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Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation

INTRODUCTION: Respiratory syncytial virus (RSV) is a common cause of morbidity among hematopoietic stem cell transplant (HSCT) recipients, with RSV-associated lower respiratory tract infection carrying high mortality rates. There have been no large studies till date, describing the incidence, clinic...

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Autores principales: Samad, Sameer Abdul, Jethani, Jyoti, Kumar, Lalit, Choudhary, Aashish, Brijwal, Megha, Dar, Lalit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552342/
https://www.ncbi.nlm.nih.gov/pubmed/36237564
http://dx.doi.org/10.4103/jgid.jgid_11_22
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author Samad, Sameer Abdul
Jethani, Jyoti
Kumar, Lalit
Choudhary, Aashish
Brijwal, Megha
Dar, Lalit
author_facet Samad, Sameer Abdul
Jethani, Jyoti
Kumar, Lalit
Choudhary, Aashish
Brijwal, Megha
Dar, Lalit
author_sort Samad, Sameer Abdul
collection PubMed
description INTRODUCTION: Respiratory syncytial virus (RSV) is a common cause of morbidity among hematopoietic stem cell transplant (HSCT) recipients, with RSV-associated lower respiratory tract infection carrying high mortality rates. There have been no large studies till date, describing the incidence, clinical features, and outcomes of RSV infection among adult HSCT recipients in India. METHODS: A prospective cohort of 100 adults who underwent HSCT was followed up for a maximum period of 18 months starting from the date of transplantation for any episode of respiratory tract infectious disease (RTID). Respiratory samples were collected for laboratory confirmation of the presence and subtyping of RSV by real-time reverse transcriptase-polymerase chain reaction. RESULTS: The study population comprised of 66% (66/100) males and 34% (34/100) females. Autologous HSCT recipients constituted 78% (78/100) and allogeneic HSCT recipients constituted 22% (22/100) of the study population. The incidence of RSV-RTID among adults after HSCT was 0.82/100 patient months. Most cases occurred during the winter season and the predominant subtype was RSV-A (9/11, 81.8%). Lower RTID was the most common clinical diagnosis made at presentation (9/11, 81.8%). Female gender was predictive of RSV-RTID (log rank P = 0.002). All the RSV-RTID episodes recovered completely without targeted therapy. CONCLUSION: RSV is a significant cause of morbidity among adult HSCT recipients in India. Prophylaxis and treatment measures need to be instituted after a proper risk-benefit assessment. Longitudinal studies with larger sample sizes are needed to confirm these results.
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spelling pubmed-95523422022-10-12 Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation Samad, Sameer Abdul Jethani, Jyoti Kumar, Lalit Choudhary, Aashish Brijwal, Megha Dar, Lalit J Glob Infect Dis Original Article INTRODUCTION: Respiratory syncytial virus (RSV) is a common cause of morbidity among hematopoietic stem cell transplant (HSCT) recipients, with RSV-associated lower respiratory tract infection carrying high mortality rates. There have been no large studies till date, describing the incidence, clinical features, and outcomes of RSV infection among adult HSCT recipients in India. METHODS: A prospective cohort of 100 adults who underwent HSCT was followed up for a maximum period of 18 months starting from the date of transplantation for any episode of respiratory tract infectious disease (RTID). Respiratory samples were collected for laboratory confirmation of the presence and subtyping of RSV by real-time reverse transcriptase-polymerase chain reaction. RESULTS: The study population comprised of 66% (66/100) males and 34% (34/100) females. Autologous HSCT recipients constituted 78% (78/100) and allogeneic HSCT recipients constituted 22% (22/100) of the study population. The incidence of RSV-RTID among adults after HSCT was 0.82/100 patient months. Most cases occurred during the winter season and the predominant subtype was RSV-A (9/11, 81.8%). Lower RTID was the most common clinical diagnosis made at presentation (9/11, 81.8%). Female gender was predictive of RSV-RTID (log rank P = 0.002). All the RSV-RTID episodes recovered completely without targeted therapy. CONCLUSION: RSV is a significant cause of morbidity among adult HSCT recipients in India. Prophylaxis and treatment measures need to be instituted after a proper risk-benefit assessment. Longitudinal studies with larger sample sizes are needed to confirm these results. Wolters Kluwer - Medknow 2022-08-26 /pmc/articles/PMC9552342/ /pubmed/36237564 http://dx.doi.org/10.4103/jgid.jgid_11_22 Text en Copyright: © 2022 Journal of Global Infectious Diseases https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Samad, Sameer Abdul
Jethani, Jyoti
Kumar, Lalit
Choudhary, Aashish
Brijwal, Megha
Dar, Lalit
Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation
title Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation
title_full Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation
title_fullStr Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation
title_full_unstemmed Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation
title_short Respiratory Syncytial Virus Infection among Adults after Hematopoietic Stem Cell Transplantation
title_sort respiratory syncytial virus infection among adults after hematopoietic stem cell transplantation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552342/
https://www.ncbi.nlm.nih.gov/pubmed/36237564
http://dx.doi.org/10.4103/jgid.jgid_11_22
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