Skip to main content
Clinical Trials/NCT03290105
NCT03290105
Completed
Not Applicable

Efficacy of Chlorhexidine Mouth Wash in ICU Ventilated Patients: Microbiological Effects and Antiseptic Residual Concentrations

Hôpital Louis Mourier0 sites30 target enrollmentStarted: January 27, 2014Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Hôpital Louis Mourier
Enrollment
30
Primary Endpoint
changes over time of bacterial growth

Overview

Brief Summary

Ventilator-associated pneumonia (VAP) is the most frequent life-threatening nosocomial infection in the ICU. Oropharyngeal colonization with bacterial pathogens is the first step toward lung infection. Oral hygiene with Chlorhexidine mouth wash (CMW) is among the most widespread preventive measure to prevent VAP. Precise microbial documentation of CMW efficacy on oropharyngeal colonization is lacking. Investigators wish to determine CMW antimicrobial efficacy in ICU ventilated patients and to measure chlorhexidine residual concentration in patients' saliva at the same time-points after CMW.

Detailed Description

Ventilator associated pneumonia (VAP) is the most frequent life-threatening nosocomial infection in the ICU. Oropharyngeal colonization with bacterial pathogens is the first step toward lung infection. Oral hygiene with Chlorhexidine mouth wash (CMW) is among the most widespread preventive measure to prevent VAP. Although many guidelines and expert opinions recommend oral hygiene with chlorhexidine, optimal conditions of CMW use remain unknown. In addition, precise microbial documentation of CMW efficacy on oropharyngeal colonization is lacking. Investigators wish to determine CMW antimicrobial efficacy in ICU ventilated patients and to measure chlorhexidine residual concentration in the saliva at the same time-points after CMW.

In the participanting unit, CMW is performed every 6 hours with a 0.12% chlorhexidine solution.

Hence, microbial oropharyngeal sampling will be performed 6h after the last CMW (and just before the next one), to assess oropharyngeal colonization and then 15 minutes, 1 hour, 2 hours, 4 hours, and 6 hours after a new CMW to assess CMW efficacy in terms of bacterial growth.

In a subset of patients, 0.5 mL of saliva will be collected with a syringe at the same time points, with an additional T30 time (at 30 minutes) to measure chlorhexidine concentration.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • critically-ill patients admitted to the ICU and receiving invasive mechanical ventilation for more than 48 hours
  • Non-inclusion criteria:
  • cervical or mouth surgery in the last 15 days;
  • history of oropharyngeal neoplasm or of cervical or oropharyngeal radiotherapy,
  • tracheotomy,
  • age under 18

Exclusion Criteria

  • Patients whose samples retrieved less than 10 to the 3 colony forming unit (CFU)/mL bacteria and those who had two or more missing microbiological samples were secondarily excluded

Outcomes

Primary Outcomes

changes over time of bacterial growth

Time Frame: 6 hours (360 minutes)

oropharyngeal colonization (i.e., amount of bacterial growth in each oropharyngeal sample) before and after a mouth wash with chlorhexidine will be measured at different time points (before (H0) and 15 minutes, 60 minutes, 120 minutes, 240 minutes, and 360 minutes after the mouth wash with chlorhexidine)

Secondary Outcomes

  • changes over time of bacterial growth of each bacterial specie(6 hours (360 minutes))
  • salivary concentration of chlorhexidine(6 hours (360 minutes))
  • susceptibility of isolates to chlorhexidine(1 hour)

Investigators

Sponsor
Hôpital Louis Mourier
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Prof Jean-Damien RICARD

Professor of Intensive Care

Hôpital Louis Mourier

Similar Trials