FRCA Notes


Anticoagulation During Renal Replacement Therapy


  • As with all extra-corporeal circuits, RRT requires anticoagulation to stop thrombus formation
  • All forms of RRT can precipitate thrombus formation by exposing blood to a non-biological surface
  • Contact between blood and either the filter itself (which has a high surface area and is the most thrombogenic component) or plastic tubing can activate the clotting cascade

  • Clot may occur in either:
    • The filter, causing trans-membrane high pressure alarms
    • The vascular access catheter, causing access high pressure alarms

  • Clotting not only leads to reduced filter efficiency, but may cause iatrogenic anaemia through loss of filter circuits

  • Ensure adequate driving pressure i.e. venous pressure

  • Ensure adequate flow rates through the vascath
    • RIJ > femoral > LIJ
    • Appropriate catheter position and care

  • Increasing pre-filter fluid (e.g. 70/30 mix instead of 50/50 mix)
    • Lowers haematocrit and reduces change of filter clot
    • Reduces efficacy of filtration process

  • Heparin can be given into the circuit before the filter, which results in less systemic anticoagulation
  • Filters are also primed with heparin, then infused with a target APTTr of <1.4
  • It can also be given systemically

  • Benefits:
    • Reversibility with protamine
    • Titratable with APTTr
    • APTTr testing is commonly performed as part of routine clotting studies
    • Cheap

  • Issues:

  • Ionised calcium is required for the function of factors 2 (prothrombin), 7a, 9a and 10/10a i.e. the vitamin K dependent clotting factors
  • Citrate chelates calcium (historically clotting factor IV)
  • The net effect is inhibition of thrombin formation
  • In order to achieve this effect, the filter must have an ionised calcium concentration of <0.4mmol/L

  • The citrate-calcium complex is removed in the filter by both convection and diffusion
  • Citrate is also rapidly metabolised in the Krebs cycle in the liver and renal cortex

  • Benefits include:
    • Generally felt to be as safe as heparin
    • Increased filter lifespan
    • Reduced need for blood products
    • Suitable in those for whom heparin is contraindicated
    • Provides a whopping 0.59kcal/mmol to help your patients get swole
    • Preferred in various countries including Australasia and Italy

  • Issues
    • Potential metabolic alkalosis by increasing the strong ion difference
    • Potential high anion gap metabolic acidosis
    • Reduced ionised calcium levels
    • Hypomagnesaemia, as magnesium binds to the citrate-calcium complex

  • PGE2 ('Flolan') can be given to inhibit platelet function
  • It benefits from a short half-life and therefore fairly rapid reversal once infusion terminated
  • Issues include:
    • Potent vasodilation → cardiovascular instability
    • Impairs HPV → hypoxia if relying on HPV to prevent excessive shunt
    • Intracranial hypertension