Dialysis Flashcards

1
Q

Drugs cleared by dialysis

A

BLAST - barbiturate, lithium, alcohol (methanol, ethylene glycol) salicylates, theophyllines

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2
Q

Types of dialysis

A

Haemodialysis
* Hameofiltration
* Haemodiafiltration
* Sustained low efficiency dialysis
* Continuous veno-veno HD, HF, HDF

Peritoneal dialysis
* Automated peritoneal dialysis
* Continuous ambulatory peritoneal dialysis

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3
Q

Main indications for dialysis in NZ/Australia

A

In order of most common
* Diabetic nephropathy
* Glomerulonephritis
* Hypertenion
* Polycystic kidney disease

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4
Q

Principles of dialysis

A

Diffusion
* Based on concentration gradient across a semi-permeable membrane
* Good for clearing small molecules
* E.g. haemodialysis and peritoneal dialysis

Convection
* Relies on hydrostatic pressure across a semi-permeable membrane
* Effective for clearing larger molecules
* E.g. haemofiltration

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5
Q

Benefits/disadvantages of haemodialysis

A

Benefits
* Rapid access - commonly used acutely
* Better for patients who require supervision
* Long-term dialysis - PD membranes often fail with time
* Can still work e.g. noctural dialysis or evening shift

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6
Q

Difference between haemodialysis and haemofiltration

A

Haemodialysis
* Dialysate added to circuit provides concentration gradient

Haemofiltration
* Replacement fluid added to dialyser = provides hydrostatic pressure
* When it is added to the circuit before it enters the dialyser = pre-dilution haemofiltration
* When it is added to the circuit after it goes through the dialyser = post-dilution haemofiltration

Haemodiafiltration
* Both dialysate and replacement fluid added to circuit - uses both diffusion and convection waste

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7
Q

Access options for haemodialysis

A

Temporary
* Non-tunneled catheter (Vascath) -> femoral or internal jugular veins
* Tunneled cather (Permacath) -> usually internal jugular veins, tip sits in SVC, cuff sits under the skin and over time the body forms scar tissue around the cuff

Complications dialysis catheters
* Infection - exit site, tunnel infection
* Malfunction - malposition, cracked/broken/kinked, fibrin sheath formation, retraction
* Central vein stenosis (when catheter has to be placed in central veins rather than internal jugular) -> can cause SVC obstruction - will see collateral veins and upper limb oedema

Permanent
AV fistula - ideal fistula -> sufficient blood flow, easy to cannulate, does not restrict blood supple, non-dominant arm, requires 6-8 weeks to mature
* Common sites -> radiocephalic, brachiocephalic, brachiobasilic
* Associated with less morbidity and moratlity compared to other alternatives
Complications
* Ischaemia - Steel syndrome
* Bruising/haematoma
* Aneursymal fistula - can cause high output heart failure - large portion of cardiac output -> fistula, also risk of bleeding
** * Loop graft** - made with synthetic material, for those with inadequate native veins, complications similar to AV fistula and catheters

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8
Q

Practicalities of haemodialysis prescription

A

See slide
* Standard outpatient prescription is 3x weeks for 4 hours at a time
* Higher the blood flow rate - the more dialysis you are getting
* Patients starting out on dialysis usually start with the small dialysier - usually for a shorter time with low blood flow rates and dialysate flow rates -> build up from there
* Ultrafiltration rate - how quickly you want to remove fluid - ?how much fluid needs to be taken off
* Anticoagulation needed to keep the circuit running - usually unfractionated or LMWH - may be omitted if patient is about to go to surgery or is bleeding
* EPO - does not cross dialysis membrane

Note time on machine main determinant of dose - blood flow, dialyslate flow, membrane charactersitics and membrane surfact area only change dose to a small degree

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9
Q

Complications of haemodialysis

A

Dialysis-dysequilibrium syndrome
* Cerebral oedema due to osmotic effects of urea
* Start dialysis slowly to avoid

Intradialytic hypotension and cramps
* Pause of cease fluid removal

Dialysis related amyloidosis
* Long-term ( > 5 years) accumulation of B2-microglobulin
* Not seen much anymore since changing to high flux dialysers

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10
Q

Principles and advantages of peritoneal dialysis

A
  • Peritoneal membrane is semipermeable membrane
  • Different types of bags - based on glucose to draw fluid
  • Sometimes used as acute therapy
  • PD catheters generally left in 2-4 weeks before using to reduce risks of leaks and malfunction

Benefits
* Lifestyle/work/travel
* Better for maintaining residual renal function

Considerations
* Not lifelong option - sclerosed membrane
* Exposure to high glucose

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11
Q

Notes on different modalities of peritoneal dialysis

A

** Continuous ambulatory PD**
- Manually change the bags throughout the day - can require 5 changes
- Connect fliuid bag in - after a few hours connect bag to drain out

Peritoneal dialysis
- Machine does the exchanges several times throughout the night

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12
Q

Notes on peritoneal dialysis prescription

A

Peritoneal membrane type
* Determined via peritoneal equilibrium test
* Assessent of solute transfer rates and how they equilbrate
* Gives you the transport status - low (slow), high (fast), average
* Slow transport status more suited to CAPD, high transport status more suited to APD

Peritoneal dialysis fluids
* Physiologic concentrations of sodium, calcium, magnesium, chloride. Lactate as buffer
* Glucose is the principal osmotic agent - concentrations of 1.5% (yellow), 2.5% (green), 4.25% (red) - higher the concentration the more filtration, but increased diabetes and membrane ultrafiltration failure
** Other solutions**
* Icodextrin - no glucose, induces higher ultrafiltration volume and can be used up to 18 hours
* Amino acid solutions

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13
Q

Notes on PD complications

A

Catheter infection
- Exit site
- Tunnel infection

Catheter malfunction
- Malposition (constipation +++), and kinks
- Pericatheter leaks

PD Peritonitis
- Present with abdominal pain and often coudy peritoneal bags
- Send PD fluid off for cell count and culture
- Most infections due to coagulase negative staph or staph aureus
- Treatment - intraperitoneal antibiotics and oral antibiotics

Pleuroperitoneal leak
- Diaphragmatic defect

Membrane sclerosis -> PD failure

Encapsulating peritoneal sclerosis
- Progressive inflammatory process -> fibrosis of the peritoneal
- Can encase the small bowel -> bowel obstruction
- High mortality

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14
Q

Contraindications to peritoneal dialysis

A

You need
- Functioning peritoneal membrane
- Home
- Willingness to do PD

Relative contraindications
- Abdominal hernia
- Previous abdominal surgery
- High BMI
- Dexterity/vision/strength

Absolute contraindications
- Non-compliance
- Major psychiatric history
- Inability to maintain hygiene /sterile environment
- Poor social circumstances

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15
Q

Measures of dialysis adequacy

A
  • Symptoms
  • Nutritional
  • Fluid balance & BP control

Biochemical
- Kt/V - represents clearance of urea in the context of time and volume - aim for 1.2 - 1.3 in haemodialysis, 1.7 in PD. Doesn’t take into account fluid clearance & middle molecule clearance
- Urea reduction radio - Urea pre-dialysis - post-dialysis/urea pre-dialysis = less prescise measure
- Peritoneal equilbtation test - also gives you a measure of creatinine clearance which you want to be > 60

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16
Q

Indications for dialysis

A

Acute
- Oligoanuria
- Fluid overload/acute pulmonary oedema
- Metabolic acidosis
- Refactory hyperkalaemia
- Uraemic encepahlopathy
- Uraemic pericarditis

Chronic
- All of the above plus presence of symptoms -> fatigue, difficulty concentrating, loss of appetite/weight loss, metallic taste, itch

Refer to a nephrologist for overall management of CKD. For dialysis access when eGFR < 20 (unless acute indication for dialysis)
Exactly when to start controversial - IDEAL study no change between GFR 10-15 anf GFR 5-7
Most people with CKD in Australia start with eGFR 6-7