Comparison of candidemia caused by Candida auris and non-auris Candida spp.: a retrospective cohort study on clinical characteristics, risk factors, and antifungal resistance profiles
摘要
Candida auris has emerged as a significant global health threat due to its resistance to multiple antifungal agents and its prominent role in healthcare-associated infections. This study aims to compare the clinical characteristics, risk factors, antifungal resistance profiles, and mortality rates of candidemia caused by C. auris and non-auris Candida spp. (NACS).
Materials and methodsThis retrospective cohort study was conducted at a tertiary care hospital from 2021 to 2024. Patients aged 18 years and older with positive blood cultures for Candida spp. were included. Demographic data, comorbidities, risk factors, mortality rates, and treatment protocols were analyzed.
ResultsA total of 1,088 candidemia cases were included in the study (C. auris: 126 cases, NACS: 962 cases). The length of hospital stay was significantly longer in the C. auris group compared to the NACS group (50.98 ± 38.79 vs. 33.05 ± 25.57 days, p < 0.001). Independent risk factors for C. auris candidemia included longer hospitalization before candidemia (OR 1.01, 95% CI 1.01–1.02, p < 0.001), chronic obstructive pulmonary disease (OR 1.89, 95% CI 1.07–3.31, p = 0.026), prior antifungal use within 30 days (OR 1.92, 95% CI 1.22–3.03, p = 0.005), and ICU admission (OR 2.08, 95% CI 1.10–3.92, p = 0.023). Antifungal resistance rates among C. auris isolates were 96.49% for fluconazole, 72.81% for amphotericin B, and 25.89% for caspofungin. The 30-day mortality rate was lower in the C. auris group (48.4%) compared to the NACS group (60.2%) (p = 0.012).
ConclusionAlthough crude 30-day mortality was lower in the C. auris group, adjusted analysis showed comparable 30-day mortality between the C. auris and NACS groups. These findings highlight the increasing clinical burden of C. auris and support accurate species identification, local antifungal susceptibility surveillance, and rigorous infection-control measures.
Clinical trial numberNot applicable.