Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy

被引:2082
作者
Shankaran, S
Laptook, AR
Ehrenkranz, RA
Tyson, JE
McDonald, SA
Donovan, EF
Fanaroff, AA
Poole, WK
Wright, LL
Higgins, RD
Finer, NN
Carlo, WA
Duara, S
Oh, W
Cotten, CM
Stevenson, DK
Stoll, BJ
Lemons, JA
Guillet, R
Jobe, AH
机构
[1] Wayne State Univ, Div Neonatal Perinatal Med, Detroit, MI USA
[2] Women & Infants Hosp Rhode Isl, Providence, RI 02908 USA
[3] Yale Univ, Sch Med, New Haven, CT USA
[4] Univ Texas, Houston, TX USA
[5] Res Triangle Inst, Res Triangle Pk, NC 27709 USA
[6] Univ Cincinnati, Coll Med, Cincinnati, OH USA
[7] Case Western Reserve Univ, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
[8] NICHHD, Bethesda, MD 20892 USA
[9] Univ Calif San Diego, San Diego, CA 92103 USA
[10] Univ Alabama, Birmingham, AL USA
[11] Univ Miami, Dept Pediat, Miami, FL 33152 USA
[12] Duke Univ, Med Ctr, Durham, NC USA
[13] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
[14] Emory Univ, Sch Med, Atlanta, GA USA
[15] Indiana Univ, Sch Med, Indianapolis, IN USA
[16] Univ Rochester, Rochester, NY USA
关键词
D O I
10.1056/NEJMcps050929
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Hypothermia is protective against brain injury after asphyxiation in animal models. However, the safety and effectiveness of hypothermia in term infants with encephalopathy is uncertain. METHODS: We conducted a randomized trial of hypothermia in infants with a gestational age of at least 36 weeks who were admitted to the hospital at or before six hours of age with either severe acidosis or perinatal complications and resuscitation at birth and who had moderate or severe encephalopathy. Infants were randomly assigned to usual care (control group) or whole-body cooling to an esophageal temperature of 33.5 degreesC for 72 hours, followed by slow rewarming (hypothermia group). Neurodevelopmental outcome was assessed at 18 to 22 months of age. The primary outcome was a combined end point of death or moderate or severe disability. RESULTS: Of 239 eligible infants, 102 were assigned to the hypothermia group and 106 to the control group. Adverse events were similar in the two groups during the 72 hours of cooling. Primary outcome data were available for 205 infants. Death or moderate or severe disability occurred in 45 of 102 infants (44 percent) in the hypothermia group and 64 of 103 infants (62 percent) in the control group (risk ratio, 0.72; 95 percent confidence interval, 0.54 to 0.95; P=0.01). Twenty-four infants (24 percent) in the hypothermia group and 38 (37 percent) in the control group died (risk ratio, 0.68; 95 percent confidence interval, 0.44 to 1.05; P=0.08). There was no increase in major disability among survivors; the rate of cerebral palsy was 15 of 77 (19 percent) in the hypothermia group as compared with 19 of 64 (30 percent) in the control group (risk ratio, 0.68; 95 percent confidence interval, 0.38 to 1.22; P=0.20). CONCLUSIONS: Whole-body hypothermia reduces the risk of death or disability in infants with moderate or severe hypoxic-ischemic encephalopathy.
引用
收藏
页码:1574 / 1584
页数:11
相关论文
共 35 条
[1]   Assessment of neonatal encephalopathy by amplitude-integrated electroencephalography [J].
al Naqeeb, N ;
Edwards, AD ;
Cowan, FM ;
Azzopardi, D .
PEDIATRICS, 1999, 103 (06) :1263-1271
[2]   Hyperthermia delayed by 24 hours aggravates neuronal damage in rat hippocampus following global ischemia [J].
Baena, RC ;
Busto, R ;
Dietrich, WD ;
Globus, MYT ;
Ginsberg, MD .
NEUROLOGY, 1997, 48 (03) :768-773
[3]   HYPOTHERMIC CEREBRAL REPERFUSION AND RECOVERY FROM ISCHEMIA [J].
BALDWIN, WA ;
KIRSCH, JR ;
HURN, PD ;
TOUNG, WSP ;
TRAYSTMAN, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (03) :H774-H781
[4]  
Barkovich AJ, 1998, AM J NEURORADIOL, V19, P143
[5]  
BAYLEY N, 1993, BAYLEY SCALES INFANT, V2
[6]   SMALL DIFFERENCES IN INTRAISCHEMIC BRAIN TEMPERATURE CRITICALLY DETERMINE THE EXTENT OF ISCHEMIC NEURONAL INJURY [J].
BUSTO, R ;
DIETRICH, WD ;
GLOBUS, MYT ;
VALDES, I ;
SCHEINBERG, P ;
GINSBERG, MD .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1987, 7 (06) :729-738
[7]   PROTECTION AGAINST HIPPOCAMPAL CA1 CELL LOSS BY POSTISCHEMIC HYPOTHERMIA IS DEPENDENT ON DELAY OF INITIATION AND DURATION [J].
CARROLL, M ;
BEEK, O .
METABOLIC BRAIN DISEASE, 1992, 7 (01) :45-50
[8]   MODERATE HYPOTHERMIA MITIGATES NEURONAL DAMAGE IN THE RAT-BRAIN WHEN INITIATED SEVERAL HOURS FOLLOWING TRANSIENT CEREBRAL-ISCHEMIA [J].
COIMBRA, C ;
WIELOCH, T .
ACTA NEUROPATHOLOGICA, 1994, 87 (04) :325-331
[9]   DELAYED AND PROLONGED POSTISCHEMIC HYPOTHERMIA IS NEUROPROTECTIVE IN THE GERBIL [J].
COLBOURNE, F ;
CORBETT, D .
BRAIN RESEARCH, 1994, 654 (02) :265-272
[10]   Specific inhibition of apoptosis after cerebral hypoxia-ischaemia by moderate post-insult hypothermia [J].
Edwards, AD ;
Yue, X ;
Squier, MV ;
Thoresen, M ;
Cady, EB ;
Penrice, J ;
Cooper, CE ;
Wyatt, JS ;
Reynolds, EOR ;
Mehmet, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 217 (03) :1193-1199