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The study consists in taking 4 tubes of blood at different times over a period of 10 days, via a catheter (central venous or arterial catheter) already in place in the usual therapeutic management. These samples will make it possible to measure blood levels of certain markers specific to invasive candidiasis. PCR will be used to quantify fungal load precisely, that is to say the quantity of yeast present in the blood and to monitor this quantity over time.
These samples will be transferred to a specialized unit and stored for a maximum of three years for use at the end of the study.
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Inclusion criteria
Patient informed about the study
Patients aged at least 18 years admitted to a medical Intensive Care or general intensive care
Patients with suspected invasive candidiasis - that is to say:
Presenting persistent sepsis despite broad-spectrum antibiotherapy for at least 48 hours or targeted antibiotherapy for a documented bacterial infection (sepsis will be defined according to:
Candida score ≥ 3 with multifocal colonization
Decision to initiate echinocandin therapy made by the clinician in charge of the patient
Exclusion criteria
80 participants in 1 patient group
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Central trial contact
Rémi BRUYERE
Data sourced from clinicaltrials.gov
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