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Relationship between platelet count and 30-day clinical outcomes after percutaneous coronary interventions. Pooled
Raisuke Iijima1, Gjin Ndrepepa, Julinda Mehilli
1Deutsches Herzzentrum, Lazarettstr. 36, 80636 Munich, Germany. raisuke329@aol.com
Insights
Baseline platelet count in patients undergoing percutaneous coronary intervention (PCI) after clopidogrel pre-treatment does not affect major adverse cardiac events (MACE). However, higher platelet counts are linked to increased 30-day mortality and Q-wave myocardial infarction.
Area of Science:
- Cardiology
- Hematology
Background:
- Platelets are crucial in major adverse cardiac events (MACE) post-percutaneous coronary intervention (PCI).
- The relationship between platelet count and outcomes in patients pre-treated with clopidogrel before PCI remains unclear.
Purpose of the Study:
- To investigate the impact of baseline platelet count on 30-day MACE and mortality in patients with coronary artery disease (CAD) undergoing PCI after clopidogrel pre-treatment.
Main Methods:
- Analysis of 5,256 patients from four randomized trials (ISAR-REACT, ISAR-SMART2, ISAR-SWEET, ISAR-REACT2).
- Patients received 600 mg clopidogrel pre-PCI, with platelet counts categorized into tertiles.
- Primary endpoint: 30-day MACE; Secondary endpoint: 30-day mortality.
Main Results:
- No significant difference in 30-day MACE incidence across platelet count tertiles (P=0.76).
- A significant increase in 30-day mortality was observed in the upper platelet count tertile (P=0.04).
- Higher incidence of Q-wave myocardial infarction in the upper tertile (P=0.02).
Conclusions:
- Baseline platelet count is an independent predictor of 30-day mortality in patients with CAD undergoing PCI after clopidogrel pre-treatment.
- While MACE rates were similar, elevated platelet counts correlate with increased mortality risk.
Abstract:
Platelets play an important role in the development of major adverse cardiac events (MACE) following percutaneous coronary intervention (PCI). The impact of platelet count on the outcome of patients undergoing PCI after pre-treatment with clopidogrel is unknown. The study included 5,256 patients enrolled in four randomized trials - ISAR-REACT, ISAR-SMART2, ISAR-SWEET, and ISAR-REACT2 - which assessed the value of abciximab in patients with coronary artery disease (CAD) undergoing PCI after pre-treatment with 600 mg of clopidogrel. Platelet count was measured at baseline before PCI. Primary endpoint was the 30-day incidence of MACE, secondary endpoint was mortality. The tertiles of platelet counts were: lower tertile (<198 x 10(9)/L; n = 1,726), middle tertile (198-244 x 10(9)/L; n = 1,750) and upper tertile (>244 x 10(9)/L; n = 1,780). The 30-day incidence of MACE was 6.7% (n = 116) among patients of the lower tertile, 6.3% (n = 111) among patients of the middle tertile, and 7.0% (n = 124) among patients of the upper tertile (P = 0.76). The 30-day mortality was 1.2% (n = 22) among patients of the upper tertile, 0.5% (n = 9) among patients of middle tertile and 0.6% (n = 11) among patients of the lower tertile (P = 0.04). Q-wave myocardial infarction occurred in 1.3% of patients (n = 23) in the upper tertile, 0.7% of patients (n = 13) in the middle tertile and 0.5% of patients (n = 8) in the lower tertile (P = 0.02). Platelet count was an independent correlate of 30-day mortality (hazard ratio 2.69, 95% confidence interval 1.08-6.67; P = 0.033 for the third vs. the first tertile). In conclusion, in patients with CAD undergoing PCI after pre-treatment with 600 mg clopidogrel, baseline platelet count predicts 30-day mortality.
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