Enalapril is an angiotensin-converting enzyme (ACE) inhibitor introduced in the 1980s as one of the first oral ACE inhibitors after captopril. It quickly became one of the most widely prescribed medicines for cardiovascular and renal disease worldwide. Enalapril is formulated as a prodrug (enalapril maleate), which is metabolised in the liver to its active form, enalaprilat. Enalaprilat is the compound responsible for inhibiting the conversion of angiotensin I to angiotensin II. This reduction in angiotensin II lowers vasoconstriction and aldosterone secretion, thereby reducing blood pressure, easing the workload of the heart, and providing kidney protection.
The pharmacokinetics of enalapril are predictable: oral bioavailability is around 60%, onset of action within one hour, peak effect 4–6 hours, and duration of effect up to 24 hours with once- or twice-daily dosing. Its long half-life allows for convenient administration, which supports patient adherence. Clinical outcome trials, such as CONSENSUS and SOLVD, established enalapril’s life-prolonging effects in heart failure with reduced ejection fraction (HFrEF), making it a cornerstone in guideline-directed therapy for decades.
In addition to lowering blood pressure, enalapril reduces afterload and preload on the heart, slows progression of heart failure, reduces hospitalisations, and provides survival benefit. In patients with diabetes or chronic kidney disease, it reduces proteinuria and slows decline of renal function, making it an essential nephroprotective agent. It is often combined with diuretics, beta-blockers, calcium channel blockers, or ARBs (though dual ACE/ARB blockade is not recommended) for comprehensive management of cardiovascular risk factors.
Because ACE inhibition increases bradykinin levels, some patients develop a persistent dry cough. Rarely, serious angioedema may occur, which is a medical emergency. The safety and effectiveness of enalapril in pregnancy is unacceptable; ACE inhibitors can cause foetal harm. Despite these risks, its proven outcome benefits make it a highly valuable and affordable therapy worldwide.
Enalapril has broad applications across cardiovascular and renal medicine, supported by decades of high-quality evidence:
Patients are advised to continue lifestyle modifications (low-salt diet, exercise, weight management, smoking cessation) to complement pharmacological therapy. Enalapril is effective long-term only if taken consistently.
Enalapril, like all ACE inhibitors, has a predictable side effect profile. While most patients tolerate it well, some adverse reactions are common enough to warrant routine counselling.
Most side effects resolve after discontinuation or dose adjustment. Alternatives such as ARBs may be used if ACE inhibitors are not tolerated.
Patients should be counselled on monitoring blood pressure, recognising signs of angioedema, and reporting new or persistent cough.
Drug interactions can significantly impact enalapril’s safety:
Herbals such as licorice (can reduce efficacy) and high-potassium diets should be discussed with healthcare providers.
Missed dose: Take as soon as remembered unless near the next scheduled dose. Do not double up. Consistency is critical for blood pressure control and heart protection.
Accidental double dose: Usually causes lightheadedness or dizziness. Rest, hydrate, and skip the next dose if necessary. Seek advice if symptoms are pronounced.
Large overdose: Can cause profound hypotension, shock, renal failure, or hyperkalaemia. Emergency medical care required. Management includes IV fluids, vasopressors, and monitoring renal/electrolyte status. Haemodialysis can partially remove enalaprilat if necessary.
Children ingesting adult doses should be evaluated urgently in hospital settings.
Carry enalapril in labelled containers when travelling; avoid exposure to extreme temperatures.
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