Department of Medicine and Neurosciences, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
Acta Neurol Scand. 2011 Jul;124(1):9-12. doi: 10.1111/j.1600-0404.2010.01429.x. Epub 2010 Sep 29.
In studies investigating foetal malformations associated with antiepileptic drug exposure during pregnancy, the common practice has been to assess the incidence and nature of the malformations at, or soon after, birth. The adequacy of this approach to determine the true incidence of the malformations has received little attention.
To compare the incidence and natures of the foetal malformations recognized by, or soon after, birth with similar data for malformations recognized in the first post-natal year.
Analysis of data from the Australian Register of Antiepileptic Drugs in Pregnancy.
Up to 25% of the malformations recognized by the end of the first post-natal year had not been detected by, or soon after, birth. There was a tendency for the late-recognized malformations to differ from the early-recognized ones in relation to the body parts involved.
Early assessment and delayed assessment of infants for the presence of foetal malformations are complementary, with the latter resulting in finding a higher incidence of malformations. However, omission of an early post-natal assessment may result in biases because of loss of subjects to follow-up.
在研究与妊娠期间抗癫痫药物暴露相关的胎儿畸形时,常见的做法是在出生时或出生后不久评估畸形的发生率和性质。这种确定畸形真实发生率的方法很少受到关注。
比较出生时或出生后不久发现的胎儿畸形的发生率和性质,以及在出生后第一年发现的类似畸形的数据。
对澳大利亚妊娠抗癫痫药物登记处的数据进行分析。
在第一年的后期,有多达 25%的畸形尚未被发现,或在出生后不久就被发现。在涉及的身体部位方面,晚期识别出的畸形与早期识别出的畸形存在一定的差异。
早期评估和后期评估婴儿是否存在胎儿畸形是相辅相成的,后者发现畸形的发生率更高。然而,如果不进行早期的产后评估,可能会因为失去随访对象而产生偏差。