Oropharyngeal Aspiration to Reduce Ventilator-Related Pneumonia

NACompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

July 1, 2015

Primary Completion Date

April 30, 2019

Study Completion Date

June 30, 2019

Conditions
Ventilator-associated Bacterial Pneumonia
Interventions
PROCEDURE

Oropharyngeal aspiration before changing the position of the patient

"Patients in the experimental group underwent oropharyngeal aspiration prior to each position change in addition to routine nursing care (Endotracheal aspiration in case of indication and oropharyngeal aspiration in the follow-up; routine and non-routine position changes every 2 hours during the day and 4 hours during the night; oral care).~Patients in this group underwent oropharyngeal aspiration at least 9 times in 24 hours with a pressure of 100-120 mmHg for 10 seconds prior to routine (2 hours a day, 4 hours a night) and non-routine position changes. After the oropharyngeal aspiration was completed, the patient's position was changed."

OTHER

Control group:

The patients in the control group received routine nursing care in the unit. (Endotracheal aspiration in case of indication and oropharyngeal aspiration in the follow-up; routine and non-routine position changes every 2 hours during the day and 4 hours during the night; oral care).

All Listed Sponsors
lead

Ayşe AKBIYIK

OTHER

NCT04107363 - Oropharyngeal Aspiration to Reduce Ventilator-Related Pneumonia | Biotech Hunter | Biotech Hunter