Electrocardiogram changes and plasma desipramine levels during treatment of depression
- 1 June 1980
- journal article
- research article
- Published by Wiley in Clinical Pharmacology & Therapeutics
- Vol. 27 (6) , 796-802
- https://doi.org/10.1038/clpt.1980.113
Abstract
Symptomatic [human] subjects (26) who met research diagnostic criteria for major affective disorder and were free of cardiovascular disease were treated for 3 wk with a fixed dosage schedule of desipramine (DMI) to a maximum of 200 mg/day. An ECG and DMI plasma level determinations were obtained before treatment and weekly thereafter. DMI levels during the trial ranged from 13.4-882.2 ng/ml. DMI treatment was associated with increase in heart rate (P < 0.001), prolongation of the PR (P < 0.001), QRS (P < 0.001) and QTc intervals (P < 0.001) and increase in T wave amplitude (P < 0.001). Significant (P < 0.001) but relatively weak correlations were noted between DMI plasma levels and heart rate (r [correlation coefficient] = 0.405), QRS interval (r = 0.346), QTc interval (r = 0.534) and T wave amplitude (r = 0.386). PR interval prolongation was independent of DMI levels (r = 0.171). DMI treatment induced no clinically significant ECG alterations or cardiovascular adverse effects. The relevance of DMI plasma level and the possible roles of other contributing factors in the production of these ECG changes are discussed.This publication has 5 references indexed in Scilit:
- Electrophysiological effects of desipramine of guinea pig papillary musclesEuropean Journal of Pharmacology, 1979
- Analysis of Tricyclic Antidepressants in Human Plasma by GLC–Chemical-Ionization Mass Spectrometry with Selected Ion MonitoringJournal of Pharmaceutical Sciences, 1978
- Effects of several tricyclic antidepressants on the hemodynamics and myocardial contractility of the anesthetized dogsEuropean Journal of Pharmacology, 1977
- Cardiac Antiarrhythmic Effect of Imipramine HydrochlorideNew England Journal of Medicine, 1977
- Tricyclic antidepressant plasma levels and adverse effects after overdoseClinical Pharmacology & Therapeutics, 1977