Comparison Between the Old Diagnostic Tools for Paediatric Undernutrition and the HAS Recommendations
NCT ID: NCT04482218
Last Updated: 2020-12-29
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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COMPLETED
100 participants
OBSERVATIONAL
2020-07-17
2020-09-30
Brief Summary
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Until now, there has been no national consensus on the criteria to be used to diagnose paediatric undernutrition. Until now, assessment focused on a range of non-consensus arguments that allowed the health care team to make its diagnosis. So, in the absence of well-defined criteria, diagnosis was based in part on experience and assesment team.
Since November 2019, the French High Authority of Health (Haute Authorité de Santé - HAS) has suggested recommendations to standardize pediatric undernutrition diagnosis.
The investigators offer to evaluate undernutrition prevalence differences diagnosed according to new HAS criteria compared to the previous diagnostic methodology.
The investigator's secondary aim is to identify profiles of children who do match between the two diagnostics methods.
Detailed Description
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Following classic patient admission in involved departments, the investigating team moves to the department to collect data.
The measurements and informations collected are no different from those taken in the context of normal care.
All anthropometric measurements correspond to recommendations of good practice. Anthropometric measurements will be carried out by the healthcare team.
With collected data the investigators will evaluate undernutrition for each child, according to the 2 diagnostics methods.
For any diagnosis of undernutrition, the department dietician will be alerted so that the patient can be taken care of so it is done normally.
Data collected are as follows:
Simple demographic characteristics: Age, sex, departmentsand principal diagnosis Anthropometry: weight, height, brachial perimeter, head circumference Birth weight and date of term of pregnancy. Clinical history: all pathologies or clinical events that may be related to a weight variation.
Assessment of ingesta. A non-opposition will be asked
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patient admitted to short and long-stay pediatric services at Montpellier University Hospital, other than maternity, neonatal, palliative care or resuscitation and rehabilitation department.
Exclusion Criteria
* Legal guardian unable to express consent
0 Years
18 Years
ALL
No
Sponsors
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University Hospital, Montpellier
OTHER
Responsible Party
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Principal Investigators
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Antoine AVIGNON, PR
Role: STUDY_DIRECTOR
University Hospital, Montpellier
Locations
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Uhmontpellier
Montpellier, , France
Countries
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Other Identifiers
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RECHMPL20_0391
Identifier Type: -
Identifier Source: org_study_id