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Postoperative Electrical Muscle Stimulation (POEMS)

Not Applicable
Conditions
Postoperative Complications
Muscle Atrophy
Interventions
Device: Electrical Muscle stimulation
Registration Number
NCT04199936
Lead Sponsor
University of Nottingham
Brief Summary

Patients lose a significant amount of muscle following major abdominal surgery. This is partly due to a catabolic response to the surgical insult and inflammation, but is also probably due to a lack of muscle use secondary to immobility.

This study will aim to assess whether some or even all of postoperative muscle loss in the upper leg muscle group is preventable through electrical muscle stimulation to mimic physical activity.

Detailed Description

Following major gastrointestinal surgery patients may loose around 6 % of their skeletal muscle mass in the first 5 days. Whilst some of this loss is as a result of inflammation and starvation, some is due to muscle disuse.

Studies have shown that patients spend 96% of their time being sedentary in the first 5 days following major abdominal surgery and by day 5 are still taking a median of less than 500 steps per day. Studies of healthy volunteers who undergo similar muscle disuse loose approximately 3.5% of skeletal muscle mass over the same time period, indicating that around half of postoperative muscle loss may be due to immobility.

Through the use of electrical muscle stimulation, this study will aim to mimic high levels of exercise in the quadriceps of patients who have undergo major gastrointestinal surgery to see whether this reduces or prevents muscle loss. Patients muscles will be measured using ultrasound and DXA and neuromuscular function will be measured using electromyography.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Adult patients undergoing major segmental colonic resections or gastric/oesophageal resection
  • Sufficient mobility and fitness to complete normal enhanced recovery protocols following surgery
  • Ability to give informed consent
Exclusion Criteria
  • Pre-existing neuromuscular disease (including parkinson's disease)
  • Pacemaker, implantable cardiac defibrillator or other implanted nerve stimulator device
  • Metalwork in both upper legs
  • Dementia
  • Inability to give informed consent
  • Disability preventing normal mobilisation after surgery
  • Symptomatic peripheral vascular disease
  • Chronic kidney failure of chronic heart failure
  • Intubation for > 24 hours post operation
  • Return to theatre for surgical complication within first 5 days post operation

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
EMG legElectrical Muscle stimulationQuadriceps muscle group of postoperative patients randomly selected leg which will undergo electrical muscle stimulation for upto 2 hours on each postoperative day
Primary Outcome Measures
NameTimeMethod
Vastus Lateralis muscle thickness (cm)5 days

Ultrasound scan (USS) measurement of Vastus Lateralis muscle thickness in stimulated vs non stimulated legs of postoperative patients

Vastus Lateralis muscle fibre length5 days

USS measurement of Vastus Lateralis muscle fibre length in stimulated vs non stimulated legs of postoperative patients

Vastus Lateralis muscle fibre pennation angle5 days

USS measurement of Vastus Lateralis muscle fibre pennation angle in stimulated vs non stimulated legs of postoperative patients

Compound muscle action potentials (CMAP) as measured by surface electromyography5 days

Changes in compound muscle action potentials (as detected by EMG) in stimulated vs non stimulated legs of postoperative patients

Near Fibre Motor Unit Potentials as measured by surface EMG5 days

Changes in motor unit potentials (as detected by EMG) in stimulated vs non stimulated legs of postoperative patients

Motor unit number estimates ((MUNE) as derived from surface EMG analysis)5 days

Changes in MUNE (as derived from surface EMG) in stimulated vs non stimulated legs of postoperative patients

Secondary Outcome Measures
NameTimeMethod
Lean muscle mass5 days

DXA measurements of lean muscle mass in upper leg of stimulated vs non stimulated legs of postoperative patients

Physical activity levels in postoperative patients5 days

Physical activity levels of patients following major gastrointestinal resection surgery on each postoperative day as measured by physical activity monitor

Dietary intake in postoperative patients5 days

Dietary intake of patients following major gastrointestinal resection surgery, as recorded by patient food diary on each postoperative day

Inflammatory response following major abdominal surgery5 days

Inflammatory response (as measured by IL6, TNFalfa and CRP) following major gastrointestinal resection surgery and its correlation with degree of skeletal muscle loss

Acceptability of electrical muscle stimulation in postoperative patients5 days

Patient experience of electrical muscle stimulation following major gastrointestinal resection surgery as measured by visual analogue score measures of patient comfort, distress, harmful effects and enjoyment.

Trial Locations

Locations (1)

Royal Derby Hospital

🇬🇧

Derby, Derbyshire, United Kingdom

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