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孕期母亲的博赫达勒克氏疝:病例报告的系统评价

Maternal Bochdalek Hernia during Pregnancy: A Systematic Review of Case Reports.

作者信息

Choi Jin-Young, Yang Song-Soo, Lee Jong-Hwa, Roh Hyun-Jin, Ahn Jun-Woo, Kim Jeong-Sook, Lee Soo-Jeong, Lee Sang-Hun

机构信息

Department of Obstetrics and Gynecology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan 44033, Korea.

Department of Surgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan 44033, Korea.

出版信息

Diagnostics (Basel). 2021 Jul 14;11(7):1261. doi: 10.3390/diagnostics11071261.

Abstract

BACKGROUND

Since the first report of a diaphragmatic hernia from Ambroise Paré's necropsy in 1610, the Bochdalek hernia (BH) of the congenital diaphragmatic hernia (CDH) has been the most common types with high morbidity and mortality in the neonatal period. Due to the nature of the disease, CDH associated with pregnancy is too infrequent to warrant reporting in the literature. Mortality of obstruction or strangulation is mostly due to failure to diagnose symptoms early.

DATA SOURCES AND STUDY SELECTION

A systematic literature search of maternal BH during pregnancy was conducted using the electronic databases (PubMed and EMBASE) from January 1941 to December 2020. Because of the rarity of the disease, this review included all primary studies, including case reports or case series that reported at least one case of maternal BH in pregnant. Searches, paper selection, and data extraction were conducted in duplicate. The analysis was performed narratively regardless of the control groups' presence due to their rarity.

RESULTS

The search retrieved 3450 papers, 94 of which were deemed eligible and led to a total of 43 cases. Results of treatment showed 16 cases in delayed delivery after hernia surgery, 10 cases in simultaneous delivery with hernia surgery, 3 cases in non-surgical treatment, and 14 cases in hernia surgery after delivery. Of 16 cases with delayed delivery after hernia surgery, 13 (81%) cases had emergency surgery and three (19%) cases had surgery after expectant management. Meanwhile, 10 cases underwent simultaneous delivery with hernia surgery, 6 cases (60%) had emergent surgery, and 4 cases (40%) had delayed hernia surgery after expectant management. 3 cases underwent non-surgical treatment. In this review, the maternal death rate and fetal/neonatal loss rate from maternal BH was 5% (2/43) and 16% (7/43), respectively. The preterm birth rate has been reported in 35% (15/43) of maternal BH, resulting from maternal deaths in 13% (2/15) of cases and 6 fetal loss in 40% (6/15) of cases; 44% (19/43) of cases demonstrated signs of bowel obstruction, ischemia, or perforation of strangulated viscera in the operative field, resulting from maternal deaths in 11% (2/19) of cases and fetal-neonatal loss in 21% (4/19) of cases.

CONCLUSION

Early diagnosis and surgical intervention are imperative, as a gangrenous or non-viable bowel resection significantly increases mortality. Therefore, multidisciplinary care should be required in maternal BH during pregnancies that undergo surgically repair, and individualized care allow for optimal results for the mother and fetus.

摘要

背景

自1610年安布鲁瓦兹·帕雷尸检首次报告膈疝以来,先天性膈疝(CDH)中的博赫dalek疝(BH)一直是新生儿期最常见的类型,发病率和死亡率都很高。由于该疾病的性质,与妊娠相关的CDH极为罕见,以至于文献中鲜有报道。梗阻或绞窄导致的死亡主要是由于未能早期诊断症状。

数据来源与研究选择

使用电子数据库(PubMed和EMBASE)对1941年1月至2020年12月期间孕期母亲的BH进行了系统的文献检索。由于该疾病罕见,本综述纳入了所有主要研究,包括报告至少一例孕期母亲BH的病例报告或病例系列。检索、论文筛选和数据提取均重复进行。由于对照组罕见,无论其是否存在,均进行叙述性分析。

结果

检索到3450篇论文,其中94篇被认为符合条件,共涉及43例病例。治疗结果显示,16例在疝修补术后延迟分娩,10例在疝修补术同时分娩,3例采用非手术治疗,14例在产后进行疝修补术。在16例疝修补术后延迟分娩的病例中,13例(81%)进行了急诊手术,3例(19%)在期待治疗后进行了手术。同时,10例在疝修补术同时分娩,6例(60%)进行了急诊手术,4例(40%)在期待治疗后延迟进行疝修补术。3例采用非手术治疗。在本综述中,母亲BH导致的母亲死亡率和胎儿/新生儿丢失率分别为5%(2/43)和16%(7/43)。据报道,35%(15/43)的母亲BH出现早产,其中13%(2/15)的病例因母亲死亡导致早产,40%(6/15)的病例因6例胎儿丢失导致早产;44%(19/43)的病例在手术视野中出现肠梗阻、缺血或绞窄内脏穿孔的迹象,其中11%(2/19)的病例因母亲死亡导致上述情况,21%(4/19)的病例因胎儿-新生儿丢失导致上述情况。

结论

早期诊断和手术干预至关重要,因为坏疽性或无法存活的肠切除会显著增加死亡率。因此对于孕期母亲BH进行手术修复时,应采取多学科护理,个体化护理有助于母亲和胎儿获得最佳结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ed/8303225/ab7993cc8c7c/diagnostics-11-01261-g001.jpg

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