Evidence map›Paper›PMID 41847887›Full record

SynthesisInfluenza and other respiratory viruses2026

Populations at Risk for Severe or Complicated Rhinovirus Illness: A Systematic Review and Meta-Analysis.

David Gou, Jessica Bartoszko, Laura Weiler, Asal Alavi Parsi, Ante Cuvalo, Sahith Rajkumar, Dominik Mertz, Mark Loeb

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Influenza and other respiratory viruses, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

David GouTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.ORCID https://orcid.org/0009-0001-7889-4177
Jessica BartoszkoDepartment of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0001-6743-3538
Laura WeilerFaculty of Engineering, McMaster University, Hamilton, Ontario, Canada.ORCID https://orcid.org/0009-0000-9827-148X
Asal Alavi ParsiFaculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
Ante CuvaloFaculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.ORCID https://orcid.org/0009-0005-6287-9473
Sahith RajkumarFaculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
Dominik MertzDepartment of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0003-4337-1613
Mark LoebDepartment of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough most rhinovirus infections are mild and subside quickly, vulnerable populations may experience severe illness. Identifying populations at risk for severe or complicated rhinovirus illness can strengthen the ongoing search for preventative and therapeutic treatments. This systematic review and meta-analysis aimed to summarize the populations at risk for the development of severe or complicated rhinovirus illness.

methodsWe searched CENTRAL, EMBASE, and MEDLINE in April 2024 for studies reporting risk factors for severe rhinovirus infection, defined as lower respiratory tract infection (LRTI), hospitalization, critical care unit (CCU) admission, mechanical ventilation, or death. We pooled odds ratios using random-effects meta-analysis, assessed risk of bias using the Newcastle-Ottawa Scale, and rated the certainty of evidence using the GRADE framework.

resultsFrom 29 observational studies (n = 13,185 participants), we analyzed 13 risk factor-outcome combinations. With high certainty, age < 1 year and premature birth are not associated with the risk of LRTI, and diabetes mellitus is not associated with mortality. With moderate certainty, any comorbidity and pulmonary comorbidity are probably associated with increased risk of LRTI, age > 18 years and malignancy are probably associated with increased risk of mortality, and malignancy is probably associated with an increased risk of CCU admission. Many risk factors lacked sufficient evidence for meta-analysis.

conclusionsIndividuals with comorbidities are at greater risk of severe rhinovirus illness. Our findings can inform clinical risk stratification and guide the development and targeted use of emerging therapies. Further comprehensive research is required to elucidate additional risk factors and strengthen the evidence.

Indexed as

Picornaviridae InfectionsRespiratory Tract InfectionsRhinovirusComorbidityHospitalizationHumansRisk Factorsmeta‐analysisrespiratory tract infectionsrhinovirusrisksystematic review

Identifiers

PMID41847887
PMCPMC13098166

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.