Interim medication-only
treatment has been suggested for the initiation of opioid maintenance treatment
(OMT) in opioid-dependent subjects, but this rarely has been studied using
buprenorphine instead of methadone. Following a pilot trial assessing interim
buprenorphine-naloxone treatment in order to facilitate transfer into OMT, we
here aimed to study retention, and potential correlates of retention, in
full-scale treatment. Thirty-six patients successfully referred from a waiting
list through an interim treatment phase were followed for nine months in OMT.
Baseline characteristics, as well as urine analyses during the interim phase
and during full-scale OMT, were studied as potential correlates of retention.
The nine-month retention in OMT was 83 percent (n = 30). While interim-phase
urine samples positive for benzodiazepines did not significantly predict
dropout from full-scale OMT (p =
0.09), urine samples positive for benzodiazepines within full-scale OMT were
significantly associated with dropout (p < 0.01), in contrast to
other substances and baseline characteristics. Retention remained high through
nine months in this pilot study sample of patients referred through
buprenorphine-naloxone interim treatment, but use of benzodiazepines is
problematic, and the present data suggest that it may be associated with
treatment dropout.
…The use of
benzodiazepines during interim treatment and during full-scale OMT was the only
variable associated with dropout in the present study. Although the number of
dropouts in this pilot study was low, urines positive for benzodiazepines in the
interim condition tended to be associated with a negative outcome once referred
to the full-scale program but did not reach statistical significance (p = 0.09). However, significantly, a
negative outcome in full-scale OMT was associated with the use of benzodiazepines
within that OMT treatment setting, which was not the case for any other
substance, suggesting that benzodiazepines may play a major role in the
clinical picture of patients with a negative treatment course in opioid
dependence.
The seemingly negative association between
retention and benzodiazepine use during treatment of opioid dependence may
require further attention in research and in clinical practice. In the present
study, at baseline, the frequency of use of benzodiazepines was comparable to
that of the main drug of these primarily opioid-dependent subjects. In contrast
to the high rates of continued benzodiazepine use, urine samples positive for
opiates were very infrequent in the full-scale OMT phase, markedly lower than
in many other studies [35,36], and
opioid-positive urines were not associated with dropout in OMT. The role of
benzodiazepines in the present results, compared to the role of opioids,
strengthens the impression that polydrug use, particularly including the use of
benzodiazepines, may present a potentially even larger challenge in the treatment
of severe opioid dependence than the actual primary opioid-related disorder.
Patients with a high level of benzodiazepine use
could represent a group with more complicated psychiatric problems and more
severe substance-related problems [29, 37]. In the present
study, patients dropping out of treatment did not report more use of
benzodiazepines during the last 30 days prior to study start, but still, this
type of substance use was associated with a negative outcome once in full-scale
treatment. It cannot be excluded that intake of benzodiazepines actually
increases when the intake of illicit opioids decreases in treatment, at least
in a subset of individuals…
Full article at: http://goo.gl/7QXGbu
By: A. Håkansson, 1 , 2 , * C. Widinghoff, 1 , 2 T. Abrahamsson, 1 , 2 and C. Gedeon 1 , 3
1Department of Clinical Sciences Lund,
Division of Psychiatry, Lund University, 221 85 Lund, Sweden
2Malmö Addiction Center, Department of
Psychiatry, 205 02 Malmö, Skane Region, Sweden
3Solstenen Outpatient Unit for Opiate
Maintenance Treatment, Östra Mårtensgatan 15, 223 61 Lund, Sweden
*A. Håkansson: Email: es.ul.dem@nossnakah.c_sredna
Academic Editor: Dennis M. Donovan
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