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Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis

OBJECTIVE: Iron deficiency (ID) has an established impact on outcomes in patients with heart failure with reduced ejection fraction; however, there is a lack of conclusive evidence in patients with heart failure with preserved ejection fraction (HFpEF). We sought to clarify the prevalence and impact...

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Autores principales: Beale, Anna L, Warren, Josephine Lillian, Roberts, Nia, Meyer, Philippe, Townsend, Nick P, Kaye, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519409/
https://www.ncbi.nlm.nih.gov/pubmed/31168385
http://dx.doi.org/10.1136/openhrt-2019-001012
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author Beale, Anna L
Warren, Josephine Lillian
Roberts, Nia
Meyer, Philippe
Townsend, Nick P
Kaye, David
author_facet Beale, Anna L
Warren, Josephine Lillian
Roberts, Nia
Meyer, Philippe
Townsend, Nick P
Kaye, David
author_sort Beale, Anna L
collection PubMed
description OBJECTIVE: Iron deficiency (ID) has an established impact on outcomes in patients with heart failure with reduced ejection fraction; however, there is a lack of conclusive evidence in patients with heart failure with preserved ejection fraction (HFpEF). We sought to clarify the prevalence and impact of ID in patients with HFpEF. METHODS: A systematic search of Cohcrane, MEDLINE, EMBASE, Web of Science and CINAHL electronic databases was performed to identify relevant studies. Included studies defined HFpEF as heart failure with an ejection fraction ≥50%. We used a random-effects meta-analysis to determine the composite prevalence of ID in patients with HFpEF across the included studies. Other outcomes were assessed with qualitative analysis due to a paucity of studies with comparable outcome measures. RESULTS: The prevalence of ID in the included studies was 59% (95% CI 52% to 65%). ID was associated with lower VO(2) max in three of four studies reporting VO(2) max as an outcome measure, lower functional status as determined by dyspnoea class or 6 min walk test in two of three studies, and worse health-related quality of life in both studies reporting on this outcome. Conversely, ID had no impact on death or hospitalisation in three of the four studies investigating this. CONCLUSIONS: ID is highly prevalent in patients with HFpEF and is associated with worse exercise capacity and functional outcomes, but not hospitalisation or mortality. Our study establishes that ID may play an important a role in HFpEF.
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spelling pubmed-65194092019-06-05 Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis Beale, Anna L Warren, Josephine Lillian Roberts, Nia Meyer, Philippe Townsend, Nick P Kaye, David Open Heart Heart Failure and Cardiomyopathies OBJECTIVE: Iron deficiency (ID) has an established impact on outcomes in patients with heart failure with reduced ejection fraction; however, there is a lack of conclusive evidence in patients with heart failure with preserved ejection fraction (HFpEF). We sought to clarify the prevalence and impact of ID in patients with HFpEF. METHODS: A systematic search of Cohcrane, MEDLINE, EMBASE, Web of Science and CINAHL electronic databases was performed to identify relevant studies. Included studies defined HFpEF as heart failure with an ejection fraction ≥50%. We used a random-effects meta-analysis to determine the composite prevalence of ID in patients with HFpEF across the included studies. Other outcomes were assessed with qualitative analysis due to a paucity of studies with comparable outcome measures. RESULTS: The prevalence of ID in the included studies was 59% (95% CI 52% to 65%). ID was associated with lower VO(2) max in three of four studies reporting VO(2) max as an outcome measure, lower functional status as determined by dyspnoea class or 6 min walk test in two of three studies, and worse health-related quality of life in both studies reporting on this outcome. Conversely, ID had no impact on death or hospitalisation in three of the four studies investigating this. CONCLUSIONS: ID is highly prevalent in patients with HFpEF and is associated with worse exercise capacity and functional outcomes, but not hospitalisation or mortality. Our study establishes that ID may play an important a role in HFpEF. BMJ Publishing Group 2019-04-03 /pmc/articles/PMC6519409/ /pubmed/31168385 http://dx.doi.org/10.1136/openhrt-2019-001012 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Heart Failure and Cardiomyopathies
Beale, Anna L
Warren, Josephine Lillian
Roberts, Nia
Meyer, Philippe
Townsend, Nick P
Kaye, David
Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
title Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
title_full Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
title_fullStr Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
title_full_unstemmed Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
title_short Iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
title_sort iron deficiency in heart failure with preserved ejection fraction: a systematic review and meta-analysis
topic Heart Failure and Cardiomyopathies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519409/
https://www.ncbi.nlm.nih.gov/pubmed/31168385
http://dx.doi.org/10.1136/openhrt-2019-001012
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