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Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes
BACKGROUND: Comorbid diabetes is common in heart failure and associated with increased hospitalization and mortality. Nonetheless, the association between glycemic control and outcomes among patients with heart failure and diabetes remains poorly characterized, particularly among low income and mino...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875651/ https://www.ncbi.nlm.nih.gov/pubmed/27206478 http://dx.doi.org/10.1186/s12872-016-0275-6 |
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author | Blecker, Saul Park, Hannah Katz, Stuart D. |
author_facet | Blecker, Saul Park, Hannah Katz, Stuart D. |
author_sort | Blecker, Saul |
collection | PubMed |
description | BACKGROUND: Comorbid diabetes is common in heart failure and associated with increased hospitalization and mortality. Nonetheless, the association between glycemic control and outcomes among patients with heart failure and diabetes remains poorly characterized, particularly among low income and minority patients. METHODS: We performed a retrospective cohort study of outpatients with heart failure and diabetes in the New York City Health and Hospitals Corporation, the largest municipal health care system in the United States. Cox proportional hazard models were used to measure the association between HbA1c levels and outcomes of all-cause hospitalization, heart failure hospitalization, and mortality. RESULTS: Of 4723 patients with heart failure and diabetes, 42.6 % were black, 30.5 % were Hispanic/Latino, 31.4 % were Medicaid beneficiaries and 22.9 % were uninsured. As compared to patients with an HbA1c of 8.0–8.9 %, patients with an HbA1c of <6.5, 6.5–6.9, 7.0–7.9, and ≥9.0 % had an adjusted hazard ratio (aHR) (95 % CI) for all-cause hospitalization of 1.03 (0.90–1.17), 1.05 (0.91–1.22), 1.03 (0.90–1.17), and 1.13 (1.00–1.28), respectively. An HbA1c ≥ 9.0 % was also associated with an increased risk of heart failure hospitalization (aHR 1.33; 95 % CI 1.11–1.59) and a non-significant increased risk in mortality (aHR 1.20; 95 % CI 0.99–1.45) when compared to HbA1c of 8.0–8.9 %. CONCLUSIONS: Among a cohort of primarily minority and low income patients with heart failure and diabetes, an increased risk of hospitalization was observed only for an HbA1c greater than 9 %. |
format | Online Article Text |
id | pubmed-4875651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48756512016-05-22 Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes Blecker, Saul Park, Hannah Katz, Stuart D. BMC Cardiovasc Disord Research Article BACKGROUND: Comorbid diabetes is common in heart failure and associated with increased hospitalization and mortality. Nonetheless, the association between glycemic control and outcomes among patients with heart failure and diabetes remains poorly characterized, particularly among low income and minority patients. METHODS: We performed a retrospective cohort study of outpatients with heart failure and diabetes in the New York City Health and Hospitals Corporation, the largest municipal health care system in the United States. Cox proportional hazard models were used to measure the association between HbA1c levels and outcomes of all-cause hospitalization, heart failure hospitalization, and mortality. RESULTS: Of 4723 patients with heart failure and diabetes, 42.6 % were black, 30.5 % were Hispanic/Latino, 31.4 % were Medicaid beneficiaries and 22.9 % were uninsured. As compared to patients with an HbA1c of 8.0–8.9 %, patients with an HbA1c of <6.5, 6.5–6.9, 7.0–7.9, and ≥9.0 % had an adjusted hazard ratio (aHR) (95 % CI) for all-cause hospitalization of 1.03 (0.90–1.17), 1.05 (0.91–1.22), 1.03 (0.90–1.17), and 1.13 (1.00–1.28), respectively. An HbA1c ≥ 9.0 % was also associated with an increased risk of heart failure hospitalization (aHR 1.33; 95 % CI 1.11–1.59) and a non-significant increased risk in mortality (aHR 1.20; 95 % CI 0.99–1.45) when compared to HbA1c of 8.0–8.9 %. CONCLUSIONS: Among a cohort of primarily minority and low income patients with heart failure and diabetes, an increased risk of hospitalization was observed only for an HbA1c greater than 9 %. BioMed Central 2016-05-20 /pmc/articles/PMC4875651/ /pubmed/27206478 http://dx.doi.org/10.1186/s12872-016-0275-6 Text en © Blecker et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Blecker, Saul Park, Hannah Katz, Stuart D. Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes |
title | Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes |
title_full | Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes |
title_fullStr | Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes |
title_full_unstemmed | Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes |
title_short | Association of HbA1c with hospitalization and mortality among patients with heart failure and diabetes |
title_sort | association of hba1c with hospitalization and mortality among patients with heart failure and diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875651/ https://www.ncbi.nlm.nih.gov/pubmed/27206478 http://dx.doi.org/10.1186/s12872-016-0275-6 |
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