SEDATIDE: Implementation and Evaluation of a Pediatric Nurse-driven Sedation Protocol in a PICU

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Completed
CT.gov ID
NCT02829710
Collaborator
(none)
200
1
26.9
7.4

Study Details

Study Description

Brief Summary

Management of analgesia and sedation is an integral component of the medical care of a critically-ill child. Its role is to assure comfort and safety to a patient undergoing painful cares and technical procedures; it can also be, in particular situations like acute respiratory distress syndrome or acute brain injury, a full processing treatment.

Sedation involves, most of the time, the association of an opioid and a sedative. The use of these drugs is difficult in children, because of a specific metabolism, inducing tolerance and withdrawal in case of prolonged administration.

The COMFORT-BEHAVIOR (COMFORT-B) scale is a validated, simple, reliable and reproducible score evaluating sedation and analgesia. Sedation scoring systems must be used regularly to avoid inadequate sedation.

Excessive sedation is associated with poor outcomes like prolonged mechanical ventilation, longer hospitalisation and more frequent withdrawal symptoms. Adult and paediatric data suggest that goal-directed sedation algorithms allow a more appropriate adaptation of the treatment to the patient's need and permit a reduction in the duration of mechanical ventilation.

The objective was to evaluate the impact of a nurse-driven sedation protocol in a paediatric intensive care unit on duration of mechanical ventilation, total doses and duration of medications, Paediatric Intensive Care Unit (PICU) length of stay, incidence of ventilator-associated-pneumonia and occurrence of withdrawal.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Nurse-driven sedation protocol

Study Design

Study Type:
Observational
Actual Enrollment :
200 participants
Time Perspective:
Retrospective
Official Title:
Implementation and Evaluation of a Paediatric Nurse-driven Sedation Protocol in a Paediatric Intensive Care Unit
Study Start Date :
Jan 1, 2013
Actual Primary Completion Date :
Mar 1, 2015
Actual Study Completion Date :
Apr 1, 2015

Arms and Interventions

Arm Intervention/Treatment
group 1 : pre implementation group

All children aged less than 18 years, requiring mechanical ventilation for at least 24 hours and admitted in PICU between January 2013 and December 2013. Prior to implementation of the protocol, analgesia and sedation were managed by the attending physician's order.

group 2 : post implementation group

All children aged less than 18 years, requiring mechanical ventilation for at least 24 hours and admitted in PICU between May 2014 and March 2015. Nurses managed analgesia and sedation following an algorithm, including COMFORT-B scale.

Behavioral: Nurse-driven sedation protocol
The nurse-driven sedation protocol included the COMFORT-B scale. Initial doses were chosen by the physicians then all changes were made by the nurses with the aim of attaining an optimal range of analgesia and sedation, which was defined as values from 11 to 17 on the COMFORT-B score.

Outcome Measures

Primary Outcome Measures

  1. Duration of mechanical ventilation (days) [Over the PICU stay of each child (Day 5)]

Secondary Outcome Measures

  1. Total doses of sedatives (unit/kg) [Over the PICU stay of each child (Day 5)]

  2. Occurrence of withdrawal symptoms [Over the PICU stay of each child (Day 5)]

  3. Length of PICU stay (days) [Over the PICU stay of each child (Day 5)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Mechanically-ventilated patients aged from 0 to 18 years receiving sedation for more than 24 hours
Exclusion Criteria:
  • Patients with tracheostomy

Contacts and Locations

Locations

Site City State Country Postal Code
1 service de réanimation pédiatrique, Hôpital Femme Mère Enfant (HFME), Hospices Civils de Lyon, 59 Boulevard Pinel Bron France 69677

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

  • Principal Investigator: Fabienne Bordet, MD, service de réanimation pédiatrique, Hôpital Femme Mère Enfant (HFME), Hospices Civils de Lyon

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT02829710
Other Study ID Numbers:
  • 69HCL15_0312
First Posted:
Jul 12, 2016
Last Update Posted:
Jul 12, 2016
Last Verified:
Jun 1, 2016

Study Results

No Results Posted as of Jul 12, 2016