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PLASMAPHERESIS
By
Dr.Mohamed Abd El Gawad
Nephrology Specialist at New Mansoura
General Hospital
Agenda
 What is Plasmapheresis ?
 INDICATIONS FOR PLASMAPHERESIS
TECHNIQUES
Replacement fluid
Vascular access
Anticoagulation
Regimens of PE
Complications
What is Plasmapheresis?
INDICATIONS FOR PLASMAPHERESIS
TECHNIQUES
A: Centrifugal plasma separation : blood cells
are separated during centrifugation , there
are two centrifugation methods Intermittent
flow device and continuous flow device
B: membrane plasma separation : plasma
separators use membranes with a molecular
weight 3 million
membrane plasma separation
 Uses highly permeable hollow fibers with membrane pores
of 0.2to 0.5 µm.
 The hollow fiber functions as a membrane, with the pore
size (0.2to 0.5 µm) allowing transport of plasma across the
membrane while retaining other blood components.
 PlasmaFlux filters contain the polysulfone-based
Plasmasulfone membrane, which has been designed to
minimise the activation of the patient’s immune system
during blood–-membrane interaction
Serum Albumin
Serum Albumin : 4 g /dL
40 g /L
40 × 3 = 120 g /L
Electrolytes
Calcium:
10 ml of calcium gluconate solution per liter
of replacement solution
Potassium :
4 mmol of Potassium to each liter of
replacement solution
Vascular access
Standard central venous catheters
 Arteriovenous(AV) fistula
 Peripheral access through large-bore, short,
intravenous cannulae
Anticoagulation
1 - Citrate
 IT is used for centrifugal plasma exchang.
 citrate has particular advantages in patients at higher
bleeding risk in view of its lack of systemic anticoagulant
actions.
 Citrate is rapidly metabolized by the liver (normal levels
within 4 hours).
Hepatic dysfunction severe hypocalcemia⇒
2–Heparin
 Used for membrane plasma filtration
 Higher doses may be needed than in hemodialysis as a
result of increased losses during the procedure (heparin
is protein bound).
 Bolus doses of unfractionated heparin 2000 to 5000 U
are given initially, and then 500 to 2000 U/h.
Plasma volume
Plasma volume =
( 0.07 × Body Weight ) × ( 1 - Hct )
( 0.07 × 70 ) × ( 1 - .4 )
= 2.9 L
Frequancy of procedures
1- Daily plasma exchange
 Most effective in rapidly depleting total body load.
 Intensity of exchanges has no major effect on
outcomes except in hemolytic-uremic syndrome.
2- Alternate-day exchanges
 proven efficacy in antineutrophil cytoplasmic
antibody (ANCA)–associated diseases.
 A single plasma volume exchange will lower
plasma macromolecule levels by
approximately 60% .
 Five exchanges during 5 to 10 days will clear
90% of the total body Immunoglobulin
Target molecule kinetics during therapeutic plasma exchange.
Mark E. Williams, and Rasheed A. Balogun CJASN
doi:10.2215/CJN.04680513
©2013by American Society of Nephrology
THANK YOU

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Plasmapheresis dr M.Elshwaf

  • 1. PLASMAPHERESIS By Dr.Mohamed Abd El Gawad Nephrology Specialist at New Mansoura General Hospital
  • 2. Agenda  What is Plasmapheresis ?  INDICATIONS FOR PLASMAPHERESIS TECHNIQUES Replacement fluid Vascular access Anticoagulation Regimens of PE Complications
  • 4.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10. TECHNIQUES A: Centrifugal plasma separation : blood cells are separated during centrifugation , there are two centrifugation methods Intermittent flow device and continuous flow device B: membrane plasma separation : plasma separators use membranes with a molecular weight 3 million
  • 11.
  • 12.
  • 13.
  • 14.
  • 15. membrane plasma separation  Uses highly permeable hollow fibers with membrane pores of 0.2to 0.5 µm.  The hollow fiber functions as a membrane, with the pore size (0.2to 0.5 µm) allowing transport of plasma across the membrane while retaining other blood components.  PlasmaFlux filters contain the polysulfone-based Plasmasulfone membrane, which has been designed to minimise the activation of the patient’s immune system during blood–-membrane interaction
  • 16.
  • 17.
  • 18. Serum Albumin Serum Albumin : 4 g /dL 40 g /L 40 × 3 = 120 g /L
  • 19. Electrolytes Calcium: 10 ml of calcium gluconate solution per liter of replacement solution Potassium : 4 mmol of Potassium to each liter of replacement solution
  • 20. Vascular access Standard central venous catheters  Arteriovenous(AV) fistula  Peripheral access through large-bore, short, intravenous cannulae
  • 21. Anticoagulation 1 - Citrate  IT is used for centrifugal plasma exchang.  citrate has particular advantages in patients at higher bleeding risk in view of its lack of systemic anticoagulant actions.  Citrate is rapidly metabolized by the liver (normal levels within 4 hours). Hepatic dysfunction severe hypocalcemia⇒
  • 22. 2–Heparin  Used for membrane plasma filtration  Higher doses may be needed than in hemodialysis as a result of increased losses during the procedure (heparin is protein bound).  Bolus doses of unfractionated heparin 2000 to 5000 U are given initially, and then 500 to 2000 U/h.
  • 23.
  • 24. Plasma volume Plasma volume = ( 0.07 × Body Weight ) × ( 1 - Hct ) ( 0.07 × 70 ) × ( 1 - .4 ) = 2.9 L
  • 25. Frequancy of procedures 1- Daily plasma exchange  Most effective in rapidly depleting total body load.  Intensity of exchanges has no major effect on outcomes except in hemolytic-uremic syndrome. 2- Alternate-day exchanges  proven efficacy in antineutrophil cytoplasmic antibody (ANCA)–associated diseases.
  • 26.
  • 27.  A single plasma volume exchange will lower plasma macromolecule levels by approximately 60% .  Five exchanges during 5 to 10 days will clear 90% of the total body Immunoglobulin
  • 28. Target molecule kinetics during therapeutic plasma exchange. Mark E. Williams, and Rasheed A. Balogun CJASN doi:10.2215/CJN.04680513 ©2013by American Society of Nephrology
  • 29.
  • 30.
  • 31.

Hinweis der Redaktion

  1. Target molecule kinetics during therapeutic plasma exchange. (A) Theoretical relationship between an increasing plasma volume exchanged relative to the patient’s plasma volume during the TPE procedure, and the percentage decrease in the concentration of the target molecule under idealized conditions. (B) Similar figure showing removal of target molecule from the beginning (closed circles) to the end of each of three TPE procedures (open circles), now taking into account factors such as biosynthesis, catabolism, and compartmental equilibration. Adapted from Kaplan (1) and Samtleben et al. (2). TPE, therapeutic plasma exchange.