Crohn's Disease Patient Experiences and Preferences With Disease Monitoring: An International Qualitative Study

被引:6
|
作者
Rohatinsky, Noelle [1 ,10 ]
Zelinsky, Sandra [2 ]
Dolinger, Michael [3 ]
Christensen, Britt [4 ,5 ]
Wilkens, Rune [6 ,7 ]
Radford, Shellie [8 ]
Dubinsky, Marla [3 ]
Novak, Kerri [9 ]
Int Bowel Ultrasound Grp IBUS
机构
[1] Univ Saskatchewan, Coll Nursing, Saskatoon, SK, Canada
[2] Univ Calgary, Calgary, AB, Canada
[3] Icahn Sch Med Mt Sinai, Div Pediat Gastroenterol, New York, NY USA
[4] Royal Melbourne Hosp, Dept Gastroenterol, Parkville, Vic, Australia
[5] Univ Melbourne Med, Parkville, Vic, Australia
[6] Copenhagen Univ Hosp, Div Med, Gastrounit, Copenhagen, Denmark
[7] Univ Copenhagen, Hvidovre Hosp, Copenhagen Ctr Inflammatory Bowel Dis Children Ado, Copenhagen, Denmark
[8] Nottingham Univ Hosp NHS Trust, Nottingham Biomed Res Ctr & Clin Res Facil, Queens Med Ctr, Nottingham, England
[9] Univ Calgary, Dept Med, Div Gastroenterol, Calgary, AB, Canada
[10] Univ Saskatchewan, Coll Nursing, 104 Clin Pl,4342 Hlth Sci, Saskatoon, SK S7N 5E5, Canada
关键词
Crohn's disease; disease monitoring; patient-oriented research; qualitative research; INFLAMMATORY-BOWEL-DISEASE; SHARED DECISION-MAKING; ULTRASONOGRAPHY; COMPLICATIONS; ENTEROGRAPHY;
D O I
10.1093/crocol/otad012
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Lay Summary This study used group interviews to understand patient experiences and preferences of Crohn's disease monitoring. Study results can be used to inform monitoring strategies, improve patient engagement, and optimize a patient-centered approach to care. Background Strategies incorporating objective disease monitoring in Crohn's disease (CD), beyond clinical symptoms are important to improve patient outcomes. Little evidence exists to explore patient understanding of CD treatment goals, nor preferences and experiences with monitoring options. This qualitative study aimed to explore patient experiences and preferences of CD monitoring to inform monitoring strategies, improve patient engagement, and optimize a patient-centered approach to care. Methods This study used a patient-oriented, qualitative descriptive design. Convenience and snowball sampling were used to recruit adult participants diagnosed with CD who had experience with at least 2 types of disease monitoring. Online focus groups were conducted and data were analyzed using thematic analysis. Results This international study included 37 participants from Australia, Canada, United Kingdom, and the United States. Overall, participants preferred more noninvasive types of monitoring [eg, intestinal ultrasound (IUS)] but were willing to undergo more invasive monitoring (eg, colonoscopy) if required. To improve disease monitoring, participants wanted increased access to IUS, establishment of a patient-centered interdisciplinary team and access to information and self-testing. Participants identified challenges with communication between patients and providers and stressed the importance of participating in shared decision making and being equal team members in their care. Conclusions It is imperative to incorporate patient-driven preferences into how we can best structure monitoring strategies, to ensure equitable access to those preferred modalities and embrace a shared decision-making approach to disease management in CD.
引用
收藏
页数:11
相关论文
共 50 条
  • [41] Aspecific ileitis: Crohn’s disease or not Crohn’s disease? A prospective study
    Cristina Bezzio
    Ilaria Arena
    Massimo Devani
    Barbara Omazzi
    Gianpiero Manes
    Simone Saibeni
    International Journal of Colorectal Disease, 2017, 32 : 1025 - 1028
  • [42] Aspecific ileitis: Crohn's disease or not Crohn's disease? A prospective study
    Bezzio, Cristina
    Arena, Ilaria
    Devani, Massimo
    Omazzi, Barbara
    Manes, Gianpiero
    Saibeni, Simone
    INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2017, 32 (07) : 1025 - 1028
  • [43] Patient perspectives on symptoms and impacts in Crohn's disease: Results from qualitative research
    Gibble, T. H.
    Kosa, K.
    Basnyat, B.
    Martin, S.
    Moses, R.
    Dubinsky, M.
    JOURNAL OF CROHNS & COLITIS, 2024, 18 : I1265 - I1266
  • [44] Patient's Perspective on Disease Burden, Remission Definition, and Symptoms Associated With Treatment Seeking: A Qualitative Study in Adult and Adolescent Patients With Crohn's Disease
    Kitchen, Helen
    Farrar, Mallory
    Al-zubeidi, Tamara
    Pegram, Hannah
    Hunter, Theresa
    Naegeli, April N.
    Delbecque, Laure
    Jairath, Vipul
    CROHNS & COLITIS 360, 2020, 2 (02)
  • [45] A rare case of thromboembolic disease in a patient with Crohn's disease
    Hutchinson, Daryl S.
    Dahche, Tarek
    Mutchnick, Milton G.
    Siddiqui, Firdous A.
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (09): : S423 - S423
  • [46] Linear IgA bullous disease in a patient with Crohn's disease
    Torres, T.
    Sanches, M.
    Selores, M.
    ACTA DERMATOVENEROLOGICA ALPINA PANNONICA ET ADRIATICA, 2010, 19 (01): : 29 - 31
  • [47] Exercise Perceptions and Experiences in Adults With Crohn's Disease Following a Combined Impact and Resistance Training Program: A Qualitative Study
    Jones, Katherine
    Naisby, Jenni
    Baker, Katherine
    Tew, Garry A.
    CROHNS & COLITIS 360, 2023, 5 (02)
  • [48] Crohn's disease experiences among a paediatric population: A qualitative study reviewing the agreement of symptoms discussed by children and adolescents
    Coskun, U.
    Kelly, K.
    Hunter, T.
    Newton, L.
    Symonds, T.
    Delbecque, L.
    JOURNAL OF CROHNS & COLITIS, 2020, 14 : S254 - S254
  • [49] A QUALITATIVE STUDY OF THE PATIENT EXPERIENCE OF PAIN AND PAIN-RELATED FUNCTIONAL IMPACTS SPECIFIC TO CROHN'S DISEASE
    Skalicky, Anne
    Gleeson, Sara
    Naegeli, April
    Kleinman, Leah
    INFLAMMATORY BOWEL DISEASES, 2018, 24 : S4 - S4
  • [50] A qualitative study to explore symptoms and impacts of pediatric and adolescent Crohn’s disease from patient and caregiver perspective
    Louise Newton
    Laure Delbecque
    Ufuk Coşkun
    Tara Symonds
    Jennifer Clegg
    Theresa Hunter
    Journal of Patient-Reported Outcomes, 5