Respiratory Syncytial Virus, Human Metapneumovirus, and Parainfluenza Virus Infections in Lung Transplant Recipients: A Systematic Review of Outcomes and Treatment Strategies.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
06 07 2022
Historique:
received: 03 08 2021
pubmed: 14 1 2022
medline: 9 7 2022
entrez: 13 1 2022
Statut: ppublish

Résumé

Respiratory syncytial virus (RSV), parainfluenza virus (PIV), and human metapneumovirus (hMPV) are increasingly associated with chronic lung allograft dysfunction (CLAD) in lung transplant recipients (LTR). This systematic review primarily aimed to assess outcomes of RSV/PIV/hMPV infections in LTR and secondarily to assess evidence regarding the efficacy of ribavirin. Relevant databases were queried and study outcomes extracted using a standardized method and summarized. Nineteen retrospective and 12 prospective studies were included (total 1060 cases). Pooled 30-day mortality was low (0-3%), but CLAD progression 180-360 days postinfection was substantial (pooled incidences 19-24%) and probably associated with severe infection. Ribavirin trended toward effectiveness for CLAD prevention in exploratory meta-analysis (odds ratio [OR] 0.61, [0.27-1.18]), although results were highly variable between studies. RSV/PIV/hMPV infection was followed by a high CLAD incidence. Treatment options, including ribavirin, are limited. There is an urgent need for high-quality studies to provide better treatment options for these infections.

Sections du résumé

BACKGROUND
Respiratory syncytial virus (RSV), parainfluenza virus (PIV), and human metapneumovirus (hMPV) are increasingly associated with chronic lung allograft dysfunction (CLAD) in lung transplant recipients (LTR). This systematic review primarily aimed to assess outcomes of RSV/PIV/hMPV infections in LTR and secondarily to assess evidence regarding the efficacy of ribavirin.
METHODS
Relevant databases were queried and study outcomes extracted using a standardized method and summarized.
RESULTS
Nineteen retrospective and 12 prospective studies were included (total 1060 cases). Pooled 30-day mortality was low (0-3%), but CLAD progression 180-360 days postinfection was substantial (pooled incidences 19-24%) and probably associated with severe infection. Ribavirin trended toward effectiveness for CLAD prevention in exploratory meta-analysis (odds ratio [OR] 0.61, [0.27-1.18]), although results were highly variable between studies.
CONCLUSIONS
RSV/PIV/hMPV infection was followed by a high CLAD incidence. Treatment options, including ribavirin, are limited. There is an urgent need for high-quality studies to provide better treatment options for these infections.

Identifiants

pubmed: 35022697
pii: 6433179
doi: 10.1093/cid/ciab969
pmc: PMC9258934
doi:

Substances chimiques

Ribavirin 49717AWG6K

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2252-2260

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Auke de Zwart (A)

University of Groningen, University Medical Center Groningen, Department of Pulmonary Medicine and Tuberculosis, Groningen, The Netherlands.

Annelies Riezebos-Brilman (A)

Laboratory for Medical Microbiology and Public Health, Hengelo, The Netherlands.

Gerton Lunter (G)

University of Groningen, University Medical Center Groningen, Department of Epidemiology, Groningen, The Netherlands.

Judith Vonk (J)

University of Groningen, University Medical Center Groningen, Department of Epidemiology, Groningen, The Netherlands.

Allan R Glanville (AR)

Lung Transplant Unit, St Vincent's Hospital, Sydney, NSW, Australia.

Jens Gottlieb (J)

Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany.

Nitipong Permpalung (N)

Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Huib Kerstjens (H)

University of Groningen, University Medical Center Groningen, Department of Pulmonary Medicine and Tuberculosis, Groningen, The Netherlands.

Jan-Willem Alffenaar (JW)

School of Pharmacy, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Westmead Hospital, Westmead, Australia.
Marie Bashir Institute of Infectious Diseases and Biosecurity, University of Sydney, Sydney, Australia.

Erik Verschuuren (E)

University of Groningen, University Medical Center Groningen, Department of Pulmonary Medicine and Tuberculosis, Groningen, The Netherlands.

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