Effect of the no-flow interval and hypothermia on cerebral blood flow and metabolism during cardiopulmonary resuscitation in dogs

被引:23
作者
Shaffner, DH [1 ]
Eleff, SM [1 ]
Koehler, RC [1 ]
Traystman, RJ [1 ]
机构
[1] Johns Hopkins Med Inst, Dept Anesthesiol & Crit Care Med, Baltimore, MD 21205 USA
关键词
cerebral blood flow; cerebral metabolism; heart arrest; hypothermia; dogs;
D O I
10.1161/01.STR.29.12.2607
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-We sought (1) to determine the effect of brief periods of no flow on the subsequent forebrain blood flow during cardiopulmonary resuscitation (CPR) and (2) to test the hypothesis that hypothermia prevents the impact of the no-flow duration on cerebral blood flow (CBF) during CPR. Methods-No-flow intervals of 1.5, 3, and 6 minutes before CPR at brain temperatures of 28 degrees C and 38 degrees C were compared in 6 groups of anesthetized dogs. Microsphere-determined CBF and metabolism were measured before and during vest CPR adjusted to maintain cerebral perfusion pressure at 25 mm Hg. Results-Increasing the no-flow interval from 1.5 to 6 minutes at 38 degrees C decreased the CBF (18.6+/-3.6 to 6.1+/-1.7 mL/100 g per minute) and the cerebral metabolic rate (2.1+/-0.3 to 0.7+/-0.2 mL/100 g per minute) during CPR. Cooling to 28 degrees C before and during the arrest eliminated the detrimental effects of increasing the no-flow interval on CBF (16.8+/-1.0 to 14.8+/-1.9 mL/100 g per minute) and cerebral metabolic rate (1.1+/-0.1 to 1.3+/-0.1 mL/100 g per minute). Unlike the forebrain, 6 minutes of preceding cardiac arrest did not affect brain stem blood flow during CPR. Conclusions-Increasing the no-flow interval to 6 minutes in normothermic animals decreases the supratentorial blood flow and cerebral metabolic rate during CPR at a cerebral perfusion pressure of 25 mm Hg. Cooling to 28 degrees C eliminates the detrimental impact of the 6-minute no-flow interval on the reflow produced during CPR. The brain-protective effects of hypothermia include improving reflow during CPR after cardiac arrest. The effect of hypothermia and the impact of short durations of no flow on reperfusion indicate that increasing viscosity and reflex vasoconstriction are unlikely causes of the "no-reflow" phenomenon.
引用
收藏
页码:2607 / 2614
页数:8
相关论文
共 32 条
[1]  
ABRAMSON NS, 1991, NEW ENGL J MED, V324, P1225
[2]  
ABRAMSON NS, 1986, NEW ENGL J MED, V314, P397
[3]   THE INCREASE IN EXTRACELLULAR POTASSIUM CONCENTRATION IN THE ISCHEMIC BRAIN IN RELATION TO THE PRE-ISCHEMIC FUNCTIONAL-ACTIVITY AND CEREBRAL METABOLIC-RATE [J].
ASTRUP, J ;
REHNCRONA, S ;
SIESJO, BK .
BRAIN RESEARCH, 1980, 199 (01) :161-174
[4]   CEREBRAL PRESERVATION DURING CARDIOPULMONARY RESUSCITATION [J].
BIRCHER, N ;
SAFAR, P .
CRITICAL CARE MEDICINE, 1985, 13 (03) :185-190
[5]   RAPID MONITORING OF CHANGES IN WATER DIFFUSION-COEFFICIENTS DURING REVERSIBLE ISCHEMIA IN CAT AND RAT-BRAIN [J].
DAVIS, D ;
ULATOWSKI, J ;
ELEFF, S ;
IZUTA, M ;
MORI, S ;
SHUNGU, D ;
VANZIJL, PCM .
MAGNETIC RESONANCE IN MEDICINE, 1994, 31 (04) :454-460
[6]   CORRELATION OF RAPID CHANGES IN THE AVERAGE WATER DIFFUSION CONSTANT AND THE CONCENTRATIONS OF LACTATE AND ATP BREAKDOWN PRODUCTS DURING GLOBAL-ISCHEMIA IN CAT BRAIN [J].
DECANNIERE, C ;
ELEFF, S ;
DAVIS, D ;
VANZIJL, PCM .
MAGNETIC RESONANCE IN MEDICINE, 1995, 34 (03) :343-352
[7]   COUPLING OF ENERGY FAILURE AND DISSIPATIVE K+ FLUX DURING ISCHEMIA - ROLE OF PREISCHEMIC PLASMA-GLUCOSE CONCENTRATION [J].
EKHOLM, A ;
KATSURA, K ;
SIESJO, BK .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1993, 13 (02) :193-200
[8]   EFFECT OF CEREBRAL BLOOD-FLOW GENERATED DURING CARDIOPULMONARY-RESUSCITATION IN DOGS ON MAINTENANCE VERSUS RECOVERY OF ATP AND PH [J].
ELEFF, SM ;
KIM, H ;
SHAFFNER, DH ;
TRAYSTMAN, RJ ;
KOEHLER, RC .
STROKE, 1993, 24 (12) :2066-2073
[9]   NO-REFLOW AFTER CARDIAC-ARREST [J].
FISHER, M ;
HOSSMANN, KA .
INTENSIVE CARE MEDICINE, 1995, 21 (02) :132-141
[10]   EFFECT OF ADRENERGIC-DRUGS ON CEREBRAL BLOOD-FLOW, METABOLISM, AND EVOKED-POTENTIALS AFTER DELAYED CARDIOPULMONARY-RESUSCITATION IN DOGS [J].
GERVAIS, HW ;
SCHLEIEN, CL ;
KOEHLER, RC ;
BERKOWITZ, ID ;
SHAFFNER, DH ;
TRAYSTMAN, RJ .
STROKE, 1991, 22 (12) :1554-1561