Home About Us Contact Us

 

Table of Content Volume 13 Issue 3- March 2020

 

 


Study of seroprevalence of hepatitis b virus infection from the patients attending tertiary care teaching hospital, Vadnagar, North Gujarat, India

 

Hitesh R Ahir1, Rakesh Rajat2*

 

1Assistant Professor, 2Associate Professor, Department of Microbiology, GMERS Medical College, Vadnagar.

Email: rakeshrjt@gmail.com

 

Abstract               Objectives: The aim of this study was to determine the prevalence of hepatitis B surface antigen (HBsAg) tested at patients attending tertiary care teaching hospital, Vadnagar, North Gujarat, India, from January 2018 till December 2018. Methods: A total of 8857 samples received from various patient groups for Hepatitis B virus antigen detection by rapid card test. All positive sample 103 were confirmed by the HbsAg ELISA test. Results: Among the 8857 samples collected, 103 were positive by HbsAg Rapid card test and HbsAg ELISA test. The Seroprevalence over one year was found to be 1.16% Conclusions: The Seroprevalence of Hepatitis B virus in this hospital in Vadnagar, North Gujarat region was considerably Lower. Reason may be due to awareness among community about this infection.

Key Words: Hepatitis B Seroprevalence, Rapid HBsag test, ELISA, Blood donors

 

 

INTRODUCTION

Hepatitis B virus (HBV) infection is a global public health problem affecting millions of people every year and causing morbidity and mortality.1 It is estimated that approximatively 257 million people are infected worldwide, particularly in low-income and middle-income countries.2 ,3 About 1 million people die each year (~2.7% of all deaths) from causes related to viral hepatitis, mostly liver disease, including liver cancer and cirrhosis.1, 4 In highly endemic areas, hepatitis B is most commonly spread vertically from mother to child at birth (perinatal transmission), or through horizontal transmission (exposure to infected blood), especially from an infected child to an uninfected child during the first 5 years of life.2 ,5 An estimated 50% to 80% of cases of primary liver cancer associated to infection with HBV.6 In sub-Saharan Africa, infections by HBV affect between 5% and 10% of the population. In many countries, HBV infection is the leading cause of liver transplants. The economic load of the disease is also important; in the terminal stage, treatments are expensive, the cost easily reaching hundreds of thousands of dollars per person.7 Following a global summit in 2015, WHO launched the international programme against hepatitis with the following goals, by 2030, to reduce by 90% the number of new cases of hepatitis B, reduce by 65% the number of hepatitis B-related deaths and treat 80% of eligible people infected with hepatitis B.8 The systematic review and meta-analysis published in Lancet by Schweitzer and colleagues in 2015 provides the global prevalence of HBV with estimate by countries.9 The purpose of our review is to provide a detailed summarisation of the data on the prevalence of HBV in the specific populations such as blood donors, pregnant women and healthcare workers in particular. Worldwide, hepatitis B virus (HBV) infection is a major cause of chronic hepatitis, liver cirrhosis, and hepatocellular carcinomas.10 and it continues to contribute to the most serious challenges currently posed by infectious diseases in public health. Although some countries, already have high immunization coverage, more than 257 million people worldwide have chronic HBV infection, with the majority of the infected people living in Africa and Asia.11 HBV and related complications result in nearly 600,000 deaths annually.12 therefore, despite the high vaccination coverage in many countries, HBV prevalence remains a major public health burden. Prior to the introduction of the national HBV vaccination program in Taiwan in 1984, approximately 15%_20% of Taiwanese adults tested positive for the HBV surface antigen (HBsAg), with mother_infant vertical transmission being the primary means of infection.13,14 The nationwide HBV vaccination program was officially implemented in July 1984 in Taiwan. During the first two years of the program, the vaccination was available free-of-charge only to infants born to HBsAg-carrier mothers. A four-dose plasma-derived vaccine regimen was provided; the doses were administered at birth and at one, two, and 12 months of age. 15 However, from July 1986 onwards, all infants were immunized against HBV by using the four-dose plasma-derived vaccine. Neonates born to highly infectious carrier mothers also received 0.5 mL of HBV immunoglobulin at birth. In addition, after November 1, 1992, the plasma-derived vaccine used for HBV vaccination was replaced by a recombinant yeast-derived vaccination with a three-dose regimen; the doses were administered at birth and at the ages of one and six months. From October 1990, the free catch-up HBV vaccination program was extended to include all children aged <7 years, all involved medical personnel, and selected groups of children (e.g., elementary-school children in aboriginal areas and offshore islands). The details of the program have been extensively documented previously. 16 The program was highly successful, and within 12 years of its implementation, over 20 million vaccinations are estimated to have been provided to neonates, children, and secondary school and college students.

 

OBJECTIVE

The aim of this study was to determine the prevalence of hepatitis B surface antigen (HBsAg) tested at patients attending tertiary care teaching hospital, Vadnagar, North Gujarat, India, from January 2018 till December 2018.

 

MATERIAL AND METHODS

Data collection:

A total of 8857 samples received from various patient groups for Hepatitis B virus antigen detection by rapid card test. All positive sample were confirmed by the HbsAg ELISA test. However, demographic variables such as sex, the first letter of the social identification number, birth date, and serological markers of HBV, including seropositivity for HBsAg, HBV surface antibody (anti-HBs), and HBV core antibody (anti-HBc), were retained.

RESULT

Table: 1: Monthwise distribution of HBSAg total and positive cases

Month

Total Sample for Hbsag

Total Positive Hbsag

January 2018

647

14

February 2018

577

8

March 2018

611

2

April 2018

592

9

May 2018

649

8

June 2018

668

6

July 2018

797

8

zAugust 2018

834

4

September 2018

883

8

October 2018

915

20

November 2018

900

12

December 2018

784

4

Total

8857

103

 


DISCUSSION

We have collected total 8857 numbers of clinical samples for HbsAg from patients attending tertiary care teaching hospital vadnagar, north Gujarat, India during January 2018 to December 2018. We have tested above samples by rapid HbsAg Kit and 103 samples were found to be positive by rapid method which were also confirmed by HbsAg ELISA kits.

CONCLUSION

We have concluded that 1.16% seroprevalence were observed for hepatitis B viral infection at tertiary care teaching hospital Vadnagar, north Gujarat, India. The Seroprevalence of Hepatitis B virus in this hospital in Vadnagar, North Gujarat region was considerably Lower. Reason may be due to awareness among community about this infection.

 

REFERENCES

  1. World Health Organization. Prévention et lutte contre l'hépatite virale: cadre pour l'action mondiale. 2012. http://www. who. int/ csr/ disease/hepatitis/ GHP_ Framework_ Fr. Pdf
  2. World Health Organization. Hepatitis B: Fact sheet. 2017. http://www. who. int/ mediacentre/ factsheets/ fs204/ en/ index. Html
  3. World Health Organization. Guidelines for the prevention, care and treatment of persons with chronic hepatitis B infection. 2015 . http://apps. who. int/ iris/ bitstream/ 10665/ 154590/ 1/ 9789241549059_ eng.pdf
  4. WHO Executive Board. Viral hepatitis. 2009. http:// apps. who. int/ gb/ebwha/ pdf_ files/ EB126/ B126_ 15- en. Pdf
  5. World Health Organization. Hepatitis B: fact Sheet. 2016. http://www.who. int/ mediacentre/ factsheets/ fs204/ en/
  6. Perz JF, Armstrong GL, Farrington LA, et al. The contributions of hepatitis B virus and hepatitis C virus infections to cirrhosis and primary liver cancer worldwide. J Hepatol 2006;45:529–38.
  7. El Khoury AC, Wallace C, Klimack WK, et al. Economic burden of hepatitis C-associated diseases: Europe, Asia Pacific, and the Americas. J Med Econ 2012;15:887–96.
  8. World Health Organization. Health topics: hepatitis. 2016. http://www. who. int/ topics/ hepatitis/ en/
  9. Schweitzer A, Horn J, Mikolajczyk RT, et al. Estimations ofworldwide prevalence of chronic hepatitis B virus infection: a systematic review of data published between 1965 and 2013. Lancet 2015;386:1546–55.
  10. Beasley RP, Hwang LY. 1984. Hepatocellular carcinoma and hepatitis B virus. Seminars in Liver Disease 4:113_121 DOI 10.1055/s-2008-1040651.
  11. World Health Organiztion (WHO). 2017. Global hepatitis report. Geneva: WHO. Available at http:// www.who.int/ hepatitis/ publications/ global-hepatitis-report2017/en/ (accessed on 29 November 2017).
  12. Perz JF, Armstrong GL, Farrington LA, Hutin YJ, Bell BP. 2006. The contributions of hepatitis B virus and hepatitis C virus infections to cirrhosis and primary liver cancer worldwide. Journal of Hepatology 45:529_538 DOI 10.1016/j.jhep.2006.05.013.
  13. Gust ID. 1996. Immunisation against hepatitis B in Taiwan. Gut 38(Suppl 2):S67_S68 DOI 10.1136/gut.38.Suppl_2.S67.
  14. Sung JL. 1984. Hepatitis B virus infection and its sequelae in Taiwan. Gastroenterologia Japonica 19:363_366.
  15. Chen DS, Hsu NH, Sung JL, Hsu TC, Hsu ST, Kuo YT, Lo KJ, Shih YT. 1987. A mass vaccination program in Taiwan against hepatitis B virus infection in infants of hep- atitis B surface antigen-carrier mothers. Journal of the American Medical Association 257:2597_2603 DOI 10.1001/jama.1987.03390190075023.
  16. Su FH, Chen JD, Cheng SH, Sung KY, Jeng JJ, Chu FY. 2008. Waning-off effect of serum hepatitis B surface antibody amongst Taiwanese university students: 18 years post- implementation of Taiwan's national hepatitis B vaccination programme. Journal of Viral Hepatitis 15:14_19 DOI 10.1111/j.1365-2893.2007.00890.x.
  17. Cochran WG. The combination of estimates from different experiments. Biometrics 1954;10:101–29.
  18. Higgins JP, Thompson SG. Quantifying heterogeneity in a metaanalysis. Stat Med 2002;21:1539–58.
  19. Egger M, Davey Smith G, Schneider M, et al. Bias in meta-analysis detected by a simple, graphical test. BMJ 1997;315:629–34.
  20. Duval S, Tweedie R. Trim and fill: a simple funnel-plot-based method of testing and adjusting for publication Bias in meta-analysis. Biometrics 2000;56:455–63.
  21. Viera AJ, Garrett JM. Understanding interobserver agreement: the kappa statistic. Fam Med 2005;37:360–3.
  22. Ankouane Andoulo F, Kowo M, Talla P, et al. Epidemiology of Hepatitis B-Associated Hepatocellular Carcinoma in Cameroon. Health Sci Dis 2013;14:16–19.
  23. Njouom R, Pasquier C, Ayouba A, et al. Low risk of mother-to-child transmission of hepatitis C virus in Yaounde, Cameroon: the ANRS 1262 study. Am J Trop Med Hyg 2005;73:460–6.
  24. Mbougua JB, Laurent C, Kouanfack C, et al. Hepatotoxicity and effectiveness of a Nevirapine-based antiretroviral therapy in HIVinfected patients with or without viral hepatitis B or C infection in Cameroon. BMC Public Health 2010;10:105.
  25. Gaynes BN, Pence BW, Atashili J, et al. Prevalence and predictors of Major depression in HIV-infected patients on antiretroviral therapy in Bamenda, a semi-urban center in Cameroon. PLoS One 2012;7:e41699.
  26. Luma HN, Eloumou SA, Malongue A, et al. Characteristics of antihepatitis C virus antibody-positive patients in a hospital setting in Douala, Cameroon. Int J Infect Dis 2016;45:53–8.
  27. Tufon KA, Meriki HD, Anong DN, et al. Genetic diversity, viraemic and aminotransferases levels in chronic infected hepatitis B patients from Cameroon. BMC Res Notes 2016;9:117.
  28. Birguel J, Ndong JG, Akhavan S, et al.[Viral markers of hepatitis B, C and D and HB vaccination status of a health care team in a rural district of Cameroon]. Med Trop 2011;71:201–2.
  29. Forbi JC, Ben-Ayed Y, Xia GL, et al. Disparate distribution of hepatitis B virus genotypes in four sub-Saharan african countries. J Clin Virol 2013;58:59–66.
  30. Abongwa LE, Clara AM, Edouard NA, et al. Sero-Prevalence of human immunodeficiency virus (HIV) and Hepatitis B virus (HBV) Co-Infection among pregnant women residing in Bamenda Health District, Cameroon. Int J Curr Microbiol App Sci 2015;4:473–83.

 



Policy for Articles with Open Access
Authors who publish with MedPulse International Journal of Microbiology(Print ISSN: 2550-7648) (Online ISSN: 2636-4646)agree to the following terms:
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
Authors are permitted and encouraged to post links to their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.