Detailed Information on Publication Record
2020
An observational study demonstrating the adherence and ease of use of the injector device, RebiSmart (R)
VALIS, Martin, Jana SARLAKOVA, Simona HALUSKOVA, Blanka KLIMOVA, Pavel POTUZNIK et. al.Basic information
Original name
An observational study demonstrating the adherence and ease of use of the injector device, RebiSmart (R)
Authors
VALIS, Martin (203 Czech Republic), Jana SARLAKOVA (203 Czech Republic), Simona HALUSKOVA (203 Czech Republic), Blanka KLIMOVA (203 Czech Republic), Pavel POTUZNIK (203 Czech Republic), Marek PETERKA (203 Czech Republic), Kamil KUCA (203 Czech Republic), Pavel ŠTOURAČ (203 Czech Republic, belonging to the institution), Jan MARES (203 Czech Republic) and Zbysek PAVELEK (203 Czech Republic)
Edition
EXPERT OPINION ON DRUG DELIVERY, ABINGDON, TAYLOR & FRANCIS LTD, 2020, 1742-5247
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30104 Pharmacology and pharmacy
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.648
RIV identification code
RIV/00216224:14110/20:00116023
Organization unit
Faculty of Medicine
UT WoS
000528167500001
Keywords in English
Multiple Sclerosis; patients; adherence; treatment; use; RebiSmart
Tags
International impact, Reviewed
Změněno: 17/7/2020 09:05, Mgr. Tereza Miškechová
Abstract
V originále
Background: Adherence to Multiple Sclerosis (MS) treatment is considered one of the crucial factors for ensuring optimal clinical outcomes. Research has shown that the use of self-injector devices improves patient compliance with treatment. Therefore, the main purpose of this study is to evaluate the ease of use of RebiSmart (R) 2.0 in clinically isolated syndrome/relapsing-remitting MS patients during 12 months treatment period. Methods: A total number of 290 subjects entered into data collection; 249 (86%) of them completed the whole 12 months study period. The primary endpoints and the secondary endpoints were assessed by the User Study Questionnaire. Adherence data were retrieved from RebiSmart (R) 2.0 (Menu - Dose History) on the respective patient's visit. Outcome measures also included Expanded Disability Status Score, Kurtzke Functional Systems, and Modified Social Support Survey, Modified Social Support Survey-5. Results: This study demonstrated a very high proportion (>95%) of patients with a positive rating of the overall ease of use and the overall convenience of RebiSmart (R). The proportion of patients with a positive rating of the ease of use by individual domains and the functions of RebiSmart (R) were also high (>80%). Conclusion: The findings demonstrate a very good perception of the usability of the device by patients overall and in its individual functions.