Synergistic effects of vasopressin plus epinephrine during cardiopulmonary resuscitation

被引:41
作者
Mulligan, KA [1 ]
McKnite, SH [1 ]
Lindner, KH [1 ]
Lindstrom, PJ [1 ]
Detloff, B [1 ]
Lurie, KG [1 ]
机构
[1] Univ Minnesota, Cardiac Arrhythmia Ctr, Minneapolis, MN 55455 USA
关键词
epinephrine; vasopressin; cardiopulmonary resuscitation; cerebral blood flow; cardiac arrest; myocardial blood flow;
D O I
10.1016/S0300-9572(97)00060-9
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Both epinephrine (Epi) and vasopressin (VP) increase coronary perfusion pressure (CPP) when administered during cardiac arrest. Given their different mechanisms of action we tested the hypothesis that during cardiopulmonary resuscitation (CPR) a combination of VP plus Epi would be superior to either agent alone. Epi(40 mu g/kg), VP(0.3 U/kg) and the combination of both agents were assessed in a porcine model of ventricular fibrillation (VF). Maximum CPP (diastolic aortic-right atrial pressures) during CPR was similar among the groups but the time course of action was different in each group: with Epi +/- VP the increase in CPP was significantly more rapid than with VP alone whereas the CPP remained significantly higher for a longer periods of time with VP or VP + Epi versus Epi alone. Left ventricular blood flow (ml/min per g) determined during CPR two min after drug administration was similar between groups: Epi 1.06 +/- 0.16; VP 0.82 +/- 0.26; Epi + VP 0.83 +/- 0.14 (P = N.S.). Post drug administration, 2 min, cerebral blood flow (ml/min per g) in the VP group (0.76 +/- 0.15) was more than two times higher compared with Epi alone (Epi:0.30 +/- 0.08, P < 0.01 versus VP) and Epi plus VP (Epi + VP:0.23 +/- 0.03, P < 0.01 versus VP). We conclude that combination of VP + Epi during cardiac arrest results in a more rapid rise in CPP when compared with VP alone and a more sustained elevation in CPP than observed with Epi alone. Thus, the synergistic effects of these two potent vasopressor agents may be of benefit during CPR. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:265 / 271
页数:7
相关论文
共 9 条
[1]   ACTIVE COMPRESSION-DECOMPRESSION CPR IMPROVES VITAL ORGAN PERFUSION IN A DOG-MODEL OF VENTRICULAR-FIBRILLATION [J].
CHANG, MW ;
COFFEEN, P ;
LURIE, KG ;
SHULTZ, J ;
BACHE, RJ ;
WHITE, CW .
CHEST, 1994, 106 (04) :1250-1259
[2]  
LINDER KH, 1997, IN PRESS LANCET
[3]  
LINDNE KH, 1994, CIRCULATION, V91, P213
[4]  
LINDNER KH, 1993, ANESTH ANALG, V77, P427
[5]   Release of endogenous vasopressors during and after cardiopulmonary resuscitation [J].
Lindner, KH ;
Haak, T ;
Keller, A ;
Bothner, U ;
Lurie, KG .
HEART, 1996, 75 (02) :145-150
[6]   STRESS HORMONE RESPONSE DURING AND AFTER CARDIOPULMONARY-RESUSCITATION [J].
LINDNER, KH ;
STROHMENGER, HU ;
ENSINGER, H ;
HETZEL, WD ;
AHNEFELD, FW ;
GEORGIEFF, M .
ANESTHESIOLOGY, 1992, 77 (04) :662-668
[7]   Vasopressin administration in refractory cardiac arrest [J].
Lindner, KH ;
Prengel, AW ;
Brinkmann, A ;
Strohmenger, HU ;
Lindner, IM ;
Lurie, KG .
ANNALS OF INTERNAL MEDICINE, 1996, 124 (12) :1061-1064
[8]   IMPROVING ACTIVE COMPRESSION-DECOMPRESSION CARDIOPULMONARY-RESUSCITATION WITH AN INSPIRATORY IMPEDANCE VALVE [J].
LURIE, KG ;
COFFEEN, P ;
SHULTZ, J ;
MCKNITE, S ;
DETLOFF, B ;
MULLIGAN, K .
CIRCULATION, 1995, 91 (06) :1629-1632
[9]   High dose and standard dose adrenaline do not alter survival, compared with placebo, in cardiac arrest [J].
Woodhouse, SP ;
Cox, S ;
Boyd, P ;
Case, C ;
Weber, M .
RESUSCITATION, 1995, 30 (03) :243-249