A qualitative inquiry into patients’ perspectives on individualized priorities for treatment outcomes in inflammatory bowel diseases
Author:
Funder
Crohn's and Colitis Foundation
Publisher
Springer Science and Business Media LLC
Subject
Public Health, Environmental and Occupational Health
Link
https://link.springer.com/content/pdf/10.1007/s11136-020-02492-8.pdf
Reference28 articles.
1. Farrell, D., McCarthy, G., & Savage, E. (2016). Self-reported symptom burden in individuals with inflammatory bowel disease. Journal of Crohn's and Colitis, 10(3), 315–322. https://doi.org/10.1093/ecco-jcc/jjv218.
2. IsHak, W. W., Pan, D., Steiner, A. J., Feldman, E., Mann, A., Mirocha, J., et al. (2017). Patient-reported outcomes of quality of life, functioning, and GI/psychiatric symptom severity in patients with inflammatory bowel disease (IBD). Inflammatory Bowel Diseases, 23(5), 798–803. https://doi.org/10.1097/MIB.0000000000001060.
3. Porter, M. E., & Lee, T. H. (2013). The strategy that will fix health care. Harvard Business Review, 91(12), 24–24.
4. Nelson, E. C., Dixon-Woods, M., Batalden, P. B., Homa, K., Van Citters, A. D., Morgan, T. S., et al. (2016). Patient focused registries can improve health, care, and science. BMJ, 354, i3319.
5. Association, A. D. (2004). The breakthrough series: IHI’s collaborative model for achieving breakthrough improvement. Diabetes Spectrum, 17(2), 97–101.
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