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ACUTE HEPATIC FAILURE Dr Jyoti Khare FCCCM, Part II PSRI Hospital, New Delhi Acute Liver Failure (ALF) ALF also known as FULMINANT HEPATIC FAILURE is a rare condition defined as the development of coagulation disturbance and encephalopathy in individuals without cirrhosis developing < 26 weeks duration. Wilson disease and Autoimmune hepatitis included as intial presentation is as acute illness. O’ GRADY CLASSIFICATION On bases of time from jaundice to encepalopathy development 1. Hyperacute - <7days 2. Acute - 8 to 28days 3. Subacute – 29 to 8 weeks ETIOLOGY (1/2) 1. Acute Viral Hepatitis – Hepatitis A,B,C,E (common in pregnancy), Cytomegalovirus ,Varicella Zoster Virus, Adenovirus, Paramyxovirus, Ebsten Barr virus, Herpes virus (more in 3rd trimester of pregnancy). 2. Metabolic Disorders- Acute fatty liver of pregnancy, HELLP, Wilson Disease, Reye syndrome. ETIOLOGY (2/2) 3. Cardiovascular disorders- Budd Chairi syndrome, Ischemic hepatitis, Hyperthermia. 4. Drugs and Toxins –Acetaminophen (most common), NSAIDS, Isoniazid, Rifampicin, Cocaine ,Herbal drugs, Halothane, Amanta phalloides (amatoxins). 5. Malignancy- lymphomas, leukemias 6. Autoimmune with ANA, Antismooth muscle antibody, Anti LKM1 positive. SIGNS and SYMPTOMS 1. 2. 3. 4. 5. 6. 7. 8. 9. Lethargy, Altered mentation Jaundice Tachypneic Hypotension Fluctuating urine output Hypoglycemia Bleeding Asterxsis Ascites EVALUATION and DIAGNOSIS History! History! Sexual contacts History! cardiac disease Risk Factors Pregnancy Medications Mushrooms Travel Toxic exposures TEST • Routine tests- ABG, CBC, LFT,PT/ INR, Ammonia, RFT, CxR, Viral makers with Anti HAV,HEV, Autoimmune markers, Ceruloplasmin levels, Toxins levels. • Blood, Urine, ascitic fluid c/s • USG abdomen. • CT SCAN Head for Cerebral oedema and Abdomen. • EEG • Echocardiography Differential Diagnosis • • • • • • Acute decompensation of cirrhosis Alcoholic hepatitis with underlying cirrhosis Autoimmune Hepatitis Eclampsia Preeclampsia Sepsis with multiorgan failure COMPLICATIONS (1/3) 1. Encephalopathy - COMPLICATIONS (2/3) Factors precipitating HE IGSCALP • I- INFECTION • G-GI BLEEDING • S-SEDATION • C-CONSTIPATION • A-ALKALOSIS • L-LOW K • P-HIGH PROTEIN COMPLICATIONS (3/3) 2. Cerebral oedema may lead to brain herniation. 3. Coagulopathy 4. Renal failure including ATN, Pre-renal renal failure, Hepato Renal syndrome 5. Metabolic Acidosis ,Hypoglycemia, Lactic acidosis, hypomagnesimia, hypophosphotemia 6. Infection –Staphylococcus, fungal . 7. Cardiovascular-Distributive shock arterial hypertension. 8. ARDS, Pleural Effusion ,Atelectasis,Intrapulmonary shunt. 9. pancreatitis PATHOPHYSIOLOGY OF CEREBRAL EDEMA (1/3) Multi factorialHyperammonia - In the brain, ammonia is detoxified to glutamine via amidation of glutamate by glutamine synthetase. The accumulation of glutamine in astrocytes results in astrocyte swelling and brain edema. The relationship between high ammonia and glutamine levels and raised ICH has been reported in humans. PATHOPHYSIOLOGY OF CEREBRAL EDEMA (2/3) Cytogenic edema - is the consequence of impaired cellular osmoregulation in the brain, resulting in astrocyte edema. Cortical astrocyte swelling is the most common observation in neuropathologic studies of brain edema in acute liver failure. PATHOPHYSIOLOGY OF CEREBRAL EDEMA (3/3) Vasogenic factors An increase in intracranial blood volume and cerebral blood flow is a factor in acute liver failure. The increased cerebral blood flow results because of disruption of cerebral autoregulation. The disruption of cerebral autoregulation is thought to be mediated by elevated systemic concentrations of nitric oxide, which acts as a potent vasodilator and BBB injury. TREATMENT (1/4) 1. General measures –identifying the severity, cause. ICU admission, securing airway, breathing ,circulation ,iv vasopressors. 2. IV antibiotics for sepsis 3. Coagulopathy correction with FFP, Vit K ,factor VII 4. Correction of Acidosis and hypoglycemia with IVF, IV dextrose. 5. Seizures control with anti epileptic drugs. 6. Correction of electrolytes. TREATMENT (2/4) 7. Renal failure –correcting cause, maintaing BP, avoiding nephrotoxic drugs and adjusting doses of antibiotics as per creatinine clearance. 8. Cerebral oedema with raised ICP- HOB 30 degree – Permissive hypernatremia (145 to 155 mmol/l) – IV mannitol (0.5 to 1.0 g/kg) and to keep osmolality <320 mosmol to avoid damage to BBB and worsening of vasogenic edema. – Hyperventilation to keep Pco2 25 to30 mmHg – Hypothermia – IV INDOMETHACIN (0.5mg/kg) – Phenobarbital, steroids role not very clear. TREATMENT (3/4) 9. Hepatic encephalopathyLactulose, L-ornithine and aspartate, non absorable antibiotic like Rifaximin, neomycin metronidazole ,oral vancomycin and quinolones. High branch chain amino acid formulae may provide protein supplimentation. TREATMENT (4/4) Diet • Patients with acute liver failure are, by necessity, on nothing by mouth (NPO) status. They may require large amounts of IV glucose to avoid hypoglycemia. • When enteral feeding via a feeding tube is not feasible (eg, as in a patient with paralytic ileus), institute total parenteral nutrition (TPN). Restricting protein (amino acids) to 0.6 g/kg body weight per day was previously routine in the setting of hepatic encephalopathy. However, this may not be necessary. • Endoscopic post-pyloric feeding tube in refractory cases. ACETAMINOPHEN TOXICITY • Intentional and Unintentional overdose. • Dose -150mg/kg • Patient with LFT derranged can have toxicity even with low doses. • Symptoms- nausea ,vomiting with derranged LFT, coagulopathy, renal failure, hypoglycemia, shock. TREATMENT • ABC • N-acetylcysteine enchances Glutathione synthesis and detoxifies N acetyl p benzoquinone imine to non toxic acetaminophen sulfate and prevent hepatic damage. • Dose-IV 150mg/kg over 15 mts followed by 50mg/kg over 4 hrs followed by 100mg/kg over 20 hrs. • Oral -140mg/kg loading dose followed by17 doses of 70mg/kg every 4hrs for 72 hrs. • Liver Transplant. HEPATORENAL SYNDROME • Is reversible acute kidney injury seen in Fulminant Liver Failure. • Renal function worsen in days to weeks. • Types – Rapidly progressive form ,doubling of s. Creat >2.5 mg/dl in <2 weeks – Moderate with slowly progressive course S. creat 1.5 to 2.5 mg/dl mostly associated with refractory ascites. TREATMENT 1. Vasoconstrictors- Terlipressin, midodrine (5to 15mg / day), octreotide (100 to 200 microgram SC three times a day) 2. IV albumin (1gm /kg /day for 3 days) 3. Transjugular intrahepati portosystemic shunt –risk of HE. 4. Heamodialysis 5. Liver transplant. ALF due to HAV and HEV • Supportive treatment - Securing airway , breathing , maintaining circulation. • Correction of coagulation parameters, cerebral oedema. • Correction of electrolytes, acidosis, Hypoglycemia, encephalopathy . • Heamodialysis in case of AKI . • Liver Transplant. LIVER TRANSPLANT CRITERIA (1/2) • Acetaminophen-induced disease • Arterial pH <7.3 (irrespective of the grade of encephalopathy) or • Grade III or IV encephalopathy, and • Prothrombin time >100 seconds, and • Serum creatinine >3.4mg/dl (301 μmol/L) LIVER TRANSPLANT CRITERIA (2/2) All other causes of fulminant hepatic failure • Prothrombin time >100 seconds (irrespective of the grade of encephalopathy) • Or • Any three of the following variables (irrespective of the grade of encephalopathy) • Age <10 years or >40 years • Etiology: non-A, non-B hepatitis, halothane hepatitis, idiosyncratic drug reactions • Duration of jaundice before onset of encephalopathy >7 days • Prothrombin time >50 seconds • Serum bilirrubin >18 mg/dl (308 μmol/L) VARIATIONS OF LIVER REPLACEMENT THERAPY Transplantation: Orthotopic LT DDLT or LDLT Auxiliary liver transplant Split liver transplant Two-stage procedures: Hepatectomy followed later by OLT Non-Transplanta Therapies Xenotransplantation Hepatocytetransplantation Hepatic assist devices CONTRAINDICATIONS FOR TRANSPLANT • Advanced cardiopulmonary dysfunction • Sepsis • Extrahepatic malignancy - Active severe infection outside the liver • HIV / AIDS • Cholangiocarcinoma • Lack of adequate family social support • Active alcoholism or drug abuse PROGNOSIS ALF carries high mortality rate with HEV infection in pregnancy. Over all mortality is high in Acute Liver Failure without Liver transplant. Thank you