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. 2015 Dec 30;2015(12):CD007394. doi: 10.1002/14651858.CD007394.pub2

Doermann 2002.

Study characteristics
Patient sampling Study design not clear
Patient characteristics and setting 423 adult participants
Age of cases ranged from 16 to 70 years; no information about gender
Haematology department
France
Inpatients, no further information provided
Index tests Platelia: no further details reported
Sera were tested twice a week in patients at risk
2 consecutive samples is positive, the rest are negative
Cut‐off = 1.5 ng/ml
Target condition and reference standard(s) Invasive aspergillosis, according to EORTC‐like criteria
Antigenaemia reported as criterion in one of the definitions for disease classifications
Acceptable reference standard? Yes
 EORTC‐like criteria; definitions of separate groups reported completely
Flow and timing All patients were evaluated according to the same criteria, but not clear whether there were withdrawals or uninterpretable results
Comparative  
No patients per category 3 proven, 9 probable, 6 possible, 405 non‐IA
Notes Language: French
Sponsoring precluded? Unclear: not 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? Yes    
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    
    Unclear Low
DOMAIN 3: Reference Standard
Is the reference standards likely to correctly classify the target condition? Unclear    
Were the reference standard results interpreted without knowledge of the results of the index tests? No    
    High Unclear
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? Unclear    
    Unclear