MycoBiomDB – Record Details (MyCo_6701)

Biomarker Record Details

Database ID: MyCo_6701
DB IDMyCo_6701
TitleMulticenter Prospective Study of Biomarkers for Diagnosis of Invasive Candidiasis in Children and Adolescents
Year2022
PMID35134165
Fungal Diseases involvedInvasive candidiasis
Associated Medical ConditionNone
GenusCandida
Speciesspp.
OrganismCandida spp.
Ethical StatementClinical Trials Registration. NCT02220790
Site of InfectionBloodstream
Opportunistic invasiveOpportunistic
Sample typeBody fluid
Sample sourceBlood
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameT2Candida
Biomarker Full NameT2Candida Assay
Biomarker TypeDiagnostic
BiomoleculeNone
Geographical LocationUSA
CohortEligible participants were aged >120 days and <18 years with clinical characteristics concerning for IC. Participants were ineligible if they (1) had possible, probable, or proven in¬vasive fungal disease according to European Organization for Research and Treatment of Cancer/Mycoses Study Group cri¬teria within the past 30 days; (2) had been previously included in the study; (3) weighed <4 kg, disallowing sufficient phle¬botomy; or (4) were receiving empirical or targeted antifungal therapy.
Cohort No.500 Patients
Age Grouppatients aged >120 days and <18 years
P ValueNone
Sensitivity0.792
Specificity0.971
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismInvasive candidiasis (IC) is a common cause of bloodstream infections in hospitalized patients and associated with in¬creased hospital lengths of stay, charges, and all-cause mortality rates. These infections can be particularly severe in chil¬dren with cancer and after organ or hematopoietic cell transplantation [6–8]. Diagnosing IC in pediatric patients is challenging. Cultures are insensitive and often take >24 hours for a preliminary positive result, delaying initial therapy and leading to in¬creased mortality rate. A single-center prediction rule to identify candidemia in pediatric intensive care unit patients found that multiple factors had a predictive probability of 46%. However, an independent multicenter study failed to vali¬date the model.
TechniqueELISA
Analysis MethodT2Candida ELISA Assay Based [FDA Approved]
ELISA kitsNone
Assay DataNone
Validation Techniques usedFDA Approved ELISA
Up Regulation Down RegulationNone
Sequence DataNone
External LinkNone