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造血干细胞移植后副粘病毒感染的抢先口服利巴韦林治疗:一项初步研究。

Pre-emptive oral ribavirin therapy of paramyxovirus infections after haematopoietic stem cell transplantation: a pilot study.

作者信息

Chakrabarti S, Collingham K E, Holder K, Fegan C D, Osman H, Milligan D W

机构信息

Department of Haematology, Birmingham Heartlands Hospital, Birmingham, UK.

出版信息

Bone Marrow Transplant. 2001 Oct;28(8):759-63. doi: 10.1038/sj.bmt.1703216.

Abstract

Infections with the paramyxoviruses, respiratory syncytial virus (RSV) and parainfluenza virus (PIV) can result in serious morbidity and mortality after haemopoietic stem cell transplant (HSCT). Once pneumonia develops, the outcome of these infections is often poor despite anti-viral therapy. Aerosolised ribavirin has been evaluated as pre-emptive therapy for post-transplant RSV infections with some success. Due to the financial and logistic burden involved with the use of aerosolised ribavirin, we explored the efficacy and toxicity of oral ribavirin for pre-emptive therapy of post-transplant RSV and PIV infections in a dose escalating schedule (15-60 mg/kg/day). Five episodes each of RSV and PIV were treated in seven patients. Five patients were receiving treatment for GVHD and two acquired the infection in the pre-engraftment period. All the episodes of RSV infection improved with oral ribavirin with dose escalation to 30-45 mg/kg in three of them. On the other hand, only two of the five PIV infections improved with oral ribavirin. Of the three non-responders, two infections were acquired in the pre-engraftment period with one death from PIV pneumonia. Reversible anaemia was the only side-effect noted in patients treated for over 2 weeks. Thus, the use of oral ribavirin was well tolerated in the post-transplant period with no untoward toxicities. There was a trend towards better response in RSV infections, which needs to be further explored in controlled studies.

摘要

副粘病毒、呼吸道合胞病毒(RSV)和副流感病毒(PIV)感染可导致造血干细胞移植(HSCT)后出现严重发病和死亡情况。一旦发生肺炎,尽管进行了抗病毒治疗,这些感染的预后往往很差。雾化利巴韦林已被评估作为移植后RSV感染的抢先治疗方法,取得了一定成功。由于使用雾化利巴韦林涉及经济和后勤负担,我们按照剂量递增方案(15 - 60毫克/千克/天)探索了口服利巴韦林对移植后RSV和PIV感染进行抢先治疗的疗效和毒性。7名患者中分别有5例RSV和PIV感染得到治疗。5名患者正在接受移植物抗宿主病(GVHD)治疗,2名患者在植入前期感染。所有RSV感染病例经口服利巴韦林治疗均有改善,其中3例剂量递增至30 - 45毫克/千克。另一方面,5例PIV感染中只有2例经口服利巴韦林治疗有改善。在3例无反应者中,2例感染发生在植入前期,1例死于PIV肺炎。接受治疗超过2周的患者中仅观察到可逆性贫血这一副作用。因此,移植后口服利巴韦林耐受性良好,无不良毒性。RSV感染有反应更好的趋势,这需要在对照研究中进一步探索。

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