Demographic and clinical characteristics of confirmed human monkeypox virus cases in individuals attending a sexual health centre in London, UK: an observational analysis.


Journal

The Lancet. Infectious diseases
ISSN: 1474-4457
Titre abrégé: Lancet Infect Dis
Pays: United States
ID NLM: 101130150

Informations de publication

Date de publication:
09 2022
Historique:
received: 31 05 2022
revised: 14 06 2022
accepted: 14 06 2022
pubmed: 6 7 2022
medline: 31 8 2022
entrez: 5 7 2022
Statut: ppublish

Résumé

Historically, human monkeypox virus cases in the UK have been limited to imported infections from west Africa. Currently, the UK and several other countries are reporting a rapid increase in monkeypox cases among individuals attending sexual health clinics, with no apparent epidemiological links to endemic areas. We describe demographic and clinical characteristics of patients diagnosed with human monkeypox virus attending a sexual health centre. In this observational analysis, we considered patients with confirmed monkeypox virus infection via PCR detection attending open-access sexual health clinics in London, UK, between May 14 and May 25, 2022. We report hospital admissions and concurrent sexually transmitted infection (STI) proportions, and describe our local response within the first 2 weeks of the outbreak. Monkeypox virus infection was confirmed in 54 individuals, all identifying as men who have sex with men (MSM), with a median age of 41 years (IQR 34-45). 38 (70%) of 54 individuals were White, 26 (48%) were born in the UK, and 13 (24%) were living with HIV. 36 (67%) of 54 individuals reported fatigue or lethargy, 31 (57%) reported fever, and ten (18%) had no prodromal symptoms. All patients presented with skin lesions, of which 51 (94%) were anogenital. 37 (89%) of 54 individuals had skin lesions affecting more than one anatomical site and four (7%) had oropharyngeal lesions. 30 (55%) of 54 individuals had lymphadenopathy. One in four patients had a concurrent STI. Five (9%) of 54 individuals required admission to hospital, mainly due to pain or localised bacterial cellulitis requiring antibiotic intervention or analgesia. We recorded no fatal outcomes. Autochthonous community monkeypox virus transmission is currently observed among MSM in the UK. We found a high proportion of concomitant STIs and frequent anogenital symptoms, suggesting transmissibility through local inoculation during close skin-to-skin or mucosal contact, during sexual activity. Additional resources are required to support sexual health and other specialist services in managing this condition. A review of the case definition and better understanding of viral transmission routes are needed to shape infection control policies, education and prevention strategies, and contact tracing. None.

Sections du résumé

BACKGROUND
Historically, human monkeypox virus cases in the UK have been limited to imported infections from west Africa. Currently, the UK and several other countries are reporting a rapid increase in monkeypox cases among individuals attending sexual health clinics, with no apparent epidemiological links to endemic areas. We describe demographic and clinical characteristics of patients diagnosed with human monkeypox virus attending a sexual health centre.
METHODS
In this observational analysis, we considered patients with confirmed monkeypox virus infection via PCR detection attending open-access sexual health clinics in London, UK, between May 14 and May 25, 2022. We report hospital admissions and concurrent sexually transmitted infection (STI) proportions, and describe our local response within the first 2 weeks of the outbreak.
FINDINGS
Monkeypox virus infection was confirmed in 54 individuals, all identifying as men who have sex with men (MSM), with a median age of 41 years (IQR 34-45). 38 (70%) of 54 individuals were White, 26 (48%) were born in the UK, and 13 (24%) were living with HIV. 36 (67%) of 54 individuals reported fatigue or lethargy, 31 (57%) reported fever, and ten (18%) had no prodromal symptoms. All patients presented with skin lesions, of which 51 (94%) were anogenital. 37 (89%) of 54 individuals had skin lesions affecting more than one anatomical site and four (7%) had oropharyngeal lesions. 30 (55%) of 54 individuals had lymphadenopathy. One in four patients had a concurrent STI. Five (9%) of 54 individuals required admission to hospital, mainly due to pain or localised bacterial cellulitis requiring antibiotic intervention or analgesia. We recorded no fatal outcomes.
INTERPRETATION
Autochthonous community monkeypox virus transmission is currently observed among MSM in the UK. We found a high proportion of concomitant STIs and frequent anogenital symptoms, suggesting transmissibility through local inoculation during close skin-to-skin or mucosal contact, during sexual activity. Additional resources are required to support sexual health and other specialist services in managing this condition. A review of the case definition and better understanding of viral transmission routes are needed to shape infection control policies, education and prevention strategies, and contact tracing.
FUNDING
None.

Identifiants

pubmed: 35785793
pii: S1473-3099(22)00411-X
doi: 10.1016/S1473-3099(22)00411-X
pmc: PMC9534773
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1321-1328

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests LSPM has consulted for or received speaker fees from bioMerieux, DNAelectronics, Eumedica, Dairy Crest, Pfizer, Profile Pharma, Umovis Lab, Kent Pharma, Pulmocide, Sumiovant, and Shionogi, and received research grants from the National Institute for Health Research, CW+ charity, and LifeArc. NG has consulted for or received speaker fees from Viiv Healthcare. JH has received a research grant from the CW+ charity. DA has consulted for or received speaker fees from Viiv Healthcare and Theratechnologies. BM-P has consulted for or received speaker fees from MSD. NM has consulted for or received speaker fees from Pfizer and Shionogi. MBo has consulted for or received speaker fees from Viiv Healthcare, Gilead, GlaxoSmithKline, Pfizer, Cypla, Mylan, and Janssen. MBo has also received research grants from Gilead, Viiv Healthcare, Mylan, Novavax, Janssen, Valneva, Moderna, and Roche. RJ has consulted for or received speaker fees from Viiv Healthcare and Gilead. GW has consulted for or received speaker fees from Viiv Healthcare and Gilead. All other authors declare no competing interests.

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Auteurs

Nicolò Girometti (N)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK. Electronic address: n.girometti@nhs.net.

Ruth Byrne (R)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Margherita Bracchi (M)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Joseph Heskin (J)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Alan McOwan (A)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Victoria Tittle (V)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Keerti Gedela (K)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Christopher Scott (C)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Sheel Patel (S)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Jesal Gohil (J)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Diarmuid Nugent (D)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Tara Suchak (T)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Molly Dickinson (M)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Margaret Feeney (M)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Borja Mora-Peris (B)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK; Imperial College Healthcare NHS Trust, London, UK.

Katrina Stegmann (K)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK; Falcon Road Clinic (Wandsworth), Central London Community Healthcare NHS Trust, London, UK.

Komal Plaha (K)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK; Falcon Road Clinic (Wandsworth), Central London Community Healthcare NHS Trust, London, UK.

Gary Davies (G)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Luke S P Moore (LSP)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK; Imperial College Healthcare NHS Trust, London, UK; Department of Infectious Diseases, Imperial College London, London, UK.

Nabeela Mughal (N)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK; Imperial College Healthcare NHS Trust, London, UK; Department of Infectious Diseases, Imperial College London, London, UK.

David Asboe (D)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Marta Boffito (M)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK; Department of Infectious Diseases, Imperial College London, London, UK.

Rachael Jones (R)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Gary Whitlock (G)

Department of HIV/GUM, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

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