MycoBiomDB – Record Details (MyCo_7246)

Biomarker Record Details

Database ID: MyCo_7246
DB IDMyCo_7246
TitleA score for predicting invasive pulmonary aspergillosis in immunocompetent critically ill patients
Year2023
PMID36920323
Fungal Diseases involvedInvasive pulmonary aspergillosis
Associated Medical ConditionNone
GenusAspergillus
Speciesspp.
OrganismAspergillus spp.
Ethical StatementThis study was approved by ethics committee of Xiangya Hospital, Central South University (No. 202104005).
Site of InfectionNone
Opportunistic invasiveInvasive
Sample typeBody fluid
Sample sourceBlood
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NamePNI
Biomarker Full NamePrognostic nutritional index
Biomarker TypeDiagnostic
BiomoleculeNone
Geographical LocationChina
CohortHere screened 2546 consecutive patients admitted to the ICU, excluding 705 patients, and enrolled 1841 patients in this study .
Cohort No.1841
Age GroupNone
P Valuep=.002
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismInvasive pulmonary aspergillosis (IPA) is a life-¬ threatening opportunistic fungal infection with a high mortality rate ranging from 45% to 90%. It mostly occurs in immuno- suppressed patients, such as those with haematological malignancies, solid organ transplants or prolonged neu- tropenia. IPA has also been accepted as an emerging in- fection in critically ill patients admitted to the intensive care unit (ICU). Critically ill patients admitted to the ICU are often exposed to many risk factors associated with IPA, such as the use of invasive devices, prolonged ex- posure to corticosteroids or broad-¬ spectrum antibiotics. The incidence of IPA in ICU settings fluctuates from 0.2% to 39%, with an overall mortality rate exceeding 60%. However, previous studies and clinical guidelines have mostly focused on immunodeficient patients and may not be applicable to patients in the ICU, because most patients in the ICU have a normal immune status at the onset of infection. Hence, there is a lack of strong clinical evidence to guide the early diagnosis of IPA and subsequent timely initial antifungal therapy in immunocompetent patients in the ICU.
TechniqueNone
Analysis MethodNone
ELISA kitsNone
Assay DataNone
Validation Techniques usedNone
Up Regulation Down RegulationPositive
Sequence DataNone
External LinkNone