Implementation of a Prospective Birth Cohort for Newborn Screening and Early Linkage to Comprehensive Sickle Cell Disease Care in a Low-Resource Setting.

IF 3.5 Q1 GENETICS & HEREDITY International Journal of Neonatal Screening Pub Date : 2026-06-16 DOI:10.3390/ijns12020042
Umma A Ibrahim, Aisha B Musa, Oiza O Aliu-Isah, Hauwa A Inuwa, Zubaida L Farouk, Khadija Bulama, Aisha Mukaddas, Khadija Kamal, Rifkatu N Auta, Nafiu Hussaini, Aisha A Galadanci, Yusuf D Jobbi, Bilya S Musa, Yvonne Carroll, Lauren J Klein, Ibrahim M Idris, Michael R DeBaun, Muktar H Aliyu
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Abstract

In sub-Saharan Africa, where approximately 75% of newborns with sickle cell disease (SCD) are born, under-five mortality remains high, partly due to the absence of newborn screening (NBS) and delayed linkage to comprehensive care. We conducted a prospective, quasi-experimental study involving two sequential newborn screening cohorts at Aminu Kano Teaching Hospital (AKTH), Kano, Nigeria (December 2022-December 2025), to evaluate the feasibility of integrating newborn screening (NBS) with early comprehensive SCD care and to identify barriers to enrollment before 3 months of age. Following an initial implementation period with suboptimal follow-up, a structured family-centered enrollment and communication strategy was introduced to improve early linkage to comprehensive care. During the pre-intervention period, 277 newborns were enrolled (33 with SCD and 244 without SCD [NSCD]), with early enrollment (≤3 months) occurring in 46.5% overall, higher among SCD than NSCD infants (72.8% vs. 43.0%). Delayed enrollment (>6 months) was more frequent among SCD infants. Following the implementation of family-centered communication strategies, 60 additional newborns were enrolled (16 SCD, 44 NSCD), and early enrollment increased to 91.7%. These findings demonstrate that low-cost, family-centered communication and tracking strategies can substantially improve early linkage to comprehensive SCD care following newborn screening in low-resource settings. Early enrollment is a critical step toward reducing morbidity and mortality among children with SCD in low-resource settings.

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在低资源环境下实施新生儿筛查和镰状细胞病综合护理早期联系的前瞻性出生队列。
在撒哈拉以南非洲,大约75%的新生儿患有镰状细胞病(SCD), 5岁以下儿童死亡率仍然很高,部分原因是缺乏新生儿筛查(NBS)以及与综合护理的联系延迟。我们于2022年12月至2025年12月在尼日利亚卡诺的Aminu Kano教学医院(AKTH)进行了一项前瞻性准实验研究,涉及两个顺序新生儿筛查队列,以评估将新生儿筛查(NBS)与早期全面SCD护理相结合的可行性,并确定3个月前入组的障碍。在最初的实施阶段随访不理想之后,引入了以家庭为中心的结构化登记和沟通策略,以改善早期与综合护理的联系。在干预前,277名新生儿入组(33名患有SCD, 244名没有SCD [NSCD]),早期入组(≤3个月)的发生率为46.5%,SCD高于NSCD婴儿(72.8%比43.0%)。延迟入组(6个月)在SCD婴儿中更为常见。在实施以家庭为中心的传播策略后,新增60名新生儿入组(16名SCD, 44名NSCD),早期入组率提高至91.7%。这些研究结果表明,低成本、以家庭为中心的沟通和跟踪策略可以大大改善低资源环境下新生儿筛查后与全面SCD护理的早期联系。早期入组是降低低资源环境下SCD患儿发病率和死亡率的关键一步。
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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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