For years, the question 'when should dialysis start?' was answered with a number — an eGFR threshold below which a patient was deemed to need it. A landmark trial dismantled that answer. Dialysis is started not when a number is crossed but when the patient develops the symptoms and indications that dialysis exists to treat, and — for the patient with a poor prognosis — only if they choose it over conservative care. The timing question is part evidence and part values, and this chapter holds both.
From a number to symptoms
The old eGFR-threshold approach — start everyone at, say, an eGFR of 10 — was overturned by the IDEAL trial, which randomised patients to an early planned start, at an eGFR of 10 to 14, or a late one, at 5 to 7 or when symptoms demanded, and found no difference in survival or complications between them. Two findings drove the conclusion. First, early initiation bought nothing — no survival, no fewer complications — while committing patients to dialysis sooner. Second, most patients assigned to the late arm actually started before reaching the low threshold, because they developed symptoms that required it. The lesson is that symptoms, not the number, identify the right moment, and that the eGFR is a guide to when symptoms are likely, not a trigger in itself. Dialysis is started when the patient clinically needs it.
The indications that trigger dialysis
If symptoms drive the decision, the clinician must know which ones. The indications to start are the manifestations of kidney failure that dialysis treats: uraemic symptoms — nausea, anorexia, vomiting, fatigue, pruritus, restless legs, and, more severely, encephalopathy, pericarditis, or bleeding; refractory fluid overload that medical therapy can no longer control; refractory hyperkalaemia or metabolic acidosis; a declining nutritional state attributable to uraemia; and the general failure of conservative measures to keep the patient well. These are clinical triggers, and when they appear and cannot be managed otherwise, they indicate dialysis regardless of the exact eGFR. In practice most patients reach this point around an eGFR of 6 to 10, but the eGFR is the company the indications keep, not the indication itself — an asymptomatic patient at eGFR 9 does not need dialysis, while a symptomatic one at eGFR 11 may.
Neither too early nor too late
The timing has two failure modes. Starting too early — on the number, before symptoms — is the error IDEAL exposed: it confers no benefit, brings forward the burden and dependence of dialysis, and exposes the patient to its complications sooner, for nothing gained. This mirrors the acute lesson from the AKI volume, where accelerated initiation also failed to help. Starting too late — letting symptoms build into a uraemic emergency — is the opposite error, risking encephalopathy, pericarditis, severe overload, and the crash start the access and pathway chapters worked to prevent. The target is the middle: watchful monitoring as the patient approaches kidney failure, with a prompt, planned start when the indications appear — the same watchful-waiting-with-prompt-initiation logic as acute dialysis, applied over months rather than days.
What is effective care, and what is the patient's
As in the other equipoise chapters, the timing question divides into what is clinically determined and what depends on values. Some elements are effective care: an emergent indication — severe refractory hyperkalaemia, uraemic pericarditis — mandates starting now, not later, and the symptom triggers themselves are clinical judgements about when dialysis is needed. But two elements are genuinely preference-sensitive. The first is the exact moment of starting within the symptom-guided window: as symptoms gather, how much the patient is willing to tolerate before beginning, weighed against their readiness and quality of life, is theirs to decide. The second, and larger, is whether to start dialysis at all — the choice between dialysis and conservative kidney management, which for a frail or poor-prognosis patient is a values decision belonging to them, developed in the conservative-care and frailty chapters. Keeping these apart — the clinical triggers from the values-laden timing and the whether — is the discipline of the chapter.
Preserving residual function and the incremental start
Residual kidney function — the urine output and clearance a patient retains as they start dialysis — is valuable: it contributes to solute and fluid clearance, eases the dialysis prescription, and is associated with better outcomes, so it is worth preserving. This underpins the incremental start: rather than beginning every patient on a full, thrice-weekly haemodialysis or full peritoneal dose, a suitable patient with meaningful residual function can begin with a reduced dose — twice-weekly haemodialysis, or a lower peritoneal dialysis dose — that supplements rather than replaces their own kidneys, reducing treatment burden while residual function lasts. Incremental dialysis requires careful monitoring of that residual function so the dose is increased as it declines, and it is not for everyone, but it reflects the principle that dialysis should do what the patient's kidneys cannot, no more, and that the transition onto it can be gradual. It also fits the symptom-guided philosophy: start with what is needed, when it is needed.
Integrating timing with the rest of the pathway
Timing does not stand alone; it is the moment the preparation of the previous chapters pays off. A symptom-driven start works well only if the patient has already chosen a modality and has working access ready, so that when the indications appear, dialysis begins electively on the planned modality rather than urgently through a catheter. This is why the predialysis pathway times preparation by risk and creates access months ahead: not to start dialysis early, but to be ready to start it promptly and well when symptoms call for it. And the timing conversation flows into, or away from, the conservative-care decision — some patients, asked when they want to start, will be asking whether they want to at all. The chapter's scripts handle both the 'when' and the 'whether,' and the answer to each belongs, ultimately, to the patient.
Where the evidence is firm, and where values govern
The firm part is IDEAL's conclusion: early initiation confers no benefit, so dialysis is started on symptoms and indications, not an eGFR threshold — grade-A evidence that reshaped practice. The value of residual function and the rationale for incremental dialysis are well supported, if still being refined. What evidence cannot settle is the exact moment within the symptom-guided window, or whether a given patient should start at all rather than choose conservative care — because those turn on the patient's values, readiness, and prognosis. So the clinician's role is to apply the IDEAL lesson firmly (no early start on the number), to recognise the clinical triggers, to preserve residual function, and then to share the timing and the whether with the patient. The proper close is a start that is symptom-driven, prepared, and chosen.