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

for the main comparison.

Antagonist‐induced compared to conventional for opioid withdrawal
Patient or population: patients with opioid withdrawal
Settings:
Intervention: Antagonist‐induced
Comparison: conventional
Outcomes Illustrative comparative risks* (95% CI) Relative effect 
 (95% CI) No of Participants 
 (studies) Quality of the evidence 
 (GRADE) Comments
Assumed risk Corresponding risk
  conventional Antagonist‐induced        
Number completing detoxification Medium risk population RR 1.42 
 (1.09 to 1.84) 100 
 (2) ⊕⊕⊝⊝ 
 low1,2  
576 per 1000 818 per 1000 
 (628 to 1060)
Number commencing naltrexone maintenance treatment ‐ Clonidine comparison Medium risk population RR 4.28 
 (2.91 to 6.3) 240 
 (3) ⊕⊕⊕⊝ 
 moderate2  
177 per 1000 758 per 1000 
 (515 to 1115)
Number commencing naltrexone maintenance treatment ‐ Buprenorphine comparison Medium risk population RR 1.29 
 (1.04 to 1.6) 72 
 (1) ⊕⊕⊕⊝ 
 moderate2  
730 per 1000 942 per 1000 
 (759 to 1168)
Retained in naltrexone maintenance treatment or abstinent at 12 weeks ‐ Tapered methadone comparison Medium risk population RR 2 
 (0.9 to 4.45) 30 
 (1) ⊕⊕⊝⊝ 
 low1,2  
333 per 1000 666 per 1000 
 (300 to 1482)
Retained in naltrexone maintenance treatment or abstinent at 12 weeks ‐ Clonidine comparison Medium risk population RR 2.77 
 (1.37 to 5.61) 240 
 (3) ⊕⊕⊕⊝ 
 moderate2  
88 per 1000 244 per 1000 
 (121 to 494)
Retained in naltrexone maintenance treatment or abstinent at 12 weeks ‐ Buprenorphine comparison Medium risk population RR 0.82 
 (0.34 to 1.97) 72 
 (1) ⊕⊕⊕⊝ 
 moderate2  
243 per 1000 199 per 1000 
 (83 to 479)
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). 
 
 CI: Confidence interval; RR: Risk ratio;
GRADE Working Group grades of evidance 
 High quality: Further research is very unlikely to change our confidence in the estimate of effect. 
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. 
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. 
 Very low quality: We are very uncertain about the estimate.

1 One study at high risk of allocation bias.

2 Less than 300 events