Angina pectoris. Angina pectoris
Conditions
Interventions
Intervention 1: In the Intervention group, after intubated by an anesthesiologist (with more work experience of 5 years) (using the touch pad cuff), by trained nurses with listed for the control group
during the first 10 minutes of anesthesia, time of admission to the intensive care unit and then in a period of 2 hours, 4 hours and 6 hours later using a handheld German construction company pressure
Treatment - Drugs
Prevention
In the Intervention group, after intubated by an anesthesiologist (with more work experience of 5 years) (using the touch pad cuff), by trained nurses with listed for the control group (during the fir
In order to collect data, demographic data and medical records endotracheal tube cuff pressure was used. In the Control group, patients with endotracheal tube cuff pressure by the anesthesiologist (wi
Sponsors
Vice chancellor for research, Shahid Sadughi University of Medical Sciences
Eligibility
Sex/Gender
All
Age
77 Years to 20 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria were: age between 18 - 75 years ; A patient for surgery was selected for the first time ; They are between 1- 4 hours ; And the duration of Intubation during surgery less than 24 hours to prevent the impact of other detrimental factors ; Risks of surgery at level 1 and 2 ; and the tracheal tube according to the sex of the patient ; As well as not having a history of head and neck surgery ; Anesthesia, medications used was similar adjustments ventilator for all patients ; And those with a history of sore throat and pharyngitis to 4 weeks prior to surgery ; And a history of respiratory problems ; Addictions, smoking and drug allergy ; As well as patients in the study were throat pain unbearable or housing request ; Inotrope drugs or vasodilator in the intensive care unit received more than 10 microns ; Longer than 30 seconds for intubation needed ; Or during the study needs to be repeated or replacing the pipes or more than 24 hours under ventilation were excluded from the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sore Throat. Timepoint: 2 hours, 6 hours, 12 and 24 hours after Extubation. Method of measurement: To search for pain from zero to 3 ; (Zero score : without sore throat ; a score of 1 : Mild sore throat (only if the person to ask) ; score 2 : moderate sore throat (pharyngitis expressed by the patient) ; grade 3 : severe sore throat (change in volume with sore throat)).;Hoarseness. Timepoint: 2 hours , 6 hours , 12 and 24 hours after Extubation. Method of measurement: As well as a change in sound quality was defined Hoarseness and its severity was determined by 4 degrees from zero to three (zero score : without hoarseness ; 1 score : violence that only by patient reported noise during the interview ; the score 2 : clear sound but mild violence ; Score 3 : violence clear sound and sharp) and transfer the patient to the intensive care unit after surgery.;Cough. Timepoint: 2 hours , 6 hours , 12 and 24 hours after Extubation. Method of measurement: To measure any cough or mild and the extreme of the scale was 0 to 4 (zero score: without coughing ; rare 1: score ; score 2 : casual less than an hour ; score 3 : repeated one or more times an hour ; the score 4 : almost unchanged). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Hassan Mondegari Bamakan
Yazd School of Nursing and Midwifery
Outcome results
None listed