Impact of bronchopulmonary dysplasia, brain injury, and severe retinopathy on the outcome of extremely low-birth-weight infants at 18 months - Results from the trial of indomethacin prophylaxis in preterms

被引:485
作者
Schmidt, B
Asztalos, EV
Roberts, RS
Robertson, CMT
Sauve, RS
Whitfield, MF
机构
[1] McMaster Univ, Dept Pediat, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON L8N 3Z5, Canada
[3] Univ Toronto, Dept Pediat, Toronto, ON, Canada
[4] Glenrose Rehabil Hosp, Child Hlth Outcomes Unit, Edmonton, AB, Canada
[5] Univ Calgary, Dept Pediat, Calgary, AB T2N 1N4, Canada
[6] Univ Calgary, Dept Community Hlth Sci, Calgary, AB T2N 1N4, Canada
[7] Univ British Columbia, Dept Pediat, Vancouver, BC V6T 1W5, Canada
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2003年 / 289卷 / 09期
关键词
D O I
10.1001/jama.289.9.1124
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Despite more than 2 decades of outcomes research after very preterm birth, clinicians remain uncertain about the extent to which neonatal morbidities predict poor long-term outcomes of extremely low-birth-weight (ELBW) infants. Objective To determine the individual and combined prognostic effects of bronchopulmonary dysplasia (BPD), ultrasonographic signs of brain injury, and severe retinopathy of prematurity (ROP) on 18-month outcomes of ELBW infants. Design Inception cohort assembled for the Trial of Indomethacin Prophylaxis in Preterms (TIPP). Setting and Participants A total of 910 infants with birth weights of 500 to 999 g who were admitted to 1 of 32 neonatal intensive care units in Canada, the United States, Australia, New Zealand, and Hong Kong between 1996 and 1998 and who survived to a postmenstrual age of 36 weeks. Main Outcome Measures Combined end point of death or survival to 18 months with 1 or more of cerebral palsy, cognitive delay, severe hearing loss, and bilateral blindness. Results Each of the neonatal morbidities was similarly and independently correlated with a poor 18-month outcome. Odds ratios were 2.4 (95% confidence interval [CI], 1.8-3.2) for BPD, 3.7 (95% CI, 2.6-5.3) for brain injury, and 3.1 (95% CI, 1.9-5.0) for severe ROP. In children who were free of BPD, brain injury and severe ROP the rate of poor long-term outcomes was 18% (95% CI, 14%-22%). Corresponding rates with any 1, any 2, and all 3 neonatal morbidities were 42% (95% CI, 37%-47%), 62% (95% CI, 53%-70%), and 88% (64%-99%), respectively. Conclusion In ELBW infants who survive to a postmenstrual age of 36 weeks, a simple count of 3 common neonatal morbidities strongly predicts the risk of later death or neurosensory impairment.
引用
收藏
页码:1124 / 1129
页数:6
相关论文
共 22 条
[1]  
[Anonymous], 1987, Arch Ophthalmol, V105, P906
[2]  
[Anonymous], 1997, Arch Dis Child Fetal Neonatal Ed, V77, pF91
[3]  
AZIZ K, 1995, PEDIATRICS, V95, P837
[4]  
Bayley N., 1993, Bayley scales of infant and toddler development, VSecond
[5]   Evaluating research in developmental disabilities: a conceptual framework for reviewing treatment outcomes [J].
Butler, C ;
Chambers, H ;
Goldstein, M ;
Harris, S ;
Leach, J ;
Campbell, S ;
Adams, R ;
Darrah, J .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 1999, 41 (01) :55-59
[6]   Evaluating "old" definitions for the "new" bronchopulmonary dysplasia [J].
Davis, PG ;
Thorpe, K ;
Roberts, R ;
Schmidt, B ;
Doyle, LW ;
Kirpalani, H .
JOURNAL OF PEDIATRICS, 2002, 140 (05) :555-560
[7]   Outcome at 5 years of age of children 23 to 27 weeks' gestation: Refining the prognosis [J].
Doyle, LW .
PEDIATRICS, 2001, 108 (01) :134-141
[8]   Neurosensory outcome and growth at three years in extremely low birthweight infants:: follow-up results from the Swedish national prospective study [J].
Finnström, O ;
Olausson, PO ;
Sedin, G ;
Serenius, F ;
Svenningsen, N ;
Thiringer, K ;
Tunell, R ;
Wesström, G .
ACTA PAEDIATRICA, 1998, 87 (10) :1055-1060
[9]  
GARNER A, 1984, PEDIATRICS, V74, P127
[10]   Neurodevelopment and predictors of outcomes of children with birth weights of less than 1000 g: 1992-1995 [J].
Hack, M ;
Wilson-Costello, D ;
Friedman, H ;
Taylor, GH ;
Schluchter, M ;
Fanaroff, AA .
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 2000, 154 (07) :725-731