Yeast Susceptibility to Fluconazole, Voriconazole, and Caspofungin
Test Codes
36271 (Susceptibility, Yeast, Limited Panel)
36268 (Culture, Yeast with Limited Susceptibility)
36270 (Culture, Yeast with Direct Fluorescent KOH and Limited Susceptibility)
Clinical Use
Clinical Background
Fungal infection is a major cause of morbidity and mortality in healthcare settings; candidiasis, an infection caused by Candida yeast species, is one of the most common types of fungal infection. Invasive candidiasis is classically considered to affect the blood, brain, bones, eyes, or heart, whereas mucosal candidiasis generally affects the mouth or throat ("thrush") or vagina ("yeast infections"). In the United States, an estimated 46,000 cases of healthcare-associated invasive candidiasis occur annually. The exact impact of invasive candidiasis can be difficult to determine, because infections often occur in people who already have medical conditions. However, 30-day, all-cause mortality is about 30% among people with candidemia, the most common type of invasive candidiasis.1
Many antifungal treatments are available, and laboratory testing can help guide treatment selection. Available therapies include 2 triazoles (fluconazole and voriconazole) and 1 echinocandin (caspofungin). However, the effectiveness of each drug depends on the species of fungus2: a particular species can be intrinsically resistant to some drugs and susceptible to others. Inadequate therapy is associated with higher in-hospital mortality.3 Thus, species identification, preferably by culture (other methods can be used as adjuncts),2 can help guide treatment decisions.
Susceptibility testing can also help guide treatment, particularly if resistance to a specific drug is more common in a species or if an isolate does not respond to treatment.4 For example, Candida glabrata resistance to triazoles and echinocandins has become more common, and resistance in Candida tropicalis and Candida parapsilosis has been reported by institutions that commonly use antifungal agents.2 Although rare, antifungal resistance among Candida albicans does occur.2 Susceptibility testing of a yeast isolate can help clinicians optimize therapy by (1) comparing susceptibility to different antifungal drugs, (2) determining the likely outcome of therapy, and (3) identifying drug resistance.4 In general, therapy response rates are 90% for isolates identified as susceptible to a certain drug in vitro and 60% for those identified as not susceptible.4
The susceptibility of a yeast isolate is measured by determining the minimum inhibitory concentration (MIC), which is the lowest drug concentration that prevents growth. An isolate can be categorized as susceptible or resistant by comparing the MIC of an isolate to established clinical breakpoints (CBPs); MICs between the breakpoints for susceptible and resistant are categorized as intermediate (or dose-dependent susceptible). CBPs for each category are specific to each species and drug.
Quest Diagnostics offers testing for antifungal drug susceptibility alone (test code 36271), with culture (test code 36268), and with culture and potassium hydroxide (KOH) (test code 36270); KOH testing identifies the presence of fungal infection, but does not provide species identification. Culture testing (test code 20541) and culture with KOH testing (test code 3968) are also offered without susceptibility testing.
Individuals Suitable for Testing
Method
Interpretive Information
A result of "susceptible" indicates that growth of the isolate is blocked by the corresponding drug(s) (caspofungin, fluconazole, and/or voriconazole) at the prescribed concentration. Because treatment outcomes are influenced by many factors (eg, drug pharmacokinetics, pharmacodynamics, and interactions; the patient's immune response; disease severity),4 a "susceptible" result does not ensure that a patient will respond to the particular drug.
A result of "resistant" indicates that growth of the isolate is not blocked by the corresponding drug(s) (caspofungin, fluconazole, and/or voriconazole) at the prescribed concentration. Because treatment outcomes are influenced by many factors (eg, drug pharmacokinetics, pharmacodynamics, and interactions; the patient's immune response; disease severity),4 a "resistant" result does not ensure that a patient will not respond to the particular drug.
A result of "intermediate" indicates that growth of the isolate is not effectively blocked by the corresponding drug(s) (caspofungin, fluconazole, and/or voriconazole) at the prescribed concentration.
References
Content reviewed 11/2023
This test is used to identify a clinically significant yeast and determine its susceptibility to a limited set of antifungal agents. Potassium hydroxide (KOH), which dissolves human cells, helps detect the presence of fungus. This test may be helpful in optimizing treatment for recurrent yeast infections.
The susceptibility of a yeast isolate is measured by determining the minimum inhibitory concentration (MIC), which is the lowest drug concentration that prevents growth. An isolate can be categorized as susceptible, intermediate, susceptible-dose dependent, or resistant by comparing the MIC of an isolate to established clinical breakpoints [1]. MIC interpretations are based on recently published guidelines from the Clinical and Laboratory Standards Institute (CLSI). When a clinical breakpoint for an antifungal agent is not established by CLSI guidelines, only the MIC value is reported. For additional guidance, please review current CLSI documents related to antifungal susceptibility testing of yeasts.
Because treatment outcomes are influenced by many factors (eg, drug pharmacokinetics, pharmacodynamics, and interactions; the patient's immune response; disease severity), a "susceptible" or a "resistant" result does not ensure that a patient will or will not respond to a particular drug.
Invasive yeast infections, commonly caused by Candida and Cryptococcus, are associated with significant morbidity and mortality especially in immunocompromised individuals [2,3]. Species of these organisms have unique virulence and antifungal susceptibility. A particular species can be resistant to some antifungal agents and susceptible to others. Therefore, species identification and antifungal susceptibility testing can help guide treatment decisions for invasive infections [4]. Yeast susceptibility testing is useful when a yeast's identity does not reliably predict its susceptibility, particularly when the identified yeast belongs to a species known to resist common antifungal agents [1].
The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.
References
1. CLSI. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts. 4th ed. CLSI guideline M27. Clinical and Laboratory Standards Institute; 2017.
2. Invasive candidiasis statistics. Centers for Disease Control and Prevention. Updated August 24, 2021. Accessed February 7, 2022. https://www.cdc.gov/fungal/diseases/candidiasis/invasive/statistics.html
3. C. neoformans Infection Statistics. Centers for Disease Control and Prevention. Updated May 26, 2020. Accessed February 7, 2022. https://www.cdc.gov/fungal/diseases/cryptococcosis-neoformans/statistics.html
4. Pappas PG, et al. Clin Infect Dis. 2016;62(4):e1-e50.
This test determines susceptibility of a rapidly growing and non-fastidious yeast isolate to a limited set of antifungal agents. This test is performed on pure yeast isolates including Candida and Cryptococcus to aid in patient management.
The susceptibility of a yeast isolate is measured by determining the minimum inhibitory concentration (MIC), which is the lowest drug concentration that prevents growth. An isolate can be categorized as susceptible, intermediate, susceptible-dose dependent, or resistant by comparing the MIC of an isolate to established clinical breakpoints [1]. MIC interpretations are based on recently published guidelines from the Clinical and Laboratory Standards Institute (CLSI). When a clinical breakpoint for an antifungal agent is not established by CLSI guidelines, only the MIC value is reported. For additional guidance, please review current CLSI documents related to antifungal susceptibility testing of yeasts.
Because treatment outcomes are influenced by many factors (eg, drug pharmacokinetics, pharmacodynamics, and interactions; the patient's immune response; disease severity), a "susceptible" or a "resistant" result does not ensure that a patient will or will not respond to a particular drug.
Invasive yeast infections, commonly caused by Candida and Cryptococcus, are associated with significant morbidity and mortality especially in immunocompromised individuals [2,3]. Species of these organisms have unique virulence and antifungal susceptibility. A particular species can be resistant to some antifungal agents and susceptible to others. Therefore, species identification and antifungal susceptibility testing can help guide treatment decisions for invasive infections [4]. Yeast susceptibility testing is useful when a yeast's identity does not reliably predict its susceptibility, particularly when the identified yeast belongs to a species known to resist common antifungal agents [1].
The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.
References
1. CLSI. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts. 4th ed. CLSI guideline M27. Clinical and Laboratory Standards Institute; 2017.
2. Invasive candidiasis statistics. Centers for Disease Control and Prevention. Updated August 24, 2021. Accessed February 7, 2022. https://www.cdc.gov/fungal/diseases/candidiasis/invasive/statistics.html
3. C. neoformans Infection Statistics. Centers for Disease Control and Prevention. Updated May 26, 2020. Accessed February 7, 2022. https://www.cdc.gov/fungal/diseases/cryptococcosis-neoformans/statistics.html
4. Pappas PG, et al. Clin Infect Dis. 2016;62(4):e1-e50.
This test is used to identify a clinically significant yeast and determine its susceptibility to a limited set of antifungal agents. This test may be helpful in optimizing treatment for recurrent yeast infections.
The susceptibility of a yeast isolate is measured by determining the minimum inhibitory concentration (MIC), which is the lowest drug concentration that prevents growth. An isolate can be categorized as susceptible, intermediate, susceptible-dose dependent, or resistant by comparing the MIC of an isolate to established clinical breakpoints [1]. MIC interpretations are based on recently published guidelines from the Clinical and Laboratory Standards Institute (CLSI). When a clinical breakpoint for an antifungal agent is not established by CLSI guidelines, only the MIC value is reported. For additional guidance, please review current CLSI documents related to antifungal susceptibility testing of yeasts.
Because treatment outcomes are influenced by many factors (eg, drug pharmacokinetics, pharmacodynamics, and interactions; the patient's immune response; disease severity), a "susceptible" or a "resistant" result does not ensure that a patient will or will not respond to a particular drug.
Invasive yeast infections, commonly caused by Candida and Cryptococcus, are associated with significant morbidity and mortality especially in immunocompromised individuals [2,3]. Species of these organisms have unique virulence and antifungal susceptibility. A particular species can be resistant to some antifungal agents and susceptible to others. Therefore, species identification and antifungal susceptibility testing can help guide treatment decisions for invasive infections [4]. Yeast susceptibility testing is useful when a yeast's identity does not reliably predict its susceptibility, particularly when the identified yeast belongs to a species known to resist common antifungal agents [1].
The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.
References
1. CLSI. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts. 4th ed. CLSI guideline M27. Clinical and Laboratory Standards Institute; 2017.
2. Invasive candidiasis statistics. Centers for Disease Control and Prevention. Updated August 24, 2021. Accessed February 7, 2022. https://www.cdc.gov/fungal/diseases/candidiasis/invasive/statistics.html
3. C. neoformans Infection Statistics. Centers for Disease Control and Prevention. Updated May 26, 2020. Accessed February 7, 2022. https://www.cdc.gov/fungal/diseases/cryptococcosis-neoformans/statistics.html
4. Pappas PG, et al. Clin Infect Dis. 2016;62(4):e1-e50.
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
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