Kunjunju A M, Gopagondanahalli K R, Chan Y, Sehgal A
Monash Newborn, Monash University Neonatologist, Monash Children's Hospital, Melbourne, VIC, Australia.
Department of Pathology, Monash Health, Melbourne, VIC, Australia.
J Perinatol. 2017 Dec;37(12):1310-1314. doi: 10.1038/jp.2017.130. Epub 2017 Sep 7.
Bronchopulmonary dysplasia (BPD) and the associated complication of pulmonary hypertension (PH) leads to increased mortality and a longer length of stay among survivors. Placental histopathology may give early clues of subsequent events. The objective was to evaluate the relationship of maternal vascular underperfusion (MVU) changes on placental histopathology with subsequent development of BPD-associated PH in a cohort of extremely premature infants.
In a cohort of preterm infants '⩽28 weeks' gestational age (GA) and with 'severe' BPD, this retrospective study evaluated specific placental histopathological changes and assessed the relationship with subsequent development of PH. 'Severe' BPD was defined as the need for ⩾30% oxygen and/or positive pressure ventilation at 36 weeks postmenstrual age. Placental and echocardiographic assessments were done by investigators masked to the grouping and clinical outcomes.
Fifty six infants with severe BPD formed the cohort; PH was noted in 22 (39.3%) infants. The GA of the infants with and without PH was comparable (25.8±1.6 vs 25.8±1.3 weeks, P=0.9). On placental histopathological examination, 13 (23%) had features of MVU. On univariate logistic regression, the presence of changes consistent with MVU increased the relative risk of subsequent BPD-associated PH by 2.75 (95% confidence interval 1.56 to 4.85, P=0.004). The significance persisted after adjustment for GA. Stratification by the presence or absence of fetal growth restriction, yielded nonsignificant associations (P=0.17).
Based on the results of the present study, specific placental histopathological changes may give early clues to the subsequent development of BPD-associated PH.
支气管肺发育不良(BPD)及相关的肺动脉高压(PH)并发症会导致死亡率增加,且存活者住院时间延长。胎盘组织病理学可能为后续事件提供早期线索。本研究旨在评估一组极早产儿中,胎盘组织病理学上母体血管灌注不足(MVU)的变化与BPD相关PH后续发生之间的关系。
在一组胎龄“≤28周”且患有“重度”BPD的早产儿中,这项回顾性研究评估了特定的胎盘组织病理学变化,并评估了其与PH后续发生之间的关系。“重度”BPD定义为在月经龄36周时需要≥30%的氧气和/或正压通气。胎盘和超声心动图评估由对分组和临床结果不知情的研究人员进行。
56例患有重度BPD的婴儿组成了该队列;22例(39.3%)婴儿出现PH。有PH和无PH的婴儿胎龄相当(25.8±1.6 vs 25.8±1.3周,P = 0.9)。胎盘组织病理学检查显示,13例(23%)具有MVU特征。单因素逻辑回归分析显示,与MVU一致的变化使后续BPD相关PH的相对风险增加2.75(95%置信区间1.56至4.85,P = 0.004)。在对胎龄进行调整后,该显著性仍然存在。根据是否存在胎儿生长受限进行分层,结果显示无显著相关性(P = 0.17)。
基于本研究结果,特定的胎盘组织病理学变化可能为BPD相关PH的后续发生提供早期线索。