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Search review questions

Each row is one question a systematic review asked: who, what, compared with what, and which outcome, with the effect it found and how certain that is. Words match anywhere in the field.

Limit to evidence status or GRADE (optional)

2,589 questions in 168 reviews · Schizophrenia

current versions
No studies 601 · 23.2%Ungraded 446 · 17.2%Very low 721 · 27.8%Low 505 · 19.5%Moderate 274 · 10.6%High 42 · 1.6%

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.

QuestionEffectEvidenceStatus / GRADE
STANDARD‐HIGHER DOSE (greater than or equal to 6‐<10 mg/day) vs ANY DOSE ‐ short term
Adverse effects: EPS: unspecified ‐ Versus high dose (greater than or equal to 10 mg) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.56 [0.31, 0.99]2 studies · 261 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Leaving the study early: insufficient response ‐ When compared with ultra low dose (<2 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.66 [0.45, 0.97]1 study · 679 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Leaving the study early: insufficient response ‐ When compared with low dose (greater than or equal to 2‐<4 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.48 [0.25, 0.92]1 study · 70 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Leaving the study early: insufficient response ‐ When compared with standard‐lower dose (greater than or equal to 4‐<6 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.64 [0.96, 2.81]2 studies · 677 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Leaving the study early: insufficient response ‐ When compared with standard‐higher dose (greater than or equal to 6‐<10 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.28 [0.82, 1.98]2 studies · 748 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Global state: 1. No clinically important improvement ‐ CGI‐I ‐ when compared with low dose (greater than or equal to 2‐<4 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.64 [0.5, 0.82]2 studies · 257 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Global state: 1. No clinically important improvement ‐ CGI‐I ‐ when compared with standard‐higher dose (greater than or equal to 6‐<10 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.18 [0.82, 1.69]2 studies · 255 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ PANSS ‐ when compared with ultra low dose (<2mg) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.89 [0.74, 1.07]1 study · 679 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ PANSS ‐ when compared with low dose (greater than or equal to 2‐<4mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.9 [0.73, 1.12]2 studies · 262 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ PANSS ‐ when compared with standard‐lower dose (greater than or equal to 4‐<6mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.11 [0.9, 1.36]1 study · 677 participantsModerate
ULTRA LOW DOSE (<2 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ as measured by PANSS ‐ when compared with standard‐low dose (greater than or equal to 4‐<6 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.24 [0.99, 1.55]1 study · 456 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ PANSS ‐ when compared with standard‐higher dose (greater than or equal to 6‐<10mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.24 [1.05, 1.47]3 studies · 941 participantsHigh
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Adverse effects: EPS: unspecified ‐ when compared with standard‐higher dose (greater than or equal to 6‐<10mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.79 [1.01, 3.18]2 studies · 261 participantsModerate
HIGH DOSE (greater than or equal to 10 mg/day) vs ANY DOSE ‐ short term
Adverse effects: EPS: unspecified ‐ when compared with low dose (greater than or equal to 2‐<4mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 2.22 [1.19, 4.14]2 studies · 262 participantsModerate
ULTRA LOW DOSE (<2 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ as measured by PANSS ‐ when compared with standard‐higher dose (greater than or equal to 6‐<10 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.32 [1.05, 1.66]1 study · 459 participantsModerate
ULTRA LOW DOSE (<2 mg/day) vs ANY DOSE ‐ short term
Mental state: 1. No clinically important improvement ‐ as measured by PANSS ‐ when compared with high dose (greater than or equal to 10 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 1.12 [0.94, 1.35]1 study · 679 participantsModerate
LOW DOSE (greater than or equal to 2‐<4 mg/day) vs ANY DOSE ‐ short term
Leaving the study early: any reason ‐ when compared with standard‐lower dose (greater than or equal to 4‐<6 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 0.75 [0.15, 3.72]1 study · 5 participantsModerate
LOW DOSE (greater than or equal to 2‐<4 mg/day) vs ANY DOSE ‐ short term
Leaving the study early: any reason ‐ when compared with standard‐higher dose (greater than or equal to 6‐<10 mg/day) · patients with schizophrenia
Risperidone dose for schizophrenia (2009) · Cochrane
RR 3.11 [1.41, 6.84]2 studies · 70 participantsModerate
Monetary reward vs no monetary reward
Target behaviour: average number of dolls assembled per day · patients with schizophrenia1
Monetary incentives for schizophrenia (2009) · Cochrane
no estimate extracted1 study · 25 participantsVery low
Intervention NR
Mental state: 1a. Overall no clinically important improvement (BPRS) ‐ short term 25‐30% change BPRS1,2 ( · people with schizophrenia
Morita therapy for schizophrenia (2007) · Cochrane
RR 0.36 [0.13, 1.03]1 study · 66 participantsLow
Intervention NR
Mental state: 1a. Overall no clinically important improvement (BPRS) ‐ medium term 25‐30% change BPRS1,2 ( · people with schizophrenia
Morita therapy for schizophrenia (2007) · Cochrane
RR 0.36 [0.14, 0.89]1 study · 76 participantsLow
Beta‐blockers vs Placebo
Global state: 1. Leaving the study early ‐ Short term · People with Schizophrenia
Beta‐blocker supplementation of standard drug treatment for schizophrenia (2001) · Cochrane
RR 1.62 [0.92, 2.83]8 studies · 274 participantsLow
Beta‐blockers vs Placebo
Global state: 2. Relapse ‐ short term · People with Schizophrenia
Beta‐blocker supplementation of standard drug treatment for schizophrenia (2001) · Cochrane
RR 3.12 [0.34, 28.36]2 studies · 68 participantsLow
Beta‐blockers vs Placebo
Adverse effects: 1. Death ‐ short term · People with Schizophrenia
Beta‐blocker supplementation of standard drug treatment for schizophrenia (2001) · Cochrane
no estimate extracted9 studies · 282 participantsUngraded
Beta‐blockers vs Placebo
Adverse effects: 1. Death ‐ medium term · People with Schizophrenia
Beta‐blocker supplementation of standard drug treatment for schizophrenia (2001) · Cochrane
no estimate extracted1 study · 20 participantsLow
Beta‐blockers vs Placebo
Adverse effect: 2. General ‐ Short term · People with Schizophrenia
Beta‐blocker supplementation of standard drug treatment for schizophrenia (2001) · Cochrane
RR 5.42 [0.27, 107.2]1 study · 48 participantsLow
Beta‐blockers vs Placebo
Adverse effects: 3. Specific ‐ cardiovascular ‐ short term · People with Schizophrenia
Beta‐blocker supplementation of standard drug treatment for schizophrenia (2001) · Cochrane
RR 1.63 [0.7, 3.84]8 studies · 274 participantsLow
INDIVIDUAL PSYCHODYNAMIC PSYCHOTHERAPY vs MEDICATION
Committed suicide by three years · patients with schizophrenia and severe mental illness
Individual psychodynamic psychotherapy and psychoanalysis for schizophrenia and severe mental illness (2001) · Cochrane
RR 0.52 [0.05, 5.56]1 study · 94 participantsLow
INDIVIDUAL PSYCHODYNAMIC PSYCHOTHERAPY vs MEDICATION
Global impression: 1. Not able to be discharged (long term) · patients with schizophrenia and severe mental illness
Individual psychodynamic psychotherapy and psychoanalysis for schizophrenia and severe mental illness (2001) · Cochrane
RR 8.35 [2.03, 34.3]1 study · 94 participantsLow
INDIVIDUAL PSYCHODYNAMIC PSYCHOTHERAPY vs MEDICATION
Global impression: 2. Given medication during 12 months to three years · patients with schizophrenia and severe mental illness
Individual psychodynamic psychotherapy and psychoanalysis for schizophrenia and severe mental illness (2001) · Cochrane
RR 0.64 [0.5, 0.81]1 study · 94 participantsLow
INDIVIDUAL PSYCHODYNAMIC PSYCHOTHERAPY vs MEDICATION
Global impression: 2. Given medication during 12 months to three years · patients with schizophrenia and severe mental illness
Individual psychodynamic psychotherapy and psychoanalysis for schizophrenia and severe mental illness (2001) · Cochrane
RR 0.85 [0.75, 0.96]1 study · 94 participantsLow
PROMPT TYPE vs NO PROMPT
Did not attend appointment ‐ telephone prompts · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 0.84 [0.66, 1.07]2 studies · 447 participantsModerate
PROMPT TYPE vs NO PROMPT
Did not attend appointment ‐ text‐based prompts · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 0.76 [0.43, 1.32]3 studies · 326 participantsModerate
PROMPT TYPE vs NO PROMPT
Did not attend appointment ‐ combination of telephone and text‐based prompts · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 0.7 [0.42, 1.17]1 study · 66 participantsVery low
TELEPHONE PROMPTS vs TEXT‐BASED PROMPTS (ORIENTATION STATEMENT)
Did not attend appointment · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 1.93 [0.98, 3.8]1 study · 75 participantsVery low
TEXT LETTER PROMPT vs TEXT ORIENTATION STATEMENT
Did not attend appointment ‐ any time before appointment · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 1.62 [0.89, 2.92]1 study · 120 participantsVery low
TEXT LETTER PROMPT vs TEXT ORIENTATION STATEMENT
Did not attend appointment ‐ one day before appointment · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 2 [0.78, 5.15]1 study · 60 participantsVery low
TEXT LETTER PROMPT vs TEXT ORIENTATION STATEMENT
Did not attend appointment ‐ three days before · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 1.38 [0.64, 2.93]1 study · 60 participantsVery low
ANY PROMPT vs NO PROMPT
Did not attend appointment · patients with serious mental illness
Prompts to encourage appointment attendance for people with serious mental illness (2001) · Cochrane
RR 0.8 [0.65, 0.98]4 studies · 789 participantsModerate