ADOPT: Improving Diagnosis of Pulmonary Hypertension With AI and Echo
NCT ID: NCT06145880
Last Updated: 2024-11-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2023-12-01
2025-12-01
Brief Summary
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In existing diagnostic pathways, evidence for the suspicion of PH is frequently overlooked, significantly delaying the time to diagnosis. Echocardiography (echo) is a quick, safe and well-tolerated test requested to investigate breathless patients, and which can provide useful information about the suspicion of PH. However, outside of specialist PH centres, doctors may not routinely look for and comment on the presence of clues to possible PH.
The investigators think that using Artificial Intelligence (AI) techniques to read echo's could make their interpretation faster and more reliable. There may also be subtle clues to the presence or severity of PH on echo, less recognisable to the human eye, which AI can identify.
In this study the investigators will gather echo images from 5 specialist PH hospitals across the UK which have all been anonymised (patient's name and personal details removed). These will all be historic scans (i.e. have already taken place) and will be grouped into those with PH present (including PH sub-type) or absent. These anonymised echo images will be used to develop and train an AI tool to identify scans where PH is present, including which specific type of PH may be present. The developed AI tool will then be tested on a separate group of scans (not used in the training stage) to validate its performance.
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Detailed Description
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These will all be historic scans (i.e. have already taken place) and will be grouped into those with PH present (including PH sub-type) or PH absent. Inclusion criteria involve patients aged ≥18 who have undergone both a transthoracic echo (TTE) and a right heart catheter (RHC) as part of their clinical care. Exclusion Criteria will involve patients aged \<18, known or suspected congenital heart disease and patients who have opted out of allowing their information to be used for research and planning (via the national data opt-out choice). A clinical case report form (CRF) will be used to capture patient demographics, clinical data with regards to the PH assessment including previous TTE results. Where available, mortality data will be recorded within 5 years of the RHC.
These anonymised echo images will be collated and labelled centrally in a core lab at the RUH Bath, who will work with Janssen to develop and train an AI tool to identify scans where PH is present, including which specific type of PH may be present.
AI tool training will be based on 5 groups (each group anticipated to contain 415 echocardiograms): mild pre-capillary PH; moderate pre-capillary PH; severe pre-capillary PH; post capillary PH; no PH. The tool will then be validated in a separate pool made up of 425 echocardiograms (a combination of pre-capillary, post capillary PH and no PH). The validation cohort will not have been used in the training stage.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Mild pre-capillary PH
Right heart catheterisation (performed as part of usual care) diagnoses pulmonary hypertension and categorises it as mild and pre-capillary.
Artificial intelligence tool for transthoracic echocardiography
Pre-defined cohorts will be used to train the artificial intelligence tool for transthoracic echocardiography to improve the diagnosis of PH on TTE.
Moderate pre-capillary PH
Right heart catheterisation (performed as part of usual care) diagnoses pulmonary hypertension and categorises it as moderate and pre-capillary.
Artificial intelligence tool for transthoracic echocardiography
Pre-defined cohorts will be used to train the artificial intelligence tool for transthoracic echocardiography to improve the diagnosis of PH on TTE.
Severe pre-capillary PH
Right heart catheterisation (performed as part of usual care) diagnoses pulmonary hypertension and categorises it as severe and pre-capillary.
Artificial intelligence tool for transthoracic echocardiography
Pre-defined cohorts will be used to train the artificial intelligence tool for transthoracic echocardiography to improve the diagnosis of PH on TTE.
Post capillary PH
Right heart catheterisation (performed as part of usual care) diagnoses pulmonary hypertension and categorises it as post-capillary.
Artificial intelligence tool for transthoracic echocardiography
Pre-defined cohorts will be used to train the artificial intelligence tool for transthoracic echocardiography to improve the diagnosis of PH on TTE.
No PH
Right heart catheterisation (performed as part of usual care) demonstrates normal pulmonary pressures (i.e. no evidence of pulmonary hypertension).
Artificial intelligence tool for transthoracic echocardiography
Pre-defined cohorts will be used to train the artificial intelligence tool for transthoracic echocardiography to improve the diagnosis of PH on TTE.
Interventions
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Artificial intelligence tool for transthoracic echocardiography
Pre-defined cohorts will be used to train the artificial intelligence tool for transthoracic echocardiography to improve the diagnosis of PH on TTE.
Eligibility Criteria
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Inclusion Criteria
* Have undergone a transthoracic echo and right heart catheter as part of their routine clinical care.
Exclusion Criteria
* Known or suspected congenital heart disease
* Patient opted out of allowing their information to be used for research and planning (via the national data opt-out choice).
18 Years
ALL
No
Sponsors
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Janssen Research & Development, LLC
INDUSTRY
Royal Free Hospital NHS Foundation Trust
OTHER
Sheffield Teaching Hospitals NHS Foundation Trust
OTHER
Papworth Hospital NHS Foundation Trust
OTHER_GOV
NHS Golden Jubilee National Hospital Glasgow
UNKNOWN
Royal United Hospitals Bath NHS Foundation Trust
OTHER
Responsible Party
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Locations
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Royal United Hospitals Bath NHS Foundation Trust
Bath, , United Kingdom
Countries
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Other Identifiers
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RUH Bath - ADOPT
Identifier Type: -
Identifier Source: org_study_id
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