2021
DOI: 10.1093/rheumatology/keab236
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Reliability, validity and responsiveness of physical activity monitors in patients with inflammatory myopathy

Abstract: Objective Idiopathic inflammatory myopathies (IIM) cause proximal muscle weakness, which affect activities of daily living. Wearable physical activity monitors (PAMs) objectively assess continuous activity with potential clinical usefulness in IIM assessment. We examined the psychometric characteristics for PAM outcomes in IIM. Methods Adult IIM patients were prospectively evaluated (baseline, 3 and 6-months) in an observatio… Show more

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Cited by 23 publications
(24 citation statements)
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“…A recent study on portable activity monitors for idiopathic inflammatory myopathies measuring average step counts/minute; peak 1-min cadence showed high compliance of patients in wearing devices (revealing a high level of patients commitment toward disease) and a very high level of concordance of these measurements with classical in-patient or ambulatory clinical evaluation. It demonstrated validity in register changes in the physical status of neuromuscular patients, with early recognition of worsening [ 28 ].…”
Section: Remote Monitoringmentioning
confidence: 99%
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“…A recent study on portable activity monitors for idiopathic inflammatory myopathies measuring average step counts/minute; peak 1-min cadence showed high compliance of patients in wearing devices (revealing a high level of patients commitment toward disease) and a very high level of concordance of these measurements with classical in-patient or ambulatory clinical evaluation. It demonstrated validity in register changes in the physical status of neuromuscular patients, with early recognition of worsening [ 28 ].…”
Section: Remote Monitoringmentioning
confidence: 99%
“…It demonstrated validity in register changes in the physical status of neuromuscular patients, with early recognition of worsening [ 28 ].…”
Section: Remote Monitoringmentioning
confidence: 99%
“…Patient-centered assessments like AL allow more regular and frequent measurements by patients at home or simpler more objective measurements during clinic follow-up may mitigate some of these limitations. Additionally, these may serve as important secondary outcomes to supplement the collection of validated CSMs in clinical trials [14].…”
Section: Discussionmentioning
confidence: 99%
“…Inclusion criteria were all adults with the diagnosis of PM or DM as per 2017 ACR/EULAR myositis classification criteria who were evaluated at rheumatology clinic between January and March of 2021. Children and those with known symptomatic ILD (dyspnoea VAS ≥ 2), PAH, or significant lower limb arthritis (pain VAS ≥ 2) were excluded due to the nature of the tests being evaluated and the pilot nature of the study [13][14][15]. Patients with other conditions interfering with their physical function, such as severe fibromyalgia, pregnancy, or fractures, were also considered ineligible for enrolment.…”
Section: Patient Populationmentioning
confidence: 99%
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