Forrester M B, Merz R D
Hawaii Birth Defects Program, Honolulu, Hawaii 96817, USA.
Teratology. 2001;64 Suppl 1:S20-5. doi: 10.1002/tera.1080.
This investigation evaluated the impact of collecting data on early fetal deaths (less than 20 weeks' gestation) on a birth defects surveillance system. Data were obtained from the Hawaii Birth Defects Program (HBDP), a statewide registry for Hawaii with active case ascertainment methodology. In 1986 through 1997, 257 early fetal deaths with birth defects were identified, representing 2.2% of the total birth defects cases. Two hundred sixteen (84.1%) of the early fetal deaths had chromosomal defects (mainly trisomies, polyploidies, and Turner syndrome) and 59 (23.0%) had structural defects. Most (65.4%) of the early fetal deaths with chromosomal defects occurred at 8-12 weeks' gestation, and 62.3% of the early fetal deaths with structural defects occurred at 16-19 weeks' gestation. For half of the 26 specific birth defects examined, early fetal deaths accounted for at least 4% of all cases. The proportion of total birth defects cases accounted for by early fetal deaths increased over the 12-year period of the study (p = 0.003). Most of this secular trend appeared to result from an increase over time in early fetal deaths where a birth defect was prenatally detected (p = 0.004). Although ascertainment of early fetal deaths is not believed to be complete, their inclusion in a birth defects registry may be beneficial because of confusion about the pregnancy outcome and/or gestational age reported in the medical record, their importance in cluster investigations, and their contribution to birth defects prevention strategies.
本研究评估了收集早期胎儿死亡(妊娠少于20周)数据对出生缺陷监测系统的影响。数据来自夏威夷出生缺陷项目(HBDP),这是夏威夷一个采用主动病例确诊方法的全州性登记处。1986年至1997年期间,共识别出257例伴有出生缺陷的早期胎儿死亡病例,占出生缺陷病例总数的2.2%。216例(84.1%)早期胎儿死亡伴有染色体缺陷(主要是三体、多倍体和特纳综合征),59例(23.0%)伴有结构缺陷。大多数(65.4%)伴有染色体缺陷的早期胎儿死亡发生在妊娠8至12周,62.3%伴有结构缺陷的早期胎儿死亡发生在妊娠16至19周。在所检查的26种特定出生缺陷中,有一半的早期胎儿死亡病例占所有病例的至少4%。在该研究的12年期间,早期胎儿死亡病例占出生缺陷病例总数的比例有所增加(p = 0.003)。这种长期趋势主要是由于产前检测到出生缺陷的早期胎儿死亡病例随时间增加所致(p = 0.004)。尽管早期胎儿死亡病例的确诊被认为并不完整,但将其纳入出生缺陷登记处可能是有益的,原因在于病历中报告的妊娠结局和/或孕周存在混淆、它们在聚集性调查中的重要性以及它们对出生缺陷预防策略的贡献。