Grosse Scott D, Van Vliet Guy
National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta GA 30333, USA.
Horm Res. 2007;67(6):284-91. doi: 10.1159/000098400. Epub 2007 Jan 3.
BACKGROUND/AIMS: Congenital adrenal hyperplasia (CAH) is increasingly being included in newborn screening programs. Screening can prevent neonatal mortality in children with salt-wasting CAH, but the number of deaths prevented is not known. Cost-effectiveness analyses of screening require estimates of the probability of mortality in CAH.
We reviewed the literature to identify cohort studies of children with CAH ascertained clinically in the absence of screening. We abstracted the numbers of infant deaths attributable to CAH. We also addressed sex ratios among children with clinically detected CAH and the contribution of ascertainment bias to unbalanced ratios.
The evidence suggests a probability of infant death due to adrenal crises in salt-wasting CAH of 4% or less in contemporary advanced economies without screening for CAH. This is lower than previous estimates, although the rate of mortality could be considerably higher in populations with limited clinical awareness or access.
Although screening for CAH is conducted in a number of countries, further research is still needed to provide reliable estimates on the numbers of prevented deaths, along with evidence-based assessments of the potential benefits, harms, and costs of screening.
背景/目的:先天性肾上腺皮质增生症(CAH)越来越多地被纳入新生儿筛查项目。筛查可预防失盐型CAH患儿的新生儿死亡,但具体预防的死亡人数尚不清楚。筛查的成本效益分析需要对CAH的死亡概率进行估计。
我们检索文献,以确定在未进行筛查的情况下临床确诊的CAH患儿的队列研究。我们提取了因CAH导致的婴儿死亡人数。我们还探讨了临床检测出的CAH患儿的性别比例以及确诊偏倚对不平衡比例的影响。
有证据表明,在当代发达经济体中,未对CAH进行筛查时,失盐型CAH患儿因肾上腺危象导致的婴儿死亡概率为4%或更低。这低于先前的估计,不过在临床意识或医疗服务有限的人群中,死亡率可能会高得多。
尽管多个国家都在开展CAH筛查,但仍需进一步研究,以提供关于预防死亡人数的可靠估计,并对筛查的潜在益处、危害和成本进行循证评估。