Efficacy of High-Dose Polyclonal Intravenous Immunoglobulin in COVID-19: A Systematic Review.

COVID-19 SARS-CoV-2 immunosuppressants intravenous immunoglobulins polyclonal antibodies

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
09 Jan 2022
Historique:
received: 08 12 2021
revised: 30 12 2021
accepted: 06 01 2022
entrez: 22 1 2022
pubmed: 23 1 2022
medline: 23 1 2022
Statut: epublish

Résumé

Although several therapeutic strategies have been investigated, the optimal treatment approach for patients with coronavirus disease (COVID-19) remains to be elucidated. This systematic review and meta-analysis aimed to evaluate the efficacy and safety of polyclonal intravenous immunoglobulin (IVIG) therapy in COVID-19. A systematic literature search using appropriate medical subject heading (MeSH) terms was performed through Medline (PubMed), EMBASE, SCOPUS, OVID and Cochrane Library electronic databases. The main outcomes considered were mortality and safety of IVIG versus placebo/standard of care. This review was carried out in accordance with Cochrane methodology including the risk bias assessment and grading of the quality of evidence. Measures of treatment effect were mean differences (MD) together with 95% confidence intervals (CIs) for continuous outcome measures and risk ratio (RR) or MD for binary outcomes. Two reviewers independently extracted data from individual studies, and disagreements were resolved by a third reviewer. A total of 2401 COVID-19 patients from 10 studies (four randomized controlled trials (RCT) and six non-randomized controlled trials (non-RCTs)) were included in the analysis. Participants received IVIG or placebo/standard of care. The use of IVIG was not associated with a significantly reduced risk of death (RR 0.50, 95% CIs 0.18-1.36, The current evidence from the literature does not support the use of IVIG in COVID-19 patients.

Sections du résumé

BACKGROUND BACKGROUND
Although several therapeutic strategies have been investigated, the optimal treatment approach for patients with coronavirus disease (COVID-19) remains to be elucidated. This systematic review and meta-analysis aimed to evaluate the efficacy and safety of polyclonal intravenous immunoglobulin (IVIG) therapy in COVID-19.
METHODS METHODS
A systematic literature search using appropriate medical subject heading (MeSH) terms was performed through Medline (PubMed), EMBASE, SCOPUS, OVID and Cochrane Library electronic databases. The main outcomes considered were mortality and safety of IVIG versus placebo/standard of care. This review was carried out in accordance with Cochrane methodology including the risk bias assessment and grading of the quality of evidence. Measures of treatment effect were mean differences (MD) together with 95% confidence intervals (CIs) for continuous outcome measures and risk ratio (RR) or MD for binary outcomes. Two reviewers independently extracted data from individual studies, and disagreements were resolved by a third reviewer.
RESULTS RESULTS
A total of 2401 COVID-19 patients from 10 studies (four randomized controlled trials (RCT) and six non-randomized controlled trials (non-RCTs)) were included in the analysis. Participants received IVIG or placebo/standard of care. The use of IVIG was not associated with a significantly reduced risk of death (RR 0.50, 95% CIs 0.18-1.36,
CONCLUSIONS CONCLUSIONS
The current evidence from the literature does not support the use of IVIG in COVID-19 patients.

Identifiants

pubmed: 35062755
pii: vaccines10010094
doi: 10.3390/vaccines10010094
pmc: PMC8779789
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Daniele Focosi (D)

North-Western Tuscany Blood Bank, Pisa University Hospital, 56124 Pisa, Italy.

Massimo Franchini (M)

Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, 46100 Mantua, Italy.

Marco Tuccori (M)

Division of Pharmacology and Pharmacovigilance, University of Pisa, 56126 Pisa, Italy.
Unit of Adverse Drug Reaction Monitoring, Pisa University Hospital, 56124 Pisa, Italy.

Mario Cruciani (M)

Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, 46100 Mantua, Italy.

Classifications MeSH