Department of Pediatrics and Cardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.
Departments of Epidemiology and Biostatistics, and Neurology, University of California San Francisco, San Francisco, CA, USA.
Pediatr Res. 2022 Feb;91(3):652-658. doi: 10.1038/s41390-021-01475-w. Epub 2021 Mar 31.
An increased risk for bronchopulmonary dysplasia (BPD) exists when moderate-to-large patent ductus arteriosus shunts (hsPDA) persist beyond 14 days.
To examine the interaction between prolonged exposures to tracheal ventilation (≥10 days) and hsPDA on the incidence of BPD in infants <28 weeks gestation.
Predefined definitions of prolonged ventilation (≥10 days), hsPDA (≥14 days), and BPD (room air challenge test at 36 weeks) were used to analyze deidentified data from the multicenter TRIOCAPI RCT in a secondary analysis of the trial.
Among 307 infants who survived >14 days, 41 died before 36 weeks. Among survivors, 93/266 had BPD. The association between BPD and hsPDA depended on the length of intubation. In multivariable analyses, prolonged hsPDA shunts were associated with increased BPD (odds ratio (OR) (95% confidence interval (CI)) = 3.00 (1.58-5.71)) when infants required intubation for ≥10 days. In contrast, there was no significant association between hsPDA exposure and BPD when infants were intubated <10 days (OR (95% CI) = 1.49 (0.98-2.26)). A similar relationship between prolonged hsPDA and length of intubation was found for BPD/death (n = 307): infants intubated ≥10 days: OR (95% CI) = 2.41 (1.47-3.95)); infants intubated <10 days: OR (95% CI) = 1.37 (0.86-2.19)).
Moderate-to-large PDAs were associated with increased risks of BPD and BPD/death-but only when infants required intubation ≥10 days.
Infants with a moderate-to-large hsPDA that persist beyond 14 days are only at risk for developing BPD if they also receive prolonged tracheal ventilation for ≥10 days. Infants who receive less ventilatory support (intubation for <10 days) have the same incidence of BPD whether the ductus closes shortly after birth or whether it persists as a moderate-to-large shunt for several weeks. Early PDA closure may be unnecessary in infants who require short durations of intubation since the PDA does not seem to alter the incidence of BPD in infants who require intubation for <10 days.
当中至大动脉导管未闭(hsPDA)持续超过 14 天时,支气管肺发育不良(BPD)的风险增加。
研究持续时间较长的气管通气(≥10 天)和 hsPDA 对胎龄<28 周的婴儿 BPD 发生率的相互作用。
使用多中心 TRIOCAPI RCT 的预先定义的长时间通气(≥10 天)、hsPDA(≥14 天)和 BPD(36 周时空气挑战试验)定义,对试验进行二次分析,对来自该试验的去识别数据进行分析。
在 307 名存活超过 14 天的婴儿中,有 41 名在 36 周前死亡。在幸存者中,有 93/266 人患有 BPD。BPD 与 hsPDA 之间的关联取决于插管时间。多变量分析显示,当婴儿需要插管≥10 天时,长时间的 hsPDA 分流与 BPD 发生率增加相关(比值比(OR)(95%置信区间(CI))=3.00(1.58-5.71))。相比之下,当婴儿插管<10 天时,hsPDA 暴露与 BPD 之间没有显著关联(OR(95%CI)=1.49(0.98-2.26))。在 BPD/死亡(n=307)方面,也发现了长时间 hsPDA 和插管时间之间的类似关系:插管≥10 天的婴儿:OR(95%CI)=2.41(1.47-3.95));插管<10 天的婴儿:OR(95%CI)=1.37(0.86-2.19))。
中至大动脉导管未闭与 BPD 和 BPD/死亡的风险增加有关-但仅在婴儿需要插管≥10 天时。
胎龄超过 14 天且存在中至大动脉导管未闭的婴儿,如果还需要气管通气≥10 天,才会有发生 BPD 的风险。接受通气支持时间较短(插管<10 天)的婴儿,无论动脉导管在出生后不久关闭还是持续存在数周作为中至大动脉导管未闭,其 BPD 发生率相同。对于需要短时间插管的婴儿,早期关闭动脉导管可能是不必要的,因为对于需要插管<10 天的婴儿,动脉导管似乎不会改变 BPD 的发生率。