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Detecting and Diagnosing Atrial Fibrillation (D2AF): study protocol for a cluster randomised controlled trial

Authors :
Nicole Verbiest-van Gurp
Henk van Weert
Steven B Uittenbogaart
Henri E J H Stoffers
Petra M. G. Erkens
Bjorn Winkens
Wim A M Lucassen
J. André Knottnerus
Graduate School
AII - Amsterdam institute for Infection and Immunity
APH - Amsterdam Public Health
General practice
CCA -Cancer Center Amsterdam
Family Medicine
FHML Methodologie & Statistiek
RS: CAPHRI School for Public Health and Primary Care
RS: CAPHRI - R5 - Optimising Patient Care
RS: CAPHRI - R6 - Promoting Health & Personalised Care
Source :
Trials, 16(1). BioMed Central, Trials, Trials, 16:478. BioMed Central Ltd
Publisher :
Springer Nature

Abstract

Background Atrial fibrillation is a common cause of stroke and other morbidity. Adequate treatment with anticoagulants reduces the risk of stroke by 60 %. Early detection and treatment of atrial fibrillation could prevent strokes. Atrial fibrillation is often asymptomatic and/or paroxysmal. Case-finding with pulse palpation is an effective screening method, but new methods for detecting atrial fibrillation have been developed. To detect paroxysmal atrial fibrillation ambulatory rhythm recording is needed. This study aims to determine the yield of case-finding for atrial fibrillation in primary care patients. In addition, it will determine the diagnostic accuracy of three different case-finding methods. Methods/Design In a multicenter cluster randomised controlled trial, we compare an enhanced protocol for case-finding of atrial fibrillation with usual care. We recruit 96 practices. We include primary care patients aged 65 years or older not diagnosed with atrial fibrillation. Within each practice, a cluster of 200 patients is randomly selected and marked. Practices are evenly randomised to intervention or control group. The allocation is not blinded. When a marked patient visits an intervention practice, the case-finding protocol starts, consisting of: pulse palpation, sphygmomanometer with automated atrial fibrillation detection and handheld single-lead electrocardiogram (ECG). All patients with at least 1 positive test and a random sample of patients with negative tests receive a 12-lead ECG. Patients without atrial fibrillation on the 12-lead ECG, undergo additional continuous Holter and use the handheld single-lead ECG at home for 2 weeks. Control practices provide care as usual. The study runs for 1 year in each cluster. The primary outcomes are the difference in detection rate of new AF between intervention and control practices and the accuracy of three index tests to diagnose AF. We are currently recruiting practices. The ‘Detecting and Diagnosing Atrial Fibrillation’ (D2AF) study will determine the yield of an intensive case-finding strategy and the diagnostic accuracy of three index tests to diagnose atrial fibrillation in a primary care setting. Trial registration Netherlands Trial Register: NTR4914, registered on the 25 of November 2014.

Details

Language :
English
ISSN :
17456215
Volume :
16
Issue :
1
Database :
OpenAIRE
Journal :
Trials
Accession number :
edsair.doi.dedup.....01afc00f4b602f0c5713a1afb5fe5345
Full Text :
https://doi.org/10.1186/s13063-015-1006-5