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# There are only two reasons to offer dialysis, and a framework for saying so out loud
- URL: https://nephspace.com/better-conversations-dialysis-decision/
- Published: 2026-11-09T10:59:00.000Z
- Updated: 2026-11-09T11:17:04.000Z
- Description: A JASN perspective names what most of us do instead of having the conversation: we describe the machine. Alongside it, a French qualitative study shows what conservative care looks like when it is actually built.
- Author: Dr Wael Hussein
- Tags: Dialysis, #story, #has-audio, #opinion, #full-story, Stories

**🎧 Listen:** [Weekly · Nov 9](https://nephspace.com/weekly-nov-9/), from 15:04.

Two stories in, you have a trial saying the dialysis-preparation default needs justifying and a scale that tells you who it applies to. Both of them land in the same place: a conversation, in a room, with a frail older patient and probably her daughter.

A JASN perspective from Jane Schell, Margaret Schwarze, Robert Arnold and Alvin Moss argues that we are mostly not having it.

### The thing we do instead

Patients describe the dialysis decision as something that simply happens when the kidneys fail, not as a choice they made. And the authors are specific about the clinician's half of that. We get lost in the technical material and the lab values. We describe what dialysis *does*, which is clean the blood and take the fluid off, instead of what it will mean for this person's life.

That is not a neutral failure. Describing the machinery quietly promises something the machine cannot deliver, which is that this will make her normal again. And offering the options impartially, without ever sharing an informed opinion, is not respect for autonomy. It can walk a patient into a burdensome treatment that was never going to meet her goals.

### The five steps

The framework comes from surgical consent and is written for all kidney replacement choices; here it is applied to long-term dialysis. Start when progression is anticipated, not when it arrives, and bring the care partner in.

**One, show your cards.** Share your inclination. Not a verdict, an opinion: for patients like you we typically do dialysis, or I am worried dialysis may do more harm than good, or there is no right path here and two options to weigh.

**Two, say what dialysis is for.** There are exactly two things on the list. To live longer, and to feel better. Then say which of them you think this patient will actually get. Their own illustration: a 68-year-old with few comorbidities should expect years; a 78-year-old with advanced heart and lung disease and frailty may get weeks to months.

**Three, present the downsides in three forms.** What happens to everyone, meaning access procedures, the time, the transport, the fatigue afterwards. What could happen, meaning access and modality complications, new problems, hospital stays. And the possibility that dialysis falls short of both its goals. Make it modality-specific.

**Four, deliberate.** Open-ended first. Given all this, what are you hoping for? What worries you most? Weigh her tolerance for the burden against the hope of more time, and put conservative management on the table as a real alternative.

**Five, make an agreement and a plan**, accepting that some patients will decide not to decide until something medical forces it.

The closing instruction is the one that keeps this from becoming paternalism: give your professional opinion, and hold your cards loosely.

### The sentence almost nobody says

Step two has a hard edge that is easy to slide past. If dialysis will not give her more time and will not make her feel better, the framework asks you to say exactly that, in plain words. I do not think dialysis will give you more time, and I do not think it will make you feel better.

That is the hardest sentence in nephrology, and it is the one she needs in order to choose anything at all. Hiding in the mechanics is what we do to avoid saying it.

### What the other side of the decision actually looks like

Saying no to dialysis only works if there is something to say yes to. A qualitative study in the same AJKD issue, published by a Lille group, describes a publicly funded home-based conservative kidney management pathway running in Hauts-de-France since 2019 under an experimental reimbursement scheme. Nephrologists refer patients with late stage 4 or stage 5 CKD once a collegial decision against dialysis has been reached, using functional and comorbidity criteria rather than an eGFR threshold.

What patients get is weekly to monthly home visits by specialised nurses, with dietitians, psychologists, social workers and adapted-physical-activity instructors, scaled by functional status, and a coordinating nurse who acts as the pivot between patient, family, nephrologist, primary care and community services, with teleconsultations from the home.

The investigators interviewed 53 people: 12 patients at a median age of 86, 12 informal caregivers, 15 nephrologists and 14 home-care professionals. Patients described declining dialysis as their own firm choice, grounded in age, values and a refusal of dependence. Home care felt seamless rather than intrusive. Nurses described their work as relational rather than technical, and counted small functional gains, walking with a cane again, as success.

Two findings should stay with you. The first is a gap in what patients had been told. One patient said plainly that what he did not know was how it ends when you do not do dialysis, and that no doctor had explained it. Choosing conservative care is not the same as understanding it.

The second is the caregivers. They monitored symptoms, organized everything, and carried a weight the system never counted. One described living with a sword hanging over her head. Families kept protective silences in both directions: patients hid pain from a daughter or a husband who had enough to deal with already, and spoke more freely to the nurse, who had no family ties. Patients without a caregiver were missing from the analysis entirely, which is its own finding.

### The editorial's argument

Barnaby Hole, a co-author of the Lancet trial, and Samantha Gelfand make the structural case. There have always been people for whom dialysis was unwarranted, unwanted or unavailable, and because the disease got conflated with its commonest treatment, those patients became invisible, either pushed to prepare for dialysis or discharged from nephrology altogether.

Their reframing is useful: conservative management as a home therapy, like PD or home haemodialysis, just without the dialysis part. Kidney failure generates multidimensional needs whether or not you treat it with a machine, and a patient should not have to start dialysis in order to see a dietitian or a social worker.

They also flag a risk in the French model's success. The program was not labeled palliative care, which may have made it easier to accept and may also have delayed specialist palliative input for the hardest parts, the complex symptoms and the conversations about dying, leaving the home team exposed. Their three lessons: embed practitioners who coordinate care and unburden families, and support those practitioners too; work out which components are actually essential; and build these services out at scale, the way dialysis and transplant services were once built.

Put the three papers together and the week has an argument. The trial removes the automatic justification for preparing a frail older patient for dialysis. The scale gives you a repeatable way to identify her. The framework gives you the words. And the French program is the honest answer to the question that follows, which is what she gets instead.

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**The source:** Schell JO, Schwarze ML, Arnold RM, Moss AH. J Am Soc Nephrol. 2026;37(11):2571-2573\. With Samyn M-C, et al. Am J Kidney Dis. 2026;88(5):692-703.e1 and Hole B, Gelfand S. Am J Kidney Dis. 2026;88(5):684-686\. [Read the original](https://doi.org/10.1681/ASN.0000001163?ref=nephspace.com)

**🎧 Listen:** [Weekly · Nov 9](https://nephspace.com/weekly-nov-9/), from 15:04.

*Physician-led, AI-assisted. Dr. Wael Hussein chooses every item NephSpace covers and reviews and edits every story before it is published. The first draft was written in our own words with AI (Claude, by Anthropic) from the full texts of the papers and checked against our reading notes; Dr. Hussein then reviewed and edited it. For education and information only, not medical advice. Please talk to your own physician or care team about your health. Clinicians: read the original before changing practice. See our* [*disclaimer*](https://nephspace.com/disclaimer/) *and* [*disclosures*](https://nephspace.com/disclosures/)*. Spotted an error?* [*Tell us*](mailto:hello@nephspace.com?subject=Correction)*.*