Bisoprolol in Hypertrophic Cardiomyopathy: Efficacy and Tolerability

Bisoprolol, a beta-blocker, is shown to be effective and well-tolerated in managing symptomatic obstructive hypertrophic cardiomyopathy (HCM), offering valuable therapeutic options for patients with this condition.

November 2022
Bisoprolol in Hypertrophic Cardiomyopathy: Efficacy and Tolerability

Highlights

  • Bisoprolol reduced the LVOT gradient to less than 30 mmHg in 36% of HCM patients.
     
  • The mean LVOT gradient reduction with bisoprolol was 28 (±14) mmHg.
     
  • Nonresponders showed a higher LVOT gradient and NYHA class than responders.
     
  • This single-center observational cohort study evaluated the role of bisoprolol in the control of symptoms and left ventricular outflow tract (LVOT) obstruction in 92 consecutive adult patients with obstructive hypertrophic cardiomyopathy (HCM). Starting at 1.25 mg daily, the dose was increased every 2 weeks to achieve an LVOT gradient <30 mm Hg and an improvement of ≥1 in NYHA class. A total of 16 patients achieved the goal; bisoprolol reduced the LVOT gradient to <30 mm Hg in 33 patients, reduced the LVOT gradient to <50 mm Hg in 57 patients, and improved NYHA class in 30 patients. However, bisoprolol failed to reduce the LVOT gradient to <50 mm Hg in 35 patients.
     
  • This study suggests that bisoprolol is an effective and well-tolerated beta-blocker in symptomatic obstructive HCM. As new therapies for HCM continue to emerge, nonvasodilator beta-blockers, such as bisoprolol, may continue to be an impactful component of a multimodal regimen.


Bisoprolol in Hypertrophic Cardiomyopathy: Efficac

Goals

To evaluate the role of bisoprolol in the control of symptoms and left ventricular outflow tract obstruction (LVOTO) in a consecutive cohort of adults with hypertrophic cardiomyopathy (HCM).

Methods and results

In this retrospective study, HCM patients with an LVOT gradient ≥50 mmHg after the Valsalva maneuver and New York Heart Association (NYHA) class II-III symptoms were assigned to receive bisoprolol (starting at 1.25 mg daily).

The initial dose was increased every two weeks to achieve the target gradient of LVOT <30 mmHg or the maximum tolerated dose. The primary endpoint was achievement of an LVOT gradient <30 mmHg and NYHA class improvement ≥1.

Secondary endpoints were the proportion of patients with an LVOT gradient <30 mmHg or <50 mmHg, the proportion of patients with NYHA class improvement ≥1, and the change from baseline in LVOT gradient.

Between December 2001 and December 2020, 92 patients were enrolled in the study. Sixteen (17%) patients on bisoprolol had the primary endpoint.

Bisoprolol reduced the LVOT gradient to less than 30 mmHg in 33 (36%) patients, to less than 50 mmHg in 57 (62%), and improved NYHA class in 30 (33%).

The mean LVOT gradient reduction with bisoprolol was 28 (±14) mmHg and the percentage reduction was 42 (±21)%.

In 35 (38%) patients, bisoprolol did not reduce the gradient to less than 50 mmHg, requiring disopyramide and/or myectomy to achieve this goal.

Conclusion

Bisoprolol treatment was well tolerated and effective in relieving obstruction and improving symptoms in a significant proportion of patients with symptomatic obstructive HCM.