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Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System
BACKGROUND: The 2022 global mpox outbreak was notable for transmission between persons outside of travel and zoonotic exposures and primarily through intimate contact. An understanding of the presentation of mpox in people with human immunodeficiency virus (HIV) and other immunocompromising conditio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644828/ https://www.ncbi.nlm.nih.gov/pubmed/38023539 http://dx.doi.org/10.1093/ofid/ofad552 |
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author | Vo, Christopher Zomorodi, Rustin Silvera, Richard Bartram, Logan Lugo, Luz Amarilis Kojic, Erna Urbina, Antonio Aberg, Judith Sigel, Keith Chasan, Rachel Patel, Gopi |
author_facet | Vo, Christopher Zomorodi, Rustin Silvera, Richard Bartram, Logan Lugo, Luz Amarilis Kojic, Erna Urbina, Antonio Aberg, Judith Sigel, Keith Chasan, Rachel Patel, Gopi |
author_sort | Vo, Christopher |
collection | PubMed |
description | BACKGROUND: The 2022 global mpox outbreak was notable for transmission between persons outside of travel and zoonotic exposures and primarily through intimate contact. An understanding of the presentation of mpox in people with human immunodeficiency virus (HIV) and other immunocompromising conditions and knowledge of the efficacy of tecovirimat continue to evolve. METHODS: This retrospective study describes clinical features and outcomes of persons with mpox who received tecovirimat. Data were obtained via medical record review of patients prescribed tecovirimat in a health system in New York City during the height of the outbreak in 2022. RESULTS: One hundred thirty people received tecovirimat between 1 July and 1 October 2022. People with HIV (n = 80) experienced similar rates of recovery, bacterial superinfections, and hospitalization compared to patients without immunocompromising conditions. Individuals determined to be severely immunocompromised (n = 14) had a higher risk of hospitalization than those without severe immunocompromise (cohort inclusive of those with well-controlled HIV, excluding those without virologic suppression, n = 101): 50% versus 9% (P < .001). Hospitalized patients (n = 18 [13% of total]) were primarily admitted for bacterial superinfections (44.4%), with a median hospital stay of 4 days. Of those who completed follow-up (n = 85 [66%]), 97% had recovery of lesions at time of posttreatment assessment. Tecovirimat was well tolerated; there were no reported severe adverse events attributed to therapy. CONCLUSIONS: There were no significant differences in outcomes between people with HIV when evaluated as a whole and patients without immunocompromising conditions. However, mpox infection was associated with higher rates of hospitalization in those with severe immunocompromise, including patients with HIV/AIDS. Treatment with tecovirimat was well tolerated. Key Points: In our mpox cohort, people with HIV had similar rates of recovery and complications as those without HIV or other immunocompromising conditions. Severe immunocompromise was associated with a higher hospitalization rate. Tecovirimat was well tolerated, with minimal side effects. |
format | Online Article Text |
id | pubmed-10644828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106448282023-11-02 Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System Vo, Christopher Zomorodi, Rustin Silvera, Richard Bartram, Logan Lugo, Luz Amarilis Kojic, Erna Urbina, Antonio Aberg, Judith Sigel, Keith Chasan, Rachel Patel, Gopi Open Forum Infect Dis Major Article BACKGROUND: The 2022 global mpox outbreak was notable for transmission between persons outside of travel and zoonotic exposures and primarily through intimate contact. An understanding of the presentation of mpox in people with human immunodeficiency virus (HIV) and other immunocompromising conditions and knowledge of the efficacy of tecovirimat continue to evolve. METHODS: This retrospective study describes clinical features and outcomes of persons with mpox who received tecovirimat. Data were obtained via medical record review of patients prescribed tecovirimat in a health system in New York City during the height of the outbreak in 2022. RESULTS: One hundred thirty people received tecovirimat between 1 July and 1 October 2022. People with HIV (n = 80) experienced similar rates of recovery, bacterial superinfections, and hospitalization compared to patients without immunocompromising conditions. Individuals determined to be severely immunocompromised (n = 14) had a higher risk of hospitalization than those without severe immunocompromise (cohort inclusive of those with well-controlled HIV, excluding those without virologic suppression, n = 101): 50% versus 9% (P < .001). Hospitalized patients (n = 18 [13% of total]) were primarily admitted for bacterial superinfections (44.4%), with a median hospital stay of 4 days. Of those who completed follow-up (n = 85 [66%]), 97% had recovery of lesions at time of posttreatment assessment. Tecovirimat was well tolerated; there were no reported severe adverse events attributed to therapy. CONCLUSIONS: There were no significant differences in outcomes between people with HIV when evaluated as a whole and patients without immunocompromising conditions. However, mpox infection was associated with higher rates of hospitalization in those with severe immunocompromise, including patients with HIV/AIDS. Treatment with tecovirimat was well tolerated. Key Points: In our mpox cohort, people with HIV had similar rates of recovery and complications as those without HIV or other immunocompromising conditions. Severe immunocompromise was associated with a higher hospitalization rate. Tecovirimat was well tolerated, with minimal side effects. Oxford University Press 2023-11-02 /pmc/articles/PMC10644828/ /pubmed/38023539 http://dx.doi.org/10.1093/ofid/ofad552 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 | Major Article Vo, Christopher Zomorodi, Rustin Silvera, Richard Bartram, Logan Lugo, Luz Amarilis Kojic, Erna Urbina, Antonio Aberg, Judith Sigel, Keith Chasan, Rachel Patel, Gopi Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System |
title | Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System |
title_full | Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System |
title_fullStr | Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System |
title_full_unstemmed | Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System |
title_short | Clinical Characteristics and Outcomes of Patients With Mpox Who Received Tecovirimat in a New York City Health System |
title_sort | clinical characteristics and outcomes of patients with mpox who received tecovirimat in a new york city health system |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644828/ https://www.ncbi.nlm.nih.gov/pubmed/38023539 http://dx.doi.org/10.1093/ofid/ofad552 |
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