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. 2014 Feb 13;2014(2):CD008544. doi: 10.1002/14651858.CD008544.pub2

Summary of findings for the main comparison. Anticonvulsants versus placebo for alcohol dependence.

Anticonvulsants versus placebo for alcohol dependence
Patient or population: patients with alcohol dependence
 Settings:Intervention: anticonvulsants versus placebo
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No. of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Control Anticonvulsants versus placebo
Dropouts 
 Follow‐up: mean 12 weeks Study population RR 0.94 
 (0.74 to 1.19) 1675
 (16 studies) ⊕⊕⊕⊝
 moderate1  
329 per 1000 309 per 1000 
 (243 to 391)
Moderate
245 per 1000 230 per 1000 
 (181 to 292)
Continuous abstinence 
 Follow‐up: mean 15.5 weeks Study population RR 1.21 
 (0.97 to 1.52) 634
 (eight studies) ⊕⊕⊕⊝
 moderate2  
299 per 1000 362 per 1000 
 (290 to 455)
Moderate
309 per 1000 374 per 1000 
 (300 to 470)
Drinks/drinking day 
 Follow‐up: mean 11.9 weeks   Mean drinks/drinking day in the intervention groups was
 1.49 lower 
 (2.32 to 0.65 lower)   1126
 (11 studies) ⊕⊕⊕⊝
 moderate3  
Heavy drinking 
 Follow‐up: mean 11.2 weeks   Mean heavy drinking in the intervention groups was
 0.35 standard deviations lower 
 (0.51 to 0.19 lower)   1129
 (12 studies) ⊕⊕⊕⊝
 moderate4  
Adverse eventswithdrawn for medical reasons 
 Follow‐up: mean 16 weeks Study population RR 1.22 
 (0.58 to 2.56) 1410
 (12 studies) ⊕⊕⊕⊝
 moderate1  
52 per 1000 64 per 1000 
 (30 to 134)
Moderate
67 per 1000 82 per 1000 
 (39 to 172)
*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 evidence.
 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.

1Heterogeneity.
 2206 events.
 3Six/11 studies with unclear allocation concealment and/or blinding or incomplete outcome data.
 4Five/12 studies with unclear allocation concealment and/or blinding or incomplete outcome data.