The value of clopidogrel administered postoperatively following a non-ST-segment elevation acute coronary syndrome.

نویسندگان

  • Ty J Gluckman
  • Jeffrey J Rade
  • Steven P Schulman
چکیده

In their recent article in CHEST (September 2004)1 on antithrombotic therapy, Stein et al recommended that clopidogrel be added to aspirin for 9 to 12 months in patients undergoing coronary artery bypass grafting (CABG) following a non-ST-segment elevation acute coronary syndrome (NSTEACS). The authors assigned this recommendation a grade of 1A, suggesting that the benefits derived from this strategy are clear and are supported by randomized clinical trial data without important limitations.2 The authors based this recommendation on data from the Clopidogrel in Unstable Angina to Prevent Recurrent Events (CURE) trial.3 Because no prospective, randomized clinical trials have specifically examined the role of clopidogrel in patients following CABG, the authors are correct in basing their recommendations on data abstracted from the CURE trial. Nevertheless, it is our opinion that currently available trial data do not support a grade 1A recommendation. In fact, recent data have suggested that postoperative treatment with clopidogrel provides no substantial clinical benefit and, if anything, increases the risk of serious bleeding. Because of this, it is our opinion that clopidogrel should not be routinely used after CABG following an NSTE-ACS. In the CURE trial,3 12,562 patients with NSTE-ACS were randomized to treatment with clopidogrel (300 mg initially followed by 75 mg daily) plus aspirin (75 to 325 mg daily) vs aspirin alone (75 to 325 mg daily). The primary outcome was a composite of cardiovascular death, nonfatal myocardial infarction, or stroke. Patients randomized to receive dual antiplatelet therapy (clopidogrel and aspirin) had a 20% relative risk reduction (RRR) in the primary end point at a mean of 9 months (9.3% vs 11.4%, respectively; p 0.001), with greater benefit (44% RRR) noted in those patients undergoing revascularization (ie, CABG or percutaneous coronary revascularization). Despite this, the CURE trial investigators cautioned against the interpretation of these latter results, “given the large numbers of subgroup analyses that were performed.” Although the CURE trial did not initially report the results of the primary end point for those who underwent CABG subsequent to study enrollment, these results were recently published by Fox et al4 In this post hoc analysis, the addition of clopidogrel to aspirin led to an insignificant 11% RRR in the primary outcome among those undergoing CABG a median of 25.5 days after randomization (14.5% vs 16.2%, respectively; 95% confidence interval [CI], 0.71 to 1.11). This sharply contrasts with the 28% RRR in the primary outcome noted in those receiving clopidogrel in association with percutaneous revascularization (95% CI, 0.57 to 0.90). Further analysis was able to demonstrate a strong trend toward benefit among those receiving clopidogrel in association with CABG during the initial hospitalization (RRR, 19%; 95% CI, 0.59 to 1.12); however, this effect was driven entirely by a reduction in the number of events prior to surgery (18% RRR in the primary outcome; 95% CI, 0.58 to 1.16), with no benefit noted in those receiving clopidogrel postoperatively (3% RRR; 95% CI, 0.74 to 1.26). Patients receiving postoperative clopidogrel also experienced a strong trend toward an excess of life-threatening bleeds (30% increased risk; 95% CI, 0.90 to 1.83). Based on these findings, clopidogrel should not be routinely used in the postoperative management of patients undergoing CABG for treatment of NSTE-ACS. In fact, available data suggest that treatment with clopidogrel should probably be limited in the postoperative period to those who are intolerant of aspirin therapy. While speculative, it is possible that short-term cessation of clopidogrel treatment after surgery (median duration, 10 days) may have contributed to the failure of study investigators to demonstrate a benefit from postoperative clopidogrel. To further explore this, though, “a dedicated randomized clinical trial of clopidogrel plus aspirin vs aspirin alone after CABG”5 is warranted.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Impact of Age on Risk Factors and Clinical Manifestations of Acute Coronary Syndrome: Observations From the Coronary Care Unit of Sulaimani, Iraq

Background: ST-segment elevation myocardial infarction (STEMI) and non-ST-segment elevation myocardial infarction (NSTEMI ) are common types of acute coronary syndrome which are associated with the risk factors of age, obesity, hypertension, and diabetes. Objective: The present study aimed to examine the effects of age on the risk factors and clinical sym...

متن کامل

Vitamin D deficiency predicts the ST elevation type of myocardial infarction in patients with acute coronary syndrome.

According to studies, a significant association exists between the low levels of vitamin D and cardiovascular diseases such as myocardial infarction (MI). In a prospective, case control study, 88 patients with acute coronary syndrome (ACS) including ST elevation myocardial infarction (STEMI) and Non-STEMI were enrolled. The plasma level of 25-hydroxy vitamin D[25(OH)D] was obtained at the time ...

متن کامل

Early, accurate, non-invasive predictors of left main or 3-vessel disease in patients with non-ST-segment elevation acute coronary syndrome.

BACKGROUND In patients with non-ST-segment elevation acute coronary syndromes (NSTE-ACS), identification of left main and/or 3-vessel disease (LM/3VD) is crucial for deciding whether to initiate early treatment with clopidogrel, which can increase the risk of surgical bleeding. METHODS AND RESULTS On admission, the clinical factors of 501 patients with NSTE-ACS, who underwent coronary angiogr...

متن کامل

Vitamin D deficiency predicts the ST elevation type of myocardial infarction in patients with acute coronary syndrome.

According to studies, a significant association exists between the low levels of vitamin D and cardiovascular diseases such as myocardial infarction (MI). In a prospective, case control study, 88 patients with acute coronary syndrome (ACS) including ST elevation myocardial infarction (STEMI) and Non-STEMI were enrolled. The plasma level of 25-hydroxy vitamin D[25(OH)D] was obtained at the time ...

متن کامل

Antiplatelet therapy in early management of non-ST-segment elevation acute coronary syndrome: the 2002 and 2007 guidelines from North America and Europe.

The American College of Cardiology, American Heart Association, and the European Society of Cardiology published updated guidelines in 2007 for patients with non-ST elevation acute coronary syndrome. In this article, we review the recommendations for antiplatelet therapy and supporting data, highlight new changes, and describe differences between the European and North American guidelines. The ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Chest

دوره 127 6  شماره 

صفحات  -

تاریخ انتشار 2005