Remote follow-up based on patient-reported outcomes in patients with chronic kidney disease: A qualitative study of patient perspectives
暂无分享,去创建一个
N. Hjollund | P. Ivarsen | A. de Thurah | Caroline Trillingsgaard Mejdahl | B. E. Grove | Liv Marit Valen Schougaard | N. H. Hjollund | B. Grove
[1] Imogen Ramsey,et al. Patients’ experiences and perspectives of patient-reported outcome measures in clinical care: A systematic review and qualitative meta-synthesis , 2022, PloS one.
[2] N. Thomas,et al. Patient perspectives and experiences of remote consultations in people receiving kidney care: A scoping review , 2022, Journal of renal care.
[3] A. Bygholm,et al. The association between patient-reported outcomes (PROs) and patient participation in chronic care: A scoping review. , 2022, Patient education and counseling.
[4] E. Gordon,et al. Perceptions of Telehealth vs In-Person Visits Among Older Adults With Advanced Kidney Disease, Care Partners, and Clinicians , 2021, JAMA network open.
[5] N. Hjollund,et al. Patient-reported outcome measures for clinical decision-making in outpatient follow-up: validity and reliability of a renal disease questionnaire , 2021, Journal of Patient-Reported Outcomes.
[6] P. Bower,et al. Routine provision of feedback from patient-reported outcome measurements to healthcare providers and patients in clinical practice. , 2021, The Cochrane database of systematic reviews.
[7] R. de Vries,et al. Adherence to Telemonitoring by Electronic Patient-Reported Outcome Measures in Patients with Chronic Diseases: A Systematic Review , 2021, International journal of environmental research and public health.
[8] M. King,et al. Perceived benefits and limitations of using patient-reported outcome measures in clinical practice with individual patients: a systematic review of qualitative studies , 2021, Quality of Life Research.
[9] L. Kayser,et al. Patient perspectives on digital patient reported outcomes in routine care of inflammatory bowel disease , 2021, Journal of Patient-Reported Outcomes.
[10] A. Bokolo,et al. Application of telemedicine and eHealth technology for clinical services in response to COVID‑19 pandemic , 2021, Health and technology.
[11] A. Bello,et al. Video Visits Using the Zoom for Healthcare Platform for People Receiving Maintenance Hemodialysis and Nephrologists: A Feasibility Study in Alberta, Canada , 2021, Canadian journal of kidney health and disease.
[12] D. Cadilhac,et al. Feedback of patient-reported outcomes to healthcare professionals for comparing health service performance: a scoping review , 2020, BMJ Open.
[13] T. Jafar,et al. Perceived barriers and facilitators to chronic kidney disease care among patients in Singapore: a qualitative study , 2020, BMJ Open.
[14] M. Carolan,et al. Web-Based Patient-Reported Outcome Measures for Personalized Treatment and Care (PROMPT-Care): Multicenter Pragmatic Nonrandomized Trial , 2020, Journal of medical Internet research.
[15] S. Ackerman,et al. Comparing Patients’ Experiences with Electronic and Traditional Consultation: Results from a Multisite Survey , 2020, Journal of General Internal Medicine.
[16] A. Coulter,et al. Satisfaction with care and adherence to treatment when using patient reported outcomes to individualize follow-up care for women with early breast cancer – a pilot randomized controlled trial , 2020, Acta oncologica.
[17] N. Hjollund,et al. Patient-reported outcome measures in the interaction between patient and clinician – a multi-perspective qualitative study , 2020, Journal of Patient-Reported Outcomes.
[18] Joanne Greenhalgh,et al. How do patient reported outcome measures (PROMs) support clinician-patient communication and patient care? A realist synthesis , 2018, Journal of Patient-Reported Outcomes.
[19] S. Thorne,et al. PRO-based follow-up as a means of self-management support – an interpretive description of the patient perspective , 2018, Journal of Patient-Reported Outcomes.
[20] K. Lomborg,et al. Experiences With Telehealth Followup in Patients With Rheumatoid Arthritis: A Qualitative Interview Study , 2018, Arthritis care & research.
[21] S. N. van der Veer,et al. Incorporating patient-reported symptom assessments into routine care for people with chronic kidney disease , 2017, Clinical kidney journal.
[22] E. Larson,et al. Unraveling the meaning of patient engagement: A concept analysis. , 2017, Patient education and counseling.
[23] E. M. Castro,et al. Patient empowerment, patient participation and patient-centeredness in hospital care: A concept analysis based on a literature review. , 2016, Patient education and counseling.
[24] N. Hjollund,et al. Use of patient-reported outcomes in outpatient settings as a means of patient involvement and self-management support – a qualitative study of the patient perspective , 2016 .
[25] Per Sidenius,et al. AmbuFlex: tele-patient-reported outcomes (telePRO) as the basis for follow-up in chronic and malignant diseases , 2016, Quality of Life Research.
[26] 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.
[27] Erik Riiskjær,et al. Use of Patient-Reported Outcome (PRO) Measures at Group and Patient Levels: Experiences From the Generic Integrated PRO System, WestChronic , 2014, Interactive journal of medical research.
[28] David Feeny,et al. Framework to assess the effects of using patient-reported outcome measures in chronic care management , 2014, Quality of Life Research.
[29] C. Douglas,et al. Symptom burden in chronic kidney disease: a review of recent literature. , 2013, Journal of renal care.
[30] Sandy Oliver,et al. Using qualitative evidence on patients’ views to help understand variation in effectiveness of complex interventions: a qualitative comparative analysis , 2013, Trials.
[31] J. Hibbard,et al. What the evidence shows about patient activation: better health outcomes and care experiences; fewer data on costs. , 2013, Health affairs.
[32] Christiane,et al. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. , 2013, JAMA.
[33] G. Velikova,et al. How do doctors refer to patient-reported outcome measures (PROMS) in oncology consultations? , 2013, Quality of Life Research.
[34] Monika Alise Johansen,et al. Electronic Symptom Reporting Between Patient and Provider for Improved Health Care Service Quality: A Systematic Review of Randomized Controlled Trials. Part 1: State of the Art , 2012, Journal of medical Internet research.
[35] Josef Coresh,et al. Chronic kidney disease , 2012, The Lancet.
[36] J. Hibbard,et al. Why Does Patient Activation Matter? An Examination of the Relationships Between Patient Activation and Health-Related Outcomes , 2012, Journal of General Internal Medicine.
[37] R. Emerson,et al. Writing Ethnographic Fieldnotes, Second Edition , 2011 .
[38] A. Carr,et al. The routine use of patient reported outcome measures in healthcare settings , 2010, BMJ : British Medical Journal.
[39] A. Bottomley,et al. Patient-reported outcomes: assessment and current perspectives of the guidelines of the Food and Drug Administration and the reflection paper of the European Medicines Agency. , 2009, European journal of cancer.
[40] P. Sainsbury,et al. Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups. , 2007, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[41] U. S. Department of Health and Human Services FDA Cen Research,et al. Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance , 2006, Health and quality of life outcomes.
[42] V. Braun,et al. Using thematic analysis in psychology , 2006 .
[43] Ethan M Balk,et al. Erratum: National Kidney Foundation practice guidelines for chronic kidney disease: Evaluation, classification, and stratification (Annals of Internal Medicine (2003) 139 (137-147)) , 2003 .
[44] K. Malterud. Qualitative research: standards, challenges, and guidelines , 2001, The Lancet.
[45] S. Thorne,et al. Interpretive description: a noncategorical qualitative alternative for developing nursing knowledge. , 1997, Research in nursing & health.
[46] Joane Nagel,et al. Constructing Ethnicity: Creating and Recreating Ethnic Identity and Culture , 1994 .