Skip to main content
Clinical Trials/NCT06038149
NCT06038149Active, not recruitingNot Applicable

Improving Pulmonary Hypertension Screening by Echocardiography

Royal United Hospitals Bath NHS Foundation Trust5 sites in 1 country200 target enrollmentStarted: November 11, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
200
Locations
5
Primary Endpoint
Analysis of the IMPULSE algorithm in the assessment of pulmonary hypertension

Study Overview

Brief Summary

This study aims to assess the application of the novel IMPULSE algorithm for the detection of pulmonary hypertension (PH) in those with a low or intermediate probability of PH according to the British Society of Echocardiography (ESC) and European Society of Cardiology (ESC) guidelines.

Detailed Description

This is a prospective, multi-centre cross-sectional study with a planned 18 month longitudinal component.

Participants will be recruited from patients referred for the first time for transthoracic echocardiography at the Royal United Hospitals Bath National Health Service (NHS) Foundation Trust, Royal Free Hospital NHS Foundation Trust, Sheffield Teaching Hospitals, Royal Papworth Hospital, and Golden Jubilee Hospital.

The investigators will prospectively recruit patients without a diagnosis of Pulmonary Hypertension.

Transthoracic echocardiographic (TTE) imaging will be performed in line with British Society of Echocardiography minimum dataset guidelines, and comprehensive right heart echocardiographic imaging and analysis will be performed following the British Society of Echocardiography recommendations for assessing right heart function, in addition to the IMPULSE algorithm;

A right ventricular free wall longitudinal strain value of less than -23%, or, right ventricular fractional area change (FAC) less than 35% in females/30% in males, in addition to a right ventricular isovolumetric relaxation time in excess of 73ms in patients with low/Intermediate probability of PH by current guidelines would categorise that patient as being IMPULSE positive.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Unexplained breathlessness
  • Risk factors for Pulmonary arterial hypertension (PAH), chronic thromboembolic pulmonary hypertension (CTEPH)
  • Unexplained elevation of B-type natriuretic peptide (BNP/proBNP)
  • Referred for catheterisation.

Exclusion Criteria

  • ESC / BSE echo high probability of PH
  • Known or suspected congenital heart disease
  • Patients unlikely to benefit from management of PH or its underlying causes.

Arms & Interventions

Low PH probability

Individuals identified as being of a low risk of pulmonary hypertension on routine echocardiography through existing British Society of Echocardiography/ European Society of Cardiology guidelines will undergo a research echocardiogram on the day of their planned right heart catheter.

Intervention: Transthoracic echocardiogram (Diagnostic Test)

Intermediate PH probability

Individuals identified as being of an intermediate risk of pulmonary hypertension on routine echocardiography through existing British Society of Echocardiography/ European Society of Cardiology guidelines will undergo a research echocardiogram on the day of their planned right heart catheter.

Intervention: Transthoracic echocardiogram (Diagnostic Test)

Outcomes

Primary Outcomes

Analysis of the IMPULSE algorithm in the assessment of pulmonary hypertension

Time Frame: 18 months

Analyse sensitivity, specificity, positive predictive value, negative predictive value, accuracy of IMPULSE algorithm on the assessment of PH.

Analysis of the IMPULSE algorithm in comparison to existing guidlines

Time Frame: 18 months

Analyse sensitivity, specificity, positive predictive value, negative predictive value, accuracy of IMPULSE algorithm in comparison with the existing ESC PH guidelines.

Secondary Outcomes

  • Analysis of additional echocardiographic measurements of right heart diastolic function not utilised in the assessment of pulmonary hypertension.(18 months)
  • Analysis of additional echocardiographic measurements of left heart function not utilised in the assessment of pulmonary hypertension.(18 months)
  • Analysis of additional echocardiographic measurements of right heart systolic function not utilised in the assessment of pulmonary hypertension.(18 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (5)

Loading locations...

Similar Trials