Symptomatic Pulmonary Arterial Hypertension After Mitral Valve Surgery

This study is currently recruiting participants. (see Contacts and Locations)
Verified March 2014 by Duke University
Sponsor:
Collaborators:
Northwestern University
Gilead Sciences
Information provided by (Responsible Party):
Duke University
ClinicalTrials.gov Identifier:
NCT01646541
First received: July 16, 2012
Last updated: March 7, 2014
Last verified: March 2014
  Purpose

Most patients with mitral valve disease are symptomatic with shortness of breath and a limited activity level prior to mitral valve surgery. Despite surgical repair or replacement of the mitral valve, many patients remain symptomatic with an impaired ability to live an active lifestyle. Often after extensive evaluation, no other pulmonary, left ventricular dysfunction, or valvular heart disease is responsible for the continued symptoms, and some of these patients will be limited by persistent pulmonary hypertension (PH) at rest or with exertion that is responsible for limiting their activity level and impacting their quality of their life.

It is our goal in the proposed study to systematically characterize symptomatic and asymptomatic patients greater than six months after mitral valve surgery using clinical data, echocardiographic evaluation, laboratory assessment, and in some patients, invasive hemodynamic measurements. The investigators will screen asymptomatic and symptomatic patients with resting echocardiography and also with echocardiography during exercise, as many patients will exhibit exercise-induced PH following mitral valve surgery. Pulmonary artery (PA) pressure will be estimated from echocardiography using Doppler-derived calculations. If elevated PA pressures are observed with echocardiography, then symptomatic patients will undergo right heart catheterization for invasive pressure measurement, which is the gold-standard for the diagnosis of PH. When PH is present and there is a normal wedge pressure (PCWP) during invasive pressure measurement, further assessment to identify potential candidates for PH therapy will be performed. This involves having patients breathe inhaled nitric oxide, a rapid-acting, pulmonary vasodilator with a short half-life. While breathing inhaled nitric oxide, blood pressure, PA pressure, PCWP, and cardiac output will be monitored to characterize individuals who could benefit symptomatically from pharmacotherapy to treat underlying PH. It is important to note that only a small minority of patients exhibit a positive vasodilator response and those with PH and a normal PCWP without an initial vasodilator response would still be identified as candidates for chronic PH therapy.

The information generated from this proposed research will make a significant contribution to the understanding of PH in a group of patients in whom it has not been previously studied. Scientific reports on the evaluation of patients with PH after mitral valve surgery are almost nonexistent from the modern era. Furthermore, patients with PH due to mitral valve disease have been excluded from clinical trials of agents currently approved by the U.S. Food and Drug Administration (FDA) to treat PH. Therefore, this work will carefully characterize PA pressures in an objective manner in a group of patients following mitral valve surgery who remain limited with respect to their activity levels. In addition, the investigators will gain a better understanding of the frequency with which patients have PH and a normal PCWP, which identifies a cohort of patients who could have an improvement in their symptoms and quality of life with chronic vasodilator treatment.


Condition
Pulmonary Hypertension
Mitral Valve Disease

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Symptomatic Pulmonary Arterial Hypertension After Mitral Valve Surgery: Pilot, Screening Study

Resource links provided by NLM:


Further study details as provided by Duke University:

Primary Outcome Measures:
  • Prevalence of pulmonary hypertension [ Time Frame: greater than 6 months after mitral valve surgery ] [ Designated as safety issue: No ]
    study evaluation period will take several hours to complete the components of the study (clinical evaluation, echocardiogram, etc.) on approximately 2 occasions


Estimated Enrollment: 100
Study Start Date: July 2012
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts
Asymptomatic
No dyspnea with exertion greater than 6 months after mitral valve surgery [New York Heart Association (NYHA) Functional Class I]
Symptomatic
Dyspnea with exertion greater than 6 months after mitral valve surgery [New York Heart Association (NYHA) Functional Class II, III, or IV]

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Patients seen in the cardiology, pulmonary hypertension, or cardiac surgery clinics at the enrolling institutions

Criteria

Inclusion Criteria:

  • Age > 18 years
  • Greater than 6 months post-mechanical or bioprosthetic mitral valve replacement or mitral valve repair (quadrangular resection, triangular resection, sliding plasty, and/or annuloplasty) surgery
  • Dyspnea at rest or with exertion (NYHA II, III, or IV) [Symptomatic Study Group]
  • Asymptomatic control group meeting criteria 1 and 2 above

Exclusion Criteria:

  • Current or prior chronic vasodilator therapy for pulmonary hypertension
  • Known collagen vascular disease
  • HIV infection: Based on self-report /historical diagnosis
  • Portal hypertension
  • Prior anorexigen use
  • History of corrected or uncorrected intracardiac shunt
  • Prior pulmonary embolism
  • Sickle cell disease
  • Left ventricular dysfunction (ejection fraction < 45%)
  • Moderate or severe mitral regurgitation
  • Moderate aortic stenosis (mean gradient > 25 mm Hg)
  • Symptomatic, non-revascularized coronary artery disease
  • Evidence of parenchymal lung disease with a TLC < 70% and an FEV1 < 65% of predicted with pulmonary function testing
  • Pregnancy - Serum pregnancy test for women of child bearing potential, if cardiac catheterization is needed
  • Unable to provide informed consent
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01646541

Contacts
Contact: Andrew Wang, M.D. 9196816197 a.wang@dm.duke.edu
Contact: Todd Kiefer, M.D. 9196816197 todd.kiefer@duke.edu

Locations
United States, Illinois
Northwestern University Medical Center Active, not recruiting
Chicago, Illinois, United States, 60611
United States, North Carolina
Duke University Medical Center Recruiting
Durham, North Carolina, United States, 27710
Sponsors and Collaborators
Duke University
Northwestern University
Gilead Sciences
Investigators
Principal Investigator: Andrew Wang, M.D. Duke University
  More Information

No publications provided

Responsible Party: Duke University
ClinicalTrials.gov Identifier: NCT01646541     History of Changes
Other Study ID Numbers: Pro00033042
Study First Received: July 16, 2012
Last Updated: March 7, 2014
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Hypertension, Pulmonary
Hypertension
Heart Valve Diseases
Lung Diseases
Respiratory Tract Diseases
Vascular Diseases
Cardiovascular Diseases
Heart Diseases

ClinicalTrials.gov processed this record on August 19, 2014