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Meta-Analysis
. 2010 Jan 20;2010(1):CD002022.
doi: 10.1002/14651858.CD002022.pub3.

Opioid antagonists under heavy sedation or anaesthesia for opioid withdrawal

Affiliations
Meta-Analysis

Opioid antagonists under heavy sedation or anaesthesia for opioid withdrawal

Linda Gowing et al. Cochrane Database Syst Rev. .

Abstract

Background: Withdrawal (detoxification) is necessary prior to drug-free treatment or as the end point of long-term substitution treatment.

Objectives: To assess the effectiveness of opioid antagonists to induce opioid withdrawal with concomitant heavy sedation or anaesthesia, in terms of withdrawal signs and symptoms, completion of treatment and adverse effects.

Search strategy: We searched the Cochrane Central Register of Controlled Trials (The Cochrane Library, Issue 3, 2009), Medline (January 1966 to 11 August 2009), Embase (January 1985 to 2009 Week 32), PsycINFO (1967 to July 2009), and reference lists of articles.

Selection criteria: Controlled studies of antagonist-induced withdrawal under heavy sedation or anaesthesia in opioid-dependent participants compared with other approaches, or a different regime of anaesthesia-based antagonist-induced withdrawal.

Data collection and analysis: One reviewer assessed studies for inclusion, undertook data extraction and assessed quality. Inclusion decisions and the overall process were confirmed by consultation between all authors.

Main results: Nine studies (eight randomised controlled trials) involving 1109 participants met the inclusion criteria for the review.Antagonist-induced withdrawal is more intense but less prolonged than withdrawal managed with reducing doses of methadone, and doses of naltrexone sufficient for blockade of opioid effects can be established significantly more quickly with antagonist-induced withdrawal than withdrawal managed with clonidine and symptomatic medications. The level of sedation does not affect the intensity and duration of withdrawal, although the duration of anaesthesia may influence withdrawal severity. There is a significantly greater risk of adverse events with heavy, compared to light, sedation (RR 3.21, 95% CI 1.13 to 9.12, P = 0.03) and probably with this approach compared to other forms of detoxification.

Authors' conclusions: Heavy sedation compared to light sedation does not confer additional benefits in terms of less severe withdrawal or increased rates of commencement on naltrexone maintenance treatment. Given that the adverse events are potentially life-threatening, the value of antagonist-induced withdrawal under heavy sedation or anaesthesia is not supported. The high cost of anaesthesia-based approaches, both in monetary terms and use of scarce intensive care resources, suggest that this form of treatment should not be pursued.

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Conflict of interest statement

Two of the authors of this review (LG, RA) were involved in one of the studies (McGregor 2002) included in this review.

Figures

1
1
Methodological quality graph: review authors' judgements about each methodological quality item presented as percentages across all included studies.
2
2
Methodological quality summary: review authors' judgements about each methodological quality item for each included study.
3
3
Forest plot of comparison: 1 Antagonist‐induced vs conventional, outcome: 1.1 Number refusing group allocation or failing to attend.
4
4
Forest plot of comparison: 1 Antagonist‐induced vs conventional, outcome: 1.2 Number completing detoxification.
5
5
Forest plot of comparison: 1 Antagonist‐induced vs conventional, outcome: 1.3 Number commencing naltrexone maintenance treatment.
6
6
Forest plot of comparison: 1 Antagonist‐induced vs conventional, outcome: 1.4 Retained in naltrexone maintenance treatment or abstinent at 12 weeks.
7
7
Forest plot of comparison: 2 Heavy vs light sedation, outcome: 2.1 Participants experiencing adverse effects.
1.1
1.1. Analysis
Comparison 1 Antagonist‐induced vs conventional, Outcome 1 Number refusing group allocation or failing to attend.
1.2
1.2. Analysis
Comparison 1 Antagonist‐induced vs conventional, Outcome 2 Number completing detoxification.
1.3
1.3. Analysis
Comparison 1 Antagonist‐induced vs conventional, Outcome 3 Number commencing naltrexone maintenance treatment.
1.4
1.4. Analysis
Comparison 1 Antagonist‐induced vs conventional, Outcome 4 Retained in naltrexone maintenance treatment or abstinent at 12 weeks.
2.1
2.1. Analysis
Comparison 2 Heavy vs light sedation, Outcome 1 Participants experiencing adverse effects.

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MeSH terms