PMID- 38129116 OWN - NLM STAT- MEDLINE DCOM- 20240318 LR - 20240324 IS - 1468-3296 (Electronic) IS - 0040-6376 (Print) IS - 0040-6376 (Linking) VI - 79 IP - 4 DP - 2024 Mar 15 TI - Low-load blood flow restriction strength training in patients with COPD: a randomised single-blind pilot study. PG - 340-348 LID - 10.1136/thorax-2023-220546 [doi] AB - OBJECTIVE: The objective of this study is to compare the effectiveness of lower limb low-load blood flow restriction training (LL-BFRT) with high-load strength training (HL-ST) as part of an outpatient pulmonary rehabilitation programme on leg strength in patients with chronic obstructive pulmonary disease (COPD). METHODS: Participants were randomised to LL-BFRT or HL-ST (24 sessions). LL-BFRT was done at 30% 1-repetition maximum (1-RM) with 70% arterial occlusion pressure. HL-ST was done at 70% 1-RM. Primary outcome was isometric strength of knee extensors and flexors. Secondary outcomes were 1-RM, functional exercise capacity, physical activity, symptom burden and health-related quality of life. Perceptions of dyspnoea and leg fatigue were recorded after every exercise. We compared groups with t-tests. RESULTS: We included 30 participants (13 women, 17 men, 64 (9) years, forced expiratory volume in 1 s 47 (18)% pred.), 24 completed the study. Isometric knee extensor strength improved to a clinically relevant degree in both legs in both groups (LL-BFRT: right leg 9 (20) Nm, left leg 10 (18) Nm; HL-ST: right leg 15 (26) Nm, left leg 16 (30) Nm, data are mean (SD)), without statistically significant or clinically relevant between-group differences (right leg mean difference= -6.4, 95% CI= -13.20 to 25.92 Nm, left leg mean difference= -5.6, 95% CI= -15.44 to 26.55 Nm). 1 min sit-to-stand test performance improved to a clinically relevant degree only in the LL-BFRT group (4 (4) vs 1 (5) repetitions). Interestingly, physical activity improved to a clinically relevant degree only in the LL-BFRT group (1506 (2441) vs -182 (1971) steps/day). LL-BFRT lowered perceived in-exercise dyspnoea and increased leg fatigue compared with HL-ST in the initial 12 trainings. CONCLUSION: In patients with stable COPD undergoing outpatient pulmonary rehabilitation, LL-BFRT was not superior to HL-ST in improving leg strength. LL-BFRT led to similar strength gains as HL-ST while reducing perceptions of dyspnoea in the initial training phase. TRIAL REGISTRATION NUMBER: NCT04151771. CI - (c) Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. FAU - Kohlbrenner, Dario AU - Kohlbrenner D AUID- ORCID: 0000-0001-6674-5193 AD - Faculty of Medicine, University of Zurich, Zurich, Switzerland dario.kohlbrenner@usz.ch. AD - Department of Pulmonology, University Hospital Zurich, Zurich, Switzerland. FAU - Kuhn, Manuel AU - Kuhn M AD - Faculty of Medicine, University of Zurich, Zurich, Switzerland. AD - Department of Pulmonology, University Hospital Zurich, Zurich, Switzerland. FAU - Manettas, Anastasios AU - Manettas A AD - Physiotherapy Occupational Therapy, University Hospital Zurich, Zurich, Switzerland. AD - Biomechanics and Ergonomics, ErgoMech Laboratory, Department of Physical Education and Sport Science, University of Thessaly, Trikala, Greece. FAU - Aregger, Celine AU - Aregger C AD - Physiotherapy Occupational Therapy, University Hospital Zurich, Zurich, Switzerland. FAU - Peterer, Matthias AU - Peterer M AD - Physiotherapy Occupational Therapy, University Hospital Zurich, Zurich, Switzerland. FAU - Greco, Nicola AU - Greco N AD - Physiotherapy Occupational Therapy, University Hospital Zurich, Zurich, Switzerland. FAU - Sievi, Noriane A AU - Sievi NA AUID- ORCID: 0000-0003-1758-4586 AD - Department of Pulmonology, University Hospital Zurich, Zurich, Switzerland. FAU - Clarenbach, Christian AU - Clarenbach C AD - Faculty of Medicine, University of Zurich, Zurich, Switzerland. AD - Department of Pulmonology, University Hospital Zurich, Zurich, Switzerland. LA - eng SI - ClinicalTrials.gov/NCT04151771 PT - Journal Article PT - Randomized Controlled Trial DEP - 20240315 PL - England TA - Thorax JT - Thorax JID - 0417353 SB - IM CIN - doi: 10.1136/thorax-2023-221218 MH - Male MH - Humans MH - Female MH - *Resistance Training MH - Pilot Projects MH - Quality of Life MH - Blood Flow Restriction Therapy MH - Single-Blind Method MH - *Pulmonary Disease, Chronic Obstructive/rehabilitation MH - Dyspnea/etiology MH - Fatigue MH - Muscle Strength PMC - PMC10958309 OTO - NOTNLM OT - exercise OT - pulmonary rehabilitation COIS- Competing interests: DK, MK, AM, CA, MP, NG and NAS have nothing to disclose. CC reports personal fees from Roche, personal fees from Novartis, personal fees from Boehringer, personal fees from GSK, personal fees from Astra Zeneca, personal fees from Sanofi, personal fees from Vifor, personal fees from Mundipharma, personal fees from Daiichi Synkyo, personal fees from CSL Behring, all outside the submitted work. EDAT- 2023/12/22 00:42 MHDA- 2024/03/18 06:44 PMCR- 2024/03/22 CRDT- 2023/12/21 21:22 PHST- 2023/06/01 00:00 [received] PHST- 2023/11/18 00:00 [accepted] PHST- 2024/03/18 06:44 [medline] PHST- 2023/12/22 00:42 [pubmed] PHST- 2023/12/21 21:22 [entrez] PHST- 2024/03/22 00:00 [pmc-release] AID - thorax-2023-220546 [pii] AID - 10.1136/thorax-2023-220546 [doi] PST - epublish SO - Thorax. 2024 Mar 15;79(4):340-348. doi: 10.1136/thorax-2023-220546.