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Effectiveness of one dose of killed oral cholera vaccine in an endemic community in the Democratic Republic of the Congo: a matched case-control study.
Malembaka, Espoir Bwenge; Bugeme, Patrick Musole; Hutchins, Chloe; Xu, Hanmeng; Hulse, Juan Dent; Demby, Maya N; Gallandat, Karin; Saidi, Jaime Mufitini; Rumedeka, Baron Bashige; Itongwa, Moïse; Tshiwedi-Tsilabia, Esperance; Kitoga, Faida; Bodisa-Matamu, Tavia; Kavunga-Membo, Hugo; Bengehya, Justin; Kulondwa, Jean-Claude; Debes, Amanda K; Taty, Nagède; Lee, Elizabeth C; Lunguya, Octavie; Lessler, Justin; Leung, Daniel T; Cumming, Oliver; Okitayemba, Placide Welo; Mukadi-Bamuleka, Daniel; Knee, Jackie; Azman, Andrew S.
Afiliação
  • Malembaka EB; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA; Centre for Tropical Diseases and Global Health (CTDGH), Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
  • Bugeme PM; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA; Centre for Tropical Diseases and Global Health (CTDGH), Université Catholique de Bukavu, Bukavu, Democratic Republic of the Congo.
  • Hutchins C; Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
  • Xu H; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA.
  • Hulse JD; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA.
  • Demby MN; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA.
  • Gallandat K; Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
  • Saidi JM; Ministère de la Santé Publique, Hygiène et Prévention, Zone de Santé d'Uvira, Uvira, Democratic Republic of the Congo.
  • Rumedeka BB; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA.
  • Itongwa M; Oxfam DRC, Uvira, Democratic Republic of the Congo.
  • Tshiwedi-Tsilabia E; Rodolphe Merieux INRB-Goma Laboratory, Goma, North Kivu, Democratic Republic of the Congo.
  • Kitoga F; Rodolphe Merieux INRB-Goma Laboratory, Goma, North Kivu, Democratic Republic of the Congo.
  • Bodisa-Matamu T; Rodolphe Merieux INRB-Goma Laboratory, Goma, North Kivu, Democratic Republic of the Congo.
  • Kavunga-Membo H; Rodolphe Merieux INRB-Goma Laboratory, Goma, North Kivu, Democratic Republic of the Congo; Institut National de Recherche Biomédicale, INRB, Kinshasa, Democratic Republic of the Congo.
  • Bengehya J; Ministère de la Santé Publique, Hygiène et Prévention, Division Provinciale de la Sante' Publique du Sud-Kivu, Bukavu, Democratic Republic of the Congo.
  • Kulondwa JC; Ministère de la Santé Publique, Hygiène et Prévention, Division Provinciale de la Sante' Publique du Sud-Kivu, Bukavu, Democratic Republic of the Congo.
  • Debes AK; Department of International Health, Johns Hopkins University, Baltimore, MD, USA.
  • Taty N; PNECHOL-MD, Community IMCI, Ministry of Health, Kinshasa, Democratic Republic of the Congo.
  • Lee EC; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA.
  • Lunguya O; Institut National de Recherche Biomédicale, INRB, Kinshasa, Democratic Republic of the Congo; Service of Microbiology, Department of Medical Biology, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
  • Lessler J; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA; University of North Carolina Population Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hil
  • Leung DT; Division of Infectious Diseases and Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
  • Cumming O; Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
  • Okitayemba PW; PNECHOL-MD, Community IMCI, Ministry of Health, Kinshasa, Democratic Republic of the Congo.
  • Mukadi-Bamuleka D; Rodolphe Merieux INRB-Goma Laboratory, Goma, North Kivu, Democratic Republic of the Congo; Institut National de Recherche Biomédicale, INRB, Kinshasa, Democratic Republic of the Congo; Service of Microbiology, Department of Medical Biology, University of Kinshasa, Kinshasa, Democratic Republic of th
  • Knee J; Department of Disease Control, London School of Hygiene & Tropical Medicine, London, UK.
  • Azman AS; Department of Epidemiology, Johns Hopkins University, Baltimore, MD, USA; Geneva Centre for Emerging Viral Diseases and Division of Tropical and Humanitarian Medicine, Geneva University Hospitals, Geneva, Switzerland. Electronic address: azman@jhu.edu.
Lancet Infect Dis ; 24(5): 514-522, 2024 May.
Article em En | MEDLINE | ID: mdl-38246191
ABSTRACT

BACKGROUND:

A global shortage of cholera vaccines has increased the use of single-dose regimens, rather than the standard two-dose regimen. There is sparse evidence on single-dose protection, particularly in children. In 2020, a mass vaccination campaign was conducted in Uvira, an endemic urban setting in eastern Democratic Republic of the Congo, resulting in largely single-dose coverage. We examined the effectiveness of a single-dose of the oral cholera vaccine Euvichol-Plus in this high-burden setting.

METHODS:

In this matched case-control study, we recruited individuals with medically attended confirmed cholera in the two cholera treatment facilities in the city of Uvira. The control group consisted of age-matched, sex-matched, and neighbourhood-matched community individuals. We recruited across two distinct periods Oct 14, 2021, to March 10, 2022 (12-17 months after vaccination), and Nov 21, 2022, to Oct 18, 2023 (24-36 months after vaccination). Study staff administered structured questionnaires to all participants to capture demographics, household conditions, potential confounding variables, and vaccination status. The odds of vaccination for the case and control groups were contrasted in conditional logistic regression models to estimate unadjusted and adjusted vaccine effectiveness.

FINDINGS:

We enrolled 658 individuals with confirmed cholera and 2274 matched individuals for the control group. 99 (15·1%) individuals in the case group were younger than 5 years at the time of vaccination. The adjusted single-dose vaccine effectiveness was 52·7% (95% CI 31·4 to 67·4) 12-17 months after vaccination and 44·7% (24·8 to 59·4) 24-36 months after vaccination. Although protection in the first 12-17 months after vaccination was similar for children aged 1-4 years and older individuals, the estimate of protection in children aged 1-4 years appeared to wane during the third year after vaccination (adjusted vaccine effectiveness 32·9%, 95% CI -30·7 to 65·5), with CIs spanning the null.

INTERPRETATION:

A single dose of Euvichol-Plus provided substantial protection against medically attended cholera for at least 36 months after vaccination in this cholera-endemic setting. Although the evidence provides support for similar levels of protection in young children and others in the short term, protection among children younger than 5 years might wane significantly during the third year after vaccination.

FUNDING:

Wellcome Trust and Gavi, the Vaccine Alliance.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Cólera / Vacinas de Produtos Inativados / Cólera Tipo de estudo: Observational_studies / Prognostic_studies / Qualitative_research Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País como assunto: Africa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Cólera / Vacinas de Produtos Inativados / Cólera Tipo de estudo: Observational_studies / Prognostic_studies / Qualitative_research Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País como assunto: Africa Idioma: En Ano de publicação: 2024 Tipo de documento: Article