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Study examines platelet function testing for guiding antithrombotic treatment before PCI procedures

Date:
September 20, 2011
Source:
JAMA and Archives Journals
Summary:
Among patients with acute coronary syndromes undergoing a procedure such as angioplasty, those who received platelet function tests before receiving antithrombotic therapy to determine appropriate clopidogrel dosing and who had high residual platelet reactivity (platelets resistant to antithrombotic therapy) were at an increased risk of an ischemic event at short- and long-term follow-up of up to two years, according to a new study.
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Among patients with acute coronary syndromes undergoing a procedure such as angioplasty, those who received platelet function tests before receiving antithrombotic therapy to determine appropriate clopidogrel dosing and who had high residual platelet reactivity (platelets resistant to antithrombotic therapy) were at an increased risk of an ischemic event at short- and long-term follow-up of up to 2 years, according to a study in the Sept. 21 issue of JAMA.

Several studies have shown that high residual platelet reactivity during clopidogrel treatment is predictive of major cardiovascular events in patients undergoing percutaneous coronary intervention (PCI; procedures such as balloon angioplasty or stent placement used to open narrowed coronary arteries). However, it has not yet been proven that the risk of thrombotic events increases markedly above a critical cut point of platelet reactivity on in vitro platelet function tests, according background information in the article.

Guido Parodi, M.D., and colleagues of Careggi Hospital, Florence, Italy, conducted a study to examine whether high residual platelet reactivity (HRPR) after clopidogrel loading (a comparatively large dose of the drug given at the beginning of treatment) is an independent prognostic marker of risk of long-term thrombotic events in patients with acute coronary syndromes (ACS) undergoing an invasive procedure and receiving long-term antithrombotic treatment adjusted according to the results of platelet function tests. The study included 1,789 patients with ACS undergoing PCI from April 2005 to April 2009 and who had platelet reactivity assessed via testing. All patients received 325 mg of aspirin and a loading dose of 600 mg of clopidogrel followed by a maintenance dosage of 325 mg/d of aspirin and 75 mg/d of clopidogrel for at least 6 months. Patients with HRPR as assessed by adenosine diphosphate test (70 percent platelet aggregation or greater) received an increased dose of clopidogrel or switched to the antiplatelet drug ticlopidine under adenosine diphosphate test guidance. The primary outcome measure was a composite of cardiac death, heart attack, any urgent coronary revascularization, and stroke at 2-year follow-up. Secondary measured outcomes were stent thrombosis and each component of the primary end point.

The researchers found that the primary end point event rate was 14.6 percent (36/247) in the HRPR group and 8.7 percent (132/1,525) in the low residual platelet reactivity group (LRPR). The difference in the event rate was driven by the difference in cardiac mortality, which was 9.7 percent in the HRPR group and 4.3 percent in the LRPR group. The stent thrombosis rate was 2-fold higher in the HRPR group (6.1 percent [15/247] vs. 2.9 percent [44/1,525]). Additional analysis indicated that HRPR was independently associated with a 49 percent increased risk of the primary end point and a 81 percent increased risk of cardiac mortality.

The authors write that "the results of this study should be considered only as hypothesis generating for further studies of tailored therapy using new antithrombotic agents."

Editorial: Applying Platelet Function Testing in Clinical Practice

Dominick J. Angiolillo, M.D., Ph.D., of the University of Florida College of Medicine-Jacksonville, comments in an accompanying editorial on the use of platelet function testing.

"… despite promising research conducted to date, currently available evidence cannot support routine use of platelet function testing [PFT] in clinical practice. Until results of appropriately powered randomized controlled trials demonstrate efficacy and safety (in particular, low bleeding risk) of adjustment of antiplatelet treatment, PFT should be reserved mostly as a research tool."


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Materials provided by JAMA and Archives Journals. Note: Content may be edited for style and length.


Journal References:

  1. G. Parodi, R. Marcucci, R. Valenti, A. M. Gori, A. Migliorini, B. Giusti, P. Buonamici, G. F. Gensini, R. Abbate, D. Antoniucci. High Residual Platelet Reactivity After Clopidogrel Loading and Long-term Cardiovascular Events Among Patients With Acute Coronary Syndromes Undergoing PCI. JAMA: The Journal of the American Medical Association, 2011; 306 (11): 1215 DOI: 10.1001/jama.2011.1332
  2. D. J. Angiolillo. Applying Platelet Function Testing in Clinical Practice: What Are the Unmet Needs? JAMA: The Journal of the American Medical Association, 2011; 306 (11): 1260 DOI: 10.1001/jama.2011.1349

Cite This Page:

JAMA and Archives Journals. "Study examines platelet function testing for guiding antithrombotic treatment before PCI procedures." ScienceDaily. ScienceDaily, 20 September 2011. <www.sciencedaily.com/releases/2011/09/110920163209.htm>.
JAMA and Archives Journals. (2011, September 20). Study examines platelet function testing for guiding antithrombotic treatment before PCI procedures. ScienceDaily. Retrieved April 18, 2024 from www.sciencedaily.com/releases/2011/09/110920163209.htm
JAMA and Archives Journals. "Study examines platelet function testing for guiding antithrombotic treatment before PCI procedures." ScienceDaily. www.sciencedaily.com/releases/2011/09/110920163209.htm (accessed April 18, 2024).

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