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. 2014 Apr 3;2014(4):CD006531. doi: 10.1002/14651858.CD006531.pub2

Summary of findings 16. Paroxetine compared with sertraline for depression.

Paroxetine compared with sertraline for depression
Patient or population: patients with depression
 Settings: in‐ and out‐patients
 Intervention: paroxetine
 Comparison: sertraline
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of Participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Sertraline Paroxetine
Failure to respond at endpoint (6‐12 weeks) 292 per 1000 340 per 1000 
 (269 to 422) OR 1.25 
 (0.89 to 1.77) 618
 (3 studies) ⊕⊕⊕⊝
 moderate1  
Failure to respond at 1‐4 weeks See comment See comment Not estimable 0
 (0) See comment No trial reported this outcome.
Failure to respond at 16‐24 weeks See comment See comment Not estimable 0
 (0) See comment No trial reported this outcome.
Failure to remit at endpoint 577 per 1000 562 per 1000 
 (478 to 647) OR 0.94 
 (0.67 to 1.34) 545
 (2 studies) ⊕⊕⊕⊝
 moderate1  
SMD at endpoint   The mean SMD at endpoint in the intervention groups was
 0.13 standard deviations lower 
 (0.34 lower to 0.07 higher)   353
 (1 study) ⊕⊕⊕⊝
 moderate1 The point estimate of the effect size corresponds to a small effect according to Cohen 1992.
Failure to complete ‐ any cause ‐ 338 per 1000 411 per 1000 
 (210 to 648) OR 1.37 
 (0.52 to 3.6) 426
 (2 studies) ⊕⊕⊕⊝
 moderate1  
Participants with at least some Side Effects See comment See comment Not estimable 0
 (0) See comment No trial reported this outcome.
*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; SMD: standardized mean difference; OR: Odds 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.

1 Blinding stated but not tested. No information on randomisation procedures and allocation concealment.