(See also Overview of Fungal Infections Overview of Fungal Infections Fungal infections are often classified as either Opportunistic Primary Opportunistic infections are those that develop mainly in immunocompromised hosts. Primary infections can develop in immunocompetent... read more , Candidiasis Candidiasis (Mucocutaneous) Candidiasis is skin and mucous membrane infection with Candida species, most commonly Candida albicans. Infections can occur anywhere and are most common in skinfolds, digital web spaces, genitals... read more , Candidal Vaginitis Candidal Vaginitis Candidal vaginitis is vaginal infection with Candida species, usually C. albicans. (See also Overview of Vaginitis.) Most fungal vaginitis is caused by C. albicans (candidiasis), which colonizes... read more , and Chronic Mucocutaneous Candidiasis Chronic Mucocutaneous Candidiasis Chronic mucocutaneous candidiasis is persistent or recurrent candidal infection due to inherited T-cell defects. Autoimmune and endocrine disorders may develop in its recessive form. Diagnosis... read more .)
Candida species are commensal organisms that inhabit the gastrointestinal (GI) tract and sometimes the skin (see etiology of mucocutaneous candidiasis Etiology Candidiasis is skin and mucous membrane infection with Candida species, most commonly Candida albicans. Infections can occur anywhere and are most common in skinfolds, digital web spaces, genitals... read more ). Unlike other systemic mycoses, candidiasis results from endogenous organisms. Most infections are caused by C. albicans; however, C. glabrata (formerly Torulopsis glabrata) and other non-albicans species are increasingly involved in fungemia, urinary tract infections, and, occasionally, other focal disease. C. glabrata is frequently less susceptible to fluconazole than other species; C. krusei is inherently resistant to fluconazole; frequency of resistance to voriconazole and amphotericin varies. C. krusei is most frequently susceptible to echinocandins. C. auris is an emerging, multidrug-resistant species that has caused recent outbreaks in hospitals and is challenging to identify and treat.
Candida species account for about 80% of major systemic fungal infections and are the most common cause of fungal infections in immunocompromised patients. Candidal infections are one of the most common hospital-acquired infections. Because resistance and transmission of C. auris in health care facilities have become a concern, special infection control precautions have been instituted for patients who are colonized or infected with C. auris.
Candidiasis of the esophagus is a defining opportunistic infection in AIDS AIDS Human immunodeficiency virus (HIV) infection results from 1 of 2 similar retroviruses (HIV-1 and HIV-2) that destroy CD4+ lymphocytes and impair cell-mediated immunity, increasing risk of certain... read more . Although mucocutaneous candidiasis is frequently present in HIV-infected patients, hematogenous dissemination is unusual unless other specific risk factors are present (see Disseminated candidiasis Disseminated candidiasis Candidiasis is infection by Candida species (most often C. albicans), manifested by mucocutaneous lesions, fungemia, and sometimes focal infection of multiple sites. Symptoms depend on the site... read more ).
Neutropenic patients (eg, complicating cancer chemotherapy) are at high risk of developing life-threatening disseminated candidiasis.
Candidemia may occur in nonneutropenic patients during prolonged hospitalization. This bloodstream infection is often related to one or more of the following:
IV lines and the GI tract are the usual portals of entry.
Candidemia often prolongs hospitalization and increases mortality due to concurrent disorders. Candidemia may occur with other forms of invasive candidiasis, such as endocarditis or meningitis, as well as focal involvement of skin, subcutaneous tissues, bones, joints, liver, spleen, kidneys, eyes, and other tissues. Endocarditis is commonly related to IV drug abuse, valve replacement, or intravascular trauma induced by indwelling IV catheters.
All forms of disseminated candidiasis should be considered serious, progressive, and potentially fatal.
Esophageal candidiasis is most often manifested by dysphagia.
Candidemia usually causes fever, but no symptoms are specific. Some patients develop a syndrome resembling bacterial sepsis Sepsis and Septic Shock Sepsis is a clinical syndrome of life-threatening organ dysfunction caused by a dysregulated response to infection. In septic shock, there is critical reduction in tissue perfusion; acute failure... read more , with a fulminating course that may include shock, oliguria, renal shutdown, and disseminated intravascular coagulation Disseminated Intravascular Coagulation (DIC) Disseminated intravascular coagulation (DIC) involves abnormal, excessive generation of thrombin and fibrin in the circulating blood. During the process, increased platelet aggregation and coagulation... read more .
Candidal endophthalmitis starts as white retinal lesions that are initially asymptomatic but can progress, opacifying the vitreous and causing potentially irreversible scarring and blindness. In neutropenic patients, retinal hemorrhages occasionally also occur, but actual infection of the eye is rare.
Papulonodular skin lesions may also develop, especially in neutropenic patients, in whom they indicate widespread hematogenous dissemination to other organs. Symptoms of other focal or invasive infection depend on the organ involved.
Because Candida species are commensal, their culture from sputum, the mouth, the vagina, urine, stool, or skin does not necessarily signify an invasive, progressive infection. A characteristic clinical lesion must also be present, histopathologic evidence of tissue invasion (eg, yeasts, pseudohyphae, or hyphae in tissue specimens) must be documented, and other etiologies must be excluded. Positive cultures of specimens taken from normally sterile sites, such as blood, cerebrospinal fluid, pericardium, pericardial fluid, or biopsied tissue, provide definitive evidence that systemic therapy is needed.
Serum beta-glucan is often positive in patients with invasive candidiasis; conversely, a negative result indicates low likelihood of systemic infection.
The T2Candida® Panel is a magnetic resonance assay that directly detects 5 Candida species (C. albicans, C. tropicalis, C. parapsilosis, C. krusei, and C. glabrata) in whole blood samples in 3 to 5 hours. It is highly sensitive and has an excellent negative predictive value (1 Diagnosis reference Candidiasis is infection by Candida species (most often C. albicans), manifested by mucocutaneous lesions, fungemia, and sometimes focal infection of multiple sites. Symptoms depend on the site... read more ). Other molecular diagnostic testing is also available, including matrix-assisted laser desorption ionization–time of flight (MALDI-TOF Mass spectroscopy Once an organism has been isolated by culture, it must be identified. Identification is important in determining management (eg, drug treatment, isolation measures). Non-nucleic acid–based identification... read more ) mass spectrometry and polymerase chain reaction (PCR)-based assays.
Ophthalmologic examination to check for endophthalmitis is recommended for all patients with candidemia.
Standard laboratory techniques often misidentify C. auris as C. haemulonii, C. famata, C. sake, or another species. MALDI-TOF mass spectrometry is a more reliable method for correct identification. A nucleic acid-based test also is now available.
(See also Antifungal Drugs Antifungal Drugs Drugs for systemic antifungal treatment include the following (see Table: Some Drugs for Systemic Fungal Infections): Amphotericin B (and its lipid formulations) Various azole derivatives (fluconazole... read more and the Infectious Diseases Society of America’s Clinical Practice Guideline for the Management of Candidiasis: 2016 Update.)
In patients with invasive candidiasis, predisposing conditions (eg, neutropenia, immunosuppression, use of broad-spectrum antibacterial antibiotics, hyperalimentation, presence of indwelling lines) should be reversed or controlled if possible.
In nonneutropenic patients, IV catheters should be removed.
When an echinocandin is indicated (if patients are moderately severely ill or critically ill [most neutropenic patients] or if C. glabrata, C. auris, or C. krusei is suspected), one of the following drugs can be used:
If fluconazole is indicated (if patients are clinically stable or if C. albicans or C. parapsilosis is suspected), loading dose is 800 mg (12 mg/kg) orally or IV once, followed by 400 mg (6 mg/kg) once a day.
If there is intolerance, limited availability, or resistance to other antifungal drugs, a lipid formulation of amphotericin B at a dosage of 3 to 5 mg/kg IV once a day can be used (1 Treatment reference Candidiasis is infection by Candida species (most often C. albicans), manifested by mucocutaneous lesions, fungemia, and sometimes focal infection of multiple sites. Symptoms depend on the site... read more ).
Treatment of invasive candidiasis is continued for 14 days after the last negative blood culture.
Esophageal candidiasis is treated with one of the following:
If these drugs are ineffective or if infection is severe, one of the following may be used:
Treatment of esophageal candidiasis is continued for 14 to 21 days.
1. Pappas PG, Kauffman CA, Andes DR, et al: Clinical practice guideline for the management of candidiasis: 2016 update by the Infectious Diseases Society of America. Clin Infect Dis 62(4):e1–e50, 2016. doi: 10.1093/cid/civ933
Unlike other fungal infections, invasive candidiasis is usually due to endogenous organisms.
Invasive infection typically occurs in immunocompromised and/or hospitalized patients, particularly those who have had surgery or been given broad-spectrum antibiotics.
Positive cultures of specimens taken from normally sterile sites (eg, blood, cerebrospinal fluid, tissue biopsy specimens) are needed to distinguish invasive infection from normal colonization; serum beta-glucan is often positive in patients with invasive candidiasis.
A T2Candida® Panel on whole blood can be used to diagnose a Candida blood infection.
Use an echinocandin if patients are severely or critically ill or if infection with C. glabrata, C. auris, or C. krusei is suspected.
Use fluconazole if patients are clinically stable or if infection with C. albicans or C. parapsilosis is suspected.
The following are English-language resources that may be useful. Please note that THE MANUAL is not responsible for the content of these resources.
Centers for Disease Control and Prevention (CDC): Infection Prevention and Control for Candida auris
Infectious Diseases Society of America: Clinical Practice Guideline for the Management of Candidiasis: 2016 Update