Key result
Among elderly patients with CAD undergoing PCI, frailty was independently associated with high on-clopidogrel (OR 2.543, P<.01) and high on-aspirin (OR 2.696, P<.01) platelet responses.
Why the study?
Although frailty is a known prognostic factor in ischemic cardiovascular disease, its effects on platelet responses to aspirin and clopidogrel remained under investigation.
Does frailty increase the risk of high on-treatment platelet reactivity to aspirin and clopidogrel in elderly patients with CAD undergoing PCI?
Observational (n=264)
Does frailty increase the risk of high on-treatment platelet reactivity to aspirin and clopidogrel in elderly patients with CAD undergoing PCI?
Odds Ratio: 2.543
Absolute Event Rate: 37.33% vs 15.79%
p-value: p=<.01
Frailty is an independent predictor of high on-treatment platelet reactivity to aspirin and clopidogrel in elderly patients undergoing PCI, suggesting a potential need for tailored antiplatelet strategies in this vulnerable population.
Frailty may flag elderly PCI patients for heightened platelet reactivity monitoring; leaves open whether adjusted regimens improve outcomes.
Frailty has been implicated as a prognostic factor for ischemic cardiovascular diseases. However, the effects of frailty on platelet responses to aspirin and clopidogrel remain under investigation. In this study, we enrolled consecutive elderly patients with coronary artery disease (CAD) who were treated by percutaneous coronary intervention (PCI) to evaluate this association. A total of 264 patients (aged 70-95 years) were included. Patients were divided into 2 groups: a nonfrail (nFR) group and a frail (FR) group according to the Clinical Frailty Scale. Platelet reactivity was assessed with a light transmittance aggregometry method, and arachidonic acid and adenosine diphosphate induced maximum platelet aggregation (AA-MPA/ADP-MPA) were calculated to evaluate the platelet response to aspirin and clopidogrel. The results showed that the AA-MPA and ADP-MPA of the FR group were significantly higher than those in the nFR group (17.49 ± 6.65 vs 15.19 ± 6.33, P < .01; 56.13 ± 10.14 vs 45.45 ± 11.59, P < .01). High on-aspirin platelet response (HAPR) and high on-clopidogrel platelet response (HCPR) were significantly more common in the FR group than in the nFR group (24.67% vs 13.16%, P = .028, 37.33% vs 15.79%, P < .01). According to multivariable regression analyses, frailty was found to be independently associated with AA-MPA (β coefficient = 1.883, P = .042) and ADP-MPA (β coefficient = 9.287, P < .001), and it was an independent predictor of HAPR (odds ratio [OR]: 2.696, P < .01) and HCPR (OR: 2.543, P < .01). It was concluded that among elderly patients with CAD undergoing PCI, frailty is an independent predictor of HAPR and HCPR, and the state of frailty is independently associated with the platelet responses to clopidogrel and aspirin.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2020) conducted an observational in Coronary artery disease undergoing percutaneous coronary intervention (n=264). Frailty vs. Nonfrail was evaluated on High on-clopidogrel platelet response (HCPR) (OR 2.543, p=<.01). Among elderly patients with CAD undergoing PCI, frailty was independently associated with high on-clopidogrel (OR 2.543, P<.01) and high on-aspirin (OR 2.696, P<.01) platelet responses.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: