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. 2022 Mar 2;2022(3):CD002795. doi: 10.1002/14651858.CD002795.pub3

Summary of findings 5. Comparison 5: SNRIs versus placebo for posttraumatic stress disorder (PTSD).

Comparison 5: SNRIs versus placebo for posttraumatic stress disorder (PTSD)
Population: adults (aged 18‐85)
Settings: multi‐centre trials
Intervention: SNRIs
Comparison: placebo
Follow‐up: for one study at week 24 or at the time of discontinuation if before week 24; the remaining study did not specify follow‐up
Outcomes Illustrative comparative risks* (95% CI) Relative effect
(95% CI) No of participants
(studies) Quality of the evidence
(GRADE) Comments
Assumed risk Corresponding risk
With placebo With SNRIs
Treatment efficacy ‐ treatment response, as measured by the Global Impressions scale change item (CGI‐I or similar): no. of responders (acute phase) N/A N/A N/A N/A N/A We found no studies that looked at the number of participants who responded to venlafaxine versus placebo.
Treatment tolerability, as measured by Dropouts due to adverse events (acute phase) Study population RR 0.98 
(0.88 to 1.10) 687
(2 studies) ⊕⊝⊝⊝
very lowa,b Dropout rates due to adverse events were low in the SNRI (4%) and placebo groups (3%)
26 per 1000 25 per 1000
(23 to 29)
Moderate
27 per 1000 26 per 1000
(24 to 30)
*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. N/A: Not applicable.
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.

aDowngraded by one level due to serious risk of bias (concerns with randomisation procedures).
bDowngraded by two levels due to considerable heterogeneity (I2 of 92%).