Risk of Infection Associated With Administration of Intravenous Iron: A Systematic Review and Meta-analysis.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 11 2021
Historique:
entrez: 12 11 2021
pubmed: 13 11 2021
medline: 12 1 2022
Statut: epublish

Résumé

Intravenous iron is recommended by many clinical guidelines based largely on its effectiveness in reducing anemia. However, the association with important safety outcomes, such as infection, remains uncertain. To examine the risk of infection associated with intravenous iron compared with oral iron or no iron. Medline, Embase, and Cochrane Central Register of Controlled Trials (CENTRAL) were searched for randomized clinical trials (RCTs) from 1966 to January 31, 2021. Ongoing trials were sought from ClinicalTrials.gov, CENTRAL, and the World Health Organization International Clinical Trials Search Registry Platform. Pairs of reviewers identified RCTs that compared intravenous iron with oral iron or no iron across all patient populations, excluding healthy volunteers. Nonrandomized studies published since January 1, 2007, were also included. A total of 312 full-text articles were assessed for eligibility. Data extraction and risk of bias assessments were performed according to the Preferred Reporting Items of Systematic Reviews and Meta-analyses (PRISMA) and Cochrane recommendations, and the quality of evidence was assessed using the GRADE (Grades of Recommendation, Assessment, Development, and Evaluation) approach. Two reviewers extracted data independently. A random-effects model was used to synthesize data from RCTs. A narrative synthesis was performed to characterize the reporting of infection. The primary outcome was risk of infection. Secondary outcomes included mortality, hospital length of stay, and changes in hemoglobin and red blood cell transfusion requirements. Measures of association were reported as risk ratios (RRs) or mean differences. A total of 154 RCTs (32 920 participants) were included in the main analysis. Intravenous iron was associated with an increased risk of infection when compared with oral iron or no iron (RR, 1.17; 95% CI, 1.04-1.31; I2 = 37%; moderate certainty of evidence). Intravenous iron also was associated with an increase in hemoglobin (mean difference, 0.57 g/dL; 95% CI, 0.50-0.64 g/dL; I2 = 94%) and a reduction in the risk of requiring a red blood cell transfusion (RR, 0.93; 95% CI, 0.76-0.89; I2 = 15%) when compared with oral iron or no iron. There was no evidence of an effect on mortality or hospital length of stay. In this large systematic review and meta-analysis, intravenous iron was associated with an increased risk of infection. Well-designed studies, using standardized definitions of infection, are required to understand the balance between this risk and the potential benefits.

Identifiants

pubmed: 34767026
pii: 2786031
doi: 10.1001/jamanetworkopen.2021.33935
pmc: PMC8590171
doi:

Substances chimiques

Hemoglobins 0
Iron E1UOL152H7

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2133935

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

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Auteurs

Akshay A Shah (AA)

Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
National Institute for Health Research Biomedical Research Centre Haematology Theme, Oxford, United Kingdom.
Adult Intensive Care Unit, Oxford University Hospitals National Health Service (NHS) Foundation Trust, Oxford, United Kingdom.

Killian Donovan (K)

Adult Intensive Care Unit, Oxford University Hospitals National Health Service (NHS) Foundation Trust, Oxford, United Kingdom.

Claire Seeley (C)

Department of Anaesthesia, Royal Berkshire Hospitals NHS Foundation Trust, Reading, United Kingdom.

Edward A Dickson (EA)

National Institute for Health Research Biomedical Research Centre in Gastrointestinal and Liver Diseases, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
Department of Colorectal Surgery, Nottingham University Hospitals NHS Trust, University of Nottingham, Nottingham, United Kingdom.

Antony J R Palmer (AJR)

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.

Carolyn Doree (C)

Systematic Review Initiative, NHS Blood & Transplant, Oxford, United Kingdom.

Susan Brunskill (S)

Systematic Review Initiative, NHS Blood & Transplant, Oxford, United Kingdom.

Jack Reid (J)

Department of Anaesthesia, Brighton and Sussex University Hospitals NHS Trust, Brighton, United Kingdom.

Austin G Acheson (AG)

National Institute for Health Research Biomedical Research Centre in Gastrointestinal and Liver Diseases, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
Department of Colorectal Surgery, Nottingham University Hospitals NHS Trust, University of Nottingham, Nottingham, United Kingdom.

Anita Sugavanam (A)

Department of Anaesthesia, Brighton and Sussex University Hospitals NHS Trust, Brighton, United Kingdom.

Edward Litton (E)

Intensive Care Unit, Fiona Stanley Hospital, Perth, Australia.

Simon J Stanworth (SJ)

Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
National Institute for Health Research Biomedical Research Centre Haematology Theme, Oxford, United Kingdom.
Systematic Review Initiative, NHS Blood & Transplant, Oxford, United Kingdom.
Department of Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

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