ZaiduMusa Aishatu, Mustapha Samaha Saleh, Abubakar Bawa Ibrahim, Lawal Nurat Oluwabunmi, Grema Mustapha Falmata, Bashir Auwal Ahmed Muhammed
Department of Paediatrics, Abubakar Tafawa Balewa University/Abubakar Tafawa Balewa University Teaching Hospital, Bauchi, Nigeria.
Department of Chemical Pathology, Abubakar Tafawa Balewa University/Abubakar Tafawa Balewa University Teaching Hospital, Bauchi, Nigeria.
Niger Med J. 2024 Nov 6;65(5):800-806. doi: 10.60787/nmj-v65i3.498. eCollection 2024 Sep-Oct.
Newborn jaundice (NNJ), especially due to ABO incompatibility, is a major global health concern. Phototherapy is standard treatment, with exchange transfusions reserved for severe cases. However, in some babies these therapies may be ineffective, requiring additional immunomodulatory treatments. Limited access to these treatments in developing countries creates a critical gap, worsening jaundice severity. A 22-hour old term neonate presented with rapidly progressive severe neonatal hyperbilirubinemia (NNJ) within 15 hours of life, consistent with ABO incompatibility based on discordant maternal and infant's blood types (mother: O, baby: B-positive). Despite aggressive initial management with phototherapy and exchange transfusions, the NNJ exhibited limited improvement. Sepsis and G6PD deficiency were considered as potential contributing factors, although confirmatory testing for G6PD deficiency was deferred due to unavailability of the diagnostic test in our setting. Given a sibling's documented successful response to methylprednisolone for a similar presentation, a brief course of low-dose intravenous methylprednisolone (1mg/kg/day in 2 divided doses) (off-label use) was cautiously initiated. This resulted in a rapid and significant improvement in the neonate's hyperbilirubinemia. Methylprednisolone was prescribed for 3 days after which it was discontinued. Following close observation for 3 days and confirmation of no neurological sequelae, the neonate was discharged home in stable condition. Managing severe, worsening NNJ, especially with multiple aetiologies, is complex. Standard therapies may be inadequate. While promising, immunomodulatory therapies like IVIG may be limited in resource-poor settings. Methylprednisolone shows potential but lacks strong clinical evidence. Well-designed studies are essential to explore its safety and efficacy, particularly in developing countries with limited treatment options.
新生儿黄疸(NNJ),尤其是由ABO血型不合引起的,是一个全球主要的健康问题。光疗是标准治疗方法,换血疗法则用于重症病例。然而,对于一些婴儿来说,这些疗法可能无效,需要额外的免疫调节治疗。在发展中国家,这些治疗方法的可及性有限,造成了关键差距,使黄疸严重程度加剧。一名22小时大的足月儿在出生后15小时内出现快速进展的严重新生儿高胆红素血症(NNJ),根据母婴血型不一致(母亲:O型,婴儿:B阳性),符合ABO血型不合。尽管最初积极采用光疗和换血疗法进行治疗,但NNJ的改善有限。脓毒症和葡萄糖-6-磷酸脱氢酶(G6PD)缺乏被认为是潜在的促成因素,不过由于我们所在地区无法进行G6PD缺乏的诊断检测,因此对G6PD缺乏的确诊检测被推迟。鉴于有记录显示一名兄弟姐妹对甲基泼尼松龙有类似表现的成功反应,谨慎地开始了一个短疗程的低剂量静脉注射甲基泼尼松龙(1毫克/千克/天,分2次给药)(超说明书用药)。这导致新生儿高胆红素血症迅速且显著改善。甲基泼尼松龙用药3天后停药。在密切观察3天并确认无神经后遗症后,新生儿病情稳定出院。管理严重且不断恶化的NNJ,尤其是病因多样的情况,很复杂。标准疗法可能并不充分。虽然有前景,但像静脉注射免疫球蛋白(IVIG)这样的免疫调节疗法在资源匮乏地区可能受限。甲基泼尼松龙显示出潜力,但缺乏有力的临床证据。精心设计的研究对于探索其安全性和有效性至关重要,特别是在治疗选择有限的发展中国家。