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先天性膈疝和肺隔离症患者的发病率和结局。

Incidence and outcomes of patients with congenital diaphragmatic hernia and pulmonary sequestration.

机构信息

Department of Pediatric Surgery, McGovern Medical School at the University of Texas Health Science Center and Children's Memorial Hermann Hospital, 6431 Fannin St, MSB 5.258, Houston, TX 77030, United States.

Department of Pediatric Surgery, McGovern Medical School at the University of Texas Health Science Center and Children's Memorial Hermann Hospital, 6431 Fannin St, MSB 5.258, Houston, TX 77030, United States.

出版信息

J Pediatr Surg. 2021 Jun;56(6):1126-1129. doi: 10.1016/j.jpedsurg.2021.02.032. Epub 2021 Feb 24.

DOI:10.1016/j.jpedsurg.2021.02.032
PMID:33752909
Abstract

BACKGROUND

Bronchopulmonary sequestration (BPS) has long been identified in patients with congenital diaphragmatic hernia (CDH), however the reported incidence in the literature varies widely and is not based on large series.

METHODS

Version 4 of the Congenital Diaphragmatic Hernia Study Group (CDHSG) included questions specifically identifying BPS-associated cases. The data were prospectively collected between 2015 and 2020. Clinical characteristics and outcomes for CDH+BPS patients were compared to patients without BPS using univariate and multiple regression analyses.

RESULTS

Out of 2118 total patients, 72 had a pulmonary sequestration (3.4%). The amount of CDH+BPS with high-risk (CDHSG type C and D) defects was significantly greater than those without BPS (68.0% vs 49.3%, respectively; p = 0.001). The need for ECLS (35/72, 48.6%) and overall mortality (21/72, 29.2%) was significantly higher in CDH+BPS. When corrected for hernia size, cardiac and chromosomal anomalies, the need for ECLS (OR 2.2, p = 0.004) and mortality (OR 2.0, p = 0.015) was significantly greater in CDH+BPS.

CONCLUSIONS

This is the largest series to look at the incidence of BPS in children with CDH. They are associated with larger defect sizes, a greater need for ECLS and higher mortality than those patients without BPS.

摘要

背景

支气管肺隔离症(BPS)在先天性膈疝(CDH)患者中早已被发现,然而文献中的报道发生率差异很大,且没有基于大系列数据。

方法

第 4 版先天性膈疝研究组(CDHSG)纳入了专门确定与 BPS 相关病例的问题。数据是在 2015 年至 2020 年期间前瞻性收集的。使用单变量和多变量回归分析比较了 CDH+BPS 患者与无 BPS 患者的临床特征和结局。

结果

在 2118 例患者中,72 例有肺隔离症(3.4%)。CDH+BPS 患者中高危(CDHSG 类型 C 和 D)缺陷的数量明显多于无 BPS 患者(分别为 68.0%和 49.3%;p=0.001)。需要体外膜肺氧合(ECLS)的患者比例(35/72,48.6%)和总体死亡率(21/72,29.2%)在 CDH+BPS 患者中明显更高。在校正疝大小、心脏和染色体异常后,ECLS 的需求(OR 2.2,p=0.004)和死亡率(OR 2.0,p=0.015)在 CDH+BPS 患者中明显更高。

结论

这是研究 CDH 患儿中 BPS 发生率的最大系列研究。与无 BPS 患者相比,BPS 与更大的缺陷大小、更需要 ECLS 和更高的死亡率相关。

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