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

Bialek 2002.

Study characteristics
Patient sampling Study design not clear
Patient characteristics and setting 17 participants
 Age ranged from 1 month to 9 years; 59% males
France or Germany
Children undergoing bone marrow transplantation (BMT), no other details reported
Paediatric bone marrow recipients; other details not reported
Index tests Platelia: screening (but not reported how often), single sample positive is positive; < 1.0 is negative and > 1.5 is positive
Target condition and reference standard(s) Invasive aspergillosis, according to EORTC criteria, EORTC website cited
They excluded the antigen detection as a microbiological criterion in the EORTC criteria
Flow and timing None very clearly reported: not clearly reported whether all patients who underwent the Platelia test also underwent the reference standard
No withdrawals reported
Uninterpretable results not clearly reported: below 1.0 ODI a sample is negative, above 1.5 ODI a sample is positive, but they do not describe how samples between 1.0 and 1.5 ODI are handled
Comparative  
No patients per category 0 proven, 1 probable, 2 possible, 14 non‐IA
Notes Research fund and university fund 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? 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? Unclear    
    Unclear