Daradkeh 1995.
Study characteristics | |||
Patient sampling | Retrospective, selected from a previous sample. | ||
Patient characteristics and setting |
N included in study: 168. N in analysis: 168. Age: Mean age onset 26.8 years (SD = 9.3) Gender: M 108, F 60. Ethnicity: Not reported. Comorbid disorders: Not reported. Duration of symptoms: Not reported. Concurrent medications used: Not reported. Inclusion criteria: Patients with major mental illnesses. Exclusion criteria: Not reported. Study aim: Prevalence and diagnostic validity of FRS for schizophrenia.. Previous treatment for schizophrenia: Not reported. Clinical setting: Unclear. Country: United Arab Emirates. |
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Index tests |
Description of FRS used: FRS's assessed through OPCRIT. Professionals performing test: Not reported. Resolution of discrepancies: Not reported. How FRS used in study: Prevalence and diagnosis. |
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Target condition and reference standard(s) |
Reference standard: ICD‐10 through OPCRIT. Target condition(s): Schizophrenia. Professionals performing test: Pair of clinicians. Resolution of discrepancies: Not reported. |
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Flow and timing |
Study process:Patients selected from a larger previous trial of ICD‐10. Most patients assessed by pairs of clinicians and two thirds had diagnostic interviews applied. OPCRIT was used to generate diagnosis and FRSs. Follow‐up: Not reported. |
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Comparative | |||
Notes | |||
Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | No | ||
Was a case‐control design avoided? | Unclear | ||
Did the study avoid inappropriate exclusions? | Unclear | ||
Unclear | Unclear | ||
DOMAIN 2: Index Test All tests | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Unclear | ||
Did the study pre‐specify whether they were using one or multiple FRSs? | No | ||
Unclear | Low | ||
DOMAIN 3: Reference Standard | |||
Is the reference standards likely to correctly classify the target condition? | Yes | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Unclear | ||
Unclear | Low | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Did all patients receive a reference standard? | Yes | ||
Did all patients receive the same reference standard? | Yes | ||
Did all patients receive an index test? | Yes | ||
Did all patients receive the same index test? | Yes | ||
Low |