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出生后延长随访期能否提高先天性异常诊断的准确性?一项基于柏林胚胎毒性项目的观察性研究。

Does extended follow-up period after birth improve precision of diagnosis of congenital anomalies? An observational study based on the Berlin Embryotox project.

作者信息

Weber-Schoendorfer Corinna, Maaß Nadia, Lohse Lukas, Beck Evelin, Schaefer Christof, Dathe Katarina

机构信息

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Institute of Clinical Pharmacology and Toxicology, Embryotox Centre of Clinical Teratology and Drug Safety in Pregnancy, Augustenburger Platz 1, 13353, Berlin, Germany.

出版信息

Eur J Pediatr. 2025 Jul 22;184(8):495. doi: 10.1007/s00431-025-06333-z.

Abstract

UNLABELLED

The aetiology of congenital anomalies is often difficult to assess. Genetic abnormalities can play a role or exogenous factors such as maternal medication during pregnancy. Observational studies require reliable data on both gestational time and dosage of drug exposure during pregnancy and, if applicable, on precise description of congenital anomalies in the infant. The Berlin Embryotox Centre carried out a questionnaire-based project to investigate whether longer follow-up periods after birth lead to more accurate diagnoses of congenital anomalies. The Berlin Embryotox Centre offers risk assessment on medication during pregnancy to health care providers and pregnant women. Follow-up questionnaires asking for course and outcome of pregnancy are routinely sent out 8 weeks after the estimated date of birth. In this project, three additional questionnaires were sent to women with a singleton live-born infant, asking for paediatric findings documented along routine examinations offered to all children in Germany at the age of approximately 6 months (U5), 1 year (U6) and 2 years (U7). In addition, parents were asked to report their observations on the child's development. Data were collected between March 2019 and May 2024. A total of 3719 parents completed at least one of the three additional follow-up questionnaires. Results of the standard questionnaire 8 weeks after birth showed 138 infants with a major defect and 13 with a genetic disorder. At the end of the extended follow-up period, 180 children were reported to have a major birth defect and 39 a genetic disorder. The rate of major birth defects increased from 3.7% to 4.8%. Gain of information was largest between the examinations at 8 weeks and 6 months.

CONCLUSION

Extending the observation period beyond the neonatal period substantially improves diagnostic accuracy in terms of completeness and specification of congenital anomalies including genetic disorders. Studies on the risk and safety of drugs in pregnancy would benefit considerably from routine follow-up for at least 6 months after birth.

WHAT IS KNOWN

• Diagnosis of congenital anomalies is often incomplete during the neonatal period. • A longer follow-up period increases the completeness of recorded congenital anomalies.

WHAT IS NEW

• Regarding major birth defects, gain of information after the neonatal period is largest up to the age of 6 months. • Only one-third of genetic diseases were diagnosed during the neonatal period, a further third up to the age of 6 months.

摘要

未标注

先天性异常的病因通常难以评估。遗传异常可能起作用,或者存在外部因素,如孕期母亲用药。观察性研究需要关于孕期用药时间和剂量的可靠数据,以及(如适用)关于婴儿先天性异常的精确描述。柏林胚胎毒性中心开展了一项基于问卷调查的项目,以调查出生后更长的随访期是否会导致对先天性异常的诊断更准确。柏林胚胎毒性中心为医疗保健提供者和孕妇提供孕期用药风险评估。在预计出生日期后8周,会定期发出询问妊娠过程和结局的随访问卷。在该项目中,向单胎活产婴儿的母亲发送了另外三份问卷,询问在德国所有儿童大约6个月(U5)、1岁(U6)和2岁(U7)时进行的常规检查中记录的儿科检查结果。此外,还要求父母报告他们对孩子发育的观察情况。数据收集时间为2019年3月至2024年5月。共有3719名父母完成了至少一份额外的随访问卷。出生后8周的标准问卷结果显示,有138名婴儿患有严重缺陷,13名患有遗传疾病。在延长随访期结束时,报告有180名儿童患有严重出生缺陷,39名患有遗传疾病。严重出生缺陷的发生率从3.7%上升到4.8%。在8周和6个月检查之间获得的信息最多。

结论

将观察期延长至新生儿期之后,在先天性异常(包括遗传疾病)的完整性和特异性方面,可显著提高诊断准确性。孕期药物风险和安全性研究将从出生后至少6个月的常规随访中受益匪浅。

已知信息

• 新生儿期对先天性异常的诊断往往不完整。• 更长的随访期可提高记录的先天性异常的完整性。

新发现

• 关于严重出生缺陷,新生儿期之后到6个月龄时获得的信息最多。• 只有三分之一的遗传疾病在新生儿期被诊断出来,另有三分之一在6个月龄之前被诊断出来。

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