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Volume 145, Issue 6, Pages 309-315 (June 2005)


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Comparison of modified Thrombelastograph and Plateletworks whole blood assays to optical platelet aggregation for monitoring reversal of clopidogrel inhibition in elective surgery patients

Robert M. Crafta, Jack J. Chaveza, Carolyn C. Snidera, Robert A. Muenchenb, Roger C. CarrollaCorresponding Author Informationemail address

Received 27 September 2004; received in revised form 11 January 2005; accepted 22 March 2005.

Clinically monitoring recovery from clopidogrel and nonsteroidal anti-inflammatory drug (NSAID) inhibition requires whole blood assays corresponding to a standard methodology such as platelet-rich plasma aggregation monitored optically (OPA). We compared OPA, using an ED50 dose of adenosine diphosphate activation, with 2 whole blood assays, Plateletworks (PWA) and modified Thrombelastograph (TEG). Two sets of assays were performed on 43 surgery patients while on clopidogrel and off clopidogrel to determine the reversal of absolute and relative inhibition. The modified TEG had Spearman correlations with OPA for absolute (ρ = .424; P = .006) and relative inhibition (ρ = .742; P < .0001). PWA correlations with OPA gave absolute (ρ = .28; P = .08) and relative inhibition (ρ = .46; P = .004) values. Bland-Altman analysis indicated agreement of both tests with OPA, showing constant biases of about 18% and some dependency on mean magnitude error. Cohen effect size thresholds defined nonresponders as < 7.7% clopidogrel inhibition relative to baseline recovery of full platelet function. Apparent nonresponse to clopidogrel or lack of platelet recovery did not correlate with statin or NSAID therapies. These PWA and modified TEG whole blood assays could prove useful for monitoring the reversal of clopidogrel and NSAID inhibition before surgery. More important, these assays done at baseline and after beginning clopidogrel therapy could monitor the effectiveness for the individual patients with cardiovascular disease and help identify the need for alternative therapies.

a Department of Anesthesiology, University of Tennessee Graduate School of Medicine, Knoxville, Tennessee

b Statistical Consulting Center, University of Tennessee, Knoxville, Tennessee

Corresponding Author InformationReprint requests: Roger C. Carroll, PhD, University of Tennessee Graduate School of Medicine, 1924 Alcoa Highway, Knoxville, TN 37920

 Supported by the University of Tennessee Anesthesiology Research Fund and Physicians’ Medical Education and Research Foundation, Knoxville, TN, and the Haemoscope Corporation, Niles, IL. Equipment provided by the Haemoscope Corporation and Helena Laboratories, Beaumont, TX.

PII: S0022-2143(05)00126-5

doi:10.1016/j.lab.2005.03.010


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