TY - JOUR
T1 - Epidemiological and clinical characteristics of patients with monkeypox in the GeoSentinel Network
T2 - a cross-sectional study
AU - GeoSentinel Network Collaborators
AU - Angelo, Kristina M.
AU - Smith, Teresa
AU - Camprubí-Ferrer, Daniel
AU - Balerdi-Sarasola, Leire
AU - Díaz Menéndez, Marta
AU - Servera-Negre, Guillermo
AU - Barkati, Sapha
AU - Duvignaud, Alexandre
AU - Huber, Kristina L.B.
AU - Chakravarti, Arpita
AU - Bottieau, Emmanuel
AU - Greenaway, Christina
AU - Grobusch, Martin P.
AU - Mendes Pedro, Diogo
AU - Asgeirsson, Hilmir
AU - Popescu, Corneliu Petru
AU - Martin, Charlotte
AU - Licitra, Carmelo
AU - de Frey, Albie
AU - Schwartz, Eli
AU - Beadsworth, Michael
AU - Lloveras, Susana
AU - Larsen, Carsten S.
AU - Guagliardo, Sarah Anne J.
AU - Whitehill, Florence
AU - Huits, Ralph
AU - Hamer, Davidson H.
AU - Kozarsky, Phyllis
AU - Libman, Michael
AU - Blumberg, Lucille
AU - Chaussade, Hélène
AU - Desclaux, Arnaud
AU - Florence, Eric
AU - Aysel Florescu, Simin
AU - Glans, Hedvig
AU - Glynn, Marielle
AU - Goorhuis, Abraham
AU - Klein, Marina
AU - Malvy, Denis
AU - McCollum, Andrea
AU - Muñoz, José
AU - Nguyen, Duc
AU - Quilter, Laura
AU - Rothe, Camilla
AU - Soentjens, Patrick
AU - Tumiotto, Camille
AU - Vanhamel, Jef
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/2
Y1 - 2023/2
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85141343419&partnerID=8YFLogxK
U2 - 10.1016/S1473-3099(22)00651-X
DO - 10.1016/S1473-3099(22)00651-X
M3 - Article
C2 - 36216018
AN - SCOPUS:85141343419
SN - 1473-3099
VL - 23
SP - 196
EP - 206
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 2
ER -