Cargando…
Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis
AIMS: Intravenous ferric carboxymaltose (FCM) has been shown to improve functional capacity and quality of life in iron deficient heart failure patients. However, FCM's effect on hospitalizations and mortality remains unclear as previous randomized controlled trials (RCTs) and their meta‐analys...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754952/ https://www.ncbi.nlm.nih.gov/pubmed/33586856 http://dx.doi.org/10.1002/ehf2.13146 |
_version_ | 1783626280323776512 |
---|---|
author | Khan, Muhammad Shahzeb Usman, Muhammad Shariq von Haehling, Stephan Doehner, Wolfram Stewart Coats, Andrew J. |
author_facet | Khan, Muhammad Shahzeb Usman, Muhammad Shariq von Haehling, Stephan Doehner, Wolfram Stewart Coats, Andrew J. |
author_sort | Khan, Muhammad Shahzeb |
collection | PubMed |
description | AIMS: Intravenous ferric carboxymaltose (FCM) has been shown to improve functional capacity and quality of life in iron deficient heart failure patients. However, FCM's effect on hospitalizations and mortality remains unclear as previous randomized controlled trials (RCTs) and their meta‐analyses have been underpowered to detect significant differences. We sought to conduct an updated meta‐analysis using recently published RCT data. METHODS AND RESULTS: Online databases were searched from inception until November 2020 for RCTs evaluating the effects of FCM on clinical outcomes in iron‐deficient heart failure patients. Outcomes of interest included heart failure hospitalizations, all‐cause mortality, and cardiovascular mortality. Meta‐analysis was performed using a fixed‐effect model and estimates were reported as odds ratios (ORs), hazard ratios, or rate ratios (RRs) along with corresponding 95% confidence intervals (CIs). A total of 1947 patients (n = 1062 in the FCM group; n = 885 in the placebo group) were included. FCM, compared with placebo, significantly reduced the risk of the composite endpoint of time to first heart failure hospitalization or cardiovascular death (hazard ratio = 0.76; 95% CI = 0.63–0.90; I (2) = 55%). FCM also significantly reduced the risk of recurrent heart failure hospitalizations (RR = 0.68; 95% CI = 0.54–0.85; I (2) = 71%) and recurrent cardiovascular hospitalizations (RR = 0.71; 95% CI = 0.59–0.86; I (2) = 56%). However, FCM had no significant effect on the risk of all‐cause (OR = 0.97; 95% CI = 0.73–1.28; I (2) = 0%) or cardiovascular mortality (OR = 0.93; 95% CI = 0.69–1.27; I (2) = 0%). CONCLUSIONS: Ferric carboxymaltose reduces heart failure hospitalizations and cardiovascular hospitalizations with no beneficial effect on all‐cause and cardiovascular mortality in iron‐deficient heart failure patients. These findings reinforce the role of FCM as a therapeutic option in heart failure patients. |
format | Online Article Text |
id | pubmed-7754952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77549522020-12-23 Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis Khan, Muhammad Shahzeb Usman, Muhammad Shariq von Haehling, Stephan Doehner, Wolfram Stewart Coats, Andrew J. ESC Heart Fail Original Research Articles AIMS: Intravenous ferric carboxymaltose (FCM) has been shown to improve functional capacity and quality of life in iron deficient heart failure patients. However, FCM's effect on hospitalizations and mortality remains unclear as previous randomized controlled trials (RCTs) and their meta‐analyses have been underpowered to detect significant differences. We sought to conduct an updated meta‐analysis using recently published RCT data. METHODS AND RESULTS: Online databases were searched from inception until November 2020 for RCTs evaluating the effects of FCM on clinical outcomes in iron‐deficient heart failure patients. Outcomes of interest included heart failure hospitalizations, all‐cause mortality, and cardiovascular mortality. Meta‐analysis was performed using a fixed‐effect model and estimates were reported as odds ratios (ORs), hazard ratios, or rate ratios (RRs) along with corresponding 95% confidence intervals (CIs). A total of 1947 patients (n = 1062 in the FCM group; n = 885 in the placebo group) were included. FCM, compared with placebo, significantly reduced the risk of the composite endpoint of time to first heart failure hospitalization or cardiovascular death (hazard ratio = 0.76; 95% CI = 0.63–0.90; I (2) = 55%). FCM also significantly reduced the risk of recurrent heart failure hospitalizations (RR = 0.68; 95% CI = 0.54–0.85; I (2) = 71%) and recurrent cardiovascular hospitalizations (RR = 0.71; 95% CI = 0.59–0.86; I (2) = 56%). However, FCM had no significant effect on the risk of all‐cause (OR = 0.97; 95% CI = 0.73–1.28; I (2) = 0%) or cardiovascular mortality (OR = 0.93; 95% CI = 0.69–1.27; I (2) = 0%). CONCLUSIONS: Ferric carboxymaltose reduces heart failure hospitalizations and cardiovascular hospitalizations with no beneficial effect on all‐cause and cardiovascular mortality in iron‐deficient heart failure patients. These findings reinforce the role of FCM as a therapeutic option in heart failure patients. John Wiley and Sons Inc. 2020-12-22 /pmc/articles/PMC7754952/ /pubmed/33586856 http://dx.doi.org/10.1002/ehf2.13146 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Articles Khan, Muhammad Shahzeb Usman, Muhammad Shariq von Haehling, Stephan Doehner, Wolfram Stewart Coats, Andrew J. Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
title | Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
title_full | Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
title_fullStr | Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
title_full_unstemmed | Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
title_short | Ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
title_sort | ferric carboxymaltose for the treatment of iron‐deficient heart failure patients: a systematic review and meta‐analysis |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754952/ https://www.ncbi.nlm.nih.gov/pubmed/33586856 http://dx.doi.org/10.1002/ehf2.13146 |
work_keys_str_mv | AT khanmuhammadshahzeb ferriccarboxymaltoseforthetreatmentofirondeficientheartfailurepatientsasystematicreviewandmetaanalysis AT usmanmuhammadshariq ferriccarboxymaltoseforthetreatmentofirondeficientheartfailurepatientsasystematicreviewandmetaanalysis AT vonhaehlingstephan ferriccarboxymaltoseforthetreatmentofirondeficientheartfailurepatientsasystematicreviewandmetaanalysis AT doehnerwolfram ferriccarboxymaltoseforthetreatmentofirondeficientheartfailurepatientsasystematicreviewandmetaanalysis AT stewartcoatsandrewj ferriccarboxymaltoseforthetreatmentofirondeficientheartfailurepatientsasystematicreviewandmetaanalysis |