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Impact of Early Lactate Dosage Compared to CK for Diagnosis of a Suspected Seizure

U

University Hospital, Clermont-Ferrand

Status

Unknown

Conditions

Epileptic Seizure
Epileptic Generalized Tonic-clonic Seizure
Lactate
Creatine Kinase

Treatments

Diagnostic Test: CK and Lactate dosages

Study type

Observational

Funder types

Other

Identifiers

NCT03163719
CHU-329

Details and patient eligibility

About

Defining the origin of a seizure remains a difficult diagnosis. The presence of witness is not systematic, the clinical examination can be little contributory, and the delay recommended by the FSN is often surpassed for the realization of Creatine kinase (4h). In the event of a suspected seizure, an initial blood test with Creatine kinase and Lactates is often done on admission of the patient in other words before the 4hours delay.

It seems interesting to harmonize the practices, to limit the patient wait in the emergencies for a deferred dosage of CK at 4 hours from the seizure and to identify an early biological marker.

Objectives:

To evaluate the value of blood CK and Lactate dosage in emergency procedures in the diagnosis of generalized seizures.

Full description

We propose to carry out a prospective, observational, monocentric study at the CHU of Clermont-Ferrand. This is a descriptive analysis of the kinetics of the Creatine kinase and Lactates rates collected at the admission of a patient consulting for strong suspicion of convulsive seizure, and at 4 hours from the generalized seizure.

A patient consulting the emergency department for suspected seizure will have an usual blood test at the admission in this context with notably ionogram, fasting glucose, venous gasometry. As the CHU purchased a venous and arterial gasometry reader for the emergency department, blood ionogram, Hb, lactates, HCO3-, pH are collected without delay.

The Creatine kinase dosage will be collected in the usual way as a "tube bottom".

As recommended by the French Society of Neurology, a new sample will be collected at 4 hours of seizure for a dosage of Creatine kinase. The determination of the lactates will be based on a "tube bottom".

It is the emergency practitioner who will decide whether or not to include the patient in the descriptive study, assisted by a standardized survey, enumerating the high probability of generalized seizure orientation characteristics (patient history, treatments including antiepileptics, anamnesis, witnesses presence, evocative clinic) The study only recruited cases of strong suspicion of generalized seizure, beginning less than 4 hours to compare the kinetics of Creatine kinase and Lactates at admission and 4 hours of the generalized seizure.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any generalized convulsive seizure defined by a transient loss of consciousness with the occurrence of tonic-clonic movements.
  • Beginning less than 4 hours.
  • In a highly evocative context of the crisis by the presence of: witnesses and/or Urine loss, Tongue bite and/or personal medical history of epilepsy and/or Favorable context: sleeping debt, drug withdrawal, lights stimulations, video games and/or Impression of "already lived", already experienced before the discomfort and/or Break contact, and/or Unusual posture with hypertonia and/or Amnesia of the episode and/or Post-episode Confusion
  • Inaugural or recurrent

Exclusion criteria

  • Patient Refusal
  • <18 years
  • Pregnancy
  • Sepsis, fever> 38 °
  • Shock State
  • Myocardial infarction
  • Unbalanced Diabetes
  • Hepatocellular insufficiency
  • Drug and Toxic Use
  • Taking Metformin
  • Significant muscle injuries
  • Myopathy

Trial design

100 participants in 1 patient group

Patients with generalized convulsive seizure
Description:
All adult patients (aged at least 18 years old) presenting to the CHU Clermont-Ferrand adult emergencies with a strong suspicion of generalized tonic-clonic seizure beginning less than 4 hours will be included. Each eligible patient will be proposed by a doctor, to participate to the study. The emergency doctor will verify the patient's inclusion and non-inclusion criteria.
Treatment:
Diagnostic Test: CK and Lactate dosages

Trial contacts and locations

1

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Central trial contact

Farès MOUSTAFA; Patrick LACARIN

Data sourced from clinicaltrials.gov

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