Division of Pulmonary Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Department of General Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Pediatr Pulmonol. 2020 Jun;55(6):1456-1467. doi: 10.1002/ppul.24736. Epub 2020 Mar 19.
Congenital diaphragmatic hernia (CDH) is associated with variable degrees of lung hypoplasia. Pulmonary support at 30 days postnatal age was found to be the strongest predictor of inpatient mortality and morbidity among CDH infants and was also associated with higher pulmonary morbidity at 1 and 5 years. It is not known, however, if there is a relationship between the need for medical therapy at 30 days of life and subsequent abnormalities in lung function as reflected in infant pulmonary function test (iPFT) measurements.
We hypothesized that CDH infants who require more intensive therapy at 30 days would have more abnormal iPFT values at the time of their first infant pulmonary function study, reflecting the more severe spectrum of lung hypoplasia.
A single-institution chart review of all CDH survivors who were enrolled in a Pulmonary Hypoplasia Program (PHP) through July 2019, and treated from 2002 to 2019 was performed. All infants were divided into groups based on their need for noninvasive (supplemental oxygen, high flow therapy, noninvasive mechanical ventilation) or invasive (mechanical ventilation, extracorporeal membrane oxygenation) respiratory assistance, bronchodilators, diuretic use, and pulmonary hypertension (PH) therapy (inhaled and/or systemic drugs) at 30 days. Descriptive and statistical analyses were performed between groups comparing subsequent lung function measurements.
A total of 382 infants (median gestational age [GA] 38.4 [interquartile range (IQR) = 37.1-39] weeks, 41.8% female, 70.9% Caucasian) with CDH were enrolled in the PHP through July 2019, and 118 infants underwent iPFT. The median age of the first iPFT was 6.6 (IQR = 5.3-11.7) months. Those requiring any pulmonary support at 30 days had a higher functional residual capacity (FRC) (z) (P = .03), residual volume (RV) (z) (P = .008), ratio of RV to total lung capacity (RV/TLC) (z) (P = .0001), and ratio of FRC to TLC (FRC/TLC) (z) (P = .001); a lower forced expiratory volume at 0.5 seconds (FEV0.5) (z) (P = .03) and a lower respiratory system compliance (Crs) (P = .01) than those who did not require any support. Similarly, those requiring diuretics and/or PH therapy at 30 days had higher fractional lung volumes, lower forced expiratory flows and Crs than infants who did not require such support (P < .05).
Infants requiring any pulmonary support, diuretics and/or PH therapy at 30 postnatal days have lower forced expiratory flows and higher fractional lung volumes, suggesting a greater degree of lung hypoplasia. Our study suggests that the continued need for PH, diuretic or pulmonary support therapy at 30 days can be used as additional risk-stratification measurements for evaluation of infants with CDH.
先天性膈疝(CDH)与不同程度的肺发育不全有关。研究发现,新生儿期 30 天后的肺支持是 CDH 婴儿住院死亡率和发病率的最强预测指标,也与 1 岁和 5 岁时更高的肺部发病率有关。然而,目前尚不清楚 30 天生命时需要医疗治疗与随后的肺功能异常之间是否存在关系,而肺功能异常反映在婴儿肺功能测试(iPFT)测量中。
我们假设在 30 天时需要更强化治疗的 CDH 婴儿在进行第一次婴儿肺功能研究时,其 iPFT 值会更异常,反映出更严重的肺发育不全。
对所有在 2002 年至 2019 年期间通过 7 月的肺发育不全计划(PHP)入组并接受治疗的 CDH 幸存者进行了一项单机构图表回顾,所有婴儿均根据其在 30 天时需要无创(补充氧气、高流量治疗、无创机械通气)或有创(机械通气、体外膜氧合)呼吸支持、支气管扩张剂、利尿剂和肺动脉高压(PH)治疗(吸入和/或全身药物)的情况分为组。比较组间后续肺功能测量的描述性和统计分析。
共有 382 名(中位胎龄 [GA] 38.4 [四分位距 [IQR] 37.1-39] 周,41.8%为女性,70.9%为白种人)患有 CDH 的婴儿通过 7 月的 PHP 入组,其中 118 名婴儿接受了 iPFT。第一次 iPFT 的中位年龄为 6.6(IQR 5.3-11.7)个月。那些在 30 天时需要任何肺支持的婴儿具有更高的功能残气量(FRC)(z)(P = 0.03)、残气量(RV)(z)(P = 0.008)、RV 与总肺容量的比值(RV/TLC)(z)(P = 0.0001)和 FRC 与 TLC 的比值(FRC/TLC)(z)(P = 0.001);用力呼气 0.5 秒时的呼气量(FEV0.5)(z)(P = 0.03)和呼吸系统顺应性(Crs)(P = 0.01)更低。同样,那些在 30 天需要利尿剂和/或 PH 治疗的婴儿的分肺容积更高,用力呼气流量和 Crs 低于未接受此类支持的婴儿(P < 0.05)。
在新生儿期 30 天后需要任何肺支持、利尿剂和/或 PH 治疗的婴儿的呼气流量更低,分肺容积更高,提示肺发育不全程度更大。我们的研究表明,在 30 天继续需要 PH、利尿剂或肺支持治疗可作为评估 CDH 婴儿的额外风险分层测量。