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. 2017 Apr 17;2017(4):CD010213. doi: 10.1002/14651858.CD010213.pub2

Hu 2013.

Study characteristics
Patient sampling Type of study: retrospective study.
 Consecutive or random sample: unclear.
Patient characteristics and setting Sample size: 80.
Females: 36 (45.0%).
Age: 57 years.
Presentation:
Inclusion criteria
  • Patients with solitary pancreatic lesions who had undergone PET scan and surgical resection.


Exclusion criteria
  • Patients with suspected malignancies in other areas of the body.


Setting: secondary care, China.
Index tests Index test: PET.
 Further details:
 Technical specifications: Biograph 16 HR PET/CT scanner (Siemens).
 Performed by: radiologist.
 Criteria for positive diagnosis: SUVmax > 3.5.
Target condition and reference standard(s) Target condition: cancerous versus benign.
 Reference standard: surgical excision.
 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? Unclear    
Was a case‐control design avoided? Yes    
Did the study avoid inappropriate exclusions? Unclear    
    Unclear High
DOMAIN 2: Index Test Cystic lesion subgroup analysis ‐ Cancerous versus benign ‐ PET
If a threshold was used, was it pre‐specified? No    
Were the index test results interpreted without knowledge of the results of the reference standard? Yes    
    High Low
DOMAIN 2: Index Test Cancerous versus benign ‐ PET (SUV max > 3.5)
If a threshold was used, was it pre‐specified? No    
Were the index test results interpreted without knowledge of the results of the reference standard? Yes    
    High 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? Yes    
    Low Low
DOMAIN 4: Flow and Timing
Was there an appropriate interval between index test and reference standard? Yes    
Did all patients receive the same reference standard? Yes    
Were all patients included in the analysis? Unclear    
    Unclear