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. 2019 Oct 21;2019(10):CD011420. doi: 10.1002/14651858.CD011420.pub3

Nakiyingi 2014.

Study characteristics
Patient sampling Cross‐sectional, prospective and consecutive enrolment
Patient characteristics and setting Presenting signs and symptoms: HIV‐infected adults suspected of tuberculosis; Presented with any of cough, fever, night sweats and weight loss
Age: median 33 (IQR 29 to 37)
Sex, female: 63%
HIV infection: 100%
Median CD4 cell count per µL: 152 (IQR 41 to 337)
History of tuberculosis: not stated
Sample size: 997
Clinical setting: inpatient and outpatient
Country: South Africa and Uganda
Tuberculosis incidence rate: 567 per 100,000 (South Africa); 201per 100,000 (Uganda)
Number (proportion) of tuberculosis cases in the study: 367 (37%)
Index tests LF‐LAM
Target condition and reference standard(s) Target condition: pulmonary tuberculosis, mycobacteraemia
Reference standard: sputum mycobacterial culture (liquid and solid), mycobacterial blood cultures; extrapulmonary specimens tested for all
Flow and timing All patients were included in the analysis
Comparative  
Notes The study authors performed sputum induction for individuals who could not expectorate. They excluded individuals without some respiratory specimen available. They attempted to identify extrapulmonary tuberculosis
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? No    
    High Low
DOMAIN 2: Index Test All tests
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 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? Yes    
    Low