Pre-existing health conditions and severe COVID-19 outcomes: an umbrella review approach and meta-analysis of global evidence.

COVID-19 Comorbidities Death Hospitalisation Pre-existing health conditions SARS-CoV-2 Umbrella review

Journal

BMC medicine
ISSN: 1741-7015
Titre abrégé: BMC Med
Pays: England
ID NLM: 101190723

Informations de publication

Date de publication:
27 08 2021
Historique:
received: 04 03 2021
accepted: 08 07 2021
entrez: 27 8 2021
pubmed: 28 8 2021
medline: 16 10 2021
Statut: epublish

Résumé

This study applies an umbrella review approach to summarise the global evidence on the risk of severe COVID-19 outcomes in patients with pre-existing health conditions. Systematic reviews (SRs) were identified in PubMed, Embase/Medline and seven pre-print servers until December 11, 2020. Due to the absence of age-adjusted risk effects stratified by geographical regions, a re-analysis of the evidence was conducted. Primary studies were extracted from SRs and evaluated for inclusion in the re-analysis. Studies were included if they reported risk estimates (odds ratio (OR), hazard ratio (HR), relative risk (RR)) for hospitalisation, intensive care unit admission, intubation or death. Estimated associations were extracted from the primary studies for reported pre-existing conditions. Meta-analyses were performed stratified for each outcome by regions of the World Health Organization. The evidence certainty was assessed using GRADE. Registration number CRD42020215846. In total, 160 primary studies from 120 SRs contributed 464 estimates for 42 pre-existing conditions. Most studies were conducted in North America, European, and Western Pacific regions. Evidence from Africa, South/Latin America, and the Eastern Mediterranean region was scarce. No evidence was available from the South-East Asia region. Diabetes (HR range 1.2-2.0 (CI range 1.1-2.8)), obesity (OR range 1.5-1.75 (CI range 1.1-2.3)), heart failure (HR range 1.3-3.3 (CI range 0.9-8.2)), COPD (HR range 1.12-2.2 (CI range 1.1-3.2)) and dementia (HR range 1.4-7.7 (CI range 1.2-39.6)) were associated with fatal COVID-19 in different regions, although the estimates varied. Evidence from Europe and North America showed that liver cirrhosis (OR range 3.2-5.9 (CI range 0.9-27.7)) and active cancer (OR range 1.6-4.7 (CI range 0.5-14.9)) were also associated with increased risk of death. Association between HIV and undesirable COVID-19 outcomes showed regional heterogeneity, with an increased risk of death in Africa (HR 1.7 (CI 1.3-2.2)). GRADE certainty was moderate to high for most associations. Risk of undesirable COVID-19 health outcomes is consistently increased in certain patient subgroups across geographical regions, showing high variability in others. The results can be used to inform COVID-19 vaccine prioritisation or other intervention strategies.

Sections du résumé

BACKGROUND
This study applies an umbrella review approach to summarise the global evidence on the risk of severe COVID-19 outcomes in patients with pre-existing health conditions.
METHODS
Systematic reviews (SRs) were identified in PubMed, Embase/Medline and seven pre-print servers until December 11, 2020. Due to the absence of age-adjusted risk effects stratified by geographical regions, a re-analysis of the evidence was conducted. Primary studies were extracted from SRs and evaluated for inclusion in the re-analysis. Studies were included if they reported risk estimates (odds ratio (OR), hazard ratio (HR), relative risk (RR)) for hospitalisation, intensive care unit admission, intubation or death. Estimated associations were extracted from the primary studies for reported pre-existing conditions. Meta-analyses were performed stratified for each outcome by regions of the World Health Organization. The evidence certainty was assessed using GRADE. Registration number CRD42020215846.
RESULTS
In total, 160 primary studies from 120 SRs contributed 464 estimates for 42 pre-existing conditions. Most studies were conducted in North America, European, and Western Pacific regions. Evidence from Africa, South/Latin America, and the Eastern Mediterranean region was scarce. No evidence was available from the South-East Asia region. Diabetes (HR range 1.2-2.0 (CI range 1.1-2.8)), obesity (OR range 1.5-1.75 (CI range 1.1-2.3)), heart failure (HR range 1.3-3.3 (CI range 0.9-8.2)), COPD (HR range 1.12-2.2 (CI range 1.1-3.2)) and dementia (HR range 1.4-7.7 (CI range 1.2-39.6)) were associated with fatal COVID-19 in different regions, although the estimates varied. Evidence from Europe and North America showed that liver cirrhosis (OR range 3.2-5.9 (CI range 0.9-27.7)) and active cancer (OR range 1.6-4.7 (CI range 0.5-14.9)) were also associated with increased risk of death. Association between HIV and undesirable COVID-19 outcomes showed regional heterogeneity, with an increased risk of death in Africa (HR 1.7 (CI 1.3-2.2)). GRADE certainty was moderate to high for most associations.
CONCLUSION
Risk of undesirable COVID-19 health outcomes is consistently increased in certain patient subgroups across geographical regions, showing high variability in others. The results can be used to inform COVID-19 vaccine prioritisation or other intervention strategies.

Identifiants

pubmed: 34446016
doi: 10.1186/s12916-021-02058-6
pii: 10.1186/s12916-021-02058-6
pmc: PMC8390115
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

212

Subventions

Organisme : German Ministry of Health
ID : project ImVaCov

Informations de copyright

© 2021. The Author(s).

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Auteurs

Marina Treskova-Schwarzbach (M)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany. TreskovaM@rki.de.

Laura Haas (L)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Sarah Reda (S)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Antonia Pilic (A)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Anna Borodova (A)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Kasra Karimi (K)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Judith Koch (J)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Teresa Nygren (T)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Stefan Scholz (S)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Viktoria Schönfeld (V)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Sabine Vygen-Bonnet (S)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Ole Wichmann (O)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

Thomas Harder (T)

Immunisation Unit, The Robert Koch Institute, Seestrasse 10, 13353, Berlin, Germany.

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