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Medical treatment to reduce total ischemic burden: total ischemic burden bisoprolol study (TIBBS), a multicenter
1Ludwig-Maximilians University Munich, Red Cross Hospital, Germany.
Insights
Bisoprolol significantly reduced transient myocardial ischemia episodes and duration in chronic stable angina patients more effectively than nifedipine. Bisoprolol also notably decreased the morning peak of ischemic activity.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Beta-adrenergic blockers and calcium antagonists are used for transient ischemic episodes.
- Few large-scale comparative studies exist for these drug classes.
Purpose of the Study:
- To compare the efficacy of bisoprolol and nifedipine in managing transient myocardial ischemia in patients with chronic stable angina.
Main Methods:
- A randomized, double-blind, controlled trial (TIBBS) involving 330 patients with chronic stable angina.
- Patients received either bisoprolol or slow-release nifedipine over two 4-week treatment phases with increasing doses.
- 48-hour Holter monitoring was conducted after each phase to evaluate ischemic episodes.
Main Results:
- Bisoprolol significantly reduced the number and duration of transient ischemic episodes compared to nifedipine (p < 0.0001).
- Bisoprolol decreased heart rate during ischemic episodes, while nifedipine did not.
- Bisoprolol demonstrated a significant reduction in the morning peak of ischemic activity.
Conclusions:
- Bisoprolol is more effective than nifedipine in reducing transient ischemic episodes in chronic stable angina patients.
- Bisoprolol offers a significant benefit in managing circadian variations of ischemic activity.
Objectives:
We compared the effects of bisoprolol on transient myocardial ischemia with those of nifedipine in patients with chronic stable angina.
Background:
Both beta-adrenergic blocking agents and calcium antagonists reduce transient ischemic episodes, but comparisons of these agents have been made in only a few larger studies.
Methods:
The Total Ischemic Burden Bisoprolol Study (TIBBS) was a randomized double-blind controlled study with two parallel groups; 330 patients from 30 centers in seven European countries with stable angina pectoris, a positive exercise test and more than two transient ischemic episodes during 48 h of Holter monitoring (central evaluation) were included. Of these patients 161 were randomized to receive bisoprolol and 169 to receive nifedipine slow release. There were two treatment phases of 4 weeks each, with 48-h Holter monitoring after each phase. During phase 1, patients received either 10 mg of bisoprolol daily or 2 x 20 mg of nifedipine slow release. During phase 2, they received either 20 mg of bisoprolol daily or 2 x 40 mg of nifedipine slow release.
Results:
In phase 1 of the trial, 4 weeks of bisoprolol therapy (10 mg daily) reduced the mean [+/- SD] number of transient ischemic episodes from 8.1 +/- 0.6 to 3.2 +/- 0.4/48 h. Nifedipine (2 x 20 mg) reduced transient ischemic episodes from 8.3 +/- 0.5 to 5.9 +/- 0.4/48 h. Total duration of ischemia was reduced from 99.3 +/- 10.1 to 31.9 +/- 5.5 min/48 h with bisoprolol and from 101 +/- 9.1 to 72.6 +/- 8.1 min/48 h with nifedipine. Reductions were statistically significant for both drugs; the difference between bisoprolol and nifedipine was also significant (p < 0.0001). Bisoprolol reduced the heart rate at onset of episodes by 13.7 +/- 1.4 beats/min from a baseline value of 99.5 +/- 1.2 beats/min (p < 0.001). Heart rate was unchanged with nifedipine. Bisoprolol had significantly higher responder rates than nifedipine. Doubling of the dose in phase 2 of the trial had small additive effects. Only bisoprolol showed a marked circadian effect by reducing the morning peak of transient ischemic episodes (by 68% at peak time, 8:00 to 8:59 AM).
Conclusions:
Both bisoprolol and nifedipine reduced the number and duration of transient ischemic episodes in patients with chronic stable angina. Bisoprolol was significantly more effective than nifedipine in both doses tested and reduced the morning peak of ischemic activity.
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