Literature DB >> 24613279

Patients' perceptions, attitudes, and experiences about the management of mild-to-moderate ulcerative colitis.

Francesc Casellas1, Daniel Ginard Vicens2, Sabino Riestra Menéndez3, Noelia Alfaro Oliver4.   

Abstract

OBJECTIVE: To establish the perceptions, attitudes, experiences, and satisfaction with clinical management of ulcerative colitis (UC) patients, particularly in aspects related to treatment.
METHODS: A qualitative, descriptive, exploratory study. A discussion group was performed in patients who were in remission according to the criteria of the Mayo index, who had never taken biologics or corticosteroids in the past year. They were selected by: course (mild/moderate), time since onset (under 5 years/ 5 to 9 years/ 10 years or more), follow-up area (primary care [PC]-hospital/PC-specialist care/hospital), treatment (yes/no), UC care unit (yes/no), belongs to patient associations (yes/no) and sex. A descriptive-interpretative content analysis was performed to detect emerging categories, providing them with an explanatory framework.
RESULTS: Diagnostic delay was detected due to lack of clinical suspicion from PC and delayed diagnostic tests. For follow-up, patients prefer care on demand, channeled through remote care, which helps to resolve questions, problems with treatment, or when a relapse occurs, minimizing visits to the hospital. They demand more information, both about UC and treatment. The expectations about treatments are limited, so they mainly requested efficacy and safety.
CONCLUSION: The results suggest the importance of developing strategies to facilitate care on demand and remote care, and to investigate on effective and safe treatments to minimize the detriment to quality of life of patients. These strategies should guarantee fast care and, together with safe and effective treatments, optimize the management of UC patients.
Copyright © 2014 European Crohn's and Colitis Organisation. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Management of the disease; Patient satisfaction; Quality of life; Treatment of the disease; Ulcerative colitis

Mesh:

Year:  2014        PMID: 24613279     DOI: 10.1016/j.crohns.2014.02.013

Source DB:  PubMed          Journal:  J Crohns Colitis        ISSN: 1873-9946            Impact factor:   9.071


  5 in total

1.  Self-assessment of treatment targets in patients with inflammatory bowel disease using a survey.

Authors:  Philipp A Reuken; Philip C Grunert; Andreas Lügering; Niels Teich; Andreas Stallmach
Journal:  Therap Adv Gastroenterol       Date:  2020-11-11       Impact factor: 4.409

Review 2.  Patient Perspectives and Expectations in Inflammatory Bowel Disease: A Systematic Review.

Authors:  Alex Al Khoury; Bhairavi Balram; Talat Bessissow; Waqqas Afif; Lorant Gonczi; Maria Abreu; Peter L Lakatos
Journal:  Dig Dis Sci       Date:  2021-05-21       Impact factor: 3.487

3.  Adapting to ulcerative colitis to try to live a 'normal' life: a qualitative study of patients' experiences in the Midlands region of England.

Authors:  Christel McMullan; Thomas D Pinkney; Laura L Jones; Laura Magill; Dmitri Nepogodiev; Shri Pathmakanthan; Rachel Cooney; Jonathan M Mathers
Journal:  BMJ Open       Date:  2017-08-21       Impact factor: 2.692

4.  Patient-reported healthcare expectations in inflammatory bowel diseases.

Authors:  Valérie Pittet; Carla Vaucher; Florian Froehlich; Michel H Maillard; Pierre Michetti
Journal:  PLoS One       Date:  2018-05-17       Impact factor: 3.240

5.  A qualitative study exploring the health-related quality of life and symptomatic experiences of adults and adolescents with ulcerative colitis.

Authors:  Louise Newton; Jason A Randall; Theresa Hunter; Shannon Keith; Tara Symonds; Roberta J Secrest; Wendy J Komocsar; Sarah E Curtis; Linda Abetz-Webb; Michael Kappelman; April N Naegeli
Journal:  J Patient Rep Outcomes       Date:  2019-10-30
  5 in total

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