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Risk of stroke in patients with high on-clopidogrel platelet reactivity to adenosine diphosphate after percutaneous
Nevio Taglieri1, Maria Letizia Bacchi Reggiani1, Tullio Palmerini1
1Istituto di Cardiologia, Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Alma Mater Studiorum Università di Bologna, Bologna, Italy.
Insights
High on-clopidogrel platelet reactivity (HPR) increases stroke risk in patients undergoing percutaneous coronary intervention (PCI). This systematic review confirms HPR as a significant risk factor for stroke in this population.
Area of Science:
- Cardiology
- Pharmacology
- Neurology
Background:
- High on-clopidogrel platelet reactivity (HPR) is a known risk factor for ischemic events after percutaneous coronary intervention (PCI).
- Previous studies lacked the power to definitively link HPR to an increased risk of stroke.
- A need exists to systematically evaluate the association between HPR and stroke incidence in PCI patients.
Purpose of the Study:
- To determine if patients undergoing PCI with HPR face an elevated risk of stroke.
- To conduct a systematic review and meta-analysis of existing prospective studies.
Main Methods:
- Systematic review and meta-analysis of 14 prospective studies.
- Inclusion criteria: patients undergoing PCI, treated with aspirin and clopidogrel, reporting on HPR to adenosine diphosphate.
- Primary endpoint: stroke rate. Investigated interactions with clinical presentation, follow-up duration, and laboratory methods.
Main Results:
- Pooled analysis of 11,959 patients revealed a higher stroke risk in patients with HPR (1.2%) compared to those without (0.7%).
- Relative risk of stroke for HPR patients was 1.84 (95% CI 1.21 to 2.80).
- No significant interaction was found between HPR and clinical presentation, follow-up duration, or laboratory methods for detecting HPR.
Conclusions:
- High on-clopidogrel platelet reactivity is a significant risk factor for stroke in patients with coronary artery disease undergoing PCI.
- The increased stroke risk associated with HPR is consistent across different clinical presentations, follow-up durations, and laboratory detection methods.
- These findings underscore the importance of monitoring and potentially managing HPR in PCI patients to mitigate stroke risk.
Abstract:
Several prospective studies have shown that high on-clopidogrel platelet reactivity (HPR) in patients undergoing percutaneous coronary intervention (PCI) is a risk factor for ischemic events. All studies were insufficiently powered to detect differences in stroke between patients with HPR and those without. Therefore, we performed a systematic review and meta-analysis of available publications aimed at determining whether patients undergoing PCI with HPR are also at increased risk of stroke. We searched for prospective studies enrolling patients undergoing PCI and treated with aspirin and clopidogrel that reported on clinical relevance of HPR to adenosine diphosphate. Study end point was the rate of stroke. We also investigated whether there was an interaction on the relative risk of stroke between HPR, clinical presentation, duration of follow-up, or laboratory methods. Fourteen studies including 11,959 patients were deemed eligible. On pooled analysis, the risk of stroke was higher in patients with HPR compared with patients with no HPR (1.2% vs 0.7%, relative risk on fixed effect 1.84, 95% confidence interval 1.21 to 2.80). There was no heterogeneity among the studies (I(2) = 0%, p = 0.5). Clinical presentation (p = 0.39 for interaction), duration of follow-up (p = 0.87 for interaction), and laboratory method for detection of HPR (p = 0.99 for interaction) did not affect the relative increase in the risk of stroke in patients with HPR compared with patients with no HPR. In conclusion, in patients with coronary artery disease undergoing PCI, the presence of HPR to adenosine diphosphate is a risk factor for stroke.
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