Heart Failure, Left Ventricular Dysfunction
Conditions
Keywords
heart failure, left sided, ventricular dysfunction, diastolic dysfunction, sildenafil
Brief summary
Sildenafil (Viagra) is known to reduce pulmonary hypertension. Heart failure patients also have pulmonary hypertension and several recent reports have shown that sildenafil leads to an improvement in their exercise capacity. In these studies sildenafil caused a reduction in the pulmonary and systemic vascular resistances, improved pulmonary gas diffusion and perhaps increased cardiac output. It is uncertain if left ventricular filling pressures are reduced and whether there is improvement in left ventricular relaxation. The investigators hypothesize that in heart failure patients the improvement in exercise capacity associated with sildenafil is related to a significant reduction in left ventricular filling pressures. The investigators propose to study 20 patients with stable but moderately symptomatic heart failure. The study design is a randomized cross-over trial of the administration of a single dose of sildenafil 50 mg or a matching placebo. Exercise capacity will be determined before and after the oral administration of sildenafil 50 mg or placebo. Left ventricular filling pressures will be assessed by Doppler echocardiography and the serum level of B-type natriuretic peptide (BNP is known to increase with higher left ventricular filling pressures). After an initial echocardiogram and performing a 6 minute walk test, the patient will then be given either sildenafil or a matching placebo in a randomized double-blind fashion. One hr later a blood sample for serum BNP, the echocardiogram and the 6 minute walk test will be repeated.
Detailed description
Sildenafil (Viagra) has been extensively studied in patients with idiopathic pulmonary hypertension. It reduces pulmonary vascular resistance, improves exercise capacity and is now an approved therapy for this condition. Heart failure (HF) patients also have pulmonary hypertension and several recent reports have shown that sildenafil leads to an improvement in their exercise capacity. In HF sildenafil causes a reduction in the pulmonary and systemic vascular resistances, improves pulmonary gas diffusion and perhaps increases cardiac output. It is uncertain if left ventricular filling pressures are reduced and whether there is improvement in left ventricular relaxation. We hypothesize that in HF patients the improvement in exercise capacity associated with sildenafil is related to a significant reduction in left ventricular filling pressures. We propose to study 10 patients with stable, symptomatic HF Class III. The study design is a randomized cross-over assignment of the administration of a single oral dose of sildenafil 50 mg or a matching placebo. Patients will be excluded if walking is impaired due to non-cardiac conditions or if they are taking nitrates. Exercise capacity will be determined before and 60 minutes after the oral administration of sildenafil 50 mg or placebo. The difference in the standardized 6 minute walk test (distance patient is able to walk over a 6 minute interval) will be used to assess exercise capacity. Left ventricular filling pressures will be assessed by Doppler echocardiography and the serum level of B-type natriuretic peptide (BNP). Evaluation of left ventricular relaxation will be determined by Doppler echocardiography techniques. Each patient will have a blood sample for BNP, an initial echocardiogram and perform a 6 minute walk test. They will then be given a single dose of either sildenafil or a matching placebo in a randomized double-blind fashion. The randomization was performed so that half of the group would receive the placebo on the initial test and sildenafil on the subsequent test and the other half would have the reverse sequence. One hr after the medication/placebo administration a blood sample for serum BNP, the echocardiogram and the 6 minute walk test will be repeated. After completion of the above protocol, the patient will return in 48 hrs and the protocol will be repeated with the predetermined assignment of either placebo or sildenafil.
Interventions
Changes in left ventricular filling pressure 1 hour after the administration of a single oral dose of sildenafil 50 mg.
Changes in left ventricular filling pressure 1 hour after oral administration of placebo
Sponsors
Study design
Eligibility
Inclusion criteria
* Adults with Class III congestive heart failure and impaired left ventricular systolic function. * A prior BNP level ≥ 200 pg/mL. * Previously documented systolic pulmonary artery pressure \>40 mmHg. * Clinically stable for a minimum of 6 weeks. * Able to give informed consent,
Exclusion criteria
* Unable to give informed consent. * Currently taking nitrates. * A HF exacerbation within the past 6 weeks. * Co-morbid conditions that could limit their walking. * Have a resting systolic blood pressure \< 110 mmHg
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Reduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil | Left ventricular filling pressure was assessed 1 hr after oral administration of sildenafil | Left ventricular filling pressure was assessed by the ratio of the velocity of early mitral inflow (E) divided by the early tissue velocity (e). E/e |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg. | Measured 1 hr after oral administration of sildenafil 50 mg | A standardized course was used to determine the distance walked (meters) during a 6 min walk supervised by a nurse trained in performance of the test. |
Countries
United States
Participant flow
Recruitment details
Patients were recruited from the Heart Failure Clinic at MetroHealth Medical Center over a 12 month interval. Recruitment was slow due to the fact that many of the patients were already perscirbed nitrates and so were ineligible for the study.
Pre-assignment details
More than 50 patients had to be excluded due to their already taking nitrates for their heart failure.
Participants by arm
| Arm | Count |
|---|---|
| Sildenafil First Placebo Second Effect of sildenafil on left ventricular filling pressures in patients with heart failure | 5 |
| Placebo First Sildenafil Second Effect of placebo on left ventricular filling pressures in patients with heart failure | 5 |
| Total | 10 |
Baseline characteristics
| Characteristic | Placebo First Sildenafil Second | Sildenafil First Placebo Second | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 2 Participants | 1 Participants | 3 Participants |
| Age, Categorical Between 18 and 65 years | 3 Participants | 4 Participants | 7 Participants |
| Age, Continuous | 64 years STANDARD_DEVIATION 12 | 64 years STANDARD_DEVIATION 12 | 64 years STANDARD_DEVIATION 12 |
| Region of Enrollment United States | 5 participants | 5 participants | 10 participants |
| Sex: Female, Male Female | 0 Participants | 1 Participants | 1 Participants |
| Sex: Female, Male Male | 5 Participants | 4 Participants | 9 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 5 | 0 / 5 |
| serious Total, serious adverse events | 0 / 5 | 0 / 5 |
Outcome results
Reduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil
Left ventricular filling pressure was assessed by the ratio of the velocity of early mitral inflow (E) divided by the early tissue velocity (e). E/e
Time frame: Left ventricular filling pressure was assessed 1 hr after oral administration of sildenafil
Population: All patients (10) that completed the protocol were analyzed.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Sildenafil First Then Placebo | Reduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil | 16.7 E/e' ratio | Standard Deviation 6.9 |
| Placebo First Then Sildenafil | Reduction of the Left Ventricular Filling Pressure in Association With Administration of Sildenafil | 16.4 E/e' ratio | Standard Deviation 6.5 |
The Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg.
A standardized course was used to determine the distance walked (meters) during a 6 min walk supervised by a nurse trained in performance of the test.
Time frame: Measured 1 hr after oral administration of sildenafil 50 mg
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Sildenafil First Then Placebo | The Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg. | 210 meters | Standard Deviation 34 |
| Placebo First Then Sildenafil | The Distance Walked During the 6-minute Walk Test 1 hr After the Oral Administration of Sildenafil 50 mg. | 219 meters | Standard Deviation 40 |