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Prevention Ventilator Associated Pneumonia

Not Applicable
Completed
Conditions
Ventilator-associated Pneumonia
Interventions
Other: Bundle implementation
Registration Number
NCT02060045
Lead Sponsor
Maria Jesus Perez
Brief Summary

The objective of the investigators work was to evaluate the impact of 4 sequentially implemented measures for preventing VAP in a major heart surgery ICU. The measures were a specific training program, aspiration of subglottic secretions (ASS), introduction of an inclinometer to improve the semirecumbent position, and reinforcement of oral care with chlorhexidine.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1534
Inclusion Criteria
  • all patients with heart surgery admitted in critical care unit during the study period
Exclusion Criteria
  • none

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
bundle implementationBundle implementationThe measures were a specific training program, aspiration of subglottic secretions (ASS), introduction of an inclinometer to improve the semirecumbent position, and reinforcement of oral care with chlorhexidine.
Primary Outcome Measures
NameTimeMethod
Change (reduction) in the incidence density of Ventilator associated pneumonia (VAP)Baseline and up to 35 months

Change (reduction) in the incidence density of VAP

Secondary Outcome Measures
NameTimeMethod
Change(length) in Intensive Care Unit (ICU) stayBaseline and up to 35 months
Change (number of days) in Mechanical Ventilator (MV) per ICU stayBaseline and up to 35 months
Change in mortality rateBaseline and up to 35 months
Change in cost of antimicrobial acquisition during ICU stayBaseline and up to 35 months
Change in compliance with the measuresBaseline and up to 35 months

Trial Locations

Locations (1)

Hopsital General Universitario Gregorio Marañon

🇪🇸

Madrid, Spain

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