Department of Pulmonary Rehabilitation, Philipps - University of Marburg, German Center for Lung Research (DZL), Marburg, Germany.
Institute for Pulmonary Rehabilitation Research, Schoen Klinik Berchtesgadener Land, Malterhoeh 1, 83471, Schoenau am Koenigssee, Germany.
Orphanet J Rare Dis. 2020 Sep 22;15(1):255. doi: 10.1186/s13023-020-01540-3.
Lymphangioleiomyomatosis (LAM) is a rare and progressive cystic lung disease with limited therapeutic options. We retrospectively analyzed the effects of a comprehensive 4-week inpatient pulmonary rehabilitation (PR) program in 58 patients with advanced LAM (FEV1: 45 ± 34%predicted, 6-min walk distance (6MWD): 338 ± 167 m). Exercise performance (6MWD: + 49 ± 50 m; p < 0.001) and quality of life (SF-36 physical component: + 2.4 ± 7.8 points; p = 0.049 and mental component: + 5.2 ± 12.1 points; p < 0.001) increased significantly after PR comparable to an COPD cohort. There were no clinical parameters that predicted changes in outcomes following PR. PR seems to be an effective therapeutic option even in patients with advanced LAM. TRIAL REGISTRATION: Clinical-Trials registration number: NCT04184193 ; date of registration: December 3, 2019.
淋巴管平滑肌瘤病(LAM)是一种罕见的进行性囊性肺疾病,治疗选择有限。我们回顾性分析了 58 例晚期 LAM 患者(FEV1:45±34%预计值,6 分钟步行距离(6MWD):338±167m)接受全面的 4 周住院肺康复(PR)计划的效果。运动表现(6MWD:+49±50m;p<0.001)和生活质量(SF-36 生理成分:+2.4±7.8 分;p=0.049 和心理成分:+5.2±12.1 分;p<0.001)在 PR 后显著增加,与 COPD 队列相当。没有临床参数可以预测 PR 后结果的变化。PR 似乎即使在晚期 LAM 患者中也是一种有效的治疗选择。试验注册:临床试验注册号:NCT04184193;注册日期:2019 年 12 月 3 日。