Assessing the Quality of Abstracts in Randomized Controlled Trials Published in High Impact Cardiovascular Journals

In the busy world of cardiovascular medicine, abstracts may be the only part of a publication that clinicians read. Therefore, it is critical for abstracts to accurately reflect article content. The extended CONSORT (Consolidated Standards of Reporting Trials) Statement for Abstracts was developed t...

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Veröffentlicht in:Circulation Cardiovascular quality and outcomes 2019-05, Vol.12 (5), p.e005260-e005260
Hauptverfasser: Khan, Muhammad Shahzeb, Shaikh, Asim, Ochani, Rohan Kumar, Akhtar, Tauseef, Fatima, Kaneez, Khan, Safi U, Mookadam, Farouk, Murad, M Hassan, Figueredo, Vincent M, Doukky, Rami, Krasuski, Richard A
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Sprache:eng
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Zusammenfassung:In the busy world of cardiovascular medicine, abstracts may be the only part of a publication that clinicians read. Therefore, it is critical for abstracts to accurately reflect article content. The extended CONSORT (Consolidated Standards of Reporting Trials) Statement for Abstracts was developed to ensure high abstract quality. However, it is unknown how often adherence to CONSORT guidelines occurs among cardiovascular journals. We searched MEDLINE for randomized controlled trials published in 3 major cardiovascular journals ( Circulation, Journal of the American College of Cardiology, and European Heart Journal) from 2011 to 2017. Post hoc, interim, and cost-effective analyses of randomized controlled trials were excluded. Two independent investigators extracted the data using a prespecified data collection form and a third investigator adjudicated the data. The primary outcome was frequency of subcategory adherence to CONSORT guidelines. A total of 478 abstracts were included in the analysis. Approximately half of the abstracts (53%; 255/478; 95% CI, 49%-57%) identified the article as randomized in the title. All abstracts detailed the interventions for both study groups (100%) and 81% (95% CI, 78%-85%) reported trial registration. Methodological quality reporting was relatively low: 9% (45/478; 95% CI, 6%-12%) described participant eligibility criteria with settings for data collection, 43% (204/478; 95% CI, 39%-47%) reported details of blinding, and
ISSN:1941-7713
1941-7705
DOI:10.1161/CIRCOUTCOMES.118.005260