Does an artificial intelligence-enabled stethoscope improve the detection of heart failure and alter diagnostic pathways in primary care?
Up to 200 primary care practices in urban North West London and rural North Wales, UK, with no patient-level inclusion or exclusion criteria
Artificial intelligence-enabled stethoscopes available for use at clinician discretion, supported by a clinical guideline
Usual care
Coprimary endpoints: (i) difference in the coded incidence (detection) of heart failure and (ii) difference in the ratio of coded incidence of heart failure via hospital admission versus community-based diagnostic pathways
The TRICORDER trial will determine if AI-enabled stethoscopes in primary care can improve the early detection and diagnostic pathways for heart failure, atrial fibrillation, and valvular heart disease.
INTRODUCTION: Early detection of cardiovascular disease in primary care is a public health priority, for which the clinical and cost-effectiveness of an artificial intelligence-enabled stethoscope that detects left ventricular systolic dysfunction, atrial fibrillation and cardiac murmurs is unproven but potentially transformative. METHODS AND ANALYSIS: TRICORDER is a pragmatic, two-arm, multi-centre (decentralised), cluster-randomised controlled trial and implementation study. Up to 200 primary care practices in urban North West London and rural North Wales, UK, will be randomised to usual care or to have artificial intelligence-enabled stethoscopes available for use. Primary care clinicians will use the artificial intelligence-enabled stethoscopes at their own discretion, without patient-level inclusion or exclusion criteria. They will be supported to do so by a clinical guideline developed and approved by the regional health system executive board. Patient and outcome data will be captured from pooled primary and secondary care records, supplemented by qualitative and quantitative clinician surveys. The coprimary endpoints are (i) difference in the coded incidence (detection) of heart failure and (ii) difference in the ratio of coded incidence of heart failure via hospital admission versus community-based diagnostic pathways. Secondary endpoints include difference in the incidence of atrial fibrillation and valvular heart disease, cost-consequence differential, and prescription of guideline-directed medical therapy. ETHICS AND DISSEMINATION: This trial has ethical approval from the UK Health Research Authority (23/LO/0051). Findings from this trial will be disseminated through publication of peer-reviewed manuscripts, presentations at scientific meetings and conferences with local and national stakeholders. TRIAL REGISTRATION NUMBER: NCT05987670.
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Mihir A Kelshiker
Patrik Bächtiger
Heart Failure & Transplant
Josephine Mansell
BMJ Open
Harvard University
Imperial College London
Lung Institute
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Kelshiker et al. (Thu,) studied this question.
synapsesocial.com/papers/6a0919c115fb758097d25568 — DOI: https://doi.org/10.1136/bmjopen-2024-098030