Why the study?
It was uncertain whether preoperative discontinuation of antiplatelet therapy has been avoided or harmful in patients with second-generation drug-eluting coronary stents undergoing noncardiac surgery.
Does preoperative discontinuation of antiplatelet therapy impact net adverse clinical events in patients with second-generation drug-eluting stents undergoing noncardiac surgery?
Does preoperative discontinuation of antiplatelet therapy impact net adverse clinical events in patients with second-generation drug-eluting stents undergoing noncardiac surgery?
Discontinuation of antiplatelet therapy during noncardiac surgery in patients with second-generation DES does not significantly increase 30-day net adverse clinical events, though prolonged discontinuation ≥9 days increases MACE risk.
Preoperative APT discontinuation was common without higher NACE; leaves open optimal perioperative strategy in second-generation DES patients.
Background Continuing antiplatelet therapy ( APT ) has been generally recommended during noncardiac surgery, but it is uncertain if preoperative discontinuation of APT has been avoided or harmful in patients with second‐generation drug‐eluting coronary stents. Methods and Results Patients undergoing noncardiac surgery after second‐generation drug‐eluting coronary stent implantation were assessed in a multicenter cohort in Korea. Net adverse clinical events within 30 days postoperatively, defined as all‐cause death, major adverse cardiac events, and major bleeding, were evaluated. Of 3582 eligible patients, 49% patients discontinued APT during noncardiac surgery. The incidence of net adverse clinical events was comparable between patients with continuation versus discontinuation (4.1% versus 3.4%; P =0.257) of APT during noncardiac surgery. Perioperative discontinuation of APT did not impact on net adverse clinical events (adjusted hazard ratio [HR], 1.00; 95% CI, 0.69–1.44; P =0.995). In subgroup analysis, patients undergoing intra‐abdominal surgery were exposed to less risk of major bleeding by discontinuing APT (adjusted HR, 0.26; 95% CI , 0.08–0.91; P =0.035). Prolonged discontinuation of APT for ≥9 days was associated with higher risk of a major adverse cardiac event compared with continuing APT (adjusted HR, 3.38; 95% CI, 1.36–8.38; P =0.009). Conclusions APT was discontinued preoperatively in almost half of patients with second‐generation drug‐eluting coronary stents. Our explorative analysis showed that there was no significant impact of discontinuing APT on the risk of perioperative adverse events except that discontinuing APT may be associated with decreased hemorrhagic risk in patients undergoing intra‐abdominal surgery. Registration URL : https://www.clinicaltrials.gov ; Unique identifier: NCT 03908463.
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Kim et al. (2020) studied this question.
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