Clinical signs predict 30-month neurodevelopmental outcome after neonatal encephalopathy

被引:98
作者
Miller, SP
Latal, B
Clark, H
Barnwell, A
Glidden, D
Barkovich, AJ
Ferriero, DM
Partridge, JC
机构
[1] Univ Calif San Francisco, Neonatal Brain Disorder Ctr, Dept Pediat, San Francisco Gen Hosp, San Francisco, CA 94110 USA
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94110 USA
[4] Univ Calif San Francisco, Dept Biostat, San Francisco, CA 94110 USA
[5] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94110 USA
关键词
neonatal encephalopathy; seizures; hypoxia-ischemia encephalopathy score;
D O I
10.1016/S0002-9378(03)00908-6
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: This study was undertaken to determine the value of a neonatal encephalopathy score (ES) and the presence of seizures for predicting 30-month neurodevelopmental outcome. Study design: In a cohort study, 68 term newborn infants with encephalopathy were evaluated with an ES based on alertness, feeding, tone, respiratory status, reflexes, and seizure activity (range: 0-6). Seizures were noted as present or absent clinically. Significant cognitive deficits (Mental Development Index <70), motor disability (spastic triplegia/quadriplegia), or death were abnormal outcomes. Results: Twenty-two newborn infants (32%) had abnormal outcomes. With the use of maximum ES and presence of seizures from days 1 to 3 of life, 87% of newborn infants were correctly classified (area under receiver operating curve 0.93). By using ES and presence of seizures on day 1 only, 87% of newborn infants were correctly classified (area under receiver operating curve 0.89). Conclusion: The severity of neonatal encephalopathy and the presence of seizures are valuable predictors of 30-month neurodevelopmental outcome, as early as the first day of life. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 99
页数:7
相关论文
共 29 条
[1]  
Badawi N, 1998, BMJ-BRIT MED J, V317, P1549, DOI 10.1136/bmj.317.7172.1549
[2]   Intrapartum risk factors for newborn encephalopathy: the Western Australian case-control study [J].
Badawi, N ;
Kurinczuk, JJ ;
Keogh, JM ;
Alessandri, LM ;
O'Sullivan, F ;
Burton, PR ;
Pemberton, PJ ;
Stanley, FJ .
BMJ-BRITISH MEDICAL JOURNAL, 1998, 317 (7172) :1554-1558
[3]  
Barkovich AJ, 1999, AM J NEURORADIOL, V20, P1399
[4]  
BAYLEY N, 1993, BAYLEY SCALES INFANT, V2
[5]   Early developmental outcomes after newborn encephalopathy [J].
Dixon, G ;
Badawi, N ;
Kurinczuk, JJ ;
Keogh, JM ;
Silburn, SR ;
Zubrick, SR ;
Stanley, FJ .
PEDIATRICS, 2002, 109 (01) :26-33
[6]   Predicting the outcome of postasphyxial hypoxic-ischemic encephalopathy within 4 hours of birth [J].
Ekert, P ;
Perlman, M ;
Steinlin, M ;
Hao, Y .
JOURNAL OF PEDIATRICS, 1997, 131 (04) :613-617
[7]   HYPOXIC-ISCHEMIC ENCEPHALOPATHY IN TERM NEONATES - PERINATAL FACTORS AND OUTCOME [J].
FINER, NN ;
ROBERTSON, CM ;
RICHARDS, RT ;
PINNELL, LE ;
PETERS, KL .
JOURNAL OF PEDIATRICS, 1981, 98 (01) :112-117
[8]   ASPHYXIAL COMPLICATIONS IN THE TERM NEWBORN WITH SEVERE UMBILICAL ACIDEMIA [J].
GOODWIN, TM ;
BELAI, I ;
HERNANDEZ, P ;
DURAND, M ;
PAUL, RH .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (06) :1506-1512
[9]   Early prediction of neurologic outcome after perinatal depression [J].
Hajnal, BL ;
Sahebkar-Moghaddam, F ;
Barnwell, AJ ;
Barkovich, AJ ;
Ferriero, DM .
PEDIATRIC NEUROLOGY, 1999, 21 (05) :788-793
[10]  
Hollingshead A.B., 1958, Social class and mental illness