Hemodialysis nursing: complete reference for nursing students

LS
By Lindsay Smith, AGPCNP
Updated October 22, 2026

Reviewed for clinical accuracy · Methodology: NIH, NCBI, AANP guidelines

Hemodialysis (HD) is the most common form of renal replacement therapy in the United States. Well over half a million Americans receive maintenance dialysis, and the large majority are treated with in-center hemodialysis. The 2024 USRDS Annual Data Report shows that in 2022, 14.0% of incident patients started on peritoneal dialysis and 0.4% on home HD; among prevalent dialysis patients, 12.1% used PD and 2.4% home HD. The in-center share has been slowly declining as home modalities and transplantation grow. It is a life-sustaining treatment for patients with end-stage renal disease (ESRD) and for those with acute kidney injury (AKI) whose kidneys can no longer maintain homeostasis. Three times per week, for 3–4 hours each session, a dialysis machine performs the filtration and solute clearance that failing kidneys cannot. Nursing students encounter hemodialysis in medical-surgical, nephrology, and critical care rotations – and it is reliably tested on the NCLEX. This reference covers every aspect the NCLEX tests: the physiological basis for HD, all three access types and their nursing assessment priorities, the complete arc of an HD session, complications and their management, continuous renal replacement therapy (CRRT) for ICU patients, diet and medication considerations, patient education, and a full comparison against peritoneal dialysis.

Quick referenceDetail
Primary indicationESRD (GFR <15) or AKI with refractory complications
Indications mnemonicAEIOU: Acidosis, Electrolytes, Intoxication, Overload, Uremia
Usual first-choice accessArteriovenous fistula (AVF) – lowest infection risk, longest patency; KDOQI 2019 chooses access by each patient's ESKD Life-Plan
Highest infection risk accessCentral venous catheter (CVC) – temporary only, last resort
Most common complicationIntradialytic hypotension (about 7% of sessions by the full EBPG definition; symptoms in about 1 in 5 sessions)
Most dangerous early complicationDialysis disequilibrium syndrome (first HD session)
Typical session3–4 hours, 3 times per week
Fluid restriction (ESRD)Commonly 500 mL/day + daily urine output (individualized)
Hepatitis B in the dialysis unitHBsAg-positive: separate room, dedicated machine, no dialyzer reuse (CDC 2001); HCV or HIV: no isolation
Priority nursing action (pre-session)Weigh patient, assess access site, check blood pressure and labs

Indications for hemodialysis

HD is indicated when the kidneys can no longer maintain safe homeostasis and conservative management has failed. For patients with ESRD from CKD, KDIGO 2024 bases the decision on a composite of symptoms, signs, quality of life, preferences, GFR and lab abnormalities, with no single GFR cutoff. Dialysis is started for uremic symptoms, acid-base or electrolyte problems that resist medical treatment, volume or blood pressure that cannot be controlled, worsening nutrition, or cognitive decline, which often but not always happens at an eGFR of 5–10 mL/min/1.73 m². Access planning starts earlier, at an eGFR below 15–20. For acute kidney injury, the decision is urgent and based on life-threatening complications rather than GFR alone.

The AEIOU mnemonic captures all dialysis indications – memorize this for the NCLEX. The numbers below are commonly taught triggers; guidelines do not set fixed cutoffs, and trials such as AKIKI used similar ones (for example potassium above 6 mmol/L or pH below 7.15).

A – Acidosis: Metabolic acidosis with pH below 7.1 that does not respond to bicarbonate therapy. Failing kidneys cannot regenerate bicarbonate or excrete acid.

E – Electrolytes: Life-threatening hyperkalemia, typically potassium above 6.5 mEq/L despite medical management (calcium gluconate, insulin/dextrose, kayexalate). Electrolyte imbalances in renal failure develop because the kidney is the primary route of potassium excretion.

I – Intoxication: Removal of dialyzable toxins and drugs – methanol, ethylene glycol, lithium, salicylates, theophylline. Water-soluble, low molecular weight, and low protein-binding drugs are most efficiently cleared by HD.

O – Overload: Refractory fluid overload (pulmonary edema, severe hypertension) unresponsive to diuretics. Fluid removal via HD ultrafiltration is both faster and more reliable than pharmacologic diuresis in oliguric or anuric patients. This overlaps significantly with heart failure management in patients who are diuretic-resistant.

U – Uremia: BUN above 100 mg/dL or symptomatic uremia at any BUN level. Uremic symptoms include encephalopathy (confusion, asterixis, seizures), pericarditis (friction rub, chest pain), platelet dysfunction with bleeding, nausea, and pruritus. Uremic pericarditis is an emergency indication.


Vascular access: types, assessment, and nursing priorities

Access is the single most important factor in safe, effective hemodialysis. The dialysis machine must pull blood from the patient at 300–500 mL/min – a flow rate impossible through a standard peripheral IV. Three access types exist, listed here from usually most to least preferred. The 2019 KDOQI vascular access guideline replaced the older “Fistula First” approach with an individualized ESKD Life-Plan, so the right access depends on the patient’s goals, vessels and expected time on HD.

Arteriovenous fistula (AVF)

An AVF is created surgically by anastomosing an artery directly to an adjacent vein, most often at the non-dominant wrist (cephalic vein to radial artery – the radiocephalic fistula) or the antecubital fossa. Arterial blood pressure causes the vein to dilate and thicken over weeks, a process called maturation or arterialization.

  • Maturation time: At least 6 weeks before first use, and often several months; many fistulas need an extra procedure before they mature
  • Patency: Longest of all access types – well-functioning AVFs can last decades
  • Infection risk: Lowest – no foreign material is implanted
  • Preferred placement: Non-dominant arm

Nursing assessment of AVF:

  • Palpate for a thrill (a continuous vibration felt at the anastomosis – indicates flow). Absence of thrill is an emergency.
  • Auscultate for a bruit (a whooshing sound over the vessel with a stethoscope). A change from continuous to only systolic bruit suggests stenosis.
  • Inspect for redness, warmth, swelling, or drainage indicating infection
  • Check capillary refill and sensation distal to the fistula (steal syndrome causes ischemia)
  • Never take blood pressure, draw blood, or place an IV in the fistula arm – compression can thrombose the access

Arteriovenous graft (AVG)

An AVG uses a synthetic tube (polytetrafluoroethylene, or PTFE) to bridge the artery and vein when the patient’s native vessels are unsuitable for fistula creation. Common sites include the upper arm (brachial artery to axillary vein) and the thigh.

  • Maturation time: Usually 2–3 weeks before use (synthetic material, no arterialization needed)
  • Patency: Shorter than AVF – synthetic material prone to stenosis and thrombosis
  • Infection risk: Higher than AVF – foreign material increases infection susceptibility
  • Thrombosis risk: Higher than AVF – grafts need more procedures to stay open

Nursing assessment of AVG: Same principles as AVF – palpate thrill, auscultate bruit, inspect for infection. Grafts are palpable as a firm, tube-like structure under the skin.

Central venous catheter (CVC)

A CVC is a large-bore, double-lumen catheter placed in the internal jugular, subclavian, or femoral vein. The right internal jugular vein is preferred. Subclavian catheters carry up to about four times the rate of central vein stenosis, which can rule out a future fistula in that arm. Femoral placement limits mobility and carries the highest infection risk.

  • Maturation time: Immediate use – no waiting period
  • Patency: Weeks to months; tunneled cuffed catheters (e.g., Permcath, Tesio) last longer than temporary non-tunneled catheters
  • Infection risk: Highest of all access types – direct bloodstream access with high-flow, repeated connections
  • Use: Temporary bridge while AVF or AVG matures, or for patients who are not candidates for surgical access

Nursing assessment of CVC:

  • Inspect catheter exit site for redness, drainage, or cuff extrusion
  • Never use the dialysis catheter for routine blood draws, IV medications, or IV fluids – reserved for dialysis only
  • Assess for signs of sepsis – a CVC-related bloodstream infection can progress to sepsis, endocarditis or death
  • Change dressing using strict aseptic technique per facility protocol
Access typeMaturationPatencyInfection riskPreferred?Key nursing assessment
AVF (arteriovenous fistula)At least 6 weeks; often monthsLongest (years to decades)LowestUsually first choice, per the ESKD Life-PlanThrill, bruit, no BP/blood draws in fistula arm
AVG (arteriovenous graft)2–3 weeksIntermediate (months to years)ModerateSecond choiceThrill, bruit, inspect for infection, thrombosis
CVC (central venous catheter)ImmediateShortest (weeks to months)HighestNo – last resortExit site inspection, strict asepsis, reserved for dialysis only

The hemodialysis session: nursing care by phase

HD sessions run 3–4 hours, three times per week (some patients do shorter daily sessions). The nurse’s role spans before, during, and after each session – each phase has distinct priorities.

Pre-session assessment

Before initiating HD, the nurse must establish a baseline and identify any conditions that require the dialysis team’s awareness.

Weight: Weigh the patient on the same scale, same clothing, each time. The difference between the patient’s current weight and their “dry weight” (euvolemic weight, established by the nephrologist) determines the ultrafiltration target – how much fluid to remove. Removing too much causes hypotension; removing too little leaves the patient fluid-overloaded.

Blood pressure and heart rate: Document bilateral blood pressure if indicated. Baseline BP guides intradialytic management. Patients on antihypertensives should often hold their morning dose before HD (see Medications section).

Access assessment: Confirm thrill and bruit for AVF or AVG. Assess CVC exit site. Inspect for signs of infection.

Labs: Review pre-session potassium, BUN, and creatinine. Note any critical values requiring urgent notification to the nephrologist. Dialysate potassium concentration is adjusted based on serum potassium.

Symptom assessment: Ask about chest pain, dyspnea, dizziness, muscle cramps from the previous session. Note any new medications, dietary changes, or hospitalizations.

During the session

The HD machine performs three simultaneous functions: diffusion (solute movement along concentration gradient – clears urea, creatinine, potassium), osmosis (water moves to the dialysate side), and ultrafiltration (controlled fluid removal via transmembrane pressure). The patient’s blood circulates through the dialyzer at 300–500 mL/min while dialysate flows counter-current on the other side of a semi-permeable membrane.

Continuous monitoring priorities:

  • Blood pressure and heart rate every 30 minutes (or continuously per protocol). Hypotension is the most common complication.
  • Patient symptoms: headache, nausea, chest pain, muscle cramps, dizziness
  • Machine alarms: blood leak detector, air detector, transmembrane pressure
  • Access site: watch for bleeding, hematoma, or needle dislodgement
  • Heparin infusion management (anticoagulation prevents circuit clotting)

Intradialytic hypotension response (most common complication):

  1. Place patient in Trendelenburg position (feet elevated)
  2. Reduce or stop ultrafiltration
  3. Administer 100–250 mL normal saline bolus per protocol
  4. Notify nephrologist if BP does not respond
  5. Do not administer antihypertensives during hypotension

Post-session care

Weight: Weigh immediately after the session using the same scale. Compare to target dry weight – confirms whether the ultrafiltration goal was met.

Blood pressure: Blood pressure is typically lower post-dialysis. Document and compare to baseline.

Access site care:

  • Apply pressure to needle sites for AVF/AVG until hemostasis is achieved (bleeding risk from heparin)
  • Do not apply tape circumferentially or place pressure dressings that could thrombose the access
  • Inspect for hematoma formation

Post-dialysis labs: Pre- and post-session BUN are used to calculate Kt/V and the urea reduction ratio (URR). For thrice-weekly HD, the 2015 KDOQI adequacy update targets a single-pool Kt/V of 1.4 per session, with a minimum delivered dose of 1.2; the older URR benchmark is at least 65%.

Patient education: Review dietary intake, fluid balance, and access self-monitoring before discharge from the dialysis center.


Complications of hemodialysis

ComplicationCauseClinical signsNursing response
Intradialytic hypotension (most common)Rapid fluid removal exceeding cardiovascular compensation; also antihypertensives taken pre-HD, low albumin, cardiac dysfunctionSBP drop >20 mmHg, dizziness, nausea, diaphoresis, muscle cramps, syncopeTrendelenburg position, reduce/stop ultrafiltration, saline bolus 100–250 mL, notify nephrologist if unresponsive
Dialysis disequilibrium syndrome (DDS)Rapid urea removal from blood creates osmotic gradient – water shifts into brain cells causing cerebral edema. Greatest risk on first HD session or after prolonged uremia.Headache, nausea, vomiting, restlessness, confusion, seizures (severe cases); onset during or within hours of sessionSlow dialysis rate (first sessions), administer mannitol or hypertonic saline per order, supportive seizure precautions, notify nephrologist immediately
Muscle crampsRapid fluid removal with resulting hypovolemia; electrolyte shifts (low sodium, low magnesium); muscle ischemiaPainful involuntary muscle contractions, most often in legsReduce ultrafiltration rate, saline bolus, warm compresses; adjust dry weight if cramps are recurrent
Air embolismAir entry into circuit via disconnected line, empty IV bag, or line breakSudden dyspnea, cough, chest pain, cyanosis, "mill wheel" murmur; can cause cardiac arrestClamp venous line immediately, place patient left lateral Trendelenburg (air rises to right ventricle apex, away from pulmonary outflow), 100% oxygen, notify team – this is an emergency
HemolysisContaminated dialysate (incorrect chloramine level, overheated), kinked blood lines, excessive negative pressurePort-wine or pink-tinged blood in venous chamber, chest/back pain, dyspnea, falling hematocritStop dialysis immediately, do not return blood to patient, discard blood in circuit, notify nephrologist; assess for hyperkalemia from lysed red cells
Clotting of the extracorporeal circuitInsufficient anticoagulation (heparin dose too low), slow blood flow, high hematocrit, excessive interruptionsDarkening of blood in tubing, decreased transmembrane pressure alarm, visible clot in dialyzer chambersFlush lines with saline per protocol, adjust heparin per order, may need to terminate session and change dialyzer; monitor patient for clotting disorders
Infection / catheter-related bloodstream infection (CRBSI)Biofilm formation on CVC; contaminated needles or access sites; skin organisms introduced at cannulationFever, chills, rigors during or after dialysis, redness/drainage at access site, positive blood culturesCollect blood cultures (peripheral and catheter), administer antibiotics per order, assess for sepsis, notify nephrologist; CVC removal may be required

Dialysis disequilibrium syndrome – NCLEX priority detail

DDS is tested frequently because it is counterintuitive – the patient feels worse as dialysis treats uremia. The mechanism: urea is cleared rapidly from the blood, but urea crosses the blood-brain barrier slowly. The resulting osmotic gradient pulls water into brain cells, causing cerebral edema. The first HD session carries the highest risk, especially in patients who have been severely uremic for a prolonged period. Prevention includes using a shorter session duration, lower blood flow rate, and higher dialysate sodium for the initial sessions. Mannitol may be given prophylactically or therapeutically to create an opposing osmotic gradient.


Infection control: hepatitis B isolation in the dialysis unit

Outside the dialysis unit, bloodborne infections need no isolation. CDC’s isolation Appendix A (updated September 11, 2026) lists Standard Precautions only for hepatitis B (acute or chronic), hepatitis C and HIV, and for hepatitis B and C it points to the separate recommendations for hemodialysis centers. Those are CDC’s 2001 recommendations for chronic hemodialysis patients (MMWR RR-5), and they contain the one bloodborne isolation rule nurses need to know: patients who are HBsAg-positive are isolated during dialysis. See the isolation precautions hub and hepatitis B nursing for the wider rules.

The reason is specific to HBV. CDC describes it as efficiently transmitted through exposure to blood and notes that it stays viable for at least 7 days on environmental surfaces at room temperature. HBsAg has been found in dialysis centers on clamps, scissors, machine control knobs and doorknobs, and CDC notes that staff can transfer the virus to patients from contaminated surfaces on their hands or gloves. CDC credits the segregation of HBsAg-positive patients and their equipment from susceptible patients with 70–80% reductions in the incidence of HBV infection among hemodialysis patients.

Patient statusWhat CDC 2001 recommends
HBsAg-positiveDialyze in a separate room with dedicated machines, equipment, instruments, supplies and medications that will not be used by HBV-susceptible patients. Staff caring for these patients should not care for susceptible patients at the same time, including the handover when one patient's treatment ends and another's begins. Dialyzers should not be reused.
HBsAg-positive, no isolation room (existing units)Separate the patient from HBV-susceptible patients in an area removed from the mainstream of activity, on a dedicated machine. Newly opened units should have isolation rooms.
HBV-immune (anti-HBs positive)May dialyze in the same area as HBsAg-positive patients. Staff can be assigned to infected and immune patients on the same shift.
Anti-HCV or HCV RNA positiveNo isolation and no dedicated machine. May take part in dialyzer reuse programs.
HIV-positiveNo isolation and no dedicated machine.

Testing and vaccination. CDC says every patient’s HBV serologic status should be known before admission to the unit, or testing completed within 7 days. HBV-susceptible patients are tested for HBsAg monthly. Hepatitis B vaccination is recommended for all susceptible patients and all staff. Patients are tested for anti-HBs 1–2 months after the last primary dose. Non-responders are revaccinated with three more doses and retested, and responders are retested every year, with a booster if anti-HBs falls below 10 mIU/mL. For HCV-negative patients, CDC suggests monthly ALT and anti-HCV every 6 months.

Practices for every patient. Isolation sits on top of strict routine precautions at every station. CDC requires gloves whenever staff care for a patient or touch the patient’s equipment, with hand hygiene after removing gloves and between patients. Unused medications or supplies taken to a station are not returned to the common area. Medications are prepared in a separate clean area and delivered to each patient individually, without common carts in the treatment area. Single-use vials are punctured only once, and environmental surfaces at the station are cleaned after each treatment.


Continuous renal replacement therapy (CRRT)

CRRT is an alternative to intermittent HD used exclusively in the intensive care unit for hemodynamically unstable patients. While conventional HD removes large amounts of fluid and solutes over 3–4 hours, CRRT operates 24 hours per day, 7 days per week, achieving the same total clearance at a fraction of the hourly rate. This slow, continuous removal is far better tolerated by patients in septic shock, after cardiac surgery, or with severe multi-organ failure.

CRRT modalities

  • CVVH (continuous venovenous hemofiltration): Removal by convection – solutes are dragged with water across a membrane via ultrafiltration. Replacement fluid is infused to maintain volume.
  • CVVHD (continuous venovenous hemodialysis): Removal by diffusion – dialysate flows counter-current to blood. Less efficient for larger molecules than convection.
  • CVVHDF (continuous venovenous hemodiafiltration): Combines both diffusion and convection – most comprehensive clearance.

CRRT nursing priorities vs intermittent HD

ParameterIntermittent HDCRRT
SettingDialysis unit or bedsideICU only
Duration3–4 hours, 3x/week24 hours/day, continuous
Hemodynamic toleranceRequires stable BPDesigned for hemodynamically unstable patients
Fluid removal rateRapid (large volume per session)Slow (net removal set hourly to the patient's tolerance)
AnticoagulationSystemic heparin or citrateCitrate preferred (regional anticoagulation avoids systemic bleeding risk)
Primary nursing concernIntradialytic hypotension, DDS, accessFilter clotting, citrate toxicity, calcium replacement, hypothermia (blood cooled outside body)
MobilityLimited during sessionPatient confined to bed during treatment

CRRT nursing priorities: Monitor hourly fluid balance (intake vs. ultrafiltration output), assess filter for clotting (darkening, falling effluent rate), monitor ionized calcium when citrate anticoagulation is used (citrate chelates calcium – hypocalcemia develops if replacement is inadequate), keep patient warm (blood in the extracorporeal circuit loses heat), and recheck electrolytes every 4–6 hours.


Diet and fluid management

Patients on HD live within significant dietary restrictions between sessions because the dialysis machine only runs three times per week. What accumulates in those intervals – fluid, potassium, phosphorus – must be manageable. Fluid and potassium excess between sessions are common, preventable reasons for emergency visits, especially after the long weekend gap.

NutrientRestrictionRationaleHigh-risk foods to avoid
FluidCommonly 500 mL/day + daily urine output (individualized)Anuric/oliguric patients cannot excrete fluid between sessions – accumulation causes hypertension, pulmonary edema, weight gainAll beverages, soups, ice, gelatin, popsicles, watermelon
Potassium40–70 mEq/day (approximately 2,000–3,000 mg)Hyperkalemia causes fatal arrhythmias; kidneys cannot excrete K+ between sessionsBananas, oranges, tomatoes, potatoes, dried fruit, nuts, salt substitutes (contain KCl)
Phosphorus800–1,000 mg/dayHyperphosphatemia binds calcium → hypocalcemia → secondary hyperparathyroidism → renal osteodystrophyDairy, cola beverages, processed foods, nuts, seeds, chocolate
SodiumUnder 2,000 mg/day (KDIGO 2024 suggests <2 g/day in CKD)Sodium drives thirst → excessive fluid intake → fluid overload between sessionsCanned foods, fast food, processed meats, soy sauce, pickled foods
Protein1.0–1.2 g/kg/day (KDOQI 2020, metabolically stable patients)HD removes amino acids – protein needs are HIGHER than non-dialysis CKD (which restricts protein). Inadequate protein → muscle wasting, malnutrition, poor outcomes.No restriction – ensure adequate intake

NCLEX distinction: Pre-dialysis CKD limits protein to reduce uremic load on failing kidneys. KDIGO 2024 suggests 0.8 g/kg/day in CKD G3–G5 and avoiding more than 1.3 g/kg/day; KDOQI 2020 allows lower intakes (0.55–0.6 g/kg/day, or 0.6–0.8 with diabetes) only under close dietitian supervision. Once on dialysis, the target rises to 1.0–1.2 g/kg/day (KDOQI 2020) because amino acids are lost in the dialysate and the uremia concern shifts to the dialysis machine.

The interdialytic weight gain target is no more than 1–2 kg between sessions (some nephrologists allow up to 3 kg for larger patients). Greater gains require faster, more aggressive ultrafiltration that increases hypotension risk.


Medications and hemodialysis

Several medication categories require adjustment or withholding around HD sessions. This is tested on the NCLEX in medication safety questions.

Medications to hold before HD

Antihypertensives: The most important category. HD removes fluid rapidly, causing blood pressure to fall physiologically during the session. Taking antihypertensives before HD compounds this – the result is severe intradialytic hypotension. Hold morning antihypertensives until after the session completes unless the nephrologist specifies otherwise.

Cardiac glycosides (digoxin): HD does not remove digoxin efficiently (high protein binding, large volume of distribution), but the rapid potassium and fluid shifts during HD alter digoxin toxicity risk. Digoxin levels and cardiac monitoring are required; dose adjustment is often needed.

Lithium: Dialyzable – HD clears lithium. Hold before sessions and check post-HD lithium levels. Lithium toxicity may unmask after the session if rebound from tissues occurs.

Drugs removed by hemodialysis (dialyzable)

Dialyzable drugs share characteristics: small molecular size, water solubility, low protein binding, and low volume of distribution. The NCLEX tests this pattern.

  • Antibiotics: Aminoglycosides (gentamicin, tobramycin, amikacin), some penicillins, cephalosporins, vancomycin (partially)
  • Water-soluble vitamins: Vitamins B1, B6, B12, C, and folate are cleared each session – patients require supplementation with dialysis-specific vitamins (Nephrocaps)
  • Electrolytes: Phosphorus binders are taken with meals to prevent absorption, not to be removed by dialysis
  • Drugs NOT significantly removed (and therefore accumulate): Fat-soluble vitamins (A, D, E, K), highly protein-bound drugs (warfarin, phenytoin), digoxin

Erythropoietin-stimulating agents (ESAs)

The kidneys normally produce erythropoietin to stimulate red blood cell production. In ESRD, EPO production falls, causing anemia (normocytic, normochromic). Patients receive injectable ESAs (epoetin alfa, darbepoetin alfa) – typically administered at the end of the HD session via the venous return line. Monitor hemoglobin against the KDIGO 2026 target: for adults on ESAs, Hb at or below 11.5 g/dL and typically 10–11.5 g/dL, and ESAs should not be used to maintain Hb at 11.5 or higher. In HD patients, targeting higher Hb (for example 13 g/dL or more) increases stroke and vascular access loss. Monitor iron stores (ferritin and transferrin saturation) to ensure adequate substrate.

Phosphate binders

Patients take phosphate binders with every meal and snack to block intestinal phosphorus absorption. The binder must be taken at the time of food ingestion. Types include calcium-based binders (calcium carbonate, calcium acetate – monitor for hypercalcemia), non-calcium binders (sevelamer, lanthanum carbonate), and iron-based binders (ferric citrate – doubles as iron supplementation).


Hemodialysis vs peritoneal dialysis

The NCLEX regularly asks students to distinguish between HD and peritoneal dialysis (PD) – including indications, mechanics, complications, and which patients are better suited for each modality.

In PD, the peritoneal membrane serves as the dialysis membrane. Dialysate is instilled into the peritoneal cavity via a surgically placed PD catheter (Tenckhoff catheter), allowed to dwell, then drained – carrying waste products and excess fluid. This cycle is called an exchange. PD can be performed manually (continuous ambulatory PD, or CAPD – 4 exchanges per day, each dwelling 4–8 hours) or by machine overnight (automated PD, or APD, sometimes called CCPD).

ParameterHemodialysisPeritoneal dialysis
MechanismDiffusion + ultrafiltration across synthetic semi-permeable membrane in dialyzerDiffusion + osmosis across peritoneal membrane (endogenous)
AccessAVF, AVG, or CVC (blood must leave the body)Tenckhoff catheter in peritoneal cavity (no blood circuit)
Session duration3–4 hours, 3 times per weekContinuous (CAPD: 24 hrs/day with exchanges; APD: nightly cycles)
Fluid removalRapid, controlled by ultrafiltration rateGradual; controlled by dialysate glucose concentration (higher dextrose = more osmotic pull = more fluid removed)
Protein lossMinimal (amino acids lost, but protein is not primary loss)Significant – 5–15 g/day lost into dialysate; protein intake of 1.0–1.2 g/kg/day (KDOQI 2020)
AnticoagulationRequired (systemic heparin or citrate to prevent circuit clotting)Not required (no extracorporeal circuit)
Hemodynamic stabilityRequires stable cardiovascular status; HD causes rapid fluid shiftsBetter tolerated hemodynamically – gradual fluid removal
Infection risk typeBacteremia / bloodstream infection (CRBSI with CVC)Peritonitis – most serious PD complication; cloudy effluent is the first sign
Home usePossible (home HD) but complex; most patients go to a dialysis centerYes – PD is home-based by design; patient performs exchanges independently
ContraindicationsLack of suitable access; severe cardiac instability during rapid fluid shiftsPrior abdominal surgeries causing adhesions, peritoneal membrane failure, hernia, inflammatory bowel disease, severe COPD (abdominal distension impairs breathing)
Key nursing priority (HD)Intradialytic hypotension monitoring, access assessment, DDS preventionPeritonitis prevention (sterile technique during exchanges), effluent monitoring, exit site care
AdvantageFaster, more efficient clearance; medically supervisedContinuous gentle clearance; home-based, preserves independence; no blood circuit

NCLEX tip on PD peritonitis: Cloudy effluent (drained dialysate) is the hallmark of peritonitis. The patient will also report abdominal pain and may have fever. Send effluent for cell count, culture, and sensitivity. ISPD 2022 prefers intraperitoneal antibiotics added to the dialysate unless the patient has signs of systemic sepsis. This is the most feared PD complication and a leading reason patients must switch to HD.


Labs to monitor in hemodialysis patients

LabNormal referenceHD patient considerationClinical significance
BUN7–20 mg/dLPre-HD: typically 60–100+ mg/dL; urea reduction ratio (URR) of at least 65%Uremia marker; elevated pre-HD is expected. Failure to reduce adequately indicates poor dialysis (low Kt/V).
Creatinine0.6–1.2 mg/dLPre-HD: typically 8–12 mg/dL in ESRDReflects muscle mass and dialysis clearance in ESRD; it is no longer a measure of residual kidney function once dialysis starts.
Potassium (K+)3.5–5.0 mEq/LPre-HD: often highest after the long weekend gap; dialysate K+ is chosen from the pre-HD valueLife-threatening hyperkalemia is the primary electrolyte emergency. Check before each session.
Phosphorus2.5–4.5 mg/dLOften elevated (5–8 mg/dL) in ESRDHyperphosphatemia → calcium-phosphorus product elevation → vascular calcification; drives secondary hyperparathyroidism
Calcium (corrected)8.5–10.5 mg/dLOften low-normal due to phosphorus binding and reduced active vitamin D productionMonitor for hypocalcemia (tetany, Chvostek's sign, Trousseau's sign); calcium carbonate and calcitriol used for correction
Hemoglobin12–17 g/dLKDIGO 2026, adults on ESAs: Hb ≤11.5 g/dL, typically 10–11.5 g/dL; do not use ESAs to maintain Hb ≥11.5Renal anemia from EPO deficiency. Higher targets raise risk: in HD, targets of 13 g/dL or more increase stroke and access loss, and TREAT (non-dialysis CKD with diabetes) found more strokes at a 13 g/dL target.
Ferritin / TSATLab- and sex-specific reference rangeKDIGO 2026: in HD patients with anemia, iron is suggested when ferritin is ≤500 ng/mL and TSAT ≤30%; it is reasonable to withhold routine iron if ferritin is >700 ng/mL or TSAT ≥40%. Systemic (formerly "absolute") iron deficiency in HD is generally ferritin <200 ng/mL with TSAT <20%Iron deficiency is common (blood loss, frequent lab draws, reduced absorption). Iron adequacy is required for ESA response; KDIGO 2026 suggests IV rather than oral iron in HD patients, with TSAT, ferritin and Hb checked every 1–3 months during IV iron therapy
PTH (intact)15–65 pg/mLKDIGO CKD-MBD suggests roughly 2–9× the upper normal limit of the assay for dialysis patients (about 130–585 pg/mL against a 65 pg/mL upper limit)Secondary hyperparathyroidism develops from chronic hypocalcemia, hyperphosphatemia, and low calcitriol; causes renal osteodystrophy. The target range is deliberately wide: over-suppression risks adynamic bone disease, so trend direction matters more than a single value.
Albumin3.5–5.0 g/dLTarget ≥4.0 g/dLAlbumin is one of the strongest predictors of mortality in dialysis patients; low albumin reflects malnutrition and chronic inflammation

Patient and family education

Patient adherence to the dialysis schedule, diet, and access care is the difference between stable ESRD and repeated hospitalizations. Education must be specific, practical, and repeated across multiple sessions.

Access protection (highest priority education point)

For AVF and AVG patients:

  • Never allow blood pressure cuffs on the fistula arm – compression can cause thrombosis
  • Never allow blood draws, IV placements, or venipunctures in the fistula arm
  • Check the fistula every day by feeling for the thrill (vibration) and listening for the bruit (with a stethoscope if trained, or by pressing gently with fingers)
  • Report to the dialysis team immediately if the thrill or bruit disappears – this indicates clotting
  • Avoid sleeping on the fistula arm or wearing tight clothing or jewelry over it
  • Do not carry heavy bags over the fistula arm
  • Show anyone in an emergency room or hospital the medical alert bracelet or card indicating the fistula arm – advocate firmly if staff attempt access there

For CVC patients:

  • Keep the catheter exit site clean and dry between sessions
  • Do not allow the catheter to be used for anything other than dialysis
  • Report fever, chills, redness, or drainage around the catheter immediately – catheter-related bloodstream infection is life-threatening

Fluid management at home

  • Weigh yourself every morning at the same time, same clothing, after urinating
  • Record the weight daily
  • Report weight gain of more than 2 kg (approximately 4–5 pounds) between sessions
  • Understand which foods contain hidden fluid (soups, gelatin, ice cream, popsicles, ice)
  • Keep a small water bottle to measure daily intake

Diet adherence

  • Avoid high-potassium foods in the days before dialysis, not just on the day of the session – potassium accumulates continuously
  • Take phosphate binders at every meal and snack – not before meals, and not after eating. The binder must be present when phosphorus from food reaches the intestine.
  • Never use salt substitutes (e.g., NoSalt, Nu-Salt) – these contain potassium chloride and can cause lethal hyperkalemia

Recognizing emergencies

Instruct patients and families to call 911 or go to the emergency department for:

  • Loss of thrill or bruit in the fistula – access thrombosis requires emergency salvage
  • Fever or shaking chills during or after dialysis
  • Severe shortness of breath (fluid overload, pulmonary edema)
  • Irregular heartbeat, chest pain (hyperkalemia)
  • Confusion, seizures (uremic encephalopathy, DDS)

NCLEX tips

  1. The AEIOU mnemonic covers all dialysis indications. Acidosis (pH <7.1), Electrolytes (K+ >6.5 mEq/L), Intoxication (lithium, methanol), Overload (fluid unresponsive to diuretics), Uremia (BUN >100 or symptomatic). Any NCLEX question asking “when is dialysis indicated?” – run through AEIOU.

  2. AVF is the usual preferred access. If a question asks which access has the lowest infection risk and longest patency, the answer is AVF. The 2019 KDOQI guideline fits the access to each patient’s ESKD Life-Plan, but a CVC remains the last resort for long-term use. If a question says the patient has a CVC “for dialysis,” expect infection to be the priority complication.

  3. Thrill and bruit assessment is mandatory before every HD session. A question that asks what the nurse should do first when caring for a dialysis patient – assess the access. Loss of thrill is an emergency.

  4. Never take blood pressure, start an IV, or draw blood from the fistula arm. This appears directly in NCLEX questions as a safety-of-care item. The wrong answer options often include these actions.

  5. Hypotension is the most common intradialytic complication. Initial response: Trendelenburg position + reduce ultrafiltration. Do not administer antihypertensives – the patient is already hypotensive.

  6. DDS occurs on the first HD session (or after prolonged uremia) and presents with headache, nausea, and confusion progressing to seizures. The mechanism is cerebral edema from rapid urea removal. Management: slow the dialysis, give mannitol.

  7. Hold antihypertensives before HD. The dialysis removes fluid, lowering BP physiologically. Antihypertensives taken before the session cause severe hypotension. This is a high-yield medication safety question.

  8. Air embolism: clamp the line, left lateral Trendelenburg. Left lateral position moves air from the pulmonary outflow tract to the right ventricular apex where it is less likely to obstruct pulmonary circulation. Do not return blood to the patient.

  9. Hemolysis: stop dialysis, do not return blood. Port-wine discoloration in the venous chamber = hemolysis. The lysed red cells release potassium – hyperkalemia is an immediate concern.

  10. Protein requirements INCREASE on dialysis. This counterintuitive point trips students. Pre-dialysis CKD limits protein (KDIGO 2024: 0.8 g/kg/day). Once on HD, requirements rise to 1.0–1.2 g/kg/day (KDOQI 2020) because amino acids are lost in the dialysate.

  11. Salt substitutes are a hidden potassium source. Potassium chloride is the active ingredient in most salt substitutes – educating patients to avoid these is a frequently tested patient education item.

  12. Peritonitis in PD presents as cloudy effluent. If a question describes a PD patient with cloudy drainage and abdominal pain – peritonitis until proven otherwise. Notify the provider, send effluent for culture.

  13. Phosphate binders must be taken with meals, not before or after. Timing is the entire point – the binder must be in the intestine simultaneously with ingested phosphorus to bind it before absorption.

  14. CRRT is for hemodynamically unstable ICU patients. When a question describes a patient in septic shock or post-cardiac surgery who needs renal replacement, CRRT is the modality – not intermittent HD, which requires cardiovascular stability.

  15. Monitor for secondary hyperparathyroidism. Hyperphosphatemia + hypocalcemia + low calcitriol → elevated PTH → renal osteodystrophy. KDIGO CKD-MBD sets the intact PTH target for dialysis patients at roughly 2–9 times the upper normal limit of the assay (about 130–585 pg/mL against a 65 pg/mL upper limit). Older sources cite a fixed 150–300 pg/mL range – that was the superseded KDOQI target. PTH should not be fully suppressed, because some PTH activity is needed for bone turnover and over-suppression risks adynamic bone disease.

  16. HBsAg-positive means isolation in the dialysis unit only. CDC’s 2001 dialysis recommendations call for a separate room, a dedicated machine and supplies, staff who are not caring for susceptible patients at the same time, and no dialyzer reuse. Patients with hepatitis C or HIV need no isolation or dedicated machine. Everywhere else in the hospital, CDC Appendix A lists hepatitis B, hepatitis C and HIV under Standard Precautions only.


Practice questions

Question 1

A patient on hemodialysis arrives for their scheduled session. During the pre-treatment assessment, the nurse palpates the left forearm arteriovenous fistula and notes absence of a thrill. The nurse’s priority action is to:

A) Proceed with the dialysis session and document the finding
B) Obtain a blood pressure measurement in the left arm to assess perfusion
C) Notify the dialysis nurse practitioner immediately
D) Apply warm compresses to the fistula site and reassess in 30 minutes

Answer: C

Rationale: Absence of thrill indicates the AVF has likely thrombosed. The fistula is the patient’s lifeline for dialysis – a thrombosed fistula requires urgent evaluation and possible thrombectomy or surgical revision within hours to maximize salvage. This is an emergency notification situation. Option A is dangerous – delaying the report risks permanent access loss. Option B is incorrect – blood pressure is never taken in the fistula arm, and this would not address the access problem. Option D wastes critical time; warm compresses may be used for spasm but loss of thrill requires immediate provider notification, not watchful waiting.


Question 2

A patient is one hour into their first hemodialysis session for severe uremia (BUN 145 mg/dL). The patient reports a severe headache and begins vomiting. The nurse’s next action is to:

A) Administer ondansetron 4 mg IV for nausea and continue the session
B) Stop the dialysis session, position the patient supine, and call the provider
C) Reduce the blood flow rate and notify the nephrologist of possible dialysis disequilibrium syndrome
D) Increase the ultrafiltration rate to clear uremic toxins more rapidly

Answer: C

Rationale: This presentation – first HD session, severe uremia, headache, and vomiting – is dialysis disequilibrium syndrome until proven otherwise. The mechanism is cerebral edema from rapid urea removal. The correct intervention is to slow the dialysis (reduce blood flow rate) to decrease the rate of urea clearance, and notify the nephrologist. The session is not necessarily stopped unless symptoms worsen to seizures or loss of consciousness. Option A treats the symptom but not the cause, and continuing full-rate dialysis could worsen the cerebral edema. Option B may be appropriate if the patient deteriorates, but the immediate response is to slow the rate, not stop. Option D is contraindicated – faster clearance worsens DDS.


Question 3

A home peritoneal dialysis patient calls the dialysis clinic and reports that today’s drained dialysate is cloudy and they have diffuse abdominal pain. The nurse’s priority action is to:

A) Instruct the patient to skip today’s exchange and rest until the next scheduled appointment
B) Ask the patient to bring the drained bag to the clinic immediately and notify the provider of suspected peritonitis
C) Advise the patient to increase the dextrose concentration of the dialysate to improve clearance
D) Instruct the patient to clamp the catheter and go to the emergency department for line removal

Answer: B

Rationale: Cloudy effluent with abdominal pain is peritonitis until proven otherwise – the most serious PD complication. The drained bag must be sent for cell count, Gram stain, and culture to guide antibiotic selection. The provider must be notified immediately so antibiotics can be initiated, typically instilled directly into the dialysate. Option A delays care and allows the infection to progress. Option C changing dialysate concentration does not address infection and could worsen abdominal discomfort. Option D is premature – catheter removal is reserved for refractory peritonitis (effluent not clearing after 5 days of appropriate antibiotics), fungal peritonitis and a few other situations; most bacterial peritonitis responds to intraperitoneal antibiotics without removing the catheter.

References

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  2. Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury Work Group. KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int Suppl. 2012;2(1):1–138. doi:10.1038/kisup.2012.1
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  7. Zepeda-Orozco D, Quigley R. Dialysis disequilibrium syndrome. Pediatr Nephrol. 2012;27(12):2205–2211. doi:10.1007/s00467-012-2199-4
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  12. Macdougall IC, Bircher AJ, Eckardt KU, et al. Iron management in chronic kidney disease: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference. Kidney Int. 2016;89(1):28–39. doi:10.1016/j.kint.2015.10.002
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  14. Ikizler TA, Burrowes JD, Byham-Gray LD, et al. KDOQI clinical practice guideline for nutrition in CKD: 2020 update. Am J Kidney Dis. 2020;76(3 Suppl 1):S1–S107. doi:10.1053/j.ajkd.2020.05.006
  15. Lok CE, Huber TS, Lee T, et al; KDOQI Vascular Access Guideline Work Group. KDOQI Clinical Practice Guideline for Vascular Access: 2019 Update. Am J Kidney Dis. 2020;75(4 Suppl 2):S1–S164. doi:10.1053/j.ajkd.2019.12.001
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  20. Centers for Disease Control and Prevention. Recommendations for preventing transmission of infections among chronic hemodialysis patients. MMWR Recomm Rep. 2001;50(RR-5):1–43. https://www.cdc.gov/mmwr/preview/mmwrhtml/rr5005a1.htm
  21. Centers for Disease Control and Prevention. Appendix A: type and duration of precautions recommended for selected infections and conditions. Isolation precautions guideline. Updated September 11, 2026. https://www.cdc.gov/infection-control/hcp/isolation-precautions/appendix-a-type-duration.html
  22. Kuipers J, Oosterhuis JK, Krijnen WP, et al. Prevalence of intradialytic hypotension, clinical symptoms and nursing interventions – a three-months, prospective study of 3818 haemodialysis sessions. BMC Nephrol. 2016;17:21. doi:10.1186/s12882-016-0231-9