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先天性肾积水开放性胎儿手术的早期经验。

Early experience with open fetal surgery for congenital hydronephrosis.

作者信息

Crombleholme T M, Harrison M R, Langer J C, Longaker M T, Anderson R L, Slotnick N S, Filly R A, Callen P W, Goldstein R B, Golbus M S

机构信息

Fetal Treatment Program, University of California, San Francisco 94143.

出版信息

J Pediatr Surg. 1988 Dec;23(12):1114-21. doi: 10.1016/s0022-3468(88)80325-7.

Abstract

The fetus with severe bilateral hydronephrosis and associated oligohydramnios in the second trimester is doomed at birth by ongoing pulmonary and renal damage. Since decompression with percutaneously placed catheters anesthetic, surgical, and tocolytic techniques for open fetal anesthetic, surgical, and tocolytic techniques for open fetal urinary tract decompression in animals, and have now applied those techniques to a small group of five patients. One had bilateral ureterostomies and the subsequent four had marsupialization of the bladder. All pregnancies proceeded to cesarean delivery at 32 to 35 weeks' gestation. There was no long-term maternal morbidity, and two mothers have since experienced normal pregnancies. Three fetuses had return of normal amniotic fluid dynamics, and all three had adequate pulmonary function at birth, suggesting that fatal pulmonary hypoplasia associated with early severe oligohydramnios had been reversed. Two neonates died at birth with pulmonary hypoplasia. One had no amniotic fluid even after decompression, and the other had some amniotic fluid after decompression but a tiny chest cavity due to the long period of severe oligohydramnios before decompression. Of the three surviving infants, one had normal renal function when she died of unrelated causes at 9 months of age. One has normal renal function at 23 months and the third had failing renal function at 2 1/2 years and has grown and developed normally, but will require renal transplantation. We have now developed selection criteria that would exclude from treatment the two fetuses who died of pulmonary hypoplasia and the one who developed renal failure.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

孕中期患有严重双侧肾积水并伴有羊水过少的胎儿,会因持续的肺和肾损伤在出生时面临死亡。自从采用经皮放置导管进行减压麻醉、手术以及用于动物开放式胎儿尿路减压的麻醉、手术和宫缩抑制技术以来,现已将这些技术应用于一小群五名患者。其中一名患者接受了双侧输尿管造口术,随后四名患者接受了膀胱造袋术。所有妊娠均在妊娠32至35周时进行剖宫产。没有长期的母体并发症,此后有两名母亲经历了正常妊娠。三名胎儿羊水动力学恢复正常,并且所有三名胎儿出生时肺功能良好,这表明与早期严重羊水过少相关的致命性肺发育不全已得到逆转。两名新生儿出生时死于肺发育不全。一名即使在减压后也没有羊水,另一名减压后有一些羊水,但由于减压前长期严重羊水过少,胸腔很小。在三名存活婴儿中,一名在9个月大时死于无关原因,当时肾功能正常。一名在23个月时肾功能正常,第三名在2岁半时肾功能衰竭,但生长发育正常,但需要肾移植。我们现在已经制定了选择标准,将死于肺发育不全的两名胎儿和一名出现肾衰竭的胎儿排除在治疗之外。(摘要截短至250字)

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