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Trends in prevalence of comorbidities in heart failure clinical trials.

Publication ,  Journal Article
Khan, MS; Samman Tahhan, A; Vaduganathan, M; Greene, SJ; Alrohaibani, A; Anker, SD; Vardeny, O; Fonarow, GC; Butler, J
Published in: Eur J Heart Fail
June 2020

AIMS: The primary objective of this systematic review was to estimate the prevalence and temporal changes in chronic comorbid conditions reported in heart failure (HF) clinical trials. METHODS AND RESULTS: We searched MEDLINE for HF trials enrolling more than 400 patients published between 2001 and 2016.Trials were divided into HF with reduced ejection fraction (HFrEF), HF with preserved ejection fraction (HFpEF), or trials enrolling regardless of ejection fraction. The prevalence of baseline chronic comorbid conditions was categorized according to the algorithm proposed by the Chronic Conditions Data Warehouse, which is used to analyse Medicare data. To test for a trend in the prevalence of comorbid conditions, linear regression models were used to evaluate temporal trends in prevalence of comorbidities. Overall, 118 clinical trials enrolling a cumulative total of 215 508 patients were included. Across all comorbidities examined, data were reported in a mean of 35% of trials, without significant improvement during the study period. Reporting of comorbidities was more common in HFrEF trials (51%) compared with HFpEF trials (27%). Among trials reporting data, hypertension (63%), ischaemic heart disease (44%), hyperlipidaemia (48%), diabetes (33%), chronic kidney disease (25%) and atrial fibrillation (25%) were the major comorbidities. The prevalence of comorbidities including hypertension, atrial fibrillation and chronic kidney disease increased over time while the prevalence of smoking decreased in HFrEF trials. CONCLUSION: Many HF trials do not report baseline comorbidities. A more rigorous, systematic, and standardized framework needs to be adopted for future clinical trials to ensure adequate comorbidity reporting and improve recruitment of multi-morbid HF patients.

Duke Scholars

Published In

Eur J Heart Fail

DOI

EISSN

1879-0844

Publication Date

June 2020

Volume

22

Issue

6

Start / End Page

1032 / 1042

Location

England

Related Subject Headings

  • United States
  • Prognosis
  • Prevalence
  • Humans
  • Heart Failure
  • Comorbidity
  • Clinical Trials as Topic
  • Chronic Disease
  • Cardiovascular System & Hematology
  • 3201 Cardiovascular medicine and haematology
 

Citation

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Khan, M. S., Samman Tahhan, A., Vaduganathan, M., Greene, S. J., Alrohaibani, A., Anker, S. D., … Butler, J. (2020). Trends in prevalence of comorbidities in heart failure clinical trials. Eur J Heart Fail, 22(6), 1032–1042. https://doi.org/10.1002/ejhf.1818
Khan, Muhammad Shahzeb, Ayman Samman Tahhan, Muthiah Vaduganathan, Stephen J. Greene, Alaaeddin Alrohaibani, Stefan D. Anker, Orly Vardeny, Gregg C. Fonarow, and Javed Butler. “Trends in prevalence of comorbidities in heart failure clinical trials.Eur J Heart Fail 22, no. 6 (June 2020): 1032–42. https://doi.org/10.1002/ejhf.1818.
Khan MS, Samman Tahhan A, Vaduganathan M, Greene SJ, Alrohaibani A, Anker SD, et al. Trends in prevalence of comorbidities in heart failure clinical trials. Eur J Heart Fail. 2020 Jun;22(6):1032–42.
Khan, Muhammad Shahzeb, et al. “Trends in prevalence of comorbidities in heart failure clinical trials.Eur J Heart Fail, vol. 22, no. 6, June 2020, pp. 1032–42. Pubmed, doi:10.1002/ejhf.1818.
Khan MS, Samman Tahhan A, Vaduganathan M, Greene SJ, Alrohaibani A, Anker SD, Vardeny O, Fonarow GC, Butler J. Trends in prevalence of comorbidities in heart failure clinical trials. Eur J Heart Fail. 2020 Jun;22(6):1032–1042.
Journal cover image

Published In

Eur J Heart Fail

DOI

EISSN

1879-0844

Publication Date

June 2020

Volume

22

Issue

6

Start / End Page

1032 / 1042

Location

England

Related Subject Headings

  • United States
  • Prognosis
  • Prevalence
  • Humans
  • Heart Failure
  • Comorbidity
  • Clinical Trials as Topic
  • Chronic Disease
  • Cardiovascular System & Hematology
  • 3201 Cardiovascular medicine and haematology