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基于州的出生缺陷登记处的病例确定:通过出生证明确定的未报告婴儿的特征及其对纽约州登记处统计数据的影响。

Case ascertainment for state-based birth defects registries: characteristics of unreported infants ascertained through birth certificates and their impact on registry statistics in New York state.

作者信息

Olsen C L, Polan A K, Cross P K

机构信息

New York State Department of Health, Albany 12203-3399, USA.

出版信息

Paediatr Perinat Epidemiol. 1996 Apr;10(2):161-74. doi: 10.1111/j.1365-3016.1996.tb00040.x.

Abstract

Cases in the New York State Congenital Malformations Registry are reported by hospitals and physicians. This study was undertaken to determine whether case finding should be expanded to include routine matching of Vital Records files to the registry in order to identify unreported children. Matching of children who were born in 1983-86 and who had a congenital malformation noted on their birth certificate yielded 2837 children who were not in the registry. The hospital of record was asked to submit a registry report if the child's medical record contained a congenital malformation. Medical records for 1267 (45%) of these children indicated that the child was normal, with no mention of a malformation. Medical records could not be located for 137. Registry reports were submitted for 1433, 67 of whom were subsequently found in the registry, leaving 1366 bona fide new cases. These new cases differ significantly from registry cases for a number of birth certificate variables and type of congenital malformation. The birth certificate cases were more likely than registry cases to have only one malformation and to have only a minor malformation. The 1366 new cases comprised 2.1% of all registry cases for 1983-86. Their addition increased the statewide prevalence of major malformations by 1.7% from 416.5 to 423.4 per 10 000 livebirths. Except for anencephaly, the prevalence of specific malformations was not altered measurably by the addition of these cases. Lengthy and continuous follow-up was required to obtain registry reports. The small number of cases found does not seem to justify the amount of resources that would be required to use birth certificates routinely to augment case finding in New York State.

摘要

纽约州先天性畸形登记处的病例由医院和医生上报。本研究旨在确定是否应扩大病例查找范围,将生命记录档案与登记处进行常规匹配,以识别未上报的儿童。对1983 - 1986年出生且出生证明上注明有先天性畸形的儿童进行匹配,结果发现有2837名儿童不在登记处。若儿童病历中有先天性畸形记录,会要求记录医院提交登记报告。其中1267名(45%)儿童的病历显示其正常,未提及有畸形。137名儿童的病历无法找到。提交了1433份登记报告,其中67份后来在登记处被找到,剩下1366例为真正的新病例。这些新病例在出生证明变量和先天性畸形类型方面与登记处病例有显著差异。出生证明病例比登记处病例更有可能仅有一种畸形且只是轻微畸形。1366例新病例占1983 - 1986年所有登记病例的2.1%。将这些病例纳入后,全州主要畸形的患病率从每10000例活产416.5例增加到423.4例,增幅为1.7%。除无脑儿外,增加这些病例后,特定畸形的患病率没有明显变化。获取登记报告需要进行长期且持续的随访。在纽约州,通过常规使用出生证明来增加病例查找所发现的病例数量较少,似乎不值得投入所需的资源。

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