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DOI 10.1093/cid/ciaf520

Медицинская библиотека · Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026

Clinical Outcomes of Mpox Disease in Patients Treated With Tecovirimat.

Leocadio Ciarra, Garcia Elizabeth A, Lash Maura, Berardi Jonathan, Chan Justin, Chasan Rachel, Esquivel Blanca, Foote Mary, Glesby Marshall J, Guerra Amiyah, Harris Alexander B, Knutsen Dorothy, Mannheimer Sharon, Mazo Dana, McLean Jacob, McPherson Tristan D, Meyerowitz Eric A, Mgbako Ofole, Patel Gopi, Pagán Pirallo Patricia M, Radix Asa E, Riska Paul F, Sayegh Mark N, Seifu Leah, Shaw Raphael, Zingman Barry S, Zomorodi Rustin, Zucker Jason, Wong Marcia

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

There is emerging literature describing clinical characteristics and outcomes in patients with mpox treated with tecovirimat.

METHODS

We analyzed retrospective deidentified data from healthcare systems in New York City with the highest number of tecovirimat prescriptions. Individuals with probable or confirmed mpox initiating tecovirimat from May to December 2022 were included. A chart abstraction instrument was used to extract demographic and clinical data from medical records. We examined factors associated with delay in treatment and hospitalization.

RESULTS

A total of 708 individuals prescribed tecovirimat for mpox were included in the analysis; median age was 36 years (IQR 31-43); 566 (80%) were cisgender men who have sex with men; and 399 (56%) were diagnosed with HIV. Side effects (100, 14%) and severe adverse events (7, 1%) were rare. The most common long-term sequela was scarring (69, 10%). One hundred and one (14%) were hospitalized. Median time from symptom onset to treatment initiation was 8 days (IQR 6-11). Non-Hispanic Black patients had higher risk of initiating tecovirimat ≥8 days after symptom onset (relative risk [RR] = 1.3, 95% CI: 1.2-1.7) and being hospitalized (adjusted relative risk [aRR] = 2.2, 95% CI: 1.4-3.5) compared with Hispanic patients, after adjusting for HIV and insurance status.

CONCLUSIONS

We described common reasons for tecovirimat initiation and hospitalization. There were racial inequities in hospitalization and treatment delays. More research and focused efforts to mitigate these inequities are needed. These findings may better inform decisions for treatment initiation and hospitalization for mpox.

Для цитирования: Leocadio Ciarra, Garcia Elizabeth A, Lash Maura, Berardi Jonathan, Chan Justin, Chasan Rachel, Esquivel Blanca, Foote Mary, Glesby Marshall J, Guerra Amiyah, Harris Alexander B, Knutsen Dorothy, Mannheimer Sharon, Mazo Dana, McLean Jacob, McPherson Tristan D, Meyerowitz Eric A, Mgbako Ofole, Patel Gopi, Pagán Pirallo Patricia M, Radix Asa E, Riska Paul F, Sayegh Mark N, Seifu Leah, Shaw Raphael, Zingman Barry S, Zomorodi Rustin, Zucker Jason, Wong Marcia. Clinical Outcomes of Mpox Disease in Patients Treated With Tecovirimat.. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2026. DOI: 10.1093/cid/ciaf520.

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