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1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach

BACKGROUND: Respiratory syncytial virus (RSV) is a common community acquired infection in lung transplant recipients (LTRs). The mortality in RSV-infected LTRs has been reported as 10–20% despite antiviral therapy; however, there is no consensus regarding treatment given limited data. METHODS: A ret...

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Autores principales: Permpalung, Nitipong, Thaniyavarn, Tany, Saullo, Jennifer, Arif, Sana, Miller, Rachel, Reynolds, John, Alexander, Barbara D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253796/
http://dx.doi.org/10.1093/ofid/ofy210.1428
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author Permpalung, Nitipong
Thaniyavarn, Tany
Saullo, Jennifer
Arif, Sana
Miller, Rachel
Reynolds, John
Alexander, Barbara D
author_facet Permpalung, Nitipong
Thaniyavarn, Tany
Saullo, Jennifer
Arif, Sana
Miller, Rachel
Reynolds, John
Alexander, Barbara D
author_sort Permpalung, Nitipong
collection PubMed
description BACKGROUND: Respiratory syncytial virus (RSV) is a common community acquired infection in lung transplant recipients (LTRs). The mortality in RSV-infected LTRs has been reported as 10–20% despite antiviral therapy; however, there is no consensus regarding treatment given limited data. METHODS: A retrospective study of all LTRs at Duke University during January 2013 and May 2017 with a positive RSV PCR respiratory specimen was performed. Baseline characteristics, sites of infection, antiviral therapy, side effects, outcomes including all-cause 1-year mortality post RSV infection, and 90-day readmission rates were analyzed. The Cox proportional hazard model was used to adjust the effect of ribavirin (RBV) on mortality. RESULTS: One hundred fourteen RSV-infected LTRs were identified: 70 received oral RBV, 32 inhaled RBV and 12 supportive care only. Baseline characteristics were similar between the 3 groups except site of infection and oxygen requirement at diagnosis (see table). Of 32 patients treated with inhaled RBV, 19 had a creatinine clearance <40 mL/minute and 8 were unable to take oral drugs. Unadjusted all-cause 1-year mortality was highest in the supportive care group [33.3% vs. 7.1% (oral RBV) vs. 25% (inhaled RBV), P = 0.01]. There were no significant differences in readmission rates among the 3 groups. The adjusted hazard ratio (HR) for death and oral RBV use was 0.27 ([0.07,1.1], P = 0.07). The adjusted HR for death and inhaled RBV use was 0.90 ([0.22, 3.68], P = 0.88). RBV was stopped prematurely in only 1 patient in the oral group due to nausea and vomiting. CONCLUSION: Oral and inhaled RBV appear to be well tolerated in LTRs. Our data support the use of oral RBV as a safe alternative to inhaled RBV in LTRs. Additional studies are required to determine whether LTRs with asymptomatic RSV infection would benefit from RBV therapy. DISCLOSURES: R. Miller, scynexis: Investigator, Research support.
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spelling pubmed-62537962018-11-28 1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach Permpalung, Nitipong Thaniyavarn, Tany Saullo, Jennifer Arif, Sana Miller, Rachel Reynolds, John Alexander, Barbara D Open Forum Infect Dis Abstracts BACKGROUND: Respiratory syncytial virus (RSV) is a common community acquired infection in lung transplant recipients (LTRs). The mortality in RSV-infected LTRs has been reported as 10–20% despite antiviral therapy; however, there is no consensus regarding treatment given limited data. METHODS: A retrospective study of all LTRs at Duke University during January 2013 and May 2017 with a positive RSV PCR respiratory specimen was performed. Baseline characteristics, sites of infection, antiviral therapy, side effects, outcomes including all-cause 1-year mortality post RSV infection, and 90-day readmission rates were analyzed. The Cox proportional hazard model was used to adjust the effect of ribavirin (RBV) on mortality. RESULTS: One hundred fourteen RSV-infected LTRs were identified: 70 received oral RBV, 32 inhaled RBV and 12 supportive care only. Baseline characteristics were similar between the 3 groups except site of infection and oxygen requirement at diagnosis (see table). Of 32 patients treated with inhaled RBV, 19 had a creatinine clearance <40 mL/minute and 8 were unable to take oral drugs. Unadjusted all-cause 1-year mortality was highest in the supportive care group [33.3% vs. 7.1% (oral RBV) vs. 25% (inhaled RBV), P = 0.01]. There were no significant differences in readmission rates among the 3 groups. The adjusted hazard ratio (HR) for death and oral RBV use was 0.27 ([0.07,1.1], P = 0.07). The adjusted HR for death and inhaled RBV use was 0.90 ([0.22, 3.68], P = 0.88). RBV was stopped prematurely in only 1 patient in the oral group due to nausea and vomiting. CONCLUSION: Oral and inhaled RBV appear to be well tolerated in LTRs. Our data support the use of oral RBV as a safe alternative to inhaled RBV in LTRs. Additional studies are required to determine whether LTRs with asymptomatic RSV infection would benefit from RBV therapy. DISCLOSURES: R. Miller, scynexis: Investigator, Research support. Oxford University Press 2018-11-26 /pmc/articles/PMC6253796/ http://dx.doi.org/10.1093/ofid/ofy210.1428 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Permpalung, Nitipong
Thaniyavarn, Tany
Saullo, Jennifer
Arif, Sana
Miller, Rachel
Reynolds, John
Alexander, Barbara D
1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach
title 1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach
title_full 1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach
title_fullStr 1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach
title_full_unstemmed 1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach
title_short 1600. An Optimal Respiratory Syncytial Virus (RSV) Treatment in Lung Transplant Recipients: Oral Ribavirin, Inhaled Ribavirin, or Conservative Approach
title_sort 1600. an optimal respiratory syncytial virus (rsv) treatment in lung transplant recipients: oral ribavirin, inhaled ribavirin, or conservative approach
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253796/
http://dx.doi.org/10.1093/ofid/ofy210.1428
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