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Low-dose enalapril in severe chronic heart failure

  • Congestive Heart Failure
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Summary

In a 3-month prospective, single-blind, controlled trial, 38 patients in New York Heart Association functional class III–IV were assigned to group E (n=19): enalapril 5 mg/day in addition to the previous therapy with digitalis and diuretics, or group C (n=19): continuation of the previous therapy.

In group E, 79% of the patients improved by at least one NYHA functional class after 3 months. In group C, the functional class did not change and four patients died. The echocardiographically determined end-diastolic diameter of the left ventricle decreased in group E from 72±8 mm to 63±6 mm (p<0.001), and the scintigraphically determined ejection fraction of the left ventricle increased from 33±18% to 40±19% (p<0.002). In contrast, no significant change was found in group C. Plasma-renin activity increased in group E from 8.2±1.8 ng/ml h to 29.7±14 ng/ml h (p<0.001), and plasma aldosterone decreased from 47.7±7.6 ng/dl to 19.9±4.8 ng/dl (p<0.01). In group C no significant change occurred. Comparing the actual changes (deltas) of the NYHA functional class (p<0.02), end-diastolic diameter and ejection fraction of the left ventricle, plasma-renin activity, and plasma aldosterone (p<0.0001), a significant difference between the two groups was found.

Thus, low-dose enalapril resulted in a significant improvement of the NYHA functional class in patients with severe chronic heart failure, accompanied by an improvement in left ventricular function and a decrease in secondary aldosteronism.

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Brilla, C.G., Krämer, B., Hoffmeister, H.M. et al. Low-dose enalapril in severe chronic heart failure. Cardiovasc Drug Ther 3, 211–218 (1989). https://doi.org/10.1007/BF01883867

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