Neuromuscular Electrical Stimulation Following Total Hip Arthroplasty

National University of Ireland, Galway, Ireland11 enrolled

Overview

Patients post total hip arthroplasty (THA) remain at high risk of developing Deep Vein Thrombosis (DVT) during the recovery period following surgery despite the availability of effective pharmacological and mechanical prophylactic methods. The use of calf muscle neuromuscular electrical stimulation (NMES) during the hospitalised recovery period on this patient group may be effective at preventing DVT. However, the haemodynamic effectiveness and comfort characteristics of NMES in post-THA patients immediately following surgery have yet to be established. The main objectives are: 1. To establish if patients in the early post-operative period have tolerance for NMES. 2. To determine if applying NMES to patients immediately post-THA increases venous outflow from the lower limb over resting conditions.

Study Type

INTERVENTIONAL

Allocation

Purpose

BASIC_SCIENCE

Masking

NONE

Enrollment

Conditions

Deep Vein Thrombosis Total Hip Arthroplasty

Interventions

Eligibility

Sex: ALLMin age: 30 YearsMax age: 90 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients who underwent total hip arthroplasty the previous day Exclusion Criteria: * Patients with Diabetes Mellitus * Patients with Peripheral Vascular Disease * Patients currently involved in another trial * Previous diagnosis of DVT

Outcomes

Primary Outcomes

Lower limb haemodynamic performance

Duplex Doppler ultrasound will be used as the outcome measure. Both legs will be measured for hemodynamic performance in the popliteal vein by placing the probe at the popliteal fossa. Measurements of peak venous velocity (cm/s), popliteal vein diameter (cm), time averaged mean velocity (TAMEAN, cm/s) and volume flow (ml/min) will be recorded. Doppler measurements will be taken initially at rest, before the application of NMES and once again when the NMES session had commenced.

Time frame: 4 hours

Secondary Outcomes

Patient comfort during application of NMES

Measurements will be taken at 3 time points (before application of NMES, after application of NMES had begun and at the end of the protocol). The measurement consists of asking patients to mark their level of comfort using a 100mm, non-hatched visual-analogue-scale (VAS). A VAS of 30 mm or less will be categorised as mild pain, between 31 and 69mm as moderate pain and scores of 70mm or greater as severe pain.