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先天性膈疝研究组登记处

The Congenital Diaphragmatic Hernia Study Group Registry.

作者信息

Morini Francesco, Lally Pamela A, Lally Kevin P, Bagolan Pietro

机构信息

Neonatal Surgery Unit, Department of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.

Department of Pediatric Surgery, University of Texas Medical School at Houston and Children's Memorial Hermann Hospital, Houston, Texas, United States.

出版信息

Eur J Pediatr Surg. 2015 Dec;25(6):488-96. doi: 10.1055/s-0035-1569151. Epub 2015 Dec 7.

Abstract

Congenital diaphragmatic hernia (CDH) is a rare anomaly with an incidence between 1/2,500 and 1/3,000 live births. The rarity of the disease makes it difficult to design powerful studies leading to accurate and meaningful evidence. For rare diseases, the development of multicenter international registries may help in collecting data and give an overall picture of the disease. In this review, we will describe the development of the CDH study group, we will describe its work methodology, and the results obtained since its birth in 1995.

摘要

先天性膈疝(CDH)是一种罕见的异常情况,活产儿中的发病率在1/2500至1/3000之间。该疾病的罕见性使得开展有力的研究以获得准确且有意义的证据变得困难。对于罕见疾病而言,多中心国际登记处的建立可能有助于收集数据并全面了解该疾病。在本综述中,我们将描述CDH研究组的发展情况,阐述其工作方法以及自1995年成立以来所取得的成果。

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