Cochrane · systematic review · CD000205

Benzodiazepines for antipsychotic‐induced tardive dyskinesia

Bergman, H, Bhoopathi, PS, Soares‐Weiser, K · Cochrane Database of Systematic Reviews · 2018 · Cochrane Library

SchizophreniaAMSTAR 2: not assessed
SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
12
current version
GRADE rated
6
No studies
6
Included studies
NR
No studies 6 · 50%Ungraded 0 · 0%Very low 6 · 50%Low 0 · 0%Moderate 0 · 0%High 0 · 0%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Questions and results

Benzodiazepines compared with placebo for antipsychotic‐induced tardive dyskinesia

Population: psychiatric patients (mainly schizophrenia) with antipsychotic‐induced tardive dyskinesia
6 questions
OutcomeEffectEvidenceStatus / GRADE
Tardive dyskinesia: no clinically important improvement
Benzodiazepines vs placebo
RR 1.12 [0.6, 2.09]2 studies · 32 participantsVery low
Downgraded: risk of bias, imprecision
Tardive dyskinesia: deterioration in symptoms
Benzodiazepines vs placebo
RR 1.48 [0.22, 9.82]2 studies · 30 participantsVery low
Downgraded: risk of bias, imprecision
Adverse effect: any adverse event
Benzodiazepines vs placebo
no estimate extractedNRNo studies
Adverse effect: no clinically significant extrapyramidal adverse effects
Benzodiazepines vs placebo
no estimate extractedNRNo studies
Acceptability of the treatment (measured by participants leaving the study early)
Benzodiazepines vs placebo
RR 2.73 [0.15, 48.04]3 studies · 56 participantsVery low
Downgraded: risk of bias, imprecision
Social confidence, social inclusion, social networks, or personalised quality of life ‐ not reported
Benzodiazepines vs placebo
no estimate extractedNRNo studies

Benzodiazepines compared with phenobarbital (as active placebo) for antipsychotic‐induced tardive dyskinesia

Population: psychiatric patients (mainly schizophrenia) with antipsychotic‐induced tardive dyskinesia
6 questions
OutcomeEffectEvidenceStatus / GRADE
Tardive dyskinesia: no clinically important improvement
Benzodiazepines vs phenobarbital (as active placebo)
RR 0.44 [0.2, 0.96]1 study · 21 participantsVery low
Downgraded: risk of bias
Tardive dyskinesia: deterioration in symptoms ‐ not measured
Benzodiazepines vs phenobarbital (as active placebo)
no estimate extractedNRNo studies
Adverse events: any
Benzodiazepines vs phenobarbital (as active placebo)
RR 1.53 [0.97, 2.41]1 study · 21 participantsVery low
Downgraded: risk of bias
Adverse effect: extrapyramidal symptoms ‐ not reported
Benzodiazepines vs phenobarbital (as active placebo)
no estimate extractedNRNo studies
Acceptability of the treatment (measured by participants leaving the study early)
Benzodiazepines vs phenobarbital (as active placebo)
no estimate extracted1 study · 21 participantsVery low
Downgraded: risk of bias
Social confidence, social inclusion, social networks, or personalised quality of life ‐ not measured
Benzodiazepines vs phenobarbital (as active placebo)
no estimate extractedNRNo studies