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. 2019 May 31;45(4):730–732. doi: 10.1093/schbul/sbz037

Table 1.

Summary of Findings: ECT Plus Standard Care Vs Standard Care for Treatment-Resistant Schizophrenia

Patient or population: people with treatment-resistant schizophrenia
Settings: hospital
Intervention: ECT plus standard care
Comparison: standard care
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.