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 |
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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 |
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Index tests | Typhidot‐M TUBEX |
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Target condition and reference standard(s) | Target condition: both Salmonella Typhi and Salmonella Paratyphi A Reference standard: peripheral blood culture (8 mL) |
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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 |