SLEEP ARCHITECTURE AND CONTINUITY MEASURES OF NEONATES WITH CHRONIC LUNG-DISEASE

被引:33
作者
SCHER, MS
RICHARDSON, GA
SALERNO, DG
DAY, NL
GUTHRIE, RD
机构
[1] UNIV PITTSBURGH,CHILDRENS HOSP PITTSBURGH,PITTSBURGH,PA 15260
[2] UNIV PITTSBURGH,DEPT PSYCHIAT & EPIDEMIOL,PITTSBURGH,PA 15260
关键词
PRETERM NEONATES; CHRONIC LUNG DISEASE; EEG SLEEP STUDIES;
D O I
10.1093/sleep/15.3.195
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Electroencephalographic (EEG) sleep studies of 25 preterm neonates with chronic lung disease (CLD) corrected to a fullterm postconceptional age were compared with recordings from two groups of neonates without CLD: a fullterm appropriate for gestational age group (9 patients) and a preterm group studied at a corrected term postconceptional age (15 patients). Electrographic/polygraphic studies were obtained using 21-channel EEG recordings. Scores were tabulated based on minute-by-minute visual analyses of sleep state, number and duration of arousals, body movements and rapid eye movements (REM). A significant reduction in the percentage of active sleep was noted in the CLD group compared to both control groups (31.15% vs. 47.01% and 52.9%, respectively). The mean percentage of indeterminate sleep was significantly increased in the study group as compared to both control groups (31.23% vs. 15.18% and 11.5%). In addition, significant differences were noted between the CLD group and the healthy preterm control group with respect to the number (0.29/minute vs. 0.13/minute) and duration (4.8 seconds vs. 2.94 seconds) of arousals as well as the total number of body movements (1.57/minute vs. 0.74/minute). These data suggest that neurophysiological organization of the immature brain, as reflected in neonatal sleep architecture and continuity measures, is adversely affected in neonates with CLD. EEG sleep architecture and continuity measures may be helpful in predicting the longitudinal outcome of infants with CLD as this group is at risk for adverse neurodevelopmental outcome.
引用
收藏
页码:195 / 201
页数:7
相关论文
共 41 条
[21]  
MEISELS SJ, 1986, PEDIATRICS, V77, P345
[22]   CEREBRAL-DYSFUNCTION AFTER CHRONIC HYPOXIA IN CHILDREN [J].
ODOUGHERTY, M ;
WRIGHT, FS ;
LOEWENSON, RB ;
TORRES, F .
NEUROLOGY, 1985, 35 (01) :42-46
[23]   ELECTROENCEPHALOGRAPHIC ABNORMALITIES IN INFANTS WITH HYPOPLASTIC LEFT HEART SYNDROME [J].
OLSON, DM ;
SHEWMON, DA .
PEDIATRIC NEUROLOGY, 1989, 5 (02) :93-98
[24]   INCIDENCE AND EVOLUTION OF SUBEPENDYMAL AND INTRA-VENTRICULAR HEMORRHAGE - STUDY OF INFANTS WITH BIRTH WEIGHTS LESS THAN 1,500 GM [J].
PAPILE, LA ;
BURSTEIN, J ;
BURSTEIN, R ;
KOFFLER, H .
JOURNAL OF PEDIATRICS, 1978, 92 (04) :529-534
[25]  
PERLMAN J, 1990, INT PEDIAT, V5, P108
[26]   NEUROPSYCHOLOGICAL TEST-PERFORMANCE IN MILDLY HYPOXEMIC PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY-DISEASE [J].
PRIGATANO, GP ;
PARSONS, O ;
LEVIN, DC ;
WRIGHT, E ;
HAWRYLUK, G .
JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1983, 51 (01) :108-116
[27]   VISUAL SIMPLE REACTION TIME IN CYANOTIC HEART DISEASE [J].
ROSENTHAL, A .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1967, 114 (02) :139-+
[28]   A DEVELOPMENTAL MARKER OF CENTRAL NERVOUS-SYSTEM MATURATION .1. [J].
SCHER, MS .
PEDIATRIC NEUROLOGY, 1988, 4 (05) :265-273
[29]   A DEVELOPMENTAL MARKER OF CENTRAL NERVOUS-SYSTEM MATURATION .2. [J].
SCHER, MS .
PEDIATRIC NEUROLOGY, 1988, 4 (06) :329-336
[30]   THE EFFECTS OF PRENATAL ALCOHOL AND MARIJUANA EXPOSURE - DISTURBANCES IN NEONATAL SLEEP CYCLING AND AROUSAL [J].
SCHER, MS ;
RICHARDSON, GA ;
COBLE, PA ;
DAY, NL ;
STOFFER, DS .
PEDIATRIC RESEARCH, 1988, 24 (01) :101-105