Effect of remote ischaemic preconditioning on walking in people with multiple sclerosis: double-blind randomised controlled trial.

exercise tolerance fatigue gait multiple sclerosis remote ischemic preconditioning

Journal

BMJ neurology open
ISSN: 2632-6140
Titre abrégé: BMJ Neurol Open
Pays: England
ID NLM: 101775450

Informations de publication

Date de publication:
2020
Historique:
received: 26 11 2019
revised: 22 01 2020
accepted: 04 02 2020
entrez: 8 3 2021
pubmed: 9 3 2021
medline: 9 3 2021
Statut: epublish

Résumé

Remote ischaemic preconditioning (RIPC) is the exposure of body parts to brief periods of circulatory occlusion and reperfusion. Recent studies have also shown that RIPC can improve exercise performance in healthy individuals. This study aimed to assess the effect of RIPC on walking in people with multiple sclerosis (MS). This was a double-blind randomised controlled clinical trial. We used three cycles of RIPC delivered by occluding the upper arm with a blood pressure (BP) cuff inflated to a pressure of 30 mm Hg above the systolic BP. In patients in the sham intervention group, the BP cuff was inflated only to 30 mm Hg below diastolic BP. Outcome measures included the Six-Minute Walk Test (6MWT), gait speed, the Borg rate of perceived exertion (RPE) scale, the tolerability of the RIPC using a Numerical Rating Scale for discomfort from 0 to 10, and adverse events. We identified responders meeting the minimal clinically important difference (MCID) established in the literature in each group. Seventy-five participants completed the study (RIPC: 38 and Sham: 37). The distance walked during the 6MWT improved by 1.9% in the sham group and 5.7% in the RIPC group (p=0.012). The number of responders meeting MCID criteria in the RIPC group was significantly greater compared with the sham intervention group. No serious adverse events occurred. Single cycle of RIPC resulted in immediate improvement in walking distances during 6MWT in people with MS. NCT03153553.

Sections du résumé

BACKGROUND BACKGROUND
Remote ischaemic preconditioning (RIPC) is the exposure of body parts to brief periods of circulatory occlusion and reperfusion. Recent studies have also shown that RIPC can improve exercise performance in healthy individuals.
OBJECTIVE OBJECTIVE
This study aimed to assess the effect of RIPC on walking in people with multiple sclerosis (MS).
METHODS METHODS
This was a double-blind randomised controlled clinical trial. We used three cycles of RIPC delivered by occluding the upper arm with a blood pressure (BP) cuff inflated to a pressure of 30 mm Hg above the systolic BP. In patients in the sham intervention group, the BP cuff was inflated only to 30 mm Hg below diastolic BP. Outcome measures included the Six-Minute Walk Test (6MWT), gait speed, the Borg rate of perceived exertion (RPE) scale, the tolerability of the RIPC using a Numerical Rating Scale for discomfort from 0 to 10, and adverse events. We identified responders meeting the minimal clinically important difference (MCID) established in the literature in each group.
RESULTS RESULTS
Seventy-five participants completed the study (RIPC: 38 and Sham: 37). The distance walked during the 6MWT improved by 1.9% in the sham group and 5.7% in the RIPC group (p=0.012). The number of responders meeting MCID criteria in the RIPC group was significantly greater compared with the sham intervention group. No serious adverse events occurred.
CONCLUSION CONCLUSIONS
Single cycle of RIPC resulted in immediate improvement in walking distances during 6MWT in people with MS.
TRIAL REGISTRATION NUMBERS BACKGROUND
NCT03153553.

Identifiants

pubmed: 33681776
doi: 10.1136/bmjno-2019-000022
pii: bmjno-2019-000022
pmc: PMC7903187
doi:

Banques de données

ClinicalTrials.gov
['NCT03153553']

Types de publication

Journal Article

Langues

eng

Pagination

e000022

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Chayaporn Chotiyarnwong (C)

Rehabilitation Medicine, Mahidol University Faculty of Medicine Siriraj Hospital, Bangkok, Thailand.
Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Krishnan Nair (K)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Lorenza Angelini (L)

Department of Mechanical Engineering and INSIGNEO, The University of Sheffield, Sheffield, Sheffield, UK.

Ellen Buckley (E)

Department of Mechanical Engineering and INSIGNEO, The University of Sheffield, Sheffield, Sheffield, UK.

Claudia Mazza (C)

Department of Mechanical Engineering and INSIGNEO, The University of Sheffield, Sheffield, Sheffield, UK.

Daniel Heyes (D)

SiTRAN, The University of Sheffield, Sheffield, Sheffield, UK.

Ridha Ramiz (R)

SiTRAN, The University of Sheffield, Sheffield, Sheffield, UK.

Kathleen Baster (K)

Statistical Services Unit, The University of Sheffield, Sheffield, Sheffield, UK.

Azza Ismail (A)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Joyutpal Das (J)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Ali Ali (A)

NIHR Sheffield Biomedical Research Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, Sheffield, UK.

Ralf Lindert (R)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Basil Sharrack (B)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Sian Price (S)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

David Paling (D)

Neurosciences, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Classifications MeSH