Management of iron‐deficiency anemia following acute gastrointestinal hemorrhage: A narrative analysis and review

Many patients experiencing acute gastrointestinal bleeding (GIB) require iron supplementation to treat subsequent iron deficiency (ID) or iron‐deficiency anemia (IDA). Guidelines regarding management of these patients are lacking. We aimed to identify areas of unmet need in patients with ID/IDA foll...

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Published inJournal of gastroenterology and hepatology Vol. 38; no. 1; pp. 23 - 33
Main Authors Lanas, Angel, Andrews, Jane M, Lau, James, Toruner, Murat, Bromley, Susan E, Gralnek, Ian M
Format Journal Article
LanguageEnglish
Published Australia Wiley Subscription Services, Inc 01.01.2023
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ISSN0815-9319
1440-1746
1440-1746
DOI10.1111/jgh.16033

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Summary:Many patients experiencing acute gastrointestinal bleeding (GIB) require iron supplementation to treat subsequent iron deficiency (ID) or iron‐deficiency anemia (IDA). Guidelines regarding management of these patients are lacking. We aimed to identify areas of unmet need in patients with ID/IDA following acute GIB in terms of patient management and physician guidance. We formed an international working group of gastroenterologists to conduct a narrative review based on PubMed and EMBASE database searches (from January 2000 to February 2021), integrated with observations from our own clinical experience. Published data on this subject are limited and disparate, and those relating to post‐discharge outcomes, such as persistent anemia and re‐hospitalization, are particularly lacking. Often, there is no post‐discharge follow‐up of these patients by a gastroenterologist. Acute GIB‐related ID/IDA, however, is a prevalent condition both at the time of hospital admission and at hospital discharge and is likely underdiagnosed and undertreated. Despite limited data, there appears to be notable variation in the prescribing of intravenous (IV)/oral iron regimens. There is also some evidence suggesting that, compared with oral iron, IV iron may restore iron levels faster following acute GIB, have a better tolerability profile, and be more beneficial in terms of quality of life. Gaps in patient care exist in the management of acute GIB‐related ID/IDA, yet further data from large population‐based studies are needed to confirm this. We advocate the formulation of evidence‐based guidance on the use of iron therapies in these patients, aiding a more standardized best‐practice approach to patient care.
Bibliography:Declaration of conflict of interest
Not applicable.
Financial support
Informed consent
This work was funded by Vifor Pharma, the Marketing Authorization Holder of Ferinject (ferric carboxymaltose). Vifor Pharma provided an unrestricted grant to support the working group and had no role in the study design, collection, analysis and interpretation of data, the writing of the paper, or the decision to submit it for publication.
Ethical approval
IMG declares payment for speaker's fees, consultancy, research support, and/or advisory board attendance from Boston Scientific, CheckCap, Clexio Bioscience, Medtronic, Motus GI, Neurogastrx, Rochlin Foundation, Symbionix, and Vifor Pharma. AL declares payment for speaker's fees and advisory board attendance from Bayer AG, Vifor Pharma, GSK, and Sysmex Ibérica. JMA declares payment for speaker's fees, research support, and advisory board attendance from Abbott, AbbVie, Allergan, Anatara, AstraZeneca, Bayer, BMS, Celgene, Celltrion, Falk, Ferring, Gilead, Hospira, Immuninc, ImmunsanT, Janssen, MSD, Nestle, Novartis, Pfizer, Sandoz, Shire, Takeda, Vifor Pharma, RAH Research Fund, The Hospital Research Fund 2020–2022, and The Helmsley Trust 2020–2023. JL declares no conflicts of interest. MT declares payment for speaker's fees, consultancy, and advisory board attendance from AbbVie, Janssen, MSD, Takeda, Pfizer, and Vifor Pharma. SB declares payment from Vifor Pharma for medical writing and research consultancy services.
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ISSN:0815-9319
1440-1746
1440-1746
DOI:10.1111/jgh.16033