Volume 30, Issue s1 pp. S160-S165

Low Doses of Intracoronary Enalaprilat Suppress Reperfusion-Associated Ventricular Arrhythmias after Primary Percutaneous Coronary Interventions for Acute Myocardial Infarction

HENDRIK BONNEMEIER M.D.

HENDRIK BONNEMEIER M.D.

Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein Campus Lübeck, Lübeck, Germany

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ULRICH SCHÄFER M.D.

ULRICH SCHÄFER M.D.

Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein Campus Lübeck, Lübeck, Germany

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JASMIN ORTAK M.D.

JASMIN ORTAK M.D.

Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein Campus Lübeck, Lübeck, Germany

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THOMAS KURZ M.D.

THOMAS KURZ M.D.

Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein Campus Lübeck, Lübeck, Germany

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HUGO A. KATUS M.D.

HUGO A. KATUS M.D.

Ruprecht-Karls-Universität Heidelberg, Innere Medizin III, Germany

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GERT RICHARDT M.D.

GERT RICHARDT M.D.

Herzzentrum Segeberger Kliniken, Bad Segeberg, Germany

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HERIBERT SCHUNKERT M.D.

HERIBERT SCHUNKERT M.D.

Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein Campus Lübeck, Lübeck, Germany

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First published: 18 January 2007
Citations: 4
Address for reprints: Hendrik Bonnemeier, M.D., Medizinische Klinik II, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, Germany. Fax: +49-451-500-2363; e-mail: [email protected]

This study was supported by a grant of the Deutsche Forschungsgemeinschaft (Ku 774/3-1), Bonn, Germany.

Abstract

Background: In the era of early reperfusion therapy, life-threatening ventricular arrhythmias (VA) remain common after recanalization of an occluded coronary artery. Experimental studies reported that angiotensin-converting (ACE) inhibitors suppress reperfusion-induced VA. However, whether ACE inhibitors lower the incidence of reperfusion clinical VA is unknown. We examined the effects of low doses of intracoronary (i.c.) enalaprilat (EN) as an adjunct to direct percutaneous coronary interventions (PCI) on reperfusion VA in the acute phase of myocardial infarction (MI).

Methods: We randomly assigned 22 patients with a first acute MI, who underwent successful direct PCI, to EN, 50 μg, i.c., or placebo (PL), administered immediately after reperfusion. VA were manually edited and counted from 24-hour Holter recordings begun upon hospital admission.

Results: There were no significant between-groups differences in clinical characteristics. Mean RR interval before and after PCI, and the incidence of VA before PCI were similar in both groups. After PCI the incidence of reperfusion-induced VA was significantly lower in the EN-treated group (VPB/h: PL 29.9 ± 12 vs EN 43.2 ± 42, P < 0.05; couplets/h: EN 0.9 ± 0.7 vs PL 4.1 ± 5.0, P < 0.01; triplets/h: EN 0.3 ± 0.2 vs PL 1.2 ± 1.5, P < 0.05; ventricular tachycardia/h: EN 0.3 ± 0.1 vs PL 0.8 ± 0.5, P < 0.01).

Conclusions: Compared with PL, i.c. EN significantly lowered the incidence of reperfusion-associated VA. This previously unrecognized antiarrhythmic effect might be an important therapeutic benefit conferred by ACE inhibitors, beyond limitation of infarct size.

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