Vancomycin-related thrombocytopenia in neonates: are Sudanese infants more prone? Case reports and literature review

IF 0.1 Q4 HEMATOLOGY
Suhair Osman Hassan
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Abstract

Background With the improvement of neonatal care in the country and survival of the preterm infants and sick neonates, many arising problems are being observed. One of these is the significant presence of neonatal thrombocytopenia and the need for lots of platelet transfusions per an infant. Many neonatal factors can cause thrombocytopenia, but we observed severe, prolonged thrombocytopenia in infants who received specifically vancomycin for sepsis or other medical/surgical conditions. Literature search revealed that vancomycin can cause immune thrombocytopenia by inducing platelet antibodies, though this is scarcely described in neonates. Participants and methods This is a hospital-based longitudinal study held in NICU during February 2017 to February 2019. All admitted neonates (term and preterm) who received vancomycin were involved, but those with maternal thrombocytopenia, systemic lupus erythematosus (SLE), maternal eclampsia/HELLP (Haemolysis, Elevated Liver enzymes, Low Platelets) syndrome, and Intr Uterine Growth Rrestriction (IUGR) were excluded. Results Of 117 infants admitted in this period, 68 infants fulfilled the inclusion criteria. The severe decline in platelet count observed on the second to third day of vancomycin treatment continued throughout the treatment and started to rise 2–3 days after discontinuation. During treatment with vancomycin, platelet transfusion 2–3 times a day was observed not to raise platelet level significantly, but it prevented serious bleeding. Conclusion Vancomycin-induced thrombocytopenia in neonate is a rising new problem in NICUs. The authors may need to add adjunctive intravenous immunoglobulins or methylprednisolone or change the dosing system to smaller frequent doses, given over longer time, to overcome this serious problem.
新生儿中与万古霉素相关的血小板减少症:苏丹婴儿更容易发生吗?病例报告和文献综述
背景随着我国新生儿护理水平的提高和早产儿及患病新生儿存活率的提高,出现了许多新问题。其中之一是新生儿血小板减少症的显著存在和每个婴儿需要大量的血小板输注。许多新生儿因素可导致血小板减少,但我们观察到,在接受万古霉素治疗败血症或其他内科/外科疾病的婴儿中,严重的、长期的血小板减少。文献检索显示万古霉素可通过诱导血小板抗体引起免疫性血小板减少症,但在新生儿中鲜有报道。这是一项以医院为基础的纵向研究,于2017年2月至2019年2月在NICU进行。所有接受万古霉素治疗的入院新生儿(足月和早产儿)均被纳入研究,但排除了伴有母体血小板减少症、系统性红斑狼疮(SLE)、母体子痫/HELLP(溶血、肝酶升高、血小板降低)综合征和子宫内生长受限(IUGR)的新生儿。结果117例患儿中,68例符合纳入标准。在万古霉素治疗的第2-3天观察到的血小板计数严重下降在整个治疗过程中持续,停药后2-3天开始上升。在万古霉素治疗期间,每天输血小板2-3次,血小板水平未明显升高,但可防止严重出血。结论万古霉素致新生儿血小板减少症是新生儿重症监护病房中一个日益突出的新问题。作者可能需要添加辅助静脉注射免疫球蛋白或甲基强的松龙,或改变给药系统,以较小的频繁剂量,给药时间更长,以克服这个严重的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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