Cochrane · systematic review · CD002022

Opioid antagonists under heavy sedation or anaesthesia for opioid withdrawal

Gowing, L, Ali, R, White, JM · Cochrane Database of Systematic Reviews · 2010 · Cochrane Library

Drugs and AlcoholAMSTAR 2: not assessed
SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
8
current version
GRADE rated
7
No studies
0
Included studies
NR
No studies 0 · 0%Ungraded 1 · 12.5%Very low 0 · 0%Low 2 · 25%Moderate 5 · 62.5%High 0 · 0%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Questions and results

Comparison

Population: patients with opioid withdrawal
6 questions
OutcomeEffectEvidenceStatus / GRADE
Number completing detoxification
RR 1.42 [1.09, 1.84]2 studies · 100 participantsLow
Downgraded: risk of bias, imprecision
Number commencing naltrexone maintenance treatment ‐ Clonidine comparison
RR 4.28 [2.91, 6.3]3 studies · 240 participantsModerate
Downgraded: risk of bias, imprecision
Number commencing naltrexone maintenance treatment ‐ Buprenorphine comparison
RR 1.29 [1.04, 1.6]1 study · 72 participantsModerate
Downgraded: risk of bias, imprecision
Retained in naltrexone maintenance treatment or abstinent at 12 weeks ‐ Tapered methadone comparison
RR 2 [0.9, 4.45]1 study · 30 participantsLow
Downgraded: risk of bias, imprecision
Retained in naltrexone maintenance treatment or abstinent at 12 weeks ‐ Clonidine comparison
RR 2.77 [1.37, 5.61]3 studies · 240 participantsModerate
Downgraded: risk of bias, imprecision
Retained in naltrexone maintenance treatment or abstinent at 12 weeks ‐ Buprenorphine comparison
RR 0.82 [0.34, 1.97]1 study · 72 participantsModerate
Downgraded: risk of bias, imprecision

Comparison

Population: patients with opioid withdrawal
2 questions
OutcomeEffectEvidenceStatus / GRADE
Participants experiencing adverse effects
RR 3.21 [1.13, 9.12]2 studies · 572 participantsModerate
Less than 300 events
no estimate extracted1 participantsUngraded