EFFECTS OF THE AT1-SELECTIVE ANGIOTENSIN-II ANTAGONIST, TELMISARTAN, ON HEMODYNAMICS AND VENTRICULAR-FUNCTION AFTER CARDIOPULMONARY-RESUSCITATION IN PIGS

Citation
Hu. Strohmenger et al., EFFECTS OF THE AT1-SELECTIVE ANGIOTENSIN-II ANTAGONIST, TELMISARTAN, ON HEMODYNAMICS AND VENTRICULAR-FUNCTION AFTER CARDIOPULMONARY-RESUSCITATION IN PIGS, Resuscitation, 35(1), 1997, pp. 61-68
Citations number
41
Categorie Soggetti
Emergency Medicine & Critical Care
Journal title
ISSN journal
03009572
Volume
35
Issue
1
Year of publication
1997
Pages
61 - 68
Database
ISI
SICI code
0300-9572(1997)35:1<61:EOTAAA>2.0.ZU;2-B
Abstract
The purpose of this study was to investigate the effects of the angiot ensin II (ANG II) antagonist, telmisartan, on hemodynamics, myocardial function and myocardial blood flow during the postresuscitation phase in a porcine model of CPR and to compare these to saline. After 4 min of ventricular fibrillation and 5 min of closed-chest CPR, defibrilla tion was performed in 16 domestic pigs to restore spontaneous circulat ion (ROSC). Ten minutes after ROSC, animals were allocated to receive either the ANG II antagonist, telmisartan, at a dose of 1 mg/kg (n = 8 ) or saline (n = 8). Hemodynamics, myocardial function and myocardial blood flow were measured prearrest and at 5, 30, 90 and 240 min after ROSC. Using a Swan-Ganz catheter with a fast responding-thermistor and a micromanometer tipped catheter, right ventricular end-diastolic and end-systolic volume, right ventricular ejection fraction, left ventri cular contractility were 67 +/- 6 ml (mean +/- S.E.M.), 42 +/- 4 mi, 3 8 +/- 2%, 2036 +/- 77 mmHg/s in the telmisartan group and 82 +/- 2 mi (P < 0.05), 59 +/- 3 mi (P < 0.01), 28 +/- 2% (P < 0.01), 1596 +/- 82 mmHg/s (P < 0.01) in the control group, at 240 min after ROSC. No sign ificant differences in mean aortic and pulmonary artery pressure, card iac index or myocardial blood flow between the two groups were found. We conclude that the ANG II antagonist telmisartan administered during the postresuscitation phase in pigs increases myocardial contractilit y without changing cardiac index, systemic vascular resistance, pulmon ary vascular resistance, or myocardial perfusion. (C) 1997 Elsevier Sc ience Ireland Ltd.