Neonatal Screening for Cystic Fibrosis in Hungary-First-Year Experiences.

IF 4 Q1 GENETICS & HEREDITY International Journal of Neonatal Screening Pub Date : 2023-08-23 DOI:10.3390/ijns9030047
Andrea Xue, István Lénárt, Judit Kincs, Hajnalka Szabó, Andrea Párniczky, István Balogh, Anna Deák, Péter Béla Monostori, Krisztina Hegedűs, Attila J Szabó, Ildikó Szatmári
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Abstract

The aim of this study is to evaluate the strategy of the cystic fibrosis newborn screening (CFNBS) programme in Hungary based on the results of the first year of screening. A combined immunoreactive trypsinogen (IRT) and pancreatitis-associated protein (PAP) CFNBS protocol (IRT/IRT×PAP/IRT) was applied with an IRT-dependent safety net (SN). Out of 88,400 newborns, 256 were tested screen-positive. Fourteen cystic fibrosis (CF) and two cystic fibrosis-positive inconclusive diagnosis (CFSPID) cases were confirmed from the screen-positive cases, and two false-negative cases were diagnosed later. Based on the obtained results, a sensitivity of 88% and a positive predictive value (PPV) of 5.9% were calculated. Following the recognition of false-negative cases, the calculation method of the age-dependent cut-off was changed. In purely biochemical CFNBS protocols, a small protocol change, even after a short period, can have a significant positive impact on the performance. CFNBS should be monitored continuously in order to fine-tune the screening strategy and define the best local practices.

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匈牙利新生儿囊性纤维化筛查的第一年经验。
本研究的目的是根据第一年的筛查结果,评估匈牙利囊性纤维化新生儿筛查(CFNBS)计划的策略。应用免疫反应性胰蛋白酶原(IRT)和胰腺炎相关蛋白(PAP)联合CFNBS方案(IRT/IRT×PAP/IRT)和IRT依赖性安全网(SN)。在88400名新生儿中,256名被检测为筛查阳性。从筛查阳性病例中确认了14例囊性纤维化(CF)和2例囊性纤维阳性非决定性诊断(CFSPID)病例,随后诊断了2例假阴性病例。根据获得的结果,计算出88%的灵敏度和5.9%的阳性预测值(PPV)。随着假阴性病例的识别,年龄相关截止值的计算方法发生了变化。在纯生物化学的CFNBS协议中,即使在短时间后,一个小的协议更改也会对性能产生显著的积极影响。应持续监控CFNBS,以微调筛选策略并确定最佳本地实践。
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来源期刊
International Journal of Neonatal Screening
International Journal of Neonatal Screening Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
20.00%
发文量
56
审稿时长
11 weeks
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