A STUDY OF THE STANDARDIZATION OF DIGITALIS. I. A METHOD FOR CLINICAL STANDARDIZATION
Open Access
- 1 November 1935
- journal article
- research article
- Published by American Society for Clinical Investigation in JCI Insight
- Vol. 14 (6), 725-731
- https://doi.org/10.1172/jci100720
Abstract
The conditions for satisfactory clinical assay of digitalis are discussed, and a standard set outlined. Attempt was made to ascertain the feasibility of separating by clinical assay different strengths of the same tincture of digitalis. In the conditions of the expts., among the phenomena observed (which included symptoms, weight, blood pressure, cardiac rate, and various aspects of the electrocardiogram), only 1 seemed clearly helpful. The effect, under standard conditions, of 3 such samples, on the "Q-T" interval of the electrocardiogram, stated in relation to the cardiac cycle length, made it possible to distinguish potencies related as 75:100:125. Aged and fresh samples of the same tincture were similarly tested.Keywords
This publication has 3 references indexed in Scilit:
- A STUDY OF THE STANDARDIZATION OF DIGITALIS. II. THE RELATIONSHIP BETWEEN LABORATORY METHODS OF ASSAY AND POTENCY AS DETERMINED BY EXPERIMENTAL CUMULATIVE POISONING AND CLINICAL STANDARDIZATIONJCI Insight, 1935
- STUDIES ON THE ELECTRICAL SYSTOLE (“Q-T” INTERVAL) OF THE HEARTJCI Insight, 1932
- STUDIES ON DIGITALIS IN AMBULATORY CARDIAC PATIENTSJCI Insight, 1929