Low-dose acyclovir for prophylaxis of varicella-zoster virus reactivation after hematopoietic stem cell transplantation in children

被引:3
|
作者
Tatebe, Yasuhisa [1 ]
Ushio, Soichiro [1 ]
Esumi, Satoru [1 ]
Sada, Hikaru [1 ]
Ochi, Motoharu [2 ]
Tamefusa, Kosuke [2 ]
Ishida, Hisashi [2 ]
Fujiwara, Kaori [2 ]
Kanamitsu, Kiichiro [2 ,3 ]
Washio, Kana [2 ]
Katsube, Risa [1 ]
Murakawa, Kiminaka [1 ]
Zamami, Yoshito [1 ]
机构
[1] Okayama Univ Hosp, Dept Pharm, Kita Ku, 2-5-1 Shikata Cho, Okayama, Japan
[2] Okayama Univ Hosp, Dept Pediat, Kita Ku, Okayama, Japan
[3] Natl Hosp Org, Okayama Med Ctr, Dept Pediat, Kita Ku, Okayama, Japan
关键词
children; low-dose acyclovir; prophylaxis; transplantation; varicella-zoster virus; BONE-MARROW-TRANSPLANTATION; HERPES-ZOSTER; RISK-FACTORS; INFECTION; DISEASE; CHEMOTHERAPY; POPULATION; PREVENTION; RECIPIENTS; LEUKEMIA;
D O I
10.1002/pbc.29979
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Varicella-zoster virus (VZV) reactivation is a serious complication of hematopoietic stem cell transplantation (HSCT). Although low-dose acyclovir can prevent VZV reactivation after HSCT in adults, the efficacy of a dose of acyclovir lower than the recommended dose, such as 60-80 mg/kg/day in children, is unclear. In this study, we aimed to evaluate the incidence of VZV reactivation after HSCT during and after low-dose acyclovir administration for preventing VZV reactivation in children. Methods This single-center retrospective study included children aged <= 15 years who received oral acyclovir (at 15 mg/kg/day) to prevent VZV reactivation after HSCT. We examined the cumulative incidence of VZV reactivation after HSCT, during and after prophylactic acyclovir administration. Results Fifty-three eligible patients were included in this study, of whom 37 underwent allogeneic HSCT. The median duration of prophylactic acyclovir therapy was 264 days (range: 69-1140 days). VZV reactivation occurred in 13 patients (24.5%, 95% confidence interval [CI]: 14.9-37.6). The cumulative incidence of VZV reactivation 1 and 2 years after HSCT was 6.26% (95% CI: 1.60-15.5) and 20.9% (95% CI: 10.3-34.0), respectively. While only one patient developed VZV reactivation during the administration of prophylactic acyclovir, the cumulative incidence of VZV reactivation increased to 24.2% (95% CI: 12.5-38.0) 1 year after the cessation of acyclovir. Conclusion Low-dose acyclovir (15 mg/kg/day) could be effective for preventing VZV reactivation after HSCT in children because VZV reactivation seldom occurs during the administration of 15 mg/kg/day acyclovir.
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页数:8
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