Cherian 2010.
Study characteristics | |||
Patient sampling | Type of study: retrospective study. Consecutive or random sample: consecutive patients. | ||
Patient characteristics and setting | Sample size: 78. Females: not stated. Age: not stated. Presentation:
Setting: secondary care, UK. |
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Index tests | Index test: EUS‐FNA. Further details: Technical specifications: Olympus GF‐UCT240‐AL5. Performed by: endoscopist and cytologist. Criteria for positive diagnosis: not stated. | ||
Target condition and reference standard(s) | Target condition: benign versus malignant. Reference standard: surgical excision and histology in people who had undergone surgery and clinical follow‐up, defined as serial imaging at 12 months that demonstrated progression of disease or patients had clinical deterioration or death. Further details: Technical specifications: not applicable. Performed by: clinicians. Criteria for positive diagnosis: not stated. | ||
Flow and timing | Number of indeterminates for whom the results of reference standard were available: not stated. Number of patients who were excluded from the analysis: not stated. | ||
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? | Yes | ||
Was a case‐control design avoided? | Yes | ||
Did the study avoid inappropriate exclusions? | Yes | ||
Low | High | ||
DOMAIN 2: Index Test Cancerous versus benign ‐ EUS FNA | |||
If a threshold was used, was it pre‐specified? | Yes | ||
Were the index test results interpreted without knowledge of the results of the reference standard? | Unclear | ||
Unclear | Low | ||
DOMAIN 3: Reference Standard | |||
Is the reference standards likely to correctly classify the target condition? | No | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Unclear | ||
High | Low | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Unclear | ||
Did all patients receive the same reference standard? | No | ||
Were all patients included in the analysis? | Yes | ||
High |