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      Impact of aerosolized ribavirin on mortality in 280 allogeneic haematopoietic stem cell transplant recipients with respiratory syncytial virus infections

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          Abstract

          Objectives

          Respiratory syncytial virus (RSV) infections are well recognized as a significant cause of morbidity and mortality in allogeneic haematopoietic stem cell transplant (allo-HSCT) recipients. We evaluated the spectrum of clinical manifestations, management (including ribavirin-based antiviral therapy) and outcomes of RSV infections and determined the risk factors associated with RSV lower respiratory tract infection (LRTI) and all-cause mortality.

          Methods

          In this retrospective study, we analysed clinical data from all laboratory-confirmed RSV infections in allo-HSCT recipients ( n = 280) who presented at our institution from January 1996 to May 2009.

          Results

          Of the 280 patients, 80 (29%) developed LRTI within 20 days (median 1 day, range 0–19 days) and 44 (16%) died within 90 days (median 26 days, range 1–82 days) from RSV diagnosis. Multivariable logistic regression analyses identified several significant risk factors associated with RSV LRTI and all-cause mortality, including age, male sex, neutropenia, lymphocytopenia and lack of ribavirin-based antiviral therapy at the upper respiratory tract infection (URTI) stage. Aerosolized ribavirin-based therapy at the URTI stage was the single most significant factor in reducing the risk of RSV LRTI (83%), all-cause mortality (57%) and RSV-associated mortality (87%) in these patients ( P < 0.05), irrespective of the year of RSV diagnosis.

          Conclusions

          Our results demonstrate that RSV infections are a significant cause of morbidity and mortality in high-risk allo-HSCT recipients and ribavirin-based antiviral therapy at the URTI stage had a positive impact on both outcomes in this vulnerable population with multiple risk factors.

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          Author and article information

          Journal
          J Antimicrob Chemother
          J. Antimicrob. Chemother
          jac
          jac
          Journal of Antimicrobial Chemotherapy
          Oxford University Press
          0305-7453
          1460-2091
          August 2013
          9 April 2013
          : 68
          : 8
          : 1872-1880
          Affiliations
          [1 ] Department of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center , Houston, TX, USA
          [2 ] The University of Texas School of Public Health , Houston, TX, USA
          [3 ] Baylor College of Medicine , Houston, TX, USA
          [4 ] Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center , Houston, TX, USA
          [5 ] Department of Laboratory Medicine, The University of Texas MD Anderson Cancer Center , Houston, TX, USA
          Author notes
          [* ]Corresponding author. Tel: +1-713-745-1116; Fax: +1-713-745-6839; E-mail: rfchemaly@ 123456mdanderson.org
          Article
          PMC6296322 PMC6296322 6296322 dkt111
          10.1093/jac/dkt111
          6296322
          23572228
          0966e1ad-d95e-4be6-80b0-7418f4a8fd77
          © The Author 2013. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com
          History
          : 8 December 2012
          : 3 January 2013
          : 26 February 2013
          : 2 March 2013
          Categories
          Original Research

          RSV,stem cell transplantation,immunocompromised,pneumonia

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