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Effective use of oral ribavirin for respiratory syncytial viral infections in allogeneic haematopoietic stem cell transplant recipients.
Gorcea, C M; Tholouli, E; Turner, A; Saif, M; Davies, E; Battersby, E; Dignan, F L.
  • Gorcea CM; Department of Clinical Haematology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK. Electronic address: Claudia.gorcea@cmft.nhs.uk.
  • Tholouli E; Department of Clinical Haematology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
  • Turner A; Department of Virology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
  • Saif M; Department of Clinical Haematology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
  • Davies E; Pharmacy Department, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
  • Battersby E; Pharmacy Department, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
  • Dignan FL; Department of Clinical Haematology, Manchester Royal Infirmary, Central Manchester NHS Foundation Trust, Manchester, UK.
J Hosp Infect ; 95(2): 214-217, 2017 Feb.
Article en En | MEDLINE | ID: mdl-28077243
ABSTRACT

BACKGROUND:

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.

AIM:

To evaluate the effectiveness of oral ribavirin in allogeneic HSCT patients with RSV infection.

METHODS:

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.

FINDINGS:

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.

CONCLUSION:

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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antivirales / Ribavirina / Trasplante Homólogo / Infecciones por Virus Sincitial Respiratorio / Trasplante de Células Madre Hematopoyéticas / Receptores de Trasplantes Tipo de estudio: Observational_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antivirales / Ribavirina / Trasplante Homólogo / Infecciones por Virus Sincitial Respiratorio / Trasplante de Células Madre Hematopoyéticas / Receptores de Trasplantes Tipo de estudio: Observational_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article