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. 2023 May 5;2023(5):CD006103. doi: 10.1002/14651858.CD006103.pub8

Summary of findings 3. Cytisine versus varenicline for smoking cessation.

Cytisine versus varenicline for smoking cessation
Patient or population: people who smoke tobacco
Setting: community, community pharmacy, participants' homes
Intervention: cytisine
Comparison: varenicline
Outcomes Anticipated absolute effects* (95% CI) Relative effect
(95% CI) № of participants
(studies) Certainty of the evidence
(GRADE) Comments
Risk with varenicline Corresponding risk with cytisine
Smoking abstinence at longest follow‐up (6+ months)
 
132 per 1000 109 per 1000
(87 to 138)
RR 0.83
(0.66 to 1.05)
2131
(2 studies) ⊕⊕⊕⊝a
Moderate
 
SAEs
 
49 per 1000 33 per 1000
(21 to 50)
RR 0.67
(0.44 to 1.03)
2017
(2 studies) ⊕⊕⊝⊝b
Low
 
Neuropsychiatric SAEs
 
No data No data No data No data No data  
Cardiac SAEs
 
No data No data No data No data No data  
*The risk in the intervention group (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). The assumed risk in the comparison group is calculated as the median risk in control groups.

CI: confidence interval; RR: risk ratio; SAE: serious adverse event
GRADE Working Group grades of evidence
 
High certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate; the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited; the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate; the true effect is likely to be substantially different from the estimate of effect.

aDowngraded one level because of imprecision: CI incorporates no difference as well as clinically significant harm.
bDowngraded two level because of imprecision: CI incorporates no difference as well as clinically significant benefit, and number of events in analysis very low (n = 82).