Department of Clinical Haematology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
Department of Clinical Haematology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
J Hosp Infect. 2017 Feb;95(2):214-217. doi: 10.1016/j.jhin.2016.11.012. Epub 2016 Nov 25.
Respiratory syncytial virus (RSV) is a frequent cause of respiratory viral infections, increasing the morbidity and mortality in allogeneic haematopoietic stem cell transplantation (HSCT) recipients. Little is known about the best management strategy in this immunocompromised group and there are very few data on oral ribavirin treatment.
To evaluate the effectiveness of oral ribavirin in allogeneic HSCT patients with RSV infection.
Twenty-three RSV cases treated with oral ribavirin were analysed retrospectively. RSV diagnosis was established by polymerase chain reaction assay. Oral ribavirin was initiated at 15 mg/kg/day in three divided doses for 10 days, with no subsequent dose escalation, as per centre policy.
At diagnosis, seven patients presented with lower respiratory tract infection (RTI), whereas 16 had upper RTI. Oral ribavirin was well tolerated with minor adverse effects. The median treatment duration was 10 days (range: 5-47). After a median follow-up of 17 months (range: 4-48), 17 patients are alive. We recorded one RSV-related and five non-related deaths.
To our knowledge, this is the largest single centre study yet performed on adult allogeneic HSCT recipients with RSV infection treated with oral ribavirin. Prompt initiation of treatment is essential and may avoid hospital admission. Our experience supports the use of oral ribavirin, but large prospective studies are needed to determine the optimal therapy in this patient group.
呼吸道合胞病毒(RSV)是一种常见的呼吸道病毒感染病原体,可增加异基因造血干细胞移植(HSCT)受者的发病率和死亡率。在免疫功能低下的这组患者中,最佳管理策略知之甚少,关于口服利巴韦林治疗的资料也很少。
评估口服利巴韦林治疗异基因 HSCT 患者 RSV 感染的疗效。
回顾性分析了 23 例接受口服利巴韦林治疗的 RSV 感染病例。通过聚合酶链反应检测法确定 RSV 诊断。根据中心政策,口服利巴韦林起始剂量为 15mg/kg/天,分 3 次服用,共 10 天,不再增加剂量。
在诊断时,7 例患者出现下呼吸道感染(RTI),16 例患者出现上呼吸道感染。口服利巴韦林耐受性良好,仅有轻微不良反应。中位治疗时间为 10 天(范围:5-47)。中位随访 17 个月(范围:4-48)后,17 例患者存活。我们记录了 1 例 RSV 相关和 5 例非相关死亡。
据我们所知,这是迄今为止针对接受口服利巴韦林治疗的异基因 HSCT 受者 RSV 感染的最大单中心研究。及时开始治疗至关重要,可避免住院。我们的经验支持使用口服利巴韦林,但需要进行大型前瞻性研究来确定该患者群体的最佳治疗方法。