White 2005.
Study characteristics | |||
Patient sampling | Study design not clear | ||
Patient characteristics and setting | 105 participants
No information about age or gender
UK Patients considered to be at high risk for invasive fungal infection, no further details provided Representative spectrum? Patients considered to be at high risk, without further information |
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Index tests | Platelia Aspergillus. One positive is positive; no positive is negative; not reported how often samples were taken. Positive result: single sample above 1.5 ODI | ||
Target condition and reference standard(s) | Invasive aspergillosis, as defined by EORTC criteria (no citation) Incorporation avoided? Not explicitly reported whether galactomannan results were excluded from EORTC criteria Acceptable reference standard? Yes: EORTC criteria (no citation) |
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Flow and timing | Timing not reported Uninterpretable results reported? No | ||
Comparative | |||
No patients per category | 1 proven, 2 probable, 4 possible, 98 no IA | ||
Notes | Sponsoring unclear; nothing reported | ||
Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | Unclear | ||
Was a case‐control design avoided? | Unclear | ||
Did the study avoid inappropriate exclusions? | Unclear | ||
Unclear | Unclear | ||
DOMAIN 2: Index Test All tests | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Unclear | ||
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? | Unclear | ||
Unclear | Low | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Unclear | ||
Did all patients receive the same reference standard? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Low |