weeks; Not discontinue abruptly, or reduce dosage, as increased seizure activity and/ or withdrawal symptoms may occur Keep a seizure log or diary to chronicle symptoms Instruct the patient to: Call for assistance when getting out of bed or attempting to walk. Remove any tripping hazards from the home environment. Instruct patient to immediately report any idiosyncratic or disabling effects. Instruct the patient or caregiver: Regarding the role of vitamins and nutrition in maintaining health. Instruct the patient to immediately report signs of vitamin deficiency. Vitamin K: easy bleeding (nasal, oral,rectal, etc.), tarry stools, bruising, pallor. Vitamin D: Joint pain, bone deformities. Vitamin B6: skin changes, dandruff (seborrhea), peripheral neuropathy, fatigue. Regarding intake of a nutrient-rich diet. Instruct the patient to: Observe for signs of toxicity: nausea, vomiting, diarrhea, rash, jaundice, abdominal pain, tenderness or distention, or change in color of stool, flank pain, hematuria. Adhere to a regular schedule of laboratory testing for liver and kidney function as ordered by the health care provider Instruct patient and caregiver: Use with caution in children, the elderly and those with pre-existing diseases, such That children respond differently because as respiratory disorders. These patients their nervous systems are not yet fully require reduced dosages. Paradoxical mature. response to drug may occur, which may The elderly are more susceptible to the cause psychomotor agitation effects of phenobarbital due to increased (hyperactivity). serum drug levels related to reduced efficiency of the liver and kidneys as a result of aging. Evaluation of Outcome Criteria Evaluate the effectiveness of drug therapy by confirming that patient goals and expected outcomes have been met (see “Planning”). Nursing Process Focus: Patients Receiving Phenytoin (Dilantin) Assessment Potential Nursing Diagnoses Prior to administration: Knowledge deficient related to drug regimen, action, and side effects Obtain complete medical history including allergies, developmental, neurological , Altered nutrition:Nutrition altered less pulmonary, cardiac, hematological, renal, than body requirements, Imbalanced biliary, and mental disorders including related to nutrient deficiency blood studies: CBC, BUN, creatinine, Oral mucous membrane, Impaired electrolytes, PT, PTT, liver enzymes, etc. related to drug effects. Obtain patient’s drug history to determine Skin integrity, Risk for impaired related possible drug interactions and allergies to adverse drug reaction Assess neurological status, including Injury, Risk for, related to drug side identification of recent seizure activity. effects Assess growth and development Planning: Patient Goals and Expected Outcomes The patient will: Report absence of seizure activity. Demonstrate understanding of drug action by accurately describing drug side effects and precautions. Demonstrate proper daily oral hygiene. Implementation Interventions and (Rationales) Patient Education/Discharge Planning During IV infusion, monitor all VS and Instruct the patient to immediately report: EKG. May need to ensure that patient’s any difficulty breathing, palpitations, chest cardiac output and central venous pressure pain, dizziness or impending syncope. be monitored according to ICU or ED protocols. Instruct the patient: Monitor neurological status, especially changes in level of consciousness and/or Report any significant change in sensorium, mental status. (At high doses, phenytoin such as slurred speech, confusion, may produce respiratory depression and hallucinations, or extreme lethargy. delirium. Report any changes in seizure quality or unexpected involuntary muscle movement, Phenytoin may have a paradoxical effect, producing involuntary movements such as such as twitching, tremor or nystagmus. dyskinesia or chorea.) Avoid driving and other activities requiring mental alertness and physical coordination until effects of the medication are known. Monitor for adverse immune reaction, such as hypersensitivity syndrome and dermatological manifestations such as purpuric dermatitis or Stevens-Johnson syndrome. Instruct the patient to: Immediately report shortness of breath, wheezing, tightness in the throat, itching or any changes in the skin such as a measleslike ("morbilliform") rash or dermatitis fever, joint pain, profound fatigue Call the health care provider immediately (before the next scheduled dose) for any adverse reaction Keep in mind that abrupt cessation of the drug can cause rebound seizures. Instruct patient to: Keep a "seizure diary" during drug initiation phase, or during dose adjustment. Take the medication exactly as ordered, including the same manufacturer's drug each time the prescription is refilled. Switching brands may result in alterations in seizure control. Take a missed dose as soon as remembered, but do not double doses to "catch up" (doubling doses could result in toxic serum level) Instruct patient to: Use cautiously in the elderly. (Diminished kidney and liver function related to aging Keep all appointments for follow-up lab result in lowered drug clearance and studies increased serum drug levels.) Report signs of toxicity to the health care provider immediately Instruct the patient to: Monitor oral health. Observe for signs of gingival hypertrophy, bleeding, Use a soft toothbrush, and oral rinses as inflammation, etc. prescribed by the dentist. Avoid mouthwashes containing alcohol, which dries mucous membranes. Brush and floss teeth after every meal; massage the gums daily. Report changes in oral health such as excessive bleeding or inflammation of the gums Maintain regular schedule of dental visits. Provide patient with information concerning Instruct the patient: contraceptive use. (Phenytoin may reduce Remain abstinent or use reliable birth the effectiveness of oral contraceptives.) control while taking this medication. Inform the health care provider if pregnancy occurs Avoid abrupt cessation of the drug; rebound seizures may cause harm to the fetus Phenytoin dose requirements increase during pregnancy. Instruct the patient to: Monitor serum glucose and observe for signs of diabetes mellitus. (Phenytoin alters Observe for subtle signs of hyperglycemia glycemic control and may cause (e.g. polydipsia, polyuria, slow wound hyperglycemia.) healing, etc.) Regularly monitor blood and/or urine glucose levels as specified by the health care provider Adhere to a calorie-controlled low refined Monitor effectiveness of drug therapy. Observe for developmental changes indicating the need for dose adjustment. (Phenytoin needs increase with initial maturing, especially at puberty, a time of rapid growth.) sugar (or ADA) diet as prescribed by the health care provider. Instruct the patient to: Monitor laboratory tests such as CBC, BUN, creatinine, electrolytes including Report shortness of breath, profound serum calcium, urinalysis and liver enzymes fatigue, pallor (signs of anemia) to determine kidney and liver function. Report nausea, vomiting, diarrhea, rash, (Phenytoin is metabolized in the liver and jaundice, abdominal pain, tenderness, excreted by the kidneys; impaired organ distention, or change in color of stool. function can increase serum drug levels.) Adhere to laboratory testing regimen for blood tests and urinalysis as directed. Include effects of phenytoin use on lab tests Inform the patient that: in teaching plan. Phenytoin may cause false positive resultsw *Reduces free thyroxine levels on tests for hypothyroidism, ant other *Reduces 17 keto-steroid levels endocrine tests. *Decreases dexamethasone suppression Should inform patient to notify laboratory values, and urine 6-b hydroxycortisol levels. personnel of phenytoin drug therapy when providing blood or urine samples. Instruct the patient to: Monitor nutritional status. (Phenytoin's action on electrolytes at the cellular level Eat well balanced meals high in vitamins [desensitizing sodium channels] contributes and nutrients. to decreased absorption of folic acid, Regularly take vitamin and mineral vitamin D, magnesium and calcium. Folic supplements (Vitamin D, folic acid, acid deficiency leads to anemia; vitamin D, magnesium, and calcium) as recommended magnesium and calcium deficiencies lead to by the health care provider. osteoporosis.) Instruct patient to: Observe patterns of elimination. (Phenytoin's central nervous system Take the drug with food to reduce depressant effects decrease gastrointestinal gastrointestinal upset. motility, producing constipation.) Immediately report any severe or persistent heartburn, upper G.I. pain, nausea or vomiting. Increase exercise, fluid and fiber intake to facilitate stool passage Consult the health care provider regarding the need for a bulk laxative or stool softener for chronic constipation. Evaluation of Outcome Criteria Evaluate the effectiveness of drug therapy by confirming that patient goals and expected outcomes have been met (see “Planning”). Nursing Process Focus: Patients Receiving Ethosuximide (Zarontin) Assessment Potential Nursing Diagnoses Prior to administration: Knowledge deficient related to drug therapy, side effects and precautions. Obtain complete medical history: neurological, hematological, pulmonary, Thought processes, Disturbed related to cardiac, renal, biliary, and mental disorders side effects of drug. including blood studies: CBC, BUN, Nutrition: less than body requirements, creatinine, electrolytes,PT, PTT, liver Imbalanced, related to weight loss enzymes, etc. Oral mucous membrane, Impaired, related Obtain patient’s drug history to determine to drug side effects. possible drug interactions and allergies Injury, Risk for related to drug side Assess neurological status, including effects. identification of recent seizure activity. Assess mental status, including affect and lucidity. Assess gastrointestinal status, including identification of biliary tract or upper digestive discomfort Assess growth and development. Planning: Patient Goals and Expected Outcomes The patient will: Experience the absence of, or a reduction in, the number or severity of seizures. Avoid physical injury related to seizure activity or medication induced sensory changes. Demonstrate understanding of the drug's action by accurately describing drug effects and precautions Maintain intact mucous membranes Implementation Interventions and (Rationales) Patient Education/Discharge Planning Instruct patient: Monitor vital signs especially temperature and respiratory patterns, especially Regarding methods to monitor vital signs at during sleep. home, especially temperature and respirations, ensuring proper use of home equipment. Elevated temperature may result from infection or indicate a blood disorder. That snoring is NOT normal; it is a sound created by obstruction in the upper respiratory tract which may signal sleep apnea and should be reported. Monitor neurological status, especially changes in level of consciousness and/or mental status. Observe for psychosis and/or labile emotions, especially mental depression. Obtain a verbal "no-self-harm" contract from patients with significant mental depression. Instruct the patient to: Report any significant change in sensorium such as visual changes (myopia), confusion, difficulty concentrating, hallucinations, or psychomotor agitation. Report dizziness, headache, lethargy, fatigue, ataxia, sleep pattern disturbances or hiccups. Report any changes in seizure quality or unexpected involuntary muscle movement. Avoid driving and other activities requiring mental alertness and physical coordination until effects of the medication are known. Instruct patient to report any severe dysphoria, especially suicidal ideation. Monitor for adverse hypersensitivity reaction, including dermatological manifestations / Stevens-Johnson syndrome. Instruct the patient to: Immediately report shortness of breath, wheezing, tightness in the throat, itching or any changes in the skin such as rash or dermatitis Call the health care provider immediately (before the next scheduled dose) for any adverse reaction Keep in mind that abrupt cessation of the drug can cause rebound seizures. Monitor immune status. Observe for signs of infection which may indicate insidious onset of blood dyscrasia: fever, sore throat, malaise, joint pain, ecchymoses, profound fatigue, shortness of breath, pallor, etc. Report immediately. Instruct the patient or caregiver Immediately report any "flu-like" symptoms: shortness of breath, fever, sore throat, malaise, joint pain, profound fatigue, etc. Flu-like symptoms may herald the "silent" onset of serious blood disorder, such as bone marrow suppression. Bruising is a sign of bleeding which can also indicate the presence of a serious blood disorder. Monitor laboratory tests such as CBC, BUN, creatinine, electrolytes, (including serum calcium), PT, PTT, liver enzymes and urinalysis, to determine kidney and liver function. (Ethosuximide is metabolized in the liver and excreted by the kidneys; impaired organ function may result.) Instruct the patient to: Immediately report any distressing symptoms to the health care provider. Adhere to laboratory testing regimen for blood tests and urinalysis as directed by the health care provider. Monitor renal function. Monitor intake & output Observe for signs of nephrotoxicity, including oliguria and pitting edema. Monitor laboratory values (see previous box above). Instruct the patient to: Monitor fluid intake and output. Immediately report changes in urine color, character or output (hematuria, oliguria, cloudiness, etc.) Immediately report nausea, fever, malaise and/or flank pain. Monitor gastrointestinal status. Observe for signs of gastrointestinal bleeding or hepatic toxicity. Monitor gastrointestinal elimination; conduct guiac stool testing for occult blood. Monitor nutritional status. Observe for weight loss secondary to anorexia. Monitor effectiveness of drug therapy. Observe for developmental changes indicating the need for dose adjustment. (Ethosuximide needs increase with initial maturing, especially at puberty, a time of rapid growth.) Use cautiously in the elderly. (Diminished kidney and liver function related to aging result in lowered drug clearance and increased serum drug levels.) Inform patient of need to use alternate forms of birth control. (Drug may decrease effectiveness of oral contraceptives.) Instruct the patient: Report any frank bleeding, abdominal pain, anorexia, heartburn, nausea, vomiting, jaundice or a change in the color or character of stools. Vomiting brown emesis that looks like coffee grounds or passing tarry stools are signs of gastrointestinal bleeding. Regarding the method of obtaining stool samples and home testing for occult blood as indicated by the health care provider. Adhere to a regimen of laboratory testing as ordered by the health care provider and keep all follow-up appoints as scheduled. Instruct patient: Measure body weight weekly Inform the health care provider of losses, especially greater than two pounds Regarding measures to enhance weight maintenance and appetite: small frequent meals, calorie-dense snacks, nutritional supplement drinks, etc. Consult with a nutritionist or dietician as ordered by the health care provider. Instruct the patient Take the medication exactly as ordered, including the same manufacturer's drug each time the prescription is refilled. Switching brands may result in alterations in seizure control. Take a missed dose as soon as remembered, but do not double doses to "catch up" (doubling doses could result in toxic serum level) Instruct the patient to report symptoms of drug toxicity such as visual changes, hallucinations, headache, or dizziness. Instruct the patient: Remain abstinent or use reliable birth control while taking this medication. Inform the health care provider if pregnancy occurs Avoid abrupt cessation of the drug; rebound seizures may result. Evaluation of Outcome Criteria Evaluate the effectiveness of drug therapy by confirming that patient goals and expected outcomes have been met (see “Planning”). Nursing Process Focus: Patients Receiving Diazepam (Valium) NOTE: this information is specific to the use of diazepam as a treatment for epilepsy only, not to other uses, such as anxiety. Assessment Potential Nursing Diagnoses Prior to administration: Airway Clearance, Ineffective related to sedative effect of drug Obtain patient’s drug history to determine possible drug interactions and allergies, Injury, Risk for related to sedative effect of including history of anti-seizure drug drug therapy and alcohol or tobacco use. Confusion, Acute related to drug side effects Assess neurological status, including Skin integrity, Risk for impaired related to LOC. Identify type and etiology of recent adverse drug reaction seizure activity. Sensory perception, Disturbed related to drug Assess growth and development, side effect including age, body mass index, and Knowledge Deficient , related to drug action, pregnancy/lactation status. side effects Assess skin integrity and identify locations for venipuncture/intravenous drug administration; insert intravenous catheter and I.V. line if not present. Obtain complete medical history: neurological ,pulmonary, cardiac, hematologic, renal, biliary, and mental disorders and including laboratory values: serum anticonvulsant level, CBC, BUN, creatinine, electrolytes, PT, PTT, and liver enzymes. Note: *Diazepam is given in response to status epilepticus, a medical emergency. Obtain as much key data as possible. Planning: Patient Goals and Expected Outcomes Patient will: Maintain a patent airway and adequate tissue perfusion. Experience the cessation of tonic-clonic seizures of status epilepticus. Avoid serious physical injury related to status epilepticus. Experience the return of normal consciousness and achieve stable neurological status. Demonstrate an understanding of the drug's action by accurately describing drug effects and precautions. Implementation Interventions and (Rationales) Patient Education/Discharge Planning Monitor respiratory rate and breathing Instruct patient and caregivers that keeping an pattern, as well as pulse oximetry and/or open airway and having sufficient oxygen is arterial blood gases. necessary to prevent permanent brain damage, which may occur related to status epilepticus. Assist with placement of an oral airway, or intubation as needed. Provide suction between seizures. Administer oxygen as ordered. Keep resuscitative equipment accessible. Instruct patient/caregivers that: During IV infusion, monitor all vital signs and EKG. May need to ensure that Status epilepticus is a life threatening emergency cardiac output and central venous and that direct IV administration of diazepam also pressure per Intensive Care Unit or has risks such as respiratory and cardiac Emergency Department protocol. depression or arrest. Observe for severe respiratory depression All necessary measures are being taken to preserve and bradycardia. (Diazepam is a CNS life and neurologic function. depressant which affects cardiorespiratory status.) Monitor neurological status. Observe for Instruct patient/caregiver to: changes in level of conscious. (Status Always take anti-seizure medication exactly as epilepticus generally causes loss of prescribed. consciousness; patients are at risk of Inform the health care provider of any other entering a coma due to increased cerebral illness; don't self-medicate with OTC medications. metabolic demand.) Avoid using alcohol, tobacco and recreational Observe for rebound seizures. (Diazepam drugs. is very short-acting.) Monitor metabolic status. (Increased Advise caregivers regarding variations in fluid and temperature increases metabolic electrolytes which may increase susceptibility to demands; lactic acidosis may follow seizures generalized motor seizures as common in status epilepticus.) Monitor fluid and electrolyte balance and intake and output. (Electrolyte imbalances may precipitate status epilepticus.) Instruct patients and caregivers to: Ensure patient safety. Place patient in semi-prone position, with head turned to Review standard safety precautions regarding reduce the risk of aspiration. Pad seizure activity siderails. Remove any restrictive Follow guidelines for seizures requiring clothing. Anchor IV lines per unit emergency intervention and transport to a protocol. hospital. Evaluation of Outcome Criteria Evaluate the effectiveness of drug therapy by confirming that patient goals and expected outcomes have been met (see “Planning”).