Patients with airway artificial lung. Other diseases of upper respiratory tract
Conditions
Interventions
Intervention 1: Experimental group: After random sampling of the patients, The standard suction method with other standard criteria will be taught to working and volunteer nurses in both control and e
Prevention
Experimental group: After random sampling of the patients, The standard suction method with other standard criteria will be taught to working and volunteer nurses in both control and experimental grou
Control group: in the control group, suction will be done based on routine standard criteria.
Sponsors
Vice chancellor for research(Science and Technology) , Zanjan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
17 Years to 80 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Having a minimum age of 18 and maximum age of 70 years? An artificial airway Having vital signs within normal limits. Exclusion criteria: Not having cardiac and pulmonary monitoring? A serve heart or lung disease? Chronic obstructive disease high intracranial pressure? Pulmonary parameters and vital signs within normal limits? Dopamine medication? Dubatomin? Nitroglycerin and increasing the blood pressure_lowering drugs? Removal of the ventilator? and the patient death during the study ? Having significant problem after the first suction or having an urgent need to have second suction? And also the patients who do not have suction problems (Airway bleeding? Fractures? et) and the patients under CMV made will not be considered in this study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean Arterial pressure. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Mm Hg, by monitoring patients.;Blood pressure. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Mm Hg, by monitoring patients.;Respiratory Rate. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: The minutes of number, by cardiac monitoring.;Saturation of arterial hemoglobin. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Percentage minutes, by cardiopulmonary monitoring.;Resistance airway. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Cm of H2O per minute, ventilator.;Heart rate. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: The minutes of number, by cardiac monitoring.;Tidal Volume. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Cc per kg; ventilator.;Compliance. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Ml cm of H2O; ventilator.;Mean airway pressure. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: ventilator.;Minute volume. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Cc per kg; ventilator. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intracranial pressure. Timepoint: Before the five minutes after opening the airway suctioning artificial. Method of measurement: Mm Hg, intracranial shunt.;And the patient death during the study. Timepoint: Before two and five minutes after opening the airway suctioning artificial. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarshid Alazmani Noodeh
Zanjan University of Medical Sciences
Outcome results
None listed