The Journal of Arthroplasty
Volume 25, Issue 4 , Pages 667-668, June 2010

In Reply

Department of Orthopaedic Surgery and Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, CA

Department of Orthopaedic Surgery, University of California, San Francisco, CA

Center for Quality of Care Research, Baystate Medical Center, Springfield, MA, and School of Public Health and Health Sciences, University of Massachusetts, Amherst, MA

Division of Hospital Medicine, University of California, San Francisco, CA

Center for Quality of Care Research, Baystate Medical Center, Springfield, MA, and Tufts University School of Medicine, Boston MA

Division of Hospital Medicine, University of California, San Francisco, CA

Received 11 October 2009; accepted 28 October 2009. published online 22 February 2010.

Article Outline

 

The authors wish to thank Dr White and his colleagues for pointing out a potential flaw in our study design. Based on their suggestion and concerns, we reran the analysis without the V12.51 code. As shown in Table 1, the results of our analysis did not change. Even when the V code was excluded from the analysis, there was no difference in the odds of any venous thromboembolic (VTE) event among total knee arthroplasty (TKA) patients who received aspirin, warfarin, or injectable drugs (low–molecular-weight heparin or synthetic pentasaccharides) for VTE chemoprophylaxis.

Table 1. Adjusted Odds of Having Any VTE Event According to VTE Chemoprophylactic Agent in TKA Patients
Model 1 (ICD-9 Secondary Diagnosis Code V12.51 Excluded From the Analysis)
Adjusted OR
(95% CI)
Original Model
Adjusted OR
(95% CI)
VTEP agent
AspirinRefRef
Injectable (LMWH or synthetic pentasaccharide)0.98 (0.59, 1.62)1.03 (0.76, 1.39)
Warfarin1.17 (0.73, 1.87)1.36* (1.02, 1.82)

ICD-9 indicates International Classification of Diseases, Ninth Revision; OR, odds ratio; CI, confidence interval; LMWH, low–molecular-weight heparin.

*P < .01 for all comparisons.

We would like to reemphasize, as we did in our article, that our results do not suggest that aspirin is more efficacious than warfarin or low–molecular-weight heparin as a VTE prophylactic agent in TKA patients. However, our results do suggest that aspirin, when used in conjunction with other modern clinical care protocols, may be an effective VTE chemoprophylactic agent in certain TKA patients. Given the observational, retrospective design of our study, our conclusions should be considered hypothesis generating, rather than conclusive evidence of the comparative safety and efficacy of aspirin for use in VTE prophylactic regimens after TKA. However, our results, along with results from other observational studies, provide justification for future trials of multimodal VTE prophylactic strategies involving aspirin and other chemoprophylactic agents in TKA patients, and evaluation of the relative risks and benefits of these strategies.

PII: S0883-5403(09)00510-5

doi:10.1016/j.arth.2009.10.016

The Journal of Arthroplasty
Volume 25, Issue 4 , Pages 667-668, June 2010