Randomized control trial.
Single center.
50 CHF patients on stable doses of ACEI.
Add-on therapy with irbesartan (300 mg/day) or continuation of conventional therapy (control group) for 1 year.
Serial clinical and echocardiographic assessment were performed as baseline, 3 months and 1 year after therapy.
There was no difference in clinical characteristics between 2 groups. Patients in the add-on therapy group had significant increase in 6-Minute Hall-Walk distance (351 ± 89 to 392 ± 84 m, P < 0.01), achieved higher METs exercise time on treadmill test (3.9 ± 1.1 to 4.6 ±1.3 METs, P = 0.01), reduction of NYHA Class (2.4 ± 0.5 to 2.0 ± 0.8, P < 0.005) and improvement of QOL score (28 ± 19 to 17 ± 18, P < 0.05). These parameters were not improved in the control group and a worsening of exercise capacity was observed (P < 0.05). A reduction of left ventricular end-systolic diameter (4.94 ± 0.85 vs 4.30 ± 1.17 cm, P < 0.05) was observed in the add-on group. At the end of 1 year, more patients have normal or abnormal relaxation pattern in the add-on group than the control group (82 % vs 53 % χ2 = 7.1, P = 0.02). Blood pressure and renal function were unchanged in both groups.
The addition of irbesartan to conventional ACEI therapy in CHF further improves symptoms, exercise capacity and quality of life without adverse effects on hemodynamics and renal function.