Table 3.
Pooled Antidepressants vs. Placebo | ||||||
---|---|---|---|---|---|---|
Continuous Outcome | N Studies | N Participants | Hedges’ g | 95% CI | p | I2% |
Total Psychopathologya | 11 | 491 | −0.27 | −0.60,0.07 | 0.12 | 65 |
Positive Symptomsa | 11 | 500 | −0.14 | −0.45,0.17 | 0.38 | 60 |
Negative Symptomsa | 11 | 500 | −0.29 | −0.62,0.05 | 0.09 | 64 |
Depression (HAM-D-predominant)a | 9 | 455 | −0.14 | −0.47,0.18 | 0.39 | 58 |
Depression (CDSS-predominant)a | 9 | 455 | −0.22 | −0.53,0.09 | 0.17 | 54 |
EPS: Any | 8 | 407 | −0.13 | −0.33,0.06 | 0.18 | 13 |
Parkinsonism | 7 | 360 | −0.11 | −0.32,0.10 | 0.30 | 21 |
Akathisiaa | 4 | 265 | −0.64 | −1.71,0.43 | 0.24 | 85b |
Dyskinesia | 3 | 230 | −0.13 | −0.39,0.13 | 0.32 | 39 |
Categorical Outcome | N | n | RR | 95% CI | p | I2% |
---|---|---|---|---|---|---|
Discontinuation: All-cause | 11 | 568 | 1.16 | 0.85,1.59 | 0.36 | 0 |
Discontinuation: Inefficacy | 10 | 540 | 0.39 | 0.12,1.33 | 0.13 | 0 |
Discontinuation: Intolerability | 10 | 540 | 1.79 | 0.75,4.27 | 0.19 | 0 |
Discontinuation: Other Reasons | 10 | 540 | 1.33 | 0.84,2.11 | 0.22 | 0 |
<50% Decrease in PANSS Total Score | 7 | 442 | 1.00 | 0.98,1.03 | 0.71 | 0 |
<20% Decrease in Any Negative Symptom Rating Scale | 7 | 236 | 0.96 | 0.87,1.06 | 0.47 | 0 |
≥20% Increase in PANSS Total Score | 4 | 163 | 2.70 | 0.47,15.32 | 0.26 | 0 |
Study-defined Inefficacy (with HAM-D) | 3 | 272 | 0.78 | 0.68,0.91 | 0.0009 | 0 |
Study-defined Inefficacy (with CDSS) | 3 | 272 | 0.76 | 0.65,0.90 | 0.0009 | 0 |
Total Neuropsychiatric Adverse Events | 4 | 312 | 1.11 | 0.96,1.28 | 0.16 | 0 |
Total Neurological Adverse Events | 4 | 312 | 1.24 | 0.83,1.85 | 0.30 | 12 |
Headache | 4 | 312 | 1.06 | 0.56,2.00 | 0.86 | 16 |
Total Psychiatric Adverse Events | 6 | 389 | 1.08 | 0.85,1.39 | 0.53 | 0 |
Suicidal Ideation | 4 | 213 | 0.50 | 0.18,1.39 | 0.19 | N/A |
Worsening of Psychosis | 5 | 168 | 3.08 | 0.65,14.54 | 0.16 | 0 |
Psychiatric Hospitalization | 4 | 359 | 1.39 | 0.43,4.49 | 0.58 | 0 |
Insomnia | 4 | 312 | 1.45 | 0.82,2.57 | 0.21 | 17 |
Sedation | 4 | 118 | 2.91 | 1.03,8.17 | 0.04 | 0 |
Weakness/Fatigue | 3 | 272 | 0.71 | 0.41,1.23 | 0.22 | 0 |
Agitation/Irritability | 4 | 319 | 1.03 | 0.44,2.41 | 0.94 | 0 |
Total GI Adverse Events | 4 | 312 | 1.17 | 0.99,1.39 | 0.06 | 0 |
Total Metabolic Adverse Eventsa | 3 | 272 | 2.67 | 0.52,13.84 | 0.24 | 62b |
Increase in Appetite | 3 | 272 | 1.34 | 0.59,3.05 | 0.48 | 0 |
Weight Gain | 4 | 300 | 2.08 | 0.87,4.97 | 0.10 | 1 |
Total Cardiorespiratory Adverse Events | 3 | 272 | 1.03 | 0.60,1.77 | 0.92 | 0 |
Total Cardiac Adverse Events | 3 | 272 | 0.93 | 0.43,2.00 | 0.85 | 0 |
Total Respiratory Adverse Events | 3 | 272 | 1.14 | 0.50,2.61 | 0.75 | 0 |
Total Ophthalmological Adverse Events | 3 | 291 | 0.36 | 0.10,1.33 | 0.13 | 15 |
For continuous outcomes, negative Hedges’ g favors treatment group; for categorical outcomes values < 1 favor treatment group; fixed effects models, except where noted
Bolded p-value: p < 0.05
Random effects
< 3 studies available per subgroup so planned subanalyses not run
Abbreviations CDSS: Calgary Depression Scale for Schizophrenia; HAM-D: Hamilton Depression Rating Scale