Non‐interventional, prospective, observational study on spasticity‐associated symptom control with nabiximols as add‐on therapy in patients with multiple sclerosis spasticity in Austria

Author:

Guger Michael1ORCID,Hatschenberger Robert2,Leutmezer Fritz3

Affiliation:

1. Department of Neurology Pyhrn‐Eisenwurzen Klinikum Steyr Steyr Austria

2. Department of Neurology Klinikum Bad Hall and Bad Schallerbach Bad Schallerbach Austria

3. Department of Neurology Medical University Vienna Vienna Austria

Abstract

AbstractBackground and purposeRandomized controlled trials and observational studies of nabiximols oromucosal spray in patients with multiple sclerosis (MS) spasticity have shown improvement in a range of associated symptoms (pain, spasms, fatigue, bladder dysfunction, and sleep disturbances). This study evaluated the effectiveness and tolerability of add‐on nabiximols in the routine management of patients with MS spasticity in Austria, with a focus on spasticity‐associated symptoms.MethodsThis was an open, prospective, multicenter, observational, non‐interventional study of patients with MS spasticity receiving add‐on treatment with nabiximols oromucosal spray. Main endpoints were patient‐reported changes from baseline in the frequency (counts) or severity (mean Numerical Rating Scale [NRS] scores) of spasticity‐associated symptoms, and patient‐reported changes from baseline in impairment of daily activities due to spasticity, after 1 and 3 months of nabiximols treatment. No analyses were conducted for statistical significance.ResultsThere were 55 patients in the effectiveness population, and 62 in the safety population. Patients reported clinically relevant reductions from baseline to month 3 in the average number of spasms/day (−68.2%) and number of urinary incontinence episodes (−69.3%) in the week prior to the clinic visit, and reductions in mean 0−10 NRS scores for sleep impairment (−47.2%), fatigue (−26.4%), pain (40.4%), and spasticity severity (39.0%). There was no change from baseline in daily activity impairment due to spasticity. The majority of patients were at least partly satisfied with add‐on nabiximols for spasticity‐associated symptoms. There were 31 adverse events (27 treatment related) reported in 19 patients, with no new safety signals.ConclusionsAdd‐on nabiximols improved the severity of MS spasticity and a range of spasticity‐associated symptoms during real‐world use in Austria. Nabiximols is an option for patients with MS spasticity who fail first‐line oral antispasticity treatment.

Publisher

Wiley

Subject

Behavioral Neuroscience

Reference24 articles.

1. Correlation between spasticity and quality of life in patients with multiple sclerosis: the CANDLE study

2. Medication Adherence: WHO Cares?

3. Bundesamt für Sicherheit im Gesundheitswesen. (2018).Wissenschaftlicher Leitfaden zur Durchführung von Nicht‐interventionellen Studien (NIS) in Österreich. Aktualisiert.https://www.jku.at/fileadmin/gruppen/88/L_I212_Leitfaden_NIS_AT.pdf

4. Review of available data for the efficacy and effectiveness of nabiximols oromucosal spray (Sativex) in multiple sclerosis patients with moderate to severe spasticity

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