Key result
Lofexidine hydrochloride for in-patient opioid detoxification resulted in 37.9% of patients remaining in treatment by day 8, with 16% requiring dose adjustments for hypotension.
Why the study?
Does lofexidine hydrochloride safely and effectively manage opioid withdrawal in an in-patient setting?
Observational (n=190)
Does lofexidine hydrochloride safely and effectively manage opioid withdrawal in an in-patient setting?
Lofexidine is a useful treatment for in-patient opioid detoxification, allowing for rapid induction to higher dosages without widespread hypotensive complications.
Answers are grounded in this paper and cite their sources.
Should not yet change inpatient opioid detox practice; hypothesis-generating for lofexidine retention and safety pending RCTs.
Over a period of 24 months, data were collected on 214 opioid detoxifications (190 patients), based on lofexidine hydrochloride. A mean maximum daily dose of 2.1 mg lofexidine was achieved by day 4 of admission. This was associated with a small fall in systolic and diastolic blood pressure, and 16% patients required adjustment to the daily dose of lofexidine or the withholding of doses. Seventy-five percent of patients were given adjunctive prescription of diazepam, and approximately a half required analgesics. By week I (day 8), 81 (37.9%) patients remained in treatment. Lofexidine appears to be a useful treatment for opioid detoxification, subject to certain limitations, and, despite a more marked reduction in both systolic and diastolic pressure than has previously been reported, hypotension does not appear to limit its usefulness—at least in an in-patient setting. Induction of lofexidine may proceed more rapidly, and to a higher dosage, than currently recommended, without any apparent widespread problems.
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Sheridan et al. (1999) conducted an observational in Opioid withdrawal (n=190). Lofexidine hydrochloride was evaluated on Retention in treatment by week 1 (day 8). Lofexidine hydrochloride for in-patient opioid detoxification resulted in 37.9% of patients remaining in treatment by day 8, with 16% requiring dose adjustments for hypotension.
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