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Effect of open and closed suction on Ventilator-associated Pneumonia and hemodynamic status

Effect of open and closed suction on Ventilator-associated Pneumonia and hemodynamic status in intensive care patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013012312251N1
Enrollment
86
Registered
2013-03-18
Start date
2013-02-28
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pneumonia. Pneumonia in diseases classified elsewhere

Interventions

Intervention 1: In the control group (open system suctioning) of tracheal tube and the ventilator was removed by entering the sterile catheter into the endotracheal tube to drain Discharge .After suct
Prevention
In the control group (open system suctioning) of tracheal tube and the ventilator was removed by entering the sterile catheter into the endotracheal tube to drain Discharge .After suctioning the patie
In the intervention group, the suctioning using a closed system( TYE CARE mark) During the first 72 hours of hospitalization in the intensive care unit and if a patient needs to be done. During endotr

Sponsors

Lorestan University of Medical Sciences, Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Criteria include: the need for endotracheal intubation and mechanical ventilation with positive pressure, age 80-15 years, the time from admission to admission to the intensive care unit of the hospital in less than 4 hours, the lack of heart disease - cardiovascular, half-sitting position, nasal tube - stomach in all patients, the level of consciousness of less than 9, but did not receive a specific antibiotic routine antibiotics (cefazolin), suctioning of secretions and require much more than. Infection, pneumonia, respiratory failure, and underlying disease that increases the risk of pneumonia. Normal cardiac rhythm, arterial oxygen saturation greater than 90%, and Heart rate between 100 to 60 beats per minute before suctioning ,and the calibration of a ventilator and monitor all devices. Exclusion criteria Patients: a history of smoking, apart from mechanical ventilation and less than 72 hours Ayntvbh of death within 48 hours, received a heart drug during the project, the need for antibiotics and certain additional antibiotics routine (cefazolin) during the project increase during the discharge plan.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ventilator-associated Pneumonia. Timepoint: After 72 hours of endotracheal intubation. Method of measurement: CIPS criteria.;Hemodynamic status. Timepoint: Before suctioning immediately, 2 and 5 minutes after suctioning. Method of measurement: Cardiorespiratory monitoring device.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactnasim alipour

Lorestan University of Medical Sciences

n.alipour@umsha.ac.ir;alipour.0289@yahoo.com+98 66 1620 0146

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026