Skip Navigation

European Heart Journal 1986 7(2):150-157;
Copyright © 1986 by the European Society of Cardiology.
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by NIEMINEN, M. S.
Right arrow Articles by FRICK, M. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by NIEMINEN, M. S.
Right arrow Articles by FRICK, M. H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1986 The European Society of Cardiology

Acute haemodynainic effects of the antiarrhythmic agent pirmenol in cardiac patients: a comparison with lidocaine

M. S. NIEMINEN, L. K. TOIVONEN, V. MANNINEN and M. H. FRICK

Cardiovascular Laboratory, First Department of Medicine, University Central Hospital Helsinki, Finland

Received 17 July 1985; revised 11 October 1985; .

Address for correspondence: Laun K. Toivonen, MD, Cardiovascular Laboratory, First Department of Medicine, Helsinki University Central Hospital, SF-00290 Helsinki 29, Finland

Abstract

The acute haemodynamic effects of pirmenol, a new Class 1 antiarrhythmic agent, were investigated in a double-blind comparison with lidocaine and placebo. Three groups of 10 patients each received either pirmenol as a 50 mg intravenous injection followed by a 2.5 mg min–1 infusion, or lidocaine as a 75 mg injection followed by a 3 mg min–1 infusion, or placebo. Mean plasma pirmenol concentrations during the 30 min infusion period were 2.3–2.5 mg l–1, and were considered to be therapeutically effective.

Compared to measurements taken during a baseline phase of 15 min duration, pirmenol increased heart rate by 10 beats min–1 (P<0.001) and mean arterial pressure (MAP) by SmmHg (P<0.001). It also increased systemic vascular (P<0.05) and pulmonary arterial resistances (P<0.01). Left ventricular end-diastolic pressure (LVEDP) was not increased significantly. Cardiac index and left ventricular work index remained unchanged. Lidocaine induced a comparable increase in MAP (6mmHg; P<0.001) and elevated LVEDP (2.8 mmHg; P<0.05) and did not affect left ventricular work index. Echocardiographic left ventricular ejection fraction was reduced more by pirmenol ( – 0.05; P<0.001) than by lidocaine (–003; P<0.05), but the greater reduction may partly be explained by the increase in heart rate. Pirmenol did not induce excessive circulatory responses or side-effects in any patient.

Intravenous administration ofpirmenol results in increased heart rate and afterload but has little effect on preload. The myocardial depressant effect is relatively slight, and comparable to that of lidocaine.

Key Words: Pirmenol • haemodynamics • heart disease • lidocaine


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.