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Published ahead of print on May 29, 2009, doi:10.1164/rccm.200901-0146OC
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American Journal of Respiratory and Critical Care Medicine Vol 180. pp. 365-370, (2009)
© 2009 American Thoracic Society
doi: 10.1164/rccm.200901-0146OC


Original Article

Fluoroquinolone Resistance in Mycobacterium tuberculosis

The Effect of Duration and Timing of Fluoroquinolone Exposure

Rose A. Devasia1, Amondrea Blackman1, Tebeb Gebretsadik2, Marie Griffin3, Ayumi Shintani2, Carolyn May1, Teresa Smith4, Nancy Hooper5, Fernanda Maruri1, Jon Warkentin6, Ed Mitchel3 and Timothy R. Sterling1,7

1 Division of Infectious Diseases and 7 Center for Health Services Research, Department of Medicine, 2 Department of Biostatistics, 3 Departments of Preventive Medicine and Medicine, Center for Education and Research on Therapeutics, Vanderbilt University School of Medicine, Nashville, Tennessee; 4 Tennessee Department of Health, Laboratory Services, Nashville, Tennessee; 5 Maryland State Laboratory, Baltimore, Maryland; and 6 Tennessee Department of Health, Nashville, Tennessee

Correspondence and requests for reprints should be addressed to Rose A. Devasia, M.D., M.P.H., Vanderbilt University School of Medicine, Division of Infectious Diseases 1161 21st Avenue, A2209 MCN, Nashville, TN 37232-2582. E-mail: devasiar09{at}gmail.com

Rationale: Fluoroquinolones are the most commonly prescribed antibiotic class in the United States. They have the potential to become first-line antituberculosis therapy, but the effect of fluoroquinolone use on fluoroquinolone resistance in Mycobacterium tuberculosis is not well characterized.

Objectives: To determine the prevalence of and risk factors for fluoroquinolone-resistant tuberculosis in a large United States population.

Methods: We identified all people with culture-confirmed tuberculosis enrolled in TennCare (Medicaid) and reported to the Tennessee Department of Health from January 2002 to December 2006. People with fluoroquinolone-resistant M. tuberculosis isolates (cases) were compared with those with susceptible isolates (control subjects). Fluoroquinolone resistance was determined by agar proportion using ofloxacin 2 µg/ml. Outpatient fluoroquinolone exposure in the 12 months before tuberculosis diagnosis was ascertained from TennCare pharmacy data.

Measurements and Main Results: Of 640 study patients, 116 (18%) had fluoroquinolone exposure in the 12 months before diagnosis, and 16 (2.5%; 95% confidence interval [CI], 1.4–4.0%) M. tuberculosis isolates were fluoroquinolone resistant. Among the 54 patients with more than 10 days of fluoroquinolone exposure, 7 (13%) had fluoroquinolone resistance. In multivariable logistic regression analyses using propensity score to control for age, sex, race, HIV serostatus, and site of disease, more than 10 days of fluoroquinolone exposure before tuberculosis diagnosis was associated with fluoroquinolone resistance (odds ratio 7.0; 95% CI, 2.3–20.6; P = 0.001). Fluoroquinolone exposure for more than 10 days that occurred more than 60 days before tuberculosis diagnosis was associated with the highest risk of resistance (20.8%; odds ratio 17.0; 95% CI, 5.1–56.8; P < 0.001 compared with no exposure).

Conclusions: Overall, fluoroquinolone resistance was relatively low. However, receipt of fluoroquinolones for more than 10 days, particularly more than 60 days before tuberculosis diagnosis, was associated with a high risk of fluoroquinolone-resistant tuberculosis.

Key Words: drug resistance • mycobacteria • antibacterial


AT A GLANCE COMMENTARY

Scientific Knowledge on the Subject
The effect of fluoroquinolone use on its resistance in Mycobacterium tuberculosis is not well characterized.

What This Study Adds to the Field
Although overall prevalence of fluoroquinolone-resistant tuberculosis was low, receipt of fluoroquinolones for more than 10 days, particularly more than 60 days before the diagnosis of tuberculosis, was associated with a high risk of fluoroquinolone-resistant tuberculosis.

 

Related articles in AJRCCM:

How Are We Creating Fluoroquinolone-resistant Tuberculosis?
John Bernardo and Wing Wai Yew
AJRCCM 2009 180: 288-289. [Full Text]  






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