Galadanci Aisha A, Ibrahim Umma A, Carroll Yvonne, Jobbi Yusuf D, Farouk Zubaida L, Mukaddas Aisha, Hussaini Nafiu, Sani Musa Bilya, Klein Lauren J, DeBaun Michael R
Department of Hematology, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.
Department of Pediatrics, Bayero University/Aminu Kano Teaching Hospital, Kano 700233, Nigeria.
Int J Neonatal Screen. 2024 Sep 30;10(4):67. doi: 10.3390/ijns10040067.
Newborn screening for sickle cell disease (SCD) is sparse in sub-Saharan Africa. The leadership of the Aminu Kano Teaching Hospital (AKTH) in Kano, Nigeria, with the support of local religious authorities, established a groundbreaking SCD newborn screening program that has become the standard of care for pregnant women and their newborns. Our program includes (1) prenatal genetic counseling for all pregnant women in the antenatal clinic, (2) newborn screening, (3) postnatal genetic counseling for parents of newborns diagnosed with SCD and SCT, and (4) referral of newborns with SCD for follow-up in the SCD Comprehensive Care Clinic by 3 months of age. From September 2020 to December 2023, the team screened 7530 infants for SCD at the AKTH, identifying 126 (1.7%) infants with SCD and 1546 (20.5%) with SCT. Of these, 93 (73.8%) newborns with SCD received individualized genetic counseling, and 43 (46%) were referred to the SCD Comprehensive Care Clinic before 3 months. Group genetic counseling was provided to the parents of 778 (50.3%) of newborns identified with SCT. The SCD newborn screening at the AKTH is now standard care, indicating the viability of sustaining an SCD newborn screening program that provides pre- and postnatal genetic counseling and comprehensive SCD care within a low-income setting.
在撒哈拉以南非洲地区,镰状细胞病(SCD)的新生儿筛查工作开展得很少。在尼日利亚卡诺的阿米努·卡诺教学医院(AKTH)的领导下,在当地宗教当局的支持下,建立了一个开创性的SCD新生儿筛查项目,该项目已成为孕妇及其新生儿的标准护理模式。我们的项目包括:(1)为产前诊所的所有孕妇提供产前遗传咨询;(2)新生儿筛查;(3)为被诊断患有SCD和SCT的新生儿的父母提供产后遗传咨询;(4)将患有SCD的新生儿在3个月龄前转诊至SCD综合护理诊所进行随访。从2020年9月到2023年12月,该团队在AKTH对7530名婴儿进行了SCD筛查,确定了126名(1.7%)患有SCD的婴儿和1546名(20.5%)患有SCT的婴儿。其中,93名(73.8%)患有SCD的新生儿接受了个性化遗传咨询,43名(46%)在3个月前被转诊至SCD综合护理诊所。为778名(50.3%)被诊断患有SCT的新生儿的父母提供了群体遗传咨询。AKTH的SCD新生儿筛查现已成为标准护理模式,这表明在低收入环境中维持一个提供产前和产后遗传咨询以及全面SCD护理的SCD新生儿筛查项目是可行的。