Why the study?
Repetitive vascular occlusion stimulus limits muscle atrophy in healthy and orthopaedic subjects, but its application to ICU patients had not been explored.
Does repetitive vascular occlusion stimulus (RVOS) improve safety, feasibility, and muscle atrophy in adult critically ill patients with multi-organ failure?
Does repetitive vascular occlusion stimulus (RVOS) improve safety, feasibility, and muscle atrophy in adult critically ill patients with multi-organ failure?
Answers are grounded in this paper and cite their sources.
RVOS application in critically ill patients with multi-organ failure appears safe and acceptable, but requires protocol modifications to improve tolerability and recruitment.
Muscle wasting is implicated in the pathogenesis of intensive care unit acquired weakness (ICU-AW), affecting 40% of patients and causing long-term physical disability. A repetitive vascular occlusion stimulus (RVOS) limits muscle atrophy in healthy and orthopaedic subjects, thus, we explored its application to ICU patients. Adult multi-organ failure patients received standard care +/− twice daily RVOS {4 cycles of 5 min tourniquet inflation to 50 mmHg supra-systolic blood pressure, and 5 min complete deflation} for 10 days. Serious adverse events (SAEs), tolerability, feasibility, acceptability, and exploratory outcomes of the rectus femoris cross-sectional area (RFCSA), echogenicity, clinical outcomes, and blood biomarkers were assessed. Only 12 of the intended 32 participants were recruited. RVOS sessions (76.1%) were delivered to five participants and two could not tolerate it. No SAEs occurred; 75% of participants and 82% of clinical staff strongly agreed or agreed that RVOS is an acceptable treatment. RFCSA fell significantly and echogenicity increased in controls (n = 5) and intervention subjects (n = 4). The intervention group was associated with less frequent acute kidney injury (AKI), a greater decrease in the total sequential organ failure assessment score (SOFA) score, and increased insulin-like growth factor-1 (IGF-1), and reduced syndecan-1, interleukin-4 (IL-4) and Tumor necrosis factor receptor type II (TNF-RII) levels. RVOS application appears safe and acceptable, but protocol modifications are required to improve tolerability and recruitment. There were signals of possible clinical benefit relating to RVOS application.
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Chhetri et al. (2022) studied this question.
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