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首页> 外文期刊>Medicine. >Varicella zoster virus infection after allogeneic hematopoietic cell transplantation in children using a relatively short duration of acyclovir prophylaxis: A retrospective study
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Varicella zoster virus infection after allogeneic hematopoietic cell transplantation in children using a relatively short duration of acyclovir prophylaxis: A retrospective study

机译:儿童阿昔洛韦预防时间较短的同种异体造血细胞移植后水痘带状疱疹病毒感染:一项回顾性研究

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Although acyclovir prophylaxis against varicella zoster virus (VZV) infection for ≥1 year is recommended after allogeneic hematopoietic cell transplantation (HCT), the emergence of acyclovir-resistant viruses and adverse drug effects cannot be ignored. We investigated the cumulative incidence of VZV infection after allogeneic HCT in children receiving a shorter duration of acyclovir prophylaxis than recommended and evaluated the appropriateness of the short duration of acyclovir prophylaxis. Medical records of 217 children who received allogeneic HCT were retrospectively reviewed until a median of 25 months (range = 1–59 months) after HCT. Acyclovir prophylaxis was given for a median of 9 weeks (range = 3–24 weeks) after HCT. VZV infection was diagnosed in 33 (15.2%) children at a median time of 5 months (range = 2–41 months) after HCT. The 1-year and 2-year cumulative incidences of VZV infection after allogeneic HCT were 11.2% and 15.5%, respectively. These incidences were between the previously reported 1-year incidence of 25% to 30% in patients not receiving prophylaxis and 1-year incidence of 4% to 5% in patients receiving ≥1 year duration of prophylaxis. Male sex and older age were significantly associated with VZV infection after allogeneic HCT. Only 1 chickenpox patient experienced severe complications because of VZV infection, and there were no deaths attributable to VZV infection. In conclusion, a shorter duration of acyclovir prophylaxis may be appropriate for children receiving allogeneic HCT, based on the rare occurrence of severe complications because of VZV infection and the expected discomfort because of daily oral medication for a long time.
机译:尽管异基因造血细胞移植(HCT)后建议使用阿昔洛韦预防水痘带状疱疹病毒(VZV)感染≥1年,但不能忽略抗阿昔洛韦的病毒的出现和药物不良作用。我们调查了接受阿昔洛韦预防时间短于推荐时间的儿童接受异基因HCT后VZV感染的累积发生率,并评估了短期阿昔洛韦预防时间的适当性。回顾性分析了接受异基因HCT的217名儿童的医疗记录,直到HCT中位值25个月(范围= 1–59个月)。 HCT后预防中位数为9周(范围= 3-24周)。在HCT后中位时间5个月(范围= 2–41个月)中,有33名(15.2%)儿童被诊断出VZV感染。异基因HCT后1年和2年VZV感染的累积发生率分别为11.2%和15.5%。这些发生率介于先前报告的未接受预防的患者的25%至30%的1年发生率与接受≥1年的预防时间的1%的发生率之间。异基因HCT后,男性和较大年龄与VZV感染显着相关。仅1名水痘患者因VZV感染而经历了严重的并发症,并且没有可归因于VZV感染的死亡。总之,基于接受VZV感染引起的严重并发症的罕见发生以及由于长时间口服口服药物带来的预期不适,较短的阿昔洛韦预防时间可能适合接受异基因HCT的儿童。

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