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. 2019 Jun 7;2019(6):CD009593. doi: 10.1002/14651858.CD009593.pub4

Tsuyuguchi 2017

Study characteristics
Patient sampling Cross‐sectional design, consecutive enrolment, prospective data collection
Patient characteristics and setting Presenting signs and symptoms: presumed TB
Age: mean 65 years (SD 17), range 23 to 94 years
Sex, female: 38%
HIV infection: not reported
History of TB: not reported
Sample size: 417
Clinical setting: not reported
Laboratory level: central
Country: Japan
World Bank Income Classification: high income
High TB burden country: no
High MDR‐TB burden country: no
High TB/HIV burden country: no
Prevalence of TB cases in the study: 55.0%
Index tests Index: Xpert MTB/RIF
Target condition and reference standard(s) Target condition: pulmonary TB
Reference standard for pulmonary TB: Ogawa and MGIT 960
Target condition: rifampicin resistance
Reference standard for rifampicin resistance: MGIT 960
Flow and timing A total of 515 sputum specimens were collected; however, 35 were ineligible due to over‐testing
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 Unclear
DOMAIN 2: Index Test Xpert MTB/RIF
Were the index test results interpreted without knowledge of the results of the reference standard? Yes
If a threshold was used, was it pre‐specified? Yes
Low Low
DOMAIN 3: Reference Standard
Is the reference standards likely to correctly classify the target condition? Yes
Were the reference standard results for TB detection interpreted without knowledge of the results of the index test? Yes
Were the reference standard results for rifampicin resistance detection interpreted without knowledge of the results of the index test? 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