Cincinnati Children's Hospital Medical Center, Division of Neonatology, University of Cincinnati College of Medicine, 3333 Burnet Ave, Cincinnati, OH 45229-3039, USA.
Pediatrics. 2010 Nov;126(5):910-6. doi: 10.1542/peds.2010-0943. Epub 2010 Oct 25.
Newborn-screening false-positive rates (FPRs) are disproportionately increased in preterm infants. The objective of this study was to determine variation in newborn screening FPRs according to birth weight and gestational age. Our secondary objective was to examine the effect of postnatal age on FPRs in preterm infants.
The Ohio State Newborn Screening Program Database was analyzed to determine the overall and birth weight-specific FPRs for 18 analytes. Data were stratified into birth weight categories (<1000 g, 1000-1499 g, 1500-2499 g, 2500-3999 g, and >4000 g). In addition, to examine the effect of postnatal age on FPRs, we examined the 2 analytes with the highest FPRs, thyrotropin with back-up thyroxine and 17-hydroxyprogesterone, in infants whose gestational age was <32 weeks, determined on the basis of postnatal age at screening.
Data from 448 766 neonates were reviewed. Infants with very low birth weight (VLBW) comprised 1.9% of the study cohort, but accounted for 18% of false-positive results. For 14 of 18 analytes studied, FPRs increased with decreasing birth weight/gestational age and were significantly increased in infants with VLBW compared with infants who weighed 2500 to 3999 g (P < .001). Thyrotropin/back-up thyroxine and 17-hydroxyprogesterone accounted for 62% of total false-positive results in VLBW infants. When blood specimens were collected at a postnatal age of ≥ 48 hours in infants born at <32 weeks, a 44% relative reduction in 17-hydroxyprogesterone false-positive results was detected.
False-positive newborn-screening rates are disproportionately increased in VLBW infants. FPRs may be reduced by delaying screening of <32 weeks' gestation, preterm infants until 24 to 48 hours' postnatal age.
早产儿的新生儿筛查假阳性率(FPR)不成比例地增加。本研究的目的是根据出生体重和胎龄确定新生儿筛查 FPR 的变化。我们的次要目标是研究早产儿出生后年龄对 FPR 的影响。
分析俄亥俄州新生儿筛查计划数据库,确定 18 种分析物的总体和特定出生体重 FPR。数据分为出生体重类别(<1000g、1000-1499g、1500-2499g、2500-3999g 和>4000g)。此外,为了研究出生后年龄对 FPR 的影响,我们检查了两种 FPR 最高的分析物,即促甲状腺素和甲状腺素后备,以及在筛查时根据出生后年龄确定胎龄<32 周的婴儿的 17-羟孕酮。
共回顾了 448766 名新生儿的数据。极低出生体重(VLBW)婴儿占研究队列的 1.9%,但占假阳性结果的 18%。在研究的 18 种分析物中,有 14 种 FPR 随着出生体重/胎龄的降低而增加,与出生体重为 2500-3999g 的婴儿相比,VLBW 婴儿的 FPR 显著增加(P<0.001)。促甲状腺素/甲状腺素后备和 17-羟孕酮占 VLBW 婴儿总假阳性结果的 62%。当在胎龄<32 周出生的婴儿出生后 48 小时以上采集血样时,17-羟孕酮假阳性结果相对减少 44%。
极低出生体重婴儿的新生儿筛查假阳性率不成比例地增加。通过将胎龄<32 周、早产儿的筛查延迟至出生后 24 至 48 小时,可能会降低 FPR。