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Clinical Assistant Professor of Pharmacy Practice, Wayne State University, Clinical Specialist, Henry Ford Hospital, Detroit, Michigan
Clinical Pharmacist in Clinical Research and Infectious Diseases, Department of Pharmacy/Clinical Research/Infections, Barnes-Jewish Hospital, 216 South Kingshighway, MS 90-52-411, St. Louis, Missouri 63110, fax 314/747-2185, psm9154{at}bjc.org
Published Online, October 2, 2007. www.theannals.com, DOI 10.1345/aph.1H516b
Concerns were raised with respect to the power to detect an association between fluconazole exposure and non-albicans vs C. albicans candidemia. As we discussed, the population studied had very low incidence of prior antifungal use. The low rate of fluconazole use would make it very impractical to study this association as a primary endpoint at this particular institution. While a patient population of this nature is certainly not universal, it is also not entirely unique, and we feel that a better understanding of risk factors in this situation can be valuable.
Finally, we appreciate the interest of Vandijck et al., as the concerns they raise are important considerations in the design of future research of Candida infections.
Footnotes
Dr. McKinnon is on the Consultancy/Speaker's Board of Pfizer, Schering-Plough, and Astellas.
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