Handing out drugs to patients you've never met may not
sound like an ideal way to practise medicine. In fact
it sounds downright unethical. But according to researchers
from the University of Washington and the Centers for
Disease Control it could be just the thing to combat partner-to-partner
sexually transmitted infections (STIs) like gonorrhea.
With STI rates threatening to explode
in North America, and with no new treatments available
to break the cycle of reinfection, the group decided
to see what a new model of partner intervention could
achieve. Their research is published in the February
17 issue of the New England Journal of Medicine (NEJM).
BUDDY
SYSTEM
"The current standard approach to gonorrhea and chlamydial
infection is to request that patients themselves notify
their sexual partners, who are then expected to seek
medical evaluation and treatment," write Baltimore specialists
Emily Erbelding and Jonathan Zenilman in an accompanying
NEJM editorial. "This has largely been a failure."
In light of this dismal record,
the researchers set out to evaluate a novel technique
for reaching the partners of patients diagnosed with
these conditions. The plan was simple. Instead of demanding
that sexual partners come in for an embarrassing interview,
the researchers gave 'partner packets' of antibiotics
to patients, or left them for pickup at the clinic reception.
|
CANADIAN STI
RATES PER 100,0000
|
| |
Chlamydia
|
Gonorrhea
|
Syphilis
|
|
1994
|
142
|
21.2
|
0.6
|
|
2004
|
208
|
27.9
|
3.8
|
| Source:
Public Health Agency of Canada (2004 rates projected) |
The trial involved 1,860 heterosexual
patients, who were randomized to either receive the
partner packets or to standard partner referral requiring
a medical evaluation. The primary measure of success
was the reinfection rate among the original patients,
and the partners themselves were never evaluated.
Persistent or recurrent infection
was found in 121 of 931 patients assigned to standard
partner referral (13%), and in 92 of 929 patients randomized
to the 'expedited partner treatment' group (10%). In
other words, patients given antibiotics for their partners
with no questions asked were only 76% as likely to suffer
recurrent infection as those processed in the normal
way.
But almost all of the clinical
benefit was seen in patients with gonorrhea, while chlamydia
patients saw minimal gains. Among gonorrhea patients,
expedited partner treatment led to recurrent or persistent
infection rates of just 3%, compared to 11% in the standard
referral group. The benefit for chlamydia patients was
less spectacular just 11% versus 13%.
ETHICAL
HURDLES
In Canada, reported chlamydia rates are only about half
those seen in the US, but there is little cause for
complacency. After years of decline, rates started rising
in the late 90s and are now on a clear upward path.
Dr Gerald Evans, director of internal
medicine at Queen's University and chief of the division
of infectious diseases at Kingston General Hospital,
thinks the researchers' revolutionary approach to partner
treatment could bring real clinical benefits. But he
predicts the method will face numerous bureaucratic
and ethical hurdles. "Here in Ontario, giving antibiotics
to people without a medical assessment would generally
be considered suboptimal treatment, and falls below
the standards of many guidelines," he says.
Canada and the US have a similar
approach to STIs. In the case of the most serious diseases,
like syphilis and HIV, staff will often make the effort
to locate partners themselves. This is particularly
true of highly-organized STI clinics. But the strain
on resources is immense, and in some areas such efforts
are impossible.
It's precisely those areas with
the fewest services for partners that have the highest
rates of STIs, say the NEJM editorialists. In
the US, no progress has been made towards goals set
in 2000 by the Health Department for reducing infection
rates.
Dr Evans says this selfsame manpower
issue could hamper the efforts of the 'partner packet'
system, were it to be initiated in clinics. "Tracking
down partners is difficult and time-consuming, but the
benefits of reaching more people must be set against
the risks of preventable adverse drug reactions," he
says. "Having said that, these antibiotics are generally
pretty well tolerated, and I notice there were no adverse
reactions in this particular trial. And of course, even
an examination can't guarantee that the potential for
adverse reactions will be spotted."
IMPERFECT
SOLUTION
Dr Evans does have a couple of concerns about the approach.
"Another issue is that we would miss the opportunity
to screen partners for more serious conditions like
HIV," he says. "A final concern is that if people didn't
comply with treatment properly, we would be increasing
antibiotic resistance for little gain. But in this case
they used a single-dose formulation, which at least
eliminates the problem of patients only taking half
their course of antibiotics."
"I think this approach deserves
further investigation, but ideally you'd want to measure
the effect on the partners, as well as the patients
who actually come in. Whatever happens, I think there
would be some persuading to do before this approach
became common in Canada."
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