Comparison Between IMV and SIMV/PS for Ventilatory Support of Children: a Randomized Clinical Trial

Last updated: June 27, 2008
Sponsor: UPECLIN HC FM Botucatu Unesp
Overall Status: Completed

Phase

3

Condition

Lung Injury

Respiratory Failure

Treatment

N/A

Clinical Study ID

NCT00549809
upeclin/HC/FMB-Unesp-04
  • Ages < 4
  • All Genders

Study Summary

Objectives: to compare intermittent mandatory ventilation (IMV) with synchronous intermittent mandatory ventilation associated with pressure support (SIMV/PS) related to duration of mechanical ventilation/weaning and length of stay in PICU (LS). Design: randomized clinical trial. Setting: Pediatric intensive care unit at a university-affiliated hospital.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Children aged between 28 days and four years, who were consecutively admitted to thePICU and required MV for more than 48h were included.

Exclusion

Exclusion Criteria:

  • Children who had chronic respiratory failure, tracheostomy, those transferred from thehospital, or died were excluded as were patients with acute respiratory distresssyndrome (ARDS).

Study Design

Total Participants: 70
Study Start date:
October 01, 2005
Estimated Completion Date:
June 30, 2007

Study Description

Objectives: to compare intermittent mandatory ventilation (IMV) with synchronous intermittent mandatory ventilation associated with pressure support (SIMV/PS) related to duration of mechanical ventilation/weaning and length of stay in PICU (LS). Design: randomized clinical trial. Setting: Pediatric intensive care unit at a university-affiliated hospital. Patients: children between 28 days and 4 years old, admitted between 10/2002 and 06/2004, and receiving mechanical ventilation (MV) for more than 48 hours. Patients were randomly assigned into two groups: IMV (IMVG; n=35) and SIMV/PS (SIMVG; n=35). Children with acute respiratory distress syndrome and tracheostomy were excluded. Ventilation and oxygenation data were recorded at admission and beginning of weaning. Results: Groups were not statistically different for age, gender, MV indications, PRISM score, COMFORT scale, sedatives, and ventilation and oxygenation parameters. Median of MV duration was 5 days for both groups (p>0.05). Also, there were no statistical differences for duration of weaning [IMVG: 1 day (1 - 6) vs. SIMVG: 1 day (1 - 6); p>0.05] and LS [IMVG: 8 days (2 - 22) vs. SIMVG: 6 days (3 - 20); p>0.05]. Conclusion: There was no statistically significant difference between IMV and SIMV/PS in these children related to MV and weaning duration, and PICU length of stay.

Connect with a study center

  • Jose Roberto Fioretto

    Botucatu, Sao Paulo 18.618-000
    Brazil

    Site Not Available

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