Clinical Monitoring Systems - PowerPoint PPT Presentation

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Clinical Monitoring Systems

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Title: Clinical Monitoring Systems Author: Baxter Last modified by: mosss Created Date: 1/20/1999 8:43:16 AM Document presentation format: On-screen Show – PowerPoint PPT presentation

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Title: Clinical Monitoring Systems


1
Principles of Peritoneal Dialysis
2
Diffusion
  • Transfer by diffusion is the passive transfer of
    solutes across the membrane, without the passage
    of solvent (water).

Blood
Membrane
Dialysate
1 - Red blood cell 2 - Bacteria
Beta 2-m (Solute PMgt5000)
3
Factors effecting diffusion
  • Membrane
  • Surface area, type, thickness
  • Blood film thickness
  • Dialysate flow configuration
  • Concentration gradient
  • Size of solute
  • Ultrafiltration
  • Temperature of dialysate
  • Qb - Blood flow rate
  • Qd - Dialysate flow rate
  • Time

4
Factors relevant to PD
  • Membrane
  • Surface area, type, thickness
  • Blood film thickness
  • Dialysate flow configuration
  • Concentration gradient
  • Size of solute
  • Ultrafiltration
  • Temperature of dialysate
  • Qb - Blood flow rate
  • Qd - Dialysate flow rate
  • Time

5
Weekly plasma clearances L/week
6
Solute Clearance in PD
  • Factors that deliver clearance
  • Total volume
  • Volume per exchange
  • Number of exchanges
  • Dwell time
  • Factors driving clearance requirements
  • Urea generation(diet, weight, metabolic rate)
  • Residual renal clearance(kidney function)
  • U.F. rate (solution tonicity, fluid intake)
  • Peritoneal membrane (permeability)

7
Osmosis
Movement of water from an area of low solute
concentration to an area of high solute
concentration.
8
Ultrafiltration
CAPD
9
Ultrafiltration
10
Ultrafiltration
11
Clearance Peritoneal Equilibration
Twardowski, University of Missouri
12
(No Transcript)
13
Process of PD
  • Exchange
  • Drain(lt20 Minutes)
  • Fill(lt10 minutes)
  • Dwell - (CAPD 4 - 8 hours)
  • - (APD 30mins 2 hours)
  • CAPD
  • Manual
  • Day Time Exchanges
  • Procedure Every 4-8 Hours

14
Outline benefits of PD
  • Medical
  • Good BP control
  • Minimal cardiovascular stress
  • Sodium and water control
  • No heparin
  • Steady state chemistries
  • No vascular access
  • Better hematocrit
  • Good middle molecule
  • clearance
  • Psycho-social
  • Self care - control
  • Fewer dietary restrictions
  • Less travel to center
  • Easier to vacation
  • Easy to learn
  • No need for electricity or
  • running water

15
Disadvantages
  • Medical
  • Risk of infection
  • Peritoneal access
  • Less effective therapy
  • Biocompatibility of solutions
  • Long term impact on peritoneal membrane
  • Protein loss
  • Glucose absorption
  • Psycho-social
  • Self Care - control
  • Constant treatment
  • Body image-catheter, girth
  • Family commitment
  • Storage requirements

16
CAPD
Continuous Therapy
Volume
Benefits
Limitations
0
24
Time
  • High transporters will have poor UF
  • 4 x per day exchange
  • IP pressure with large volumes
  • Optimum dialysis for low permeability
  • No night time Tx
  • Can perform anywhere

Ambulatory Anywhere 4 - 5 Exchanges Long Dwells
17
APD
Intermittent Therapy
Volume
Benefits
Limitations
0
24
Time
  • Optimum dialysis for High permeability
  • No night time Tx
  • Can perform anywhere
  • Low transporter will have poor clearance
  • Exchange burden
  • IP Pressure with large volumes

Ambulatory Anywhere 4 - 5 Exchanges Shorter
Dwells Dry night
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