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November 12, 1983BMJ49 citationsOpen Access

Enalapril in the treatment of hypertension with renal artery stenosis.

GHG P HodsmanJBJ. J. BrownACA M Cumming

Structured PICO

Does enalapril reduce blood pressure in hypertensive patients with renal artery stenosis?

P
Population
20 hypertensive patients with renal artery stenosis
I
Intervention
Enalapril 10-40 mg single daily dose for up to 3 months
O
Outcome
Blood pressure reduction at 6 hours and 3 monthssurrogate

Enalapril effectively controls blood pressure in patients with hypertension and renal artery stenosis, though it is associated with increases in serum potassium, creatinine, and urea.

Abstract

The converting enzyme inhibitor enalapril, in single daily doses of 10-40 mg, was given to 20 hypertensive patients with renal artery stenosis. The blood pressure fall six hours after the first dose of enalapril was significantly related to the pretreatment plasma concentrations of active renin and angiotensin II and to the concurrent fall in angiotensin II. Blood pressure fell further with continued treatment; the long term fall was not significantly related to pretreatment plasma renin or angiotensin II concentrations. At three months, 24 hours after the last dose of enalapril, blood pressure, plasma angiotensin II, and converting enzyme activity remained low and active renin and angiotensin I high; six hours after dosing, angiotensin II had, however, fallen further. The rise in active renin during long term treatment was proportionally greater than the rise in angiotensin I; this probably reflects the fall in renin substrate that occurs with converting enzyme inhibition. Enalapril alone caused reduction in exchangeable sodium, with distinct increases in serum potassium, creatinine, and urea. Enalapril was well tolerated and controlled hypertension effectively long term; only two of the 20 patients required concomitant diuretic treatment.

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Cite This Study

Hodsman et al. (1983) studied this question.

synapsesocial.com/papers/6a1be904ea84844e355f2a9chttps://doi.org/10.1136/bmj.287.6403.1413
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