Cirrhosis is a diffuse process characterized by fibrosis and nodular regeneration, which lead to the disorganization of liver architecture. Cirrhosis was long thought to be irreversible and associated with limited life expectancy. However, it is now considered a dynamic condition, which can be reversed if adequately treated.

According to data from the Brazilian Unified Health System, between 2001 and 2010, liver diseases were the eighth leading cause of death in Brazil[1]. Cirrhosis was the main cause of hospital admissions and death from liver disease in Brazil, especially in the South region of the country. Little is known about its incidence in children.

Studies of the natural history of cirrhosis have found that the disease tends to present with a silent clinical course, followed by the onset of liver dysfunction and portal hypertension. The most important predictor of decompensation is the increase in hepatic venous pressure gradient (HVPG), which is seldom measured routinely in children and adolescents. In clinical practice, mortality risk is generally estimated on the basis of albuminemia, MELD (Model for End-Stage Liver Disease)/PELD (Pediatric End-Stage Liver Disease)/Child-PughTurcotte scores and body mass index. Advances in diagnostic and treatment technology, especially liver transplant surgery, have contributed significantly to the management of these cases. Currently, the majority of children diagnosed with cirrhosis in the first years of life can grow, develop and reach adulthood.

Biliary atresia and inherited syndromes of intrahepatic cholestasis are the most frequent causes of chronic liver disease in children[2]. The most common causes of cirrhosis in the first years of life are biliary atresia and genetic-metabolic diseases, whereas in older children, cirrhosis is usually caused by chronic viral hepatitis and autoimmune diseases (Table 1). Cirrhosis can be classified in several ways, based on morphological, histological, etiological and clinical criteria. As cirrhosis is the final stage of several types of progressive liver disease, etiological classification is often crucial for treatment planning. Despite the long list of possible etiologies shown in Table 1, the cause of cirrhotic disease is not always possible to determine. As a result, the condition is considered cryptogenic in 5%-15% of cases. Cryptogenic cirrhosis in pediatric patients may result from the progression of fatty liver disease or from the effects of complex metabolic syndromes, such as mitochondriopathies[3].

Biliary atresia (BA) occurs exclusively in childhood, and is the most common cause of chronic cholestasis and liver transplantation in children. It occurs in the first weeks of life and is characterized by complete obstruction of the biliary tract. Portal hypertension and biliary cirrhosis tend to occur early in the course of illness, and can be detected by 2 to 3 mo of age. Two forms of the disease have been identified: the congenital or “fetal” form, which accounts for 10% to 20% of cases of BA, and the perinatal or “acquired” form, which is responsible for 80% to 90% of cases. The fetal form usually manifests as jaundice at birth, and, in 15%-30% of patients, may also involve extrahepatic anomalies (vascular malformations, variant abdominal organ positioning, heart disease, etc.). In acquired BA, jaundice occurs later, after the first or second week of life, resulting in a jaundice-free period between the onset of physiological jaundice and biliary obstruction. Congenital extrahepatic anomalies are rare in this form of the disease. Studies involving the surgical removal of biliary obstruction have revealed that, in most cases, the preformed bile ducts are affected by inflammatory processes, the causes of which are still poorly understood. BA may represent a phenotype resulting from factors which lead to biliary obstruction and include developmental anomalies, infections, vascular alterations and exposure to toxins[2,4,5]. Treatment for this condition is surgical (Kasai portoenterostomy and its modifications, performed before the first 8 wk of life). The degree of restoration of biliary flow is inversely proportional to the age when surgery is performed. Without treatment, patients do not generally survive past 18-24 mo.

This condition consists of congenital dilatation of the biliary ducts. Choledochal cysts are rare, with a prevalence of 1 per 13000-15000 live births in Western countries, although they are more common in Japan. Choledochal cysts are more common in females (5:1) and can be diagnosed antenatally by ultrasound. The cysts can be classified into five types: I, cystic dilatation of the common bile duct; II, diverticulum of the common bile duct; III, choledochocele; IV, multiple cysts; and V, intrahepatic fusiform dilatation[6]. Most patients present with the typical symptom triad of abdominal pain, jaundice and palpable masses in the right upper quadrant. Surgical treatment consisting of cyst excision and bilioenteric anastomosis have produced excellent results, although a small percentage of patients may develop cholangiocarcinoma in the remaining biliary tract.

Alagille syndrome is the most common cause of familial progressive intrahepatic cholestasis[7], and occurs in approximately 1:100000 live births. Most patients have mutations in the JAG1 gene, located on the short arm of chromosome 20. The syndrome is diagnosed on the basis of clinical symptoms, which can be difficult to detect in the first months of life, especially if the clinical picture is not yet clear. Histological examination may reveal a reduction of interlobular bile ducts in addition to cholestasis. Its main clinical features are cholestasis, a characteristic facies, cardiac abnormalities, vertebral arch defects and posterior embryotoxon. Supportive management is required in approximately 50% of cases. Alagille syndrome progresses to secondary biliary cirrhosis in 20%-25% of cases. The differential diagnosis must include other causes of ductopenia such as alpha-1-antitrypsin deficiency; the Zellweger, Ivemark and Williams syndromes; cystic fibrosis; chromosomal alterations (trisomy 18 or 21); and HIV.

Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of hereditary autosomal diseases characterized by mutations in genes governing intrahepatic biliary transport, comprising PFIC 1 (ATP8B1), PFIC 2 (ABCB11) and PFIC 3 (ABCB4). These conditions manifest in the first year of life, usually as cholestasis and its associated consequences. These are rare but universally occurring conditions, whose exact prevalence is unknown. Although phenotypes may vary, the following clinical characteristics are often present: cholestatic jaundice, choluria and hypocholia, severe itching in the first months of life, delayed weight gain, malnutrition and progression to cirrhosis and associated complications (Table 2).

Hepatitis B/D are the most common viral causes of cirrhosis in children and adolescents. Although Hepatitis C may also be acquired in childhood, it only tends to lead to cirrhosis later in life[8]. According to a study of the population-based prevalence of infections by the hepatitis B and C viruses (HBV and HCV), conducted between 2005 and 2009 in all Brazilian capitals and the Federal District, the frequency of viral hepatitis B and C in people between the ages of 10 and 69 was 7.4% and 1.38% respectively, which is consistent with low endemicity of these conditions[9].

Few studies have attempted long-term outcome of children with hepatitis B[10,11]. At least 50% of children infected by the vertical route (mother-to-child) test positive for viral replication in adulthood. The use of medication (telbivudine, lamivudine or tenofovir) by HBsAG-positive mothers with high levels of viremia (serum HBV DNA 10^5-7 IU/mL) during the last trimester of pregnancy reduces the risk of intra-uterine and perinatal transmission of HBV if given in addition to hepatitis B immunoglobulin (HBIg) and HBV vaccine[12].

The hepatitis delta virus consists of an RNA genome enveloped by the HBV surface antigen (HBsAg). The rates of progression to chronicity in hepatitis delta are similar to those observed in hepatitis B, since HDV depends on the persistence of HBV. Chronicity rates are high when infection is acquired in the neonatal period (80%-90%), intermediate (25%-50%) when it occurs between 1 and 5 years of age, and low when acquired in later childhood (2%-6%).

The natural history of hepatitis C in children is very different from that seen in adults, and although the progression of chronic hepatitis to cirrhosis is unlikely, it may even progress to hepatocellular carcinoma[13]. Since viral screening began to be used routinely in blood donors, vertical transmission became the main cause of hepatitis C in children. Vertical transmission occurs in approximately 5% of HIV-negative mothers and in up to 25% of mothers co-infected with HIV[14]. In a study conducted by Bortolotti et al[15], only 6 (1.8%) of the 332 children evaluated developed cirrhosis after a period of 10 years. The incidence of hepatitis symptoms and severe liver disease was low[15]. In a separate study performed in 80 Spanish and Italian children, only one presented with cirrhosis[16]. More recently, a study of 121 children with chronic hepatitis C and a mean age of 10 years found that cirrhosis was only present in 2% of the sample[17].

Alpha-1-antitrypsin (AAT) is a glycoprotein produced in large quantities in the liver to inhibit the neutrophil proteases associated with inflammation. The classical form of the disease is caused by homozygosity for the Z mutation (“PiZZ” genotype for SERPINA1). Over 100 mutations in the AAT gene have been described, although the Z mutant is that most closely associated with liver disease[18]. The clinical course is variable, and may involve neonatal cholestasis, liver dysfunction, liver failure and cirrhosis. Liver transplantation is often required. Approximately 20% of “PiZZ” patients develop cholestasis in the first weeks of life, and have a 5% risk of developing more severe forms of the disorder in childhood/adolescence. These patients are also more likely to develop hepatocellular carcinoma. There is no specific treatment or prevention against this condition, save for liver transplantation.

This autosomal recessive disease affects 1 in every 30000 live births. It is caused by mutations in the ATP7B gene (chromosome 13), which encodes the protein responsible for the metabolism, transport and biliary excretion of copper. The clinical presentation of Wilson’s disease (WD) involves abnormal liver function tests, acute hepatitis, liver failure, portal hypertension, gallstones and cirrhosis. Copper accumulates in the liver, brain and cornea, and hepatic manifestations occur after the first 3 years of life. In adolescents, the diagnosis of WD is often based on signs and symptoms of chronic liver disease. Patients often have a family history of WD, and approximately 25% of cases are diagnosed as a result of the investigation of asymptomatic relatives. If left untreated, WD usually carries a bad prognosis.

This autosomal recessive disease occurs in approximately 1 in 2000-4000 live births in Caucasian populations. Cystic fibrosis (CF) is caused by mutations in the CFTR transmembrane regulator gene, which is expressed in the apical membrane of biliary epithelial cells. This condition leads to severe and progressive impairment in the respiratory and digestive systems. Most patients do not present with liver damage in the early phase of the disease, although hepatic impairment is present in 10%-30% of cases. In older children and adolescents, CF liver disease manifests as hepatosplenomegaly and/or portal hypertension. Gallstones and micro-gallbladder are the most common biliary abnormalities in these patients. Portal hypertension is the major hepatic complication in CF.

Given the high prevalence of obesity and metabolic syndrome in the general population, non-alcoholic fatty liver disease has become the most common cause of liver disease in both adults and children[19]. It is a common, albeit under diagnosed, condition. Most cases are associated with obesity and type 2 diabetes mellitus. The risk of liver disease tends to increase with weight[20]. Most patients are asymptomatic, and the disease is often discovered during routine examinations (by ultrasound or biochemical screening). Progression to cirrhosis is not common in childhood, but may occur in young adults.

Autoimmune liver diseases include sclerosing cholangitis, primary biliary cirrhosis, and autoimmune hepatitis (AIH), with the latter being the most autoimmune liver condition in children and adolescents. Primary biliary cirrhosis is rare in this age range, although sclerosing cholangitis has been increasing in prevalence, often accompanied by inflammatory bowel disease.

AIH is a chronic inflammatory liver disease, with variable onset and duration. The prevalence of this condition in children is not yet known. There are few publications regarding this disease in patients from South America. In Brazil, AIH is still considered unusual, accounting for only 5%-10% of cases of liver disease in the major medical centers of the country[21]. There are particular human leukocyte antigen (HLA) specificities associated with AIH in Latin Americans. HLA-DQ2 and DR52 seem to be risk factors, whereas DR5 and DQ3 appear to have a protective effect in this population[22]. The trigger of the autoimmune process is not yet known. AIH can be classified into two subtypes, according to the non-organ specific antibodies present: typeI(AIH-1) is associated with anti-nuclear (ANA) and anti-smooth muscle (ASMA) antibodies, whereas type II (AIH-2) is associated with positivity for anti-liver/kidney microsomal (LKM-1) antibodies. AIH-2 manifests earlier, in the first years of life, while AIH-1 generally occurs in older children and adolescents[23].

Primary sclerosing cholangitis (PSC) is a chronic, progressive liver disease of unknown cause. There is strong evidence to suggest that PSC is the result of alterations in the immune response to certain antigens. Cases with a well-defined etiology (e.g., cytomegalovirus infection, trauma, ischemic lesion) are diagnosed as “secondary sclerosing cholangitis”. PSC is characterized by obliterative fibrosis of the intra- and/or extrahepatic biliary tree. Concentric fibrosis is very common, and may lead to narrowing of the bile ducts and, eventually, to biliary cirrhosis and its complications. Sclerosing cholangitis may present soon after birth, in which case it must be distinguished from other causes of neonatal cholestasis, or later, with manifestations ranging from asymptomatic to decompensated cirrhosis[24].

Mitochondrial diseases, or mitochondriopathies, are inherited disorders of energy metabolism associated with a vast range of presentations, symptoms, severities and outcomes. Combined, they form one of the commonest groups of inherited metabolic diseases[25]. Mitochondrial diseases occur due to dysfunction of the respiratory chain (RC) with resultant cellular ATP deficiency, increased production of reactive oxygen species and toxic metabolites and, ultimately, cell death. Disorders of mitochondrial energy metabolism result from mutations of nuclear or mitochondrial DNA. The exact prevalence of hepatic mitochondrial disease is not known, although it has been estimated that 10%-20% of patients with RC deficiencies have hepatic dysfunction. The three main defects associated with liver disease are almost always fatal: deficiency of RC enzymes, DNA depletion syndrome and Alpers syndrome[26]. Liver involvement occurs frequently in childhood-onset mitochondrial disease, particularly in cases presenting in the neonatal period and early infancy[27]. Liver transplantation is contraindicated in children with severe, life-threatening multiorgan extrahepatic mitochondrial disease due to poor post transplant neurological outcome.

Ultrasound is the ideal imaging method for the initial investigation of chronic liver disease in children and adolescents. The size of the spleen may provide indirect evidence of the presence or absence of portal hypertension, although it is not directly associated with measures of portal hypertension and is not an accurate indicator of the presence or absence of varices[31]. Ultrasound examination may also contribute to the diagnosis of gallstones, choledochal cysts and Caroli disease[47]. The use of Doppler techniques can complement ultrasound evaluations and help determine the perfusion and direction of blood flow in the portal system and hepatic artery. This method also allows identification of portal malformations. Cavernous transformation of the portal vein is a diagnostic feature of portal vein thrombosis.

Endoscopy is the best method for evaluation of the presence, size and extension of gastric, esophageal and, more rarely, duodenal varices, and can help diagnose hypertensive gastropathy[48,49]. A prospective study of endoscopic findings in children with BA found that the presence of red signs and gastric varices was associated with increased risk of gastrointestinal bleeding[50]. Gastric mucosal damage, or hypertensive gastropathy, is characterized by the dilatation or ectasia of vessels in the mucosa and submucosa in the absence of inflammatory alterations, as identified by endoscopy or histological examination[51,52]. Although these criteria are not always used in children, a study of endoscopic findings in 51 children with portal hypertension found this condition in 59% of 28 children with cirrhosis[53]. Endoscopy is also important to exclude other causes of gastrointestinal bleeding, such as gastric or duodenal ulcers and Mallory-Weiss tears[31]. In a study of 76 children with cirrhosis candidates for liver transplantation, gastric or duodenal ulcers were diagnosed in 8/21 (38%) of children with gastrointestinal bleeding[54]. Studies of noninvasive methods to identify high risk of esophageal varices in children with chronic liver disease found that splenomegaly and hypoalbuminemia[55], as well as platelet counts, Z scores of spleen size and albumin levels, predicted the presence of varices in patients with cirrhosis[56].

Liver biopsy is still considered the gold-standard diagnostic method for cirrhosis. When required, it should be performed after through laboratory tests and imaging. The biopsy specimen should be evaluated by a pediatric hepatology specialist. The interpretation of results may be limited by several factors, especially when suction biopsy is performed. These include small specimen size, sampling error or fragmented biopsy specimens[57].

In adults, HVPG measurements are the best method of assessing the presence and severity of portal hypertension, and can be used to monitor the efficacy of medical treatment[58,59]. However, this is still not a routine procedure in children.

Miraglia et al[60] consider multidetector computed tomography scans and abdominal MRI crucial for the pretransplant assessment of patients with BA[60]. These imaging modalities permit identification of congenital anomalies or cirrhosis-related alterations (portosystemic shunts, portal thrombosis) which may require modification of surgical techniques[60]. Most of these methods have not been studied extensively in children due to their invasive nature. Angiographic examinations are usually only performed in children as part of the preoperative assessment of surgical portosystemic shunts or liver transplantation[61].

Malnutrition is an important prognostic factor, which may influence the clinical course of chronic liver disease[62] and is associated with greater morbidity and mortality in both the pre- and posttransplant periods[63]. In children and adolescents, the increased energy demands associated with anorexia and nausea may complicate the management of malnutrition[64-66].

A comprehensive clinical history and general physical examinations of the child/adolescent must be included in routine clinical practice[67], and special attention must be paid to changes in muscle mass and body fat depots, both of which reflect important aspects of patient nutritional status. In clinical practice, anthropometry is the most widely used method for nutritional diagnosis. Regular patient follow-up also enables early detection of nutritional impairments. Given the high prevalence of water retention and organomegaly in pediatric cirrhosis, body weight is an unsatisfactory marker of nutritional status. In addition to measuring the weight, height/length and head circumference of children younger than 3 years, it is important to follow their long-term growth using reference curves. Triceps skinfold thickness and upper arm circumference measurements are also important to assess fat and protein reserves and can allow early detection of alterations in the nutritional status of pediatric patients with liver disease[68,69]. Subjective global assessments of nutritional status, performed on the basis of interview and physical examination findings, can also help identify factors which may influence the progression or regression of nutritional abnormalities[70].

Children or adolescents with chronic liver disease have increased nutritional needs. Patients at risk of malnutrition require 20%-80% more calories than healthy children to achieve normal growth[26]. These recommendations aim to ensure that children have sufficient energy to meet daily requirements, address the nutritional deficits caused by the increased energy demands of cirrhotic liver disease and prevent protein catabolism[71].

Protein intake should not be restricted in the absence of hyperammonemia[26]. Cirrhotic infants with cholestasis require a protein intake of approximately 2-3 g/kg per day to achieve normal growth and endogenous synthesis. Supplementation with up to 4 g/kg per day is generally safe and necessary to maintain normal growth and avoid excessive catabolism.

Lipids are an especially important dietary component in children with liver disease, and should account for approximately 30%-35% of total calories in the diet. Medium-chain triglycerides (MCTs) should account for 30%-50% of lipid intake, as these are absorbed directly by the intestinal epithelium and do not require bile salts for digestion and absorption[65-72]. Although MCT supplementation is crucial for the nutritional management of children with cholestasis, long-chain triglycerides should not be eliminated from the diet, as these substances provide essential fatty acids and contribute to the absorption of lipid-soluble molecules.

Deficiency of lipid-soluble vitamins is a common problem, especially in children with cholestasis; therefore, levels of these nutrients must be carefully monitored[73,74].

Oral nutrition should always be preferred, although enteral or parenteral supplementation may be necessary if not all nutritional requirements can be met by oral feeding[69]. Enteral supplementation is generally recommended when oral intake provides less than 60% of recommended energy needs or in cases of severe malnutrition[75].

Patients with cirrhosis are especially susceptible to infection, the most common of which is spontaneous bacterial peritonitis (SBP)[76]. Urinary and respiratory infections are also common[31]. In patients with cirrhosis, infections can lead to complications such as encephalopathy, ascites and hepatorenal syndrome.

Recommended preventive measures include nutritional supplementation, vaccination and prophylactic antibiotics for invasive procedures[37]. Pneumococcal and meningococcal vaccines are recommended for children with functional asplenia due to portal hypertension[37]. In children with cirrhosis candidates for liver transplantation, accelerated vaccination programs should be considered[77].

Rupture of gastroesophageal varices is the most common cause of gastrointestinal bleeding in children with cirrhosis. It is the most severe complication of the disease, and is considered a medical emergency[33]. Gastrointestinal bleeding caused by gastroesophageal varices in children and adolescents is generally treated using statements developed for adults. These statements were adapted for use in children by an expert committee (Baveno V Consensus), which also proposed a set of guidelines for the treatment of children with portal hypertension[78]. Treatments can be classified as pharmacological, endoscopic, mechanical and surgical[78,79].

Ascites is a common complication in pediatric cirrhosis, especially in younger children with terminal liver disease[37]. This is generally associated with a poor prognosis[80]. Pediatric patients with a sudden increase in ascites or new episodes of water retention should undergo paracentesis[34]. Analysis of the ascitic fluid enables differentiation of ascites from portal hypertension of other causes of ascites. A serum-ascites albumin gradient - calculated by subtracting the albumin concentration of the ascitic fluid from the serum albumin level - greater than 1.1 g/dL can diagnose portal hypertension with 97% accuracy[81]. Tests such as amylase, cytology, polymerase chain reaction and mycobacterial cultures should also be performed in case of diagnostic uncertainty or when pancreatic ascites, malignant tumors or tuberculosis are suspected[81].

In most cases, cirrhotic ascites is resolved through dietary sodium restriction and the use of diuretics[31]. However, children and adolescents ingesting low-sodium diets must be carefully monitored, since these restrictions often make the diet unpalatable and reduce food intake. Fluid restriction is strongly recommended in case of hyponatremia with serum sodium levels below 125 mEq/L[31]. When diuretics are required, spironolactone (1-6 mg/kg per day) should be preferred and, if necessary, combined with a loop diuretic such as furosemide (1-6 mg/kg per day). The combination with furosemide lowers the risk of hyperkalemia due to increased potassium excretion. Thiazide diuretics can be used for treatment maintenance[31]. During diuretic treatment and until the patient is stable, frequent laboratory testing should be performed to verify serum electrolytes, creatinine, blood urea nitrogen and urinary sodium levels. Excess fluid loss can lead to plasma depletion and deterioration of renal function.

Patients with refractory ascites or respiratory impairment can be treated by large-volume paracentesis. Up to 100 mL/kg of liquid can be removed at one time with the help of a post-paracentesis albumin infusion (25% albumin at 1 g/kg)[31]. Albumin and furosemide infusions can be used to treat patients with serum albumin below 2 mg/dL[33]. In severe or recurrent refractory ascites, a transjugular intrahepatic portosystemic shunt may be performed as a bridge to liver transplantation[31]. However, this procedure may be associated with increased risk of renal failure and encephalopathy[31].

Some medications should be avoided by patients with ascites. Aminoglycoside antibiotics, for instance, may increase the risk of renal failure, and non-steroidal anti-inflammatory drugs pose a high risk of sodium retention, hyponatremia and renal failure[81].

SBP refers to a bacterial infection of ascites without evidence of intestinal perforation or other intra-abdominal sources of infection[31]. Infection is usually monomicrobial and caused by E. coli, Klebsiella spp. and Enterococcus faecalis[31]. Polymicrobial infections are indicative of intestinal perforation or secondary peritonitis[31]. SBP is a relatively common and potentially fatal complication in children with ascites[33]. The presence of portal hypertension in patients with cirrhosis increases susceptibility to bacteremia and SBP[82]. These phenomena are likely caused by the translocation of intestinal bacteria and of immune system deficits associated with cirrhosis, such as alterations in complement fixation and opsonization, decreased Kupffer cell function and neutropenia[34]. Bacterial overgrowth and alterations in intestinal permeability probably play a role in bacterial translocation[83]. Studies have found that detection of bacterial DNA in the ascitic fluid of children with portal hypertension is superior to cell cultures in diagnosing SBP, but cannot differentiate between infection and ascitic fluid colonization[84].

SBP must always be considered in children with cirrhosis and ascites who present with fever, abdominal pain or leukocytosis[33]. Risk factors for SBP include ascites, hypoalbuminemia, gastrointestinal bleeding, pediatric intensive care unit admission and recent endoscopic examinations[34].

Children with SBP are usually treated with a third-generation intravenous cephalosporin, such as cefotaxime, for 14 d. As a preventive measure, antibiotics should always be used during invasive procedures. If SBP recurs, the use of oral prophylactic antibiotics such as co-trimoxazole, ciprofloxacin or norfloxacin can be considered[34].

Hepatic encephalopathy (HE) is an alteration in brain function caused by liver insufficiency and/or portosystemic shunts[85]. Infection is the main cause of HE. Gastrointestinal bleeding, excessive doses of diuretics, electrolyte imbalance and constipation are also commonly associated with this condition[85]. HE can also be caused by excess protein intake, anesthetics and sedatives[86]. Patients with HE may present with several neurological and psychiatric manifestations, ranging from subclinical alterations to coma[85]. In children and adolescents, the first symptoms of HE are subtle, and include developmental delays, academic difficulties, lethargy or sleep inversion. Older children may also exhibit personality changes, intellectual impairments, obtundation (clouding of consciousness), stupor and coma.

Diagnosis of HE in children involves a high index of suspicion. Mild HE is even more difficult to diagnose, given the difficulty of administering psychometric tests to children and the absence of measures validated for use in this age range. Children are usually diagnosed on the basis of clinical symptoms. Psychometric tests evaluate memory and neuromotor function, and have been widely used to assess patients with mild encephalopathy. In children and adolescents, the most commonly used such tests are the Wechsler Intelligence Scales and the Dutch Child Intelligence test[87]. The critical flicker frequency test, a simple and reliable test for the assessment of low-grade HE, can also be used in children older than 8 years[87].

Neuroimaging studies are important to exclude other causes of encephalopathy, but cannot be used to diagnose the condition[88]. MR spectroscopy has proved to be as useful as neuropsychometric tests for the diagnosis of mild HE in adults[89]. According to Foerster et al[90], the alterations in cerebral metabolism observed in pediatric patients with suspected mild HE are similar to those observed in adults.

Sedatives (especially benzodiazepines and opiates) should be avoided, as these drugs may worsen encephalopathy. Identification and treatment of the underlying cause of HE are crucial for the cure of the disease in approximately 90% of cases[85]. Prolonged use of low-protein diets should be avoided. When protein restriction is required, protein intake should be reduced to 2-3 g/kg per day[37]. Nonabsorbable disaccharides are the treatment of choice for patients with HE[31,87]. In children, the optimal dose of lactulose is 0.3-0.4 mL/kg, two to three times a day[31]. In adolescents and adults, the ideal dose can range from 10-30 mL three times a day, although treatment may begin with 25 mL/kg twice daily[85]. A study of lactulose therapy in 22 children with cirrhosis and HE revealed complete recovery in 73% of patients[91]. Several antibiotics, such as neomycin, vancomycin, metronidazole and rifaximin, have been used to reduce the number of ammonia-producing bacteria in the gastrointestinal tract[87]. A case report of a 9-year-old girl with cirrhosis and HE described positive clinical results with the use of rifaximim[92].

Acute-on-chronic liver failure (ACLF) is the acute deterioration of liver function in patients with cirrhosis resulting from extra- or intrahepatic causes. Data on the epidemiology of ACLF are rare[93]. In a study that evaluated a cohort of 192 patients admitted to the emergency department of a Brazilian tertiary hospital due to acute decompensation of cirrhosis, 46 (24%) fulfilled the EASL-CLIF Consortium criteria for ACLF. Bacterial infections were observed in 50%[94]. In children, the most common precipitating factor is infection. ACLF can progress to decompensation and multiple organ failure, resulting in high mortality rates. Mortality among inpatients with cirrhosis is strongly associated with infection. Patients with cirrhosis who acquire viral hepatitis, for instance, exhibit very rapid deterioration of liver function.

Hepatopulmonary syndrome (HPS) is a common complication in patients with portal hypertension and cirrhosis. It is characterized by intrapulmonary vasodilation, which results in insufficient oxygenation[95]. The diagnosis of HPS should only be made when clinical suspicion is high, since clinical manifestations are subtle in the early stages of the disease. The presence of three symptoms – liver dysfunction, arteriovenous shunts and reduced O2 saturation - is required for diagnosis[95]. The clinical picture can be reversed by liver transplantation, although the presence of HPS may interfere with tolerance to anesthesia and preclude transplant[96].

HPS is distinct from pulmonary hypertension, another underdiagnosed circulatory condition associated with pediatric cirrhosis. Pulmonary hypertension (also known in this setting as portopulmonary hypertension) has a vasoconstrictive etiology. Mild to moderate hypertension can be corrected by liver transplantation[97].

Patients with cirrhosis exhibit a progressive deterioration of renal function. Two types of hepatorenal syndrome (HRS) have been described: Type 1 HRS is associated with rapidly progressive kidney failure and a very low survival expectancy, the median survival time being only 2 wk if it is not treated; type 2 HRS is associated with slowly progressive kidney failure and has a better prognosis than type 1 HRS. Children also could exhibit alterations in renal function after liver transplantation, especially due to treatment with calcineurin inhibitors[98].

The basic laboratory tests of coagulation used to evaluate the risk of hemorrhage, such as prothrombin time and partial activated thromboplastin time, are only weakly associated with the incidence or duration of bleeding after liver biopsy or other potentially hemorrhagic procedures[99]. Nevertheless, patients with cholestatic disease and prolonged prothrombin time should receive parenteral vitamin K supplementation. The recommended dosage for children is 2-10 mg IV once daily for 3 d, or 5 to 10 mg IM per week[100]. Fresh frozen plasma infusions (5-10 mL/kg) and cryoglobulin and/or platelet transfusions can also be used as treatment for bleeding episodes or prophylaxis against bleeding during procedures such as liver biopsy[100].

Chronic anemia is common in patients with cirrhosis, and can be caused by blood loss, iron deficiency and low folic acid levels due to sodium and water retention and hemolysis secondary to hypersplenism[31].

Hepatocellular carcinoma (HCC) is also observed in patients with chronic liver disease. In pediatric patients, HCC can result from the progression of cholestatic, metabolic or viral diseases[101]. Its pathogenesis is complex and involves both genetic and environmental factors. The usual symptoms are abdominal discomfort and distention and eating difficulties. Abdominal masses may also be detected on physical or ultrasound examinations[102]. Alpha-fetoprotein levels may be elevated[102].

An Italian study found HCC to be present in 2% of 103 children with cirrhosis who underwent primary liver transplantation. Despite the early age of onset, prognosis after liver transplantation was excellent, and recurrence was not observed[103]. HCC has also been reported in children with BA and Alagille syndrome[104,105] and in adolescents with chronic hepatitis B[106,107] or C[108]. Children with cirrhosis of any etiology should undergo abdominal ultrasound examinations and alpha-fetoprotein measurements every 6 mo or at least on a yearly basis[101,109].