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1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida

BACKGROUND: Candida species are the most common cause of invasive fungal infections in hospitalized patients. Children with hematological malignancies are at increased risk. The epidemiology of species implicated in invasive candidiasis (IC) has changed over the past 25 years with non-albicans Candi...

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Autores principales: Said, Amira, Afridi, Faraz, Daignault, Chelsea, O’Farrell, Candelaria, Scheurer, Michael E, Redell, Michele S, Garnes, Natalie J Dailey, Gramatges, Maria, Dutta, Ankhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679075/
http://dx.doi.org/10.1093/ofid/ofad500.1534
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author Said, Amira
Afridi, Faraz
Daignault, Chelsea
O’Farrell, Candelaria
Scheurer, Michael E
Redell, Michele S
Garnes, Natalie J Dailey
Gramatges, Maria
Dutta, Ankhi
author_facet Said, Amira
Afridi, Faraz
Daignault, Chelsea
O’Farrell, Candelaria
Scheurer, Michael E
Redell, Michele S
Garnes, Natalie J Dailey
Gramatges, Maria
Dutta, Ankhi
author_sort Said, Amira
collection PubMed
description BACKGROUND: Candida species are the most common cause of invasive fungal infections in hospitalized patients. Children with hematological malignancies are at increased risk. The epidemiology of species implicated in invasive candidiasis (IC) has changed over the past 25 years with non-albicans Candida (NAC) species now prevailing. These changes have therapeutic and prophylactic implications as some species carry intrinsic resistance to widely-used antifungal medications. METHODS: Patients ages 0-18 with hematologic malignancy and at least one episode of IC from 2011-2022 from two institutions were included. Patients who had received a bone marrow transplant were excluded. Information related to demographics, host factors, clinical risk factors, Candida species and antifungal minimum inhibitory concentrations (MICs), treatment and outcomes was collected via retrospective chart review. RESULTS: 53 cases of IC were identified. Sixty percent were males. Thirty (57%) were of Hispanic ethnicity. The median age at diagnosis was 9 years (range 2 months-18 years). Seventy percent (37/53) had B-cell acute lymphoblastic leukemia. The median time to IC from diagnosis of cancer was 95 days (IQR 20-277). C. tropicalis (n=17; 32%) and C. albicans (n=14; 26%) were the most common species followed by C. glabrata and C. parapsilosis. Thirty-five percent (18/53) had concurrent bacteremia. The most common sites of dissemination were the lungs (n=24, 45%), kidneys (n=17; 32%), liver (n=15, 28%) and spleen (n=14; 27%). Of the 35 patients who underwent dilated eye exams, 23% (n=8) had ophthalmologic involvement. NAC were more likely to disseminate to the eyes, skin and spleen than C. albicans (p< 0.05). Fourteen isolates (26%) demonstrated increased MICs to fluconazole and six demonstrated increased MICs to voriconazole. Most (59%) required more than 6 weeks of antifungals. Sixteen patients died, of which six were attributed to IC. CONCLUSION: NAC accounted for most of the IC in hematological malignancies with C.tropicalis being the most common. The implications of NAC being predominant in this high-risk group is concerning due to the higher MIC to azoles and the potential for azole resistance in the future. Antifungal prophylaxis and treatment both need to be reevaluated periodically based on these findings. DISCLOSURES: Natalie J Dailey Garnes, MD, MPH, AlloVir: Grant/Research Support
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spelling pubmed-106790752023-11-27 1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida Said, Amira Afridi, Faraz Daignault, Chelsea O’Farrell, Candelaria Scheurer, Michael E Redell, Michele S Garnes, Natalie J Dailey Gramatges, Maria Dutta, Ankhi Open Forum Infect Dis Abstract BACKGROUND: Candida species are the most common cause of invasive fungal infections in hospitalized patients. Children with hematological malignancies are at increased risk. The epidemiology of species implicated in invasive candidiasis (IC) has changed over the past 25 years with non-albicans Candida (NAC) species now prevailing. These changes have therapeutic and prophylactic implications as some species carry intrinsic resistance to widely-used antifungal medications. METHODS: Patients ages 0-18 with hematologic malignancy and at least one episode of IC from 2011-2022 from two institutions were included. Patients who had received a bone marrow transplant were excluded. Information related to demographics, host factors, clinical risk factors, Candida species and antifungal minimum inhibitory concentrations (MICs), treatment and outcomes was collected via retrospective chart review. RESULTS: 53 cases of IC were identified. Sixty percent were males. Thirty (57%) were of Hispanic ethnicity. The median age at diagnosis was 9 years (range 2 months-18 years). Seventy percent (37/53) had B-cell acute lymphoblastic leukemia. The median time to IC from diagnosis of cancer was 95 days (IQR 20-277). C. tropicalis (n=17; 32%) and C. albicans (n=14; 26%) were the most common species followed by C. glabrata and C. parapsilosis. Thirty-five percent (18/53) had concurrent bacteremia. The most common sites of dissemination were the lungs (n=24, 45%), kidneys (n=17; 32%), liver (n=15, 28%) and spleen (n=14; 27%). Of the 35 patients who underwent dilated eye exams, 23% (n=8) had ophthalmologic involvement. NAC were more likely to disseminate to the eyes, skin and spleen than C. albicans (p< 0.05). Fourteen isolates (26%) demonstrated increased MICs to fluconazole and six demonstrated increased MICs to voriconazole. Most (59%) required more than 6 weeks of antifungals. Sixteen patients died, of which six were attributed to IC. CONCLUSION: NAC accounted for most of the IC in hematological malignancies with C.tropicalis being the most common. The implications of NAC being predominant in this high-risk group is concerning due to the higher MIC to azoles and the potential for azole resistance in the future. Antifungal prophylaxis and treatment both need to be reevaluated periodically based on these findings. DISCLOSURES: Natalie J Dailey Garnes, MD, MPH, AlloVir: Grant/Research Support Oxford University Press 2023-11-27 /pmc/articles/PMC10679075/ http://dx.doi.org/10.1093/ofid/ofad500.1534 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Said, Amira
Afridi, Faraz
Daignault, Chelsea
O’Farrell, Candelaria
Scheurer, Michael E
Redell, Michele S
Garnes, Natalie J Dailey
Gramatges, Maria
Dutta, Ankhi
1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida
title 1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida
title_full 1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida
title_fullStr 1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida
title_full_unstemmed 1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida
title_short 1701. Trends in Invasive Candidiasis in Children with Hematologic Malignancies: Increased Risk of Dissemination with Non-albicans Candida
title_sort 1701. trends in invasive candidiasis in children with hematologic malignancies: increased risk of dissemination with non-albicans candida
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679075/
http://dx.doi.org/10.1093/ofid/ofad500.1534
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