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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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