Current guidelines for the treatment of syphilis in patients
with HIV are based on limited clinical data, investigators show in the online
edition of Sexually Transmitted
Infections.
Even though their systematic review had broad inclusion
criteria, they were only able to identify 23 studies examining the outcomes of
HIV-positive patients treated for syphilis. Only two of these studies were
rated as “high quality” by the investigators.
Rates of treatment failure varied considerably, and were as
high as 31% for latent syphilis. However, the investigators believe that
confounding factors rather than the poor efficacy of treatment are the likely
explanation for this.
Since its development the 1940s, penicillin has remained the
favoured treatment for syphilis. Current UK and US guidelines recommend that
the infection should be treated with intramuscular injection of long-lasting
benzathine penicillin G. The oral antibiotic doxycycline is an alternative
therapy for patients with allergy to penicillin.
Azithromycin is another oral
antibiotic that is also active against syphilis. However, its routine use is
not recommended because the Street 14 strain of syphilis is naturally resistant
to this antibiotic. For patients with neurosyphilis, high-dose intravenous
aqueous crystalline penicillin if the preferred therapy.
Current US guidelines recommend the same therapies for
HIV-positive patients, but with more intensive follow-up.
Nevertheless, there is uncertainty about the best treatment
for syphilis for patients with HIV. Indeed, a survey of US doctors revealed
that two-thirds used non-standard treatments for this group of patients. There
are also anecdotal reports from the UK of HIV-positive patients with high CD4
cell counts and early syphilis being treated with 14 days of intramuscular
injections, a therapy that is likely to involve considerable inconvenience and
discomfort for patients.
Because of this uncertainty, investigators from Baltimore
systematically reviewed the literature regarding syphilis treatment for patients
with HIV.
They set broad inclusion criteria:
·
Syphilis diagnosis made on the basis of
serology or microscopy.
·
Studies involved ten or more patients, at least
one of which was HIV-positive.
·
The HIV status of patients was known at or near
(within a year) of the syphilis diagnosis.
·
Both the type and duration of antibiotic therapy
were documented.
·
Outcomes were reported at least six months after
treatment for early syphilis and twelve months after the completion of therapy
for late latent and neurosyphilis.
Their initial literature search identified 1380 studies.
However, only 23 met their inclusion criteria, and just two of these studies
were deemed to be of good quality.
“Our study entry criteria were not overly restrictive. In
fact, we chose criteria that would allow for the least restrictive clinically
meaningful interpretation of the data”, comment the investigators.
They continue, “even high-quality randomised trials did not
evaluate the efficacy of syphilis treatment in HIV-positive patients as their
primary outcome.”
The failure rates of treatment for early syphilis ranged
from 7% to 22%. The failure rate of therapy for latent syphilis ranged from 19%
to 31%, and between 27% and 28% of patients did not respond to treatment for
neurosyphilis.
“Of the studies summarised…only a few had HIV-uninfected
controls”, note the authors. Although these studies HIV-positive patients were
more likely to experience treatment failure than HIV-negative patients, “most
comparisons were not statistically significant owing to small numbers.”
Historically, failure rates of penicillin treatment for
early and latent syphilis in HIV-negative patients range between 3% and 10%.
Although the investigators consider the possibility that
this treatment is less effective in patients with HIV, they believe that there
are other explanations for the high failure rates seen in the studies.
Follow-up in most of the studies was below the 24 months
recommended in guidelines, and “this might have inflated the rates of
seriological failure.”
Underlying cerebrospinal fluid abnormalities unrelated to
syphilis may also have complicated the interpretation of results for the
outcome of neurosyphilis. “The main clinical measure of syphilis disease
activity, serological titres, are not specific for treponemes and may not
reflect the underlying microbiology”, note the researchers.
The authors conclude that the best treatment for syphilis
for HIV-positive patients is unknown. Therefore, “any guideline recommendations
in this population are ultimately based on limited objective data.”