Early Recognition of Pulmonary Arterial Hypertension in Myelodysplastic and Myeloproliferative Diseases

Completed

• Conditions: Myelodysplastic Syndromes; Pulmonary Hypertension; Myeloproliferative Disorder
• Interventions: Other: echocardiography, right heart catheterisation

• Registration Number: NCT00909467
• Lead Sponsor: Medical University of Graz

Brief Summary

Myelodysplastic and myeloproliferative Disease represent conditions with increased risk for pulmonary hypertension. However, the exact prevalence of pulmonary hypertension in these conditions is not known. The effects of pulmonary hypertension on the clinical picture and the symptoms of patients in these conditions needs also further exploration. This exploratory study is designed to describe the prevalence of pulmonary hypertension in the population with such hematologic diseases, and the stages of pulmonary hypertension as well its effect on exercise capacity at time of diagnosis.

Detailed Description

For early recognition of pulmonary hypertension exercise doppler echocardiography will be used in all patients. Patients with elevated pulmonary arterial pressure at rest or during exercise (estimated by echocardiography), or with decreased exercise capacity (as a potential sign of pulmonary hypertension) are advised to undergo right heart catheterisation. Cardiopulmonary exercise testing and six-minute walk distance measurement are performed to measure exercise capacity. The described work-up of patients allows precise and objective hemodynamic and clinical evaluation.

Study Timeline

• Study Start: 2009-04
• Study First Submitted: 2009-05-27
• Study First Submitted QC: 2009-05-27
• Study First Posted: 2009-05-28
• Primary Completion: 2011-11
• Study Completion: 2011-11
• Status Verified: 2012-03
• Last Update Submitted: 2012-03-08
• Last Update Posted: 2012-03-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

• myelodysplastic disease or myeloproliferative diseases

Exclusion Criteria

• known pulmonary hypertension
• relevant pulmonary disease
• relevant left cardiac or valvular disease
• recent major operations
• recent changes in medications
• relevant anaemia
• inability to exercise

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
myeloproliferative, -dysplastic disease	echocardiography, right heart catheterisation	-

Primary Outcome Measures

Name	Time	Method
mean pulmonary arterial pressure at rest and during exercise	at baseline and after 1 year

Secondary Outcome Measures

Name	Time	Method
exercise capacity	at baseline and after 1 year

Trial Locations

Locations (1)

Medical University of Graz, Pulmonology; 🇦🇹 Graz, Austria