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Author Notes:

Dr Kristina M Angelo, Division of Global Migration and Quarantine, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA. Email;kangelo@cdc.gov

KMA was involved in conceptualising the study, data curation, formal analysis, methodology, funding acquisition, project administration, resources, supervision, validation, visualisation, writing of the original draft, and review and editing the manuscript. TS was involved in conceptualising the study, data curation, formal analysis, methodology, resources, software, validation, visualisation, and writing, reviewing, and editing the manuscript. DC-F, LB-S, MDM, GS-N, SB, AD, KLBH, AC, EB, CG, MG, DMP, CPP, CM, CL, AdF, ES, MB, SL, CL, LB, HC, Ade, EF, SAF, HG, AG, MK, DM, AM, JM, DN, CR, PS, CT, and JVH were involved in data collection, resources, writing, and reviewing and editing the manuscript. HA was involved in conceptualising the study, data collection, data methodology, resources, and writing, reviewing, and editing the manuscript. SAJG was involved in conceptualising the study, data curation, formal analysis, methodology, resources, software, supervision, validation, visualisation, and writing, reviewing, and editing the manuscript. FW was involved in conceptualising the study, methodology, resources, and writing, reviewing, and editing the manuscript. RH, DHH. and PK were involved in conceptualising the study, methodology, funding acquisition, resources, visualisation, and writing, reviewing, and editing the manuscript. ML was involved in conceptualising the study investigation, methodology, funding acquisition, resources, supervision, visualisation, and writing, reviewing, and editing the manuscript. MG was involved with data visualization, and writing, reviewing, and editing the manuscript. LQ was involved in conceptualising the study, data curation, and writing, reviewing, and editing the manuscript. TS and SG directly assessed and verified data. All authors had full access to these data, read and approved the final version of the manuscript, and accept responsibility for publication.

he authors would like to thank the European Network for Tropical Medicine and Travel Health (TropNet) for their collegiality and collaboration. We would also like to thank Alba Antequera, (Barcelona, Spain; patient care), John T Brooks (Atlanta, GA, USA; manuscript review), Jaclyn Chabot (Montreal, QC, Canada; data entry), Maria Agustina Dal Molin (Barcelona, Spain; patient care), Cindy Friedman (Atlanta, GA, USA; protocol and manuscript review), Irene Fuertes De Vega, (Barcelona, Spain; patient care), Santiago Garro (Buenos Aires, Argentina; patient care), Miguel J Martinez (Barcelona, Spain; laboratory testing), Miguel Martinez-Lacalzada (Barcelona, Spain; patient care), Hansi Peiris (Montreal, QC, Canada; data entry), Mary G Reynolds (Atlanta, GA, USA; sample size calculations review), Aisha Rizwan (Atlanta, Georgia, USA; programme management), Natalia Rodriguez-Valero (Barcelona, Spain; patient care), Julie Rushmore (Atlanta, GA, USA; questionnaire development), and Lisa Owusu Sarpong (Montreal, QC, Canada; data entry). The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the US CDC.

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Research Funding:

This project was funded through a Cooperative Agreement between the US Centers for Disease Control and Prevention (CDC) and the International Society of Travel Medicine (1 U01CK000632-01-00).

Keywords:

  • Male
  • Humans
  • Adolescent
  • Young Adult
  • Adult
  • Middle Aged
  • Aged
  • Female
  • HIV Infections
  • Homosexuality, Male
  • Cross-Sectional Studies
  • Smallpox
  • Monkeypox
  • Sexual and Gender Minorities
  • Exanthema

Epidemiological and clinical characteristics of patients with monkeypox in the GeoSentinel Network: a cross-sectional study

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Journal Title:

The Lancet Infectious Diseases

Volume:

Volume 23, Number 2

Publisher:

, Pages 196-206

Type of Work:

Article | Final Publisher PDF

Abstract:

Background: The early epidemiology of the 2022 monkeypox epidemic in non-endemic countries differs substantially from the epidemiology previously reported from endemic countries. We aimed to describe the epidemiological and clinical characteristics among individuals with confirmed cases of monkeypox infection. Methods: We descriptively analysed data for patients with confirmed monkeypox who were included in the GeoSentinel global clinical-care-based surveillance system between May 1 and July 1 2022, across 71 clinical sites in 29 countries. Data collected included demographics, travel history including mass gathering attendance, smallpox vaccination history, social history, sexual history, monkeypox exposure history, medical history, clinical presentation, physical examination, testing results, treatment, and outcomes. We did descriptive analyses of epidemiology and subanalyses of patients with and without HIV, patients with CD4 counts of less than 500 cells per mm3 or 500 cells per mm3 and higher, patients with one sexual partner or ten or more sexual partners, and patients with or without a previous smallpox vaccination. Findings: 226 cases were reported at 18 sites in 15 countries. Of 211 men for whom data were available, 208 (99%) were gay, bisexual, or men who have sex with men (MSM) with a median age of 37 years (range 18–68; IQR 32–43). Of 209 patients for whom HIV status was known, 92 (44%) men had HIV infection with a median CD4 count of 713 cells per mm3 (range 36–1659; IQR 500–885). Of 219 patients for whom data were available, 216 (99%) reported sexual or close intimate contact in the 21 days before symptom onset; MSM reported a median of three partners (IQR 1–8). Of 195 patients for whom data were available, 78 (40%) reported close contact with someone who had confirmed monkeypox. Overall, 30 (13%) of 226 patients were admitted to hospital; 16 (53%) of whom had severe illness, defined as hospital admission for clinical care rather than infection control. No deaths were reported. Compared with patients without HIV, patients with HIV were more likely to have diarrhoea (p=0·002), perianal rash or lesions (p=0·03), and a higher rash burden (median rash burden score 9 [IQR 6–21] for patients with HIV vs median rash burden score 6 [IQR 3–14] for patients without HIV; p<0·0001), but no differences were identified in the proportion of men who had severe illness by HIV status. Interpretation: Clinical manifestations of monkeypox infection differed by HIV status. Recommendations should be expanded to include pre-exposure monkeypox vaccination of groups at high risk of infection who plan to engage in sexual or close intimate contact. Funding: US Centers for Disease Control and Prevention, International Society of Travel Medicine.

Copyright information:

Published by Elsevier Ltd.

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