November 25, 2014
2 min read
Save

Beta-blockers lowered all-cause mortality in patients with HFpEF

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

Patients with HF with preserved ejection fraction who received treatment with beta-blockers had lower rates of all-cause mortality, according to new study results.

However, the same trend was not observed with beta-blocker use and combined all-cause mortality and hospitalization for HF in this patient population.

Lars H. Lund, MD, PhD, from Karolinska University Hospital in Stockholm, and colleagues conducted a propensity score-matched cohort study to test the hypothesis that beta-blockers are associated with lower all-cause mortality in patients with HF with preserved ejection fraction (HFpEF). The researchers reviewed data on 41,976 consecutive patients with clinician-judged HF enrolled in the Swedish Heart Failure Registry from July 1, 2005, to Dec. 30, 2012. For this study, HFpEF was defined as EF of ≥40%.

In total, 19,083 patients had HFpEF (mean age, 76 years; 46% women). Patients with HFpEF were matched 2:1 for beta-blocker use (5,496 treated patients, 2,748 untreated patients). The overall patient population was followed for a median of 755 days and the matched cohort was followed for a median of 709 days.

Among the patients with HFpEF, those treated with beta-blockers had a 1-year survival rate of 80% compared with 79% for those who were untreated. The 5-year survival rate was 45% in the treated group vs. 42% in the untreated group. Overall, 2,279 total deaths (41%; 177 per 1,000 patient-years) occurred in patients with HFpEF treated with beta-blockers vs. 1,244 total deaths (42%; 191 per 1,000 patient-years) in the patients who were untreated (HR=0.93; 95% CI, 0.86-0.996).

The researchers found no reduction in combined mortality or HF hospitalization related to beta-blocker use. The treated group experienced 3,368 (61%) total first events vs. 1,753 (64%) total first events in the untreated group. There were 371 first events per 1,000 patient-years in the treated group vs. 378 first events per 1,000 patient-years in the untreated group (HR=0.98; 95% CI, 0.92-1.04).

Lund and colleagues also studied 22,893 patients with HF with reduced EF (HFrEF) for a positive-control consistency analysis. Of those, 6,081 were matched (4,054 treated patients, 2,027 untreated patients). In the matched group of patients with HFrEF, the researchers observed an association between beta-blocker use and decreased mortality (HR=0.89; 95% CI, 0.82-0.97) and with reduced combined mortality or HF hospitalization (HR=0.89; 95% CI, 0.84-0.95).

According to the researchers, the lack of reduction in combined all-cause mortality or HF hospitalization was unexpected and may be related to non-CV comorbidity in patients with HFpEF patients or a paradoxical relationship between mortality and rehospitalization.

“Beta-blockers in HFpEF should be studied in a sufficiently powered randomized clinical trial,” they concluded.

Disclosure: The researchers report no relevant financial disclosures.