Atelectasis. Pulmonary collapse
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria including: Patients candidate for non emergency open heart surgery (coronary artery bypass and heart valve surgery by sternotomy and cardiopulmonary bypass); Aged from 18 until 65 years; No ejection fraction less than 30% in the angiography form, preoperative; No history of chronic airway obstruction disease and lung trauma; No history of open heart surgery or lung surgery; No history of rib fractures and chest tube insertion; No history of trauma in the head or nose, neurologic disease and frequent sinus infections; No history of chemotherapy and using immunosuppressants three months prior to the surgery; No serum creatinine greater than 3.5 mg/Dl; No body mass index greater than 40 kg/m2; Consciousness level at 15 before surgery; Exclusion criteria including: Arterial systolic pressure less than 90 mmHg despite of fluid intake; Arterial blood pH less than 7.30; Arterial carbon dioxide pressure greater than 50 mmHg; Arterial oxygen saturation less than 80% despite of supplemental oxygen intake; Hemoglobin concentration less than 7 gr/dL; Aortic cross clamp time longer than 150 minutes; Cardiopulmonary bypass time longer than 240 minutes; Using intra aortic balloon pump (IABP) intraoperative and postoperative; Intubation over 24 hours; Also, the patient will be excluded from the study when he/she retransfers to the operating room or when he/she needs ventilator therapy protocols apart from of research protocols.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Atelectasis. Timepoint: Two hours after extubation, the third day after surgery (72 hours of operation). Method of measurement: Chest x-rays. | — |
Secondary
| Measure | Time frame |
|---|---|
| Respiratory variable of arterial blood gas (arterial oxygen tension, arterial carbon dioxide tension, arterial oxygen saturation, arterial bicarbonate and arterial blood PH). Timepoint: Before the intervention, one and four hours after the starting of the intervention, before extubation. Method of measurement: ABG test.;Arterial systolic pressure, diastolic blood pressure and mean arterial pressure. Timepoint: Before the intervention, one and four hours after the starting of the intervention, before extubation. Method of measurement: Advanced vital signs monitoring devices.;Heart rate. Timepoint: Before the intervention, one and four hours after the starting of the intervention, before extubation. Method of measurement: Advanced vital signs monitoring devices.;Respiratory rate. Timepoint: Before the intervention, one and four hours after the starting of the intervention, before extubation. Method of measurement: Counting the number of breaths per minute.;Tempreture. Timepoint: Before the intervention, one and four hours after the starting of the intervention, before extubation. Method of measurement: Advanced vital signs monitoring devices thermometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Mazandaran University of Medical Sciences