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挪威医学出生登记处 1970-2016 年肢体减少缺陷的流行病学:基于人群的研究。

Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study.

机构信息

Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.

Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.

出版信息

PLoS One. 2019 Jul 17;14(7):e0219930. doi: 10.1371/journal.pone.0219930. eCollection 2019.

Abstract

BACKGROUND

Following the Thalidomide disaster, the Medical Birth Registry of Norway (MBRN) was established in 1967, with epidemiological surveillance of congenital anomalies as one main aim. Limb reduction defects (LRD) constitute a rare and heterogeneous anomaly group, where correct registration and classification is important for surveillance and research. We aimed at reviewing and recoding LRD cases in the MBRN using the same classification system for all years, and evaluate time trends, characteristics and risk factors, 1970-2016.

METHODS

After reviewing and recoding LRD cases using International Classification of Diseases (ICD), 10th version, for all years, time trends, association with major anomalies, risk factors and infant outcomes were calculated. Generalized linear models for the binomial family with log link gave relative risks (RR) with 95% confidence intervals (CI). Classification of LRD as suggested by European surveillance of congenital anomalies (EUROCAT) was attempted.

RESULTS

Overall LRD prevalence, 1970-2016, was 4.4 per 10 000, slightly increasing during 1970-1981, followed by relatively stable rates. There were more defects in upper than lower limbs. Defects in hands/fingers were most common, but unspecific descriptions prevented classification of LRD according to EUROCAT. A majority of cases had associated anomalies, the most common being other limb defects, followed by cardiac defects and anomalies in the nervous and digestive systems. From 1999, 26% of LRD cases were terminated, more than 90% of these had associated major anomalies. Stillbirth, neonatal and infant mortality were higher among infants with LRD, also related to associated anomalies. Pre-gestational diabetes was associated with a more than three times increased risk of offspring total LRD, while no association with maternal epilepsy was found. Taking folate/multivitamin supplements before and/or during pregnancy was associated with lower risk of offspring LRD (adjusted RR 0.7; 95% CI 0.6-0.9), while daily smoking did not significantly increase the risk.

CONCLUSION

The MBRN now has information on LRD coded by ICD-10 from 1970, but information is not specific enough to use other recommended classification systems. Collecting radiographic descriptions and/or more details from hospital records would improve the quality of the registry data. Taking folate supplements before/during pregnancy may reduce the risk of offspring LRD.

摘要

背景

在沙利度胺灾难之后,挪威医学出生登记处(MBRN)于 1967 年成立,其主要目的之一是对先天畸形进行流行病学监测。肢体减少缺陷(LRD)是一种罕见且异质性的畸形群体,正确的登记和分类对于监测和研究很重要。我们旨在使用相同的分类系统对 MBRN 中的 LRD 病例进行回顾和重新编码,评估 1970-2016 年的时间趋势、特征和危险因素。

方法

使用国际疾病分类(ICD)第 10 版对所有年份的 LRD 病例进行回顾和重新编码,计算时间趋势、与主要畸形的关系、危险因素和婴儿结局。使用二项式家族的对数链接广义线性模型给出了 95%置信区间(CI)的相对风险(RR)。尝试根据欧洲先天畸形监测(EUROCAT)对 LRD 进行分类。

结果

1970-2016 年,LRD 的总体患病率为每 10000 例 4.4 例,1970-1981 年略有增加,随后相对稳定。上肢缺陷比下肢缺陷更常见。手部/手指缺陷最常见,但由于描述不明确,无法按照 EUROCAT 对 LRD 进行分类。大多数病例都有相关畸形,最常见的是其他肢体缺陷,其次是心脏缺陷和神经系统及消化系统的畸形。自 1999 年以来,26%的 LRD 病例被终止,其中超过 90%的病例有相关的主要畸形。LRD 患儿的死产、新生儿和婴儿死亡率较高,这也与相关畸形有关。妊娠前和/或妊娠期间服用叶酸/多种维生素补充剂与后代总 LRD 的风险增加三倍以上相关,而妊娠前和/或妊娠期间服用叶酸/多种维生素补充剂与母亲癫痫无关联。每天吸烟并不会显著增加患 LRD 的风险。

结论

MBRN 现在有了从 1970 年开始按照 ICD-10 编码的 LRD 信息,但信息不够具体,无法使用其他推荐的分类系统。从医院记录中收集放射学描述和/或更多详细信息将提高登记处数据的质量。妊娠前和/或妊娠期间服用叶酸补充剂可能会降低后代患 LRD 的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e8a/6636750/40c23a82b54b/pone.0219930.g001.jpg

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