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Optimising a Digital Diagnostic Pathway for Heart Failure in the Community

Completed
Conditions
Heart Failure
Interventions
Diagnostic Test: Echocardiogram
Registration Number
NCT04724200
Lead Sponsor
NHS Greater Glasgow and Clyde
Brief Summary

This is a prospective, observational study. The primary aim is to assess the diagnostic accuracy of Artificial Intelligence (AI) analysis of Point of Care (POC) handheld transthoracic echocardiogram images (POC handheld echocardiogram) compared to the current gold-standard of transthoracic echocardiogram images acquired and analysed by a British Society of Echocardiography (BSE) accredited operator, using a standard echocardiogram machine (standard TTE), for the diagnosis of Heart Failure with reduced Ejection Fraction (HFrEF), in patients referred from the community for investigation of suspected new Heart Failure (HF).

Detailed Description

1. Demonstrate that in comparison to using the current gold standard of BSE accredited operator echocardiography within a HFDP, using AI enhanced analysis of POC handheld echocardiography is accurate and safe. This has the potential to improve access to timelier echocardiography in order to achieve earlier HF diagnosis and treatment, which is known to delay/prevent progression to HF hospitalisation. It will also provide useful information regarding the future feasibility of using AI enhanced analysis of POC handheld echocardiography in the community, for investigation of people with suspected new HF.

2. Facilitate the digitisation of an NHS Heart Failure diagnostic service in order to standardise and improve the quality of data collection and clinical care provided within the service.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
867
Inclusion Criteria
  • Adult individuals referred from the community who are awaiting HF diagnostic investigations, including echocardiography, to investigate for a suspected new diagnosis of HF
Exclusion Criteria
  1. Individuals less than 18 years of age
  2. Individuals who have had an interim echocardiogram for another clinical reason, whilst on the outpatient echocardiogram waiting list for investigation of HF
  3. Individuals with a previous ICD-10 diagnosis of HF in any coding position
  4. Inability of the participant, in the opinion of the investigators, to understand and/or comply with study procedures, or any conditions that, in the opinion of the investigators, may render the participant unable to understand, attend and/or undergo study visit investigations
  5. Inability to read and understand the PIS (provided in English only), and understand the research team

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Referred from primary care for investigation of suspected heart failureEchocardiogramAll patients recruited to the OPERA trial will have been referred from their primary care clinician for investigation of a suspected diagnosis of heart failure.
Primary Outcome Measures
NameTimeMethod
False negative1 day

A result that wrongly indicates heart failure is not present in the OPERA patient

sensitivity1 day

the ability of a diagnostics test to correctly identify those with heart failure

specificity1 day

the ability of a diagnostic test to correctly identify those without heart failure

False positive1 day

A results that wrongly indicates heart failure is present in the OPERA patient

Area under curve1 day

area under receiver operator curve comparison of the standard TTE Vs AI analysed POC echocardiogram for the diagnosis of HFrEF in people referred from the community for investigation of suspected new HF

Negative and positive predictive value (NPV and PPV)1 day

NPV and PPV describe the proportions of postive and negative results that are true results

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

NHS Louisa Jordan

🇬🇧

Glasgow, United Kingdom

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