TY - JOUR
T1 - Use of cidofovir in a patient with severe mpox and uncontrolled HIV infection
AU - Stafford, Adam
AU - Rimmer, Stephanie
AU - Gilchrist, Mark
AU - Sun, Kristi
AU - Davies, Ella P.
AU - Waddington, Claire S.
AU - Chiu, Christopher
AU - Armstrong-James, Darius
AU - Swaine, Thomas
AU - Davies, Frances
AU - Gómez, Carlos H.M.
AU - Kumar, Vagish
AU - ElHaddad, Ahmad
AU - Awad, Zaid
AU - Smart, Christopher
AU - Mora-Peris, Borja
AU - Muir, David
AU - Randell, Paul
AU - Peters, Joanna
AU - Chand, Meera
AU - Warrell, Clare E.
AU - Rampling, Tommy
AU - Cooke, Graham
AU - Dhanji, Sara
AU - Campbell, Vivienne
AU - Davies, Carys
AU - Osman, Sana
AU - Abbara, Aula
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/6
Y1 - 2023/6
N2 - A 48-year-old man with poorly controlled HIV presented with severe human monkeypox virus (hMPXV) infection, having completed 2 weeks of tecovirimat at another hospital. He had painful, ulcerating skin lesions on most of his body and oropharyngeal cavity, with subsequent Ludwig's angina requiring repeated surgical interventions. Despite commencing a second, prolonged course of tecovirimat, he did not objectively improve, and new lesions were still noted at day 24. Discussion at the UK National Health Service England High Consequence Infectious Diseases Network recommended the use of 3% topical and then intravenous cidofovir, which was given at 5 mg/kg; the patient made a noticeable improvement after the first intravenous dose. He received further intravenous doses at 7 days and 21 days after the dose and was discharged at day 52. Cidofovir is not licensed for use in treatment of hMPXV infection. Data for cidofovir use in hMPXV are restricted to studies in animals. Four other documented cases of cidofovir use against hMPXV have been reported in the USA in 2022, but we present its first use in the UK. The scarcity of studies into the use of cidofovir in this condition clearly shows the need for robust studies to assess efficacy, optimum dosage, timing, and route of administration.
AB - A 48-year-old man with poorly controlled HIV presented with severe human monkeypox virus (hMPXV) infection, having completed 2 weeks of tecovirimat at another hospital. He had painful, ulcerating skin lesions on most of his body and oropharyngeal cavity, with subsequent Ludwig's angina requiring repeated surgical interventions. Despite commencing a second, prolonged course of tecovirimat, he did not objectively improve, and new lesions were still noted at day 24. Discussion at the UK National Health Service England High Consequence Infectious Diseases Network recommended the use of 3% topical and then intravenous cidofovir, which was given at 5 mg/kg; the patient made a noticeable improvement after the first intravenous dose. He received further intravenous doses at 7 days and 21 days after the dose and was discharged at day 52. Cidofovir is not licensed for use in treatment of hMPXV infection. Data for cidofovir use in hMPXV are restricted to studies in animals. Four other documented cases of cidofovir use against hMPXV have been reported in the USA in 2022, but we present its first use in the UK. The scarcity of studies into the use of cidofovir in this condition clearly shows the need for robust studies to assess efficacy, optimum dosage, timing, and route of administration.
UR - http://www.scopus.com/inward/record.url?scp=85150174079&partnerID=8YFLogxK
U2 - 10.1016/S1473-3099(23)00044-0
DO - 10.1016/S1473-3099(23)00044-0
M3 - Review article
C2 - 36773621
AN - SCOPUS:85150174079
SN - 1473-3099
VL - 23
SP - e218-e226
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 6
ER -