Complete Hemodialysis Procedure
Overview and Principle
Hemodialysis (HD) substitutes an artificial filter (the dialyzer) for the glomerulus to produce an ultrafiltrate of plasma. Blood is withdrawn from the patient, circulated through the dialyzer where waste products and excess fluid are removed, and returned to the patient. The core mechanism relies on:
- Diffusion - solutes move down a concentration gradient across a semipermeable membrane (removes urea, potassium, creatinine, phosphate)
- Ultrafiltration (UF) - fluid removal driven by a controlled hydrostatic pressure gradient across the membrane
- Convection (in high-flux/hemodiafiltration) - solute drag carried with water movement, improving middle-molecule clearance
Blood and dialysate flow countercurrently on opposite sides of the membrane to maximize the concentration gradient throughout the entire length of the dialyzer. - Brenner and Rector's The Kidney
Phase 1: Pre-Dialysis Assessment
Patient Evaluation Before Each Session
Before connecting the patient, the following are assessed:
| Parameter | Details |
|---|
| Dry weight (target weight) | Estimated weight with no excess fluid; guides total UF volume |
| Interdialytic weight gain | Compared to last session's post-dialysis weight; excess = fluid to remove |
| Blood pressure and heart rate | Pre-dialysis BP documented; guides UF rate |
| Temperature | Fever may indicate access infection |
| Access site inspection | AV fistula/graft: auscultate for bruit, palpate for thrill; catheter: check exit site for redness/discharge |
| Symptoms | Dyspnea, chest pain, nausea, neurological changes |
| Recent labs | Pre-dialysis BUN, potassium, bicarbonate, phosphate, hemoglobin; reviewed to adjust prescription |
The HD prescription must be individualized for each patient based on these clinical parameters. - Brenner and Rector's The Kidney
Phase 2: Vascular Access
Three types of access are used, in order of preference:
1. Arteriovenous (AV) Fistula (Preferred)
- Surgically created connection between an artery and vein (usually radial artery + cephalic vein at the wrist, or brachial artery + cephalic/basilic vein)
- Takes 6-12 weeks to "mature" (dilate and thicken) before use
- Cannulation technique: two 15-gauge large-bore needles inserted - one arterial (blood withdrawal, upstream) and one venous (blood return, downstream); placed 5-8 cm apart using the rope-ladder or buttonhole technique
- Preferred because of lowest infection rate, longest longevity, and best outcomes
2. AV Graft
- A synthetic (polytetrafluoroethylene, PTFE) or biological tube bridging artery to vein
- Can be used within 2-4 weeks of creation
- Cannulated with the same 15-gauge needle technique as a fistula
- Higher complication rate than native fistula (thrombosis, infection, stenosis)
3. Tunneled-Cuffed Central Venous Catheter (Last resort)
Used when AV access is not available or not yet mature.
Insertion procedure (as described in Brenner and Rector's The Kidney):
- Strict sterile technique and topical 1% Xylocaine; conscious sedation often used
- Access to the right internal jugular vein under real-time ultrasound guidance using a 21-gauge needle
- A guide wire is passed down to the inferior vena cava under fluoroscopy
- A skin pocket (~1 cm) is created at the insertion site
- A subcutaneous tunnel is created laterally and inferiorly, under the clavicle, approximately 5-7 cm from the needle insertion point
- The catheter tip is fed to the junction of the superior vena cava and right atrium
- The cuff is positioned 2 cm from the exit site
- Final X-ray confirms position and checks for kinks
Catheter sizes: 14.5 or 16 French; lengths: 24 cm (right IJ), 28 cm (left IJ), 36-42 cm (femoral)
Tunneled hemodialysis catheter placement - the catheter tunneled from upper chest to the internal jugular entry site. - Brenner and Rector's The Kidney
Phase 3: The Dialysis Prescription
The complete dialysis prescription consists of the following individualized components (Box 63.1, Brenner and Rector's The Kidney):
| Prescription Component | Standard Values |
|---|
| Duration | 3-4 hours per session (US average ~3.5 hr) |
| Frequency | 3 times per week (Monday/Wednesday/Friday or Tuesday/Thursday/Saturday) |
| Vascular access type | AV fistula > AV graft > tunneled catheter |
| Dialyzer | Selected by membrane type, surface area, flux (low vs. high), biocompatibility |
| Blood flow rate (Qb) | 300-500 mL/min |
| Dialysate flow rate (Qd) | 500-800 mL/min (countercurrent to blood) |
| Ultrafiltration rate (UFR) | Calculated from weight gain ÷ session time; typically 0.5-1 L/hr |
| Dialysate composition | Tailored (see table below) |
| Anticoagulation | Heparin (most common) |
| Dialysate temperature | 35-37°C (cooling can reduce intradialytic hypotension) |
| Intradialytic medications | ESAs, IV iron, vitamin D analogs as needed |
Dialysate Composition
| Solute | Typical Concentration | Purpose |
|---|
| Sodium | 135-145 mEq/L | Fluid balance, BP control |
| Potassium | 1-4 mEq/L | Removes excess potassium |
| Bicarbonate | 33-40 mEq/L | Corrects metabolic acidosis |
| Calcium | 2.5-3.5 mEq/L | Bone disease management |
| Magnesium | 0.5-1.0 mEq/L | Prevents hypomagnesemia |
| Glucose | 100-200 mg/dL | Prevents hypoglycemia |
Dialysate concentrations mirror those normally maintained by the native kidneys. - Brenner and Rector's The Kidney
Phase 4: Anticoagulation
Anticoagulation prevents clotting within the extracorporeal circuit.
Standard Protocol - Unfractionated Heparin (UFH):
- Small amounts of IV heparin (1,000-2,000 units) prevent thrombosis at the vascular access site - Tintinalli's Emergency Medicine
- Loading dose: ~40 U/kg IV bolus at the start
- Continuous infusion: ~20 U/kg/hour, adjusted to maintain adequate circuit anticoagulation
- Target: activated clotting time (ACT) 200-250 seconds within the circuit
Alternatives when heparin is contraindicated (e.g., heparin-induced thrombocytopenia):
- Regional citrate anticoagulation - citrate infused pre-filter creates regional hypocalcemia in the circuit; calcium replaced post-filter
- Hirudin/lepirudin - direct thrombin inhibitors
- Heparin-free dialysis - frequent saline flushes of circuit; used in active bleeding
Phase 5: Machine Setup and Circuit Priming
Before connecting the patient:
- Dialyzer inspection - check for integrity, correct membrane type, expiry
- Blood tubing set - arterial and venous lines connected to dialyzer
- Circuit priming - the extracorporeal circuit is flushed with ~500-1000 mL normal saline to remove air and manufacturing preservatives (e.g., glycerine), and to check for leaks
- Dialysate preparation - machine mixes concentrated dialysate with purified water to achieve the prescribed ionic composition; online conductivity monitoring ensures correct preparation
- Water treatment - incoming water undergoes softening, activated carbon filtration, and reverse osmosis to remove ions, organic compounds, and endotoxins; standards for water purity are strict because microbe-generated impurities such as endotoxins can cross the dialyzer membrane and cause inflammation - Brenner and Rector's The Kidney
- Alarms set - arterial pressure, venous pressure, TMP (transmembrane pressure), air detector, conductivity, temperature, and blood leak detector alarms confirmed
Phase 6: Initiating Dialysis (Patient Connection)
For AV Fistula/Graft:
- Skin cleaned with antiseptic; sterile drape placed
- Local anesthetic (optional) applied over needle sites
- Arterial needle (16G or 15G) inserted first, bevel up, at 25-45° angle, in the direction of blood flow upstream
- Venous needle inserted downstream, 5-8 cm from the arterial needle
- Needles secured with tape/dressing
- Blood lines connected; clamps released
- Blood pump started at a slow initial rate (~100-150 mL/min), then gradually increased to target (300-500 mL/min) over several minutes
For Catheter:
- Sterile technique; mask and gloves mandatory
- Catheter caps removed; lumens aspirated to check blood return
- Locked anticoagulant solution (heparin lock) aspirated and discarded
- Blood lines connected to arterial (red) and venous (blue) ports
- Blood pump started
Once connected:
- Heparin loading dose administered
- Heparin infusion started
- UF rate set per prescription
- Dialysate circuit opened
Phase 7: During the Dialysis Session (Monitoring)
The patient is monitored continuously throughout the 3-4 hour session:
| Parameter | Frequency | Action if Abnormal |
|---|
| Blood pressure | Every 30 min (or continuous) | If hypotensive: reduce UFR, give normal saline bolus, recline patient |
| Heart rate | Every 30 min | |
| Symptoms | Continuous nursing observation | |
| Arterial/venous pressures | Continuous (machine alarm) | Access dysfunction or needle dislodgement |
| Transmembrane pressure (TMP) | Continuous | Clotting or filter fouling |
| Blood leak detector | Continuous | Dialyzer membrane rupture |
| Air detector (venous trap) | Continuous | Air embolism prevention |
| Conductivity and pH | Continuous | Incorrect dialysate preparation |
| Temperature | Continuous | |
| Blood glucose (diabetics) | Each session | |
Common Intradialytic Complications and Management
| Complication | Frequency | Cause | Management |
|---|
| Hypotension | Most common (~25% of sessions) | Excessive/rapid fluid removal, low serum osmolality | Reduce UF rate, saline bolus 100-200 mL, trendelenburg position, cool dialysate |
| Muscle cramps | Common | Rapid fluid removal, low sodium dialysate | Reduce UF rate, saline bolus, hypertonic saline or glucose |
| Nausea and vomiting | Common | Hypotension, dialysis disequilibrium | Treat hypotension; antiemetics if needed |
| Headache | Common | Dialysis disequilibrium syndrome | Reduce blood flow rate, shorten session |
| Fever/chills | Occasional | Access infection, endotoxin contamination | Blood cultures, IV antibiotics; evaluate water quality |
| Chest pain | Occasional | Angina, air embolism, hemolysis | Stop dialysis; ECG, oxygen, evaluate cause |
| Air embolism | Rare | Air in circuit | Clamp lines, left lateral decubitus position, 100% oxygen |
| Hemolysis | Rare | Overheated dialysate, incorrect osmolality, kinking | Stop dialysis; do NOT return blood |
| Arrhythmia | Occasional | Electrolyte shifts (K+), myocardial disease | ECG monitoring; adjust dialysate K+ |
Dialysis Disequilibrium Syndrome - occurs especially in first sessions or after long gaps; caused by rapid removal of urea creating transient cerebral edema from osmotic shift. Prevented by using lower blood flow rates and shorter first sessions.
Phase 8: Terminating Dialysis (Takedown)
At end of session:
- Blood pump slowed to ~100 mL/min
- Blood lines rinsed with ~200-300 mL normal saline to return all blood to the patient (saline rinse-back)
- Blood pump stopped
- Lines clamped
- Needles removed from AV fistula/graft; firm pressure held for 5-10 minutes until hemostasis achieved
- For catheter: each lumen flushed with saline, then locked with heparin solution (1000-5000 U/mL per lumen volume); caps replaced with strict sterile technique
- Access site inspected and dressed
Post-Dialysis Assessment
- Post-dialysis weight recorded and compared to target dry weight
- Blood pressure and heart rate (supine and sitting) - watch for orthostatic hypotension
- Post-dialysis symptoms: fatigue, lightheadedness, dyspnea
- Blood samples drawn for post-dialysis BUN (to calculate Kt/V)
- Patient monitored for 10-15 minutes before discharge from the unit
Phase 9: Assessing Dialysis Adequacy (Kt/V)
Adequacy is measured by urea kinetic modeling, specifically Kt/V:
K = urea clearance (mL/min)
t = dialysis time (min)
V = volume of distribution of urea = total body water (liters)
Calculation (simplified):
From pre- and post-dialysis BUN:
URR (Urea Reduction Ratio) = [(Pre-BUN - Post-BUN) / Pre-BUN] × 100
A URR ≥65% is considered adequate. - Washington Manual of Medical Therapeutics
For more accurate Kt/V, formal urea kinetic modeling accounts for:
- Fluid removal during the session (which reduces V)
- Urea generation during treatment
- Post-dialysis urea rebound (the "double-pool effect" - urea rebounds ~30 min after dialysis ends as intracellular urea equilibrates with the blood)
Adequacy Targets (KDOQI Guidelines):
- Single-pool Kt/V ≥ 1.4 per session (minimum 1.2)
- Standard Kt/V ≥ 2.1/week for thrice-weekly dialysis
- For AKI: Kt/V ≥ 3.9/week (KDIGO recommendation) - Brenner and Rector's The Kidney
Residual kidney function (Ku) contributes additional continuous clearance between sessions and should be incorporated into the overall adequacy calculation - it confers a survival advantage far in excess of an equivalent dialyzer clearance. - Brenner and Rector's The Kidney
Phase 10: Machine Disinfection After Session
After each patient:
- Dialyzer (if for reuse program) rinsed, tested for volume/clearance, and chemically disinfected
- Blood tubing discarded as biohazardous waste
- Machine exterior wiped with appropriate disinfectant
- Dialysate pathways disinfected (heat or chemical)
- Reuse of dialyzers is prohibited by law in some countries (e.g., Egypt) and not practiced in others (Saudi Arabia, Libya, Iran) - Brenner and Rector's The Kidney
Summary: Complete HD Session Timeline
BEFORE SESSION
├── Patient assessment (weight, BP, labs, access inspection)
├── Prescription review & adjustment
└── Machine setup, priming, dialysate preparation
INITIATING DIALYSIS
├── Vascular access cannulation (AV needles) or catheter connection
├── Heparin loading dose
└── Blood pump started slow → ramp to target Qb
DURING SESSION (3-4 hours)
├── Continuous machine monitoring (pressures, alarms)
├── Vital signs every 30 min
├── UFR adjusted per fluid removal target
└── Intradialytic complications managed as they arise
TERMINATING DIALYSIS
├── Saline rinse-back of extracorporeal blood
├── Needles/catheter disconnected with sterile technique
├── Hemostasis (needles) or heparin lock (catheter)
└── Post-dialysis weight, BP, symptom check
POST-SESSION
├── Post-dialysis BUN for Kt/V calculation
├── Machine disinfection
└── Patient education and next appointment
Sources: Brenner and Rector's The Kidney, 2-Volume Set; Tintinalli's Emergency Medicine, A Comprehensive Study; Washington Manual of Medical Therapeutics; Comprehensive Clinical Nephrology, 7th ed.; Brenner and Rector's The Kidney (KDIGO AKI guidelines chapter)