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. 2020 Jun;13(3):317-325.
doi: 10.1007/s40271-019-00407-5.

A Qualitative Research for Defining Meaningful Attributes for the Treatment of Inflammatory Bowel Disease from the Patient Perspective

Affiliations

A Qualitative Research for Defining Meaningful Attributes for the Treatment of Inflammatory Bowel Disease from the Patient Perspective

Edouard Louis et al. Patient. 2020 Jun.

Abstract

Introduction: Crohn's disease (CD) and ulcerative colitis (UC) are chronic, inflammatory bowel diseases (IBD). Each class and type of medication available for the treatment of IBD has distinct characteristics and long-term effects that a patient may consider. We present the results of qualitative research that aimed to develop a descriptive framework that outlines the most relevant disease and/or treatment attributes for IBD treatment decisions and focuses on the patient perspective.

Methods: This research employed a three-step approach: a literature review to identify a broad list of attributes, a focus group meeting including patients and clinicians to assess the relevance of the attributes, and two rounds of voting to name and define each attribute. The literature review was used to develop the initial list of attributes. Although the same attributes were defined for both UC and CD, the relative importance of each attribute to UC or CD was considered. The list of attributes was discussed and evaluated in the focus group meeting, which included eight patient representatives and nine gastroenterologists. Using feedback elicited from the focus group meeting, the research team developed a draft of the descriptive framework that grouped the attributes into domain subsets. All members of the focus group participated in two subsequent rounds of structured, online voting, which was used to refine the wording to name and define each attribute. Additionally, participants ranked all the attributes included in the descriptive framework to suggest which attributes were less relevant and could be omitted.

Results: Among 574 publications retrieved from the databases and registries, we identified 32 eligible publications, and an initial list of attributes was developed. This list was refined during the focus group meeting, resulting in a draft descriptive framework of attributes within subsets of domains. The final descriptive framework was developed based on structured rounds of online voting to further refine attribute names and definitions. In the final descriptive framework, a total of ten attributes were identified: abdominal pain, other disease-related pain, bowel urgency, fatigue, risk of cancer and serious infections within the next 10 years, risk of mild to moderate complications, aesthetic complications related to treatment, emotional status, sexual life, and social life and relationships. These attributes were distributed across three domains: efficacy, complications and risk, and health-related quality of life.

Conclusions: Through the identification of the ten most relevant attributes that influence patient decision making for IBD treatments, we developed a descriptive framework that should be considered by physicians when discussing IBD treatment options with their patients. The results of our qualitative research may also be helpful for the development of future IBD clinical studies and quantitative research.

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Conflict of interest statement

E. Louis has received consulting and/or lecture fees from AbbVie, Ferring, MSD, Falk, Takeda, Hospira, Janssen, Pfizer, and Celgene; research grants from Takeda and Pfizer; and educational grants from AbbVie, Takeda, and Janssen; and has served on advisory boards for AbbVie, Ferring, MSD, Takeda, Celgene, Hospira, and Janssen. J.M. Ramos-Goñi has received consulting fees from AbbVie for conducting this research work. However, J.M. Ramos-Goñi does not have any conflict of interest with the results of this research. J. Cuervo has received consulting fees from AbbVie for conducting this research work. However, J. Cuervo does not have any conflict of interest with respect to the results of this research. U. Kopylov has received research grants from Janssen, Takeda, and Medtronic; speaker fees from Janssen, AbbVie, Takeda, MSD, and CTS; and advisory fees from Janssen, AbbVie, and Takeda. M. Barreiro-de Acosta has received financial support from AbbVie for this research. S. McCartney has received consulting, lecturing, or advisory board fees from AbbVie, Ferring, MSD, Falk, Takeda, and Janssen. A. Hart has served as consultant, advisory board member, or speaker for AbbVie, Atlantic, Bristol-Myers Squibb, Celltrion, Falk, Ferring, Janssen, MSD, Napp Pharmaceuticals, Pfizer, Pharmacosmos, Shire, and Takeda. She also serves on the Global Steering Committee for Genentech. G. Rosenfeld has received financial support for research projects and speaking engagements, and consulting fees from several pharmaceutical companies. This support was not anticipated to impact this study. He also received support to enable him to attend the in-person meeting that formed a part of this study. K. Novak has received honoraria from AbbVie for participating in this research. D. Easton and E. Tzur have participated in AbbVie-sponsored research. R. Saldaña has not received any benefit from participating in this study. However, the patient association for which he works has received honoraria from AbbVie. D. Bettenworth is on the advisory board or has been a consultant for AbbVie, Amgen, Falk Foundation, Ferring, MSD, Pharmacosmos, Pfizer, Roche, Takeda, Tillotts Pharma, and Vifor. X. Donnet has received support for travel to meetings for this research study from AbbVie Inc. The non-profit patient association “Association Crohn-RCUH”, for which X. Donnet volunteers (as a Crohn patient), is sponsored by AbbVie, Dr Falk, Ferring, Janssen, Janssens, Pfizer, Takeda, and UCB. K. Protze has received consulting fees from AbbVie for participating in this research. However, K. Protze does not have any conflict of interest with respect to the results of this research. F. Casellas has received research funding from AbbVie, MSD, Shire, Ferring, and Zambon and speaker fees from AbbVie, MSD, Shire, Ferring, Zambon, Gebro, Chiesi, and Takeda. G. Alperovich is an AbbVie employee and may own AbbVie stock and/or options.

Figures

Fig. 1
Fig. 1
Literature flow diagram. *Used as a complementary source to confirm that all the relevant endpoints in clinical investigation had been identified. ISPOR International Society for Pharmacoeconomics and Outcomes Research, NIH National Institutes of Health
Fig. 2
Fig. 2
Frequencies of stated attributes dropped by patients. *Used as a complementary source to confirm that all the relevant endpoints in clinical investigation had been identified

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