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564. Nocardiosis in Portugal: a single-center experience

BACKGROUND: Nocardiosis is a rare opportunistic infection with increasing incidence. Given its rarity, data on the prognosis and distribution are scarce and essential. METHODS: Retrospective study reviewing all nocardiosis cases diagnosed at our tertiary care hospital from January 2019 to January 20...

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Autores principales: Besteiro, Bruno, Coutinho, Daniel, Fragoso, Joana, Figueiredo, Cristovão, Nunes, Sofia, Azevedo, Carlos, Teixeira, Tiago, Selaru, Aurelia, Lameirão, Angelina, Malheiro, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676892/
http://dx.doi.org/10.1093/ofid/ofad500.633
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author Besteiro, Bruno
Coutinho, Daniel
Fragoso, Joana
Figueiredo, Cristovão
Nunes, Sofia
Azevedo, Carlos
Teixeira, Tiago
Selaru, Aurelia
Lameirão, Angelina
Malheiro, Luis
author_facet Besteiro, Bruno
Coutinho, Daniel
Fragoso, Joana
Figueiredo, Cristovão
Nunes, Sofia
Azevedo, Carlos
Teixeira, Tiago
Selaru, Aurelia
Lameirão, Angelina
Malheiro, Luis
author_sort Besteiro, Bruno
collection PubMed
description BACKGROUND: Nocardiosis is a rare opportunistic infection with increasing incidence. Given its rarity, data on the prognosis and distribution are scarce and essential. METHODS: Retrospective study reviewing all nocardiosis cases diagnosed at our tertiary care hospital from January 2019 to January 2023. RESULTS: A positive Nocardia spp. culture was identified in 20 patients. Nocardia isolation was considered colonization in 2 patients, but the other 18 cases were considered as disease, 6 (33.3%) of which were classified as disseminated nocardiosis (DN). The mean age was 64.0±14.05 years-old and 75% were males. One or more immunosuppressive conditions were identified in 70% of patients, including diabetes mellitus (n=9), active solid tumors (n=3), autoimmune diseases (n=3) and HIV infection with CD4+ < 200 cel/uL (n=2). Among the immunocompromised patients, 28,6% were being treated with high-dose corticosteroid therapy. The lung was the most common site of infection (85%) and most cultures were initially retrieved for lower respiratory tract samples (85%) evaluated for mycobacteria in modified Middlebrook 7H9 Broth. Lymphopenia was observed in 38.9% of patients.The most frequently isolated species were N.nova/africana (n=7), N.cyriacigeorgica (n=4) and N.pseudobrasiliensis (n=3). N.cyriacigeorgica was identified in the two cases considered colonization. Most patients (94.4%) were treated with antimicrobials, 50.0% in monotherapy and 44.4% in combination therapy. The most frequently prescribed antibiotics were co-trimoxazole (94.4%), imipenem (22.2%) and linezolid (16.7%). Selected antimicrobial agents were generally effective, with linezolid and co-trimoxazole having the highest susceptibility rates (100% susceptibility). The median [IQR] duration of treatment was 238 [45–720] and 170 [5–360] days for localized and DN, respectively. The overall one- year case fatality was 25% and was higher in patients with DN (80%). CONCLUSION: Nocardiosis is an uncommon but emerging disease which can occur both in immunocompetent and immunocompromised patients. The present study reports a case series on Nocardiosis from Portugal and provides important information of this disease. As the outcomes are poor, early recognition and prompt treatment are essential to improve the outcome. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106768922023-11-27 564. Nocardiosis in Portugal: a single-center experience Besteiro, Bruno Coutinho, Daniel Fragoso, Joana Figueiredo, Cristovão Nunes, Sofia Azevedo, Carlos Teixeira, Tiago Selaru, Aurelia Lameirão, Angelina Malheiro, Luis Open Forum Infect Dis Abstract BACKGROUND: Nocardiosis is a rare opportunistic infection with increasing incidence. Given its rarity, data on the prognosis and distribution are scarce and essential. METHODS: Retrospective study reviewing all nocardiosis cases diagnosed at our tertiary care hospital from January 2019 to January 2023. RESULTS: A positive Nocardia spp. culture was identified in 20 patients. Nocardia isolation was considered colonization in 2 patients, but the other 18 cases were considered as disease, 6 (33.3%) of which were classified as disseminated nocardiosis (DN). The mean age was 64.0±14.05 years-old and 75% were males. One or more immunosuppressive conditions were identified in 70% of patients, including diabetes mellitus (n=9), active solid tumors (n=3), autoimmune diseases (n=3) and HIV infection with CD4+ < 200 cel/uL (n=2). Among the immunocompromised patients, 28,6% were being treated with high-dose corticosteroid therapy. The lung was the most common site of infection (85%) and most cultures were initially retrieved for lower respiratory tract samples (85%) evaluated for mycobacteria in modified Middlebrook 7H9 Broth. Lymphopenia was observed in 38.9% of patients.The most frequently isolated species were N.nova/africana (n=7), N.cyriacigeorgica (n=4) and N.pseudobrasiliensis (n=3). N.cyriacigeorgica was identified in the two cases considered colonization. Most patients (94.4%) were treated with antimicrobials, 50.0% in monotherapy and 44.4% in combination therapy. The most frequently prescribed antibiotics were co-trimoxazole (94.4%), imipenem (22.2%) and linezolid (16.7%). Selected antimicrobial agents were generally effective, with linezolid and co-trimoxazole having the highest susceptibility rates (100% susceptibility). The median [IQR] duration of treatment was 238 [45–720] and 170 [5–360] days for localized and DN, respectively. The overall one- year case fatality was 25% and was higher in patients with DN (80%). CONCLUSION: Nocardiosis is an uncommon but emerging disease which can occur both in immunocompetent and immunocompromised patients. The present study reports a case series on Nocardiosis from Portugal and provides important information of this disease. As the outcomes are poor, early recognition and prompt treatment are essential to improve the outcome. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10676892/ http://dx.doi.org/10.1093/ofid/ofad500.633 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
Besteiro, Bruno
Coutinho, Daniel
Fragoso, Joana
Figueiredo, Cristovão
Nunes, Sofia
Azevedo, Carlos
Teixeira, Tiago
Selaru, Aurelia
Lameirão, Angelina
Malheiro, Luis
564. Nocardiosis in Portugal: a single-center experience
title 564. Nocardiosis in Portugal: a single-center experience
title_full 564. Nocardiosis in Portugal: a single-center experience
title_fullStr 564. Nocardiosis in Portugal: a single-center experience
title_full_unstemmed 564. Nocardiosis in Portugal: a single-center experience
title_short 564. Nocardiosis in Portugal: a single-center experience
title_sort 564. nocardiosis in portugal: a single-center experience
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676892/
http://dx.doi.org/10.1093/ofid/ofad500.633
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