A systematic literature review and meta-analysis of the incidence of serious or severe hypersensitivity reactions after administration of ferric derisomaltose or ferric carboxymaltose

Background Intravenous iron is the preferred treatment for patients with iron deficiency anemia in a variety of clinical situations. Although uncommon, administration of modern IV iron formulations can result in hypersensitivity reactions (HSRs) and, rarely, anaphylactic or anaphylactoid reactions....

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Veröffentlicht in:International journal of clinical pharmacy 2023-06, Vol.45 (3), p.604-612
Hauptverfasser: Kennedy, Nicholas A., Achebe, Maureen M., Biggar, Patrick, Pöhlmann, Johannes, Pollock, Richard F.
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container_title International journal of clinical pharmacy
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creator Kennedy, Nicholas A.
Achebe, Maureen M.
Biggar, Patrick
Pöhlmann, Johannes
Pollock, Richard F.
description Background Intravenous iron is the preferred treatment for patients with iron deficiency anemia in a variety of clinical situations. Although uncommon, administration of modern IV iron formulations can result in hypersensitivity reactions (HSRs) and, rarely, anaphylactic or anaphylactoid reactions. Aim The objective of the present study was to systematically review the literature to identify and analyze data on the incidence of HSRs after administration of ferric derisomaltose (FDI) or ferric carboxymaltose (FCM). Method A prospectively-registered systematic literature review was conducted to identify prospective randomized controlled trials comparing FDI and FCM with other intravenous iron formulations or oral iron. Searches were conducted in PubMed (including MEDLINE), EMBASE, and the Cochrane Library in November 2020. The relative incidence of serious or severe HSRs occurring on the day or day after dosing of intravenous iron, recorded under the standardized Medical Dictionary for Regulatory Activities query for anaphylactic reaction. Results Data were obtained from seven randomized controlled trials of FCM (N = 2683) and ten of FDI (N = 3474) enrolling 10,467 patients in total. The number of patients experiencing any serious or severe HSR event was 29/2683 (1.08%) with FCM versus 5/3474 with FDI (0.14%). Bayesian inference of proportions showed the event rates to be significantly lower with FDI relative to FCM. Conclusion HSR events were uncommon with both intravenous iron formulations; however, the present study showed a significantly lower incidence of HSRs with FDI relative to FCM. Further large-scale, head-to-head trials of the iron formulations would be required to confirm this finding.
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Although uncommon, administration of modern IV iron formulations can result in hypersensitivity reactions (HSRs) and, rarely, anaphylactic or anaphylactoid reactions. Aim The objective of the present study was to systematically review the literature to identify and analyze data on the incidence of HSRs after administration of ferric derisomaltose (FDI) or ferric carboxymaltose (FCM). Method A prospectively-registered systematic literature review was conducted to identify prospective randomized controlled trials comparing FDI and FCM with other intravenous iron formulations or oral iron. Searches were conducted in PubMed (including MEDLINE), EMBASE, and the Cochrane Library in November 2020. The relative incidence of serious or severe HSRs occurring on the day or day after dosing of intravenous iron, recorded under the standardized Medical Dictionary for Regulatory Activities query for anaphylactic reaction. Results Data were obtained from seven randomized controlled trials of FCM (N = 2683) and ten of FDI (N = 3474) enrolling 10,467 patients in total. The number of patients experiencing any serious or severe HSR event was 29/2683 (1.08%) with FCM versus 5/3474 with FDI (0.14%). Bayesian inference of proportions showed the event rates to be significantly lower with FDI relative to FCM. Conclusion HSR events were uncommon with both intravenous iron formulations; however, the present study showed a significantly lower incidence of HSRs with FDI relative to FCM. Further large-scale, head-to-head trials of the iron formulations would be required to confirm this finding.</description><identifier>ISSN: 2210-7703</identifier><identifier>EISSN: 2210-7711</identifier><identifier>DOI: 10.1007/s11096-023-01548-2</identifier><identifier>PMID: 37010731</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Administration, Intravenous ; Analysis ; Anaphylactoid reactions ; Anaphylaxis ; Anaphylaxis - diagnosis ; Anaphylaxis - drug therapy ; Anaphylaxis - epidemiology ; Anemia, Iron-Deficiency - drug therapy ; Anemia, Iron-Deficiency - epidemiology ; Anemia, Iron-Deficiency - etiology ; Bayes Theorem ; Bayesian analysis ; Clinical trials ; Complications and side effects ; Ferric carboxymaltose ; Foreign investments ; Humans ; Hypersensitivity ; Incidence ; Internal Medicine ; Intravenous administration ; Iron ; Iron - therapeutic use ; Iron compounds ; Iron deficiency ; Iron deficiency anemia ; Literature reviews ; Medicine ; Medicine &amp; Public Health ; Meta-analysis ; Nutrient deficiency ; Patients ; Pharmacy ; Prospective Studies ; Review ; Review Article ; Systematic review</subject><ispartof>International journal of clinical pharmacy, 2023-06, Vol.45 (3), p.604-612</ispartof><rights>The Author(s) 2023</rights><rights>2023. 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Although uncommon, administration of modern IV iron formulations can result in hypersensitivity reactions (HSRs) and, rarely, anaphylactic or anaphylactoid reactions. Aim The objective of the present study was to systematically review the literature to identify and analyze data on the incidence of HSRs after administration of ferric derisomaltose (FDI) or ferric carboxymaltose (FCM). Method A prospectively-registered systematic literature review was conducted to identify prospective randomized controlled trials comparing FDI and FCM with other intravenous iron formulations or oral iron. Searches were conducted in PubMed (including MEDLINE), EMBASE, and the Cochrane Library in November 2020. The relative incidence of serious or severe HSRs occurring on the day or day after dosing of intravenous iron, recorded under the standardized Medical Dictionary for Regulatory Activities query for anaphylactic reaction. Results Data were obtained from seven randomized controlled trials of FCM (N = 2683) and ten of FDI (N = 3474) enrolling 10,467 patients in total. The number of patients experiencing any serious or severe HSR event was 29/2683 (1.08%) with FCM versus 5/3474 with FDI (0.14%). Bayesian inference of proportions showed the event rates to be significantly lower with FDI relative to FCM. Conclusion HSR events were uncommon with both intravenous iron formulations; however, the present study showed a significantly lower incidence of HSRs with FDI relative to FCM. 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Although uncommon, administration of modern IV iron formulations can result in hypersensitivity reactions (HSRs) and, rarely, anaphylactic or anaphylactoid reactions. Aim The objective of the present study was to systematically review the literature to identify and analyze data on the incidence of HSRs after administration of ferric derisomaltose (FDI) or ferric carboxymaltose (FCM). Method A prospectively-registered systematic literature review was conducted to identify prospective randomized controlled trials comparing FDI and FCM with other intravenous iron formulations or oral iron. Searches were conducted in PubMed (including MEDLINE), EMBASE, and the Cochrane Library in November 2020. The relative incidence of serious or severe HSRs occurring on the day or day after dosing of intravenous iron, recorded under the standardized Medical Dictionary for Regulatory Activities query for anaphylactic reaction. Results Data were obtained from seven randomized controlled trials of FCM (N = 2683) and ten of FDI (N = 3474) enrolling 10,467 patients in total. The number of patients experiencing any serious or severe HSR event was 29/2683 (1.08%) with FCM versus 5/3474 with FDI (0.14%). Bayesian inference of proportions showed the event rates to be significantly lower with FDI relative to FCM. Conclusion HSR events were uncommon with both intravenous iron formulations; however, the present study showed a significantly lower incidence of HSRs with FDI relative to FCM. Further large-scale, head-to-head trials of the iron formulations would be required to confirm this finding.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>37010731</pmid><doi>10.1007/s11096-023-01548-2</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9873-7507</orcidid><oa>free_for_read</oa></addata></record>
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subjects Administration, Intravenous
Analysis
Anaphylactoid reactions
Anaphylaxis
Anaphylaxis - diagnosis
Anaphylaxis - drug therapy
Anaphylaxis - epidemiology
Anemia, Iron-Deficiency - drug therapy
Anemia, Iron-Deficiency - epidemiology
Anemia, Iron-Deficiency - etiology
Bayes Theorem
Bayesian analysis
Clinical trials
Complications and side effects
Ferric carboxymaltose
Foreign investments
Humans
Hypersensitivity
Incidence
Internal Medicine
Intravenous administration
Iron
Iron - therapeutic use
Iron compounds
Iron deficiency
Iron deficiency anemia
Literature reviews
Medicine
Medicine & Public Health
Meta-analysis
Nutrient deficiency
Patients
Pharmacy
Prospective Studies
Review
Review Article
Systematic review
title A systematic literature review and meta-analysis of the incidence of serious or severe hypersensitivity reactions after administration of ferric derisomaltose or ferric carboxymaltose
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