Table 1.
Patient or population: people with treatment-resistant schizophrenia Settings: hospital Intervention: ECT plus standard care Comparison: standard care |
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Outcomes | Anticipated Absolute Effects a (95% CI) | Relative Effect (95% CI) | No. of Participants (Studies) | Quality of the Evidence (GRADE) | Comments | |
Risk With Placebo (No Treatment) | Risk With ECT (Add-on) | |||||
Response to treatment (medium term)
Clinically important response to treatment as defined by each study Follow-up: 8–12 weeks |
308 per 1000 | 635 per 1000 (539 to 746) | RR 2.06 (1.75 to 2.42) | 819 (9 studies) | ⊕⊕⊕⊝ moderateb | |
Cognitive functioning (short term)—memory deterioration Follow-up: 3–4 weeks |
0 per 1000 | 13 per 1000 (1 to 219) |
RR 27 (1.67 to 437.68) |
72 (1 study) | ⊕⊝⊝⊝ very lowb,c,d | Data for predefined outcome “clinically important change” not reported |
Satisfaction and acceptability of treatment (medium term)—leaving the study early Follow-up: 8–12 weeks |
23 per 1000 | 27 per 1000 (9 to 82) | RR 1.18 (0.38 to 3.63) | 354 (3 studies) | ⊕⊝⊝⊝ very lowa,d | |
Mental state (medium term)—total scores (BPRS, high = poor) Follow-up: 8–12 weeks |
The mean mental state—average scores (BPRS, high = poor, medium term) was 33.4 | MD 11.18 lower (12.61–9.76 lower) | — | 345 (2 studies) | ⊕⊕⊝⊝ Lowb,c |
Data for predefined outcome “clinically important change” not reported |
General functioning (medium term)—average scores (GAF, high = good) Follow-up: 12 weeks–6 months |
The mean mental state—average scores (GAF, high = good, medium term) was 47.3. | MD 10.66 higher (6.98–14.34 higher) | — | 97 (2 studies) | ⊕⊝⊝⊝ very lowb,c,e,f | Data for predefined outcome “clinically important change” not reported |
Service use—hospitalization | See comment | See comment | See comment | See comment | See comment | No studies reported this outcome, so there is no evidence to support or refute benefits of the intervention. |
Adverse event/effect(s)—death | See comment | See comment | See comment | See comment | See comment | No studies reported this outcome, so there is no evidence to support or refute benefits of the intervention |
* |
Note: BPRS, Brief Psychiatric Rating Scale; CI, confidence interval; ECT, electroconvulsive therapy; GAF, Global Assessment of Functioning; MD, mean difference; RR, risk ratio. GRADE Working Group grades of evidence. High quality: we are very confident that the true effect lies close to that of the estimate of the effect. Moderate quality: we are moderately confident in the effect estimate; the true effect is likely to be close to the estimate of effect, but there is a possibility that it is substantially different. Low quality: our confidence in the effect estimate is limited; the true effect may be substantially different from the estimate of the effect. Very low quality: we have very little confidence in the effect estimate; the true effect is likely to be substantially different from the estimate of effect.
a 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).
bDowngraded by one level due to risk of bias: high risk of bias with blinding of participants and personnel.
cDowngraded by one level due to indirectness: scores from scale were employed as a surrogate index of the intended outcome.
dDowngraded by two levels due to imprecision: low event rate.
eDowngraded by one level due to heterogeneity.
fDowngraded by one level due to imprecision: small sample size.