Advocating for in-center hemodialysis patients via anonymous survey

• Published in: Medicine (Baltimore) Vol. 101; no. 41; p. e30937
• Main Authors: Rajasekaran, Arun, Prakash, Anand, Hatch, Spencer, Lu, Yan, Cutter, Gary R., Zarjou, Abolfazl
• Format: Journal Article
• Language: English
• Published: United States Lippincott Williams & Wilkins 14.10.2022
• Subjects: Hospice Care; Humans; Observational Study; Palliative Care; Patient Satisfaction; Renal Dialysis - psychology; Surveys and Questionnaires
• ISSN: 1536-5964; 0025-7974; 1536-5964
• DOI: 10.1097/MD.0000000000030937

We conducted an anonymous survey in 9 of our university affiliated outpatient dialysis units to address the concern that many in-center hemodialysis patients may not feel comfortable sharing their experiences. Major goals of this studyInvestigating level of patient satisfaction with their care; Evaluating the subjective perception of the level of understanding of patients regarding pertinent issues of their disease and its management; Identifying potential avenues for care improvement. Survey was conducted in English, paper-based, with answer choices to individual questions for patient satisfaction and education graded using a 5-point Likert scale. Regarding potential areas of improvement, patients were asked to choose as many areas as deemed appropriate. To ensure anonymity, the completed surveys were folded and dropped into a box. Overall, 253 out of 516 (49%) screened patients were eligible and completed the survey. Patients expressed favorable responses regarding satisfaction (mean rating > 4 in each of 14 questions) and education (mean rating > 4 in 8 questions, > 3.5 in 2 questions) regarding hemodialysis. About 62% of overall study participants identified at least one area where they felt additional information would result in improvement of care. Our results indicate that patients undergoing outpatient hemodialysis were overall satisfied and had a good perceptive understanding about their health. Based on the patients’ input, strategies focused on addressing pain and discomfort, privacy, providing information about palliative care/hospice, mental health resources, and the process of kidney transplantation may promote improvement in overall quality of care.