Self‐administered non‐invasive vagus nerve stimulation therapy for severe pharmacoresistant restless legs syndrome: outcomes at 6 months

Author:

Hartley Sarah1ORCID,Bao Guillaume23,Russo Ashley23,Zagdoun Marine23,Chevallier Sylvain4ORCID,Lofaso Frédéric125,Leotard Antoine15,Azabou Eric23

Affiliation:

1. Sleep Unit, Department of Physiology Raymond Poincaré Hospital, Assistance Publique‐Hôpitaux de Paris (AP‐HP) Paris France

2. Clinical Neurophysiology and Neuromodulation Unit, SMART_VNS Platform, Department of Physiology Raymond Poincaré Hospital, Assistance Publique‐Hôpitaux de Paris (AP‐HP) Paris France

3. Laboratory of Infection and Inflammation (2I) INSERM UMR 1173 University of Versailles Saint‐Quentin‐en‐Yvelines (UVSQ), Paris‐Saclay University Paris France

4. Versailles Engineering Systems Laboratory (LISV) University of Versailles Saint‐Quentin‐en‐Yvelines (UVSQ) Vélizy France

5. Laboratory « End:icap », INSERM UMR 1179 University of Versailles Saint‐Quentin‐en‐Yvelines (UVSQ), Paris‐Saclay University Paris France

Abstract

SummarySevere pharmacoresistant restless legs syndrome (RLS) is difficult to manage and a source of suffering to patients. We studied the effectiveness at 6 months of an innovative treatment: transauricular vagus nerve stimulation (taVNS) in the left cymba concha in a case series of 15 patients, 53% male, mean (SD) age 62.7 (12.3) years with severe pharmacoresistant RLS (mean [SD] International Restless Legs Rating Scale [IRLS] score of 31.9 [2.9]) at baseline. Following an 8‐week non‐randomised hospital‐based study with eight 1‐h sessions of taVNS, patients were trained to administer taVNS at home and were followed up for 6 months. The primary outcome measure was the IRLS score, secondary outcome measures were quality of life, mood disorders using the Hospital Anxiety and Depression scale (HAD) subscales for depression (HADD) and anxiety (HADA). At the 6‐month follow‐up 13/15 patients continued to use weekly taVNS. Symptom severity decreased (mean [SD] IRLS score 22.2 [9.32] at 6 months, p = 0.0005). Four of the 15 patients had an IRLS score of <20 at 6 months and two an IRLS score of 5. Quality of life significantly improved compared to baseline (mean [SD] score at baseline 49.3 [18.1] versus 65.66 [22.58] at 6 months, p = 0.0005) as did anxiety and depression symptoms (mean [SD] HADA score at baseline 8.9 [5.4] versus 7.53 [4.42] at 6 months, p = 0.029; and HADD score at baseline 5.2 [4.5] versus 4.73 [4.44] at 6 months, p = 0.03). Treatment was well tolerated, and no adverse events were reported. Our case series shows a potential role for self‐administered taVNS in patients with severe pharmacoresistant RLS. Randomised controlled trials are needed to confirm the utility of taVNS.

Funder

Association France Ekbom

Publisher

Wiley

Subject

Behavioral Neuroscience,Cognitive Neuroscience,General Medicine

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