Abstract

BackgroundDisease modifying treatments (DMT) for MS such as interferon beta (IFNβ) have been shown to reduce the risk for disease progression. Therefore adherence to treatment is essential for treatment outcome.Here we want to evaluate if participation in a patient management program (PMP) improves adherence to DMT as well as health and cost outcomes associated with MS.MethodsIn this open-label multicentre prospective observational study, German MS patients treated with once weekly intramuscular (IM) IFNβ-1a (Avonex ®), were offered participation in a PMP and followed for up to 12 months. The PMP included injection trainings, support and quarterly visits for up to 12 months after initiation of therapy. Utilisation of health care services was evaluated.The primary endpoint was to evaluate the direct and indirect cost associated with MS from payer, patient and societal perspective, in patients who participate in the PMP. Secondary endpoint was the clinical outcome in patients who participate in the PMP (differentiated in adherent versus non-adherent patients).ResultsIn total 731 patients (mean age: 38.2, 73.7 % female) were enrolled, 640 (88 %) were observed for twelve months. After six months 34 % of patients had participated in the PMP continuously and 21 % temporarily; 39 % had not participated. After twelve months, the proportions of participants were: 37 % continuously and 19 % temporarily; 40 % had not participated.After 6 months, mean reduction in cost per patient in the participants group (€ 2151) was almost twice as high as the cost reduction amongst non-participants (€ 1131).After twelve months, the annual relapse rate was reduced by 58 % compared to baseline in both the participant and non-participant groups.ConclusionsIn a real-world-setting, participation in a patient management program was associated with improved medication adherence and lower total MS-related direct and indirect cost over time.

Highlights

  • Disease modifying treatments (DMT) for Multiple sclerosis (MS) such as interferon beta (IFNβ) have been shown to reduce the risk for disease progression

  • Adult patients with a clinically isolated syndrome (CIS), or with a diagnosis of relapsing-remitting MS (RRMS) who had received a prescription for once weekly IM IFNb-1a for at least one month before inclusion were included in the non-interventional study

  • Data from 731 patients with CIS or RRMS on once weekly IM IFNb-1a were included in the analysis

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Summary

Introduction

Disease modifying treatments (DMT) for MS such as interferon beta (IFNβ) have been shown to reduce the risk for disease progression. MS usually begins with an acute inflammatory demyelinating episode (clinically isolated syndrome, CIS) turning to relapsing-remitting MS (RRMS) characterized by discrete acute attacks of worsening neurological function (relapses) that are followed by partial or complete recovery (remission). Therapeutic options in MS include treatment of acute relapses, immunomodulating disease-modifying drugs (DMD), and symptomatic therapy. A large number of randomized clinical trials showed that DMDs reduce relapse rates, decrease the occurrence of new lesions on magnetic resonance imaging (MRI), and reduce disease progression in patients with MS [2,3,4,5,6,7]. Apart from recently introduced oral drugs, first-line DMDs are self-administered parenterally (subcutaneously or intramuscularly) on a regular basis by the patient and are given daily to once weekly, depending on the product

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