Seher Satar - Ataturk Chest Diseases and Surgery Education and Research Hospital, Ankara, Turkey.
Ipek Candemir - Ataturk Chest Diseases and Surgery Education and Research Hospital, Ankara, Turkey.
Pinar Ergun - Ataturk Chest Diseases and Surgery Education and Research Hospital, Ankara, Turkey.

Objectives: Idiopathic pulmonary fibrosis (IPF) is characterized by progressively worsening lung function, ventilation capacity, dyspnea, and finally reduced exercise intolerance. All of these have a significant negative impact on functional capacity and quality of life. In this study, we aim to evaluate the effects of pulmonary rehabilitation (PR) in IPF and assess the predictors of success. Methods: Data from ۱۷ IPF patients who completed the program from the total of ۲۷ patients who applied to PR were used in our study. We evaluated their pulmonary function tests, exercise capacity, peripheral-respiratory muscle strength, body composition, quality of life, and psychological states before and after PR. Results: Following the PR program, improvements over the minimal clinically important differences were observed in almost all parameters compared to the baseline; however, statistically significant improvements were only observed in the medical research council (P=۰.۰۲۰), the St. George respiratory questionnaire (P=۰.۰۰۲), the maximal inspiratory pressure (P=۰.۰۲۴), the anxiety score (P=۰.۰۰۱), the depression score (P=۰.۰۰۲), and the right quadriceps muscle strength (P=۰.۰۴۶). There was only a statistically significant negative correlation between the initial forced vital capacity and the forced expiratory volume in one-second value with the increase in patients’ maximal inspiratory pressure values after PR.  Discussion: After a multidisciplinary, comprehensive PR program, dyspnea sensation, exercise capacity, endurance time, quality of life, respiratory and peripheral muscle strengths, and psychological status were improved regardless of age, gender, antifibrotic treatment, and comorbidities. Therefore, patients should be referred to PR units before the deterioration in the quality of life in the early stages of the disease.

Pulmonary rehabilitation, Idiopathic pulmonary fibrosis, Quality of life, Muscle strength, Improvements