Successful prevention of syphilis infection with azithromycin in both HIV-negative and HIV-positive individuals, San Francisco, 1999-2003. - PowerPoint PPT Presentation

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Successful prevention of syphilis infection with azithromycin in both HIV-negative and HIV-positive individuals, San Francisco, 1999-2003.

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Title: Successful prevention of syphilis infection with azithromycin in both HIV-negative and HIV-positive individuals, San Francisco, 1999-2003.


1
Successful prevention of syphilis infection with
azithromycin in both HIV-negative and
HIV-positive individuals, San Francisco,
1999-2003.
  • J. D. Klausner,1,2 K. Steiner,1 R. Kohn11San
    Francisco Dept Public Health, San Francisco, CA
    2University of California, San Francisco, San
    Francisco, CA.

2
Background Syphilis trends in San Francisco
3
Background Current syphilis epidemic in San
Francisco
4
BackgroundPrevious studies on azithromycin and
syphilis
  • Hook EW, Stephens J, Ennis DM, Ann Intern Med,
    1999
  • randomized trial of 1 gram azithromycin vs. 2.4
    mu benzathine penicillin for incubating disease
  • no reactive FTA-ABS at 3 months in either group
  • Hook EW et al., Sex Trans Dis, 2001
  • RCT of azithromycin vs. benzathine penicillin for
    syphilis cases
  • 2 grams of azithromycin as effective as
    benzathine penicillin for treating disease

5
BackgroundSyphilis treatment in San Francisco
  • Contacts new cases versus epi treatment
  • 2.4 mu benzathine penicillin G I.M. (bicillin)
  • 100 mg doxycycline P.O. BID for 14 days
  • 1 gram azithromycin P.O.
  • Field-delivered therapy with Azithromycin began
    March, 1999

6
Objective
  • Compare observed success in treating incubating
    syphilis using azithromycin to success with other
    treatments in order to justify continued use of
    azithromycin

7
MethodsSan Francisco STD Registry
  • STD clinic medical record data
  • Reported morbidity and reactive STS
  • Interview data and field activity
  • Screening data

8
Methods Sample
  • Data from 1999 through 2003
  • Non-reactive RPR or VDRL with any syphilis
    treatment (n3812)
  • Follow-up titer between 30 and 90 days after
    initial titer (n151)

9
Methods Measurements
  • Outcome any reactive titer defines treatment
    failure
  • Biological false positives excluded from analysis
  • HIV status measured from multiple sources,
    including self-reported status

10
ResultsAll patients
11
Results By HIV Status
12
Conclusions
  • Failure rate for azithromycin was not
    significantly greater than rate for bicillin
  • Since no resistance to bicillin has been
    documented, apparent treatment failures likely
    indicate re-exposure
  • Success in treatment did not vary between
    HIV-negative and HIV-positive clients

13
Limitations
  • No way to distinguish treatment failure from
    re-exposure
  • Not all exposed will develop disease
  • No randomization
  • penicillin allergies
  • field versus clinic
  • Small number of follow-up titers
  • Wide confidence limits for negative results

14
Limitations
  • No power to assess temporal trends
  • Azithromycin epi-treatment failures
  • November 2002
  • April 2003
  • July 2003
  • Bicillin epi-treatment failure
  • April 1999

15
Further research
  • Another randomized trial of azithromycin vs.
    bicillin
  • HIV-positive clients only
  • San Francisco Los Angeles
  • Five years later than 1999 study by Hook

16
Thank you ...
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