SYSTEMIC HYPOTHERMIA IN TREATMENT OF SEVERE BRAIN INJURY - A REVIEW AND UPDATE

被引:63
作者
CLIFTON, GL
机构
[1] Department of Neurosurgery, The University of Texas Houston Health Science Center, Houston
关键词
HYPOTHERMIA; NORMOTHERMIA; BRAIN INJURY; GLASGOW COMA SCALE (GCS); MODERATE; SYSTEMIC;
D O I
10.1089/neu.1995.12.923
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Laboratory studies of moderate hypothermia (30-33 degrees C) after injury show diminished neuronal loss after ischemia, diminished excessive neurotransmitter release after ischemia, prevention of blood-brain barrier disruption after ischemia and brain injury, and behavioral improvement after brain injury. Clinical literature suggests that brief periods of moderate hypothermia (greater than or equal to 30 degrees C) in humans are not associated with cardiovascular, hematologic, metabolic, or neurological toxicity, Clinical studies were, therefore, organized to investigate the potential application of moderate systemic hypothermia in patients after severe brain injury. A study of 21 elective craniotomy patients and 11 patients with severe brain injury led to the conclusion that 32 to 33 degrees C was the lowest safe temperature in patients with severe brain injury. A randomized study of moderate hypothermia in 46 patients with Glasgow Coma Score (GCS) 4-7 gave an indication of improved neurologic outcome in the hypothermia group. A multicenter, randomized protocol to test the effect of moderate systemic hypothermia in patients with severe brain injury is in progress. Funded by the National Institutes of Health. The National Acute Brain Injury Study: Hypothermia tests the hypothesis that systemic hypothermia to 32-33 degrees C if rendered within 6 h of injury improves Glasgow Outcome Scores (GOS) at 6 months after injury in patients with severe brain injury (GCS 3-8).
引用
收藏
页码:923 / 927
页数:5
相关论文
共 39 条
[11]  
CLIFTON GL, 1992, J NEUROTRAUM, V9, pS487
[12]   CONDITIONS FOR PHARMACOLOGIC EVALUATION IN THE GERBIL MODEL OF FOREBRAIN ISCHEMIA [J].
CLIFTON, GL ;
TAFT, WC ;
BLAIR, RE ;
CHOI, SC ;
DELORENZO, RJ .
STROKE, 1989, 20 (11) :1545-1552
[13]   A PHASE-II STUDY OF MODERATE HYPOTHERMIA IN SEVERE BRAIN INJURY [J].
CLIFTON, GL ;
ALLEN, S ;
BARRODALE, P ;
PLENGER, P ;
BERRY, J ;
KOCH, S ;
FLETCHER, J ;
HAYES, RL ;
CHOI, SC .
JOURNAL OF NEUROTRAUMA, 1993, 10 (03) :263-271
[14]   MARKED PROTECTION BY MODERATE HYPOTHERMIA AFTER EXPERIMENTAL TRAUMATIC BRAIN INJURY [J].
CLIFTON, GL ;
JIANG, JY ;
LYETH, BG ;
JENKINS, LW ;
HAMM, RJ ;
HAYES, RL .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1991, 11 (01) :114-121
[15]   MECHANISM OF VENTRICULAR FIBRILLATION IN HYPOTHERMIA [J].
COVINO, BG ;
DAMATO, HE .
CIRCULATION RESEARCH, 1962, 10 (02) :148-&
[16]  
DRAKE CG, 1962, CAN MED ASSOC J, V87, P887
[17]   EFFECT OF HYPOTHERMIA OF 2-HOURS TO 24-HOURS ON OXYGEN CONSUMPTION AND CARDIAC OUTPUT IN THE DOG [J].
FISHER, B ;
RUSS, C ;
FEDOR, EJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1957, 188 (03) :473-476
[18]  
GRAY TC, 1957, LANCET, V1, P383
[19]  
HENDRICK EB, 1959, ARCH SURG-CHICAGO, V79, P362
[20]  
JENNETT B, 1975, LANCET, V1, P480