SouthEast Asia Encephalitis Project

Encephalitis Clinical Trial

— SEAe  

Official title:

The Threat of Infectious Encephalitis in Southeast Asia: SouthEast Asia Encephalitis Project

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04089436
• Other study ID #: 2013-024
• Status: Active, not recruiting
• Start date: July 15, 2014
• Est. completion date: December 31, 2019

Study information

• Verified date: September 2019
• Source: Institut Pasteur
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Encephalitis, an acute inflammation of the central nervous system associated with neurologic dysfunction is of public health concern worldwide, because of its high mortality and neurological sequelae rates. In Asia where many of the possible etiologies are of major public health concerns (i.e. dengue, Japanese encephalitis, West Nile virus, EV71), acute encephalitis is among the most frequent and severe causes of pediatric hospitalization.

Despite extensive microbiological investigations, no pathogen is identified for a significant proportion of encephalitis patients in both industrialized and developing countries (28-85% of cases remain unconfirmed). Unknown and sometimes new emerging infectious agents may be responsible for cases of currently unknown etiology and an intensive effort to identify and characterize them is to be done. From this perspective, the Southeast Asian region, a particularly significant biodiversity hotspot, is at high risk for new pathogen emergence.

Surveillance and diagnostic capabilities for encephalitis remain poor and still suffer from serious shortcomings in most Southeast Asian countries and beyond. Although the burden of non-infectious encephalitis in this region remains to be ascertained, the best laboratories only identify etiological infective agents in less than half of patients. Systematic data regarding the contribution of these diseases are lacking and to define the burden of these infections, to describe the full clinical spectrum and characteristics of acute central nervous system infections, and to develop diagnostic and therapeutic algorithms to improve patient care.

The proposed project is an ambitious and multidisciplinary research consortium that aims to reduce the morbidity and mortality associated with infectious encephalitis in Southeast Asia (Cambodia, Laos, Vietnam and Myanmar) by improving diagnosis and medical care for patients.

The SEAe project specific objectives are:

• To fill‐in the biomedical knowledge gaps regarding acute encephalitis syndrome;

• To strengthen hospital laboratories capacities to enhance health by improving diagnosis and care for patients;

• To identify unknown pathogens responsible for encephalitis;

• To provide reliable information and a sustainable regional and sub‐regional surveillance network to clinicians and public health stakeholders that will help them to better define prevention policies, vaccination strategy, and build preparedness to emerging infectious risks.

Description:

Background:

Encephalitis is defined as an acute inflammation of the central nervous system associated with neurologic dysfunction. The most common etiologies are infections by either viruses or bacteria although parasites and fungi can also be occasionally detected, especially in immunocompromised patients. Because of high mortality and long-term neurological sequelae, encephalitis is of public health concern worldwide. Reported incidences range between 3.5 and 7.4 cases per 100,000 patient-years with higher incidences in children than adults. Various encephalitis outbreaks have recently emerged in Asia such as the fatal outbreak of enterovirus 71 (EV71) that occurred in mid-2012 in Cambodia affecting very young children (most below 3 years, all below 12 years). In Asia where many of the possible etiologies are of major public health concerns (i.e. dengue, Japanese encephalitis, West Nile virus, EV71), acute encephalitis is among the most frequent and severe causes of pediatric hospitalization.

Despite extensive microbiological investigations and the use of the most advanced molecular biology-based assays, no pathogen is identified for a significant proportion of encephalitis patients in both industrialized and developing countries (28-85% of cases remain unconfirmed). Previous studies support the hypothesis that unknown and sometimes new emerging infectious agents may be responsible for cases of currently unknown etiology and strongly argue for an intensive effort to identify and characterize them. This hypothesis is also strengthened by the recent apparent increase in emerging infectious diseases, many of which have been linked to human activities that impact the environment and to the spreading of pathogens to new geographic regions. From this perspective, the Southeast Asian region, a particularly significant biodiversity hotspot, is at high risk for new pathogen emergence. Indeed, growing human populations, increasing urbanization and frequent contact with wildlife and domesticated animals have created novel opportunities for the emergence of pathogens such as SARS at the end of 2002, and highly facilitated the spread of infectious diseases such as H5N1 high-pathogenicity avian influenza virus since 2004, and H1N1 pandemic influenza virus in 2009. The population in developing Southeast Asian countries is particularly at risk for the circulation of emerging or reemerging infectious agents and for this reason the surveillance and investigation of acute encephalitis syndrome in this region is of utmost public health importance, both locally and globally.

Surveillance and diagnostic capabilities for encephalitis remain poor and still suffer from serious shortcomings in most Southeast Asian countries and beyond. Although the burden of non-infectious encephalitis in this region remains to be ascertained, the best laboratories only identify etiological infective agents in less than half of patients. Moreover, because of the absence of reliable microbiological diagnostic capacity in the majority of public referral hospitals, local clinicians have to treat acute encephalitis syndromes mostly empirically, with little evaluation of the effectiveness of their clinical approach. Even if some of the most common causes of acute encephalitis syndrome may be vaccine-preventable, systematic data regarding the contribution of these diseases are lacking and no reliable data are available to define the burden of these infections, to describe the full clinical spectrum and characteristics of acute central nervous system infections, and to develop diagnostic and therapeutic algorithms to improve patient care. Besides, whatever the nature and magnitude of the encephalitis burden in Southeast Asia and the criteria used to assess it (i.e. morbidity, mortality, handicap, impact on families' budget or livelihood), this burden is borne principally by underprivileged populations with limited access to prevention and health care.

Project partners The proposed project is an ambitious and multidisciplinary research consortium associating: (i) national health authorities in Cambodia, Lao PDR, Vietnam and Myanmar; (ii) local major university and clinical sites (national hospitals and provincial health centers); (iii) key French stakeholders of life and health sciences with research activities carried out in the Southeast Asian region such as: Institut Pasteur and the Institut Pasteur International Network, Institut National de la Santé et de la Recherche Médicale (Inserm), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad), Institut de Recherche pour le Développement (IRD) ‐ Aix‐Marseille University ‐ Ecole des Hautes Etudes en Santé Publique (EHESP); and (iv) teams from the Southeast Asian Wellcome Trust Oxford University Major Overseas Programme.

Objectives:

The SEAe project aims to reduce the morbidity and mortality associated with infectious encephalitis in Southeast Asia by improving diagnosis and medical care for patients.

The SEAe project specific objectives are:

• To fill‐in the biomedical knowledge gaps regarding acute encephalitis syndrome;

• To strengthen hospital laboratories capacities to enhance health by improving diagnosis and care for patients;

• To identify unknown pathogens responsible for encephalitis;

• To document and analyze factors related to clusters of encephalitis cases integrating human health, animal health and environment through a "One Health" approach;

• To provide reliable information and a sustainable regional and sub‐regional surveillance network to clinicians and public health stakeholders that will help them to better define prevention policies, vaccination strategy, and build preparedness to emerging infectious risks.

Population study: patient with suspected encephalitis hospitalized in in 4 different Hospitals, Kantha Bopha IV children's Hospital, Phnom Penh, Cambodia, National paediatrics Hospital, Hanoi, Vietnam and Mahosot Hospital, Vientiane, Lao PDR, Yangon Children Hospital, Yangon, Myanmar. Inclusion criteria were adapted from the International Encephalitis Consortium 2013: all patients should be older than 28 days and presenting an altered mental status (i.e. confusion or inability to talk, decreased or altered level of consciousness or personality change) lasting more than 24 hours without alternative cause identified. These criteria should be associated with at least one of the following: (i) fever (>=38°C axillary) for less than 72 hours before or after presentation; (ii) seizure (febrile seizure excluded); (iii) focal neurologic finding.

Data collection:

Clinical data entries are required for this study.

Data entries:

A single data entry person (a medical doctor) enters clinical information and fill in a paper form at admission, at 24 hours, at discharge and one year after discharge and enter the data into an OpenClinica (hosted in CIRAD server, Montpellier, France ) anonymized online database.

Laboratory data is entered into a customized ACCESS (Microsoft database). The results are entered into dedicated tabs for the different techniques.

A data manager dedicated to the study is in charge of the database. The CIRAD and the Institut Pasteur share the co-ownership of the database.

First statistical analysis will be performed in Institut Pasteur du Cambodge, Phnom Penh, under epidemiology unit responsibility. Continuous data will be described with descriptive statistics, including mean ±SD and/or median (range) as appropriate and categorical data with frequencies (%). Categorical data will be analyzed by univariate analysis with χ2 or Fisher exact test as appropriate and continuous data by nonparametric Mann-Whitney test. Statistical analyses will involve use of R software. Relationships between clinical, biological, radiological variables, etiologies and outcome will be assessed by using a univariate and multivariate logistic regression analyses to identify determinants for poor outcome.

Study Calendar

• Provisional inclusion starting date: July 2014

• Provisional inclusion duration: 3 years and half

• Patient participation duration: 1 year

• Study provisional duration: 5 years

• Data archiving duration: 15 years

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 800
• Est. completion date: December 31, 2019
• Est. primary completion date: September 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• presenting altered mental status (i.e. confusion or inability to talk, decreased or altered level of consciousness or personality change AND lasting 24 hours or more AND no alternative cause identified);

AND at least one of minor inclusion criteria must be met before patient inclusion:

• presenting fever (38°C axillary) for less than 72 hours before or after presentation;

• seizure (febrile seizure excluded);

• focal neurologic finding.

Exclusion Criteria:

• None

Related Conditions & MeSH terms

• Encephalitis

Intervention

Diagnostic Test:
• CSF sampling
CSF sampling by lumbar puncture
• Blood sampling
Blood sampling by blood test
• Nasopharyngeal and rectal sampling
Nasopharyngeal and rectal sample by swabbing

Locations

Country	Name	City	State
Cambodia	Institut Pasteur of Cambodia	Phnom Penh
Cambodia	Kantha Bopha IV children Hospital	Phnom Penh
Lao People's Democratic Republic	Mahidol Oxford Tropical Medicine Research Unit	Vientiane
Myanmar	National Health Laboratory	Yangon
Myanmar	Yangon children hospital	Yangon
Vietnam	National Hospital of Pediatrics	Hanoi
Vietnam	National Institute of Hygiene Epidemiology	Hanoï

Sponsors (8)

Lead Sponsor	Collaborator
Institut Pasteur	Centre De Coopération International En Recherche Agronomique Pour Le Développement, Institut de Recherche pour le Developpement, Institut National de la Santé Et de la Recherche Médicale, France, Institut Pasteur, Cambodia, National Health Laboratory, Myanmar, National Institute of Hygiene and Epidemiology, Vietnam, University of Oxford

Countries where clinical trial is conducted

Cambodia,  Lao People's Democratic Republic,  Myanmar,  Vietnam, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Identify etiologies of encephalitis in South East Asia (Vietnam, Laos, Cambodia and Myanmar).	Proportion of patients with confirmed or probable etiologies and proportion with unidentified pathogen	August 2019
Secondary	Describe clinical and biological features of patients with encephalitis	Proportion of participants by demographic data (geographic origin, age), by clinical and biological features assessed by physician (general symptoms, neurological symptoms, length of symptoms, blood pressure, blood pulse, weight, height, white blood cells, platelets counts, hemoglobin, CSF cells, protein glucose levels).	August 2019
Secondary	describe clinical outcomes of encephalitis in general and by etiology	Proportion of patient who died or had neurological sequelae or recovered during hospitalization and at one year	December 2019
Secondary	Identify factors associated with death or severe neurological sequelea in patients with confirmed infectious encephalitis (survival analyses, sequelea score).	Estimation of risk ratio for death or severe neurological sequelae in patients with confirmed infectious encephalitis by demographic, clinical, and biological data	December 2019