Feasibility and safety of two weeks of blood flow restriction exercise in individuals with spinal cord injury

被引:1
|
作者
Jonsson, Anette Bach [1 ,2 ]
Krogh, Soren [1 ,2 ]
Severinsen, Kare Eg [2 ,3 ]
Aagaard, Per [4 ]
Kasch, Helge [2 ,5 ]
Nielsen, Jorgen Feldbaek [1 ,2 ,3 ]
机构
[1] Spinal Cord Injury Ctr Western Denmark, Viborg, Denmark
[2] Aarhus Univ, Dept Clin Med, Hlth, Palle Juul Jensens Blvd 11, DK-8200 Aarhus N, Denmark
[3] Hammel Neurorehabil Ctr & Univ Clin, Hammel, Denmark
[4] Univ Southern Denmark, Inst Sports Sci & Clin Biomech, Muscle Physiol & Biomech Res Unit, Odense, Denmark
[5] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark
关键词
Feasibility; Safety; Blood flow restriction exercise; Spinal cord injury; OCCLUSION PRESSURE; STRENGTH; PEOPLE; MUSCLE;
D O I
10.1080/10790268.2024.2408052
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ContextReduced muscle strength and function are common after spinal cord injury (SCI). While low-load blood flow restriction exercise (BFRE) enhances muscle strength in healthy and clinical populations, its safety and feasibility in individuals with SCI remain underexplored.ObjectivesTo investigate the feasibility and safety of low-load BFRE in individuals with incomplete SCI.Study DesignCase series.SettingSCI rehabilitation center.ParticipantsSix participants with motor incomplete SCI were enrolled in the study.InterventionA two-week BFRE intervention for the lower limbs was conducted twice weekly at 40% total arterial occlusion pressure, using 30-40% of 1-repetition maximum loads.Outcome MeasuresFeasibility measures, specifically recruitment and eligibility rates and intervention acceptability, were collected. Blood pressure (BP) responses and specific coagulation markers for deep vein thrombosis (DVT) were assessed as safety measures.ResultsRecruitment and eligibility rates were 2.8% and 6.6% for individuals admitted for first-time rehabilitation (subacute SCI) and 8.3% and 13.9% for 4-week readmission rehabilitation stays (chronic SCI), respectively. Intervention acceptability was high, characterized by 95.8% training adherence and low-to-moderate self-reported pain levels. BP responses and changes in C-reactive protein, Fibrinogen, and D-dimer during the intervention remained within clinically acceptable levels.ConclusionBFRE was feasible in an SCI rehabilitation setting despite a low recruitment rate. BFRE imposed no heightened risk of DVT or severe BP fluctuations in the present case series. Additionally, no severe adverse events occurred, and only mild complaints were reported. More extensive safety considerations warrant larger-scale exploration.Trial registrationClinicalTrials.gov identifier: NCT03690700.
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页数:10
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