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Published on: July 7, 2016
Antiischemic effect of intracoronary diltiazem on myocardial ischemia during PTCA
Insights
Intracoronary diltiazem significantly reduced chest pain and ST elevation during percutaneous transluminal coronary angioplasty (PTCA). This pretreatment with diltiazem may allow for longer balloon inflations, improving patient outcomes.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Myocardial ischemia is a significant concern during percutaneous transluminal coronary angioplasty (PTCA).
- Effective management of ischemia during PTCA is crucial for patient outcomes.
Purpose of the Study:
- To evaluate the efficacy of intracoronary diltiazem in mitigating myocardial ischemia during PTCA.
- To assess the impact of diltiazem on chest pain and electrocardiographic (ECG) markers of ischemia.
Main Methods:
- A double-blind study involving 38 patients undergoing PTCA.
- Patients were randomized to receive placebo, low-dose (1 mg), or high-dose (2-3 mg) intracoronary diltiazem.
- Chest pain scores and ST-segment elevation on standard and intracoronary ECGs were measured before and after treatment during balloon inflation.
Main Results:
- Intracoronary diltiazem significantly reduced chest pain scores in both low-dose and high-dose groups (P < 0.01).
- ST-segment elevation, a marker of ischemia, was significantly attenuated in diltiazem groups compared to placebo (P < 0.01).
- No significant correlation was found between ST elevation changes and rate-pressure product, despite a slight decrease in blood pressure.
Conclusions:
- Intracoronary diltiazem effectively attenuates myocardial ischemia and chest pain during PTCA.
- This pharmacological approach may facilitate longer balloon inflation times, potentially improving procedural success and patient safety.
Abstract:
To evaluate the effect of intracoronary diltiazem on myocardial ischemia during percutaneous transluminal coronary angioplasty (PTCA), 38 patients were randomly assigned to receive inactive placebo (n = 19; group C) or a low dose (1 mg, n = 10; group D1), or a high dose (2 or 3 mg, n = 9; group D2) of diltiazem in a double-blind manner. The agent was administered directly into the coronary artery via a balloon catheter following a control balloon inflation. Chest pain score (maximum, 10) and the magnitude of ischemic ST elevation on standard and intracoronary electrocardiograms (ECGs) during a balloon inflation were assessed in the control and posttreatment periods. After the administration of diltiazem, the chest pain score was significantly decreased in group D1 (control: 5.1 +/- 3.6, posttreatment: 3.8 +/- 3.1, P < 0.01) and group D2 (3.4 +/- 2.5 vs 2.5 +/- 2.0, P < 0.01), but not in group C (4.1 +/- 3.1 vs 3.7 +/- 3.3, difference not significant). The magnitude of ST elevation relative to the control on standard and intracoronary ECGs was significantly smaller in groups D1 and D2 than in group C (standard ECG; D1: 51.8 +/- 10.6% of control, D2: 41.6 +/- 28.7% vs C: 93.3 +/- 15.6% and intracoronary ECG; D1: 47.1 +/- 11.7% of control, D2: 27.5 +/- 26.9% vs C: 94.6 +/- 29.3%, all P < 0.01). Although systolic blood pressure decreased slightly in groups D1 and D2, there was no significant correlation between the change in ST elevation and the change in the rate-pressure product. Pretreatment with a small dose of intracoronary diltiazem attenuated myocardial ischemia during PTCA and this pretreatment may enable us to perform balloon inflation for a longer period.
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