Study characteristics | |||
Patient sampling | Cross‐sectional design, random enrolment, prospective data collection | ||
Patient characteristics and setting | Presenting signs and symptoms: people with microbiologically or clinically diagnosed TB for detection of rifampicin resistance Age: 18 years and older Sex, female: not reported HIV infection: 57% History of TB: not reported Sample size: 188 Clinical setting: outpatient Laboratory level: central Country: Malawi World Bank Income Classification: low income High TB burden country: no High MDR‐TB burden country: no High TB/HIV burden country: yes |
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Index tests | Index: Xpert MTB/RIF | ||
Target condition and reference standard(s) | Target condition: rifampicin resistance Reference standard for rifampicin resistance: MTBDRplus |
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Flow and timing | |||
Comparative | |||
Notes | Xpert run especially in sputum smear‐negative and HIV‐positive people. Study used frozen specimens | ||
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 | Low | ||
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? | Unclear | ||
Were the reference standard results for rifampicin resistance detection interpreted without knowledge of the results of the index test? | Unclear | ||
Unclear | 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? | Yes | ||
Low |