Ventilator Associated Pneumonia. Postprocedural respiratory disorder, unspecified
Conditions
Interventions
Intervention 1: In the Intervention group, the upper respiratory care program was carried out, which included oral and subglottic secretion suction with 100-140 mmHg before each change position, hea
Prevention
In the Intervention group, the upper respiratory care program was carried out, which included oral and subglottic secretion suction with 100-140 mmHg before each change position, head elevation ever
In control group patients were taken under routine upper respiratory care, including oral and subglottic secretion suction every two hours for patients under mechanical ventilation independent of the
Sponsors
Vice chancellor for research, Isfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: inclusion criteria: Patients above 18,mechanical ventilation more than 24 hr,free of pneumonia or hospital infections before and in the first 48 hr of intubation, free of invasive antibiotics, free of limitations due to head position of medical bed, Exclusion Criteria: Death before the end of the study, extubation before the end of the study,Transfer to other wards or hospitals before the end of the study, undergoing surgery during the study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of Ventilator Associated Pneumonia. Timepoint: Before intervention, day 3, day 4, day 5,. Method of measurement: Clinical Pulmonary Infection Score, CPIS. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactnasim bahrami
Isfahan University of Medical Science
Outcome results
None listed