Assessment of Adults Epidemiological Characteristics of Status Epilepticus in the French West Indies and in French Guiana
NCT ID: NCT05246566
Last Updated: 2024-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
241 participants
OBSERVATIONAL
2022-05-15
2025-01-30
Brief Summary
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The morbidity of SE is significant, associating neurological disorders with impaired consciousness, respiratory, hemodynamic and cardiac rhythm disorders, as well as metabolic disorders such as acidosis. SE-related mortality in the acute phase ranges from 3-40% across studies and regions, while long-term mortality ranges from 17-80% depending on age, cause of SE, comorbidities and the occurrence of complications.
The prognosis of this pathology has however improved in recent years in developed countries or countries with a high level of health system. On the other hand, the morbidity and mortality of SE in the French overseas departments is not known, even if these territories are supposed to be at an equivalent level in terms of health system to that of mainland France.
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Detailed Description
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The epidemiological, clinical, etiological and prognostic characteristics of epilepsy and SE vary depending on the continent and region, mainly linked to the exposing or favoring factors as well as the socio-economic level of the population, the healthcare offer of the patient health system and accessibility to care for the population.
In France, the management of SE has been codified by Formalized Expert Recommendations (RFE) from learned societies in Emergencies and Resuscitation. The last updated RFE was published in 2018. However, very few studies have been carried out on SE in prehospital or emergencies department. There are no national epidemiological data on SE. To our knowledge, there is no data on the prevalence of SE in the French West Indies (FWI) and French Guiana and even less on the main aetiologies and prognosis of this acute neurological complication.
The interest of this prospective study is to evaluate, through the emergency system, the incidence, the modes of clinical presentation, the etiologies, the therapeutic modalities and finally the prognosis of SE in French overseas departments. This study is of scientific interest for the new knowledge it will bring, because there is no data concerning this relatively common pathology in these regions.
The results of the study would contribute to the improvement of scientific knowledge, to the highlighting of potential particularities and specificities of this pathology in the FWI and French Guiana, and would contribute to improving medical practice and the management of these patients.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Subjects covered for suspected or SE diagnosis
Patients covered for suspected or SE diagnosis defined by one of the following:
* a prolonged generalized tonic-clonic crisis lasting more than 5 minutes and accompanied by impaired consciousness or at least 2 generalized tonic-clonic crisis without return to normal consciousness between crisis.
* a focal convulsive crisis (motor or not) with disturbances of consciousness which lasts beyond 10 minutes or crisis which are repeated (≥ 2) at short intervals without recovery of interictal consciousness.
* a focal convulsive crisis (motor or not) without alteration of consciousness that lasts beyond 10 to 15 minutes.
* an absence-type crisis that lasts longer than 10 to 15 minutes.
* a myoclonic, clonic and tonic crisis that lasts longer than 10 to 15 minutes.
* a coma with an epileptic cause diagnosed on an EEG.
Routine care
The investigator takes care of the patient according to the protocol in force in his department and decides on the final orientation of the patient (transfer to intensive care unit/ICU, hospitalization or home discharge).
No recommendations or instructions are given to the investigators. Each investigator is free to decide on his care and the terms of transfer, hospitalization and discharge.
Interventions
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Routine care
The investigator takes care of the patient according to the protocol in force in his department and decides on the final orientation of the patient (transfer to intensive care unit/ICU, hospitalization or home discharge).
No recommendations or instructions are given to the investigators. Each investigator is free to decide on his care and the terms of transfer, hospitalization and discharge.
Eligibility Criteria
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Inclusion Criteria
* Covered for suspected or SE diagnosis defined by one of the following:
* a prolonged generalized tonic-clonic crisis lasting more than 5 minutes and accompanied by impaired consciousness or at least 2 generalized tonic-clonic crisis without return to normal consciousness between crisis.
* a focal convulsive crisis (motor or not) with disturbances of consciousness which lasts beyond 10 minutes or crisis which are repeated (≥ 2) at short intervals without recovery of interictal consciousness.
* a focal convulsive crisis (motor or not) without alteration of consciousness that lasts beyond 10 to 15 minutes.
* an absence-type crisis that lasts longer than 10 to 15 minutes.
* a myoclonic, clonic and tonic crisis that lasts longer than 10 to 15 minutes.
* a coma with an epileptic cause diagnosed on an EEG.
* Patient if he is able to, or representative of the patient in case of incapacity, having given his agreement for the use of his medical data for this research.
Exclusion Criteria
* Absence of consent from the patient, or representative to the use of the data for the research.
* Patient whose main residence is not in the department where the study is taking place (vacationer for example).
18 Years
ALL
No
Sponsors
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University Hospital Center of Martinique
OTHER
Responsible Party
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Principal Investigators
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Florian Negrello, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital Center of Martinique
Locations
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Hospital of Cayenne
Cayenne, French Guiana, France
Hospital of Basse-Terre
Basse-Terre, Guadeloupe, France
University Hospital Center of Guadeloupe
Pointe à Pitre, Guadeloupe, France
University Hospital Center of Martinique
Fort-de-France, Martinique, France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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21_RIPH3-05
Identifier Type: -
Identifier Source: org_study_id
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