Respiratory Syncytial Virus Sequelae Among Adults in High-Income Countries: A Systematic Literature Review and Meta-analysis.

Adults RSV Respiratory syncytial virus Sequelae Systematic review

Journal

Infectious diseases and therapy
ISSN: 2193-8229
Titre abrégé: Infect Dis Ther
Pays: New Zealand
ID NLM: 101634499

Informations de publication

Date de publication:
06 May 2024
Historique:
received: 24 01 2024
accepted: 05 04 2024
medline: 25 5 2024
pubmed: 25 5 2024
entrez: 24 5 2024
Statut: aheadofprint

Résumé

Respiratory syncytial virus (RSV) can cause severe respiratory infections in adults; however, information on associated sequelae is limited. This systematic literature review aimed to identify sequelae in adults within 1 year following RSV-related hospitalization or resolution of acute infection. Studies were identified from Embase, MEDLINE, LILACS, SciELO, and grey literature. Random-effects meta-analyses using restricted maximum likelihood were used to calculate the proportions and relative risks of sequelae in patients with RSV compared with controls (patients with RSV-negative influenza-like illness, influenza, and parainfluenza) per follow-up period, population, and treatment setting, where possible. Twenty-one relevant studies covering the period from 1990 to 2019 were included. Among the general population, the most frequent clinical sequela was sustained function loss (33.5% [95% CI 27.6-39.9]). Decline in lung function and cardiovascular event or congestive heart failure were also identified. Utilization sequelae were readmission (highest at > 6 months after discharge) and placement in a skilled nursing facility. The only subpopulation with data regarding sequelae was transplant patients. Among lung transplant patients, the most frequently reported clinical sequelae were decline in lung function, followed by graft dysfunction and bronchiolitis obliterans syndrome. Pooled relative risks were calculated for the following sequela with controls (primarily influenza-positive patients): cardiovascular event (general population) and pulmonary impairment (hematogenic-transplant patients) both 1.4 (95% CI 1.0-2.0) and for readmission (general population) 1.2 (95% CI 1.1-1.3). Although less data are available for RSV than for influenza or other lower respiratory tract infections, RSV infection among adults is associated with medically important sequelae, with a prevalence similar to other respiratory pathogens. RSV sequelae should be included in disease burden estimates.

Identifiants

pubmed: 38789901
doi: 10.1007/s40121-024-00974-7
pii: 10.1007/s40121-024-00974-7
doi:

Types de publication

Journal Article Review

Langues

eng

Informations de copyright

© 2024. The Author(s).

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Auteurs

Egbe Ubamadu (E)

P95 Pharmacovigilance and Epidemiology, Louvain, Belgium.

Estefania Betancur (E)

P95 Pharmacovigilance and Epidemiology, Louvain, Belgium.

Bradford D Gessner (BD)

Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA, USA.
Pfizer Vaccines, 9 Riverwalk, Citywest Business Campus, Dublin 24, Ireland.

Sonia Menon (S)

P95 Pharmacovigilance and Epidemiology, Louvain, Belgium.

Hilde Vroling (H)

P95 Pharmacovigilance and Epidemiology, Louvain, Belgium.

Daniel Curcio (D)

Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA, USA.
Pfizer Vaccines, 9 Riverwalk, Citywest Business Campus, Dublin 24, Ireland.

Mark Rozenbaum (M)

Value and Evidence, Patient and Health Impact, Pfizer Inc., Capelle a/d Ijssel, The Netherlands.

Samantha K Kurosky (SK)

Value and Evidence, Patient and Health Impact, Pfizer Inc., New York, NY, USA.

Zuleika Aponte (Z)

P95 Pharmacovigilance and Epidemiology, Louvain, Belgium.

Elizabeth Begier (E)

Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA, USA. Elizabeth.Begier@pfizer.com.
Pfizer Vaccines, 9 Riverwalk, Citywest Business Campus, Dublin 24, Ireland. Elizabeth.Begier@pfizer.com.

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