Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)

Elena Didenko Pedersen,1,2 Egon Stenager,3,4 JL Vadgaard,5 MB Jensen,6 R Schmid,7 N Meland,8 G Magnussen,9 Jette L Frederiksen10,11 1Akershus University Hospital, Department of Neurology, Loerenskog, Norway; 2Sandvika Nevrosenter, Sandvika, Norway; 3MS Clinic of Southern Jutland, Department of Neur...

Full description

Bibliographic Details
Main Authors: Pedersen ED, Stenager E, Vadgaard JL, Jensen MB, Schmid R, Meland N, Magnussen G, Frederiksen JL
Format: Article
Language:English
Published: Dove Medical Press 2018-04-01
Series:Patient Preference and Adherence
Subjects:
Online Access:https://www.dovepress.com/adherence-to-subcutaneous-interferon-beta-1a-treatment-using-an-electr-peer-reviewed-article-PPA
_version_ 1831645141649063936
author Pedersen ED
Stenager E
Vadgaard JL
Jensen MB
Schmid R
Meland N
Magnussen G
Frederiksen JL
author_facet Pedersen ED
Stenager E
Vadgaard JL
Jensen MB
Schmid R
Meland N
Magnussen G
Frederiksen JL
author_sort Pedersen ED
collection DOAJ
description Elena Didenko Pedersen,1,2 Egon Stenager,3,4 JL Vadgaard,5 MB Jensen,6 R Schmid,7 N Meland,8 G Magnussen,9 Jette L Frederiksen10,11 1Akershus University Hospital, Department of Neurology, Loerenskog, Norway; 2Sandvika Nevrosenter, Sandvika, Norway; 3MS Clinic of Southern Jutland, Department of Neurology, Hospital of Southern Denmark, Odense, Denmark; 4Institute of Regional Research, University of Southern Denmark, Odense, Denmark; 5Department of Neurology, Sjællands University Hospital, Roskilde NeuroCenter, Roskilde, Denmark; 6Department of Neurology, Nordsjaellands Hospital, Hilleroed, Denmark; 7MS Clinic, Department of Neurology, Vejle Hospital, Vejle, Denmark; 8Smerud Medical Research, Oslo, Norway; 9Merck Norway, An Affiliate of Merck AB (Merck AB NUF), Oslo, Norway; 10Department of Neurology, Rigshospitalet Glostrup, Faculty of Health and Medical Science, Glostrup, Denmark; 11Institute of Clinical Medicine, Copenhagen University, Copenhagen, Denmark Background: Disease modifying drugs help control the course of relapsing remitting multiple sclerosis (RRMS); however, good adherence is needed for long-term outcomes.Objective: To evaluate patient adherence to treatment with subcutaneous interferon beta-1a using RebiSmart® and assess injection-site reactions and treatment satisfaction.Methods: This prospective, single-arm, open-label, noninterventional multicenter Phase IV trial included disease modifying drug-experienced mobile patients with RRMS. Adherence was measured over 12 weeks. Items 13–23, 35, 37, and 38 of the Multiple Sclerosis Treatment Concerns Questionnaire (injection-site reactions and treatment satisfaction) were recorded at 12 weeks.Results: Sixty patients were recruited (mean age 43.7 [±SD 7.9] years; 83% female; mean years since multiple sclerosis diagnosis 6.7 [SD 4.5]). Adherence data were obtained in 54 patients only due to technical problems with six devices. Over 12 weeks, 89% (n=48) of patients had ≥90% adherence to treatment. Most patients experienced mild influenza-like symptoms and injection-site reactions, and global side effects were minimal. Most patients (78%) rated the convenience as the most important aspect of the device, and most experienced no or mild pain.Conclusion: RRMS patients treated with subcutaneous interferon beta-1a, administered with RebiSmart, demonstrated generally good adherence, and the treatment was generally well tolerated. Keywords: adherence, multiple sclerosis, relapsing remitting MS, subcutaneous interferon beta-1a, RebiSmart, trial
first_indexed 2024-12-19T13:30:29Z
format Article
id doaj.art-ba6de3766026433ca6b9d37f0feaa6b6
institution Directory Open Access Journal
issn 1177-889X
language English
last_indexed 2024-12-19T13:30:29Z
publishDate 2018-04-01
publisher Dove Medical Press
record_format Article
series Patient Preference and Adherence
spelling doaj.art-ba6de3766026433ca6b9d37f0feaa6b62022-12-21T20:19:23ZengDove Medical PressPatient Preference and Adherence1177-889X2018-04-01Volume 1256957537872Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)Pedersen EDStenager EVadgaard JLJensen MBSchmid RMeland NMagnussen GFrederiksen JLElena Didenko Pedersen,1,2 Egon Stenager,3,4 JL Vadgaard,5 MB Jensen,6 R Schmid,7 N Meland,8 G Magnussen,9 Jette L Frederiksen10,11 1Akershus University Hospital, Department of Neurology, Loerenskog, Norway; 2Sandvika Nevrosenter, Sandvika, Norway; 3MS Clinic of Southern Jutland, Department of Neurology, Hospital of Southern Denmark, Odense, Denmark; 4Institute of Regional Research, University of Southern Denmark, Odense, Denmark; 5Department of Neurology, Sjællands University Hospital, Roskilde NeuroCenter, Roskilde, Denmark; 6Department of Neurology, Nordsjaellands Hospital, Hilleroed, Denmark; 7MS Clinic, Department of Neurology, Vejle Hospital, Vejle, Denmark; 8Smerud Medical Research, Oslo, Norway; 9Merck Norway, An Affiliate of Merck AB (Merck AB NUF), Oslo, Norway; 10Department of Neurology, Rigshospitalet Glostrup, Faculty of Health and Medical Science, Glostrup, Denmark; 11Institute of Clinical Medicine, Copenhagen University, Copenhagen, Denmark Background: Disease modifying drugs help control the course of relapsing remitting multiple sclerosis (RRMS); however, good adherence is needed for long-term outcomes.Objective: To evaluate patient adherence to treatment with subcutaneous interferon beta-1a using RebiSmart® and assess injection-site reactions and treatment satisfaction.Methods: This prospective, single-arm, open-label, noninterventional multicenter Phase IV trial included disease modifying drug-experienced mobile patients with RRMS. Adherence was measured over 12 weeks. Items 13–23, 35, 37, and 38 of the Multiple Sclerosis Treatment Concerns Questionnaire (injection-site reactions and treatment satisfaction) were recorded at 12 weeks.Results: Sixty patients were recruited (mean age 43.7 [±SD 7.9] years; 83% female; mean years since multiple sclerosis diagnosis 6.7 [SD 4.5]). Adherence data were obtained in 54 patients only due to technical problems with six devices. Over 12 weeks, 89% (n=48) of patients had ≥90% adherence to treatment. Most patients experienced mild influenza-like symptoms and injection-site reactions, and global side effects were minimal. Most patients (78%) rated the convenience as the most important aspect of the device, and most experienced no or mild pain.Conclusion: RRMS patients treated with subcutaneous interferon beta-1a, administered with RebiSmart, demonstrated generally good adherence, and the treatment was generally well tolerated. Keywords: adherence, multiple sclerosis, relapsing remitting MS, subcutaneous interferon beta-1a, RebiSmart, trialhttps://www.dovepress.com/adherence-to-subcutaneous-interferon-beta-1a-treatment-using-an-electr-peer-reviewed-article-PPAAdherencemultiple sclerosisrelapsing remitting MSsubcutaneous interferon beta-1aRebiSmart®trial
spellingShingle Pedersen ED
Stenager E
Vadgaard JL
Jensen MB
Schmid R
Meland N
Magnussen G
Frederiksen JL
Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)
Patient Preference and Adherence
Adherence
multiple sclerosis
relapsing remitting MS
subcutaneous interferon beta-1a
RebiSmart®
trial
title Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)
title_full Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)
title_fullStr Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)
title_full_unstemmed Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)
title_short Adherence to subcutaneous interferon beta-1a treatment using an electronic injection device: a prospective open-label Scandinavian noninterventional study (the ScanSmart study)
title_sort adherence to subcutaneous interferon beta 1a treatment using an electronic injection device a prospective open label scandinavian noninterventional study the scansmart study
topic Adherence
multiple sclerosis
relapsing remitting MS
subcutaneous interferon beta-1a
RebiSmart®
trial
url https://www.dovepress.com/adherence-to-subcutaneous-interferon-beta-1a-treatment-using-an-electr-peer-reviewed-article-PPA
work_keys_str_mv AT pedersened adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT stenagere adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT vadgaardjl adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT jensenmb adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT schmidr adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT melandn adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT magnusseng adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy
AT frederiksenjl adherencetosubcutaneousinterferonbeta1atreatmentusinganelectronicinjectiondeviceaprospectiveopenlabelscandinaviannoninterventionalstudythescansmartstudy