Burden of Candidemia in the United States, 2017
Open accessAbstract
Background: Candidemia is a common healthcare-associated bloodstream infection with high morbidity and mortality. There are no current estimates of candidemia burden in the United States (US). Methods: In 2017, the Centers for Disease Control and Prevention conducted active population-based surveillance for candidemia through the Emerging Infections Program in 45 counties in 9 states encompassing approximately 17 million persons (5% of the national population). Laboratories serving the catchment area population reported all blood cultures with Candida, and a standard case definition was applied to identify cases that occurred in surveillance area residents. Burden of cases and mortality were estimated by extrapolating surveillance area cases to national numbers using 2017 national census data. Results: We identified 1226 candidemia cases across 9 surveillance sites in 2017. Based on this, we estimated that 22 660 (95% confidence interval [CI], 20 210–25 110) cases of candidemia occurred in the US in 2017. Overall estimated incidence was 7.0 cases per 100 000 persons, with highest rates in adults aged ≥ 65 years (20.1/100 000), males (7.9/100 000), and those of black race (12.3/100 000). An estimated 3380 (95% CI, 1318–5442) deaths occurred within 7 days of a positive Candida blood culture, and 5628 (95% CI, 2465–8791) deaths occurred during the hospitalization with candidemia. Conclusions: Our analysis highlights the substantial burden of candidemia in the US. Because candidemia is only one form of invasive candidiasis, the true burden of invasive infections due to Candida is higher. Ongoing surveillance can support future burden estimates and help assess the impact of prevention interventions.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
6 of 10 cited sources checked · 2 supported · 0 flagged · accuracy not yet measured
- Study design and conductown data
In 2017, CDC conducted active population-based surveillance for candidemia through the Emerging Infections Program in 45 counties in 9 states covering approximately 17 million persons (5% of the national population).
“In 2017, the Centers for Disease Control and Prevention conducted active population-based surveillance for candidemia through the Emerging Infections Program in 45 counties in 9 states encompassing approximately 17 million persons (5% of the national population).”
- Also stated in: § METHODS · plain
“In 2017, surveillance for candidemia was conducted in 45 counties in 9 states (California, Colorado, Georgia, Maryland, Minnesota, New Mexico, New York, Oregon, and Tennessee) with a total catchment area population of 17 million persons.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [6] Toda, 2019, Population-based active surveillance for culture-confirmed candidemia—four sites, United States, 2012–2016, MMWR Surveill Summ source
The Abstract’s Public Health Action section and the Conclusion state that candidemia surveillance expanded to nine sites in 2017. The Methods’ Data Source section describes the earlier 2012–2016 surveillance area, not the expanded 2017 area. Our copy does not substantiate the claim’s 45 counties, approximately 17 million persons, or 5% of the national population. (LLM, conf=0.88)
Experimental — accuracy not yet measured
- Also stated in: § METHODS · plain
- Study design and conductreasoning
Because the populations under surveillance in the 9 EIP sites are diverse, EIP findings can and have been used to extrapolate to national estimates of other infections.
“Furthermore, because the populations under surveillance in the 9 sites are diverse (by age distribution, race, urban/rural, and other factors), EIP findings can and have been used to extrapolate to national estimates of other infections [33,34].”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [33] Dantes, 2013, National burden of invasive methicillin-resistant Staphylococcus aureus infections, United States, 2011, JAMA Intern Med source
The Discussion describes diverse populations in several metropolitan surveillance areas, and Methods > Statistical Analysis explains how EIP-ABCs data were extrapolated to national estimates of invasive MRSA. The paper does not establish that the sites are diverse by urban/rural status or that EIP findings have been used to estimate other infections nationally. It also cautions that the sites were not randomly selected to be representative. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [34] Lessa, 2015, Burden of Clostridium difficile infection in the United States, N Engl J Med source
The Methods (Surveillance Population and Definition; Statistical Analysis) describe geographically varied EIP surveillance areas and use EIP data to estimate the national burden of C. difficile infection, accounting for demographic factors. This supports the cited paper as an example of national extrapolation. It studied 10 EIP sites, however, not the nine sites named in the citing sentence, and does not establish that site diversity was the reason extrapolation was possible. (LLM, conf=0.85)
Experimental — accuracy not yet measured
- Findingown data
In this analysis, the burden of candidemia among black individuals was disproportionately high.
“In this analysis, we found that the burden of candidemia among black individuals was disproportionately high.”
Quote in the paperSubstantial claim - Findingown data
An estimated 5628 deaths (95% CI, 2465-8791) occurred during hospitalization with candidemia in the United States in 2017.
“An estimated 3380 (95% CI, 1318-5442) deaths occurred within 7 days of a positive Candida blood culture, and 5628 (95% CI, 2465-8791) deaths occurred during the hospitalization with candidemia.”
- Also stated in: § RESULTS · hedged
“An estimated 3380 (95% CI, 1318-5442) deaths occurred within 7 days of positive culture for candidemia and 5628 (95% CI, 2465-8791) deaths occurred during the hospitalization with candidemia.”
Quote in the paperNot a substantial claim - Also stated in: § RESULTS · hedged
- Findingown data
Candida parapsilosis accounted for 14% of Candida isolates.
“The most frequent Candida species isolated from culture was Candida albicans (38%), followed by Candida glabrata (30%), Candida parapsilosis (14%), and Candida tropicalis (7%).”
Quote in the paperNot a substantial claim
- Findingown data
The overall estimated incidence of candidemia was 7.0 cases per 100,000 persons.
“Overall estimated incidence was 7.0 cases per 100 000 persons, with highest rates in adults aged ≥ 65 years (20.1/100000), males (7.9/100 000), and those of black race (12.3/100 000).”
- Also stated in: § RESULTS · hedged
“The overall estimated incidence of candidemia was 7.0 cases per 100 000 persons.”
Quote in the paperNot a substantial claim - Also stated in: § RESULTS · hedged
- Findingown data
The most frequent Candida species isolated was Candida albicans, accounting for 38% of isolates.
“The most frequent Candida species isolated from culture was Candida albicans (38%), followed by Candida glabrata (30%), Candida parapsilosis (14%), and Candida tropicalis (7%).”
Quote in the paperNot a substantial claim - Findingown data
Among racial groups, estimated incidence was highest among black patients, at 12.3 per 100,000.
“Overall estimated incidence was 7.0 cases per 100 000 persons, with highest rates in adults aged ≥ 65 years (20.1/100000), males (7.9/100 000), and those of black race (12.3/100 000).”
- Also stated in: § RESULTS · plain
“Among racial groups, incidence was highest among black patients (12.3 per 100 000), accounting for nearly a quarter of all cases (5366 [95% CI, 4055-6677]).”
Quote in the paperNot a substantial claim - Also stated in: § RESULTS · plain
- Findingown data
An estimated 22,660 candidemia cases (95% CI, 20,210-25,110) occurred in the United States in 2017.
“Based on this, we estimated that 22 660 (95% confidence interval [CI], 20 210-25 110) cases of candidemia occurred in the US in 2017.”
- Also stated in: § RESULTS · hedged
“We estimated that 22 660 candidemia cases (95% CI, 20 210-25 110) occurred in the US in 2017.”
Quote in the paperSubstantial claim - Also stated in: § RESULTS · hedged
- Findingown data
Six percent of all Candida isolates were resistant to fluconazole.
“Six percent of all Candida isolates were resistant to fluconazole, with rates ranging from 0.5% in C. albicans to 7% in C. glabrata and 9% in C. parapsilosis.”
Quote in the paperNot a substantial claim - Findingown data
Candida glabrata accounted for 30% of Candida isolates.
“The most frequent Candida species isolated from culture was Candida albicans (38%), followed by Candida glabrata (30%), Candida parapsilosis (14%), and Candida tropicalis (7%).”
Quote in the paperNot a substantial claim - Findingown data
Two percent of Candida isolates were resistant to an echinocandin antifungal.
“Two percent of Candida isolates were resistant to an echinocandin antifungal, of which most were C. glabrata.”
Quote in the paperNot a substantial claim - Findingown data
Estimated incidence was highest among adults aged 65 years or older, at 20.1 per 100,000.
“Overall estimated incidence was 7.0 cases per 100 000 persons, with highest rates in adults aged ≥ 65 years (20.1/100000), males (7.9/100 000), and those of black race (12.3/100 000).”
- Also stated in: § RESULTS · plain
“Incidence was highest among adults aged ≥ 65 years (20.1 per 100 000), accounting for nearly half of all candidemia cases (10 205 [95% CI, 8305-12 104]).”
Quote in the paperNot a substantial claim - Also stated in: § RESULTS · plain
- Findingown data
All-cause in-hospital mortality within 7 days of candidemia was 15%.
“All-cause in-hospital mortality within 7 days of candidemia was 15%, and mortality during the entire hospitalization with candidemia was 25%.”
Quote in the paperNot a substantial claim - Findingown data
All-cause in-hospital mortality during the entire hospitalization with candidemia was 25%.
“All-cause in-hospital mortality within 7 days of candidemia was 15%, and mortality during the entire hospitalization with candidemia was 25%.”
Quote in the paperNot a substantial claim - Findingown data
An estimated 3380 deaths (95% CI, 1318-5442) occurred within 7 days of a positive Candida blood culture in the United States in 2017.
“An estimated 3380 (95% CI, 1318-5442) deaths occurred within 7 days of a positive Candida blood culture, and 5628 (95% CI, 2465-8791) deaths occurred during the hospitalization with candidemia.”
- Also stated in: § RESULTS · hedged
“An estimated 3380 (95% CI, 1318-5442) deaths occurred within 7 days of positive culture for candidemia and 5628 (95% CI, 2465-8791) deaths occurred during the hospitalization with candidemia.”
Quote in the paperNot a substantial claim - Also stated in: § RESULTS · hedged
- Premisecitation
Previous studies of autopsy-proven invasive candidiasis suggest that blood cultures are positive in 21%-71% of cases.
“Previous studies of autopsy-proven invasive candidiasis suggest that blood cultures are positive in 21%-71% of cases [9], which suggests that the estimated burden of invasive candidiasis would be even higher, although further evaluation of the relative burden of candidemia in overall invasive candidiasis is needed.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [9] Clancy, 2013, Finding the “missing 50%” of invasive candidiasis: how nonculture diagnostics will improve understanding of disease spectrum and transform patient care, Clin Infect Dis source
- Interpretationreasoning
The overall burden of candidemia in the United States was likely underestimated.
“For these reasons, we have likely underestimated the overall burden of candidemia in the US.”
Quote in the paperSubstantial claim - Interpretationnone given
This analysis represents the first population-based estimate of candidemia burden in the United States.
“Despite these limitations, this analysis represents the first population-based estimate of candidemia burden in the United States and will serve as a starting point for evaluating future rates and epidemiology, in addition to the impact of interventions aimed at preventing candidemia.”
Quote in the paperSubstantial claim
- Classified as probably not a substantial claim. 15
- May combine two claims. 4
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationCandidemia is a common healthcare-associated bloodstream infection in the United States with significant morbidity and 25%-40% all-cause in-hospital mortality.
“Candidemia is one of the most common healthcare-associated bloodstream infections in the United States (US) [1,2].It is associated with significant morbidity and 25%-40% all-cause in-hospital mortality [3].”
Quote in the paperNot a substantial claim3 of 3 sources checked- cites [1] Magill, 2014, Multistate point-prevalence survey of health care-associated infections, N Engl J Med source
- cites [2] Magill, 2018, Changes in prevalence of health care-associated infections in U.S. hospitals, N Engl J Med source
- cites [3] Pfaller, 2007, Epidemiology of invasive candidiasis: a persistent public health problem, Clin Microbiol Rev source
In “The Burden of Disease: Perspectives from the NHDS” (page not supplied), the paper identifies Candida as the fourth leading cause of nosocomial bloodstream infection in the United States and describes a substantial disease burden. It uses 40% crude mortality as an assumption for estimating deaths, but the cited passages do not establish a 25%–40% range or specify all-cause in-hospital mortality. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThirty-two percent of candidemia cases occurred in black patients.
“Overall, 64% of cases occurred in white patients, and 32% of cases occurred in black patients (Table 1).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataFifty-five percent of candidemia cases occurred in males.
“Fifty-five percent of cases occurred in males.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThree percent of candidemia cases were among children aged 18 years or younger.
“Forty-two percent of cases occurred in patients aged ≥ 65 years, and 3% were among children (≤ 18 years).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataIn 2017, 1226 candidemia cases were identified in 1140 patients across 9 EIP sites.
“In 2017, we identified 1226 cases of candidemia in 1140 patients in 9 EIP sites, with 7% of cases being recurrent in the same patient.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataForty-two percent of candidemia cases occurred in patients aged 65 years or older.
“Forty-two percent of cases occurred in patients aged ≥ 65 years, and 3% were among children (≤ 18 years).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataSixty-four percent of candidemia cases occurred in white patients.
“Overall, 64% of cases occurred in white patients, and 32% of cases occurred in black patients (Table 1).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataCandida tropicalis accounted for 7% of Candida isolates.
“The most frequent Candida species isolated from culture was Candida albicans (38%), followed by Candida glabrata (30%), Candida parapsilosis (14%), and Candida tropicalis (7%).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataSeven percent of candidemia cases were recurrent in the same patient.
“In 2017, we identified 1226 cases of candidemia in 1140 patients in 9 EIP sites, with 7% of cases being recurrent in the same patient.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
PremisecitationEstimates of mortality attributable to candidemia range from 5% to 71%, varying based on setting, age group, and study design.
“Estimates of mortality attributable to candidemia range from 5% to 71%, varying based on setting, age group, and study design [10].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [10] Falagas, 2006, Attributable mortality of candidemia: a systematic review of matched cohort and case-control studies, Eur J Clin Microbiol Infect Dis source
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataMultiple imputation was performed for missing patient race information based on the distribution of known values for 2017 cases, stratified by age and sex.
“To address missing patient race information, we performed multiple imputations based on the distribution of known values for 2017 cases, stratified by age and sex.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenPeriodic audits were conducted at each laboratory to ensure completeness of reporting.
“Periodic audits were conducted at each laboratory to ensure completeness of reporting.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningCandidemia represents only a portion of the burden of invasive candidiasis; other forms of invasive disease may not manifest with positive blood cultures but also have severe sequelae and contribute to morbidity and mortality.
“Candidemia represents only a portion of the burden of invasive candidiasis; other forms of invasive disease include intra-abdominal candidiasis, hepatosplenic candidiasis, endophthalmitis, osteomyelitis, and meningitis, which may not manifest with positive blood cultures, but also have severe sequelae and contribute to morbidity and mortality.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationAvailable Candida isolates from incident blood cultures were sent to CDC for species confirmation and antifungal susceptibility testing using Clinical and Laboratory Standards Institute guidelines.
“Available Candida isolates from incident blood cultures were sent to CDC for species confirmation and antifungal susceptibility testing using Clinical and Laboratory Standards Institute guidelines [8].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] Clinical and Laboratory Standards Institute
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
InterpretationreasoningThe 2017 resistance rates of 6% to fluconazole and 2% to echinocandins correspond to more than 1400 fluconazole-resistant and 340 echinocandin-resistant bloodstream infections nationally in 2017.
“Although we did not include an extrapolation of drug-resistant infections in our national estimates, resistance rates found in 2017, 6% to fluconazole and 2% to echinocandins, correspond to > 1400 fluconazole-resistant and 340 echinocandin-resistant bloodstream infections nationally in 2017.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductown dataA standard case definition was applied to identify candidemia cases in surveillance area residents.
“a standard case definition was applied to identify cases that occurred in surveillance area residents.”
- Also stated in: § METHODS · plain
“A case of candidemia was defined as a blood culture positive for Candida species in a surveillance area resident.”
Quote in the paperSubstantial claim- Also stated in: § METHODS · plain
May combine two claims.
Study design and conductown dataSampling weights were calculated by dividing the 2017 US Census population estimate by estimated EIP site populations, stratified by age, sex, and race, and used to estimate national candidemia burden.
“We calculated sampling weights by dividing the Census Bureau 2017 US population estimate by estimated EIP site populations, stratified by age, sex, and race.We then weighted 2017 case numbers, stratified by demographic characteristics, to estimate the national burden of candidemia and generate 95% confidence intervals (CIs).”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
PremisecitationThirteen percent of the US population was black in 2017 Census Bureau estimates.
“Thirteen percent of the US population was black in 2017 Census Bureau estimates [19], whereas nearly a quarter of all estimated candidemia cases occurred among black individuals.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [19]
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
The paper relies on this without support.
There are no current estimates of candidemia burden in the United States.
“There are no current estimates of candidemia burden in the United States (US).”
The authors state this as an assumption.
The bloodstream infection with Candida species contributed, at least in part, to death within 7 days of a positive Candida blood culture.
“Therefore, we used a conservative estimate of death within 7 days of positive blood culture for Candida, assuming that the bloodstream infection with Candida species contributed, at least in part, to death in these cases.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The proportion of C. albicans was 70-80% in the 1980-1990s and has now declined to 40-60% in most geographic areas.
“While the proportion of C. albicans was 70–80% in the 1980–1990s,54 it has now declined to 40–60% in most geographic areas.25,55,56”
From Epidemiology of Invasive Candidiasis (2024) · cites this paper as [25]
The Results report that C. albicans accounted for 38% of Candida isolates in the paper’s 2017 US surveillance, supporting a substantially lower contemporary proportion. The paper does not establish the cited 40–60% range across most geographic areas; the historical 70–80% figure is attached to a different citation in the citing sentence. (LLM, conf=0.84)
Experimental — accuracy not yet measuredActive population-based surveillance showed the incidence of candidemia decreased from 2008 to 2017 across multiple US sites, with a coincident increase in the incidence of invasive candidiasis from non-blood sources, including abdominal sterile sites, from 2009-2017.
“A more nuanced assessment using data from active population-based surveillance showed the incidence of candidemia decreased from 2008 to 2017 across multiple US sites,25,27,35 with a coincident increase in the incidence of IC from non-blood sources, including abdominal sterile sites, from 2009–2017.34”
From Epidemiology of Invasive Candidiasis (2024) · cites this paper as [25]
Split into 2 atoms — 0 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 1 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredIn the United States, all-cause mortality of invasive candidiasis was highest among older adults and lowest among children.
“In the US, all-cause mortality was highest among older adults and lowest among children.25,27,52”
From Epidemiology of Invasive Candidiasis (2024) · cites this paper as [25]
The Results report that all-cause in-hospital mortality among patients with candidemia was highest at age ≥65 (31%) and lowest at age ≤18 (9%). The paper also states that candidemia is only one form of invasive candidiasis, so these age-specific findings do not establish the pattern for invasive candidiasis as a whole. (LLM, conf=0.88)
Experimental — accuracy not yet measuredCandidemia causes an estimated 22,000 infections annually in the United States.
“Candidemia causes an estimated 22,000 infections annually in the United States.25”
From Epidemiology of Invasive Candidiasis (2024) · cites this paper as [25]
There has been a clear worldwide trend of decreasing proportions of C. albicans as the causative pathogen of invasive candidiasis or candidemia.
“Independent of these geographic variations, there has been a clear worldwide trend of decreasing proportions of C. albicans as the causative pathogen.”
From Epidemiology of Invasive Candidiasis (2024) · cites this paper as [25]
The Results report that C. albicans accounted for 38% of isolates in the US surveillance sites in 2017, but give no comparison over time. The Discussion says limited earlier site participation prevented national-level trend estimation; the copy does not address a worldwide decline in the proportion of C. albicans. (LLM, conf=0.78)
Experimental — accuracy not yet measured
The proportion of C. glabrata has increased particularly in the United States, Australia, and Northern Europe.
“The proportion of C. glabrata has increased particularly in the US, Australia, and Northern Europe.25,40,41,55,61”
From Epidemiology of Invasive Candidiasis (2024) · cites this paper as [25]
The Results report that C. glabrata accounted for 30% of US Candida isolates in 2017, but give no evidence that its proportion increased. The Discussion says the surveillance data limit national-level trend estimates; our copy does not address C. glabrata trends in Australia or Northern Europe. Searched for increasing C. glabrata proportions and those regions. (LLM, conf=0.76)
Experimental — accuracy not yet measuredThese rates are higher than the observed mortality rates for candidemia/invasive candidiasis, which are estimated to be 25% overall and 31%, respectively, for patients ≥65 years of age.
“These rates are higher than the observed mortality rates for candidemia/invasive candidiasis, which are estimated to be 25% overall and 31%, respectively, for patients ≥65 years of age (9).”
Invasive candidiasis remains a significant cause of patient morbidity and death.
“Invasive candidiasis remains a significant cause of patient morbidity and death.”
Cites
Unequal treatment: confronting racial and ethnic disparities in health care
(2003) · Choice Reviews Online · doi:10.5860/choice.40-5843 · Cited by 7,043 · see citing works
Antibiotic resistance threats in the United States, 2019
(U.S.), C. F. D. C. A. P. (2019) · doi:10.15620/cdc:82532 · Cited by 5,782 · see citing works
Pappas, P. G., Kauffman, C. A., Andes, D. R., Clancy, C. J., Marr, K. A., Ostrosky-Zeichner, L., Reboli, A. C., Schuster, M. G., Vazquez, J. A., Walsh, T. J., et al. (2016) · Clinical Infectious Diseases · doi:10.1093/cid/civ933 · Cited by 4,200 · see citing works
Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem
Pfaller, M. A., & Diekema, D. J. (2007) · Clinical Microbiology Reviews · doi:10.1128/cmr.00029-06 · Cited by 4,174 · see citing works
Multistate point-prevalence survey of health care-associated infections
Magill, S. S., Edwards, J. R., Bamberg, W., Beldavs, Z. G., Dumyati, G., Kainer, M. A., Lynfield, R., Maloney, M., McAllister-Hollod, L., Nadle, J., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1306801 · Cited by 3,931 · see citing works
Self-citationKlevens, R. M. (2007) · JAMA · doi:10.1001/jama.298.15.1763 · Cited by 3,726 · see citing works
Burden of <i>Clostridium difficile</i> Infection in the United States
Lessa, F. C., Mu, Y., Bamberg, W. M., Beldavs, Z. G., Dumyati, G. K., Dunn, J. R., Farley, M. M., Holzbauer, S. M., Meek, J. I., Phipps, E. C., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1408913 · Cited by 2,641 · see citing works
Self-citationKullberg, B. J., & Arendrup, M. C. (2015) · New England Journal of Medicine · doi:10.1056/nejmra1315399 · Cited by 1,315 · see citing works
Pappas, P. G., Kauffman, C. A., Andes, D. R., Clancy, C. J., Marr, K. A., Ostrosky-Zeichner, L., Reboli, A. C., Schuster, M. G., Vazquez, J. A., Walsh, T. J., et al. (2016) · Clinical Infectious Diseases · doi:10.1093/cid/civ1194 · Cited by 1,298 · see citing works
Changes in prevalence of health care-associated infections in U.S. hospitals
Magill, S. S., O’Leary, E., Janelle, S. J., Thompson, D. L., Dumyati, G., Nadle, J., Wilson, L. E., Kainer, M. A., Lynfield, R., Greissman, S., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1801550 · Cited by 1,249 · see citing works
Self-citationGarey, K. W., Rege, M., Pai, M. P., Mingo, D. E., Suda, K. J., Turpin, R. S., & Bearden, D. T. (2006) · Clinical Infectious Diseases · doi:10.1086/504810 · Cited by 1,171 · see citing works
Zaoutis, T. E., Argon, J., Chu, J., Berlin, J. A., Walsh, T. J., & Feudtner, C. (2005) · Clinical Infectious Diseases · doi:10.1086/496922 · Cited by 784 · see citing works
Alexander, B. D., Johnson, M. D., Pfeiffer, C. D., Jiménez-Ortigosa, C., Catania, J., Booker, R., Castanheira, M., Messer, S. A., Perlin, D. S., & Pfaller, M. A. (2013) · Clinical Infectious Diseases · doi:10.1093/cid/cit136 · Cited by 778 · see citing works
Clancy, C. J., & Nguyen, M. H. (2013) · Clinical Infectious Diseases · doi:10.1093/cid/cit006 · Cited by 688 · see citing works
Hicks, L. A., Bartoces, M. G., Roberts, R. M., Suda, K. J., Hunkler, R. J., Taylor, T. H., & Schrag, S. J. (2015) · Clinical Infectious Diseases · doi:10.1093/cid/civ076 · Cited by 559 · see citing works
Dantes, R. (2013) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2013.10423 · Cited by 452 · see citing works
Risk Factors for Hospital-Acquired Candidemia: A Matched Case-Control Study
Wey, S. B. (1989) · Archives of Internal Medicine · doi:10.1001/archinte.1989.00390100145030 · Cited by 369 · see citing works
Ruiz‐Gaitán, A., Moret, A. M., Tasias‐Pitarch, M., Aleixandre‐López, A. I., Martínez‐Morel, H., Calabuig, E., Salavert‐Lletí, M., Ramírez, P., López‐Hontangas, J. L., Hagen, F., et al. (2018) · Mycoses · doi:10.1111/myc.12781 · Cited by 343 · see citing works
Attributable mortality of candidemia: a systematic review of matched cohort and case-control studies
Falagas, M. E., Apostolou, K. E., & Pappas, V. D. (2006) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-006-0159-2 · Cited by 294 · see citing works
Toda, M., Williams, S. R., Berkow, E. L., Farley, M. M., Harrison, L. H., Bonner, L., Marceaux, K. M., Hollick, R., Zhang, A. Y., Schaffner, W., et al. (2019) · MMWR Surveillance Summaries · doi:10.15585/mmwr.ss6808a1 · Cited by 198 · see citing works
Self-citationVallabhaneni, S., Cleveland, A. A., Farley, M. M., Harrison, L. H., Schaffner, W., Beldavs, Z. G., Derado, G., Pham, C. D., Lockhart, S. R., & Smith, R. M. (2015) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofv163 · Cited by 187 · see citing works
Self-citationEpidemiology of hospitalizations associated with invasive candidiasis, United States, 2002-20121
Strollo, S., Lionakis, M. S., Adjemian, J., Steiner, C. A., & Prevots, D. R. (2016) · Emerging Infectious Diseases · doi:10.3201/eid2301.161198 · Cited by 129 · see citing works
Vallabhaneni, S., Benedict, K., Derado, G., & Mody, R. K. (2017) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofw268 · Cited by 98 · see citing works
Self-citationGualandi, N., Mu, Y., Bamberg, W. M., Dumyati, G., Harrison, L. H., Lesher, L., Nadle, J., Petit, S., Ray, S. M., Schaffner, W., et al. (2018) · Clinical Infectious Diseases · doi:10.1093/cid/ciy277 · Cited by 60 · see citing works
Self-citationChang, D. C., Burwell, L. A., Lyon, G. M., Pappas, P. G., Chiller, T. M., Wannemuehler, K. A., Fridkin, S. K., & Park, B. J. (2008) · Infection Control & Hospital Epidemiology · doi:10.1086/524324 · Cited by 51 · see citing works
Self-citationTrends in antifungal use in US hospitals, 2006–12
Vallabhaneni, S., Baggs, J., Tsay, S., Srinivasan, A. R., Jernigan, J. A., & Jackson, B. R. (2018) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dky270 · Cited by 45 · see citing works
Self-citationClinical features and risk factors for blood stream infections of Candida in neonates
LIU, M., HUANG, S., GUO, L., LI, H., WANG, F., ZHANG, Q., & SONG, G. (2015) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2015.2626 · Cited by 23 · see citing works
378. <i>Candida auris</i> Fungemia: Risk Factors and Outcome
Adam, R., Okinda, N., Revathi, G., Fontaine, M., Kagotho, E., Castanheira, M., Pfaller, M. A., & Maina, D. (2018) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofy210.389 · Cited by 4 · see citing works
Zhang, A. Y., Shrum, S., Williams, S., Vonbank, B., Hillis, S., Barter, D., Petnic, S., Harrison, L. H., Dumyati, G., Phipps, E. C., et al. (2018) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofy209.128 · Cited by 2 · see citing works
Self-citation
Flagged first, then by citations
1 of the 30 references couldn’t be matched to a known paper.
Research works printed but not linked: 6
- Centers for Disease Control and Prevention, Emerging Infections Program (EIP)
- Clinical and Laboratory Standards Institute, Reference method for broth dilution antifungal susceptibility testing of yeasts, 4th ed
- Centers for Disease Control and Prevention, Candida auris
- QuickFacts
- Centers for Disease Control and Prevention, Active Bacterial Core surveillance report, Emerging Infections Program Network, Streptococcus pneumoniae, 2017.
- Centers for Disease Control and Prevention, Active Bacterial Core surveillance report, Emerging Infections Program Network, group A Streptococcus, 2017.
Cited by
Sorted by citations
Diagnosis of invasive fungal infections: challenges and recent developments
Fang, W., Wu, J., Cheng, M., Zhu, X., Du, M., Chen, C., Liao, W., Zhi, K., & Pan, W. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00926-2 · Cited by 363 · see citing works
“T2 Candida for rapid diagnosis of candidemia in whole blood With an estimated death rate ranging from 25 to 40%, candidemia is the fourth most common cause of hospital-associated bloodstream infections [99].”
BackgroundLass‐Flörl, C., Kanj, S. S., Govender, N. P., Thompson, G. R., Ostrosky‐Zeichner, L., & Govrins, M. A. (2024) · Nature Reviews Disease Primers · doi:10.1038/s41572-024-00503-3 · Cited by 317 · see citing works
Thompson, G. R., Soriano, A., Cornely, O. A., Kullberg, B. J., Kollef, M., Vazquez, J., Honore, P. M., Bassetti, M., Pullman, J., Chayakulkeeree, M., et al. (2023) · The Lancet · doi:10.1016/s0140-6736(22)02324-8 · Cited by 192 · see citing works
Biofilm formation in medically important Candida species
Malinovská, Z., Čonková, E., & Váczi, P. (2023) · Journal of Fungi · doi:10.3390/jof9100955 · Cited by 167 · see citing works
“It is necessary to focus on differentiating biofilm-forming isolates because the mortality rate caused by biofilm formation in Candida -related infections has been shown to be increased almost two-fold when compared to planktonic infections [33].”
BackgroundBranco, J., Miranda, I. M., & Rodrigues, A. G. (2023) · Journal of Fungi · doi:10.3390/jof9010080 · Cited by 133 · see citing works
Arendrup, M. C., Arıkan-Akdağlı, S., Jørgensen, K. M., Barac, A. M., Steinmann, J., Toscano, C., Arsić-Arsenijević, V. S., Sartor, A., Lass‐Flörl, C., Hamprecht, A. G., et al. (2023) · Journal of Infection · doi:10.1016/j.jinf.2023.08.001 · Cited by 130 · see citing works
Prevalence of biofilms in Candida spp. bloodstream infections: A meta-analysis
Atiencia-Carrera, M. B., Cabezas-Mera, F. S., Tejera, E., & Machado, A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0263522 · Cited by 112 · see citing works
Epidemiology of Invasive Candidiasis
Bays, D., Jenkins, E., Lyman, M., Chiller, T., Strong, N., Ostrosky-Zeichner, L., Hoenigl, M., Pappas, P., & Thompson, G. (2024) · Clinical Epidemiology · doi:10.2147/clep.s459600 · Cited by 109 · see citing works
“25,40,41,55,61 Comparatively, the proportion of C. parapsilosis has increased in Asia (including Japan and China), Latin America (including Brazil) and Southern Europe, 31,62–65 and the proportion of C. tropicalis has increased particularly in Latin America, and large parts of Asia.”
BackgroundInfluentialSelf-citationRecent Trends in the Epidemiology of Fungal Infections
Seagle, E. E., Williams, S., & Chiller, T. M. (2021) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2021.03.001 · Cited by 96 · see citing works
Self-citationVazquez, J. A., Pappas, P. G., Boffard, K., Paruk, F., Bien, P. A., Tawadrous, M., Ople, E., Wedel, P., Oborska, I., & Hodges, M. R. (2023) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01419-22 · Cited by 92 · see citing works
Schroeder, M. L., Weber, T., Denker, T., Winterland, S., Wichmann, D., Rohde, H., Ozga, A., Fischer, M., & Kluge, S. (2020) · Annals of Intensive Care · doi:10.1186/s13613-020-00755-8 · Cited by 90 · see citing works
Zhang, S. X., Babady, N. E., Hanson, K. E., Harrington, A., Larkin, P. M. K., Leal, S. M., Luethy, P. M., Martin, I. W., Pancholi, P., Procop, G. W., et al. (2021) · Journal of Clinical Microbiology · doi:10.1128/jcm.01784-20 · Cited by 87 · see citing works
Thompson, G. R., Soriano, À., Honoré, P. M., Bassetti, M., Cornely, O. A., Kollef, M. H., Kullberg, B. J., Pullman, J. R., Hites, M., Fortün, J., et al. (2023) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(23)00551-0 · Cited by 83 · see citing works
Thomaz, D. Y., Negro, G. M. B. D., Ribeiro, L. B., da Silva, M., Carvalho, G. O. M. H., Camargo, C. H., de Almeida, J. N., Motta, A. L., Siciliano, R. F., Sejas, O. N. E., et al. (2022) · Journal of Fungi · doi:10.3390/jof8020100 · Cited by 65 · see citing works
Pappas, P. G., Vazquez, J. A., Oren, I., Rahav, G., Aoun, M., Bulpa, P., Ben-Ami, R., Ferrer, R., Mccarty, T., Thompson, G. R., et al. (2023) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkad256 · Cited by 65 · see citing works
Evaluation of the biofilm life cycle between Candida albicans and Candida tropicalis
Atiencia-Carrera, M. B., Cabezas-Mera, F. S., Vizuete, K. S., Debut, A., Tejera, E., & Machado, A. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.953168 · Cited by 61 · see citing works
“tropicalis is now considered the most important emerging fungal pathogen, and recent reports have identified several strains resistant to standard empirical treatments, such as fluconazole (Tsay et al., 2020; Atiencia-Carrera et al., 2022).”
BackgroundRace and ethnicity: Risk factors for fungal infections?
Jenks, J. D., Aneke, C. I., Al-Obaidi, M. M., Egger, M., Garcia, L., Gaines, T., Hoenigl, M., & Thompson, G. R. (2023) · PLOS Pathogens · doi:10.1371/journal.ppat.1011025 · Cited by 55 · see citing works
Antifungal therapy of Candida biofilms: Past, present and future
Ajetunmobi, O. H., Badali, H., Romo, J. A., Ramage, G., & Lopez-Ribot, J. L. (2023) · Biofilm · doi:10.1016/j.bioflm.2023.100126 · Cited by 52 · see citing works
Augmenting Azoles with Drug Synergy to Expand the Antifungal Toolbox
Kane, A., & Carter, D. A. (2022) · Pharmaceuticals · doi:10.3390/ph15040482 · Cited by 55 · see citing works
Bibi, M., Murphy, S., Benhamou, R. I., Rosenberg, A., Ulman, A., Bicanic, T. A., Fridman, M., & Berman, J. G. (2021) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.0c00721 · Cited by 40 · see citing works
Pinto, H., Simões, M. V., & Borges, A. D. S. (2021) · Antibiotics · doi:10.3390/antibiotics10070825 · Cited by 44 · see citing works
Minority report: the intestinal mycobiota in systemic infections
Rolling, T., Hohl, T. M., & Zhai, B. (2020) · Current Opinion in Microbiology · doi:10.1016/j.mib.2020.05.004 · Cited by 42 · see citing works
Public Health Research Priorities for Fungal Diseases: A Multidisciplinary Approach to Save Lives
Smith, D. J., Gold, J. A. W., Benedict, K., Wu, K., Lyman, M., Jordan, A., Medina, N., Lockhart, S. R., Sexton, D. J., Chow, N. A., et al. (2023) · Journal of Fungi · doi:10.3390/jof9080820 · Cited by 39 · see citing works
“Invasive Candida infections are a common cause of healthcare-associated infections, with an estimated 22,660 infections occurring annually in the United States, and they are associated with a high morbidity rate [44].”
BackgroundSelf-citationBiofilm-Associated Candidiasis: Pathogenesis, Prevalence, Challenges and Therapeutic Options
Amann, V., Kissmann, A., Firacative, C., & Rosenau, F. (2025) · Pharmaceuticals · doi:10.3390/ph18040460 · Cited by 41 · see citing works
Novel Therapeutic Approaches to Invasive Candidiasis: Considerations for the Clinician
Lamoth, F. (2023) · Infection and Drug Resistance · doi:10.2147/idr.s375625 · Cited by 37 · see citing works
“The Evolving Landscape of Invasive Candidiasis While the global epidemiological trends of IC are difficult to assess and may vary between different geographical areas, its incidence remains high and data from North America and Europe suggest an increased burden of the disease among the elderly and immunocompromised po…”
BackgroundZeng, Z., Ding, Y., Tian, G., Yang, K., Deng, J. M., Li, G., & Liu, J. (2020) · Antimicrobial Resistance and Infection Control · doi:10.1186/s13756-020-00798-3 · Cited by 34 · see citing works
“Candidaemia is associated with significant morbidity and mortality [3].”
BackgroundCopper in infectious disease: Using both sides of the penny
Culbertson, E. M., & Culotta, V. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.12.003 · Cited by 34 · see citing works
Gallic Acid Leads to Cell Death of Candida Albicans by the Apoptosis Mechanism
Liberato, I., Lino, L. A., Souza, J. K. D., Neto, J. B., Sá, L. G. D. A. V., Cabral, V. P. D. F., da Silva, C. R., Cavalcanti, B. C., de Moraes, M. O., Freire, V. N., et al. (2022) · Future Microbiology · doi:10.2217/fmb-2021-0139 · Cited by 31 · see citing works
Kajihara, T., Yahara, K., Nagi, M., Kitamura, N., Hirabayashi, A., Hosaka, Y., Abe, M., Miyazaki, Y., & Sugai, M. (2022) · Medical Mycology · doi:10.1093/mmy/myac071 · Cited by 29 · see citing works
Chevecich, C. C., Müller-Sepúlveda, A., Jara, J. A., López‐Muñoz, R., Santander, R., Budini, M., Escobar, A. F., Quijada, R., Criollo, A., Díaz‐Dosque, M., et al. (2022) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-022-03518-z · Cited by 35 · see citing works
“Recent global reports estimate that yeasts from the genus Candida are responsible for 400,000 new cases of life-threatening candidiasis each year, with mortality rates of up to 40–60%, even with antifungal treatment [4, 5].”
BackgroundDerkacz, D., Bernat, P., & Krasowska, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031631 · Cited by 31 · see citing works
“albicans remains the dominant species isolated from the patient population [2,3].”
BackgroundEpidemiology of Candidemia in Kuwait: A Nationwide, Population-Based Study
Alobaid, K., Ahmad, S., Asadzadeh, M., Mokaddas, E. M., Al‐Sweih, N., Benwan, K. A., Alfouzan, W. A., Al‐Obaid, I., Jeragh, A., Al-Roomi, E., et al. (2021) · Journal of Fungi · doi:10.3390/jof7080673 · Cited by 30 · see citing works
Antifungal Activity of Minocycline and Azoles Against Fluconazole-Resistant Candida Species
Tan, J., Jiang, S., Tan, L., Shi, H., Yang, L., Sun, Y., & Wang, X. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.649026 · Cited by 28 · see citing works
Locke, J. B., Pillar, C. M., Castanheira, M., Carvalhaes, C. G., Andes, D. R., Aram, J. A., Andrzejewski, C., Bartizal, K. F., Das, A., Sandison, T., et al. (2024) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01584-23 · Cited by 27 · see citing works
Albahar, F., Alhamad, H., Assab, M. A., et al. (2023) · Tropical Medicine and Infectious Disease · doi:10.3390/tropicalmed9010008 · Cited by 26 · see citing works
“For example, in the United States, candidemia is only a small fraction of the burden caused by invasive candidiasis [22].”
BackgroundRodrigues, D. K. D. B., Bonfietti, L. X., Garcia, R. A., Araújo, M. R., Rodrigues, J. S., Gimenes, V. M. F., & Melhem, M. D. S. C. (2021) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2020e10928 · Cited by 27 · see citing works
Increasing morbidity and mortality of candidemia over one decade in a Swiss university hospital
Battistolo, J., Glampedakis, E., Damonti, L., Poissy, J., Grandbastien, B., Kalbermatter, L., Pagani, J., Eggimann, P., Bochud, P., Calandra, T., et al. (2021) · Mycoses · doi:10.1111/myc.13376 · Cited by 23 · see citing works
“Renal replacement therapy 9 (13) 22 (22) .”
Antimicrobial therapy during cancer treatment: Beyond antibacterial effects
Ghanem, S., Kim, C. J., Dutta, D., Salifu, M. O., & Lim, S. H. (2020) · Journal of Internal Medicine · doi:10.1111/joim.13238 · Cited by 22 · see citing works
Badiee, P., Boekhout, T., Haddadi, P., Mohammadi, R., Ghadimi-Moghadam, A., Soltani, J., Mahmoudabadi, A. Z., Mousavi, S. A. A., Najafzadeh, M. J., Diba, K., et al. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.02453-22 · Cited by 22 · see citing works
“0 mg/mL, and MIC50 and MIC90 values were 1 and 2 mg/mL, respectively (29).”
BackgroundRisk Factors and Clinical Outcomes of Candidemia Associated With Severe COVID-19
Dixit, D., Jen, P., Maxwell, T. D., Smoke, S. M., McCracken, J. A., Cardinale-King, M., Haribhakti, A., Patel, P. R., Cani, E., Choi, S., et al. (2022) · Critical Care Explorations · doi:10.1097/cce.0000000000000762 · Cited by 25 · see citing works
“In previous studies, in-hospital mortality in patients with candidemia ranged from 25% to 40% (22, 23), whereas our study found a higher mortality rate of 68% in patients with candidemia and COVID-19, which was also significantly higher than the mortality rate of COVID-19 patients without candidemia (p < 0.”
ResultInflammatory ER stress responses dictate the immunopathogenic progression of systemic candidiasis
Awasthi, D., Chopra, S., Cho, B. A., Emmanuelli, A., Sandoval, T. A., Hwang, S., Chae, C.-S., Salvagno, C., Tan, C., Vasquez-Urbina, L., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci167359 · Cited by 24 · see citing works
“In patients, invasive candidiasis causes high mortality despite the availability of antifungal drugs (80, 81).”
BackgroundGold, J. A. W., Seagle, E. E., Nadle, J., Barter, D. M., Czaja, C. A., Johnston, H., Farley, M. M., Thomas, S., Harrison, L. H., Fischer, J., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab512 · Cited by 20 · see citing works
Self-citationDemin, K. A., Refeld, A. G., Bogdanova, A. A., Prazdnova, E. V., Popov, I. V., Kutsevalova, O. Y., Ermakov, A. M., Bren, A. B., Rudoy, D. V., Chistyakov, V. A., et al. (2021) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-021-09776-6 · Cited by 24 · see citing works
Candida glabrata: A Tale of Stealth and Endurance
Askari, F., & Kaur, R. (2024) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.4c00477 · Cited by 21 · see citing works
Pfaller, M. A., Carvalhaes, C. G., DeVries, S. D., Huband, M. D., & Castanheira, M. (2021) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2021.115627 · Cited by 20 · see citing works
Invasive Candidiasis in the Intensive Care Unit: Where Are We Now?
Vázquez, J. A., Whitaker, L., & Zubovskaia, A. (2025) · Journal of Fungi · doi:10.3390/jof11040258 · Cited by 24 · see citing works
“…(ECMO), the development of acute renal failure with hemodialysis, mechanical ventilation (>3 days), and severe acute pancreatitis [4–6 , 21– 23] A subset of postsurgical patients, particularly those with recurrent gastrointestinal perforation, anastomotic leaks, or acute necrotizing…”
Mallick, D. C., Kaushik, N., Goyal, L., Mallick, L., & Singh, P. K. (2025) · Diseases · doi:10.3390/diseases13040093 · Cited by 26 · see citing works
“More recent data indicate an escalating burden, with Candida albicans now accounting for approximately 40–50% of isolates in many regions, reflecting its continued prominence [6].”
Emerging and re‐emerging fungal threats in Africa
Dangarembizi, R., Wasserman, S. A., & Hoving, J. C. (2022) · Parasite Immunology · doi:10.1111/pim.12953 · Cited by 17 · see citing works
Augmenting Azoles with Drug Synergy to Expand The Antifungal ToolboxPreprint
Kane, A., & Carter, D. A. (2022) · Preprints.org · doi:10.20944/preprints202203.0262.v1 · Cited by 17 · see citing works
Arastehfar, A. A., Marcet‐Houben, M., Daneshnia, F., Taj‐Aldeen, S. J., Batra, D. G., Lockhart, S. R., Shor, E., Gabaldón, T., & Perlin, D. S. (2021) · Studies in Mycology · doi:10.1016/j.simyco.2021.100133 · Cited by 15 · see citing works
Govender, N. P., Todd, J., Nel, J. S., Mer, M., Karstaedt, A., Cohen, C., & GERMS-SA1, F. (2021) · Emerging infectious diseases · doi:10.3201/eid2706.210128 · Cited by 17 · see citing works
Stewart, A. G., Laupland, K. B., Edwards, F., Koo, S., Hammond, S. P., Harris, P. N. A., Paterson, D. L., Slavin, M. A., & Chen, S. C.-A. (2025) · Journal of Infection · doi:10.1016/j.jinf.2025.106513 · Cited by 20 · see citing works
Fais, R., Rizzato, C., Franconi, I., Tavanti, A., & Lupetti, A. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.01240-22 · Cited by 15 · see citing works
Activity of rezafungin against Candida auris
Locke, J. B., Andes, D. R., Flanagan, S., Redell, M. A., Ong, V. S., Aram, J. A., Pappas, P. G., Castanheira, M., & Thompson, G. R. (2025) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkaf124 · Cited by 17 · see citing works
Bourassa‐Blanchette, S., Biesheuvel, M. M., Lam, J. C., Kipp, A. J., Church, D. L., Carson, J. A., Dalton, B., Parkins, M. D., Barkema, H. W., & Gregson, D. B. (2023) · BMC Infectious Diseases · doi:10.1186/s12879-023-08050-0 · Cited by 15 · see citing works
Benedict, K., Gold, J. A. W., Jenkins, E. N., Roland, J., Barter, D., Czaja, C. A., Johnston, H. L., Clogher, P., Farley, M. M., Revis, A., et al. (2022) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofac461 · Cited by 14 · see citing works
Self-citationRecurrent Candidemia: Trends and Risk Factors Among Persons Residing in 4 US States, 2011–2018
Seagle, E. E., Jackson, B. R., Lockhart, S. R., Jenkins, E. N., Revis, A., Farley, M. M., Harrison, L. H., Schaffner, W., Markus, T. M., Pierce, R. A., et al. (2022) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofac545 · Cited by 11 · see citing works
Self-citationAjetunmobi, O. H., Wall, G., Bonifácio, B. V., Delgado, L., Chaturvedi, A. K., Najvar, L. K., Wormley, F. L., Patterson, H. P., Wiederhold, N. P., Patterson, T. F., et al. (2023) · Journal of Fungi · doi:10.3390/jof9090879 · Cited by 11 · see citing works
“Infections caused by opportunistic pathogenic fungi within the genus Candida represent an increasing threat to an expanding population of immune- and medically compromised patients [1,2].”
Chesdachai, S., Baddour, L. M., Sohail, M. R., Palraj, R., Madhavan, M., Tabaja, H., Fida, M., Challener, D. W., & DeSimone, D. C. (2023) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofad318 · Cited by 11 · see citing works
“These high rates are, in part, related to the advanced age and multiple comorbid conditions that typically characterize patients with candidemia as was seen in the present cohort [6, 14].”
BackgroundOkamoto, M., Nakano, K., Takahashi-Nakaguchi, A., Sasamoto, K., Yamaguchi, M., Teixeira, M. C., & Chibana, H. (2023) · Journal of Fungi · doi:10.3390/jof9020240 · Cited by 11 · see citing works
Candida auris : host interactions, antifungal drug resistance, and diagnostics
Chowdhary, A., Lionakis, M. S., & Chauhan, N. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00187-22 · Cited by 13 · see citing works
“For example, Candida auris , Candida glabrata ( Nakaseomyces glabratus ), Candida parapsilosis , Candida tropicalis , and Candida krusei ( Pichia kudriavze vii ) are frequently isolated from human bloodstream infections (20–23).”
Sahoo, B., Goyal, R., Dutta, S., Joshi, P., & Sanyal, K. (2025) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.5c00079 · Cited by 12 · see citing works
Yu, S. N., Hong, S. I., Park, J. W., Jeon, M. H., & Cho, O. (2025) · Journal of Fungi · doi:10.3390/jof11030217 · Cited by 10 · see citing works
“The rate of micafungin resistance in the Asia–Pacific region was lower than that in North America, with C. glabrata showing a resistance rate of 0.4% while other Candida species showed no resistance [16].”
InfluentialStress contingent changes in Hog1 pathway architecture and regulation in Candida albicans
Day, A. M., Cao, M., Dantas, A. D. S., Ianieva, O., Herrero-de-Dios, C. M., Brown, A. J. P., & Quinn, J. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012314 · Cited by 13 · see citing works
Candida albicans Recovered From Persistent Candidemia Exhibits Enhanced Virulence Traits
Ribeiro, F. D. C., Kemmerich, K. K., Gonçale, J. C., Junqueira, J. C., Mannan, M. A., Nabeela, S., Colombo, A. L., & Uppuluri, P. (2024) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiae631 · Cited by 11 · see citing works
“Hematogenous candidiasis is a major cause of fungal infections in hospitalized patients globally [1, 2].”
Kantroo, H. A., Mubarak, M. M., Chowdhary, R., Rai, R., & Ahmad, Z. (2024) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.4c00476 · Cited by 10 · see citing works
Antifungal Stewardship Interventions in Patients with Hematologic Malignancies
Vergidis, P. I., Stevens, R. W., & Agrawal, S. G. (2023) · Current Fungal Infection Reports · doi:10.1007/s12281-023-00465-1 · Cited by 10 · see citing works
Rauseo, A. M., Olsen, M. A. A., Stwalley, D. L., et al. (2022) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofac447 · Cited by 10 · see citing works
What ‘Omics can tell us about antifungal adaptation
Ribeiro, G. F., Denes, E., Heaney, H., & Childers, D. S. (2021) · FEMS Yeast Research · doi:10.1093/femsyr/foab070 · Cited by 9 · see citing works
“…candidiasis is estimated at ∼5100 individuals per year in the UK and ∼25 000 patients per year in the USA, and in particular affects patients on intensive chemotherapy, immunosuppressive drugs or long-term hospital stays (Bongomin et al. 2017; Pegorie, Denning and Welfare 2017; Tsay et al. 2020).”
BackgroundCortés, J. A., Valderrama-Ríos, M. C., Pietrobom, P. M. P., Silva, M., Díaz‐Brochero, C., Robles-Torres, R. R., Espinosa‐Almanza, C. J., Nócua-Báez, L. C., Nucci, M., Álvarez, C., et al. (2024) · The Brazilian Journal of Infectious Diseases · doi:10.1016/j.bjid.2024.104495 · Cited by 10 · see citing works
Soriano, À., Honoré, P. M., Cornely, O. A., Chayakulkeeree, M., Bassetti, M., Haihui, H., Dupont, H., Kim, Y. K., Kollef, M. H., Kullberg, B. J., et al. (2024) · Clinical Infectious Diseases · doi:10.1093/cid/ciae363 · Cited by 9 · see citing works
“Candidemia and invasive candidiasis (IC) are common health-care facility–associated fungal infections that have a substantial impact on patient morbidity and mortality and a high economic burden [1– 5].”
Naicker, S. D., Shuping, L., Zulu, T. G., Mpembe, R. S., Mhlanga, M., Tsotetsi, E., Maphanga, T. G., Govender, N. P., MMed, F. P. S., Black, J., et al. (2023) · Medical Mycology · doi:10.1093/mmy/myad057 · Cited by 8 · see citing works
Clinical Sensitivity of the (1–3)-β-D-glucan Test for Predicting Candidemia
Lee, Y. W., Lim, S. Y., Jin, S., Park, H. J., Sung, H., Kim, M., Bae, S., Jung, J., Kim, M. J., Kim, S., et al. (2023) · Annals of Laboratory Medicine · doi:10.3343/alm.2023.43.4.381 · Cited by 9 · see citing works
Cheng, L., Liang, Z., Liu, F., et al. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1126580 · Cited by 9 · see citing works
Grant, V. C., Nguyen, K., Rodriguez, S., et al. (2022) · Tropical Medicine and Infectious Disease · doi:10.3390/tropicalmed7020023 · Cited by 9 · see citing works
Rapid detection of biofilm‐producing Candida species via MALDI‐TOF mass spectrometry
de Aguiar, P. A. D. F., Menezes, R. D. P., Penatti, M. P. A., et al. (2021) · Journal of Applied Microbiology · doi:10.1111/jam.15066 · Cited by 9 · see citing works
Macrophage pyroptosis induced by Candida albicans
Zhang, F.-Y., Lian, N., & Li, M. (2024) · Pathogens and Disease · doi:10.1093/femspd/ftae003 · Cited by 8 · see citing works
Nickels, T. J., & Cunningham, K. W. (2025) · mSphere · doi:10.1128/msphere.00270-25 · Cited by 8 · see citing works
Invasive fungal infections in non-neutropenic patients
Kreitmann, L., Blot, S. I., & Nseir, S. (2024) · Intensive Care Medicine · doi:10.1007/s00134-024-07683-2 · Cited by 7 · see citing works
“C. albicans remains the dominant strain, but the epidemiology of IC is changing towards an increase of non-albicans strains [2], driven in part by exposure to antifungals [3].”
Pseudolaric Acid A: A Promising Antifungal Agent Against Prevalent Non-albicans Candida Species
Li, Z., Zhu, B., Chen, W., Hu, J., Xue, Y., Yin, H., Hu, X., & Liu, W. (2023) · Infection and Drug Resistance · doi:10.2147/idr.s419646 · Cited by 7 · see citing works
“6,7 While a recent study on C. glabrata in Germany found that the resistance rate to FLC was 38%, and cross-resistance rate to FLC and echinocandin was 14%.”
BackgroundAjetunmobi, O. H., Chaturvedi, A. K., Badali, H., Vaccaro, A., Najvar, L. K., Wormley, F. L., Wiederhold, N. P., Patterson, T. F., & Lopez-Ribot, J. L. (2023) · Apmis · doi:10.1111/apm.13342 · Cited by 8 · see citing works
“Candidiasis, infections caused by Candida spp, constitutes a growing threat to human health, particularly for immune-and medically compromised individuals [1, 2].”
Kovács, R., Majoros, L., Stemler, J., Cornely, O. A., & Salmanton‐García, J. (2023) · Therapeutic Advances in Infectious Disease · doi:10.1177/20499361231219315 · Cited by 7 · see citing works
Souza, L. A. L., Dias, L. P., Araújo, N. M. S., Carneiro, R. F., Nagano, C. S., Teixeira, C. S., Silva, R. G. G., Oliveira, J. T. A., & Sousa, D. O. B. (2022) · Biochimie · doi:10.1016/j.biochi.2022.05.014 · Cited by 6 · see citing works
Forster, J., Dichtl, K., & Wagener, J. (2022) · Mycoses · doi:10.1111/myc.13421 · Cited by 7 · see citing works
“Persistence of a positive (1,3)- β- Glucan test after clearance of Candidemia in hematopoietic stem cell transplant recipients.”
BackgroundCandidemia and Severe Coronavirus Disease 2019: Which Risk Factors Are Modifiable?
McCarty, T. P. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab635 · Cited by 8 · see citing works
“The bulk of candidemia occurs in hospitalized patients with a large proportion of patients having central venous access [4, 5].”
BackgroundOvercoming antifungal resistance in Candida albicans via RNA interference: a therapeutic perspective
Mundhe, A. K., & Rajkumari, R. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1675921 · Cited by 6 · see citing works
Feng, Y., Feng, W., Yang, J., & Ma, Y. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1578749 · Cited by 6 · see citing works
Heterogeneity of Candida bloodstream isolates in an academic medical center and affiliated hospitals
Scott, N. E., Wash, E., Zajac, C., Erayil, S. E., Kline, S. E., & Selmecki, A. M. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.00464-25 · Cited by 6 · see citing works
“Our data are relatively consistent with nationwide studies from 2012 to 2017, albeit with slightly lower frequencies of C. parapsilosis and C. tropicalis (9, 46).”
Cugnata, S., Sacheli, R., Layios, N., & Hayette, M. (2025) · Journal of Fungi · doi:10.3390/jof11060465 · Cited by 6 · see citing works
Carneiro, J. N. P., dos Santos, A. T. L., Fonseca, V. J. A., de Freitas, M. A., Silva, F. D. S., Lopes, L. A., Araújo, N. M. S., Sousa, D. O. B., Silva, R. G. G., Neto, J. X. D. S., et al. (2025) · Current Microbiology · doi:10.1007/s00284-025-04133-0 · Cited by 7 · see citing works
Eicosapentaenoic acid as an antibiofilm agent disrupts mature biofilms of Candida albicans
Wang, S., Xie, S., Li, T., Liu, J., Wang, P., Wang, Y., Gu, L., Luo, D., & Wei, M. (2024) · Biofilm · doi:10.1016/j.bioflm.2024.100251 · Cited by 6 · see citing works
“The metabolic activity was assessed with the XTT [2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide] reduction assay as previously described by Manoharan et al. [27].”
Al‐Obaidi, M. M., Ostrosky‐Zeichner, L., & Nix, D. E. (2023) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofad345 · Cited by 6 · see citing works
“Other factors related to social and health disparities involving this region may lead to increased use of antifungal against certain fungal infections; as reported before that, candidemia cases are the highest in the south central and south Atlantic regions among 9 of the evaluated sites [27].”
BackgroundRacial disparities among candidemic patients at a Southern California teaching hospital
Grant, V. C., Zhou, A. Y., Tan, K. K., et al. (2023) · Infection Control and Hospital Epidemiology · doi:10.1017/ice.2023.74 · Cited by 6 · see citing works
Ryder, J. H., Schooneveld, T. C. V., Lyden, E. R., Ramahi, R. E., & Stohs, E. J. (2022) · Infection Control and Hospital Epidemiology · doi:10.1017/ice.2022.209 · Cited by 6 · see citing works
Oliveira, A. D. S., Farias, J. R., Franco, D. C. G., da Costa, A. A. C., Santos, P. G., Silva, M. C. P. D., do Nascimento, F. R. F., & Guerra, R. N. M. (2024) · Preprints.org · doi:10.20944/preprints202404.1065.v1 · Cited by 4 · see citing works
Changes in Epidemiology of Candidemia in the United States With a Focus on Candida auris
Pérez, M. A., Patel, K., Rasmy, L., Yoshida, H., Arias, C. A., Nigo, M., & Adelman, M. W. (2026) · Clinical Infectious Diseases · doi:10.1093/cid/ciag312 · Cited by 5 · see citing works
Thompson, G. R., Huang, H., Feng, S., Yu, Y., Soriano, À., Cornely, O. A., Kullberg, B. J., Pappas, P. G., Kollef, M. H., Vázquez, J. A., et al. (2025) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofaf555 · Cited by 4 · see citing works
“In the USA and Europe, the incidence of candidemia is 4–9 cases per 100 000 inhabitants [1, 6–8], while in China it is 26 per 100 000 admissions [9].”
Caniff, K. E., Musawa, M. A., Judd, C., Shupp, M., Veve, M. P., Alangaden, G. J., Claeys, K. C., Scipione, M. R., Walsh, T. J., & Rybak, M. J. (2025) · Journal of Clinical Microbiology · doi:10.1128/jcm.00043-25 · Cited by 4 · see citing works
Stack, M. A., Ostrosky-Zeichner, L. L., Hasbun, R., Park, S. O., Babic, J. T., & Kapadia, M. (2025) · IDCases · doi:10.1016/j.idcr.2025.e02232 · Cited by 7 · see citing works
“Invasive candidiasis is a common and serious healthcare-associated infection with substantial morbidity and mortality [1].”
Association between CTX-1 and Fibulin-1 Serum Levels with Pathogenesis of Multiple Myeloma Cancer
Al-Janabi, A. M. A. A., Momeni, H. R., & Al-Harbi, H. J. (2024) · Asian Pacific Journal of Cancer Prevention · doi:10.31557/apjcp.2024.25.5.1599 · Cited by 4 · see citing works
“in the United States each year, and nearly 13,000 patients die from it [4].”
Background
- Authors
- Tsay, S. V., Mu, Y., Williams, S., Epson, E., Nadle, J., Bamberg, W. M., Barter, D. M., Johnston, H. L., Farley, M. M., Harb, S., Thomas, S., Bonner, L. A., Harrison, L. H., Hollick, R., Marceaux, K., Mody, R. K., Pattee, B., Shrum Davis, S., Phipps, E. C., Tesini, B. L., Gellert, A. B., Zhang, A. Y., Schaffner, W., Hillis, S., Ndi, D., Graber, C. R., Jackson, B. R., Chiller, T., Magill, S., & Vallabhaneni, S.
- Affiliations
- Centers for Disease Control and Prevention (US)
- California Emerging Infections Program, Oakland, California,
- Colorado Department of Public Health and Environment (US)
- Emory University (US)
- Georgia Emerging Infections Program , Atlanta, Georgia,
- Maryland Emerging Infections Program, Baltimore, Maryland,
- Johns Hopkins University (US)
- Minnesota Department of Health (US)
- New Mexico Emerging Infections Program , Albuquerque, New Mexico,
- University of New Mexico (US)
- University of Rochester (US)
- New York Emerging Infections Program , Rochester, New York,
- Oregon Health Authority (US)
- Vanderbilt University (US)
- Tennessee Emerging Infections Program , Nashville, Tennessee,
- Corresponding author
- Tsay, Sharon V
- ORCID
- Venue
- Clinical Infectious Diseases
- Publisher
- Oxford University Press (OUP)
- Published
- 2020-02-28
- Volume
- 71
- Issue
- 9
- Pages
- e449-e453
- ISSN
- 1058-4838 (ISSN-L)
- 1537-6591
- OpenAlex
- W3007919525
- Semantic Scholar
- b8d45dbf43a735b9527e8366a98207b38030b225
- Cited by
- 163
- References
- 30
- Citations by year
- 2026: 13 · 2025: 37 · 2024: 22 · 2023: 35 · 2022: 26 · 2021: 21 · 2020: 9
- FWCI
- 2.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- public-domain
- Locations
- Clinical Infectious Diseases (publishedVersion, public-domain)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Health Sciences › Medicine › Epidemiology › Infective Endocarditis Diagnosis and Management
- Keywords
- candidemia, invasive candidiasis, Candida, healthcare-associated bloodstream infections, disease burden, incidence, mortality, Emerging Infections Program, population-based surveillance, United States
- MeSH terms
- Adult, Aged, Candida, Cross Infection, Humans, Male, Population Surveillance, United States, Incidence, Candidemia
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