Department of Obstetrics and Gynaecology and the School of Population and Public Health, University of British Columbia and the Children's and Women's Health Centre of British Columbia, Vancouver, BC, Canada.
BJOG. 2011 Dec;118(13):1617-29. doi: 10.1111/j.1471-0528.2011.03128.x. Epub 2011 Sep 6.
To identify the disease processes underlying the increasing rate of gestational age-specific perinatal mortality observed under the fetuses-at-risk model.
Retrospective cohort study.
USA and Nova Scotia, Canada.
Births in the USA (1995 and 2005) and Nova Scotia, Canada (1988-2007).
Incidence rates of perinatal death and serious neonatal morbidity were calculated using the fetuses-at-risk approach (e.g. cumulative incidence of stillbirth during any gestational week per 1000 fetuses at risk of stillbirth).
Perinatal mortality and serious neonatal morbidity.
Perinatal mortality rates increased with advancing gestation. Rates of bronchopulmonary dysplasia, intraventricular haemorrhage, periventricular leucomalacia and retinopathy of prematurity were highest in early gestation, whereas rates of meconium aspiration syndrome and aspiration pneumonitis were highest at late term and post-term gestation. Respiratory depression (i.e. delay in initiating and maintaining respiration after birth, low 5-minute Apgar score or seizures caused by neonatal encephalopathy) showed an increase from 34 weeks onwards. The increase in perinatal mortality rates at late gestation was congruent with increases in respiratory depression. Other findings included a high incidence of respiratory distress syndrome at late gestation, a nonspecific pattern in the gestational age-specific rates of necrotising enterocolitis and high rates of sudden infant death syndrome at late gestation.
The natural history of pregnancy is characterised by diseases of early and late gestation, with the latter largely determining patterns of gestational age-specific perinatal mortality. These findings have implications for obstetric theory and provide insight into various contemporary phenomena, including the rise in iatrogenic late preterm birth.
确定高危儿模型下观察到的特定胎龄围产儿死亡率增加的潜在疾病过程。
回顾性队列研究。
美国和加拿大新斯科舍省。
美国(1995 年和 2005 年)和加拿大新斯科舍省(1988-2007 年)的分娩。
使用高危儿方法计算围产儿死亡和严重新生儿发病率的发生率(例如,每 1000 例有死胎风险的胎儿在任何妊娠周的死胎累积发生率)。
围产儿死亡率和严重新生儿发病率。
围产儿死亡率随胎龄的增加而增加。支气管肺发育不良、脑室内出血、脑室周围白质软化和早产儿视网膜病变的发生率在早期最高,而胎粪吸入综合征和吸入性肺炎的发生率在晚期和过期妊娠最高。呼吸抑制(即出生后开始和维持呼吸的延迟、低 5 分钟 Apgar 评分或新生儿脑病引起的癫痫发作)从 34 周开始增加。晚期妊娠围产儿死亡率的增加与呼吸抑制的增加一致。其他发现包括晚期妊娠呼吸窘迫综合征的发病率较高,坏死性小肠结肠炎的胎龄特异性发生率无特异性模式,以及晚期妊娠突然婴儿死亡综合征的高发生率。
妊娠的自然史以早、晚期妊娠疾病为特征,后者在很大程度上决定了胎龄特异性围产儿死亡率的模式。这些发现对产科理论有影响,并为各种当代现象提供了深入了解,包括医源性晚期早产的增加。