Neonatal Hyperbilirubinemia: A Case of Complex Management Involving ABO Incompatibility, Sepsis, and Suspected G6PD Deficiency treated with Methyl Prednisolone.

Aishatu ZaiduMusa, Samaha Saleh Mustapha, Bawa Ibrahim Abubakar, Nurat Oluwabunmi Lawal, Mustapha Falmata Grema, Auwal Ahmed Muhammed Bashir
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Abstract

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.

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新生儿高胆红素血症:一例复杂的管理涉及ABO不相容,败血症,并怀疑G6PD缺乏症与甲基强的松龙治疗。
新生儿黄疸(NNJ),特别是由于ABO血型不合,是一个主要的全球卫生问题。光疗是标准的治疗方法,重症患者需进行换血。然而,在一些婴儿中,这些疗法可能无效,需要额外的免疫调节治疗。发展中国家获得这些治疗的机会有限,造成了严重的差距,加剧了黄疸的严重程度。一个22小时出生的足月新生儿在15小时内出现了快速进展的严重新生儿高胆红素血症(NNJ),符合基于母婴血型不一致(母亲:O型,婴儿:b阳性)的ABO不相容。尽管最初进行了积极的光疗和交换输血治疗,但NNJ的改善有限。脓毒症和G6PD缺乏被认为是潜在的影响因素,尽管由于在我们的环境中无法获得诊断测试,G6PD缺乏的确证测试被推迟。鉴于一位兄弟姐妹对甲基强的松龙治疗类似症状的成功反应,我们谨慎地开始了一个短疗程的低剂量静脉注射甲基强的松龙(1mg/kg/天,分2次使用)(标签外使用)。这导致了新生儿高胆红素血症的快速和显著改善。甲强的松龙开了3天,之后停药。密切观察3 d,确认无神经系统后遗症,病情稳定出院。管理严重、恶化的NNJ,特别是多种病因的NNJ,是复杂的。标准疗法可能是不够的。虽然很有希望,但像IVIG这样的免疫调节疗法在资源贫乏的环境中可能受到限制。甲基强的松龙显示出潜力,但缺乏强有力的临床证据。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。
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