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利巴韦林治疗骨髓移植受者的病毒性呼吸道感染

Ribavirin therapy in bone marrow transplant recipients with viral respiratory tract infections.

作者信息

Sparrelid E, Ljungman P, Ekelöf-Andström E, Aschan J, Ringdén O, Winiarski J, Wåhlin B, Andersson J

机构信息

Department of Infectious Diseases, Karolinska Institute, Huddinge Hospital, Stockholm, Sweden.

出版信息

Bone Marrow Transplant. 1997 May;19(9):905-8. doi: 10.1038/sj.bmt.1700752.

Abstract

Treatment with ribavirin was instituted in 12 allogeneic and one autologous bone marrow transplant (BMT) recipients with proven respiratory syncytial virus (RSV), influenza B virus or parainfluenza virus infections. RSV was diagnosed in six cases, influenza B virus in four and parainfluenza virus in three patients. Ribavirin was given orally or intravenously (15-20 mg/kg/day in three divided doses) and in nine cases with the addition of ribavirin inhalations (6 g/day). Three patients required ventilator support. Three out of seven patients with pneumonia, including one patient with RSV who developed pulmonary infiltrates 10 days after the start of therapy, died despite treatment with ribavirin (two RSV, one influenza B). Multiple etiological agents were found in the fatal cases. The clinical condition improved in 10 of 13 patients during therapy. No serious adverse effects of systemic ribavirin were noticed. Two patients had reversible signs of hemolysis but only one patients required more erythrocyte transfusions than expected after BMT. Obstructive respiratory distress was often observed (6/9 patients receiving ribavirin inhalation therapy), which resulted in discontinuation of aerosolized therapy in four cases. Time to engraftment (WBC < 0.2 x 10(9)/l) did not differ from other non-treated BMT patients. We conclude that ribavirin is well tolerated both orally and intravenously and it may, if instituted before development of hypoxia, reduce morbidity and mortality of RSV, influenza B and parainfluenza in this group of patients.

摘要

对12例异基因和1例自体骨髓移植(BMT)受者进行了利巴韦林治疗,这些患者已确诊感染呼吸道合胞病毒(RSV)、乙型流感病毒或副流感病毒。6例诊断为RSV感染,4例为乙型流感病毒感染,3例为副流感病毒感染。利巴韦林通过口服或静脉给药(15 - 20mg/kg/天,分3次给药),9例患者还加用了利巴韦林雾化吸入(6g/天)。3例患者需要呼吸机支持。7例肺炎患者中有3例死亡,其中包括1例RSV感染患者,该患者在治疗开始10天后出现肺部浸润,尽管接受了利巴韦林治疗(2例RSV感染,1例乙型流感病毒感染)。在死亡病例中发现了多种病原体。13例患者中有10例在治疗期间临床状况改善。未发现全身性利巴韦林的严重不良反应。2例患者出现可逆性溶血迹象,但只有1例患者在BMT后需要比预期更多的红细胞输血。经常观察到阻塞性呼吸窘迫(9例接受利巴韦林雾化吸入治疗的患者中有6例),4例因此停止了雾化治疗。植入时间(白细胞<0.2×10⁹/L)与其他未接受治疗的BMT患者无差异。我们得出结论,利巴韦林口服和静脉给药耐受性良好,在缺氧发生前开始使用,可能会降低该组患者中RSV、乙型流感病毒和副流感病毒感染的发病率和死亡率。

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