Med Practicum
Pharmacology Study Notes
NPH Insulin
Generic and Trade Names:
Generic: NPH Insulin
Trade: HumuLIN N, HumuLIN N KwikPen, NovoLIN N, NovoLIN N FlexPen
Dosage and Route:
Depends on blood glucose and other factors.
Administration: SUBQ (Subcutaneous)
Dosage: 0.5-1 unit total insulin/kg/day
Onset, Peak, Duration:
Onset:
SUBQ: 2-4 hours
70% NPH/30% R Insulin mixture: 30 min
Peak:
SUBQ: 4-10 hours
70% NPH/30% R Insulin mixture: 2-12 hours
Duration:
SUBQ: 10-16 hours
70% NPH/30% R Insulin mixture: 24 hours
Therapeutic Class:
Antidiabetics
Hormones
Pharmacologic Class:
Pancreatics
Indications:
Control of hypoglycemia in patients with diabetes mellitus.
Mechanism of Action (MOA):
Lowers blood glucose by stimulating glucose uptake in skeletal muscle and fat; inhibits hepatic glucose production.
Nursing Considerations:
Assess for symptoms of hypoglycemia, including:
Anxiety, restlessness, tingling in hands, feet, lips.
Monitor body weight; changes may necessitate adjustments in insulin dose.
Administer PO medication 1-2 hours prior to meals.
Medication can be crushed for patients with swallowing difficulties.
Medication may be dissolved in 25-100 mL of water; shake for 5 minutes and administer within 30 minutes.
Patient Family Teaching:
Instruct on proper administration technique.
Demonstrate mixing technique for insulin.
Caution against sharing pen devices (risk of bloodborne pathogens).
Explain the importance of medication in controlling hyperglycemia without curing diabetes (long-term therapy).
Adverse Effects:
Local: Cutaneous amyloidosis, erythema, lipodystrophy, pruritus, swelling.
Endocrine: Hypoglycemia.
Miscellaneous: Hypersensitivity reactions, anaphylaxis, hypokalemia.
Drug Interactions:
Beta-blockers and clonidine may mask symptoms of hypoglycemia.
Corticosteroids, thyroid supplements, estrogens, isoniazid, niacin, phenothiazines, rifampin increase insulin requirements.
Alcohol, ACE inhibitors, MAO inhibitors, Octreotide, oral hypoglycemic agents, and salicylates may decrease insulin requirements.
Pioglitazone may increase risk of fluid retention and worsening heart failure.
Lab Considerations:
Monitor glucose every 6 hours.
A1C levels.
Serum potassium.
Captopril
Generic and Trade Names:
Generic: Captopril
Trade: No specific trade name provided.
Dosage and Route:
Maximum dosage: 450 mg/day.
Administration: PO (by mouth).
Onset, Peak, Duration:
Onset:
PO: 15-60 min
Peak:
60-90 min
Duration:
6-12 hrs
Therapeutic Class:
Antihypertensives
Pharmacologic Class:
ACE Inhibitors
Indications:
Treatment of hypertension.
Heart failure (HF).
Treatment for diabetic nephropathy in patients with type 1 diabetes and retinopathy.
Mechanism of Action (MOA):
ACE inhibitors block the conversion of angiotensin I to angiotensin II (a vasoconstrictor), thereby lowering blood pressure.
They increase plasma renin levels and decrease aldosterone levels.
Nursing Considerations:
Monitor blood pressure and pulse.
Assess the patient for signs of angioedema (e.g., swelling of face, extremities, eyes, lips, tongue, difficulty swallowing or breathing).
Monitor weight for resolution of fluid overload.
Patient Family Teaching:
Educate the patient to take the medication consistently at the same time each day.
Advise to take missed doses immediately unless close to next dose (do not double dose).
Instruct them to continue taking the medication even if feeling better; do not discontinue without consulting a provider.
Educate on the proper technique for taking blood pressure.
Caution against salt substitutes or potassium-rich foods.
Advise to change positions slowly to minimize risk of hypotension.
Adverse Effects:
CNS: Dizziness, fatigue, headache, insomnia.
Respiratory: Cough.
Cardiovascular: Hypotension, chest pain, palpitations, tachycardia.
Gastrointestinal: Taste disturbance, abdominal pain, anorexia, constipation, diarrhea, nausea, vomiting.
Genitourinary: Proteinuria, renal impairment.
Dermatological: Rash, pruritus.
Miscellaneous: Angioedema, fever.
Hematological: Agranulocytosis, neutropenia.
Drug Interactions:
Concurrent use with sacubitril increases the risk of angioedema (do not use within 36 hours of switching).
Hypotension may occur when using potassium supplements or potassium-sparing diuretics.
Increased risk of hyperkalemia, renal dysfunction, hypotension, and syncope with angiotensin II receptor blockers.
NSAIDs and COX-2 inhibitors may inhibit the antihypertensive effect and increase the risk for renal dysfunction.
Food may decrease the absorption of captopril; must be taken 1 hour before meals.
Lab Considerations:
Monitor aldosterone levels.
BUN and serum creatinine levels.
Electrolytes and serum potassium.
Complete blood count with differential prior to therapy, then every 2 weeks for 3 months, and then periodically to monitor for neutropenia (discontinue if neutrophil count <1000/mm³).
Increased levels of AST, ALT, alkaline phosphatase, bilirubin, uric acid, and glucose may occur.
Urine protein should be monitored periodically for one year for patients with renal impairment or those receiving >150 mg/day.