In general, avoidance of exposure to fungal pathogens is not realistic; but avoidance of circumstances likely to lead to prolonged heavy exposure (e.g., contact with pigeon guano [Cryptococcus neoformans] or disturbed soil in highly endemic areas [Cryptococcus immitis, Histoplasma capsulatum]) is reasonable, especially for immunosuppressed patients.
Antiretroviral therapy
Early and effective antiretroviral therapy in patients with HIV may prevent occurrence of fungal meningitis.
Antiretroviral therapy remains the most effective prophylaxis to prevent HIV-associated cryptococcal disease.
Antifungal therapy
Patients presenting with advanced HIV infection, a CD4 count <100 cells/microliter, and who have a positive cryptococcal antigen test result should be given preemptive antifungal therapy to prevent the development of invasive cryptococcal disease before initiating or reinitiating antiretroviral therapy.[71]World Health Organization. Guidelines for diagnosing, preventing and managing cryptococcal disease among adults, adolescents and children living with HIV. June 2022 [internet publication].
https://www.who.int/publications/i/item/9789240052178
http://www.ncbi.nlm.nih.gov/pubmed/35797432?tool=bestpractice.com
[72]National Institutes of Health, Centers for Disease Control and Prevention, HIV Medicine Association of the Infectious Disease Society of America. Guidelines for the prevention and treatment of opportunistic infections in adults and adolescents with HIV. September 2022 [internet publication].
https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-opportunistic-infections
Antifungal therapy may also be considered at a higher CD4 count threshold of <200 cells/microliter.[71]World Health Organization. Guidelines for diagnosing, preventing and managing cryptococcal disease among adults, adolescents and children living with HIV. June 2022 [internet publication].
https://www.who.int/publications/i/item/9789240052178
http://www.ncbi.nlm.nih.gov/pubmed/35797432?tool=bestpractice.com
Although primary antifungal prophylaxis with either fluconazole or itraconazole reduces the incidence of cryptococcal meningitis in patients with advanced HIV disease and reduces deaths due to cryptococcal disease, it has no clear effect on overall mortality.[73]Awotiwon AA, Johnson S, Rutherford GW, et al. Primary antifungal prophylaxis for cryptococcal disease in HIV-positive people. Cochrane Database Syst Rev. 2018 Aug 29;(8):CD004773.
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD004773.pub3/full
http://www.ncbi.nlm.nih.gov/pubmed/30156270?tool=bestpractice.com
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What are the effects of primary antifungal prophylaxis for cryptococcosis in HIV‐positive people?/cca.html?targetUrl=https://www.cochranelibrary.com/cca/doi/10.1002/cca.2297/fullShow me the answer In settings where antigen screening is not available, the World Health Organization recommends initiating fluconazole primary prophylaxis in people with HIV infection and a CD4 count <100 cells/mm³.[71]World Health Organization. Guidelines for diagnosing, preventing and managing cryptococcal disease among adults, adolescents and children living with HIV. June 2022 [internet publication].
https://www.who.int/publications/i/item/9789240052178
http://www.ncbi.nlm.nih.gov/pubmed/35797432?tool=bestpractice.com
Prophylaxis for histoplasmosis with itraconazole is recommended in HIV-infected patients with CD4 cell counts <150 cells/microliter who are at high risk because of occupational exposure, or who are resident in specific endemic areas where the incidence is >10 cases per 100 patient-years.[72]National Institutes of Health, Centers for Disease Control and Prevention, HIV Medicine Association of the Infectious Disease Society of America. Guidelines for the prevention and treatment of opportunistic infections in adults and adolescents with HIV. September 2022 [internet publication].
https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-opportunistic-infections
Prophylaxis with itraconazole may also be appropriate in specific circumstances in other immunosuppressed patients, such as organ transplant patients or those taking immunosuppression medicine such as corticosteroids.
For patients with HIV living in the coccidioidal-endemic region, primary antifungal prophylaxis is not recommended to prevent coccidioidomycosis.[74]Galgiani JN, Ampel NM, Blair JE, et al. 2016 Infectious Diseases Society of America (IDSA) clinical practice guideline for the treatment of coccidioidomycosis. Clin Infect Dis. 2016 Sep 15;63(6):e112-46.
https://academic.oup.com/cid/article/63/6/e112/2389093
http://www.ncbi.nlm.nih.gov/pubmed/27470238?tool=bestpractice.com
Fluconazole prophylaxis is, however, recommended for organ transplant patients without active coccidioidomycosis who are in the endemic area.[74]Galgiani JN, Ampel NM, Blair JE, et al. 2016 Infectious Diseases Society of America (IDSA) clinical practice guideline for the treatment of coccidioidomycosis. Clin Infect Dis. 2016 Sep 15;63(6):e112-46.
https://academic.oup.com/cid/article/63/6/e112/2389093
http://www.ncbi.nlm.nih.gov/pubmed/27470238?tool=bestpractice.com
Primary prophylaxis against invasive candidiasis is indicated in selected high-risk patient groups.[75]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. 2016 Feb 15;62(4):e1-50.
https://academic.oup.com/cid/article/62/4/e1/2462830
http://www.ncbi.nlm.nih.gov/pubmed/26679628?tool=bestpractice.com
Primary prophylaxis may be indicated in patients with prolonged neutropenia or high-risk bone marrow, and in solid-organ transplant recipients and selected intensive care unit patients where there are high rates of disease. Fluconazole, and azole antifungals with additional activity against mold infections, have been used in these settings. In very low birthweight infants (<1.5 kg), chemoprophylaxis with fluconazole and oral nystatin is considered to be an effective practice to prevent neonatal fungal infections.[76]Blyth CC, Barzi F, Hale K, Isaacs D. Chemoprophylaxis of neonatal fungal
infections in very low birthweight infants: efficacy and safety of fluconazole
and nystatin. J Paediatr Child Health. 2012 Sep;48(9):846-51.
http://www.ncbi.nlm.nih.gov/pubmed/22970680?tool=bestpractice.com
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What are the benefits and harms of systemic prophylactic antifungal agents to prevent invasive fungal infection in very low birth weight infants?/cca.html?targetUrl=https://cochranelibrary.com/cca/doi/10.1002/cca.1163/fullShow me the answer
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What are the benefits and harms of prophylactic oral antifungal agents to prevent invasive fungal infection in very low birth weight infants?/cca.html?targetUrl=https://cochranelibrary.com/cca/doi/10.1002/cca.1164/fullShow me the answer