Cocaine users have poorer adherence to HIV pre-exposure prophylaxis (PrEP)
and engagement with care, according to research published in the online edition of the Journal
of Acquired Immune Deficiency Syndromes. Even light cocaine use doubled the
odds of having blood levels of tenofovir, a key PrEP drug, that were
insufficient to protect against infection with HIV. Individuals with
moderate/heavy cocaine use were three times more likely to drop out of PrEP
care than individuals who did not use cocaine.
“These findings
underscore the importance of providing comprehensive care at the time of PrEP
initiation that includes assessment of cocaine use and other potential barriers
to optimal adherence,” comment the investigators. “Expanded efforts are needed
to assist persons who use cocaine with completing routine follow-up visits that
allow for regular monitoring and present an opportunity to support adherence,
discuss risk reduction, and address co-occurring stimulant use.”
Providers have reported that a
significant proportion of PrEP users drop out of care. Little is known about the
association between the use of stimulant drugs such as cocaine and adherence to
PrEP and retention in PrEP programmes. This is an important gap in knowledge as
stimulant use is increasing among men who have sex with men (MSM), with a recent study showing
that a quarter of MSM in San Francisco used cocaine in the previous three
months.
Investigators therefore designed a study which analysed data from 400 MSM and
transgender women who took PrEP as part of the iPrEx OLE study.
Cocaine use was
measured by establishing measuring concentrations of the drug in hair
samples at the first quarterly study visit. Hair analysis indicates drug use in the previous three months. Cocaine levels between 500-3000ph/mg
corresponded to light use (perhaps once or twice a month), with concentrations above this level indicating
moderate or heavy use of the drug (perhaps weekly to daily use).
Blood concentrations
of tenofovir were assessed in the first three months after starting PrEP. The
adherence outcome was blood concentration of the medication below the level of
quantification. This was selected because levels of tenofovir above this are associated with greater than 90% protection against infection with HIV.
The study
population consisted of 358 MSM (90%) and 42 transgender women (10%).
Three-quarters were Hispanic/Latino and the median age at PrEP initiation was
29 years.
Just over a fifth
(21%) of participants tested positive for recent cocaine use. The median
concentration was 2513pg/mg. Of those with evidence of cocaine use, there was
an approximately 50-50 split between light (52%) and moderate/heavy (48%)
users.
A quarter of
participants had blood concentrations of tenofovir below the level of
quantification in the first three months of therapy. After taking into account
factors such as age, ethnicity and transgender status, individuals with
evidence of light (aOR = 2.10; 95% CI, 1.07-4.14) or moderate/heavy (aOR =
2.32; 95% CI, 1.08-5.00) cocaine use were significantly more likely to have undetectable
levels of tenofovir than individuals with no evidence of cocaine use.
“We found that
cocaine use at any level was associated with lower odds of achieving
prevention-effective adherence in the first three months after starting PrEP,”
note the authors. “The first few months following PrEP initiation is a
particularly critical period as adherence during this time is predictive of
future adherence patterns.”
A total of 60
participants (15%) dropped out of care (had a four-month gap in follow-up). In adjusted analysis,
individuals with evidence of moderate/heavy cocaine were three times more
likely to drop out of care compared to individuals who didn’t use cocaine (aHR
= 2.90; 95% CI, 1.48-5.66).
Cocaine use has
been associated with kidney damage, which is also a possible side-effect of
tenofovir. Creatinine clearance was therefore analysed in participants and
compared according to evidence of cocaine use. However, there was no evidence
that taking cocaine increased the risk of renal toxicity.