共 20 条
Cardiopulmonary resuscitation with a novel chest compression device in a porcine model of cardiac arrest - Improved hemodynamics and mechanisms
被引:116
作者:

Halperin, HR
论文数: 0 引用数: 0
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机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA

Paradis, N
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA

Ornato, JP
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA

Zviman, M
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA

LaCorte, J
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA

Lardo, A
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA

Kern, KB
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA
机构:
[1] Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ Hosp, Dept Med, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ Hosp, Dept Biomed Engn, Baltimore, MD 21205 USA
[4] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
[5] Virginia Commonwealth Univ, Richmond, VA USA
[6] Univ Arizona, Tucson, AZ USA
关键词:
D O I:
10.1016/j.jacc.2004.08.061
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
OBJECTIVES The goal of this study was to determine the magnitude and mechanisms of hemodynamic improvement of an automated, load-distributing band device (AutoPulse, Revivant Corp., Sunnyvale, California) compared with conventional cardiopulmonary resuscitation (C-CPR). BACKGROUND lmproved blood flow during cardiopulmonary resuscitation (CPR) enhances survival from cardiac arrest. METHODS AutoPulse CPR (A-CPR) and C-CPR were performed on 30 pigs (16 +/- 4 kg) 1 min after induction of ventricular fibrillation. Aortic and right atrial pressures were measured with micromanometers. Regional flows were measured with microspheres; A-CPR and C-CPR were performed with 20% anterior-posterior chest compression, with (n = 10) and without (n = 10) epinephrine. A pressure transducer was advanced down the airways during chest compressions (n = 10), and magnetic resonance imaging (MRI) was performed. RESULTS AutoPulse CPR improved coronary perfusion pressure (CPP) (aortic - right atrial pressure) without epinephrine (A-CPR 21 +/- 8 mm Hg vs. C-CPR 14 +/- 6 mm Hg, mean +/- SD, p < 0.0001) and with epinephrine (A-CPR 45 +/- 11 mm Hg vs. C-CPR 17 +/- 6 min Hg, p < 0.0001). AutoPulse CPR improved myocardial flow without epinephrine and cerebral and myocardial flow with epinephrine (p < 0.05). AutolPulse CPR also produced greater myocardial flow at every CPP (p < 0.01). With A-CPR, high airway pressure was noted distal to the carina, which corresponded to an area of airway collapse on MRI, and which was not present with C-CPR. CONCLUSIONS AutoPulse CPR improved hemodynamics over C-CPR in this pig model. AutoPulse CPR with epinephrine can produce pre-arrest levels of myocardial and cerebral flow. The improved hemodynamics with A-CPR appear to be mediated through airway collapse, which likely impedes airflow and helps maintain higher levels of intrathoracic pressure. (C) 2004 by the American College of Cardiology Foundation.
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页码:2214 / 2220
页数:7
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h-index: 0
机构:
JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

GUERCI, AD
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

CHANDRA, N
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

HERSKOWITZ, A
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

TSITLIK, JE
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

NISKANEN, RA
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

WURMB, E
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205

WEISFELDT, ML
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JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205 JOHNS HOPKINS MED INST,DEPT MED,DIV CARDIOL,PETER BELFER LAB MYOCARDIAL RES,BALTIMORE,MD 21205