Clinical use of a calcium antagonistic agent (nifedipine) in acute pulmonary edema.

Abstract

Nifedipine induces vascular smooth muscle relaxation through a calcium antagonistic action. The possibility of clinical use of the drug as a ventricular unloading agent has been explored in this study. In patients with hypertensive (seven cases), primary (seven cases) or rheumatic (aortic insufficiency five cases, mitral regurgitation five cases) cardiac disease, nifedipine, administered in a single sublingual dose (10 mg), relieved acute pulmonary edema. Circulatory variations from control were the following: decrease of systemic and pulmonary arterial pressures, and of vascular resistances, of pulmonary wedge pressure, of left ventricular diastolic and systolic dimensions (echocardiography); increase of cardiac and stroke index, of left ventricular mean rate of circumferential fiber shortening, of left and right mean pre-ejection delta P/delta t and mean rate of ejection; improvement of forward output in primary and rheumatic disease. Nifedipine benefits acute congestive heart failure by sustained fall of both preload and afterload and, possibly, by an enhanced contractility. It seems to have an appropriate indication in cases in which left ventricular afterload reduction is desirable.

• Authors: A Polese, C Fiorentini, M T Olivari, M D Guazzi
• Journal: The American journal of medicine (Am J Med) Vol. 66 Issue 5 Pg. 825-30 (May 1979) ISSN: 0002-9343 [Print] United States
• PMID: 443258 (Publication Type: Journal Article)

Chemical References

• Pyridines
• Nifedipine
• Calcium

Topics

• Adult
• Aged
• Blood Pressure (drug effects)
• Calcium (antagonists & inhibitors)
• Cardiomyopathies (complications)
• Female
• Humans
• Hypertension (complications)
• Male
• Middle Aged
• Muscle, Smooth (drug effects)
• Myocardial Contraction (drug effects)
• Nifedipine (therapeutic use)
• Pulmonary Edema (drug therapy, etiology)
• Pyridines (therapeutic use)
• Rheumatic Heart Disease (complications)
• Stroke Volume (drug effects)
• Vascular Resistance (drug effects)