10

HEMODIALYSIS & EXTRACORPOREAL THERAPY

Chapter 10

Dialysis Adequacy & Kt/V

Beyond the Number

Orientation & KnowledgeVisualise & MapClinical ReasoningSafety & EvidencePatient DecisionsApply & Test
Chapter Preamble

This preamble records the dynamic decisions the master makes for this chapter.

Signals declared

  • Sig-D diagnostic (primary) — the chapter measures and interprets the delivered dialysis dose.
  • Sig-V evidence-dense — dose targets and their limits rest on randomised evidence.

Levels populated and omitted

  • Eighteen levels are built — a measurement-and-evidence chapter.
  • Omitted: L6 concept maps and L9 implications triads — no mechanistic-physiology signal (clearance physics lives in the prescription chapter). L15 and L16 — adequacy assessment is effective-care, not preference-sensitive.
  • Included by author decision (L17, optional-dynamic): an adequacy review produces a real chart note, which is the framework's true inclusion test for documentation.
Phase A Orientation & Knowledge
01
Phase A · Level 1

Learning Objectives

The contract between this chapter and the reader.

  1. 1. Define adequacy as more than a single dose number.
  2. 2. Calculate and interpret the urea reduction ratio and single-pool Kt/V.
  3. 3. Explain post-dialysis urea rebound and equilibrated Kt/V.
  4. 4. Use standard weekly Kt/V to compare dose across frequencies.
  5. 5. Sample post-dialysis blood correctly.
  6. 6. Incorporate residual kidney function into the delivered dose.
  7. 7. Apply dose targets without shortening time to meet them.
  8. 8. Recognise what Kt/V does not measure.
  9. 9. Construct an adequacy-assessment schedule and act on it.
02
Phase A · Level 2

Executive Summary

A sixty-second reading. Each bullet stands alone.

  • Adequacy is euvolemia, clearance, nutrition, mineral-bone health, symptoms, and survival together — not a single number.
  • Small-solute dose is a minimum to clear, not the goal of dialysis.
  • The urea reduction ratio is (pre minus post) over pre; the usual minimum is at least 65%.
  • Single-pool Kt/V is derived from pre- and post-dialysis urea, time, and ultrafiltration; the minimum is about 1.2 per session, often targeted near 1.4.
  • After dialysis, urea rebounds from tissues into blood, so equilibrated Kt/V — about 0.2 lower — reflects the true dose better.
  • Standard weekly Kt/V allows dose to be compared fairly across different frequencies.
  • Correct post-dialysis sampling (a slow-flow or stop-pump method) is essential; sloppy sampling falsely inflates the dose.
  • Residual kidney clearance adds to dose and can justify a lower prescribed dose or incremental HD when substantial.
  • Do not shorten treatment time just because a Kt/V target is met — time has value beyond small-solute clearance.
  • Kt/V measures urea only; it captures nothing about middle molecules, phosphate, volume, or blood pressure.
  • Randomised evidence shows a higher dose does not improve survival — meet the floor and attend to the clinical domains.
  • Twice-weekly HD is acceptable only with substantial residual function.
  • A normal Kt/V in an overloaded, wasting, or symptomatic patient is not adequate dialysis.
03
Phase A · Level 3

Main Narrative

The medical core. An expert should agree adequacy assessment is fully covered here.

Why it matters at the bedside

Kt/V is the number every unit reports and the one most likely to mislead. It measures how much urea was cleared — useful, but a floor, not the goal. Read it for what it is, sample it honestly, and never let it stand in for the fuller question: is this dialysis keeping the patient well?

What adequacy means

  • Adequate dialysis is clinical: a euvolemic, well-nourished patient with controlled mineral-bone disease, few uraemic symptoms, and a clearance that meets a minimum. Each domain can fail on its own, so each is judged in its own right; a patient above every numeric target can still be inadequately dialysed.

Measuring the dose: URR and Kt/V

  • The simplest measure is the urea reduction ratio — the fractional fall in urea across a session — with a usual minimum of at least 65%. The standard measure is the single-pool Kt/V, computed from pre- and post-dialysis urea with treatment time and ultrafiltration; the minimum for thrice-weekly HD is about 1.2 per session, often targeted nearer 1.4.

Single-pool, rebound, and equilibrated Kt/V

  • The single-pool model assumes urea sits in one compartment, but in reality it rebounds: after dialysis, urea redistributes from cells and poorly-perfused tissues back into the blood over 30–60 minutes, so the post sample taken immediately understates true urea. Equilibrated Kt/V corrects for this and runs about 0.2 below the single-pool value — a better reflection of the dose actually delivered.

Standard weekly Kt/V and frequency

  • Per-session Kt/V cannot fairly compare a thrice-weekly schedule with a daily or nocturnal one. The standard weekly Kt/V converts any schedule to a common weekly figure, which is how frequent and nocturnal regimens are dosed and compared.

Sampling correctly

  • Dose is only as honest as the post-dialysis sample. Drawing it at full blood-flow contaminates it with dialysed blood and access recirculation, falsely raising the apparent dose; a slow-flow or stop-pump technique with consistent timing gives the true value. A surprisingly good Kt/V often means a sampling error, not good dialysis.

Residual kidney function

  • Residual renal urea clearance adds to the delivered dose and, when substantial, can justify a lower prescribed dialysis dose or an incremental schedule — even twice-weekly. As in PD, it is worth preserving and measuring; in anuric patients it is absent and the dialysis must do all the work.

Targets and the value of time

  • Meet the minimum — a single-pool Kt/V of at least 1.2 and a URR of at least 65% — but do not treat the number as the ceiling, and never shorten the session below a minimum time just because the target is met. Time clears middle molecules and phosphate, allows gentler fluid removal, and carries value the urea number cannot see.

What Kt/V does not measure

  • Kt/V is a urea number. It says nothing about middle molecules, phosphate, fluid removal, blood pressure, or nutrition. The randomised dose trial drove the point home: raising the small-solute dose above target did not improve survival, because the things that matter most are not what Kt/V counts.

When you feel the dialysis is inadequate

  • A symptomatic patient with an adequate Kt/V is a prompt to look elsewhere — volume overload, anaemia, acidosis, mineral-bone disease, depression, or intercurrent illness — each of which can mimic underdialysis and each of which has its own treatment.

Evidence base

  • The minimum dose targets rest on guideline consensus anchored to outcome data; the futility of exceeding them rests on a large randomised trial; the rebound correction rests on kinetic studies; and the survival value of residual function rests on consistent cohort data.
04
Phase A · Level 4

Reference Tables

Five fully-built tables.

Table A — Domains of adequacy

DomainWhat to assessTarget / sign
Solute clearanceURR / single-pool Kt/VURR ≥ 65%; spKt/V ≥ 1.2
VolumeBP, weight, oedemaEuvolemia
NutritionAppetite, weight trend, albuminNo protein-energy wasting
Mineral-bonePhosphate, PTH, calciumPer CKD-MBD goals
Symptoms / wellbeingUraemic symptoms, energyPatient feels well

Table B — Dose measures

MeasureHowTarget
URR(pre − post)/pre × 100≥ 65%
Single-pool Kt/VPre/post urea, time, UF, weight≥ 1.2 (target ~1.4)
Equilibrated Kt/VSingle-pool minus rebound~0.2 below spKt/V
Standard weekly Kt/VFrequency-adjusted~2.1–2.3 / week
+ Residual renal clearanceTimed urineAdds to total

Table C — Kinetic measures

MeasureCapturesUse
spKt/VSingle-pool, per sessionRoutine thrice-weekly
eKt/VCorrects for reboundTrue delivered dose
stdKt/VWeekly, frequency-independentCompare schedules

Table D — Post-dialysis sampling

DoAvoid
Slow-flow / stop-pump post-sampleSampling at full blood flow
Draw from the correct portAccess recirculation contaminating the sample
Consistent timingDelayed sampling that misses the true value
A standardised techniqueAd hoc methods that inflate Kt/V

Table E — Frequency and residual function

ScenarioApproach
Anuric, thrice-weeklyspKt/V ≥ 1.2; minimum time ≥ ~3.5 h
Substantial residual functionIncorporate it; consider incremental HD
Twice-weeklyOnly with substantial residual function
Frequent / nocturnalUse standard weekly Kt/V to compare

Visualise & Map

Phase B Visualise & Map
05
Phase B · Level 5

Imaging and Algorithm Flowcharts

Figure 10.1 — Post-dialysis urea rebound
Figure 10.1 — Post-dialysis urea rebound
Figure 10.2 — The adequacy dashboard
Figure 10.2 — The adequacy dashboard
Flowchart 10.A — The adequacy assessment
Flowchart 10.A — The adequacy assessment
Flowchart 10.B — The surprisingly high Kt/V
Flowchart 10.B — The surprisingly high Kt/V
07
Phase B · Level 7

Clinical Decision Pathways

Numbered rules. These numbers are the cross-reference handle for the cases and flowcharts.

R1
IF assessing adequacy, THEN evaluate clearance, volume, nutrition, mineral-bone health, and symptoms — not Kt/V alone.
R2
IF measuring dose, THEN report URR and/or single-pool Kt/V from correctly sampled pre- and post-dialysis urea.
R3
IF spKt/V < 1.2 (thrice-weekly) or URR < 65%, THEN increase the prescription (Chapter 9) and recheck.
R4
IF comparing dose across frequencies, THEN use standard weekly Kt/V.
R5
IF interpreting dose, THEN account for post-dialysis rebound (eKt/V) and do not be misled by spKt/V.
R6
IF sampling post-dialysis urea, THEN use a slow-flow or stop-pump technique to avoid recirculation error.
R7
IF residual function is substantial, THEN incorporate it and consider incremental (or twice-weekly) HD.
R8
IF a Kt/V target is met, THEN do not shorten time below the minimum to “save” the number.
R9
IF the patient is unwell with an adequate Kt/V, THEN look beyond dose — volume, anaemia, acidosis, mineral-bone, nutrition.

Clinical Reasoning

Phase C Clinical Reasoning
08
Phase C · Level 8

Clinical Cases

Four cases. Each stops you at a decision before it answers it.

CASE 1STANDARD

A routine adequacy reviewReading the whole picture

Presentation

A stable patient has a single-pool Kt/V of 1.4 and URR 72%, is euvolemic, eats well, and has controlled phosphate. The team asks whether to change anything.

Pause and reflect

Before reading on: is this adequate — and should the dose be pushed higher?

Analysis

Every domain is satisfied: clearance above the floor, euvolemic, nourished, mineral-bone controlled. Raising the dose further has no evidence of benefit. Adequate means leave it alone and schedule the next review.

Management plan

  1. Confirm all adequacy domains (R1).
  2. Note dose above the floor; do not escalate (R8).
  3. Schedule the next assessment; track residual function.

Teaching points

  • Meeting the floor with a well patient is success, not a reason to push the number.

Cross-reference: exercises R1, R8.

CASE 2COMPLEX

Good number, unwell patientWhy Kt/V is not adequacy

Presentation

A patient has a Kt/V of 1.3 but is oedematous and hypertensive, with stubborn hyperphosphataemia and falling appetite.

Pause and reflect

Before reading on: the urea dose is met — is this adequate dialysis?

Analysis

Volume, mineral-bone, and nutrition are all failing, so the dialysis is inadequate despite an acceptable Kt/V. The overload and phosphate point to time and volume (Chapters 9 and 11), and the appetite loss prompts a search for causes; the Kt/V is a distraction here.

Management plan

  1. Recognise failing domains despite the dose (R1).
  2. Address volume and phosphate (more time/frequency); investigate appetite (R9).
  3. Do not be reassured by the Kt/V alone.

Teaching points

  • A failing domain means inadequacy even when Kt/V is met.

Cross-reference: exercises R1, R9.

CASE 3COMPLEX

Too good to be trueThe sampling error

Presentation

A patient's reported Kt/V jumps to 2.0 on an unchanged prescription. The post-dialysis sample was drawn at full blood flow from the venous line.

Pause and reflect

Before reading on: a sudden high Kt/V with no prescription change — do you believe it?

Analysis

A dose that leaps without a prescription change is almost always a sampling artefact: a post sample taken at full flow is diluted by freshly dialysed blood and access recirculation, falsely inflating the number. Re-sampling with a slow-flow or stop-pump method gives the true, lower value.

Management plan

  1. Distrust the unexplained high dose; re-sample correctly (R6).
  2. Recompute; if still discrepant, investigate access recirculation.
  3. Act on the corrected value.

Teaching points

  • A surprisingly high Kt/V usually means a sampling error, not good dialysis.

Cross-reference: exercises R6.

CASE 4COMPLEX

Plenty of urineUsing residual function

Presentation

A new patient starting HD still passes substantial urine with meaningful residual clearance. The default is a full thrice-weekly prescription.

Pause and reflect

Before reading on: should residual function change the dialysis dose?

Analysis

Substantial residual renal clearance adds to the delivered dose, so a full thrice-weekly schedule may over-treat. Incorporating residual function allows an incremental approach — even twice-weekly while it lasts — with close monitoring as it declines, mirroring the incremental logic of PD.

Management plan

  1. Measure residual clearance and incorporate it (R7).
  2. Consider incremental / twice-weekly while function is substantial (R7).
  3. Reassess frequently and step up as it falls.

Teaching points

  • Substantial residual function can justify incremental HD — only while it lasts.

Cross-reference: exercises R7.

10
Phase C · Level 10

Clinical Pearls

Exhaustive. Every threshold and rule in the chapter is here.

Adequacy = clearance + volume + nutrition + mineral-bone + symptoms.
Small-solute dose is a floor, not the goal.
URR ≥ 65%; single-pool Kt/V ≥ 1.2 (target ~1.4).
Urea rebounds post-dialysis; eKt/V ≈ 0.2 below spKt/V.
Standard weekly Kt/V compares across frequencies (~2.1–2.3).
Correct post-sampling (slow-flow/stop-pump) is essential.
A surprisingly high Kt/V usually means a sampling error.
Residual clearance adds to dose — enables incremental HD.
Never shorten time just to meet a Kt/V.
Kt/V ignores middle molecules, phosphate, volume, and BP.
Higher dose above target gives no survival benefit.
Twice-weekly only with substantial residual function.
A normal Kt/V with overload/wasting is not adequate dialysis.
Unwell with adequate Kt/V → look beyond dose.

Safety & Evidence

Phase D Safety & Evidence
11
Phase D · Level 11

Red Flags and NEVER DO

Panel A — Red flags

A Kt/V that jumps without a prescription change — a sampling error.
A normal Kt/V with overload, hyperphosphataemia, or wasting — inadequacy beyond the number.
Twice-weekly schedule in an anuric patient — underdialysis.
Time being shortened to ‘save’ a met Kt/V — loss of time's benefit.

Panel B — NEVER DO

NEVER — shorten treatment time below the minimum just because a Kt/V target is met.
NEVER — declare adequacy from the Kt/V number alone.
NEVER — trust a dose computed from a post sample taken at full blood flow.
NEVER — run twice-weekly HD in an anuric patient.
NEVER — chase a Kt/V above target expecting a survival benefit.
12
Phase D · Level 12

Common Pitfalls

Anti-patterns clinicians fall into. Each becomes a Level 22 distractor.

WRONG Shortening time because the Kt/V target is met.
RIGHT Keep the minimum time.
WHY Time clears middle molecules and phosphate and aids tolerance.
WRONG Declaring adequacy from Kt/V alone.
RIGHT Assess all adequacy domains.
WHY Outcomes are multidimensional; one domain can fail in isolation.
WRONG Trusting a high Kt/V from a full-flow post sample.
RIGHT Re-sample with a slow-flow/stop-pump method.
WHY Recirculation and dilution inflate the apparent dose.
WRONG Running twice-weekly HD in an anuric patient.
RIGHT Reserve twice-weekly for substantial residual function.
WHY Without residual clearance, twice-weekly underdialyses.
WRONG Treating single-pool Kt/V as the true dose.
RIGHT Account for rebound with equilibrated Kt/V.
WHY Single-pool overestimates the delivered dose.
WRONG Blaming all malaise on the dialysis dose.
RIGHT Exclude anaemia, volume, acidosis, and other causes.
WHY Many conditions mimic underdialysis.
13
Phase D · Level 13

Evidence Grading

The grade reflects strength of evidence, not importance.

GRADE

A

HIGH CONFIDENCE

The effect is real and the estimate is stable.

RCTs at low risk of bias; multiple concordant prospective cohorts; meta-analyses.

GRADE

B

MODERATE CONFIDENCE

The effect is likely real but may shift with new data.

Observational studies, registries, mechanistic human studies.

GRADE

C

LOW CONFIDENCE

Rests on physiology, reasoning, or consensus rather than outcomes.

Pathophysiological reasoning; extrapolation; consensus without outcomes.

StatementGradeRationale for the grade
Raising small-solute dose above target does not improve survival.ALarge randomised trial.
A single-pool Kt/V ≥ 1.2 / URR ≥ 65% is an appropriate minimum.BGuideline consensus anchored to outcome data.
Equilibrated Kt/V better reflects the true dose (rebound).BKinetic studies.
Minimum treatment time matters beyond Kt/V.BObservational data and consensus.
Residual function adds to dose and enables incremental HD.BObservational data.
Standard weekly Kt/V allows fair comparison across frequencies.CConsensus and kinetic modelling.

Patient Decisions

Phase E Patient Decisions
14
Phase E · Level 14

Absolute-Risk Presentation

Outcomes as natural frequencies. Figures are representative; the direction of effect is given where precise numbers are uncertain.

OutcomeOption AOption BDifferenceEvidence
Survival, higher vs target Kt/Vhigher Kt/Vtarget Kt/VNo meaningful differenceSee L13 — Grade A
Outcomes, below-floor vs adequate dosebelow flooradequateWorse below the floorSee L3 — Grade B
Survival, preserved vs lost residual functionlost RKFpreservedBetter with preserved RKFSee L13 — Grade B

Reading the table

The shape is a floor, not a ladder: falling below the minimum harms, but climbing above it does not help — which is why effort goes to the clinical domains and to residual function. Where exact frequencies are uncertain, the direction of effect is given; the evidence column points to where the detail lives.

Apply & Test

Phase F Apply & Test
17
Phase F · Level 17

Documentation Templates

Included by author decision: an adequacy review is a real chart note.

Template 1 — Adequacy review note

  • Dose: URR ___; spKt/V ___; eKt/V ___; (stdKt/V if non-thrice-weekly) ___.
  • Sampling verified (slow-flow/stop-pump): yes/no.
  • Volume: BP ___; weight/oedema ___ — euvolemic? yes/no.
  • Nutrition ___; mineral-bone (phosphate/PTH) ___; symptoms ___.
  • Residual renal clearance: ___ — incorporated? yes/no.
  • Assessment: adequate / inadequate (domain ___); action and next review ___.

Template 2 — Dose / sampling discrepancy note

  • Reported dose and change from prior: ___.
  • Sampling technique used: ___ (full-flow error suspected? yes/no).
  • Re-sampled correctly: result ___.
  • Access recirculation assessed: ___.
  • Corrected dose acted upon; prescription change (if any): ___.
18
Phase F · Level 18

High-Yield Cheat Sheet

Pre-rounds compression. Numbers and rules only.

Adequacy = clearance + volume + nutrition + MBD + symptoms.
URR ≥ 65%; spKt/V ≥ 1.2 (target ~1.4).
eKt/V ≈ spKt/V − 0.2 (rebound).
stdKt/V ~2.1–2.3/week to compare frequencies.
Sample post-urea slow-flow/stop-pump.
Surprise-high Kt/V = sampling error.
Residual clearance counts → incremental HD.
Never shorten time to a Kt/V.
Kt/V ≠ middle molecules/phosphate/volume/BP.
Above target = no survival gain.
Twice-weekly only with substantial RKF.
Unwell + good Kt/V → look beyond dose.
19
Phase F · Level 19

Flashcards

Active recall. At least one card per objective.

CARD 1

Q. What does dialysis adequacy comprise?

Show answer

A. Clearance, volume, nutrition, mineral-bone health, and symptoms together — not a single number.

DETAILED. Each domain can fail independently.

CLINICAL. A patient above every numeric target can still be inadequately dialysed.

CARD 2

Q. Define URR and single-pool Kt/V and their minimums.

Show answer

A. URR = (pre − post)/pre, minimum ≥ 65%; single-pool Kt/V from pre/post urea, time, and UF, minimum ≥ 1.2 (target ~1.4).

DETAILED. Both quantify small-solute (urea) removal.

CLINICAL. They are floors, not goals.

CARD 3

Q. What is urea rebound, and how does eKt/V differ?

Show answer

A. After dialysis, urea redistributes from tissues into blood over 30–60 minutes; equilibrated Kt/V corrects for this and is ~0.2 below single-pool.

DETAILED. Single-pool overestimates the true dose.

CLINICAL. eKt/V better reflects what was delivered.

CARD 4

Q. Why use standard weekly Kt/V?

Show answer

A. It converts any schedule to a common weekly figure, allowing fair comparison across frequencies.

DETAILED. Per-session Kt/V cannot compare thrice-weekly with daily or nocturnal.

CLINICAL. Target around 2.1–2.3 per week.

CARD 5

Q. How should the post-dialysis urea be sampled?

Show answer

A. With a slow-flow or stop-pump technique and consistent timing.

DETAILED. Full-flow sampling is contaminated by dialysed blood and recirculation.

CLINICAL. A surprisingly high Kt/V usually means a sampling error.

CARD 6

Q. How does residual kidney function affect the dose?

Show answer

A. It adds to the delivered dose and, when substantial, justifies a lower prescribed dose or incremental (even twice-weekly) HD.

DETAILED. It is measured from a timed urine collection.

CLINICAL. Reassess as it declines and step up dialysis.

CARD 7

Q. How are dose targets applied with respect to time?

Show answer

A. Meet the minimum, but never shorten the session below the minimum time to ‘save’ a met Kt/V.

DETAILED. Time clears middle molecules and phosphate and aids tolerance.

CLINICAL. Time has value the urea number cannot capture.

CARD 8

Q. What does Kt/V fail to measure?

Show answer

A. Middle molecules, phosphate, fluid removal, blood pressure, and nutrition.

DETAILED. The dose trial showed exceeding the target gives no survival benefit.

CLINICAL. Adequacy is clinical, with Kt/V only a floor.

CARD 9

Q. A patient feels unwell with an adequate Kt/V. What now?

Show answer

A. Look beyond dose — volume overload, anaemia, acidosis, mineral-bone disease, depression, intercurrent illness.

DETAILED. Each can mimic underdialysis.

CLINICAL. Treat the actual problem rather than raising the dose.

20
Phase F · Level 20

One-Minute Preceptor

Micro-teaching for rounds. Two scenarios, five steps each.

SCENE 1
Good number, swollen patient
GET A COMMITMENTAsk: “Kt/V is 1.3 but he's oedematous and hyperphosphataemic — adequate?”
PROBE“Which adequacy domains are failing?”
TEACHVolume and mineral-bone — adequacy is multidimensional; the Kt/V doesn't capture them.
REINFORCE“Right — treat the failing domains, not the number.”
CORRECT ERRORSIf they were reassured by the Kt/V, point to the overload and phosphate.
SCENE 2
The Kt/V that jumped
GET A COMMITMENTAsk: “Kt/V suddenly reads 2.0 with no change — do you believe it?”
PROBE“How was the post sample taken?”
TEACHFull-flow sampling inflates the dose — re-sample slow-flow/stop-pump.
REINFORCE“Exactly — a surprise-high Kt/V is a sampling error until proven otherwise.”
CORRECT ERRORSIf they accepted the number, point to recirculation and dilution.
21
Phase F · Level 21

Reflective Prompts

Metacognition anchored to this chapter's tensions. No answers provided.

  1. 1. A single number is easy to chart and audit; how do you keep Kt/V from quietly becoming the definition of ‘good dialysis’ on your unit?
  2. 2. Time helps most and is the easiest to cut when a Kt/V is already met; how do you protect it against the pressure to shorten sessions?
  3. 3. A flattering dose can come from a careless sample; how confident are you that your unit's post-sampling is honest, and how would you check?
  4. 4. Residual function lets you do less, yet it is rarely measured once a patient is established; what would it take to make incremental HD routine?
  5. 5. When a patient with a perfect Kt/V still feels terrible, where do you look first — and what does that say about what dialysis is for?
22
Phase F · Level 22

Board-Style Q&A

Nine items, each anchored in this chapter. At least one per objective.

Q 01
A patient has spKt/V 1.4 and URR 72% but is oedematous and hyperphosphataemic. Is the dialysis adequate?

Tap an option to check your answer

  • AYes — the dose target is met
  • BNo — volume and mineral-bone domains are failing
  • CYes — reduce the dose
  • DNo — raise the Kt/V
Q 02
What is the usual minimum single-pool Kt/V and URR for thrice-weekly HD?

Tap an option to check your answer

  • AspKt/V 0.8; URR 50%
  • BspKt/V ≥ 1.2; URR ≥ 65%
  • CspKt/V ≥ 2.0; URR ≥ 90%
  • DspKt/V ≥ 1.2; URR ≥ 40%
Q 03
How does equilibrated Kt/V relate to single-pool Kt/V?

Tap an option to check your answer

  • AIt is higher because of rebound
  • BIt is about 0.2 lower, correcting for rebound
  • CIt is identical
  • DIt cannot be estimated
Q 04
A patient's reported Kt/V jumps to 2.0 with no prescription change; the post sample was taken at full blood flow. The best action is:

Tap an option to check your answer

  • AAccept it and shorten the session
  • BRe-sample with a slow-flow/stop-pump method
  • CIncrease the prescription
  • DSwitch to twice-weekly
Q 05
A Kt/V target is comfortably met. Which action is inappropriate?

Tap an option to check your answer

  • AContinue the current prescription
  • BShorten the session below the minimum time to save the number
  • CKeep monitoring the clinical domains
  • DTrack residual function
Q 06
When is twice-weekly haemodialysis acceptable?

Tap an option to check your answer

  • AIn any stable patient
  • BOnly with substantial residual kidney function
  • CIn anuric patients to reduce burden
  • DWhenever the Kt/V is met on two sessions
Q 07
Which interpretation of the dose evidence is correct?

Tap an option to check your answer

  • AHigher Kt/V above target improves survival
  • BAbove target, a higher dose gives no survival benefit; below the floor harms
  • CDose has no effect at any level
  • DLower than target is safe
Q 08
Which is NOT captured by Kt/V?

Tap an option to check your answer

  • ASmall-solute (urea) clearance
  • BPhosphate, middle molecules, volume, and blood pressure
  • CThe fractional fall in urea
  • DSingle-pool urea kinetics
Q 09
In Flowchart 10.A, the dose is at target but the patient is overloaded and hyperphosphataemic. The pathway directs you to:

Tap an option to check your answer

  • ADeclare adequate and schedule review
  • BTreat the failing domains and exclude non-dialysis causes
  • CIncrease the Kt/V
  • DStop assessing — the number is fine