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

Weisser 2005.

Study characteristics
Patient sampling Prospective; consecutive series of patients. Episode‐based analysis
Patient characteristics and setting 161 participants
Age ranged from 16 to 78 years
 51% males
 Switzerland
Adults undergoing autologous or allogeneic haematopoietic stem cell transplantation (HSCT) or receiving chemotherapy Inpatients; monitoring clinical course
Representative spectrum? Yes: adults undergoing autologous or allogeneic HSCT or receiving chemotherapy
Index tests Platelia Aspergillus. Sera were tested twice weekly. 2 consecutives positive was considered positive. Cut‐off = 0.5 ODI
Target condition and reference standard(s) Invasive aspergillosis, as defined by EORTC criteria
Incorporation avoided? Not explicitly reported whether galactomannan results were excluded from EORTC criteria
 Acceptable reference standard? Yes: EORTC criteria
Flow and timing Timing not reported
Partial verification avoided? Not clear
 Withdrawals explained? Not reported
 Uninterpretable results reported? Not reported
Comparative  
No patients per category 20 proven or probable, 32 possible, 109 no IA
Notes Sponsoring: Science Grant reported
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? 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? Unclear    
    Unclear