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Childhood encephalitis in the Greater Mekong region (the SouthEast Asia Encephalitis Project): a multicentre prospective study.
Pommier, Jean David; Gorman, Chris; Crabol, Yoann; Bleakley, Kevin; Sothy, Heng; Santy, Ky; Tran, Huong Thi Thu; Nguyen, Lam Van; Bunnakea, Em; Hlaing, Chaw Su; Aye, Aye Mya Min; Cappelle, Julien; Herrant, Magali; Piola, Patrice; Rosset, Bruno; Chevalier, Veronique; Tarantola, Arnaud; Channa, Mey; Honnorat, Jerome; Pinto, Anne Laure; Rattanavong, Sayaphet; Vongsouvath, Manivanh; Mayxay, Mayfong; Phangmanixay, Sommanikhone; Phongsavath, Khounthavy; Tin, Ommar Swe; Kyaw, Latt Latt; Tin, Htay Htay; Linn, Kyaw; Tran, Thi Mai Hung; Pérot, Philippe; Thuy, Nguyen Thi Thu; Hien, Nguyen; Phan, Phuc Huu; Buchy, Philippe; Dussart, Philippe; Laurent, Denis; Eloit, Marc; Dubot-Pérès, Audrey; Lortholary, Olivier; de Lamballerie, Xavier; Newton, Paul N; Lecuit, Marc.
Affiliation
  • Pommier JD; Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia; Institut Pasteur, Biology of Infection Unit, Paris, France; Inserm U1117, Paris, France; Intensive Care Department, University Hospital of Guadeloupe, Guadeloupe, France.
  • Gorman C; Virology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Crabol Y; Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Bleakley K; Université Paris-Saclay, CNRS, Inria, Laboratoire de Mathématiques d'Orsay, Orsay, France.
  • Sothy H; Kantha Bopha IV Children's Hospital, Phnom Penh, Cambodia.
  • Santy K; Kantha Bopha IV Children's Hospital, Phnom Penh, Cambodia.
  • Tran HTT; National Children's Hospital, Hanoi, Vietnam.
  • Nguyen LV; National Children's Hospital, Hanoi, Vietnam.
  • Bunnakea E; Kantha Bopha IV Children's Hospital, Phnom Penh, Cambodia.
  • Hlaing CS; Yangon Children's Hospital, Yangon, Myanmar.
  • Aye AMM; Yangon Children's Hospital, Yangon, Myanmar.
  • Cappelle J; Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia; French Agricultural Research Centre for International Development (CIRAD), Montpellier, France.
  • Herrant M; International Department, Institut Pasteur, Paris, France.
  • Piola P; Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Rosset B; French Agricultural Research Centre for International Development (CIRAD), Montpellier, France.
  • Chevalier V; Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia; French Agricultural Research Centre for International Development (CIRAD), Montpellier, France.
  • Tarantola A; Epidemiology and Public Health Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Channa M; Virology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Honnorat J; French Reference Center for Paraneoplastic Neurological Syndromes and Autoi mmune Encephalitis, Hospices Civils de Lyon, Synatac Team, NeuroMyoGene Institute, Inserm U1217/CNRS UMR5310, Université de Lyon, Lyon, France.
  • Pinto AL; French Reference Center for Paraneoplastic Neurological Syndromes and Autoi mmune Encephalitis, Hospices Civils de Lyon, Synatac Team, NeuroMyoGene Institute, Inserm U1217/CNRS UMR5310, Université de Lyon, Lyon, France.
  • Rattanavong S; Lao-Oxford-Mahosot Hospital, Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos.
  • Vongsouvath M; Lao-Oxford-Mahosot Hospital, Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos.
  • Mayxay M; Lao-Oxford-Mahosot Hospital, Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos; Unité des Virus Émergents, Marseille, France.
  • Phangmanixay S; National Children's Hospital, Vientiane, Laos.
  • Phongsavath K; National Children's Hospital, Vientiane, Laos.
  • Tin OS; National Health Laboratory, Yangon, Myanmar.
  • Kyaw LL; National Health Laboratory, Yangon, Myanmar.
  • Tin HH; National Health Laboratory, Yangon, Myanmar.
  • Linn K; Yangon Children's Hospital, Yangon, Myanmar.
  • Tran TMH; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
  • Pérot P; Laboratory for Pathogen Discovery, Institut Pasteur, Paris, France.
  • Thuy NTT; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
  • Hien N; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
  • Phan PH; National Children's Hospital, Hanoi, Vietnam.
  • Buchy P; Virology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Dussart P; Virology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
  • Laurent D; Kantha Bopha IV Children's Hospital, Phnom Penh, Cambodia.
  • Eloit M; Laboratory for Pathogen Discovery, Institut Pasteur, Paris, France; Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
  • Dubot-Pérès A; Lao-Oxford-Mahosot Hospital, Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos; Unité des Virus Émergents, Marseille, France; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Churchill Hospital, Oxford, UK.
  • Lortholary O; Université Paris Cité, Department of Infectious Diseases and Tropical Medicine, Necker-Enfants Malades University Hospital, Institut Imagine, Assistance Publique-Hôpitaux de Paris, Paris, France; Institut Pasteur, CNRS, Molecular Mycology Unit, National Reference Center for Mycoses and Antifungals,
  • de Lamballerie X; Unité des Virus Émergents, Marseille, France.
  • Newton PN; Lao-Oxford-Mahosot Hospital, Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Churchill Hospital, Oxford, UK.
  • Lecuit M; Institut Pasteur, Biology of Infection Unit, Paris, France; Inserm U1117, Paris, France; Université Paris Cité, Department of Infectious Diseases and Tropical Medicine, Necker-Enfants Malades University Hospital, Institut Imagine, Assistance Publique-Hôpitaux de Paris, Paris, France. Electronic addr
Lancet Glob Health ; 10(7): e989-e1002, 2022 07.
Article in En | MEDLINE | ID: mdl-35714649
BACKGROUND: Encephalitis is a worldwide public health issue, with a substantially high burden among children in southeast Asia. We aimed to determine the causes of encephalitis in children admitted to hospitals across the Greater Mekong region by implementing a comprehensive state-of-the-art diagnostic procedure harmonised across all centres, and identifying clinical characteristics related to patients' conditions. METHODS: In this multicentre, observational, prospective study of childhood encephalitis, four referral hospitals in Cambodia, Vietnam, Laos, and Myanmar recruited children (aged 28 days to 16 years) who presented with altered mental status lasting more than 24 h and two of the following minor criteria: fever (within the 72 h before or after presentation), one or more generalised or partial seizures (excluding febrile seizures), a new-onset focal neurological deficit, cerebrospinal fluid (CSF) white blood cell count of 5 per mL or higher, or brain imaging (CT or MRI) suggestive of lesions of encephalitis. Comprehensive diagnostic procedures were harmonised across all centres, with first-line testing was done on samples taken at inclusion and results delivered within 24 h of inclusion for main treatable causes of disease and second-line testing was done thereafter for mostly non-treatable causes. An independent expert medical panel reviewed the charts and attribution of causes of all the included children. Using multivariate analyses, we assessed risk factors associated with unfavourable outcomes (ie, severe neurological sequelae and death) at discharge using data from baseline and day 2 after inclusion. This study is registered with ClinicalTrials.gov, NCT04089436, and is now complete. FINDINGS: Between July 28, 2014, and Dec 31, 2017, 664 children with encephalitis were enrolled. Median age was 4·3 years (1·8-8·8), 295 (44%) children were female, and 369 (56%) were male. A confirmed or probable cause of encephalitis was identified in 425 (64%) patients: 216 (33%) of 664 cases were due to Japanese encephalitis virus, 27 (4%) were due to dengue virus, 26 (4%) were due to influenza virus, 24 (4%) were due to herpes simplex virus 1, 18 (3%) were due to Mycobacterium tuberculosis, 17 (3%) were due to Streptococcus pneumoniae, 17 (3%) were due to enterovirus A71, 74 (9%) were due to other pathogens, and six (1%) were due to autoimmune encephalitis. Diagnosis was made within 24 h of admission to hospital for 83 (13%) of 664 children. 119 (18%) children had treatable conditions and 276 (42%) had conditions that could have been preventable by vaccination. At time of discharge, 153 (23%) of 664 children had severe neurological sequelae and 83 (13%) had died. In multivariate analyses, risk factors for unfavourable outcome were diagnosis of M tuberculosis infection upon admission (odds ratio 3·23 [95% CI 1·04-10·03]), coma on day 2 (2·90 [1·78-4·72]), supplementary oxygen requirement (1·89 [1·25-2·86]), and more than 1 week duration between symptom onset and admission to hospital (3·03 [1·68-5·48]). At 1 year after inclusion, of 432 children who were discharged alive from hospital with follow-up data, 24 (5%) had died, 129 (30%) had neurological sequelae, and 279 (65%) had completely recovered. INTERPRETATION: In southeast Asia, most causes of childhood encephalitis are either preventable or treatable, with Japanese encephalitis virus being the most common cause. We provide crucial information that could guide public health policy to improve diagnostic, vaccination, and early therapeutic guidelines on childhood encephalitis in the Greater Mekong region. FUNDING: Institut Pasteur, Institut Pasteur International Network, Fondation Merieux, Aviesan Sud, INSERM, Wellcome Trust, Institut de Recherche pour le Développement (IRD), and Fondation Total.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Encephalitis / Hashimoto Disease Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Lancet Glob Health Year: 2022 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Encephalitis / Hashimoto Disease Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Lancet Glob Health Year: 2022 Document type: Article Affiliation country: Country of publication: