Previous Page  11 / 21 Next Page
Information
Show Menu
Previous Page 11 / 21 Next Page
Page Background

Nursing Education 2018

Journal of Nursing and Health Studies

ISSN: 2574-2825

Page 63

April 23-25, 2018

Rome, Italy

27

th

Edition of World Congress on

Nursing Education &

Research

R

emoval of uremic waste products and excess of accumulated

body fluid are the goals of peritoneal dialysis (PD) in the

treatment of patients with chronic renal failure. The peritoneum

used as a dialysis membrane consists of the mesothelial layer

and interstitial tissue, in which blood- and lymphatic vessels are

present. The microvessels allow transport of solutes and water

from the blood to the dialysis fluid in the peritoneal cavity. Solutes

like urea are transported by diffusion across the vascular wall;

fluid removal (ultrafiltration) requires a pressure gradient. The

latter consists of the intravascular hydrostatic pressure, which

drives fluid out of the microvessels to the interstitium through

interendothelial pores, but also of an osmotic pressure gradient.

The latter is created by adding high dosages of glucose to the

dialysis fluid.This is only effective, because the transcellular water

channel aquaporin-1 (AQP-1) is present in peritoneal endothelial

cells. AQP-1 is permeable towater only, not to solutes like glucose

and Na+. Consequently AQP-1 allows free water (water only)

transport (FWT). The osmotic gradient contributes to SPFT to a

limited extent only. During the first few years of PD about 40% of

the ultrafiltered volume consists of FWT and 60% of small-pore

fluid transport (SPFT). Loss of ultrafiltration capacity occurs

especially in long-term PD patients. It is mostly associated with

high solute transport rates, suggestive of an enlarged vascular

surface area leading to rapid disappearance of the osmotic

gradient. This affects especially SPFT. A longitudinal study

showed a marked reduction of SPFT after 4 years of PD, possibly

due to vascular abnormalities. FWT is markedly decreased in

patients who develop encapsulating peritoneal sclerosis. Binding

of free water by a collagen increase is the most likely explanation.

Determination of both SPFT and FWT are essential in the follow-

up of PD patients.

r.t.krediet@amc.uva.nl

Fluid removal in peritoneal dialysis

Raymond T Krediet

Academic Medical Centre, Netherlands

J Nurs Health Stud 2018, Volume 3

DOI: 10.21767/2574-2825-C1-003