Nephrologists Should Voluntarily Divulge Survival Data to Potential Dialysis Patients: A Questionnaire Study
Abstract
Background: For many dialysis patients, survival is no different than with certain cancers. Yet, it appears that most nephrologists do not give detailed information about survival prior to obtaining informed consent for chronic dialysis. There are no published data on whether patients wish to be so informed. Objective: To assess whether patients would want voluntary disclosure by their physician of their survival should they need dialysis, and if so, why? Method: A questionnaire was completed by 100 general nephrology patients during their first visit to a nephrologist. Results: The vast majority of patients (97%) would want to be given life-expectancy information, and for the physician to do so without having to be prompted. Furthermore, the majority of patients would want as much information as possible, both good and bad. Conclusions: Virtually all patients want, and therefore should receive from their physician, prognostic information about dialysis to facilitate informed decision-making. This is in accordance with current practice guidelines.
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Several studies show that older dialysis patients retain their mental quality of life.
“In several studies, although physical aspects of quality of life are reduced compared with younger ESRD patients or healthy elderly, mental aspects of quality of life are preserved [22,23].”
From Should there be an expanded role for palliative care in end-stage renal disease? (2010) · cites this paper as [23]
Quality-of-life studies in older chronic dialysis patients suggest that dialysis is not always unsatisfactory for older people.
“studies of quality of life in elderly patients receiving chronic dialysis offer reason to believe that dialysis therapy is not uniformly unsatisfactory in the elderly.”
From Should there be an expanded role for palliative care in end-stage renal disease? (2010) · cites this paper as [23]
Several studies show that older dialysis patients have lower physical quality of life than younger ESRD patients or healthy older adults.
“In several studies, although physical aspects of quality of life are reduced compared with younger ESRD patients or healthy elderly, mental aspects of quality of life are preserved [22,23].”
From Should there be an expanded role for palliative care in end-stage renal disease? (2010) · cites this paper as [23]
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- Authors
- Fine, A., Fontaine, B., Kraushar, M. M., & Rich, B. R.
- Affiliations
- University of Manitoba (CA)
- Corresponding author
- Fine, Adrian
- Venue
- Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis
- Publisher
- SAGE Publications
- Published
- 2005-05
- Volume
- 25
- Issue
- 3
- Pages
- 269-273
- ISSN
- 0896-8608 (ISSN-L)
- 1718-4304
- OpenAlex
- W2188945950
- Cited by
- 84
- References
- 17
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 1 · 2023: 1 · 2022: 5 · 2021: 1 · 2020: 1 · 2019: 6 · 2018: 2 · 2017: 7 · 2016: 4 · 2015: 7 · 2014: 4 · 2013: 10 · 2012: 8
- FWCI
- 2.09
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Peritoneal Dialysis International (publishedVersion)
- PubMed (publishedVersion)
- DigitalGeorgetown (Georgetown University Library) (submittedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
- Health Sciences › Medicine › Nephrology › Dialysis and Renal Disease Management
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics and bioethics in healthcare
- Keywords
- dialysis, survival prediction, informed consent, patient preferences, nephrologists, end-stage renal disease, prognostic information, informed decision-making, physician-patient communication
- MeSH terms
- Aged, Female, Renal Dialysis, Humans, Kidney Diseases, Life Expectancy, Male, Middle Aged, Patient Participation, Physician-Patient Relations, Quality of Life, Surveys and Questionnaires, Truth Disclosure, Cohort Studies
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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