Integrated care pathways for cancer survivors – a role for patient-reported outcome measures and health informatics
暂无分享,去创建一个
[1] L. Staetsky,et al. The health and well-being of cancer survivors in the UK: findings from a population-based survey , 2011, British Journal of Cancer.
[2] M. Hampshire,et al. Patient reported late effects of gynecological cancer treatment. , 2012, Gynecologic oncology.
[3] Joanne Greenhalgh,et al. Implementing patient-reported outcomes assessment in clinical practice: a review of the options and considerations , 2012, Quality of Life Research.
[4] D. Berwick. The science of improvement. , 2008, JAMA.
[5] Roma Maguire,et al. What is the value of the routine use of patient-reported outcome measures toward improvement of patient outcomes, processes of care, and health service outcomes in cancer care? A systematic review of controlled trials. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[6] I. Higginson,et al. Implementing patient reported outcome measures (PROMs) in palliative care - users' cry for help , 2011, Health and quality of life outcomes.
[7] G. Velikova,et al. How do doctors refer to patient-reported outcome measures (PROMS) in oncology consultations? , 2013, Quality of Life Research.
[8] E. Maher. Managing the consequences of cancer treatment and the English National Cancer Survivorship Initiative , 2013, Acta oncologica.
[9] R. Grol,et al. Integrated care programmes for chronically ill patients: a review of systematic reviews. , 2005, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[10] C. Earle,et al. Associations among cancer survivorship discussions, patient and physician expectations, and receipt of follow-up care. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[11] L. Batehup,et al. Towards a personalised approach to aftercare: a review of cancer follow-up in the UK , 2011, Journal of cancer survivorship : research and practice.
[12] D. Forman,et al. Integrating cancer survivors' experiences into UK cancer registries: design and development of the ePOCS system (electronic Patient-reported Outcomes from Cancer Survivors) , 2011, British Journal of Cancer.
[13] Amy P Abernethy,et al. Supporting clinical practice decisions with real-time patient-reported outcomes. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[14] Martin Knapp,et al. Exploring barriers to participation and adoption of telehealth and telecare within the Whole System Demonstrator trial: a qualitative study , 2012, BMC Health Services Research.
[15] J. Coebergh,et al. The Patient Reported Outcomes Following Initial treatment and Long term Evaluation of Survivorship registry: scope, rationale and design of an infrastructure for the study of physical and psychosocial outcomes in cancer survivorship cohorts. , 2011, European journal of cancer.
[16] P. Selby,et al. Patients report improvements in continuity of care when quality of life assessments are used routinely in oncology practice: secondary outcomes of a randomised controlled trial. , 2010, European journal of cancer.
[17] G. Lyman,et al. Screening, assessment, and management of fatigue in adult survivors of cancer: an American Society of Clinical oncology clinical practice guideline adaptation. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[18] Deborah Schrag,et al. Feasibility of long-term patient self-reporting of toxicities from home via the Internet during routine chemotherapy. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[19] Peter Bower,et al. Support for self care for patients with chronic disease , 2007, BMJ : British Medical Journal.
[20] A. Bezjak,et al. Cancer patients' preferences for communicating clinical trial quality of life information: A qualitative study , 2003, Quality of Life Research.
[21] Peter Murchie,et al. Using technology to deliver cancer follow-up: a systematic review , 2014, BMC Cancer.
[22] D Brewster,et al. Cancer prevalence in the United Kingdom: estimates for 2008 , 2009, British Journal of Cancer.
[23] Galina Velikova,et al. Measuring quality of life in routine oncology practice improves communication and patient well-being: a randomized controlled trial. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[24] David Forman,et al. Integrating Patient Reported Outcomes With Clinical Cancer Registry Data: A Feasibility Study of the Electronic Patient-Reported Outcomes From Cancer Survivors (ePOCS) System , 2013, Journal of medical Internet research.
[25] R. DeRubeis,et al. Screening, assessment, and care of anxiety and depressive symptoms in adults with cancer: an American Society of Clinical Oncology guideline adaptation. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[26] A. Abernethy,et al. PCN122 DEVELOPMENT OF THE PATIENT-REPORTED VERSION OF THE COMMON TERMINOLOGY CRITERIA FOR ADVERSE EVENTS (PRO-CTCAE) , 2010 .
[27] Richard Jones,et al. Management of cancer pain in the community: Perceptions of current UK information technology systems and implications for future development , 2012, Health Informatics J..
[28] T. Skolarus,et al. American Cancer Society prostate cancer survivorship care guidelines , 2014, CA: a cancer journal for clinicians.
[29] C. Gotay,et al. Exercise interventions on health-related quality of life for cancer survivors. , 2012, The Cochrane database of systematic reviews.
[30] P. Selby,et al. Impact of patient-reported outcomes in oncology: a longitudinal analysis of patient-physician communication. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[31] R. Grol,et al. Personal paper: Beliefs and evidence in changing clinical practice , 1997 .
[32] Elizabeth Ercolano,et al. Self‐management: Enabling and empowering patients living with cancer as a chronic illness , 2011, CA: a cancer journal for clinicians.
[33] V. Lemmens,et al. Quantifying fatigue in (long-term) colorectal cancer survivors: a study from the population-based patient reported outcomes following initial treatment and long term evaluation of survivorship registry. , 2013, European journal of cancer.
[34] A. Bryant,et al. Patient-reported outcome measures for follow-up after gynaecological cancer treatment. , 2013, The Cochrane database of systematic reviews.
[35] M. Swan. Emerging Patient-Driven Health Care Models: An Examination of Health Social Networks, Consumer Personalized Medicine and Quantified Self-Tracking , 2009, International journal of environmental research and public health.