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. 2017 May 25;2017(5):CD008892. doi: 10.1002/14651858.CD008892.pub2

Dong 2007.

Study characteristics
Patient sampling Prospective multicentre study as part of a vaccine surveillance programme
Healthcare settings: primary, secondary, and tertiary centres (85 in total)
Point of recruitment: inpatient and outpatient
Patient characteristics and setting Countries: China
Level of typhoid endemicity (Crump 2004): medium
Age: not specified
Gender distribution: not specified
Entry criteria: aged between 5 and 60 years with a history of fever ≥ 3 days
Sample size: 1874
Index tests Typhidot‐M
TUBEX
Target condition and reference standard(s) Target condition: both Salmonella Typhi and Salmonella Paratyphi A
Reference standard: peripheral blood culture (8 mL)
Flow and timing Prospective multicentre study as part of a vaccine surveillance programme. Index tests performed in real time during patient recruitment.
Comparative  
Notes Reported diagnostic test accuracy for detecting cases of Salmonella Paratyphi A as well as Salmonella Typhi.
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 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? No    
    Low