Williamson 2000.
Study characteristics | |||
Patient sampling | Prospective; consecutive series of patients; blood samples re‐analysed later for ELISA | ||
Patient characteristics and setting | 104 participants Age ranged from 3 months to 56 years No information about gender UK Children and adults undergoing bone marrow transplantation (BMT) or chemotherapy for haematological malignancy with severe neutropenia Inpatients Monitoring clinical course |
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Index tests | Platelia Aspergillus Serum samples were collected and tested twice weekly One positive is positive; no positive at all is negative Cut‐off value not reported |
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Target condition and reference standard(s) | Invasive aspergillosis, as defined by EORTC‐like criteria, no reference; 3 groups Galactomannan ELISA was not mentioned as part of the reference criteria |
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Flow and timing | All patients were classified according to the same reference criteria Withdrawals explained? Yes Uninterpretable results reported? No |
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Comparative | |||
No patients per category | 7 proven, no probables, 9 possible, 88 no IA | ||
Notes | Nothing reported on conflicts of interest or sponsoring | ||
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? | Unclear | ||
Unclear | Low | ||
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? | Unclear | ||
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? | Yes | ||
Unclear | Unclear | ||
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 | ||
Low |