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The Patient and Clinician Assessment of Gastrointestinal (GI) Related Adverse Events Associated with Oral Disease-Modifying Therapies in Multiple Sclerosis: A Qualitative Study by Farah Jivraj; Sha Kang; Scott Reedie; Shivani Kapadia; Sara Strzok; Emma Elliott; Stefan Cano; Marvin Rock is a Medicine article available to read on EtoBox.

What is The Patient and Clinician Assessment of Gastrointestinal (GI) Related Adverse Events Associated with Oral Disease-Modifying Therapies in Multiple Sclerosis: A Qualitative Study about?

## Introduction Current guidelines for relapsing-remitting multiple sclerosis (RRMS) call for treatment with disease-modifying therapies (DMTs) early in the disease to prevent relapses and accumulation of neurologic impairment and disability. However, patients taking certain oral DMTs may experience gastrointestinal (GI)-related adverse events (AEs), particularly at dose titration. We conducted qualitative research with healthcare professionals (HCPs) and patients in Canada to contextualize their experiences with three oral DMTs: dimethyl fumarate (Tecfidera^®^), fingolimod (Gilenya^®^), and teriflunomide (Aubagio^®^). The objectives of this study were to (1) gather qualitative data to better understand the patient and HCP experience of GI AEs in oral MS DMT treatment in Canada and (2) determine to what extent two patient-reported outcome (PRO) instruments used in recent oral DMT trials capture what is important to patients regarding GI AEs in oral MS DMT treatment (content validity) and to provide qualitative data to help interpret PRO scores. ## Methods This was a qualitative, non-interventional, descriptive, cross-sectional study comprising HCP and patient interviews conducted i

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Author
Farah Jivraj; Sha Kang; Scott Reedie; Shivani Kapadia; Sara Strzok; Emma Elliott; Stefan Cano; Marvin Rock
Publisher
Springer Science and Business Media LLC
Published
2022
Language
EN
Field
Medicine (Health Sciences)

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