Business Wire India
Viral hepatitis is a leading cause of death worldwide (1.46 million deaths, a toll higher than that from HIV, tuberculosis or malaria, and on the increase since 1990). More than 90% of this burden is due to the sequelae of liver infections with the hepatitis B virus (HBV
) and hepatitis C virus (HCV
). The liver is a vital organ that processes nutrients, filters the blood, and fights infections. When the liver is inflamed or damaged, its function can be affected. Heavy alcohol use, toxins, some medications, and certain medical conditions can cause hepatitis. However, hepatitis is most often caused by a virus.
Worldwide, mortality attributed to viral hepatitis has increased by 22% since 2000 despite decline in deaths caused by other infectious diseases, including HIV, tuberculosis, and malaria. World Health Organisation
(WHO) estimates that in 2015, viral hepatitis was responsible for 1.34 million deaths per year2
. In 2016, in light of the public health burden of viral hepatitis, and persisting gaps in prevention and response, the World Health Assembly approved WHO’s first Global Health Sector Strategy on Viral Hepatitis
This strategy sets the first global targets for eliminating HBV and HCV infections as public health threats by 2030 (defined as a 90% reduction in incidence and a 65% reduction in deaths) and establishes indicators to monitor implementation of necessary interventions to reach these goals.
According to Dr. Akash Shukla, Consultant Hepatologist & Liver Transplant Physician, Global Hospital
, “The challenge in eliminating chronic viral hepatitis is due to the infected person being unaware of their chronic carrier status and to the potential for them to continue to infect others for decades. Eventually the society is burdened with loss of productive workforce, and the health care system with expenses of treating liver failures, chronic liver diseases, and cancers. A large study from India has shown that out of 18,589 people screened, HBV infection was detected in 303 (prevalence 1.63%) and HCV infection in 56 (prevalence 0.3%)
Screening and prevention can reduce the rate of new infections, but the number of those already infected would remain high for a generation. Prevention of hepatitis B virus (HBV) transmission from infected mothers to their new-borns is critical to HBV control and eventual eradication. Mother-to-child perinatal transmission causes the highest chronic carrier rate (>85%) with a high rate of subsequent chronic liver disease and hepatocellular carcinoma. This risk is reduced by 90% with HBV vaccine given along with hepatitis B immune globulin (HBIG) starting at birth. In the absence of additional efforts, 19 million hepatitis-related deaths can be anticipated from 2015 to 2030. However, advances in medicine have made it possible prevent deaths.
Further Dr. Ameet Mandot, Consultant Gastroenterologists, Hepatologist & Endoscopist, The Gut Clinic,
added, “Access to HCV and HBV therapy begins with screening to identify infected persons, followed by referral to a skilled provider; together, these essential prevention steps are known as the 'HBV care cascade' and the 'HCV cure cascade'. Males contributed to about three-fourths of detected HBV
(77%) or HCV
(73%) infection. Screening detected a higher overall HBV/HCV infection rate in rural
(2.52%) than in urban
(P<0.0001). Slum areas had an HBV prevalence of
With constant evolution in the medicine world, new therapies and drugs are helping doctors and patients with disease management. These advances have now made hepatitis C a curable infection in most instances. Progress has been made with the development and introduction of Tenofovir Alafenamide Fumarate
(TAF) a potent and safe option for the long-term treatment of hepatitis B. Patients appropriately managed may avoid the complication of chronic hepatitis like cirrhosis, inflammation and liver failure.
Awareness and screening is the first step to eradicating this infection. A simple blood test is all it takes.
Weekly Epidemiology Rec. 2017 Sep 15;92(37):537-56.
2017 Nov;50:3-19. doi: 10.1016/j.biologicals.2017.08.008.
Eur J Gastroenterol Hepatol. 2018 Jun 8. doi: 10.1097/MEG.0000000000001180.
J Family Med Prim Care. 2018 Jan-Feb;7(1):157-161.