BCC4: David anderson on Acute Liver Failure
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David Anderson gives an entertaining and informative talk about Acute Liver Failure at BCC4. He covers thinking about diagnosis, management and prognosis of acute liver failure. The podcast for this presentation is found at www.intensivecarenetwork.com
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BCC4: David anderson on Acute Liver Failure
- 1. Acute liver Failure David Anderson Advanced Trainee in Intensive Care Medicine Advanced Trainee in Palliative Medicine
- 7. Case
- 9. Jaundice Definition Encephalopathy A short time after the onset of Coagulopathy http://www.capitalpath.com.au/about-us/laboratory-information.aspx http://patient.co.uk Encephalopathy
- 12. Full Blood Count Biochemistry LFTs Coags (incl fibrinogen) Group and Screen Blood Gas (with Lactate) Paracetamol Level Viral Hepatitis Serologybeta HCG* Ammonia Autoimmune Screen HIV Amylase/Lipase Send Labs http://www.npsg.uwaterloo.ca/people/daniel/rendering/
- 14. ICU Housekeeping http://allposters.com.au http://mooselicker.wordpress.com/2012/09/24/continuations/
- 22. TEG Patton et al, 2012 http://www.aacc.org/publications/cln/2011/April/Pages/PlateletFunction.aspx
- 25. Cholongitas et al, 2012 Prognosis
- 26. Palliative Care
Notas do Editor
- Acute Liver Failure (ALF), also known as fulminant hepatic failure, can be a scary condition to deal with for those who don’t work in specialist liver units. This is a simple guide for emergency physicians and intensivists to the assessment and management of these complex patients with acute liver failure while awaiting transfer to the liver transplant center.
- A more australian ALF
- Lets look at a case. You are the intensivist in a small regional hospital and are called to see a 30 year old woman with jaundice and confusion She is warm and vasodilated, tachycardic and hypotensive, She is deeply jaundiced with gingival bleeding, but no stigmata of chronic liver disease A VBG which shows a severe metabolic acidosis with a lactate of 8, and a Glucose of 2.5
- They don’t always present like this of course, and sometimes you have to do quite a bit of detective work
- There is no single accepted definition of ALF but most societies’ definitions include the development of coagulopathy and/or encephalopathy within a short period after the onset of symptoms or development of jaundice in someone with no previous liver disease. While the latency between onset of jaundice and onset of encephalopathy is typically only a few days, the most commonly used definition (the O’Grady criteria) allow up to 26 weeks.
- It is important to establish the aetiology, as different aetiologies have different clinical courses and chances of spontaneous regeneration of hepatic tissue. Common aetiologies are; Paracetamol poisoning Acute viral hepatitis Idiosyncratic drug reactions Other causes such as death cap mushrooms and wilsons disease up to 1/4 of cases have no cause found
- - Once you have identified a patient with ALF, you should contact the regional liver transplant center for advice and to arrange referral if appropriate - Most patients are sick enough to justify medical retrieval
- While most centers wont be able to run all of these tests, a thorough blood workup is essential, as there are often multiple derangements. At the least you should send; full blood count full biochemistry liver function tests coagulation including fibrinogen arterial or venous blood gas with lactate Blood group and screen Paracetamol level
- Lets look at management now N-Acetyl cysteine (NAC) should be administered to all patients where paracetamol poisoning is confirmed or suspected Regardless of time interval since paracetamol ingestion It should be continued until the patient receives a liver transplant or leaves ICU It is very safe Consider administering NAC to all patients May be beneficial in early grade encephalopathy
- As with all patients, good general ICU housekeeping is vital Be vigilant for, and promptly correct hypoglycaemia which is common in ALF, an infusion of 50% dextrose may be required to maintain euglycaemia All patients should have stress ulcer prophylaxis Enteral feeding should be commenced early, unless contra-indicated Consider low protein feeds and Consider concentrated feeds if neutral or negative fluid balance is difficult to maintain
- A vasodilated, high cardiac output state is very common in ALF and almost all patients will require invasive monitoring and vasopressor support Place invasive lines early. ultrasound guided internal jugular lines should be placed by the most experienced person available. If you have a TEG, this should be used to guide correction of coagulopathy Consider inserting a dialysis catheter at the time of central line insertion
- Consider using CO monitoring if available Consider aiming for a higher than normal MAP to help ensure adequate cerebral perfusion Use fluid boluses initially but norad plus or minus vasopressin or terlipressin will likely be required Very occasionally an inotrope will be required Consider low dose corticosteroids if vasopressor requirements are significant Have a high index of suspicion for occult sepsis in addition to vasoplegia if vasopressor requirements are high or rising rapidly
- Encephalopathy develop very rapidly. Intracranial hypertension (ICH) is a common cause of death. Much of the intensive care management of patients with ALF is aimed at preventing or treating ICH Ventilate to a low normal ETCO2 Try to avoid high PEEP as it can increase ICP and cause hepatic venous congestion Keep well sedated Assess neurology hourly Take standard measures to prevent intracranial hypertension Essentially - treat like a TBI, including use of therapeutic hypothermia, bearing in mind that this may worsen coagulopathy. Some centers routinely use therapeutic hypothermia in acute liver failure, and an RCT is underway
- Lactulose is not routinely indicated While useful in early encephalopathy, there is no good evidence to support its use in high grade encephalopathy and it may interfere with fluid balance and make transplant technically more difficult Seizures should be treated promptly with a benzodiazepine and phenytoin There is no role for prophylactic phenytoin Signs of increased ICP such as anisicoria or drop in GCS should be treated with osmotherapy +/- therapeutic hypothermia
- Limit all fluid intake, Aim for neutral or slightly negative daily fluid balance Avoid hypotonic fluids wherever possible Avoid nephrotoxins Consider Commencing CRRT in all intubated patients, regardless of renal function to reduce ammonia levels and maintain neutral or negative fluid balance Aim for a high normal sodium - 145-155 Hyponatraemia should be treated with HTS
- Ammonia levels can be monitored and used to stratify risk of intracranial hypertension Arterial ideally Ammonia <75 = low risk of ICH Ammonia >100 = high risk of ICH Ammonia >200 = almost certain to have ICH - commence appropriate management
- Despite an elevated INR being part of the definition of ALF, clinically significant bleeding is rare. This is probably because hepatic production of anticoagulant factors is impaired together with procoagulant factors An elevated INR should not be routinely corrected, If the patient is bleeding, used small amounts of FFP to correct coagulopathy, aiming for an INR of <7 Administer vitamin K Keep platelets >10,000/mm3 unless bleeding
- Bedside tests of coagulation, such as TEG or ROTEM should be used if available, they are much better indicators of the need to treat coagulopathy than traditional tests and can guide the products required.
- Be vigilant for infection Administer broad spectrum antibiotics and an antifungal to all patients with grade III or IV encephalopathy There is less evidence for routine antibiotic prophylaxis for patients with a lesser grade of encephalopathy Treat fever early and aggressively in order to avoid spikes in ICP
- - While many patients, particularly those with paracetamol induced ALF will recover with NAC alone, many require OLT. As mentioned earlier, the Kings College Criteria are traditionally used to guide management. Sometimes the liver service will decide not to accept a patient, either because they are too sick and not likely to survive or because they aren’t sick enough. In which case they may remain in the local hospital. It is still wise in this case to stay in touch with the liver service in case of any deterioration
- - While the KCH criteria are commonly used to prognosticate transplant free survival, others are being investigated. The KCH are the most specific but the least sensitive. Lactate alone is most sensitive but least specific and SOFA has moderate sensitivity and specificity, giving it the highest AUC on a ROC.
- If a patient is declined by the liver service because they are too sick, they still need meticulous intensive and palliative care at the referring center. The commonest cause of a patient being declined or dying while awaiting transplant is refractory ICH. As with all palliative patients in the ED or ICU, excellent communication with the family and judicious use of analgesia and sedation to ensure comfort and dignity are essential.
- - Extracorporeal hepatic support relies on a similar principle to CRRT, but aims to clear albumin bound, water soluble molecules (like ammonia) using a variety of albumin based techniques. Biological systems using hepatocytes have also been investigated. Trials have shown mixed results and extracorporeal systems currently have no role outside of the clinical trial setting.
- So, in summary - Find out the cause - Call for help - Take lots of bloods - Give NAC - Good housekeeping - Get lines in early, including a vascath - Treat the high output, vasodilated circulation - Treat the brain like a TBI - Measure ammonia if you can - Start CRRT early - Use TEG if you’ve got it - Be vigilant for infection - Accept that not everyone gets a transplant - Provide excellent palliative care to those too sick to transfer