Volume 24, Issue 5 pp. 636-642

Lower risk of urinary tract infection with low-dose trimethoprim/sulfamethoxazole compared to dapsone prophylaxis in older renal transplant patients on a rapid steroid-withdrawal immunosuppression regimen

Jeffrey Allen Giullian

Jeffrey Allen Giullian

South Denver Nephrology Associates, Denver, CO

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Kerri Cavanaugh

Kerri Cavanaugh

Division of Nephrology, Vanderbilt University Medical Center, Nashville, TN, USA

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Heidi Schaefer

Heidi Schaefer

Division of Nephrology, Vanderbilt University Medical Center, Nashville, TN, USA

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First published: 18 November 2009
Citations: 22
Corresponding author: Jeffrey Giullian, MD, 950 East Harvard Ave, Suite 240, Denver, CO 80210, USA.
Tel.: (303) 871 0977; fax: (303) 733 2387;
e-mail: [email protected]

Abstract

Giullian JA, Cavanaugh K, Schaefer H. Lower risk of urinary tract infection with low-dose trimethoprim/sulfamethoxazole compared to dapsone prophylaxis in older renal transplant patients on a rapid steroid-withdrawal immunosuppression regimen.
Clin Transplant 2009 DOI: 10.1111/j.1399-0012.2009.01129.x
© 2009 John Wiley & Sons A/S.

Abstract: Background: Urinary tract infections (UTI) are common in renal transplant recipients. Trimethoprim/sulfamethoxazole (TMP/SMZ) in moderate to high daily doses prevents Pneumocystis jiroveci (PCP) and reduces the risk of UTI in renal transplant patients. Low-dose TMP/SMZ also reduces the risk of PCP, although its ability to reduce the risk of UTI is uncertain.

Design: Retrospective review of 158 patients who received a renal transplant without corticosteroids for maintenance immunosuppression.

Results: Forty percent of patients initially prescribed TMP/SMZ ultimately stopped this medication early because of an adverse reaction. Urinary infection occurred in 16% without a significant difference in the risk of UTI between those treated with dapsone vs. those treated with TMP/SMZ (HR [95%CI]: 1.7 [0.75, 3.9], p = 0.2). In the subset of patients who were older than age 47 yr (mean age for this cohort, SD ± 6.2 yr), those treated with dapsone originally or who switched from TMP/SMZ to dapsone had a greater risk of UTI compared to patients who remained on TMP/SMZ (HR [95%CI]: 4.3 [1.2, 15.5], p = 0.024).

Conclusions: For renal transplant recipients over the age of 47 yr, treated without long-term glucocorticoids, our retrospective data suggest that low-dose TMP/SMZ is associated with a lower risk of UTI compared to dapsone prophylaxis.

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