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Human monkeypox outbreak: Epidemiological data and therapeutic potential of topical cidofovir in a prospective cohort study - 14/04/23

Doi : 10.1016/j.jaad.2022.10.043 
Tristán Gabriel Sobral-Costas, MD a, , Rafael Escudero-Tornero, MD a, Guillermo Servera-Negre, MD a, Jose I. Bernardino, MD, PhD b, Almudena Gutiérrez Arroyo, MD c, Marta Díaz-Menéndez, MD, PhD d, Jose Manuel Busto-Leis, MD a, Patricia Roces Álvarez, MD c, Pedro Herranz Pinto, MD, PhD e, Elena Sendagorta Cudos, MD, PhD e
a Dermatology Department, La Paz University Hospital, Madrid, Spain 
b HIV&Infectious Disease Unit, La Paz University Hospital, Idipaz, CIBERINFEC, Madrid, Spain 
c Microbiology Department, La Paz University Hospital, Madrid, Spain 
d National Referral Centre for Tropical Diseases and International Health, La Paz University Hospital, Idipaz, CIBERINFEC, Madrid, Spain 
e Dermatology Department, La Paz University Hospital, Idipaz, CIBERINFEC, Madrid, Spain 

Correspondence to: Tristán Gabriel Sobral-Costas, MD, Dermatology Department, La Paz University Hospital, Castellana 261, 28046, Madrid, Spain.Dermatology DepartmentLa Paz University HospitalCastellana 261Madrid28046Spain

Abstract

Background

Human monkeypox has become increasingly frequent worldwide since the outbreak was first reported in May 2022.

Objectives

As cidofovir is effective against vaccinia and other Orthopoxvirus diseases, we hypothesize that its topical use could be an effective treatment for monkeypox skin lesions, avoiding the adverse effects of systemic administration.

Methods

We conducted a prospective study to collect data on the clinical and virologic course of patients with monkeypox. All patients were offered symptomatic treatment. They were also offered treatment with topical cidofovir on a compassionate use basis. Twelve patients received treatment with topical cidofovir 1%, while the others received only symptomatic treatment. Prospective visits were scheduled for the collection of clinical and virological data.

Results

Lesions cleared quicker in the cidofovir-treated group (hazard ratio, 4.572; P = .0039). The median time to resolution was 12 (11.5-15) and 18 (16-21) days, respectively. On day 14, polymerase chain reaction-positive skin lesions were detected in 10% of the cidofovir sample, compared with 62.5% of the non-treated group (P = .019). Local adverse effects were frequent (50%), especially in the anogenital region. No systemic adverse effects were reported.

Limitations

The study is not a clinical trial and lacks a placebo-controlled arm.

Discussion

Topical cidofovir is a potentially relevant therapy in patients with skin lesions but mild systemic involvement. Reducing time to resolution could shorten isolation time and improve the cosmetic impact in areas such as the face.

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Key words : cidofovir, monkeypox, skin, topical

Abbreviations used : PCR, STD


Mappa


 Funding sources: None.
 IRB approval status: The study has received approval from the local ethics committee, which is available for submission to the journal.
 Consent informed: Consent for the publication of recognizable patient photographs or other identifiable material has been obtained by the authors and are available for submission to the journal.
 Reprints not available from the authors.


© 2022  American Academy of Dermatology, Inc.. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 88 - N° 5

P. 1074-1082 - maggio 2023 Ritorno al numero
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