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Peritoneal dialysis (PD): overview
AKA: automated peritoneal dialysis (APD)/continuous cycler peritoneal dialysis (CCPD), continuous ambulatory peritoneal dialysis (CAPD), continuous optimized peritoneal dialysis (COPD), intermittent peritoneal dialysis (IPD), nightly intermittent peritoneal dialysis (NIPD), tidal peritoneal dialysis (TPD)
A general overview of the principles of peritoneal dialysis therapy in pediatric patients
Fundamentals
- Sterile dialysate fluid is introduced into the peritoneal cavity via a catheter and exchanged at intervals
- Typically, the dialysate is infused, allowed to dwell for a period of time, and then drained; this cycle is repeated a number of times
- Exception: continuous flow peritoneal dialysis
- Typically, the dialysate is infused, allowed to dwell for a period of time, and then drained; this cycle is repeated a number of times
- Rather than using an extracorporeal dialyzer/filter, the patient’s peritoneal membrane serves as the semipermeable membrane
- The presence of small pores aquaporin channels allow water to move through the membrane.
- The peritoneum is highly vascular and the presence of capillaries allows for transfer of solutes.
Peritoneal membrane as filter
Why it works
- Within the peritoneal membrane (between the abdominal wall and the peritoneal cavity) there are capillaries, lymphatic vessels, and interstitial spaces
- These enable the absorption of particles from the dialysate (in the peritoneal cavity) into the rest of the body
- The peritoneal capillaries enable the movement of water (by
) into the peritoneal cavity
- Transport in PD is an interaction of diffusion,
, and fluid absorption
Peritoneal transport: “three pore” conceptual model
- Large pores (>20 nm [>200 Å] diameter)
- <10% of the pores in the peritoneal membrane
- Permit transport of proteins (e.g., immunoglobulins) and other large molecules
- Can be increased with significant inflammation such as peritonitis
- Small pores (4-6 nm [40-60 Å] diameter)
- ~90% of pores in the peritoneal membrane
- Transport most small molecules
- Ultra small pores (0.3-0.5 nm [3-5 Å] aquaporins)
- 1-2% of pores in the peritoneal membrane
- Responsible for nearly half of water transport
Diffusion in PD: key factors
- Concentration gradient of solute: dialysate/plasma (D/P) ratio
- Mass transfer area coefficient (MTAC)
- Effective peritoneal surface area (analogous to the K0A in
) - Surface area of the peritoneal membrane
- Vascularity: how many peritoneal capillaries are in the peritoneum
- Diffusive characteristics of membrane for solute in question (permeability)
- Varies from patient to patient
- Changes in individuals over time
- Effective peritoneal surface area (analogous to the K0A in
- Particle size:
- Small molecules diffuse rapidly
- Large molecules take a longer time to diffuse across the peritoneal membrane
Ultrafiltration in PD: key factors
- Osmotic gradient: fluid removal (
) is accomplished using osmotic pressure rather than hydrostatic pressure - The osmotic gradient is created by including an osmotic agent (e.g., dextrose, icodextrin) in the dialysate
- Increasing the concentration of the osmotic agent generates a greater osmotic gradient and results in more fluid removal
- Using dialysate with higher dextrose concentration generates a greater osmotic gradient and results in more fluid removal
- The osmotic gradient is created by including an osmotic agent (e.g., dextrose, icodextrin) in the dialysate
- Reflection coefficient: how resistant a particle in the dialysate is to being absorbed (i.e., how well it stays in the dialysate), on a scale of 0 to 1
- An osmotic agent with a reflection coefficient of 1 would be an ideal osmotic agent: it would draw water into the peritoneal cavity without being absorbed
- Ultrafiltration coefficient (of the membrane): depends on the surface area and the number of pores
- Hydrostatic pressure
- Filling the peritoneal cavity with dialysate increases the hydrostatic pressure
- Oncotic pressure gradients
- Related to changes of protein levels inside the bloodstream as water is removed from the peritoneal cavities
Fluid absorption
- Peritoneal fluid, including dialysate, is absorbed during peritoneal dialysis:
- Direct lymphatic absorption
- Tissue absorption (into the interstitium) of peritoneal fluid
- Fluid absorption limits
and mass transfer - Higher levels of peritoneal absorption reduces the net
- Higher levels of peritoneal absorption reduces the net
Comparison with HD
- PD is generally the preferred chronic dialysis modality in pediatrics
- Depends on patient and family preference, institutional practice and availability
Advantages of PD
- Vascular access is not required
- Better outcomes (vs
) in the US -
Gentler fluid removal over longer time period avoids cardiac stunning seen in
- Better preservation of remaining kidney function
- Better outcomes after kidney transplantation
- Better growth
- Improved fluid balance
- Also reduces need for antihypertensive medications
-
Gentler fluid removal over longer time period avoids cardiac stunning seen in
- Daily clearance
- Less accumulation of toxins (e.g., phosphorus, potassium) between sessions
- Better quality of life
- Home treatment (less frequent travel to the dialysis unit)
- Self control of the therapy
- No needles
- Facilitates school attendance/employment
- Extended travel is possible
- Fewer dietary restrictions
- Less technically difficult, especially in babies
- Teaching usually takes 3-5 days
Disadvantages of PD
- Risk of infection: peritonitis, exit site, and tunnel infections
- Hernias
- Decreased appetite
- Body image disturbance
- Labor intensive
- Drawbacks of home PD:
- Caregiver burden
- Requires a lot of physical space to keep supplies
- Requires a savvy family
- However, even with poor educational background (e.g., illiteracy) can be trained to be competent
Contraindications to PD
- Anatomical
- Multiple prior abdominal surgeries with lots of scarring
- Compromised diaphragm with communication between abdominal and thoracic cavities (e.g., diaphragmatic hernia, surgical complication)
- Other congenital abnormalities: omphalocele, gastroschisis, bladder exstrophy
- ≥2 prior episodes of peritonitis
- Obliterated peritoneal cavity
- E.g., from prior surgeries, trauma, infections
- Peritoneal membrane failure
Relative contraindications
- Presence of ileostomies/colostomies
- Ideally would locate as far away as possible from the PD exit site to avoid contamination
- Infants with significant organomegaly
- Impending abdominal surgery
-
If expecting transplant soon (typically <3-6 months), usually prefer to initiate
- Significant time investment of planning surgery, waiting for tract to mature, training of patient/family
- Lack of appropriate caregiver(s)
- Lack of appropriate home environment