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Chronic Hepatitis B infection
Chronic Hepatitis B infection is defined as having
persistent Hepatitis B surface antigen (HBsAg) and detectable serum
Hepatitis B virus for more than 6 months. Risk of being chronic carriers depends on the age
of infection. The younger the age of infection, the higher the risk
of being a chronic carrier after an acute infection. About 90% of patients who acquire Hepatitis B from
birth will become chronic Hepatitis B carriers, while less than 5%
of adult patients become carriers after an acute infection Immunotolerant phase: Patients often had high amount
of Hepatitis B virus but despite that, there is little inflammation
in the liver and patients' liver panel are normal. It is because patient's
immune system does not recognize the virus. Immunoclearance phase: Patients' immune system started
to recognize the virus and begin to kill the viruses. As Hepatitis
B virus live in the liver, such killing also causes the liver cells
to die. Patients often has abnormal liver panel at this stage. If
this stage persists for prolonged period, patients progress to complications
faster. Inactive carrier stage: At this stage, patients have
low amount of Hepatitis B virus and there is little liver damage.
Risk of progression decreases but may still occur. Reactivation phase: At this stage, patients' Hepatitis
B virus becomes reactivated and increases in amount, with active liver
damage. Chronic Hepatitis (inflammation of the liver) Hepatitis Flare (sudden increase of the ALT , > 5 times upper
limit of normal) Cirrhosis (hardening of the liver) Ascites (fluid accumulation in the abdomen) Bleeding of the esophageal or gastric varices (Burst of vessels in
gullet or stomach) Liver cancer Liver failure (confusion and coma due to poor liver function) Spontaneous Bacterial Peritonitis (SBP) - infection of ascites fluid
by bacteria Hepatorenal Symdrome (HRS) - Kidney failure secondary to liver failure
Rate of progression among patients with chronic Hepatitis B
Among patients with abnormal liver panel, risk of
developing liver cirrhosis occurs at a rate of 2-10% yearly. Risk factors for development of liver cirrhosis include
older age, male gender, active liver inflammation, high amount of
Hepatitis B virus in blood, and alcohol abuse. Risk of development of liver cancer is about 0.6%
in carriers of Hepatitis B, but increases to about 2% once liver cirrhosis
occurs. Once a patient develops liver cancer, even if it is treated,
rate of recurrence is high, at about 10% yearly. Although patients with flares may develop liver failure
and progress to cirrhosis faster, they may not have symptoms in the
early stage and the only sign is abnormal liver panel. Once they are
jaundiced (yellowing of eyes), it may already be late. Liver cirrhosis (or liver hardening) is divided into
early and late. Patients with early cirrhosis do not feel any symptoms,
but once they progress to late cirrhosis (or what doctors called decompensated
cirrhosis), they will have symptoms such as yellowing of eyes, ascites
(abdomen filled with fluid), ankle edema, vomiting of blood, reduced
energy level, and even confusion and coma. In other words, patients
with early cirrhosis cannot tell they have cirrhosis. Patients with liver cancer also do not have any symptoms
till the late stage. Patients with advanced liver cancer often have
jaundice (yellowing of eyes), ascites (accumulation of fluid in the
abdomen), and lack of energy and weight loss. By the time patients
have these symptoms, it is often too late and is beyond the curative
stage. Patients with chronic Hepatitis B but without complications
such as cirrhosis or cancer can lead a normal life, without any symptoms.
Their lifespan is often similar to those without Hepatitis B. However, once cirrhosis develops, their lifespan
may be affected. Patients with early cirrhosis still have >80% chance
of survival 5 years later, but once late complications (such as jaundice,
ascites, and confusion) occur, less than 20% are still alive after
5 years.
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