Current Trends -- Recommendations for Diagnosing and Treating
Syphillis in HIV-Infected Patients
The clinical manifestations, serologic responses, efficacy of
treatment, and occurrence of complications of syphilis may be
altered
in patients coinfected with human immunodeficiency virus (HIV).
Because
syphilis is a disease with a broad range of manifestations and
variable
course, assessing reports of unusual clinical or lab- oratory
findings
in HIV-coinfected patients is difficult (1). On March 21 and 22,
1988,
experts* from academic medical centers and state and local health
departments met at CDC to discuss the diagnosis and treatment of
syphilis in HIV-infected patients. The following recommendations
were
developed based on these discussions.
DIAGNOSIS OF SYPHILIS IN HIV-INFECTED PATIENTS
Most HIV-infected patients appear to have a normal serologic
response
to Treponema pallidum infection (2). However, in some HIV-infected
patients with biopsy- confirmed secondary syphilis, both
nontreponemal
and treponemal tests for syphilis are negative (3). In addition,
some
patients infected with both T. pallidum and HIV have had unusually
high
titers on nontreponemal serologic tests for syphilis (CDC,
unpublished
data, 1987-88), possibly because of HIV-related polyclonal B-cell
stimulation. The frequency of unusual clinical and laboratory
manifestations of syphilis in patients coinfected with HIV is
unknown.
Recommendations
Persons with HIV infection acquired through sexual contact or
intravenous (IV)- drug abuse should be tested for syphilis, and all
sexually active persons with syphilis should be tested for HIV
(with
the informed consent of the patient). HIV test results are
clinically
important in managing patients with syphilis and, with appropriate
confidentiality safeguards, should be made available to medical
per-
sonnel who care for these patients.
When clinical findings suggest syphilis is present, but
serologic
tests are negative, other tests should be used to determine if
syphilis
is present. These tests include dark-field microscopy and direct
fluorescent antibody for T. pallidum (DFA-TP) staining of lesion
exudate and examination of biopsy tissue using DFA-TP or Steiner
stain
(4).**
Laboratories should titrate nontreponemal tests to a final
endpoint,
rather than reporting results as greater than an arbitrary cutoff
(e.g.,greater than 1:512). Specific results permit more accurate
determination of response to therapy and also help identify unusual
serologic responses to syphilis.
Neurosyphilis should be considered in the differential diagnosis
of
neurologic disease in HIV-infected persons.
Consultation should be obtained to evaluate unusual serologic
test
results in patients suspected of having syphilis or in those being
followed for response to treatment.
TREATMENT AND FOLLOW-UP
Case reports have suggested that treatment failures, including
progression to neurosyphilis, may occur more frequently in patients
coinfected with HIV than in those with syphilis alone (5,6). This
has
not yet been confirmed, but because an intact cellular immune
response
is important in the host response to T. pallidum infection (7) and
because HIV infection impairs cellular immune response in some
patients, an increased frequency of treatment failure is plausible.
Recommended treatment schedules for neurosyphilis have included
benzathine penicillin (8), although treatment with benzathine
penicillin in currently recommended dosages does not achieve
treponemicidal antibiotic levels in the cerebrospinal fluid (CSF)
of
most patients with syphilis, and rare treatment failures have been
reported (9-11).
Recommendations
No change in therapy for early syphilis for HIV-coinfected
patients
is recommended. However, there is disagreement on this issue, and
some
authorities have advised CSF examination and/or treatment with a
regimen appropriate for neurosyphilis for all patients coinfected
with
syphilis and HIV, regardless of the clinical stage of syphilis
(12). In
all cases, careful follow-up is necessary to assure adequacy of
treatment.
Serologic testing after treatment for early syphilis is
important
for all patients, regardless of HIV infection status. In patients
coinfected with HIV, quantitative nontreponemal tests should be
repeated at 1, 2, and 3 months and at 3-month intervals thereafter
until a satisfactory serologic response to treatment occurs. If the
titer does not decrease appropriately (two-dilution decrease by 3
months for primary syphilis or by 6 months for secondary syphilis)
(13)
or if a sustained two-dilution or greater increase occurs, the
patient
should be reevaluated to consider the possibility of treatment
failure
or reinfection, and CSF should be examined. Sexually transmitted
disease (STD) clinics and others providing STD treatment should
assure
adequate follow-up.
A CSF examination should precede and guide treatment of
HIV-infected
patients with latent syphilis present for longer than 1 year or for
unknown duration. If an examination is not possible, patients
should be
treated for presumed neuro- syphilis.
Benzathine penicillin regimens should not be used to treat
either
asymptomatic or symptomatic neurosyphilis in HIV-infected patients.
Patients should be treated for at least 10 days with either aqueous
crystalline penicillin G, 2-4 million units IV every 4 hours (12-24
million units each day), or aqueous procaine penicillin G, 2.4
million
units intramuscularly daily, plus probenecid 500 mg orally 4 times
daily (8).
Reported by: Div of Sexually Transmitted Diseases, Center for
Prevention Svcs; AIDS Program and Sexually Transmitted Diseases
Laboratory Program, Center for Infectious Diseases, CDC.
Editorial Note
Editorial Note: The expert consultants also highlighted the
following
research priorities related to the diagnosis and treatment of
syphilis
in HIV-coinfected patients:
The effect of HIV infection on initial clinical and laboratory
manifestations of syphilis and on the efficacy of current syphilis
therapy should be prospectively studied.
A surveillance system should be developed to detect
complications of
syphilis, especially neurosyphilis, and unusual clinical and
laboratory
manifestations of syphilis in patients with and without
HIV-coinfection.
The importance of CNS involvement in early syphilis should be
determined in patients with and without HIV coinfection.
Better laboratory methods should be developed for detecting T.
pallidum or T. pallidumantigens in CSF, blood, and lesions.
A better animal model of T. pallidum infection is needed to
examine
the effect of immunosuppression on the course of syphilis.
So that the frequency of unusual manifestations of syphilis can be
determined, health-care providers are requested to notify their
state
epidemiologists of HIV- infected patients who meet one of the
following
conditions:
Neurosyphilis confirmed by CSF examination or histopathology;
Negative serologic tests for syphilis (nontreponemal (VDRL, RPR)
or
treponemal (FTA-ABS, MHA-TP, HATTS) tests) during secondary
syphilis
diagnosed by dark- field microscopy or histopathology of lesion
material.
The state epidemiologists will forward these reports without
personal
identifiers to the Division of Sexually Transmitted Diseases,
Center
for Prevention Services, CDC.
References
Beck-Sague CM, Alexander ER, Jaffe HW. Neurosyphilis and HIV
infection (Letter). N Engl J Med 1987;317:1473.
Schultz S, Araneta MRG, Joseph SC. Neurosyphilis and HIV
infection
(Letter). N Engl J Med 1987;317:1474.
Hicks CB, Benson PM, Lupton GP, Tramont EC. Seronegative
secondary
syphilis in a patient infected with the human immunodeficiency
virus
(HIV) with Kaposi sarcoma: a diagnostic dilemma. Ann Intern Med
1987;107:492-4.
Swisher BL. Modified Steiner procedure for microwave staining of
spirochetes and nonfilamentous bacteria. J Histotechnol
1987;10:241-3.
Berry CD, Hooton TM, Collier AC, Lukehart SA. Neurologic relapse
after benzathine penicillin therapy for secondary syphilis in a
patient
with HIV infection. N Engl J Med 1987; 316:1587-9.
Johns DR, Tierney M, Felsenstein D. Alteration in the natural
history of neurosyphilis by concurrent infection with the human
immunodeficiency virus. N Engl J Med 1987; 316:1569-72.
Pavia CS, Folds JD, Baseman JB. Cell-mediated immunity during
syphilis: a review. Br J Vener Dis 1978;54:144-50.
Greene BM, Miller NR, Bynum TE. Failure of penicillin G
benzathine
in the treatment of neurosyphilis. Arch Intern Med 1980;140:1117-8.
Mohr JA, Griffiths W, Jackson R, Saadah H, Bird P, Riddle J.
Neurosyphilis and penicillin levels in cerebrospinal fluid. JAMA
1976;236:2208-9.
Cuddy PG. Benzathine penicillin G in the treatment of
neurosyphilis. Drug Intell Clin Pharm 1982;16:205-10.
Tramont EC. Syphilis in the AIDS era. N Engl J Med
1987;316:1600-1.
Brown ST, Zaidi A, Larsen SA, Reynolds GH. Serological response
to
syphillis treatment: a new analysis of old data. JAMA
1985;253:1296-9.
*Expert consultants: M Rein, MD, Univ of Virginia School of
Medicine; G
Bolan, MD, San Francisco Dept of Public Health; W Boyd, Georgia
Dept of
Human Resources; D Burke, Tennessee Dept of Health and Environment;
W
Greaves, MD, Howard Univ Hospital; V Mesa, MD, Detroit Dept of
Health;
E Hook, III, MD, Johns Hopkins Univ School of Medicine; J Hadler,
MD,
Connecticut State Dept of Health Svcs; D Des Jarlais, PhD, State of
New
York Div of Substance Abuse Svcs; S Lukehart, PhD, Univ of
Washington
School of Medicine; M Lovett, MD, Univ of California, Los Angeles,
School of Medicine; R Magana, PhD, Orange County (California)
Health
Dept; W McCormack, MD, Downstate Medical Center, Brooklyn, New
York; S
Schultz, MD, New York City Dept of Health; E Tramont, MD, Walter
Reed
Army Medical Center; H Jaffe, MD, CDC.
**In evaluating biopsy specimens, histologic stains (Warthin Starry
Silver, Steiner) must be interpreted with caution since other
spirochetes and artifacts may be misidentified as T. pallidum with
these silver stains.
Disclaimer
All MMWR HTML documents published before January 1993 are electronic conversions from ASCII text into HTML. This conversion may have resulted in character translation or format errors in the HTML version. Users should not rely on this HTML document, but are referred to the original MMWR paper copy for the official text, figures, and tables. An original paper copy of this issue can be obtained from the Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact GPO for current prices.
**Questions or messages regarding errors in formatting should be addressed to [email protected].
