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严重程度的胎儿超声标志物可预测先天性膈疝肺动脉高压的消退情况。

Fetal ultrasound markers of severity predict resolution of pulmonary hypertension in congenital diaphragmatic hernia.

作者信息

Lusk Leslie A, Wai Katherine C, Moon-Grady Anita J, Basta Amaya M, Filly Roy, Keller Roberta L

机构信息

Division of Neonatology, Department of Pediatrics, Benioff Children's Hospital, University of California, San Francisco, CA.

School of Medicine, University of California, San Francisco, CA.

出版信息

Am J Obstet Gynecol. 2015 Aug;213(2):216.e1-8. doi: 10.1016/j.ajog.2015.03.036. Epub 2015 Mar 19.

Abstract

OBJECTIVE

Congenital diaphragmatic hernia (CDH) results in morbidity and death from lung hypoplasia and persistent pulmonary hypertension (PH). We sought to define the relationship between fetal ultrasound markers of severity in CDH and the time to resolution of neonatal PH.

STUDY DESIGN

We conducted a retrospective study of fetuses with an antenatal ultrasound scan and left-sided CDH cared for at the University of California San Francisco (2002-2012). Fetal liver position was classified on ultrasound scan as abdominal (entire liver within the abdomen) or thoracic (any portion of the liver within the thorax). Fetal stomach position was classified from least to most aberrant: abdominal, anterior left chest, mid-posterior left chest, or retrocardiac (right chest). Lung-to-head ratio (LHR) was determined from available scans at 20-29 weeks of gestational age (GA). Routine neonatal echocardiograms were performed weekly for up to 6 weeks or until PH resolved or until discharge. PH was assessed by echocardiogram with the use of a hierarchy of ductus arteriosus level shunt, interventricular septal position, and tricuspid regurgitant jet velocity. Days to PH-free survival was defined as the age at which pulmonary artery pressure was estimated to be <2/3 systemic blood pressure. Cox proportional hazards models adjusted for GA at birth, era of birth, fetal surgery, and GA at ultrasound scan (LHR model only), with censoring at 100 days.

RESULTS

Of 118 patients, the following fetal markers were available: LHR (n = 53), liver position (n = 112), and stomach position (n = 80). Fewer infants experienced resolved PH if they had LHR <1 (P = .006), thoracic liver position (P = .001), or more aberrant stomach position (P < .001). There was also a decreased rate of resolution of PH in infants with LHR <1 (hazard ratio, 0.30; P = .007), thoracic liver position (hazard ratio, 0.38; P < .001), and more aberrant stomach position (hazard ratios, 0.28 [P = .002]; 0.1 [P < .001]; and 0.07 [P < .001]).

CONCLUSION

Fetal ultrasound markers of CDH severity are predictive not only of death but also of significant morbidity. LHR <1, thoracic liver, and aberrant stomach position are associated with delayed time to resolution of PH in infants with CDH and may be used to identify fetuses at high risk of persistent PH.

摘要

目的

先天性膈疝(CDH)会导致肺发育不全和持续性肺动脉高压(PH),进而引发发病和死亡。我们试图明确CDH严重程度的胎儿超声标志物与新生儿PH消退时间之间的关系。

研究设计

我们对在加利福尼亚大学旧金山分校接受治疗(2002 - 2012年)的产前超声检查发现患有左侧CDH的胎儿进行了一项回顾性研究。在超声检查中,将胎儿肝脏位置分类为腹部(整个肝脏位于腹部)或胸部(肝脏的任何部分位于胸腔内)。胎儿胃的位置从异常程度最小到最大进行分类:腹部、左前胸、左胸后中部或心后(右胸)。在孕20 - 29周(GA)时,根据可用扫描确定肺头比(LHR)。每周进行常规新生儿超声心动图检查,最长持续6周,或直至PH消退或直至出院。通过超声心动图,利用动脉导管水平分流、室间隔位置和三尖瓣反流喷射速度的分级来评估PH。无PH存活天数定义为估计肺动脉压<2/3体循环血压时的年龄。Cox比例风险模型针对出生时的GA、出生年代、胎儿手术以及超声检查时的GA(仅LHR模型)进行了调整,并在100天时进行删失。

结果

118例患者中,可获得以下胎儿标志物:LHR(n = 53)、肝脏位置(n = 112)和胃位置(n = 80)。LHR<1(P = 0.006)、肝脏位于胸部(P = 0.001)或胃位置异常更严重(P < 0.001)的婴儿中,经历PH消退的较少。LHR<1(风险比,0.30;P = 0.007)、肝脏位于胸部(风险比,0.38;P < 0.001)以及胃位置异常更严重(风险比,0.28 [P = 0.002];0.1 [P < 0.001];和0.07 [P < 0.001])的婴儿中,PH消退率也降低。

结论

CDH严重程度的胎儿超声标志物不仅可预测死亡,还可预测严重发病情况。LHR<1、肝脏位于胸部以及胃位置异常与CDH婴儿PH消退时间延迟相关,可用于识别持续性PH高危胎儿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4731/4519413/6f47491b0ebd/nihms689434f1.jpg

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