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Hepatitis

Hepatitis is a gastroenterological disease, featuring inflammation of the liver. The clinical signs and prognosis, as well as the therapy, depend on the cause. more...

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Signs and symptoms

Hepatitis is characterised by fatigue, malaise, joint aches, abdominal pain, vomiting 2-3 times per day for the first 5 days, loss of appetite, dark urine, fever, hepatomegaly (enlarged liver) and jaundice (icterus). Some chronic forms of hepatitis show very few of these signs and only present when the longstanding inflammation has led to the replacement of liver cells by connective tissue; the result is cirrhosis. Certain liver function tests can also indicate hepatitis.

Types of hepatitis

Viral

Most cases of acute hepatitis are due to viral infections:

  • Hepatitis A
  • Hepatitis B
  • Hepatitis C
  • D-agent (requires presence of the hepatitis B virus)
  • Hepatitis E
  • Hepatitis F (discredited)
  • Hepatitis G
Please see the respective articles for more detailed information

Hepatitis A

Hepatitis A is an enterovirus transmitted by the orofecal route, such as contaminated food. It causes an acute form of hepatitis and does not have a chronic stage. The patient's immune system makes antibodies against Hepatitis A that confer immunity against future infection. People with Hepatitis A are usually advised to rest, stay hydrated and avoid alcohol. A vaccine is available that will prevent infection from hepatitis A for life.

Hepatitis B

Hepatitis B causes both acute and chronic hepatitis in some patients who are unable to eliminate the virus. Identified methods of transmission include blood (blood transfusion, now rare), tattoos (both amateur and professionally done), sexually or vertically (from mother to her unborn child). However, in about half of cases the source of infection cannot be determined. Blood contact can occur by sharing syringes in intravenous drug use, shaving accessories such as razor blades, or touching wounds on infected persons. Needle-exchange programmes have been created in many countries as a form of prevention. In the United States, 95% of patients clear their infection and develop antibodies against Hepatitis B virus. 5% of patients do not clear the infection and develop chronic infection; only these people are at risk of long term complications of Hepatitis B. Patients with chronic hepatitis B have antibodies against Hepatitis B, but these antibodies are not enough to clear the infection that establishes itself in the DNA of the affected liver cells. The continued production of virus combined with antibodies is a likely cause of immune complex disease seen in these patients. A vaccine is available that will prevent infection from hepatitis B for life. Hepatitis B infections result in 500,000 to 1,200,000 deaths per year worldwide due to the complications of chronic hepatitis, cirrhosis, and hepatocellular carcinoma. Hepatitis B is endemic in a number of (mainly South-East Asian) countries, making cirrhosis and hepatocellular carcinoma big killers. There are three, FDA-approved treatment options available for persons with a chronic hepatitis B infection: alpha-interferon, adefovir and lamivudine. In about 45% of persons on treatment achieve a sustained response.

Read more at Wikipedia.org


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Outcomes of Lung Transplant Recipients previously infected with hepatitis C virus
From CHEST, 10/1/05 by Hina Sahi

PURPOSE: Outcomes of Lung Transplant in Hepatitis C virus (HCV) positive Recipients is not known. We describe our experience with 5 such patients.

METHODS: Charts of LTR known to be HCV positive prior to transplantation were reviewed for demographics, HCV etiology, HCV RNA viral load pre and post transplantation, liver biopsy results, transaminase levels during various points post transplantation, the development of acute hepatitis and survival.

RESULTS: 454 lung transplants were performed during a 14 year period, only five patients (1%) [age (yrs [+ or -] SD): 48 [+ or -] 9.7, 3 females], were anti-HCV seropositive. Etiology of HCV infection included IVDA (n=l), unknown causes (n=4), and two patients had concomitant liver disease due to alpha-1-antitrypsin deficiency and cystic fibrosis. All patients were diagnosed with HCV prior to transplantation and confirmed with HCV qualitative RNA testing. All recipients had disease severity documented by liver biopsy (minimal peri portal fibrosis n=3, no cirrhosis n=5). The median duration from HCV diagnosis to transplantation was 2 years [inter quartile range, 1 to 8.2 yrs). Pre transplantation median quantitative HCV RNA levels were 50,300 IU/ml [inter quartile range, 16,897 to 200,780,000 IU/ml]. Post transplantation median quantitative HCV RNA level were noted to markedly increase [level (IU/ml): 2,470,000 IU/ml (inter quartile range, 646,825 to 2,897,500 IU/ml)]. There was no statistically significant increase in transaminase levels pre and post LTX despite increase in HCV RNA levels. The longest surviving_patient in this cohort is 5 yrs post transplantation, the shortest survival being 8 months. The patient died of respiratory complications with no evidence of hepatic failure at the time of death [mean survival (months [+ or -] SD): 32.6 [+ or -] 23.9].

CONCLUSION: Although viral loads tended to significantly increase post transplantation, there was no significant difference in the episodes of acute hepatitis, hepatic failure or cirrhosis during the duration of follow up. Post transplant monitoring of quantitative RNA HCV levels was not of any prognostic value.

CLINICAL IMPLICATIONS: Further studies are needed to provide guidelines for monitoring of this population post transplantation.

DISCLOSURE: Hina Sahi, None.

Hina Sahi MD * Marie Budev DO Holli Blazey Other Atul Mehta MBBS Cleveland Clinic Foundation, Cleveland, OH

COPYRIGHT 2005 American College of Chest Physicians
COPYRIGHT 2005 Gale Group

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