Chávez G F, Mulinare J, Edmonds L D
Birth Defects and Genetic Disease Branch, Centers for Disease Control, Atlanta, GA 30333.
JAMA. 1991 Jun 26;265(24):3270-4. doi: 10.1001/jama.1991.03460240066029.
Nationwide surveillance of Rh hemolytic disease of the newborn (RhHDN) indicates that, after a substantial decline in incidence, reported rates reached a plateau in the late 1970s. We conducted a study designed to validate RhHDN surveillance data, to obtain corrected incidence estimates, and to identify potential reasons for the reported plateau. We obtained data from the Birth Defects Monitoring Program, a national surveillance system that collects data from public and private hospitals participating voluntarily. We asked hospitals for copies of the medical records for all infants discharged with a code for RhHDN and for a sample of the medical records of infants discharged with a code for other and unspecified hemolytic disease during 1986. The estimated incidence rate of RhHDN was 10.6 per 10,000 total births, with some regional variations. Our findings indicate that, despite the availability of an effective preventive measure, RhHDN continues to contribute significantly to infant morbidity and mortality in the United States.
全国范围内对新生儿Rh溶血病(RhHDN)的监测表明,在发病率大幅下降之后,报告的发病率在20世纪70年代末达到了平稳状态。我们开展了一项研究,旨在验证RhHDN监测数据,获得校正后的发病率估计值,并确定报告发病率平稳的潜在原因。我们从出生缺陷监测项目获取数据,这是一个全国性监测系统,从自愿参与的公立和私立医院收集数据。我们向医院索要1986年所有出院诊断为RhHDN的婴儿以及一部分出院诊断为其他及未特指溶血病的婴儿的病历副本。RhHDN的估计发病率为每10000例总出生数中有10.6例,存在一些地区差异。我们的研究结果表明,尽管有有效的预防措施,但在美国,RhHDN仍然是婴儿发病和死亡的一个重要原因。