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通过新生儿筛查发现的囊性纤维化患者发病率降低。

Reduced morbidity in patients with cystic fibrosis detected by neonatal screening.

作者信息

Wilcken B, Chalmers G

出版信息

Lancet. 1985 Dec 14;2(8468):1319-21. doi: 10.1016/s0140-6736(85)92623-6.

Abstract

The effects of neonatal diagnostic screening on cystic-fibrosis (CF) -related morbidity were evaluated by comparing hospital admissions for CF-related illness in the first 2 years of life in 40 patients detected by means of neonatal screening and 56 patients born in the 3 years before screening began. Unscreened patients without meconium ileus had a mean of 27.25 hospital days for CF-related illness, and screened patients a mean of 3.9 days. There was no trend with time towards fewer days spent in hospital: the change was sudden. The difference was significant and could not be attributed to non-comparability of groups, changes in admission policy, or changes in management. In patients with meconium ileus there was no significant difference in hospital admissions between the groups. Neonatal screening significantly reduces CF morbidity in the first 2 years of life.

摘要

通过比较40例经新生儿筛查确诊的患者和筛查开始前3年出生的56例患者出生后头两年因囊性纤维化(CF)相关疾病的住院情况,评估了新生儿诊断筛查对CF相关发病率的影响。未筛查且无胎粪性肠梗阻的患者因CF相关疾病平均住院27.25天,而筛查患者平均住院3.9天。住院天数没有随时间减少的趋势:变化是突然的。差异具有显著性,且不能归因于组间不可比性、入院政策变化或管理变化。对于有胎粪性肠梗阻的患者,两组间的住院情况没有显著差异。新生儿筛查显著降低了出生后头两年的CF发病率。

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