Thygesen Sandra Kruchov, Olsen Morten, Østergaard John R, Sørensen Henrik Toft
Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus N, Denmark.
Department of Paediatrics, Aarhus University Hospital, Aarhus N, Denmark.
BMJ Open. 2016 Oct 11;6(10):e011643. doi: 10.1136/bmjopen-2016-011643.
Infant respiratory distress syndrome (IRDS) is a known risk factor for intracerebral haemorrhage/intraventricular haemorrhage (ICH/IVH) and periventricular leucomalacia. These lesions are known to increase the risk of cerebral palsy (CP). Thus, we wanted to examine the long-term risk of CP following IRDS in moderately late and late preterm infants.
Population-based cohort study.
All hospitals in Denmark.
We used nationwide medical registries to identify a cohort of all moderately and late preterm infants (defined as birth during 32-36 full gestational weeks) born in Denmark in 1997-2007 with and without hospital diagnosed IRDS.
We followed study participants from birth until first diagnosis of CP, emigration, death or end of follow-up in 2014. We computed the cumulative incidence of CP before age 8 years and used Cox's regression analysis to compute HRs of IRDS, comparing children with IRDS to those without IRDS. HRs were adjusted for multiple covariates.
We identified 39 420 moderately late and late preterm infants, of whom 2255 (5.7%) had IRDS. The cumulative incidence of CP was 1.9% in infants with IRDS and 0.5% in the comparison cohort. The adjusted HR of CP was 2.0 (95% CI 1.4 to 2.9). The adjusted HR of CP was 12 (95% CI 4.5 to 34) in children with IRDS accompanied by a diagnosis of ICH/IVH. After restriction to children without diagnoses of perinatal breathing disorders other than IRDS, congenital heart disease and viral or bacterial infections occurring within 4 days of birth, the overall adjusted HR was 2.1 (95% CI 1.4 to 3.1).
The risk of CP was increased in moderately late and late preterm infants with IRDS compared with infants without IRDS born during the same gestational weeks.
婴儿呼吸窘迫综合征(IRDS)是脑内出血/脑室内出血(ICH/IVH)和脑室周围白质软化的已知危险因素。已知这些病变会增加脑瘫(CP)的风险。因此,我们想研究中度晚期和晚期早产儿患IRDS后患CP的长期风险。
基于人群的队列研究。
丹麦所有医院。
我们使用全国性医疗登记系统,确定了1997年至2007年在丹麦出生的所有中度和晚期早产儿(定义为孕32 - 36足周出生)队列,这些婴儿有或没有医院诊断的IRDS。
我们对研究参与者从出生开始随访,直至首次诊断为CP、移民、死亡或2014年随访结束。我们计算了8岁前CP的累积发病率,并使用Cox回归分析计算IRDS的风险比(HRs),将患IRDS的儿童与未患IRDS的儿童进行比较。HRs针对多个协变量进行了调整。
我们确定了39420名中度晚期和晚期早产儿,其中2255名(5.7%)患有IRDS。患IRDS婴儿的CP累积发病率为1.9%,对照组为0.5%。CP的调整后HR为2.0(95%置信区间1.4至2.9)。伴有ICH/IVH诊断的患IRDS儿童的CP调整后HR为12(95%置信区间4.5至34)。在将研究对象限制为除IRDS外无围产期呼吸障碍、先天性心脏病以及出生后4天内发生的病毒或细菌感染诊断的儿童后,总体调整后HR为2.1(95%置信区间1.4至3.1)。
与相同孕周出生的未患IRDS婴儿相比,中度晚期和晚期早产儿患IRDS后患CP的风险增加。