The American public health agency, the Centers for Disease
Prevention and Control (CDC), today released guidelines for the use of Truvada by HIV-negative gay and bisexual
men wishing to reduce their risk of HIV infection. While the CDC highlights a
number of uncertainties and concerns about pre-exposure prophylaxis (PrEP),
they have issued their ‘interim guidance’ just two months after the first
positive results of a research trial into the approach.
They have done this, they say, because: “Concerns exist
that without early guidance, various unsafe and potentially less effective
PrEP-related practices could develop among health-care providers and MSM
beginning to use PrEP in the coming weeks and months.”
Prescriptions should only be given for 90 days at a time, with HIV
testing, adherence counselling, sexually transmitted infection check-ups,
sexual risk counselling and condoms provided before new prescriptions are
issued.
The guidelines state that PrEP should only be provided for men who
have sex with men, specifically those who are “at substantial, ongoing, high
risk for acquiring HIV infection”.
Pre-exposure prophylaxis involves HIV-negative people taking
antiretroviral medications in order to reduce their risk of acquiring HIV. In
November, a study conducted with gay and bisexual men in six countries showed
that daily use of the two drugs tenofovir and FTC (combined in one pill as Truvada) reduced the risk of infection
by 44%. However many of the gay and bisexual men participating in the trial did
not take the pills each day, as prescribed. In men who did take the drugs
consistently, results seemed to be much better. In men with very poor
adherence, results were worse.
However extensive analysis of the adherence data from the trial
has not yet been completed, nor have the trial results been replicated in other
settings.
The CDC only endorses a model of Truvada prescribing that is very close to that carried out in the
trial setting. That is why its use is limited to high-risk gay and bisexual men.
The guidance gives quite a broad indication of which men PrEP may
be suitable for, citing only lack of condom use in combination with “frequent
partner change or concurrent partners in a geographic setting with high HIV
prevalence” as examples.
The CDC says that antiretrovirals other than Truvada should not be used for PrEP and that the same daily dosing
schedule that was employed in the trial must be followed. Therefore,
‘intermittent’ dosing (i.e., before or after sex) is not endorsed.
Moreover adherence support must be a “routine component of any
PrEP program”. It should be provided before PrEP is issued, and then at least
every 90 days.
Similarly, PrEP should only be delivered “as part of a
comprehensive set of prevention services” that includes risk-reduction
counselling, ready access to condoms and the diagnosis and treatment of
sexually transmitted infections. These activities should take place each 90
days, before a new prescription is issued.
Before PrEP is provided, clinicians must also check that the
patient is HIV-negative. If he has any signs or symptoms that may be linked to
HIV seroconversion, RNA testing is recommended. He must also be screened for
sexually transmitted infections and hepatitis B, and have his kidney function
assessed (Truvada can sometimes harm
the kidneys).
Other tests for side-effects are required after three months and
then annually. Any serious adverse events should be reported to the Food &
Drug Administration (FDA).
Cost remains a central concern. As Truvada is only approved by the FDA for the treatment of HIV and
not its prevention, insurance companies are unlikely to pay for PrEP. Doctors
are allowed to prescribe it if men have the means to pay for it themselves. A
month’s supply of the drug costs around $1000, to which must be added the costs
of counselling, side-effects monitoring and medical appointments.
The CDC’s document provides ‘interim guidance’. Further
guidelines, with more involvement from stakeholders, are in the process of
being developed.