Body Volume Regulation in Pulmonary Arterial Hypertenison With Right Ventricular Failure

Condition(s) targeted: Right Heart Failure; Pulmonary Hypertension

Intervention: Spironolactone and conivaptan (Drug); usual care (Other)

Phase: N/A

Status: Not yet recruiting

Sponsored by: University of Colorado, Denver

Official(s) and/or principal investigator(s):
Shweta Bansal, MD, Principal Investigator, Affiliation: UCHSC

Overall contact:
Shweta Bansal, MD, Phone: 303-266-9220, Email: shweta.bansal@uchsc.edu

Secondary hyperaldosteronism and the non-osmotic release of arginine vasopressin (AVP) are the major factors in sodium and water retention in pulmonary arterial hypertension with right ventricular failure. Natriuretic doses of mineralocorticoid antagonist and aquaretic doses of V2 receptor antagonist will attenuate the sodium and water retention respectively, and be associated with clinical improvement.

Official title: Body Volume Regulation in Pulmonary Arterial Hypertenison With Right Ventricular Failure

Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Cross sectional study: Correlation between severity of pulmonary hypertension and neurohumoral activation, RBF & TPV. Acute study:electrolyte-free water and sodium excretion. Cohort Study: Composite of CI, BNP and RAP

Secondary outcome: Cross-sectional Study: correlations between mean pulmonary artery pressure, pulmonary vascular resistance; and neurohumoral activation, GFR and TPV. Acute study:correlation between response to drug and severity of disease.

Detailed description: Much has been learned about the pathophysiological state that underlies the development of increased total body volume and edema in left ventricular failure. Very little, however, is known about the mechanism underlying systemic hypervolemia in patients with isolated right ventricular dysfunction. Patients with pulmonary arterial hypertension (PAH) represent a model of isolated right ventricular dysfunction in which these mechanisms may be elucidated. Aldosterone has now been shown to have many properties that are likely to be detrimental in congestive heart failure (CHF) and that are not shared by angiotensin II. Aldosterone blockade has been associated with improved mortality in patients with left ventricular failure, already receiving an angiotensin converting enzyme inhibitor. But its role in isolated right ventricular failure has not been elucidated. The plasma arginine vasopressin levels are disproportionately elevated for the degree of serum osmolarity in patients with heart failure and result in water retention and hyponatremia. Conivaptan, a vasopressin receptor antagonist, appears to reduce body weight and improve signs of left heart failure, though there is no study to evaluate its role in right ventricular failure with edema.

This study will examine the role of spironolactone and conivaptan in patients with right ventricular failure and pathophysiology of sodium and water retention in these patients.

Minimum age: 18 Years. Maximum age: 75 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

1. Patients with WHO group 1 pulmonary arterial hypertension [51], excluding patients with portal hypertension, meeting the following hemodynamic parameters:

- Mean pulmonary artery pressure (mPAP) >35 mmHg at rest, and

- Pulmonary capillary wedge pressure (PCWP) <15 mmHg, and

- Pulmonary vascular resistance (PVR) >1. 5 wood units, and 2. Age 18 to 75 years 3.

Right ventricular failure defined by right atrial pressure >7 mmHg along with either dilated right ventricle, or absence of inferior vena cava collapse or BNP >100 pg/ml 4. Patients of childbearing age must be practicing effective birth control. 5. Normal left ventricular function as assessed by echocardiogram, multiple gated acquisition (MUGA) cardiac scan, or invasive left ventriculography.

Exclusion Criteria:

1. Group 2-5 pulmonary hypertension as defined by WHO.

- Pulmonary hypertension with left heart failure (as assessed by echocardiogram,

multiple gated acquisition (MUGA) cardiac scan, or invasive left ventriculography).

- Pulmonary hypertension associated with lung disease and/or hypoxemia (e. g. chronic

obstructive pulmonary disease, interstitial lung disease, sleep disordered breathing, chronic exposure to high altitude, alveolar hypoventilation syndrome.

- Pulmonary hypertension due to chronic thrombotic and/or embolic diseases

- Miscellaneous such as sarcoidosis, compression of pulmonary vessels by adenopathy,

tumor 2. Systemic hypertension, defined as a systolic pressure >140 mmHg or a diastolic blood pressure >90mmHg 3. Patients taking angiotensin converting enzyme (ACE) inhibitor or angiotensin receptor blockers (ARBs) 4. Pregnancy 5. Chronic kidney disease (serum creatinine > 2. 5mg/dl, proteinuria >500 mg/day, hematuria) 6. Cirrhosis or portal hypertension 7. Inability to provide informed consent. 8. Allergy to conivaptan or spironolactone. 9. Active malignancy 10. Patients receiving spironolactone 11. Enrollment in other interventional studies. 12. Patients on HAART

Shweta Bansal, MD, Phone: 303-266-9220, Email: shweta.bansal@uchsc.edu

University of Colorado at Denver and Health Sciences Center General Clinical Research Center, Denver, Colorado 80262, United States

Starting date: January 2009
Last updated: December 18, 2008