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Peritoneal dialysis

Peritoneal dialysis. Jana Fialová Martina Peiskerová Klinika nefrologie 1. LF a VFN Praha 10/2007. Modalities of renal replacement therapy. Interchangeable, depends on residual renal function. Ramesh Khanna & Karl D. Nolph. Peritoneal dialysis - outline. Principles of PD PD solutions

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Peritoneal dialysis

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  1. Peritoneal dialysis Jana Fialová Martina Peiskerová Klinika nefrologie 1. LF a VFN Praha 10/2007

  2. Modalities of renal replacement therapy Interchangeable, depends on residual renal function Ramesh Khanna & Karl D. Nolph

  3. Peritoneal dialysis - outline • Principles of PD • PD solutions • PD catheter • Indication / contraindication of PD • PD schemes : CAPD, CCPD • Assessement of PD adequacy, ultrafiltration • Assessement of peritoneal function • Complications • Perspectives – new dialysis solutions

  4. Peritoneal dialysis – introduction • method of RRT for 100.000 patients worldwide • complementary to hemodialysis Principles: • peritoneum (capillary endothelium, matrix, mesothelium) = semipermeable dialysis membrane through which fluid and solute move from blood to dialysis solution via diffusion and convection • effective peritoneal surface area = perfused capillaries closed to peritoneum (↓ in peritonitis) • ultrafiltration (movement of water) enabled by osmotic gradient generated by glucose or glucose polymers (isodextrin)

  5. Principles of peritoneal dialysis

  6. Scheme of peritoneal solute transport by diffusion through the pores of capillary wall

  7. Model of transport - 3 sorts of pores Ramesh Khanna & Karl D. Nolph

  8. Composition of standard peritoneal dialysis solution Na 132 mmol/l Ca 1,25mmol/l Mg 0,5 mmol/l Cl 100 mmol/l lactate 35 mmol/l ev. lactate/bicarbonate glukose 1,36-4,25 g/dl osmolarity 347-486 pH 5,2 GDP (degradation products of glucose) Ramesh Khanna & Karl D. Nolph

  9. Urea concentration in dialysate, rate of equalization of solute concentration depends on molecular size of solute

  10. Concentration of Creatinin in dialysate equilibrium of concentrations between dialysate and blood is slower than for urea

  11. Peritoneal catheter • implanted via laparoscopy, punction or laparotomy (total anesthesy) • PD is started 3 weeks following the impantation of catheter

  12. Types of peritoneal catheters

  13. Why to start with PD ? 1. better maintenance of residual renal function

  14. Why to start with PD ? • clinical outcomes comparable to HD, no difference in 2 year and 5 year mortality vs. HD (study NECOSAD) • saves vascular access • preferred for children (APD) • modality choice is a lifestyle issue

  15. Indication / Contraindications of PD 80% of patients have no contra-indication to any of the dialysis methods and may choose according to their life style between HD a PD Absolute contra-indications of PD: 1.peritoneal fibrosis and adhesions following intraabdominal operations 2.inflammatory gut diseases Ramesh Khanna & Karl D. Nolph

  16. Relative contraindications of PD • * diverticulosis • colostomy • obesity • blindness • pleuro-peritoneal leakage • hernias • significant loin pain • big polycystic kidneys • severe deformant arthritis • psychosis • significant decrease of lung functions

  17. CAPD – continual ambulatory peritoneal dialysis • manual exchanges

  18. NIPD – night intermitent peritoneal dialysis (cycler)

  19. CCPD – continual cyclic PD

  20. Assessement of PD adequacyPET (peritoneal equilibrium test) 1 • determines quick or slow passage of toxins from the blood into the dialysis fluid • ‘high-fast transporters’ v.s. ‘low-slow transporters’ • helps to decide about the PD scheme (dwell duration and intervals, CAPD vs. CCPD) • performed in hospital, takes 5 hours • involves doing a CAPD exchange using a 2.27% G, samples of PD fluid and blood are taken at set times

  21. PET (peritoneal equilibration test) 2

  22. Interpretation of peritonal equilibration test ??

  23. Results of baseline PET Ramesh Khanna & Karl D. Nolph

  24. Choice of PD scheme depends of BSA and type of transport

  25. Assessement of peritoneal function • PET- peritoneal equilibration test (type of transport and ultrafiltration after 4 hours) • weekly clearance of creatinine and urea • daily UF • dicrease of Na in dialysis fluid after 60 minutes using 3,8% G (test of aquaporines)

  26. Ratio D/P for Na, upper curve – 1,27% glucose, lower curve - 3,86% G (initial drop due to transcellular UF of water through aquaporins)

  27. Ultrafiltration during PD • Depends on: • - type of transporter – low transporters have better UF • - concentration and type of osmotic agent in PD fluid: • Fluids with glucosis (1,27%, 2,5% a 3,8% ), higher concentration – higher osmotic pressure and UF • Fluid with icodextrin (Extraneal) = glucose polymer with a large molecule, resorbs only 10-20%, offers longtime UF, suitable for long night exchanges, 8-12 hours) • - time between exchanges, using glucose-based fluids, maximal UF obtained after 2-3 hours, using longer spaces UF dicreases.

  28. Ultrafiltration in different types of PD solutions

  29. Criteria of PD adequacy

  30. Complications of PD 1 • Infectious: • exit-site inflammation (flare, suppurative secretion, • granulation) • peritonitis (turbid dialysate, abdominal pain, fever) • Non-infectious: • hernias • hydrothorax • sclerosing encapsulating peritonitis (rare, life threatening complication, mostly after ≥ 6 years on PD, peritoneum is massively thickened and calcificated, leading to intestinal obstruction)

  31. Complications of PD 2 • Non-infectious: • Leakage of dialysate along the peritoneal catheter • Drainage failure of dialysate (dislocation or catheter obstruction by fibrin) • Morphologic changes of peritoneum following long-lasting PD (peritoneal fibrisis, mesotelial damage, vasculopathy and neo-angiogenesis) leading to loss of UF capacity – reason for PD cessation in 24% of all patients, and in 51% of patients treated above 6 years.

  32. Causes of UF failure • Large vascular surface of peritoneum (due to neo-angiogenesis, vasodilation), leading to high (fast) type of transport including fast loss of osmotic glucose pressure • Decreased function of aquaporins • High lymfatic absorption

  33. Morphologic changes of peritoneum due to PD (1) Obr.1-before starting PD, norm. peritoneum (omentum)

  34. Morphologic changes of peritoneum due to PD (2) Obr.2-after 3 years of PD, submesotelial fibrosis and neo-angiogenesis (enlargement of vascular surface of peritoneum)

  35. Peritonitis • Clinical features: cloudy PD effluent, abdominal pain, nausea, vomiting, • Laboratory: leucocytosis, CRP, > 100wbc/ mm3, PD fluid culture • Bacteriology: Gram + cocci (incl. S.aureus) in 75%, Gram – (incl. Pseudomonas) in 25%, culture negative, mycobacterial (1%), fungal (3%), allergic (Icodextrin) • Complications: relapses, antibiotic treatment failure, acute and chronic UF failure • Treatment for. 14-21 days : Gram + cocci: Vankomycin / cephalosporin, Gram -: aminoglycoside / cephalosporin III. Generation (+ antimycotics, metronidazole) • Goal: < peritonitis / 18 months

  36. From PD gudelines (ISPD) • biocompatible PD solutions - normal pH, low concentration of glucose • insertion of PD catheter – 10 days-6 weeks before RRT • urea / creatinine clearance measured every 6 months • PET: 6 weeks after commencing treatment + annually • avoid routine use of high glucose concentrations )use of icodextrin, aminoacids instead) • preserve residual diuresis, obtain UF above 750 ml/day • peritonitis and exit-site infection rates, regular revision of technique • invasive procedures cover by ATB prophylaxis • topical ATB administration if needed (S.aureus, Ps. aeruginosa) • beware central obesity

  37. Perspectives - New dialysis solutions protect peritoneal membrane •  GDPs and AGEs •  Lactate • Physiologic pH and pCO2 •  Membrane and immune cell function Physioneal1 Extraneal2 • Isosmolar to plasma • No glucose exposure • GDPs and AGEs •  Membrane and immune cell function Nutrineal2 • No glucose exposure • No GDPs or AGEs • Membrane and immune cell function 1Skoufos, et al. Kidney Int. 2003;64(suppl 88):S94-S99. 2Vardhan, et al. Kidney Int. 2003;64(suppl 88):S114-S123.

  38. Clinical advantages of new dialysis solutions Physioneal Infusion pain Peritonitis  Glycemic control Appetite Patient acceptance No  UF Extraneal Glucose load Glycemic control UF, control of fluid status Dyslipidemia Quality of life  Time on PD Nutrineal Glucose load Glycemic control Protein intake, nutritional status Pecoits-Filho, et al. Kidney Int. 2003;64(suppl 88):S100-S104. Vardhan, et al. Kidney Int. 2003;64(suppl 88):S114-S123.

  39. Glucose absorbed = 159 g/day 2.5 L Physioneal 1.36% 2.5 L Physioneal 1.36% 2.5 L Physioneal 1.36% 2.5 L Physioneal 3.86% Glucose absorbed = 50 g/day 2.5 L Physioneal 1.36% 2.5 L Physioneal 1.36% 2.5 L Nutrineal 2.5 L Extraneal Absorbtion of glucose from peritoneal solutions • Solutions containing glucose (green) lead to significant glucose absorbtion • Solutions based on another osmotic agent (blue, violet) do not lead to glucose absorbtion, so decrease total daily glucose load). 1 2

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