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VACTERL 综合征,流行病学定义与描述。

VACTERL association, epidemiologic definition and delineation.

作者信息

Rittler M, Paz J E, Castilla E E

机构信息

ECLAMC: Latin-American Collaborative Study of Congenital Malformations, WHO Collaborating Centre for the Prevention of Birth Defects, ECLAMC at Hospital Maternoinfantil Ramón Sardá, Buenos Aires, Brazil.

出版信息

Am J Med Genet. 1996 Jun 28;63(4):529-36. doi: 10.1002/(SICI)1096-8628(19960628)63:4<529::AID-AJMG4>3.0.CO;2-J.

Abstract

This study departed from a preconceived definition of VACTERL, including more than one of these six anomalies in the same infant: V (vertebral anomalies), A (anal atresia), C (congenital heart disease), TE (tracheoesophageal fistula or esophageal atresia), R (reno-urinary anomalies), and L (radial limb defect). Under this definition, 524 infants were ascertained by ECLAMC from almost 3,000,000 births examined from 1967 through 1990. Observed association rates among VACTERL components as well as between VACTERL and other defects were compared against randomly expected values obtained from 10,084 multiply malformed infants (casuistic method) from the same birth sample. Conclusions were: 1) Cardiac defects are not a part of VACTERL. 2) Single umbilical artery, ambiguous genitalia, abdominal wall defects, diaphragmatic hernia, and anomalies that are secondary to VACTERL components (intestinal and respiratory anomalies, and oligohydramnios sequence defects) are frequent enough to be considered an "extension" of VACTERL, and cardiac defects should be included in this category. 3) Neural tube defects are negatively associated with VACTERL which could not be explained by selection bias or any other operational artifact. High embryonic lethality or mutually exclusive pathogenetic mechanisms could be suitable explanations. 4) Results were not clear enough to determine whether VACTERL should be defined by at least two or three component defects.

摘要

本研究背离了VACTERL的先入为主的定义,该定义包括同一婴儿出现这六种异常中的不止一种:V(脊柱异常)、A(肛门闭锁)、C(先天性心脏病)、TE(气管食管瘘或食管闭锁)、R(肾泌尿异常)和L(桡骨肢体缺陷)。根据这一定义,欧洲先天性畸形监测中心(ECLAMC)从1967年至1990年检查的近300万例出生病例中确定了524例婴儿。将观察到的VACTERL各组成部分之间以及VACTERL与其他缺陷之间的关联率与从同一出生样本中10084例多重畸形婴儿(病例法)获得的随机预期值进行比较。结论如下:1)心脏缺陷不是VACTERL的一部分。2)单脐动脉、生殖器模糊、腹壁缺陷、膈疝以及继发于VACTERL各组成部分的异常(肠道和呼吸异常以及羊水过少序列缺陷)出现频率足够高,可被视为VACTERL的“扩展”,心脏缺陷应归入此类。3)神经管缺陷与VACTERL呈负相关,这无法用选择偏倚或任何其他操作假象来解释。高胚胎致死率或相互排斥的致病机制可能是合适的解释。4)结果不够明确,无法确定VACTERL是否应由至少两种或三种组成缺陷来定义。

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