4.7 Article

Platelet Reactivity and Outcomes after Off-Pump Coronary Surgery in Acute Coronary Syndrome Patients

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JOURNAL OF CLINICAL MEDICINE
卷 11, 期 12, 页码 -

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MDPI
DOI: 10.3390/jcm11123285

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acute coronary syndrome; dual anti-platelet therapy; off-pump coronary artery bypass surgery; P2Y(12) antagonist

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This study investigated the association between preoperative platelet reactivity to P2Y(12) antagonists and ischemic and hemorrhagic complications in ACS patients undergoing coronary surgery. The results showed no correlation between platelet inhibitory response to P2Y(12) antagonists and ischemic or hemorrhagic complications.
Ischemic and hemorrhagic complications are major determinants of survival in acute coronary syndrome (ACS) patients undergoing coronary surgery. We investigated the association of preoperative platelet reactivity to P2Y(12) antagonists with ischemic and hemorrhagic complications after Off-Pump Coronary Artery Bypass surgery (OPCAB) in ACS patients who received dual anti-platelet therapy (DAPT) within 5 days prior to surgery. This prospective, observational study with 177 patients compared the incidence of perioperative major bleeding and major adverse cardiac events (MACEs) in relation to the tertile distribution of the % inhibitory response to P2Y(12) antagonists, as measured by a thromboelastography platelet mapping assay. The incidences of perioperative major bleeding and MACEs were similar in relation to the tertile distribution of inhibitory response to P2Y(12) antagonists. The % inhibitory responses to P2Y(12) antagonists between patients who did or did not exhibit MACEs, and with or without major bleeding, were 58 +/- 20% and 56 +/- 20% (p = 0.578) and 57 +/- 19% and 56 +/- 21% (p = 0.923), respectively. In ACS patients who received DAPT close to OPCAB, the platelet inhibitory response to P2Y(12) antagonists was not associated with ischemic or hemorrhagic complications. OPCAB may obviate the need for routine platelet function testing for ACS patients requiring DAPT and surgical revascularization. Clinical Registration Number: NCT02184884.

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