Hemodynamic and metabolic effects of carvedilol: a meta-analysis approach

✍ Scribed by Stienen, U. ;Meyer-Sabellek, W.

• Publisher: Springer-Verlag
• Year: 1992
• Tongue: English
• Weight: 512 KB
• Volume: 70
• Category: Article
• ISSN: 1432-1440
• DOI: 10.1007/bf00207614

✦ Synopsis

Establishing the overall efficacy or safety of a drug requires a unified methodological approach and analysis of all clinical trials to be included. As an example, this paper presents the aggregated dose-response relationship of efficacy data and a last-value analysis of laboratory data across all studies of the antihypertensive drug project carvedilol. Hemodynamic endpoints were calculated as change from the baseline blood pressure and pulse after an average treatment of 2-4 weeks whereas metabolic endpoints were calculated as changes from the baseline until the last day with respect to glucose, potassium, creatinine, lipids and liver function (median duration of treatment was 8-12 weeks). All antihypertensive trials were reanalyzed using an intent-to-treat principle. Aggregated efficacy data (mean, standard deviation, sample size) for each allocated group within each study were combined by means of meta-analysis separately for o.d. or b.i.d. dose regimens. Laboratory data were aggregated similarly within each study, using the last active drug as a grouping factor. The results showed that the patient population was treated adequately with 25 mg carvedilol o.d. The dose response curve for o.d. regimens shows a typical sigmoid shape: a steeper increase from 12.5 mg to 25 mg carvedilol, which then flattens (25 mg, 50 mg, 100 mg carvedilol o.d.). No superiority of a b.i.d. dose regimen over a o.d. dose regimen by means of BP lowering could be detected. There was a considerable variation in the results between studies, much bigger than the dose-response effect, most due to monocentric trials.(ABSTRACT TRUNCATED AT 250 WORDS)