TABLE 5

Study Quality Assessment with Methodologic Quality Criteria Guidelines*

GuidelineStudyGuideline (%)
Rege et al. (5)Kole et al. (16)Hanasono et al. (13)Greven et al. (15)Lassen et al. (8)Gupta et al. (12)Aassar et al. (35)Bohuslavizki et al. (6)Jungehülsing et al. (36)
Guideline 1: description of study design and patient selection criteria
 1.Study designAAAAAPAAAA = 70.37 P = 25.93 N = 3.85
 2.Patient selection criteriaPAPPAPPAA
 3.Exclusion of patients from study’s final analysisAAAAANPAA
Guideline 2: characteristics of patient population finally studied
 1.Mean age with range and sexAANNAPAAAA = 55.55 P = 4.44 N = 40.00
 2.Comorbid conditionsNNNNNNNNN
 3.Diabetes mellitusNNNNNNNPN
 4.Localization of metastasis of UPTAAAAAAAAA
 5.Special institution characteristicsAAAAAAAAA
Guideline 3: patient indications leading to use of 18F-FDG PET
 1.Reasons for use of 18F-FDG PETAAAAAAAAAA = 100.00
 2.Reasons for use of 18F-FDG PET correlated with specific 18F-FDG PET findingsAAAAAAAAA
 3.Extent of metastatic disease in every patientAAAAAAAAA
Guideline 4: details of technologies used during study and image-interpretation issues
 1.Imaging techniques used in study and resolutionAAPAPAAAAA = 62.50 P = 16.67 N = 20.83
 2.Patient preparationNANAAAAAA
 3.Minimum 4-h fasting before 18F-FDG injectionNANAAAAAA
 4.Blood glucose level checked before 18F-FDG injectionNNNNPNNNA
 5.Attenuation correctionAPAAPAAPA
 6.Explanation of special characteristics of interpretersANAAAPANN
 7.Definition of positive and negative 18F-FDG PET findingsAAAAAPPPN
 8.Additional scansAAAAPAAPA
Guideline 5: final diagnostic confirmation
 1.Final confirmationAAAAAAAAAA = 82.22 P = 6.67 N = 11.11
 2.Association between specific 18F-FDG PET finding and final confirmation technique usedAAPAAAAAA
 3.Histopathologic confirmationAAAAAAAAA
 4.Nonhistopathologic confirmationNAAAPAAAA
 5.Patients lost to clinical follow-up confirmationNNNAANPAA
Guideline 6: sensitivity and specificity data
 1.Description of TP, FP, TN, and FNPPAAAPAAPA = 57.14 P = 22.22 N = 20.63
 2.Qualitative explanation of FP and FNNANAPPAPA
 3.Specific region studied by 18F-FDG PETPAAPAAPAP
 4.Location and no. of primary tumors and other metastatic lesions detected by 18F-FDG PETAAPAAAAAA
 5.Confidence intervalsNNNNNNNNN
 6.Equivocal 18F-FDG PET findingsNANAAPAAA
 7.Data reported in patients and in corresponding lesionsAAPAAAAAA
Guideline 7: change-in-management information
 1.18F-FDG PET-directed change in managementN/AAN/AN/AAPN/AAAA = 77.14 P = 17.14 N = 5.71
 2.Diagnostic tool used to make initial treatment decisionN/APN/AN/AAPN/APA
 3.Diagnostic tool used to make final treatment decisionN/AAN/AN/AAPN/AAA
 4.Medical treatment made both initially and after 18F-FDG PETN/APN/AN/AANN/ANA
 5.Correct or incorrect 18F-FDG PET-directed management changeN/AAN/AN/AAAN/AAA
 6.Upstaging and downstagingN/AAN/AN/AAAN/AAA
 7.18F-FDG PET in management algorithmN/AAN/AN/AAAN/AAA
Percentage of scores for each article
 A (%)58.0673.6851.6177.4276.3155.2670.9771.0581.58
 P (%)9.6810.5316.136.4515.7928.9516.1315.795.26
 N (%)32.2615.7932.2616.137.8915.7912.9013.1613.16
  • * Methodologic quality criteria guidelines formulated by Huebner et al. (25) and adapted for review of studies of patients with UPT in which 18F-FDG PET is performed to detect primary tumor.

  • A = adequate adherence; P = partial adherence; N = not addressed; N/A = not applicable; TP = true-positive; FP = false-positive; TN = true-negative; FN = false-negative.