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

Summary of findings 4. Cytisine versus nicotine replacement therapy for smoking cessation.

Cytisine versus nicotine replacement therapy for smoking cessation
Patient or population: people who smoke tobacco
Setting: participants' homes (participants were callers to a national Quitline)
Intervention: cytisine
Comparison: nicotine replacement therapy (NRT)
Outcomes Anticipated absolute effects* (95% CI) Relative effect
(95% CI) № of participants
(studies) Certainty of the evidence
(GRADE) Comments
Risk with NRT Corresponding risk with cytisine
Smoking abstinence at longest follow‐up (6+ months)
 
153 per 1000 218 per 1000
(173 to 275)
RR 1.43
(1.13 to 1.80)
1310
(1 study) ⊕⊕⊝⊝a,b
Low
 
SAEs
 
60 per 1000 68 per 1000
(45 to 104)
RR 1.15
(0.76 to 1.75)
1310
(1 study) ⊕⊝⊝⊝a,c
Very 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; NRT: nicotine replacement therapy; 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 risk of bias: sole study at high risk.
bDowngraded one level because of imprecision: fewer than 300 events in the analysis.
cDowngraded two levels because of imprecision: CI incorporates clinically significant benefit and clinically significant harm.