PEDIASED: Reduce Pediatric Sedation to Reduce Mechanical Ventilation Complication in ICU

Sponsor
Nantes University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02040168
Collaborator
(none)
106
1
61
1.7

Study Details

Study Description

Brief Summary

Mechanical ventilation is a common procedure used in pediatric intensive care units (ICU). Its use requires almost always the establishment of a sedation. Sedation is a generic term for all procedures, pharmacological or not, ensuring physical and psychological comfort and the safety of patient admitted in intensive care units.

An inadequate sedation, insufficient or excessive, has common side effects, as increase of the duration of mechanical ventilation and of hospital-acquired infections (in particular, ventilator associated pneumonia), of hemodynamic disorders, of extubation failure or accidental extubation, of withdrawal syndrome, and of post-traumatic stress disorder (PTSD). All these complications increase mechanical ventilation time and ICU length of stay. Several studies in adult's population have shown that the implementation of a sedation algorithm allowed to decrease the incidence of these complications.

We hypothetized that the duration of mechanical ventilation would be reduced by a nurse-implemented sedative management protocol.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    1. During the first period (15 months), no protocol is used. This period consists to assess current analgesia-sedation procedure used in the pediatric intensive care unit (PICU), associated with the collection of medical and socio-demographical data about mechanical ventilation duration, sedation complications, PTSD development. The severity of pathology can be evaluated using PIM2 and POPC scores. The sedation deepness will be determined using COMFORT-B scale. Eight weeks after hospitalization, families will be phoned to assess children memories, anxious troubles, and PTSD symptoms for the patients of more than 18 months old.

    2. During the transition period (6 months), nurses and physicians develop the protocol and undergo training in its use.

    During the third period, a nurse-implemented sedation is used. The collected data are the same that the collected data during the first period

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    106 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of the Interest of a Nurse-implemented Sedation Protocol for the Reduction of the Duration of Mechanical Ventilation Complication Associated With Extended Sedation in Pediatric Intensive Care Unit.
    Actual Study Start Date :
    Oct 1, 2010
    Actual Primary Completion Date :
    Dec 31, 2014
    Actual Study Completion Date :
    Oct 31, 2015

    Arms and Interventions

    Arm Intervention/Treatment
    28 days - 18 yo

    Children requiring mechanical ventilation for at least 24h from 28 days to 18 yo

    18 months - 18 yo

    Post traumatic stress disorder evaluation in children requiring mechanical ventilation for at least 24h from 18 month to 18 Years old

    Outcome Measures

    Primary Outcome Measures

    1. Duration of the ventilation period [Hospitalization + 8 weeks]

      30% decrease of the ventilation period

    Secondary Outcome Measures

    1. evaluate the impact of sedation protocol on short-term consequences of prolonged sedation [Hospitalization + 8 weeks]

      Hospitalization length reduction PTSD incidence reduction of 50% Weaning syndrom incidence decrease Sedation drugs total dose decrease Decrease of mechanical ventilation related infections Decrease of accidental or self extubation frequency Required amine total dose decrease Correlation between sedation level and PTSD frequency Analysis of PTSD risk factors

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    28 Days to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Children aged 28 days to 18 years

    • Admitted in pediatric intensive care unit

    • Necessity of mechanical ventilation > 24 hours.

    Exclusion Criteria:
    • Sedation started in another intensive care unit > 24 hours

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Nantes University Hospital Nantes Loire-Atlantique France 44093

    Sponsors and Collaborators

    • Nantes University Hospital

    Investigators

    • Principal Investigator: Liet Jean Michel, Nantes UH

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nantes University Hospital
    ClinicalTrials.gov Identifier:
    NCT02040168
    Other Study ID Numbers:
    • PROG/10/53
    First Posted:
    Jan 20, 2014
    Last Update Posted:
    Sep 16, 2021
    Last Verified:
    Sep 1, 2021
    Keywords provided by Nantes University Hospital

    Study Results

    No Results Posted as of Sep 16, 2021