Assessment of Patient Experience of Care in Home Dialysis Around the World: Enhancing the Patient’s Voice in Home Dialysis Care and Research

Authors

DOI:

https://doi.org/10.25796/bdd.v4i3.62803

Keywords:

Home dialysis, Peritoneal dialysis, hemodialysis, PREM, PROM, treatment choice, Patient reported outcome, end stage renal disease, quality of life

Abstract

With the global growth in the use of home dialysis modalities, there is a need to better understand patients’ experiences with their home dialysis care.  Patient-reported experience measures or PREMs, are standardized survey questionnaires that allow patients to provide input on processes and experiences of care in a confidential and validated manner.  Until recently, no validated PREM has been available for assessment of patient-reported experience of care for home dialysis modalities, including peritoneal dialysis or home hemodialysis.  The Home Dialysis Care Experience instrument (Home-DCE) is a newly developed and content-valid PREM for use among patients treated with home dialysis modalities.  The survey instrument includes 26 core survey questions and 20 demographic questions, and is now available in English, Spanish, and French.  Domains of care assessed in the Home-DCE include staff education and patient-centered communication, care coordination, patient safety, concern and helpfulness of the care team, and staff care proficiency.  Worldwide use of the Home-DCE will allow incorporation of patients’ experiences and preferences in initiatives to enhance quality of care for home dialysis patients globally.  Translation and deployment of a PREM in additional languages should be done using established cultural adaptation methods, the gold standard for which is termed linguistic validation.  Translation and linguistic validation are hurdles to global use of the Home-DCE, but challenges that should be met to enhance home dialysis patients’ voice in clinical kidney care.

References

Liyanage T, Ninomiya T, Jha V, et al. Worldwide access to treatment for end-stage kidney disease: a systematic review. The Lancet. 2015;385(9981):1975-1982. doi:10.1016/S0140-6736(14)61601-9

Li PK-T, Chow KM, Van de Luijtgaarden MWM, et al. Changes in the worldwide epidemiology of peritoneal dialysis. Nat Rev Nephrol. 2017;13(2):90-103.

Rivara MB, Mehrotra R. The changing landscape of home dialysis in the United States. Curr Opin Nephrol Hypertens. 2014;23(6):586-591.

Karopadi AN, Mason G, Rettore E, Ronco C. Cost of peritoneal dialysis and haemodialysis across the world. Nephrol Dial Transplant. 2013;28(10):2553-2569.

Executive Order on Advancing American Kidney Health. The White House. Accessed July 29, 2019. https://www.whitehouse.gov/presidential-actions/executive-order-advancing-american-kidney-health/

Gura V, Rivara MB, Bieber S, et al. A wearable artificial kidney for patients with end-stage renal disease. JCI Insight. 2016;1(8). Accessed November 26, 2018. https://insight.jci.org/articles/view/86397

Lee DBN, Roberts M. A peritoneal-based automated wearable artificial kidney. Clin Exp Nephrol. 2008;12(3):171-180.

US Centers for Medicare and Medicaid Services: End Stage Renal Disease (ESRD) Quality Initiative. Medicare program; end-stage renal disease prospective payment system and quality incentive program; ambulance fee schedule; durable medical equipment; and competitive acquisition of certain durable medical equipment prosthetics, orthotics and supplies. Final rule. Fed Regist. 2011;76(3):70228-70316.

Veer SN van der, Jager KJ, Visserman E, et al. Development and validation of the Consumer Quality index instrument to measure the experience and priority of chronic dialysis patients. Nephrol Dial Transplant. 2012;27(8):3284-3291.

Kirchgessner J, Perera-Chang M, Klinkner G, et al. Satisfaction with care in peritoneal dialysis patients. Kidney Int. 2006;70(7):1325-1331.

Patient Reported Experience of Kidney Care in the UK 2019. Kidney Care UK & The Renal Association; 2019. Accessed December 5, 2020. https://renal.org/sites/renal.org/files/PREM-report-2019-final-web-copy.pdf

Rivara MB, Edwards T, Patrick D, Anderson L, Himmelfarb J, Mehrotra R. Development and Content Validity of a Patient-Reported Experience Measure for Home Dialysis. Clin J Am Soc Nephrol. 2021;16(4):588-598.

Weidmer BA, Cleary PD, Keller S, et al. Development and evaluation of the CAHPS (Consumer Assessment of Healthcare Providers and Systems) survey for in-center hemodialysis patients. Am J Kidney Dis. 2014;64(5):753-760.

McKown S, Acquadro C, Anfray C, et al. Good practices for the translation, cultural adaptation, and linguistic validation of clinician-reported outcome, observer-reported outcome, and performance outcome measures. J Patient-Rep Outcomes. 2020;4(1):89. doi:10.1186/s41687-020-00248-z

Wild D, Grove A, Martin M, et al. Principles of Good Practice for the Translation and Cultural Adaptation Process for Patient-Reported Outcomes (PRO) Measures: Report of the ISPOR Task Force for Translation and Cultural Adaptation. Value Health. 2005;8(2):94-104.

Published

2021-09-15

How to Cite

1.
Rivara M. Assessment of Patient Experience of Care in Home Dialysis Around the World: Enhancing the Patient’s Voice in Home Dialysis Care and Research. Bull Dial Domic [Internet]. 2021 Sep. 15 [cited 2024 Apr. 18];4(3):151-63. Available from: https://bdd.rdplf.org/index.php/bdd/article/view/62803