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出境医 / 临床实验 / Accuracy and rEliabilitY of the vEstibuLo-ocular ExAmination Performed by inteRNs IN the emerGency Department (EYE LEARNING)

Accuracy and rEliabilitY of the vEstibuLo-ocular ExAmination Performed by inteRNs IN the emerGency Department (EYE LEARNING)

Study Description
Brief Summary:

Dizziness, loss of balance, and unsteadiness of gait are common symptoms reported by Emergency Department (ED) patients. The incidence of acute vestibular syndrome (AVS) is increasing and reaches 2-4% of ED visits. In the ED of the Paris Saint Joseph Hospital Group, its incidence was 5% during the year 2019 and 2% during the year 2020 (COVID-19 pandemic period).

Emergency medicine is based on a dichotomous principle for any acute pathology in the initial phase. For AVS, the diagnostic dilemma for emergency physicians is usually to differentiate a benign vestibular cause from a potentially serious cerebral cause such as ischemic stroke of the vertebro-basilar territory. The majority of AVS are related to acute vestibulopathies, yet it is necessary to recognize and distinguish a benign paroxysmal positional vertigo (BPPV) from a vestibular neuritis, a vestibular migraine, or a labyrinthine hydrops, to exclude with certainty a cerebral involvement. However, posterior fossa strokes mimic 5% of BPPV and 25% of vestibular neuritis. Among these strokes, about 20% are therefore revealed by a VAS without associated localizing neurological sign. In the absence of a clear neurological sign, the emergency physician must therefore decide whether to treat the patient as an outpatient when he or she suspects a AVS of "peripheral" origin (otolaryngology), or as an inpatient when he or she suspects a "central" origin, in particular a stroke.


Condition or disease
Acute Vestibular Syndrome Emergencies

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Study Design
Layout table for study information
Study Type : Observational
Estimated Enrollment : 200 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Accuracy and rEliabilitY of the vEstibuLo-ocular ExAmination Performed by inteRNs IN the emerGency Department
Actual Study Start Date : May 7, 2021
Estimated Primary Completion Date : June 3, 2022
Estimated Study Completion Date : December 31, 2022
Arms and Interventions
Outcome Measures
Primary Outcome Measures :
  1. To determine the diagnostic accuracy of the STANDING algorithm performed by ED medical student to distinguish central from peripheral causes of isolated AVS in the ED. [ Time Frame: Day 1 ]
    Sensitivity and specificity of the STANDING algorithm performed by ED medical student.


Secondary Outcome Measures :
  1. To determine the inter-rater reliability of each items of the STANDING algorithm, between an ED medical student and a senior emergency physician for each patient. [ Time Frame: Day 1 ]
    Inter-observer agreement measured by the overall Fleiss Kappa coefficient (K) and by the K each item of the STANDING algorithm performed by the ED medical student and by the senior emergency physician

  2. To evaluate the changing opinions of ED medical students on vestibulo-ocular examination between the beginning and the end of their internship in the ED [ Time Frame: Day 1 ]
    Changing confidences of the ED medical students regarding each item of the STANDING algorithm measured on a survey with a 5-points Likert scale, at the beginning and at the end of their ED internship


Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
This is a prospective diagnostic monocentric cohort study. These patients consulted the SU for symptoms integrated in an isolated AVS, i.e.: vertigo, balance disorder, instability on walking, present for at least one hour and less than one week, as defined by the Barany Society. The study will be reported using the STARD Statement criteria.
Criteria

Inclusion Criteria:

  • Patient whose age is ≥ 18 years
  • French-speaking patient.
  • Patient presenting on admission to the emergency department with an isolated AVS defined by a course of more than one hour and less than one week and the presence of at least one symptom among:

    1. vertigo: an illusion of displacement of the subject in relation to surrounding objects or surrounding objects in relation to the subject, a sensation of rotation, displacement of the body in the vertical plane, instability described as pitching or as a "spinning head", sometimes associated with vegetative signs (nausea, vomiting, pallor, sweating, slowing of the heart rate)
    2. and/or spontaneous or positional nystagmus,
    3. and/or a gait disorder: such as imbalance with lurching, or a shaky gait, or simple instability.
  • A patient may be included several times during the study period provided that they are distinct acute episodes of isolated AVS.

Exclusion Criteria:

  • Patient under guardianship or curatorship
  • Patient deprived of liberty
  • Patient under court protection
  • Patient objecting to the use of his/her data for this research
  • Patient with focal neurological signs concomitant with AVS: a language or writing disorder, a speech disorder such as dysarthria, a disorder in the execution of voluntary movements, a sensory, motor or visual deficit, involuntary abnormal movements
  • Patient with a history of oculomotor paralysis.
Contacts and Locations

Contacts
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Contact: Camille GERLIER, MD 01 44 12 33 33 ext + 33 cgerlier@ghpsj.fr

Locations
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France
Groupe Hospitalier Paris Saint Joseph Recruiting
Paris, Ile-de-France, France, 75014
Contact: BEAUSSIER Helene, PhD, PharmD       hbeaussier@ghpsj.fr   
Contact: CRC    +33 1 44 12 70 33    crc@ghpsj.fr   
Sponsors and Collaborators
Groupe Hospitalier Paris Saint Joseph
Investigators
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Principal Investigator: Camille GERLIER, MD Groupe Hospitalier Paris Saint Joseph
Tracking Information
First Submitted Date April 30, 2021
First Posted Date June 9, 2021
Last Update Posted Date June 9, 2021
Actual Study Start Date May 7, 2021
Estimated Primary Completion Date June 3, 2022   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: June 2, 2021)
To determine the diagnostic accuracy of the STANDING algorithm performed by ED medical student to distinguish central from peripheral causes of isolated AVS in the ED. [ Time Frame: Day 1 ]
Sensitivity and specificity of the STANDING algorithm performed by ED medical student.
Original Primary Outcome Measures Same as current
Change History No Changes Posted
Current Secondary Outcome Measures
 (submitted: June 2, 2021)
  • To determine the inter-rater reliability of each items of the STANDING algorithm, between an ED medical student and a senior emergency physician for each patient. [ Time Frame: Day 1 ]
    Inter-observer agreement measured by the overall Fleiss Kappa coefficient (K) and by the K each item of the STANDING algorithm performed by the ED medical student and by the senior emergency physician
  • To evaluate the changing opinions of ED medical students on vestibulo-ocular examination between the beginning and the end of their internship in the ED [ Time Frame: Day 1 ]
    Changing confidences of the ED medical students regarding each item of the STANDING algorithm measured on a survey with a 5-points Likert scale, at the beginning and at the end of their ED internship
Original Secondary Outcome Measures Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Accuracy and rEliabilitY of the vEstibuLo-ocular ExAmination Performed by inteRNs IN the emerGency Department
Official Title Accuracy and rEliabilitY of the vEstibuLo-ocular ExAmination Performed by inteRNs IN the emerGency Department
Brief Summary

Dizziness, loss of balance, and unsteadiness of gait are common symptoms reported by Emergency Department (ED) patients. The incidence of acute vestibular syndrome (AVS) is increasing and reaches 2-4% of ED visits. In the ED of the Paris Saint Joseph Hospital Group, its incidence was 5% during the year 2019 and 2% during the year 2020 (COVID-19 pandemic period).

Emergency medicine is based on a dichotomous principle for any acute pathology in the initial phase. For AVS, the diagnostic dilemma for emergency physicians is usually to differentiate a benign vestibular cause from a potentially serious cerebral cause such as ischemic stroke of the vertebro-basilar territory. The majority of AVS are related to acute vestibulopathies, yet it is necessary to recognize and distinguish a benign paroxysmal positional vertigo (BPPV) from a vestibular neuritis, a vestibular migraine, or a labyrinthine hydrops, to exclude with certainty a cerebral involvement. However, posterior fossa strokes mimic 5% of BPPV and 25% of vestibular neuritis. Among these strokes, about 20% are therefore revealed by a VAS without associated localizing neurological sign. In the absence of a clear neurological sign, the emergency physician must therefore decide whether to treat the patient as an outpatient when he or she suspects a AVS of "peripheral" origin (otolaryngology), or as an inpatient when he or she suspects a "central" origin, in particular a stroke.

Detailed Description

Unfortunately, the diagnostic evaluation of an isolated AVS is often frustrating because patients with vertigo tend to be uncertain and imprecise when describing their symptoms. Examination of the vestibulo-ocular pathway, by assessing eye movements in different head positions, is an essential step in the clinical examination to reliably and quickly predict the origin of a AVS. The 3-step clinical rule "HINTS" (Head Impulse, Nystagmus, Test of Skew) was developed in 2009 by "neuro-ophthalmologists" in the USA. It evaluates the vestibulo-ocular reflex by the Head Impulse Test (pathological with the presence of ocular saccades for a peripheral AVS), the characteristics of the nystagmus (multidirectional and/or vertical for a central AVS), and looks for ocular misalignment (Test of Skew with cover-test, pathognomonic of a central involvement). In patients at high cardiovascular risk, HINTS is 100% sensitive and 96% specific in predicting posterior fossa stroke within 2 minutes at the bedside, compared with the Gold-Standard. The "STANDING" (SponTAneous, Nystagmus, Direction, head Impulse test, STANDING) clinical rule is a structured bedside diagnostic algorithm in four clinical steps. It is based on the evaluation of two eye movements (Head Impulse Test and nystagmus), an evaluation of gait (search for ataxia) and the search for positional nystagmus (Dix Hallpike test for the posterior canal and Panigni test or "supine and roll test" for the lateral canal). In the ED, with patients at heterogeneous cardiovascular risk, the STANDING is more interesting than the HINTS. Indeed, it allows the detection of BPPV in pauci-symptomatic patients at the time of their clinical evaluation (i.e., those without spontaneous nystagmus). It had also shown excellent performance (sensitivity:95%, specificity:87-96%) in diagnosing any central cause of VAS in the hands of emergency physicians. However, the 2017 validation study of STANDING had an audit bias. The gold standard test, brain imaging, had only been performed when deemed appropriate (ie, in 34% of peripheral diagnoses, and for only 5% of these by brain MRI).

In the EYE-ECG study conducted at the GhPSJ SU from October 2019 to January 2021, the invesitgators determined the diagnostic performance of these two clinical rules performed by emergency physicians to 300 patients with isolated VAS, comparing it to the Gold-Standard. The article resulting from this study is submitted to the journal Annals of Emergency Medicine. Its originality was to evaluate the performance of the tests in the hands of emergency physicians and on a population not selected for its risk of stroke. The investigators showed that the HINTS and STANDING tests had excellent sensitivities (97% and 94% respectively) and negative predictive values (99% and 98% respectively) for predicting any central cause of VAS on brain MRI. They thus allowed emergency physicians to exclude a central cause in a rapid manner (on average 5±3 minutes) with very acceptable false-negative rates (3% and 6%, respectively), and with a potential impact on the reduction of unnecessary brain imaging (-33% and -32%, respectively). For predicting MRI normality, STANDING was more specific than HINTS (75% vs. 67%). This is explained by the addition of a clinical item dedicated to positional nystagmus in the STANDING, and by the high prevalence of BPPV among VAS of ENT origin in SU patients (40%). Indeed, among the false-positives of the HINTS test (erroneously predicted as a central cause for benign vestibular disease), one third of the diagnoses were BPPVs.

The major limitation of the EYE-ECG study was that it did not assess interindividual variability of the HINTS and STANDING tests between different emergency physicians. The STANDING validation study was the only study that assessed global and individual agreement of the algorithm item scores in a binary "central or peripheral" mode between two senior emergency physicians. The inter-observer agreement of the STANDING was good globally (K=0.83) and also at each step of the algorithm (distinction between spontaneous and positional nystagmus: K=0.83, interpretation of a multidirectional or vertical nystagmus: K=0.95, normal Head Impulse Test: K=0.74, recognition of a walking ataxia: K=0.81)18.

Each semester, an average of 7 medical students in general medicine and one in emergency medicine complete an internship at the GhPSJ. In routine practice, the medical students interview and examine their patients alone. They document their clinical examination in the patient's medical record and then present the patient's clinical record to a senior emergency physician. In a second step, the patient is clinically reassessed by the senior emergency physician who becomes responsible for the patient's diagnostic and therapeutic strategy. The accuracy of the vestibulo-ocular examination performed by medical students has never been described in the literature.

The hypothesis of the investigators is that after standardized theoretical training and with the clinical experience gained during their semester in the ED, medical students should be able to examine and interpret the vestibulo-ocular examination of patients with isolated AVS as accurately as seniors.

Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population This is a prospective diagnostic monocentric cohort study. These patients consulted the SU for symptoms integrated in an isolated AVS, i.e.: vertigo, balance disorder, instability on walking, present for at least one hour and less than one week, as defined by the Barany Society. The study will be reported using the STARD Statement criteria.
Condition
  • Acute Vestibular Syndrome
  • Emergencies
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Recruiting
Estimated Enrollment
 (submitted: June 2, 2021)
200
Original Estimated Enrollment Same as current
Estimated Study Completion Date December 31, 2022
Estimated Primary Completion Date June 3, 2022   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Patient whose age is ≥ 18 years
  • French-speaking patient.
  • Patient presenting on admission to the emergency department with an isolated AVS defined by a course of more than one hour and less than one week and the presence of at least one symptom among:

    1. vertigo: an illusion of displacement of the subject in relation to surrounding objects or surrounding objects in relation to the subject, a sensation of rotation, displacement of the body in the vertical plane, instability described as pitching or as a "spinning head", sometimes associated with vegetative signs (nausea, vomiting, pallor, sweating, slowing of the heart rate)
    2. and/or spontaneous or positional nystagmus,
    3. and/or a gait disorder: such as imbalance with lurching, or a shaky gait, or simple instability.
  • A patient may be included several times during the study period provided that they are distinct acute episodes of isolated AVS.

Exclusion Criteria:

  • Patient under guardianship or curatorship
  • Patient deprived of liberty
  • Patient under court protection
  • Patient objecting to the use of his/her data for this research
  • Patient with focal neurological signs concomitant with AVS: a language or writing disorder, a speech disorder such as dysarthria, a disorder in the execution of voluntary movements, a sensory, motor or visual deficit, involuntary abnormal movements
  • Patient with a history of oculomotor paralysis.
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts
Contact: Camille GERLIER, MD 01 44 12 33 33 ext + 33 cgerlier@ghpsj.fr
Listed Location Countries France
Removed Location Countries  
 
Administrative Information
NCT Number NCT04919187
Other Study ID Numbers EYE LEARNING
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement Not Provided
Responsible Party Groupe Hospitalier Paris Saint Joseph
Study Sponsor Groupe Hospitalier Paris Saint Joseph
Collaborators Not Provided
Investigators
Principal Investigator: Camille GERLIER, MD Groupe Hospitalier Paris Saint Joseph
PRS Account Groupe Hospitalier Paris Saint Joseph
Verification Date April 2021