HEPATITIS
NIDA SEHAR Noman
MS (Pharmacology) & MBA (Finance)
nidasehar19@yahoo.com
what is hepatitis?
Cause
Anyother cause?
Hepatitis viruses are the most common cause of hepatitis in the world
Hepatitis is an inflammation of the liver
Other infections.
Toxic substances (e.g. alcohol, certain drugs)
Autoimmune diseases.
Types of hepatitis
350 million hepatitis B
virus carriers
worldwide.
600,000 death due to
HBV complications
annually.
one of the major cause
of liver cancer
globally.
HEPATITIS B
Transmission
• It is transmitted by
• body fluids
• Hepatitis B exposure
• Intravenous drug user
• Patient immunocompromised
• Fetal or neonatal effect of maternal
infection
• Surgical procedure
• Healthcare Worker, or
• Transfusion of blood product.
• There are three surface antigen
HBsAg most abundant persistence past 6 months
after initial detection corresponds to chronic infection and
indicates an increased risk for cirrhosis and HCC.
HBeAg present in an acute infection and is replaced by
antibodies (anti-HBeAg ) once an infection is resolved.
HBcAgnucleocapsid protein that,when expressed on
hepatocytes,promotes immune-mediated cell ldeath.
Stages of HBV
Immunotolerant Immunoactive Seroconversion
HBeAg +
HBV DNA >20000IU/ml
ALT normal
HBeAg +,-
usually HBV DNA
>20000IU/ml
ALT elevated
HBeAg -
Normal ALT
Anti HBeAg
• Loss ofAppetite.
• Fatigue.
• Nausea and vomiting.
• Itching all over the body.
• Pain over the location of
the liver.
• Jaundice (skin and the
whites of the eyes turn
yellow in color)
• Dark urine (the color of
cola or tea)
• Pale-colored stools
SIGN AND
SYMPTOMS
Diagnosis is done by serological assay and liver enzymes test (LFT).
 Acute HBV infection is characterized by the presence of HBsAg and
immunoglobulin M (IgM) antibody to the core antigen, HBcAg.
During the initial phase of infection, patients are also seropositive
for hepatitis B e antigen (HBeAg). HBeAg is usually a marker of
high levels of replication of the virus. The presence of HBeAg
indicates that the blood and body fluids of the infected individual
are highly infectious.
 Chronic infection is characterized by the persistence of HBsAg for at
least 6 months (with or without concurrent HBeAg). Persistence of
HBsAg is the principal marker of risk for developing chronic liver
disease and liver cancer (hepatocellular carcinoma) later in life.
Diagnosis
Hepatitis b (1)
Hepatitis b (1)
T
R
E
A
T
M
E
N
T
Interferon
 IFN-alfa therapy was the first approved therapy for
treatment of HBV.
 Improves long-term outcomes and survival.
 It has antiviral,antiproliferative,and immunomodulatory
effects
 Most effective in pateints with increased ALT and HBV
DNA levels,high histologic activity score at biopsy,and
being non-Asian.
 It enhance the host immune system to defense against
HBV.
Lamivudine
 Lamivudine, a nucleoside analog,work by incorporating
into growing HBV DNA chain causing premature chain
termination.
 Nose is 100mg daily orally.
 No definite duration of therapy
 And there is chance of resistance
 It's not recommended as first-line therapy
Adefovir
 Adefovir,an analog of adenosine monophosphate,act by inhibiting
HBV reverse transcriptase and DNA polymerase.
 effective in lamivudine resistent patients
 30mg/day of adenofovir was found nephrotoxic in clinical trials.
 serum creatinine monitoring is recommended in patients with risk
of renal insuffeincy and, treated with adefovir for more than one
year.
 dose is 10mg daily for one year.
 the risk of adefovir resistence is high in lamivudine resistenent
patients.
 but no drug resistence has been seen in first year of therapy.
 not first line therapy for HBV.
Entecavir
 Entecavir is a guanosine nucleoside analog that inhibit
HBV replication at three stages.
 More potent than both lamivudine and adefovir.
 Effective in lamuvidine resistent patients.
 Dose 0.5 mg daily and 1mg in lamivudine resistent pts.
 No resistence has been seen but the risk of resistence
high in lamuvidine and adefovir resistent patients.
 Available by the name of Baraclude
Telbivudine
 Telbivudine is HBV specific nucloside analog act as
competitive inhibitor of viral reverse transcriptase and
DNA polymerase.
 As compare to lamivudine ;telbivudine is more potent
suppressor of HBV DNA.
 Telbivudine resistant mutations are cross-resistant with
lamivudine.
 Because of resistance concerns telbivudine monotherapy
has a limited role in the treatment of HBV.
Tenofovir
 Tenofovir is a nucleotide analog approved f or HBV in
2008.
 equally effective in both HBeAg positive and HBeAg
negative patients.
 not nephrotoxic.
 found effective in both lamuvidine and adefovir resistent
patients.
 Daily dose is 300mg orally.
 First line therapy.

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Hepatitis b (1)

  • 1. HEPATITIS NIDA SEHAR Noman MS (Pharmacology) & MBA (Finance) [email protected]
  • 2. what is hepatitis? Cause Anyother cause? Hepatitis viruses are the most common cause of hepatitis in the world Hepatitis is an inflammation of the liver Other infections. Toxic substances (e.g. alcohol, certain drugs) Autoimmune diseases.
  • 4. 350 million hepatitis B virus carriers worldwide. 600,000 death due to HBV complications annually. one of the major cause of liver cancer globally. HEPATITIS B
  • 5. Transmission • It is transmitted by • body fluids • Hepatitis B exposure • Intravenous drug user • Patient immunocompromised • Fetal or neonatal effect of maternal infection • Surgical procedure • Healthcare Worker, or • Transfusion of blood product.
  • 6. • There are three surface antigen HBsAg most abundant persistence past 6 months after initial detection corresponds to chronic infection and indicates an increased risk for cirrhosis and HCC. HBeAg present in an acute infection and is replaced by antibodies (anti-HBeAg ) once an infection is resolved. HBcAgnucleocapsid protein that,when expressed on hepatocytes,promotes immune-mediated cell ldeath.
  • 7. Stages of HBV Immunotolerant Immunoactive Seroconversion HBeAg + HBV DNA >20000IU/ml ALT normal HBeAg +,- usually HBV DNA >20000IU/ml ALT elevated HBeAg - Normal ALT Anti HBeAg
  • 8. • Loss ofAppetite. • Fatigue. • Nausea and vomiting. • Itching all over the body. • Pain over the location of the liver. • Jaundice (skin and the whites of the eyes turn yellow in color) • Dark urine (the color of cola or tea) • Pale-colored stools SIGN AND SYMPTOMS
  • 9. Diagnosis is done by serological assay and liver enzymes test (LFT).  Acute HBV infection is characterized by the presence of HBsAg and immunoglobulin M (IgM) antibody to the core antigen, HBcAg. During the initial phase of infection, patients are also seropositive for hepatitis B e antigen (HBeAg). HBeAg is usually a marker of high levels of replication of the virus. The presence of HBeAg indicates that the blood and body fluids of the infected individual are highly infectious.  Chronic infection is characterized by the persistence of HBsAg for at least 6 months (with or without concurrent HBeAg). Persistence of HBsAg is the principal marker of risk for developing chronic liver disease and liver cancer (hepatocellular carcinoma) later in life. Diagnosis
  • 13. Interferon  IFN-alfa therapy was the first approved therapy for treatment of HBV.  Improves long-term outcomes and survival.  It has antiviral,antiproliferative,and immunomodulatory effects  Most effective in pateints with increased ALT and HBV DNA levels,high histologic activity score at biopsy,and being non-Asian.  It enhance the host immune system to defense against HBV.
  • 14. Lamivudine  Lamivudine, a nucleoside analog,work by incorporating into growing HBV DNA chain causing premature chain termination.  Nose is 100mg daily orally.  No definite duration of therapy  And there is chance of resistance  It's not recommended as first-line therapy
  • 15. Adefovir  Adefovir,an analog of adenosine monophosphate,act by inhibiting HBV reverse transcriptase and DNA polymerase.  effective in lamivudine resistent patients  30mg/day of adenofovir was found nephrotoxic in clinical trials.  serum creatinine monitoring is recommended in patients with risk of renal insuffeincy and, treated with adefovir for more than one year.  dose is 10mg daily for one year.  the risk of adefovir resistence is high in lamivudine resistenent patients.  but no drug resistence has been seen in first year of therapy.  not first line therapy for HBV.
  • 16. Entecavir  Entecavir is a guanosine nucleoside analog that inhibit HBV replication at three stages.  More potent than both lamivudine and adefovir.  Effective in lamuvidine resistent patients.  Dose 0.5 mg daily and 1mg in lamivudine resistent pts.  No resistence has been seen but the risk of resistence high in lamuvidine and adefovir resistent patients.  Available by the name of Baraclude
  • 17. Telbivudine  Telbivudine is HBV specific nucloside analog act as competitive inhibitor of viral reverse transcriptase and DNA polymerase.  As compare to lamivudine ;telbivudine is more potent suppressor of HBV DNA.  Telbivudine resistant mutations are cross-resistant with lamivudine.  Because of resistance concerns telbivudine monotherapy has a limited role in the treatment of HBV.
  • 18. Tenofovir  Tenofovir is a nucleotide analog approved f or HBV in 2008.  equally effective in both HBeAg positive and HBeAg negative patients.  not nephrotoxic.  found effective in both lamuvidine and adefovir resistent patients.  Daily dose is 300mg orally.  First line therapy.