BRAIN RESUSCITATION BY EXTRACORPOREAL-CIRCULATION AFTER PROLONGED CARDIAC-ARREST IN CATS

被引:18
作者
IIJIMA, T [1 ]
BAUER, R [1 ]
HOSSMANN, KA [1 ]
机构
[1] MAX PLANCK INST NEUROL RES,DEPT EXPTL NEUROL,GLEUELER STR 50,W-5000 COLOGNE 4,GERMANY
关键词
BRAIN RESUSCITATION; EXTRACORPOREAL CIRCULATION; REPERFUSION INJURY; CEREBROVASCULAR CIRCULATION; NO REFLOW; POSTISCHEMIC HYPOPERFUSION;
D O I
10.1007/BF01708367
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: Brain reanimation after prolonged ischemia is limited by post-ischemic reperfusion deficits (no-reflow phenomenon). The present study was undertaken to establish whether after 30 min cardiac arrest extracorporeal circulation is able to restore brain reperfusion and to promote functional and metabolic recovery. Design: Adult normothermic cats were submitted to 30 min cardiac arrest by KCl-induced cardioplegia. Resuscitation was carried out by extracorporeal circulation (ECC) until spontaneous heart function returned. The quality of brain recovery was assessed 3 h later by electrophysiological recording and by imaging of the regional distribution of brain energy metabolites. Results: In 6 of 10 cats cardiac sinus rhythm returned after 32+/-15 min. In the other 4 cats cardiac function did not return or only intermittently returned during the 3 h observation period. Cerebral blood flow measured by laser Doppler flowmetry returned to 102%+/-40% of control immediately after the beginning of resuscitation but then gradually declined to 43%+/-32% after 3 h despite normotensive perfusion. In all cats pupils started to constrict within less than 5 min of recirculation but in 2 animals they secondarily dilated 1.5 and 2 h later, respectively. Spontaneous EEG activity reappeared in 4 of the 6 successfully resuscitated cats after 111+/-40 min but failed to recover in the others. Bioluminescent imaging of ATP after 3 h recirculation revealed near-complete depletion throughout the brain in all 4 cats without cardiac recovery. Of the 6 successfully resuscitated cats 5 exhibited patchy areas of low ATP, glucose and pH in 22%-92% of the cross sectional area of brain; in one cat recovery of energy metabolism and acid-base homoiostasis was homogenous without any focal deficits. The cross sectional area of ATP recovery correlated directly with CBF and hematocrit and inversely with the plasma lactate level. Conclusions: This study demonstrates for the first time that ECC is able to restore electrophysiological and metabolic brain function after cardiac arrest of as long as 30 min, but recovery is heavily restricted by delayed postischemic disturbances of recirculation. Progress in cardiac resuscitation by ECC requires substantial improvement in the efficiency of cerebrovascular reperfusion.
引用
收藏
页码:82 / 88
页数:7
相关论文
共 34 条
[1]  
AMES A, 1968, AM J PATHOL, V52, P437
[2]  
ANDERSEN K, 1985, J THORAC CARDIOV SUR, V90, P570
[3]   A COMPARISON OF CARDIOPULMONARY-RESUSCITATION WITH CARDIOPULMONARY BYPASS AFTER PROLONGED CARDIAC-ARREST IN DOGS - REPERFUSION PRESSURES AND NEUROLOGIC RECOVERY [J].
ANGELOS, M ;
SAFAR, P ;
REICH, H .
RESUSCITATION, 1991, 21 (2-3) :121-135
[4]   PULSATILE REPERFUSION AFTER CARDIAC-ARREST IMPROVES NEUROLOGIC OUTCOME [J].
ANSTADT, MP ;
STONNINGTON, MJ ;
TEDDER, M ;
CRAIN, BJ ;
BROTHERS, MF ;
HILLEREN, DJ ;
RAHIJA, RJ ;
MENIUS, JA ;
LOWE, JE .
ANNALS OF SURGERY, 1991, 214 (04) :478-490
[5]  
Blauth C, 1989, Eur J Cardiothorac Surg, V3, P135, DOI 10.1016/1010-7940(89)90091-2
[6]   PUMP PERFUSION ABOLISHES AUTO-REGULATION POSSIBLY VIA PROSTAGLANDIN RELEASE [J].
BORGDORFF, P ;
SIPKEMA, P ;
WESTERHOF, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (02) :H280-H287
[7]  
CANALE SD, 1990, J THORAC CARDIOVASC, V99, P327
[8]   THE EFFECT OF CARDIOPULMONARY BYPASS RESUSCITATION ON CARDIAC-ARREST INDUCED LACTIC-ACIDOSIS IN DOGS [J].
CARDEN, DL ;
MARTIN, GB ;
NOWAK, RM ;
FOREBACK, CC ;
TOMLANOVICH, MC .
RESUSCITATION, 1989, 17 (02) :153-161
[9]   A TOPOGRAPHIC QUANTITATIVE METHOD FOR MEASURING BRAIN-TISSUE PH UNDER PHYSIOLOGICAL AND PATHOPHYSIOLOGICAL CONDITIONS [J].
CSIBA, L ;
PASCHEN, W ;
HOSSMANN, KA .
BRAIN RESEARCH, 1983, 289 (1-2) :334-337
[10]  
FIACCADORI E, 1989, CRIT CARE MED, V17, P1286, DOI 10.1097/00003246-198912000-00008