先天性膈疝的临床表现及预后。

R Hentschel, L Wiethoff, G Hülskamp, S Tercanli, W Holzgreve, C Becker, G Jorch
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引用次数: 0

摘要

我们对36例早期甚至出生前发现的先天性膈肌缺损患者的资料进行了回顾性分析。分析患者的妊娠过程、妊娠风险、产前检查结果、分娩方式、临床参数、产前、围产期和产后程序、手术检查结果和手术治疗与预后的关系。以下因素影响预后:相关异常、产前诊断、年龄成熟度、体重、Apgar评分、缺陷的大小和肺发育不全的程度(以及与此相关的患者术前心肺状况),可能还有性别。手术前存活的患者死亡率为28%。对于在出生前就知道的膈肌缺陷,我们的标准程序是在孩子第一次自主呼吸之前进行初级插管。我们也考虑延迟手术的做法,直到稳定已经实现,特别是在病房的培养箱的行动过程中,从患者的角度来看,目前并发症最少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Manifestations and prognosis of congenital diaphragmatic hernia].

We conducted a retrospective examination of the data of 36 patients with congenital diaphragm defects detected at an early stage or even before birth. The course of pregnancy, pregnancy risks, prenatal findings, mode of delivery, clinical parameters, prenatal, perinatal and postnatal procedures, findings at surgery and surgical therapy were analyzed with respect to the patients' outcome. The following factors were seen to influence the prognosis: associated anomalies, prenatal diagnosis, maturity for age, weight, Apgar score, the size of the defect and the extent of the pulmonary hypoplasia (and--linked to this--the patient's cardiorespiratory condition prior to surgery), and possibly sex. The mortality of patients surviving until surgery became possible was 28%. Our standard procedure in case of diaphragm defects known before birth is primary intubation before the child's first spontaneous breath. We also consider the practice of delaying surgery until stabilization has been achieved and especially in the incubator on the ward the course of action with the fewest complications at present from the patient's point of view.

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