OPTIMIZE-HF Registry analysis shows that patients with heart failure prescribed carvedilol at discharge had better survival than patients not on a beta-blocker
Patients with heart failure who were prescribed
carvedilol at discharge had better survival rates at 60-90 days
than patients who were eligible but were not prescribed a beta-blocker,
according to an analysis of data from the US heart failure registry
OPTIMIZE-HF, according to a presentation at the annual meeting of
the American College of Cardiology.
OPTIMIZE-HF, funded by the drug’s manufacturer,
is the only hospital-based heart failure registry with 60-90 day
follow-up data on this patient population in the USA.
Data were collected at 60 to 90 days following
hospital discharge on patients with heart failure to measure the
associations with clinical outcomes in eligible patients with left
ventricular systolic dysfunction who received carvedilol prior to
hospital discharge versus patients who were eligible but who received
no beta-blocker at discharge.
Of the 720 patients with left ventricular systolic dysfunction,
2,373 (87.2%) were eligible to receive a beta-blocker at discharge.
Carvedilol was prescribed at discharge for 1,146 patients, 94.2
percent of whom remained on therapy for the duration of the follow-up
period.
Data analysis showed that patients prescribed carvedilol at discharge
had a significantly decreased risk for death and for rehospitalization
or death, a sign that the drug had improved the early post-discharge
risk for recurrent heart failure.
"This analysis adds to the evidence supporting the benefits
and tolerability of prescribing carvedilol at hospital discharge
for patients admitted with heart failure," said Gregg C. Fonarow,
MD, chairman of the OPTIMIZE-HF Committee and director of Ahmanson
- UCLA Cardiomyopathy Center in Los Angeles. "Based on this
analysis and earlier studies, carvedilol should be started when
medically advisable at the time of hospital discharge in all eligible
heart failure patients since the difference in survival and re-hospitalizations
emerges in just weeks among patients who receive carvedilol as opposed
to those who don't have a beta-blocker added to their treatment
regimen."
The registry was launched in 2003 as an improvement in care program
to analyze patient outcomes based on evidence-based, guideline-driven
patient management. Carvedilol is currently the only beta-blocker
approved in the US for patients who had a myocardial infarction
resulting in left ventricular dysfunction. Carvedilol is also approved
to increase survival in patients with mild-to-severe heart failure.
|