Including: Anticoagulation Prescribing Protocol

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Presentation transcript:

Including: Anticoagulation Prescribing Protocol Concepts of Continuous Renal Replacement Therapy in Adult critical care at LTHT Including: Anticoagulation Prescribing Protocol

Introduction The machine used at Leeds Teaching Hospitals to deliver Continuous Renal Replacement Therapy (CRRT) is the Fresenius MultiFiltrate machine The mode of treatment we use is continuous veno-venous haemodialysis (CVVHD) The first line anticoagulation is Regional Citrate Anticoagulation (RCA)

Indications for CRRT High serum potassium Acidosis Pulmonary Oedema WHEN TO USE High serum potassium Acidosis Pulmonary Oedema Control of uremic symptoms Hyperpyrexia Filter metabolites/Septic mediators Drug poison removal Hyperkalaemia k⁺ >6.5mmol/L Metabolic Acidosis Ph <7.1 Pulmonary Oedema (not responsive to diuretics) Uremic Encephalopathy/Neuropathy Non emergency initiation Fluid management Solute control Pre-existing ESRF Lactate is not removed by dialysis

CVVHD During CVVHD diffusion of molecules takes place between blood in one fluid compartment of the dialyser and dialysis fluid in the other fluid compartment Haemodialysis utilizes counter current flow where the dialysate is flowing in the opposite direction to blood flow in the extracorporeal circuit Counter-current flow maintains the concentration gradient across the membrane at a maximum and increases the efficiency of the dialysis

Anticoagulation Anticoagulation of blood is required to avoid clotting in the filter circuit The default choice of anticoagulation at Leeds is Regional Citrate Anticoagulation (RCA) This reflects a change from historic practice where heparin was used RCA offers longer filter life and may reduce complications, it also avoids systemic anticoagulation

Alternative anticoagulation options Unfractionated heparin None if INR >2.5 and platelets <80 Prostacycline used rarely

Regional Citrate Anticoagulation Negatively charged ion Binds with ionised calcium Forms a single negatively charged chelate complex Concentration of free ionised calcium in blood is reduced in the circuit Ionised calcium is essential to the coagulation cascade – reducing it reduces clotting Some of the citrate-calcium complex is removed by the filter and rest passes into patient where it is metabolised by the liver

Regional Citrate Anticoagulation Clotting cascade cannot function if ionised calcium in bloods falls <0.5 mml/L <0.3 mmol/L clotting abolished Target calcium concentration in the circuit for optimal function is 0.25-0.34

Fresenius Multifiltrate This is the machine used in Leeds It can be used with RCA or heparin Ci-Ca is the system for RCA Multibic with heparin (separate protocol)

Fresenius Ci-Ca system 4 3 5 2 1

Fresenius Ci-Ca System 4+2 pump-system Citrate infusion is coupled to the blood flow Citrate and calcium infusion is automatically taken into account for fluid balancing Dedicated Zero-Ca, Low- Bicarb dialysate and Ci-Ca cassette with pre-connected citrate and calcium lines

Fresenius Ci-Ca System

Dialysate Fluid Sodium and Bicarbonate reduced in order to compensate for the systemic infusion of Sodium Citrate Calcium free to avoid unnecessary increase of citrate requirements. It is a double chamber bag Fluid is stable for 24 hours once mixed At Leeds we only use K⁺ 4 mmol/L bags if patient has hyperkalaemia use 35mL/Kg/Hr dialysis dose Fluid Constitution Na⁺ 133 mmol/L K⁺ 4 mmol/L Mg⁺⁺ 0.75 mmol/L Ca⁺⁺ 0 mmol/L HCO3⁺ 20 mmol/L Cl⁻ 116.5 mmol/L Glucose 1 g/L

Core safety concepts Protocol must be followed Prescription must be written before patient connected to system and then daily RCA interferes with normal calcium homeostasis - maintain a safe serum ionised calcium level

Core safety concepts Safety check via T:I ratio – this is the total:ionised calcium ratio and is a marker of citrate accumulation RCA interferes with acid-base balance - be aware that the blood flow and dialysate flow need to be balanced (1:20 ratio) to prevent iatrogenic acidosis or alkalosis Liver patients may not tolerate RCA – separate guidance

Limits Maximum treatment duration is 120 hours per filter Washback, recirculation and disconnection - circuit can be reconnected up to four hours Recirculation with blood – circuit can be reconnected up to 30 mins

Dose choice Dialysis dose can be chosen as 25 ml/kg/hr or 35 ml/kg/hr – weight based guidance charts in protocol 25 is the default choice 35 should be chosen in patients with: Severe hyperkalaemia (>7mmol/l) Severe acidosis (pH <7.0) Ethylene glycol poisoning Inadequate treatment on 25 ml/kg/hr

Calcium Management Refer to the protocol for guidance in calcium management Around 60% of patients in critical care need to be pre-treated with calcium Be mindful that in all patients the systemic ionised calcium will drop in the first 24-48 hours, this is not a citrate accumulation unless the T:I ratio is > 2.5 Calcium management is the single most important factor of citrate anticoagulation

Fluid management CRRT is a powerful tool for correcting fluid balance Prescription should state a range of removal rates and a target fluid balance Start the removal rate based upon current input and target balance and adjust in response to changes over the course of the day

Fluid management example Hourly input total 50ml (propofol/alfentanil/feed) 50x24=1200 Anuric, no drains/loose stools etc Target balance –ve 1000ml/24 hours Set initial removal at 100ml/hr (approximated) 1200+1000=2200 2200/24=92 After 12 hours patient given 500ml blood Balance, before blood, at 12 hours is -600ml [(50x12)-(100x12)] After blood is -100ml with 12 hours left, input still 50ml/hr Aim remains -1000ml Set removal at 125ml/hr -100 + (50x12) = +500 500+1000=1500; 1500/12=125

Acid-Base Management Citrate is metabolised in the liver The by-product of citrate metabolism is bicarbonate One molecule of citrate produces 3 molecules of bicarbonate You require a prescription at a 20:1 (dialysate flow:blood flow) ratio to maintain homeostasis Any derangement in acid-base must be assessed to ascertain if it is a due to patient pathology or due to the RCA itself

Metabolic acidosis potential causes Is it the patients underlying condition? Has therapy been running long enough? Inadequate dialysis dose? May need to increase dialysis to 35mL/kg/hr Dialysate flow rate too high in relation to blood flow rate, i.e. not 20:1 (was the prescription previously written for metabolic alkalosis?) Citrate accumulation due to impaired metabolism. T:I ratio will be >2.5

Prescribing for Metabolic Acidosis Either: Decrease dialysate flow Less removal of citrate by filter therefore effectively increased bicarbonate delivered to patient Increase blood flow (increases citrate flow) More citrate delivered to system without increased removal by filter, therefore also effectively increasing bicarbonate delivery Could consider increasing dialysis to 35mL/kg/hr Increased dose of dialysis will aid clearance of pathological acidosis This should be done if there is no other reason for the patient to be acidotic.

Metabolic alkalosis potential causes Check patients underlying condition Dialysate flow rate too low in relation to blood flow rate (<20:1) Check for medications that may cause alkalosis Filter age As treatment continues the filter slowly blocks resulting in reduced clearance and a greater proportion of citrate reaching patient This increased delivery of citrate is converted to bicarbonate

Prescribing for Metabolic Alkalosis Decrease blood flow (this should be the first action) Decreased citrate into the system so effectively less bicarbonate delivered to patient Increase dialysate flow Increased clearance of citrate by filter so effectively less bicarbonate delivered to patient Consider changing the filter set if >72 hours old This should be done if there is no other reason for the patient to have an alkalosis

Citrate Accumulation Problems may occur if the patient is unable to adequately metabolise citrate in the presence of acute severe liver failure and/or severe lactic acidosis Signs include T:I ratio >2.5 Marked drop in systemic Ca2+ Elevated total calcium (>3) Anion gap acidosis Protocol dictates management if suspected

Liver Patients Altered protocol if lactate >8 and total to ionised (TI) calcium ratio >2 Always pretreat with calcium Increased initial calcium flow rates At increased risk of citrate accumulation. Vigilance required

Summary Main indications for CRRT are hyperkalaemia, acidosis or fluid overload Anticoagulation is usually with citrate which works by binding to ionised calcium which prevents activation of the clotting cascade You must monitor and control patients and filters Ca2+ levels Fluid balance targets must be adhered to Be aware that the system can both cause and correct an acid-base imbalance T:I ratio is an essential safety check – risk of citrate accumulation

Points of contact Charlotte Trumper – Clinical Nurse Specialist James Beck – ICM Consultant Andy Lewington – Renal Consultant