Table 1.
Studies Involving β-Blockers
Source | Drugs Studieda | No. of Patients (Age Mean or Range, y)/ Duration | Study Design | Population (Setting) | Jadad or Newcastle-Ottawa Scoreb | Results | Listed Source of Funding |
---|---|---|---|---|---|---|---|
Ahrens et al,25 2007 | Toprol XL vs 8 versions of long-acting metoprolol | 49673 (56)/4 y | Retrospective cohort study | Patients affiliated with 3 German health insurers (non-US) | 8 | No excess risk of hospitalization for cardiovascular events after adjustment for confounding (OR, 1.04–1.06; 95% CI, 0.89–1.21) | Generic manufacturers |
Portoles et al,26 2005 | Coreg vs carvedilol | 24 (22.8)/1 dose of each with washout | RCT with crossover | Healthy subjects (non-US) | 2 | No significant differences in HR, BP, PR length, tolerability | Not listed |
Mirfazaelian et al,27 2003 | Tenormin vs atenolol | 12 (NA)/1 dose of each with washout | Bioequivalency study: double-blind RCT with crossover | Healthy subjects (non-US) | 2 | No significant differences in reductions of HR, BP | Not listed |
Bongers and Sabin,28 1999 | Toprol XL vs long-acting metoprolol | 52 (62)/4 wk for each product | Double-blind RCT with crossover | Outpatients with stable angina and 6 proven ST-segment depressions on ambulatory ECG (non-US) | 3 | Both significantly reduced ischemic events; no significant difference in reductions of HR or BP, signs of ischemia on telemetry (P = .21), anginal attacks (P = .34), nitrate use (P = .13), or adverse events (P = .08); median HR slightly less for brand-name (P = .05) | Brand-name manufacturer |
Chiang et al,29 1995 | Tenormin vs atenolol | 23 (59)/4 wk of each with washout | Double-blind RCT with crossover | Outpatients with hypertension (non-US) | 3 | No significant differences in reductions of HR, BP | Not listed |
Sarkar et al,30 1995 | Tenormin vs atenolol | 31 (NA)/1 dose of each with washout | Bioequivalency study: RCT with crossover | Healthy subjects (US) | 2 | No significant differences in reductions of HR, BP | Generic manufacturer |
Carter et al,31 1989 | Inderal vs Inderal LA (long-acting) vs propranolol | 15 (46)/4 wk of each with washout | Single-blind RCT with crossover | Outpatients with hypertension (US) | 3 | No significant differences in reductions of HR, reductions of BP, tolerability | National Institutes of Health |
el-Sayed and Davies,32 1989 | Inderal vs propranolol vs placebo | 12 (NA)/1 dose of each with washout | Double-blind RCT with crossover | Healthy subjects (non-US) | 2 | No significant differences in change in resting HR, SBP, postexercise values | Not listed |
Sanderson and Lewis,33 1986 | Inderal vs propranolol | 1700 (68)/Half switched to Inderal LA for 4 wk; then all switched for 4 wk | Retrospective cohort study | Outpatients with multiple indications for β-blocker (non-US) | 3 | Increased incidence of self-reported adverse effects among group taking generic at initiation of study (P < .001) (difference extinguished after all switched to Inderal LA, P = .15) | Not listed |
Abbreviations: BP, blood pressure; CI, confidence interval; ECG, electrocardiogram; HR, heart rate; NA, not available; OR, odds ratio; RCT, randomized controlled trial; SBP, systolic blood pressure.
Toprol XL and Tenormin are manufactured by AstraZeneca, Wilmington, Delaware; Coreg, GlaxoSmithKline, London, England; and Inderal, Ayerst Laboratories, Radnor, Pennsylvania.
The Jadad score range is 1–5 for RCTs; the Newcastle-Ottawa score range, 1–9 stars for observational studies.