The Effect of Pulmonary Rehabilitation on Bronchoscopic Volume Reduction Process Success
- Conditions
- EmphysemaPulmonary RehabilitationBronchoscopic Lung Volume Reduction
- Interventions
- Other: Pulmonary RehabilitationOther: Standart care
- Registration Number
- NCT04347044
- Lead Sponsor
- Istanbul Medipol University Hospital
- Brief Summary
The data of patients undergoing bronchoscopic volume reduction procedure will be analyzed retrospectively. Patients will be divided into two groups as patients with and without Pulmonary Rehabilitation before the procedure, and changes in functional levels of patients will be compared.
- Detailed Description
The data of patients who underwent bronchoscopic volume reduction between January 2013 and March 2019 will be examined.
Patients will be divided into two groups as pulmonary rehabilitation applied (PR group) and not applied (Control group) before the procedure.
Changes in the parameters of initial and rehabilitation follow-up will be examined.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 80
- Between the ages of 18-75
- Patients with a diagnosis of emphysema and bronchoscopic procedures
• Patients who develop complications related to the procedure after bronchoscopic procedure.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Pulmonary Rehabilitation Group Pulmonary Rehabilitation Optimal medication and clinical follow-up plus Pulmonary rehabiltation Pulmonary Rehabilitation Group Standart care Optimal medication and clinical follow-up plus Pulmonary rehabiltation Non-Pulmonary Rehabilitation Group Standart care Optimal medication and clinical follow-up
- Primary Outcome Measures
Name Time Method Six minute walking test 20 minutes The test was conducted in a 30-meter corridor in line with American Thoracic Society (ATS) guidelines. Patients were asked to walk as far as they can. Prior to and following the test, oxygen saturation, heart rate and Borg fatigue rating were measured, and the walking distance were recorded
Pulmonary Function Tests 15 minutes PFTs were performed by using the Sensormedics model 2400 (Yorba Linda, CA, USA) spirometry device, and according to the American Thoracic Society (ATS) guidelines
- Secondary Outcome Measures
Name Time Method Carbonmonoxide diffusion test 15 minutes It will performed in the pulmonary function test laboratory using Cosmed Quark PFT (USA) with single-breath technique
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