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

Rovira 2004.

Study characteristics
Patient sampling Prospective; consecutive series of patients
Patient characteristics and setting 74 participants
 Age ranged from 15 to 60 years
 61% males
 Spain
Adults undergoing allogeneic haematopoietic stem cell transplantation in institution and adult outpatients receiving immunosuppressive therapy. Inpatients were screened twice weekly; outpatients weekly, if possible
Representative spectrum? Yes: adults undergoing allogeneic haematopoietic stem cell transplantation
Index tests Platelia. Serum was monitored twice a week until discharge or death. Outpatients were monitored weekly where possible. Positive was above 1.5 and negative was below 1.0. In between was undetermined. Total of 832 samples from 74 patients. Positive was one or more positive; negative was all negative
Target condition and reference standard(s) Invasive aspergillosis, as defined by EORTC criteria (Ascioglu 2002)
Incorporation avoided? Yes: Aspergillus galactomannan antigen test results were excluded as microbiologic criteria
 Acceptable reference standard? Yes: EORTC criteria (Ascioglu 2002)
Flow and timing Time interval not reported
Partial verification avoided? Yes: all patients were classified according to reference criteria
 Withdrawals explained? Unclear
 Uninterpretable results reported? Yes: when a sample was undetermined, an additional sample was immediately tested
Comparative  
No patients per category 1 proven, 5 probable, 2 possible, 66 no IA
Notes Clinical course and timelines for 8 patients
Sponsoring? Governance funds and a leukaemia foundation
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? Yes    
    Low 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