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Generation of Fluorescent Protein Fusions in Candida Species
Published on: March 4, 2017
Outcomes attributable to neonatal candidiasis.
Theoklis E Zaoutis1, Kateri Heydon, Russell Localio
1Division of Infectious Diseases, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA. zaoutis@email.chop.edu
Summary
Invasive candidiasis significantly increases mortality and costs in extremely low birth weight neonates. For larger neonates, it leads to longer hospital stays and higher costs but not increased mortality.
Area of Science:
- Neonatal Medicine
- Infectious Diseases
- Healthcare Economics
Background:
- Neonatal intensive care units (NICUs) face rising rates of candidiasis.
- Invasive candidiasis in neonates causes significant morbidity and mortality.
- Limited data exist on outcomes directly attributed to neonatal candidiasis.
Purpose of the Study:
- To estimate the incidence of systemic candidiasis in hospitalized US neonates.
- To determine the attributable mortality, length of hospital stay, and costs.
- To analyze outcomes stratified by birth weight, focusing on extremely low birth weight (ELBW) neonates.
Main Methods:
- Utilized the 2003 Kid's Inpatient Database for analysis.
- Defined systemic candidiasis and comorbidities using ICD-9-CM codes.
- Employed propensity score methods to balance covariates, with separate analyses for ELBW neonates (<1000g).
Main Results:
- Overall incidence of invasive candidiasis: 15 per 10,000 neonatal admissions.
- ELBW neonates with candidiasis had a 2.2-fold increased mortality risk (11.9% attributable mortality) and $39,045 in excess charges.
- Neonates >1000g with candidiasis experienced a 16-day longer stay and $122,302 in excess charges, without increased mortality.
Conclusions:
- Invasive candidiasis significantly elevates death risk and hospital charges in ELBW neonates.
- For neonates weighing >=1000g, candidiasis increases hospital stay duration and costs but not mortality.
- Findings highlight the substantial burden of neonatal candidiasis, particularly in vulnerable ELBW infants.
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