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Difficulties in using 1,3-beta-D-glucan as the screening test for the early diagnosis of invasive fungal infections in patients with haematological malignancies--high frequency of false-positive results and their analysis
Zdenek Racil, Iva Kocmanova, Martina Lengerova, Barbora Weinbergerova, Lucie Buresova, Martina Toskova, Jana Winterova, Shira Timilsina, Isa Rodriguez, Jiri Mayer
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NS10442
MZ0
CEP - Centrální evidence projektů
NS10441
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
Zdroj
NLK
Free Medical Journals
od 1968 do Před 1 rokem
PubMed
20488937
DOI
10.1099/jmm.0.019299-0
Knihovny.cz E-zdroje
- MeSH
- beta-glukany krev MeSH
- hematologické nádory komplikace farmakoterapie MeSH
- imunoanalýza MeSH
- imunokompromitovaný pacient MeSH
- lidé MeSH
- mykózy krev diagnóza imunologie MeSH
- oportunní infekce chemicky indukované diagnóza MeSH
- prediktivní hodnota testů MeSH
- protinádorové látky škodlivé účinky terapeutické užití MeSH
- senzitivita a specificita MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
We have evaluated the contribution of the 1,3-beta-d-glucan (BG) assay for the screening of invasive fungal infections (IFIs) in patients with haematological malignancies. Serum samples from patients at risk of IFI were collected twice a week and retrospectively tested using the BG assay. BG screening was performed on 1143 samples from 91 patients during 104 anticancer treatment cycles. Proven and probable cases of IFI occurred in 9 (8.7 %) treatment cycles. Depending on the criterion of positivity used (1x >60 pg ml(-1), 1x >80 pg ml(-1), 2x >60 pg ml(-1) or 2x >80 pg ml(-1)) the sensitivity and specificity were 89, 89, 67 and 44 %, and 20, 48, 33 and 56 %, respectively. Although the test was marked as positive in 82, 68, 54 and 45 % of all the treatment cycles, in the majority of cases, these positivities were probably false. The major limit of the BG test was an extremely low positive predictive value (10 to 12 %). We have analysed mucositis, candida colonization, bacteraemia, use of antimicrobials, erythrocyte and thrombocyte filtered blood products, collecting tubes or sampling via venous catheters. Even though no factor is a major source of BG, it could at least partially influence BG assay performance. Thus, BG detection has a limited usefulness as a screening method for IFIs in patients with haematological malignancies.
Department of Microbiology University Hospital Brno Brno Czech Republic
Citace poskytuje Crossref.org
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