Abstract
Background
Viral hepatitis is a serious public health problem affecting billions of people globally with maternal-fetal transmission on the rise.
Objectives
This study sought to determine the prevalence and factors associated with hepatitis B virus (HBV) and hepatitis C virus (HCV) infections among pregnant women in the Asante Akim North Municipality, in the Ashanti region of Ghana.
Methods
In this cross-sectional study 168 pregnant women were recruited from the Agogo Presbyterian hospital. Blood samples were collected for the detection of Hepatitis B Surface Antigen (HBsAg) and anti-HCV antibodies. A pretested questionnaire was used to obtain demographic data and identify the risk factors associated with the two infections.
Results
Of the 168 participants studied, 16 (9.5%) tested positive for HBV and 13 (7.7%) tested positive for HCV representing 9.5% and 7.7% respectively. A participant tested positive for both HBV and HCV co-infection representing 0.6%. Undertaking blood transfusion, tattooing and sharing of needles were associated with hepatitis C infection (P=0.001). HBV was not associated with any of the risk factors (P>0.05).
Conclusion
Our findings suggest a high prevalence of hepatitis B and hepatitis C among pregnant women; blood transfusion, tattooing and sharing of hypodermic needles were associated with hepatitis C infection. Measures to reduce the disease and transmission burden must be introduced.
Keywords: Hepatitis B, Hepatitis C, pregnant women, seroprevalence, risk factors, Ghana
Introduction
Hepatitis B virus (HBV) and hepatitis C virus (HCV) infections are serious public health issues with different prevalence rates worldwide. About one fifth of the 2 billion people infected with HBV across the globe have chronic infection1,2. World Health Organization (WHO) estimates indicate that about 200 million people have HCV infection across the globe3,4. HBV and HCV are contagious diseases that can be transmitted vertically from mothers to their neonates or horizontally through blood products and body secretions5. Mother-to-child transmission remains one of the commonest routes by which HBV infection is contracted worldwide.6. The World Health Organization (WHO) estimates that 3% of the world's population has chronic hepatitis C infection. Most of these cases occur in Africa, which has the highest HCV infection prevalence rate7. Between 1999 and 2002, an estimated 4.1 million people in the United States were infected with HCV, and of these, 3.2 million had chronic infection8.
Acute HBV infection during pregnancy is less severe and is not directly associated with increased mortality or teratogenicity9,10. However, increased incidences of low birth weight and prematurity in infants born to mothers with acute HBV infection have been recorded9,11. Furthermore, acute HBV infection in early pregnancy has been associated with a 10% perinatal transmission rate11. Transmission rates (as high as 60%) have been reported to increase significantly if acute infection occurs at or near the time of delivery10.
In light of the aforementioned this study sought to determine the prevalence and factors associated with HBV and HCV infections among pregnant women at the Agogo Presbyterian hospital in the Ashanti region of Ghana. Screening pregnant women for hepatitis B and C can give a reliable prevalence of the disease in this population and provide an avenue for preventing mother to child transmission of the virus.
Subjects and methods
Study design/study site
This cross-sectional hospital based study was conducted at the Agogo Presbyterian hospital from December 2012 to February 2013. The hospital is a referral centre located in the Asante Akim North District of the Ashanti region of Ghana. It provides antenatal and other specialized obstetric services for the inhabitants of the district and beyond. This district is a predominantly farming community.
Study population/sampling technique
The study population comprised all pregnant women receiving antenatal care at the Agogo Presbyterian hospital, in the Asante Akim North municipality. We used consecutive sampling to recruit 168 eligible pregnant women after we had explained the significance of the study to the participants who visited the health facility within the study period. Women with a previous history of any form of liver disease, diabetes and pre-eclampsia were excluded from the study.
Socio-demographic data
We obtained informed written consent from participants of the study and administered a pre-tested questionnaire to obtain socio-demographic and obstetric information, such as age, parity, educational background and marital status. Other data on the risk factors of possible routes of transmission of HBV and HCV like sharing of toothbrush, haemodialysis treatment, history of abortions, multiple sexual partners, history of previous blood transfusions and other blood products, history of intravenous drug use, history of tattooing, history of HBV vaccination was obtained.
Laboratory methods
Blood sample collection
Three milliliters (3mls) of venous blood was collected from each participant through venipuncture, dispensed into serum separator tubes, allowed to clot and centrifuged at a relative centrifugal force (RCF) of 1000–1500g for 10 minutes. The serum aliquots were stored at −20°C until ready for use.
HBV and HCV testing
Separate strips (Dia Spot Rapid One-step Test Strip, United Kingdom) were used to detect HBsAg and anti-HCV antibodies in the serum of participants in accordance with the manufacturers' instructions.
Statistical analysis
Data was entered into Excel worksheet and analyzed using SPSS version 16 (Statistical Package for Social Sciences). Also Chi - square model was conducted to determine the significance of the associations between the possible risk factors and their infections due to the non-parametric nature of the data P-value <0.05 was considered significant.
Ethical approval
Ethical consent was sought from the Institutional Review Board of the University Cape Coast (UCCIRB) and the hospital ethical committee. Informed consent was obtained from each participant prior to commencement of the study.
Results
Table 1 shows the prevalence of HBV and HCV infection among the study participants. For HBV 16 participants (9.5%) tested positive whereas 13 (7.7%) tested positive for HCV. Only 1 participant (0.6%) had mixed infection of HbsAg and HCV.
Table 1.
Variable | N (%) (n = 168) |
Age group n (%) | |
10–14 | 2 (1.2) |
15–19 | 12 (7.1) |
20–24 | 43 (25.6) |
25–29 | 55 (32.7) |
30–34 | 30 (17.9) |
35–40 | 26 (15.5) |
Education n (%) | |
None | 15 (8.9) |
Primary | 105 (62.5) |
Secondary | 24 (14.3) |
Tertiary | 24 (14.3) |
Occupation n (%) | |
None | 30 (17.9) |
Formal | 17 (10.1) |
Informal | 121 (72.0) |
Hepatitis Status n (%) | |
HBV | |
Positive | 16 (9.5) |
Negative | 152 (90.5) |
HCV | |
Positive | 13 (7.7) |
Negative | 155 (92.3) |
HBV + HCV | |
Positive | 1 (0.6) |
Negative | 167 (99.4) |
HBV=hepatitis B virus;HCV=hepatitis C virus
Table 2 shows the factors associated with HBV and HCV infection among the study participants. None of the risk factors showed a significant association with HBV infection. However, blood transfusion (OR=13.91; P=0.012), tattooing and sharing of needles (OR=7.21; P=0.004) were associated with HCV infection. Factors such as diagnosis with STD'S, history of healthcare needle stick injury, exposure to human blood, and family history of HCV were not significantly associated with HCV infection (P>0.05).
Table 2.
Variable | HBV | HCV | ||
OR (95% CI) | P-value | OR (95% CI) | P-value | |
Diagnosed with STD's | ||||
Yes | 1.93 (0.66–5.69) | 0.231 | 2.83 (0.89–8.97) | 0.077 |
No * | 1* | 1* | ||
Multiple Sexual partners | ||||
Yes* | 1* | 1* | ||
No | 1* | |||
Receipt of clotting factor concentrates | ||||
Yes* | 1* | 1* | ||
No | 0.11 (0.00–5.63) | 0.270 | 0.09 (0.00–4.55) | 0.226 |
Contact with blood/open sores of infected person |
||||
Yes* | 1* | 1* | ||
No | 0.11 (0.00–5.63) | 0.270 | 0.09 (0.00–4.55) | 0.226 |
Due to the fact that most of the participants answered no to exposure to some risk factors (multiple sexual partners, haemodialysis treatment, usage of illegal drugs, sharing of toothbrush with HCV affected person, receiving blood clotting factors concentrates and contact with blood or open sores), no association was found to exist between such factors and HCV infection.
Discussion
HBV and HCV infections are both contagious diseases that can be transmitted vertically from mothers to their neonates or horizontally through blood products and body secretions5. This study determined the prevalence and risk factors associated with hepatitis B and C infection among pregnant women in the Ashanti Akim-north municipality in the Ashanti region of Ghana. The study revealed 9.5% and 7.7% prevalence of hepatitis B and hepatitis C infection respectively among the participants. Only one participant (0.6%) was a carrier of both viruses. Also, no association was found between hepatitis B infections and the risk factors. Blood transfusion, tattooing, body piercing and sharing of needles were associated with transmission of hepatitis C virus infection among the participants.
The prevalence observed in this study is consistent with the findings of earlier studies which reported a higher hepatitis B infection rate than hepatitis C among pregnant women in Nigeria12. The above findings are also similar to the study of Murad et al13, who recorded a prevalence of 10.8%, 8.5% and 0% of HBV, HCV and HBV-HCV co-infection respectively among 400 participants in Saana Yemen. However, our prevalence is higher than the 5% and less than one percent recorded in studies in Sudan7. The prevalence in our study is higher because we used immunochromatographic methods whereas ELISA technique was used in the Sudanese study. Immunochromatographic methods have lower specificity compared to the more specific ELISA techniques. In contrast with earlier studies in Sudan7 and Malawi14 0.6% of our participants had both HCV and HBV infection.
The prevalence of hepatitis C infection in this study was higher (7.7%) than the prevalence (0.2% and 6.25%) reported in Lorestan (West of Iran) and Ahvaz by Mohebbi et al.,5 and Motlagh et al,15 respectively. These inconsistencies could be attributed to the differences in sample size as well as the fact that Mohebbi et al., conducted their study across multiple centres in rural and urban communities whereas our single-centre study was conducted in a predominantly rural community. Moreover, in the cross-sectional study by Mohebbi et al,5 samples were first screened for anti-HBc and anti-HCV using commercially available ELISA kits before those which were reactive for anti-HBc were tested for HBsAg. Similarly, the prevalence rate of HBV infection recorded in this study is higher than that observed in earlier studies among pregnant women in Sudan16, Saudi Arabia17 and Libya18. Geographical differences have been identified as the main reason for the variation of seroprevalence rates of HBV infection among pregnant women in different countries19. Furthermore, as in the studies in Lorestan and Ahaz, positive cases in Egypt, Saudi Arabia and Libya were confirmed with ELISA techniques. However, studies conducted by Eke et al,20 from Nigeria recorded a prevalence (8.3%) comparable with what is recorded in our study.
In consonance with earlier studies21, we observed a sig nificant association between some risk factors (tatooing and body piercing, history of sharing of hypodermic needles and blood transfusion) and HCV infection. Ward et al.,21 had earlier identified an association between illicit drug use and body piercing (chiefly for ear rings) and HCV infection in the multiethnic population in London. In agreement with the findings of Eke et al,20 and Akani et al,22 from studies conducted in Nnewi and Port Harcourt respectively, we recorded no significant association between hepatitis B infection and the risk factors. Interestingly, this observation contradicts the results of studies conducted in Nigeria and Palestine23,24. Though no reason could readily be assigned for this observation, the small sample size employed in this study coupled with the method of testing for the infection could account for the lack of association between hepatitis B infection and the risk factors.
The outcome of this study justifies the establishment of a national HBV and HCV screening program for all pregnant women in antenatal clinics throughout Ghana. In addition, a national policy to vaccinate all pregnant women who test negative for hepatitis B must be adopted so as to reduce the risk of mother to child transmission within the population. Although this study is relevant it has major limitations. Investigation into a similar population of non-pregnant women to compare the findings was not done. Also, the study did not employ ELISA for the sero-analysis but rather used rapid test strips which may not yield 100% accuracy especially for HCV. Furthermore, the viral load was not determined for HBV and HCV positive pregnant women.
Conclusion
The prevalence of HBV and HCV infection in this study was 9.5% and 7.7% respectively. History of sharing hypodermic needles, tattooing and body piercing, and blood transfusion were associated with HCV infection. The Ghana Health Service policy of screening all pregnant women in Ghana during their routine antena tal visit is therefore justified and a policy to vaccinate women who test negative for HBV must be promulgated to reduce the future risk of mother to child transmission.
Acknowledgement
The authors are grateful to the staff of the laboratory and antenatal departments of the Agogo Presbyterian hospital
Competing interests
None declared
References
- 1.Lok AS. Chronic hepatitis B. N Engl J Med. 2002;346(22):1682–1683. doi: 10.1056/NEJM200205303462202. [DOI] [PubMed] [Google Scholar]
- 2.Drosten C, Nippraschk T, Manegold C, Meisel H, Brixner V, Roth WK, et al. Prevalence of hepatitis B virus DNA in anti-HBc-positive/HBsAg-negative sera correlates with HCV but not HIV serostatus. J Clin Virol. 2004;29(1):59–68. doi: 10.1016/s1386-6532(03)00090-8. [DOI] [PubMed] [Google Scholar]
- 3.Parry J. At last a global response to viral hepatitis. Bull World Health Organ. 2010;88(11):801–802. doi: 10.2471/BLT.10.011110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Te HS, Jensen DM. Epidemiology of hepatitis B and C viruses: a global overview. Clin Liver Dis. 2010;14(1):1–21. vii. doi: 10.1016/j.cld.2009.11.009. [DOI] [PubMed] [Google Scholar]
- 5.Mohebbi SR, Sanati A, Cheraghipour K, Rostami Nejad M, Shalmani HM, Zali MR. Hepatitis C and hepatitis B virus infection: epidemiology and risk factors in a large cohort of pregnant women in Lorestan, West of Iran. Hepat Mon. 2012;11(9):736–739. doi: 10.5812/kowsar.1735143X.749. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Petrova M, Kamburov V. Breastfeeding and chronic HBV infection: clinical and social implications. World J Gastroenterol. 2010;16(40):5042–5046. doi: 10.3748/wjg.v16.i40.5042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Elsheikh RM, Daak AA, Elsheikh MA, Karsany MS, Adam I. Hepatitis B virus and hepatitis C virus in pregnant Sudanese women. Virol J. 2007;4:104. doi: 10.1186/1743-422X-4-104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Armstrong GL, Arase Y, Ikeda K, Murashima N, Chayama K, Tsubota A, et al. The prevalence of hepatitis C virus infection in the United States, 1999 through 2002. Ann Intern Med. 2006;144:705–714. doi: 10.7326/0003-4819-144-10-200605160-00004. [DOI] [PubMed] [Google Scholar]
- 9.Hieber JP, Dalton D, Shorey J, Combes B. Hepatitis and pregnancy. J Pediatr. 1977;91(4):545–549. doi: 10.1016/s0022-3476(77)80499-x. [DOI] [PubMed] [Google Scholar]
- 10.Sookoian S. Liver disease during pregnancy: acute viral hepatitis. Ann Hepatol. 2006;5(3):231–236. [PubMed] [Google Scholar]
- 11.Jonas MM. Hepatitis B and pregnancy: an under-estimated issue. Liver Int. 2009;29 Suppl 1:133–139. doi: 10.1111/j.1478-3231.2008.01933.x. [DOI] [PubMed] [Google Scholar]
- 12.Ugbebor O, Aigbirior M, Osazuwa F, Enabudoso E, Zabayo O. The prevalence of hepatitis B and C viral infections among pregnant women. N Am J Med Sci. 2011;3(5):238–241. doi: 10.4297/najms.2011.3238. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Murad EA, Babiker SM, Gasim GI, Rayis DA, Adam I. Epidemiology of hepatitis B and hepatitis C virus infections in pregnant women in Sana'a, Yemen. BMC Pregnancy Childbirth. 2013;13:127. doi: 10.1186/1471-2393-13-127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Ahmed SD, Cuevas LE, Brabin BJ, Kazembe P, Broadhead R, Verhoeff FH, et al. Seroprevalence of hepatitis B and C and HIV in Malawian pregnant women. J Infect. 1998;37(3):248–251. doi: 10.1016/s0163-4453(98)91983-1. [DOI] [PubMed] [Google Scholar]
- 15.Motlagh M, Makvandi M, Jalali M. Prevalence of anti-HCV among pregnant women. J Qazvin Univ Med Sci. 2001;5(2):59–63. [Google Scholar]
- 16.EL-Shabrawi M, Mohamed M, El Din Hamdi M, Ehab M, Khamiss S, EL Karasky H. Prevalence of Hepatitis B Virus Infection among Egyptian Pregnant Women - A Single Center. Study international journal of tropical disease & health. 2013;3(2):157–168. [Google Scholar]
- 17.Alrowaily MA, Abolfotouh MA, Ferwanah MS. Hepatitis B virus sero-prevalence among pregnant females in Saudi Arabia. Saudi J Gastroenterol. 2008;14(2):70–72. doi: 10.4103/1319-3767.39621. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.El-Magrahe H, Furarah AR, El-Figih K, El-Urshfany S, Ghenghesh KS. Maternal and neonatal seroprevalence of Hepatitis B surface antigen (HBsAg) in Tripoli, Libya. J Infect Dev Ctries. 2010;4(3):168–170. doi: 10.3855/jidc.609. [DOI] [PubMed] [Google Scholar]
- 19.Vazquez-Martinez JL, Coreno-Juarez MO, Montano-Estrada LF, Attlan M, Gomez-Dantes H. Seroprevalence of hepatitis B in pregnant women in Mexico. Salud Publica Mex. 2003;45(3):165–170. doi: 10.1590/s0036-36342003000300005. [DOI] [PubMed] [Google Scholar]
- 20.Eke AC, Eke UA, Okafor CI, Ezebialu IU, Ogbuagu C. Prevalence, correlates and pattern of hepatitis B surface antigen in a low resource setting. Virol J. 2011;8:12. doi: 10.1186/1743-422X-8-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Ward C, Tudor-Williams G, Cotzias T, Hargreaves S, Regan L, Foster GR. Prevalence of hepatitis C among pregnant women attending an inner London obstetric department: uptake and acceptability of named antenatal testing. Gut. 2000;47(2):277–280. doi: 10.1136/gut.47.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Akani CI, Ojule AC, Opurum HC, Ejilemele AA. Sero-prevalence of hepatitis B surface antigen (HBsAg) in pregnant women in Port Harcourt, Nigeria. Niger Postgrad Med J. 2005;12(4):266–270. [PubMed] [Google Scholar]
- 23.Nazzal Z, Sobuh I. Risk factors of hepatitis B transmission in northern Palestine: a case -control study. BMC Res Notes. 2014;7:190. doi: 10.1186/1756-0500-7-190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Obienu O, Nwokediuko S, Malu A, Lesi OA. Risk factors for hepatitis C virus transmission obscure in nigerian patients. Gastroenterol Res Pract. 2011 doi: 10.1155/2011/939673. [DOI] [PMC free article] [PubMed] [Google Scholar]