Incentive Spirometry Prehabilitation Study
Purpose
Postoperative pulmonary complications (PPCs) are the most common complication following thoracic surgery. PPCs are associated with prolonged hospital stay, increased morbidity, mortality, ICU admission, and healthcare costs (Azhar, 2015). Current preoperative optimization in this patient group includes smoking cessation and management of Chronic Obstructive Pulmonary Disease with inhaled bronchodilators and inhaled steroids as indicated. There have been studies using preoperative incentive spirometry in patients undergoing laparotomy with conflicting results, but scant data on its use in patients undergoing one-lung ventilation (Tyson, et al., 2015; Cattano, et al., 2010). A study from 2013 investigated the effectiveness of incentive spirometry in patients following thoracotomy and found conflicting results, without significant improvement in lung function or reduction in PPCs, but a larger difference in frequency of PPC was noted, indicating possible benefit to intervention and a need for further study (Agostini, et al., 2013). Volume-based incentive spirometry pre- and postoperatively has also been found to improve pulmonary function and diaphragm excursion in patients undergoing laparoscopic surgery (Alaparthi, et al., 2016). Patients customarily receive an incentive spirometer for use postoperatively in the PACU. There is scant data in the thoracic surgery population concerning prehabilitation by dispensing the incentive spirometer at the PACT evaluation.
Condition
- Pulmonary Disease
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Patients scheduled for thoracic surgery procedures involving one-lung ventilation - open thoracotomy - Video-assisted thoracoscopic surgery (VATS) - Robotic-assisted thoracoscopic surgery (RATS) - Procedures to include: Lung resection for any purpose, esophagectomy, thymectomy - Patients undergoing esophagectomy performed by a general surgeon - Patients willing and able to independently perform incentive spirometry
Exclusion Criteria
- Trauma patients - Lung Volume reduction surgery (LVRS) - In-Patients - Patients not undergoing one-lung ventilation - Patients undergoing thoracoabdominal aortic aneurysm repair - Transhiatal esophagectomy (does not involve one-lung ventilation) - Lung transplantation
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Supportive Care
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
No Intervention Control |
|
|
Experimental Spirometry Group |
|
More Details
- Status
- Completed
- Sponsor
- University of Alabama at Birmingham