The American Journal of Medicine
Volume 121, Issue 10 , Pages 903-908 , October 2008

Primary Syphilis: Serological Treatment Response to Doxycycline/Tetracycline versus Benzathine Penicillin

  • Tom Wong, MD, MPH

      Affiliations

    • Centre for Infectious Disease Prevention and Control, Public Health Agency of Canada, Ottawa, Ontario, Canada
  • ,
  • Ameeta E. Singh, BMBS, MSc

      Affiliations

    • Alberta Health and Wellness, Edmonton, Canada
    • Department of Medicine, University of Alberta, Edmonton, Canada
    • Corresponding Author InformationRequests for reprints should be addressed to Ameeta Singh, BMBS, MSc, Infectious Diseases Consultant, Alberta Health and Wellness, P.O. Box 1360 Stn Main, 10025 Jasper Ave., Edmonton, AB T5J 2N3, Canada
  • ,
  • Prithwish De, MHSc, PhD

      Affiliations

    • Department of Epidemiology and Biostatistics, McGill University, Montreal, Quebec, Canada

  • Image Result

    Case selection for analysis and treatment protocol for all first-time primary syphilis cases reported in Alberta, Canada, 1980-2001.

    Case selection for analysis and treatment protocol for all first-time primary syphilis cases reported in Alberta, Canada, 1980-2001.

  • Image Result

    Serological treatment success according to treatment with benzathine penicillin G or doxycycline/tetracycline. Note: Serological treatment success was defined as a decrease in the baseline rapid plasm

    Serological treatment success according to treatment with benzathine penicillin G or doxycycline/tetracycline. Note: Serological treatment success was defined as a decrease in the baseline rapid plasma reagin test titer since treatment initiation by ≥4-fold by 6 months, or ≥8-fold decrease within 12 months, or ≥16-fold decrease within 24 months. If rapid plasma reagin test titer was 1:4, 1:2, or 1:1 at baseline, a serofast stable serology (ie, ±1 dilution from baseline) between 6 months and 12 months (184 days to 365 days) of treatment initiation also was considered treatment success. Treatment was considered to have failed if none of the above conditions were met, including if the rapid plasma reagin test titer increased from baseline by at least 4-fold between 1 month and 6 months (31 days to 183 days).

 This study was supported by funding from Alberta Health and Wellness and from the Public Health Agency of Canada, and approved by the University of Alberta Health Research and Ethics Board.

PII: S0002-9343(08)00610-4

doi: 10.1016/j.amjmed.2008.04.042

The American Journal of Medicine
Volume 121, Issue 10 , Pages 903-908 , October 2008