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实验性先天性梗阻性尿路病

Experimental congenital obstructive uropathy.

作者信息

Peters C A, Mandell J

机构信息

Department of Surgery, Children's Hospital, Boston, Massachusetts.

出版信息

Urol Clin North Am. 1990 May;17(2):437-47.

PMID:2186545
Abstract

Continued experimental work in congenital obstructive uropathy is essential to support the rapidly advancing field of fetal medicine. It is possible to reproduce the clinically relevant obstructive lesions in an experimental model. On the basis of data from these models, the tentative conclusion is that in utero intervention is beneficial in severe congenital obstructive uropathy associated with oligohydramnios. The limited human experience provides insufficient data to confirm this hypothesis but has demonstrated the technical feasibility of prenatal interventions. There is a critical need for further refinement in understanding the complex pathophysiology of congenital obstructive uropathy, not only the renal consequences, but also the pulmonary and systemic effects. There remains the particular need to resolve the determinants and indicators of functional salvageability of the kidneys and lungs in congenital obstructive uropathy.

摘要

先天性梗阻性尿路病的持续实验工作对于支持快速发展的胎儿医学领域至关重要。在实验模型中重现临床相关的梗阻性病变是可能的。基于这些模型的数据,初步结论是,宫内干预对与羊水过少相关的严重先天性梗阻性尿路病有益。有限的人类经验提供的数据不足以证实这一假设,但已证明产前干预在技术上是可行的。迫切需要进一步完善对先天性梗阻性尿路病复杂病理生理学的理解,不仅要了解肾脏后果,还要了解肺部和全身影响。尤其需要解决先天性梗阻性尿路病中肾脏和肺部功能可挽救性的决定因素和指标。

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