Hepatitis B and C viruses’ infection and associated factors among pregnant women in the Amhara region, Ethiopia: implications for prevention of vertical transmission.

doi:10.21203/rs.3.rs-30519/v1

Background

Hepatitis virus infection is a major public health burden and silent killer disease in sub-Saharan Africa, including Ethiopia. Despite the recommendations of the World Health Organization, screening for hepatitis B virus (HBV) and hepatitis C virus (HCV) in pregnant women is not done routinely in public health institutions. Therefore, this study aimed to determine the burden of HBV and HCV and its associated factors among pregnant women in the Amhara region, Ethiopia.

Methods

A total of 1121 pregnant women were enrolled in the study. Data on sociodemographic and associated factors were collected using a structured questionnaire. Blood was collected from the pregnant women, and serum samples were tested for HBsAg and anti-hepatitis C virus antibody (anti-HCV) using ELISA. The status of HIV-infected pregnant women was collected from the records of their charts. SPSS version 20 was used for data analysis, and a binary logistic regression model was used to assess the relationship between factors associated with HBV and HCV infection.

Results

The seroprevalence of HBsAg and anti-HCV antibody were 4.6% and 1.6, respectively. The co-infection rate of HBV/HCV was 1.4% (1/69). Ten out of 52 HBV positive cases (19.2%) were co-infected with HIV. Only 20 (1.8%) pregnant women had the HBV vaccine. Interestingly, pregnant women with a history of multiple sexual partners (AOR = 3.2,95% CI,1.7–7.6), blood transfusion (AOR = 7.6,95% CI,2.9–16.9), family history of HBV (AOR = 3.5, 95% CI,1.7–7.6), being HIV-positive (AOR = 2.5, 95% CI,1-5.9), and tattooing (AOR = 2, 95% CI, 1-3.8) were significant predictors of HBV infection.

Conclusions

HBV and HCV infections were intermediate among pregnant women; risk factors were responsible for the majority of cases. Infants born from these infected mothers are at risk of infection. This calls for integration of HBV prevention into the PMTC of HIV. Thus, the provision of health education on HBV and HCV transmission, vaccination, and screening of all pregnant women routinely is essential for PMTCT.

Infectious Diseases

Maternal & Fetal Medicine

Pregnant women

HBV

HCV

Associated factors

Amhara region

Viral hepatitis is a major public health burden all over the world. It is responsible for an estimated 1.4 million deaths, which is greater than the death toll of 1.2 million to that of HIV. Globally, 248 million and 150 million people have chronic HBV and HCV infections and the cause of death for 780,000 and 350,000 people, respectively [1]. HBV and HCV infections are highly endemic in developing regions of Asia and Africa. The highest seroprevalence of hepatitis B surface antigen (HBsAg) > 8% and anti-hepatitis C virus (anti-HCV) antibody > 3.5% have been reported in these regions [2, 3]. Despite its high prevalence of HBV and HCV, it remains under-reported and lacks of reliable epidemiological data in most African countries, including Ethiopia. Globally, less than 5% of people are aware of infected by hepatitis virus infection [1]. The majority of hepatitis infected individuals remain asymptomatic or apparently healthy, transmit the virus to other persons, and die of the infection without notice; it is a silent killer [4].

HBV is highly contagious and hundred times more infectious than HIV, transmitted horizontally through infected blood, blood products, unprotected sex, unsafe injection, tattooing, and from infected mother-to-child vertically, before birth, during birth and after birth [5, 6]. Mother-to-child transmission (MTCT) of HBV remains a major source of chronic infection in endemic countries [7]. A pregnant woman positive for HBsAg, hepatitis B e antigen (HBeAg), and HBV viral load of deoxyribonucleic acid (DNA) (> 200,000 IU/mL, equivalent to 6 log copies/mL), the chance of MTCT increases and reaches 90% [8]. In Africa, about 70–90% of infants infected before 1 year of age develop chronic HBV infection, liver cirrhosis, hepatocellular carcinoma, and early death in children [9]. To prevent MTCT, screening, early case detection, initiation of treatment of pregnant women, and provision of active birth dose HBV and passive hepatitis B immunoglobulin (HBIG) vaccines within 24 hours are widely recommended for infants born to HBsAg-positive pregnant mothers [9, 10] .

HCV is transmitted mainly through parenteral routes such as infected blood transfusion, intravenous drug use or blood product, therapeutic injection, intravenous drug use, acupuncture, tattooing, ear piercing and transmission during sexual contact and vertically from infected-mother-to-child [5, 11, 12].Vertical transmission of HCV from mother-to-child contributes to 10% of cases and lower than other viral pathogens such as HIV and HBV [13]. Drugs like direct-acting antiviral agents (DAA) are effective for curing up to 70% of HCV-infected persons; however, contraindicated during pregnancy [11, 13]. Currently, there is no effective vaccine for HCV and no effective means of preventing MTCT of HCV.

Viral hepatitis during pregnancy is associated with a high risk of maternal, fetal, and neonatal complications such as still birth, abortion, premature birth, and low birth weight [14]. Despite the significant health burden, it places on communities, viral hepatitis is an ignored health problem and has given little attention in Ethiopia. In Ethiopia, there is a lack of reliable national and sub-national epidemiological data on both HBV and HCV among pregnant women. Though few studies have been conducted in our country with small sample sizes. The prevalence of HBsAg among pregnant women varies considerably from 2.4–8.4% and anti-HCV antibody 0.6–8.1%, respectively [15–18]. In Ethiopia, the co-endemicity of HBV, HCV, and HIV and the same route of transmission and co-infections in pregnancy resulted in increased morbidity, mortality and vertical transmission of these viruses [4, 19] .

Screening for hepatitis during pregnancy is important for both the mother and the fetus, widely recommended and giving prophylaxis for those who are positive [1, 20, 21]. HIV and syphilis are routinely screened in Ethiopia. There is a well-organized and standard PMTCT of HIV in the country. Moreover, the World Health Organization (WHO) recommended PMTCT for HIV, syphilis and HBV [22]. Despite this recommendation, Ethiopia has not scaled up HBV PMTCT in the country. Currently, screening for these viruses is not a routine practice in health institutions in Ethiopia due to a lack of diagnostic kits and high cost of treatment. There are no current multicenter studies with large sample sizes on HBV and HCV among pregnant women in Ethiopia, specifically in the Amhara region, Ethiopia. Therefore, this study aimed to assess the magnitude of HBV and HCV infections and associated factors in the first trimester of pregnant women in the Amhara region, northwest Ethiopia.

Study area, design, and period

A cross-sectional study was conducted in the Amhara regional referral hospitals, namely, the University of Gondar Comprehensive Specialized Hospital, Felege Hiwot Specialized Hospital, and Debre Markos Hospital. The University of Gondar Comprehensive Specialized Hospital is located in Gondar, 750 km northwest of Addis Ababa. The hospital serves more than 5 million inhabitants in the Amhara region. The Felege Hiwot Comprehensive Specialized Hospital is located in Bahir Dar, the capital city of the Amhara region. It serves as a referral hospital in the Amhara region. Debre Markos Hospital is Zonal Hospital, which serves two million people in the East Gojam Zone. The study was conducted from May1,2018 to September 30,2019.

Study population, sample size, and sampling technique

The study population were all pregnant women who were attending the University of Gondar Compressive Specialized Hospital (UOGCSH), Felege Hiwot Comprehensive Specialized Hospital (FHCSH) in Bahir Dar and Debre Markos Hospital (DMH) during the study period. All pregnant women whose urine tests positive for human gonadotrophic hormone (HCG) and first trimester were included in the study. Those pregnant women with unknown gestational age and seriously ill were excluded from the study. The sample size was calculated using a single proportion formula. The formula is n = z²/d²(p(1-q)/w2. The assumption 95% confidence interval, 1.96%, margin of error 2%, and prevalence of 50%. Including 5% of the 1067 nonresponse rates. Finally, the sample size was 1121. A systematic sampling technique was used to select pregnant women in the antenatal clinic (ANC).

Data collection

Sociodemographic and clinical characteristics of pregnant women and associated factors were collected using a pretested structured questionnaire by trained experienced senior Midwifery nurses.

Sample collection, transportation, and processing

After getting permission from the pregnant women, five mL of venous blood was collected from each pregnant woman by a trained experienced senior laboratory technologist. Serum was separated within 8 h by centrifugation of whole blood at 3000 rpm for 10 min. Serum samples were separated and transferred to a nuck tube and stored at -80 0_C in a refrigerator until being processed by Enzyme Linked Immuno Sorbent Assay (ELISA). Serum samples collected from Felege Hiwot Comprehensive Specialized and Debre Markos Hospital were transported to the University of Gondar Comprehensive Specialized Hospital using cold boxes with dry ice. Hepatitis B surface antigen (HBsAg) from the serum of each pregnant woman was determined using ELISA according to the manufacturer’s instructions (Linear Chemicals, S.L.U., Spain). Anti-HCV antibodies were tested using commercially available ElISA kits (DIALB Diagnostics GmbH, Vienna, Austria) according to the manufacturer instructions. The results were read in a microplate reader at 450 nm within 30 min. In addition, the HIV test results of the pregnant women were also collected from their medical records. The HIV test was performed using rapid test kits following the national test algorithm. HIV1/2 STAT PACK was used as a screening test kit, followed by ABBON. If both test kits were discordant, repeated again. If both were positive, the third test (tie breaker BIOLINE) will be performed if positive the result reported as positive.

Data quality

The data collectors were trained on the study protocol (client approach, data collection procedures, and quality issues) prior to the start of the study. To ensure the quality of the data, questionnaires were prepared in English and translated into Amharic and retranslated back into English. The questionnaires were pretested before two weeks in the study time among 5% of pregnant women in the Poly Health Center in Gondar Town. The collected data were checked for consistency and accuracy. The standard operating procedures were strictly followed during blood sample collection, storage, and analytical process. The storage conditions and expiration date of the reagents were checked. The ELISA test was controlled by house internal known positive and negative controls processed using Wanti. Both positive and negative controls were run along with samples prepared by the manufacturer and following the manufacturer’s instructions.

Data Analysis

Before data entry, the collected data were checked for completeness, consistency, and coded manually. Data were entered into SPSS version 20, cleaned, and recoded. Sociodemographic characteristics were analyzed using descriptive statistics such as frequencies, mean, and standard deviation. Bivariate logistic regression was used to determine the association between the outcome variable and explanatory variables. All variables in the bivariate logistic regression model whose p-value less than or equal to 0.2 were included in the multivariate logistic regression model. The adjusted odds ratio (AOR) with a 95% confidence interval was used to check the strength of the association. Model fitness was done using Hosmer and Lemeshow statistics. Variables with a p-value < 0.05 were considered statistically significant with a 95% confidence interval.

Sociodemographic characteristics

A total of 1121 pregnant women participated in the study. Of these, 593 (52.9%) of participants were from the University of Gondar Comprehensive Specialized Hospital and the rest were from Bahir Dar Comprehensive Specialized Hospital and Debre Markos Hospital. The mean age of study participants was 27.2 years with a standard deviation of 4.8 years. A large proportion of pregnant women 1094 (97.6%) were married. Majority,895(79.8%) of participants were from urban. Most of the study participants 1064 (94.9%) were Orthodox Christians. More than half of the pregnant women 732 (65.3%) were housewives. Only 20 (1.8%) pregnant women were vaccinated for HBV before the study period (Table 1).

Seroprevalence of HBV and HCV

In this study,69 (6.2%) pregnant women had serological evidence of either infections of HBV or co-infection with HCV. The overall prevalence of HBsAg among pregnant women was 52/1121, 4.6% (95% CI, 3.4–5.8%). The prevalence of HBsAg was 7.2% (32/447) and 2.8% (17/593), 3.7% (3/81) at Felege Hiwot Comprehensive Specialized Hospital, University of Gondar Comprehensive Specialized Hospital, and Debre Markos Hospital, respectively. While the overall seroprevalence of HCV antibody was 18/1121,1.6% (95% CI, 0.9–2.4%). The highest HCV seroprevalence was 9.8% (8/81) at Debre Makos Hospital, followed by the University of Gondar Comprehensive Referral Hospital 1% (6/593), and Felege Hiwot Comprehensive Referral Hospital 0.9% (4/448). The co-infection rates of HBV and HCV were 1.4% (1/69).

The highest seroprevalence of HBsAg was 21.7% observed among unmarried pregnant women, followed by low income 9.4% and 6.2% rural residence; respectively (Table 2). Ten of 52 HBV positive cases (19.2%) were coinfected with HIV. The overall HBV/HIV coinfection rate was 0.89% (10/1121). There was no co-infection of HCV with HIV in this study. Three hundred and fifty-two (31.3%) pregnant women had tattoos in their body parts. The highest seroprevalence among the associated factors was blood transfusion 7/34 (20.6%), followed by multiple sexual partners 7/61(11.5%) (Table 3).

Factors associated with HBV infection in pregnant women

Multivariate analysis showed that some of the variables were significantly associated with HBV infection (Table 3). Pregnant women who had HIV infection were (AOR 2.5; 95% CI: 1-5.9) times more likely to develop HBV infection than their counterparts. Similarly, pregnant women with a history of blood transfusion were (AOR 7.4; 95% CI 2.5–21.3) more likely to have HBV infection than those who were not transfused blood. Pregnant women who had a history of sharing their tooth brush to others were 4.5 times (AOR 4. 5, 95% CI: 1.1–18) more likely to have HBV infection than those who did not share their tooth brush. Other variables like history of abortion, ear piercing, nose piercing, and surgery had no significant association with HBV infection.

The World Health Organization has an ambitious plan to eliminate hepatitis viruses as a public health treat in 2030 [1]. Despite this, screening for HBV and HCV among apparently healthy pregnant women in Ethiopia is poor. Globally, more than 95% of hepatitis infected persons do not aware of their infection[1]. This number is substantial in developing countries where there is no routine screening for hepatitis. To eliminate hepatitis virus’s early detection, prevention of transmission and initiation of treatment is very crucial. Screening of apparently healthy pregnant women is key for the prevention of vertical transmission. Thus, this study has a paramount significance and calls for Amhara regional health officials and even to the country level to work on screening for HBV and HCV among pregnant women routinely in public health institutions and integrate into the PMTCT of HIV.

This is the first large-scale study that examined seroprevalence of HBsAg and anti-HCV antibody and associated factors among pregnant women in the Amhara region, Ethiopia. Our study revealed that 4.6% of pregnant women were infected with HBV. This finding is in line with the WHO intermediate classification of HBsAg prevalence, which is 2–7% [23]. Moreover, it is similar to other studies conducted previously in Bahir Dar 4.4%, Arba Minch 4.3%, Dessie 4.9%, and Egypt 5%, South Africa 4.5% [17, 24–27].

However, our findings are higher than those of studies done in the east Wolega zone 2.4%, Dawuro 3.5%, Addis Ababa 3%, Eritrea 3.2%, Germany 0.48%, Turkey 2.1%, and China 3.2% [28–34]. On the other hand, our findings are lower than those studies done in Dire Dewa 8.4%, Mekele 8%, Hawasa 7.8%, Yirgalem 7.2%, Gambella 7.9%, Harar 6.9%, Tigray 5.5%, Gambia 9.2%, Tazania 8.03%, Cameroon 6.6%, and Ghana 12.9% [16, 18, 35–43]. There is a variation among the prevalence’s of our study with the studies that were conducted around the globe. The differences might be due to differences in cultural practices, socioeconomic status, availability of medical services, vaccination status, and diagnostic test kit employed in the study.

The overall seroprevalence of anti-HCV antibody in the present study was found to be 1.6%. This finding is in agreement with the WHO intermediate criteria. According to WHO classification criteria graded as low, the HCV seroprevalence is < 1.5%, intermediate 1.5%-3.5%, and high > 3.5% [12]. This finding is comparable to a study conducted in southern Ethiopia 1.8% [44]. However, our result is higher than Tazania 0.3% [45] and Bahir Dar 0.6% [17]. In contrast, our finding is lower than studies done in East Wolega 8.1% and Egypt 6.1% [29, 46]. On the other hand, anti-HCV antibody seroprevalence was 8.9% in Debre Markos Hospital, which is unexpectedly highest. This finding calls further study in Debre Markos Hospital and around the area in the community to further explore risk factors for a high prevalence of HCV. Variations in seroprevalence in Ethiopia and elsewhere might be due to the diagnostic test kit employed, awareness of transmission of HCV, exposure to risk factors, and geographic location.

Studies have documented that there was co-infection of HBV and HCV among pregnant women, similar to our findings [37, 44]. In contrast to this finding, no co-infection of these viruses was detected in studies conducted in Ethiopia and elsewhere [17, 29, 45].

Of the sociodemographic characteristics, younger age, and unmarried pregnant women had a significant association with HBsAg prevalence (Table 3). This might be due to, at younger age sexual activity being higher compared than in age groups of 25 years and above. This finding agrees with other studies in Gambella, Addis Ababa in Ethiopia [4, 41]. In contrast, studies have reported a high prevalence of HBsAg in pregnant women with increasing age [4]. Moreover, the probability of getting HBV infection in unmarried women is higher than that in their counterparts. This in line with a study conducted in Ethiopia [18]. This might be due to in Ethiopia, unmarried pregnant women have the possibility of having more than one sexual partner to get job opportunities and to get money as compared to married pregnant women. To the contrary of this study, a high positive HBsAg more likely in married pregnant women than in single and divorced [36]. The observed differences could be due to the sample size of the study participant, geographic location difference, and culture of population living in.

Among the various risk factors assessed, having multiple sexual partners, HIV, sharing toothbrush, family history of HBV, history of tattooing, and previous history of blood transfusion were significantly associated with HBV infection (Table 3). Pregnant women with multiple sexual partners had 3 times (AOR3.2; 95% CI: 1.3–7.6%) more likely to develop HBV infection than their counterparts. This finding is similar to other studies [17, 24, 40–43]. Blood transfusion has been recognized as a major risk factor for transmission of HBV throughout the world. Pregnant women with a history of blood transfusion previously had almost 8 times (AOR 7.6, 95% CI 2.9–16.9) more likely to develop HBV infection than compared to pregnant women with no history of blood transfusion. This is similar to previous studies done elsewhere [17, 18, 34]. However, inconsistent with other studies [40–42]. In fact, in Ethiopia, blood and blood products have been screened for HBV, HCV, HIV, syphilis, and malaria since 2001 [6]. However, in our country, screening for HBV from blood and blood products using ELISA may not detect the virus in the window period and occult hepatitis, which needs molecular techniques for accurate detection of the virus. Evidence showed that a study done in Taiwan, among 10,727 seronegative blood donations, 12 HBV DNA was detected [47]. Therefore, it is advisable to evaluate HBsAg ELISA against molecular techniques.

Participants with a history of tattooing on their body parts (AOR 2, 95%CI:1.1–3.7) had more chance of being infected with HBV than pregnant women who did not have tattooing on their body parts. This is in line with studies done in Addis Ababa and Arba Minch, Ethiopia [4, 24]. However, this is contrary to other studies [39, 40]. The observed differences might be due to variations in sample size of study participants, safety precaution, and culture.

Moreover, study participants with a family history of HBV infection (AOR 3.5,95% CI:1.7–3.7) had more likely to be infected with HBV than compared to their counterparts. This is similar to the study done in Tigray, Ethiopia [43]. In contrast, this is inconsistent with other studies [24, 40]. The variations might be due to differences, sample size, and awareness of study participants regarding transmission methods. In Ethiopia, there is a belief that hepatitis disease is not transmitted from person to person; rather, it is Bat’s disease or ``Yewef Beshita`` in Amharic language [6].

In relation to HIV, pregnant women who had HIV in their blood two times (AOR 2.5, 95% CI,1-5.9) more likely develop HBV as compared to HIV-negative pregnant women. HIV is significantly associated with HBV infection. This finding is similar to studies done in Ethiopia and other African countries [4, 18, 36]. This is explained by HBV and HIV shared routes of transmission. HIV and HBV not only share routes of transmission but also, they have reverse transcriptase in a common, target for reverse transcriptase inhibitors. Viral hepatitis is a growing cause of mortality among people living with HIV. In sub-Saharan Africa (SSA), an estimated 10% of HIV-infected individuals are co-infected with HBV [48]. The co-infection rate of HBV and HIV in Ethiopia is a common phenomenon, which leads to increased morbidity and mortality than mono infection of both viruses. HIV negatively impacts the HBV life cycle by increasing persistent HBV infection, having a higher HBV viral load, lower rates of HBeAg loss, increased cirrhosis ,and increased risk of hepatocellular carcinoma [49]. Moreover, HIV-HBV co-infected pregnant women are twice as likely to test positive for HBeAg, three times more likely to have detectable HBV DNA, and have higher HBV DNA serum concentrations as compared to those who are HBV mono-infected, thereby greatly increasing the risk of MTCT [50].

Moreover, in Ethiopia, a systematic review and meta-analysis revealed that the HIV prevalence among pregnant women was 5.7%. This review also reported that HIV in the Amhara region, among pregnant women, was 9.5% [19]. Despite the recommendation of many international and national HIV guidelines to test HBV among HIV-positive pregnant women before ART initiation, screening uptake is generally poor in Ethiopia. Therefore, screening for HBV among HIV-positive pregnant women is very essential for the mother and the child for prevention of vertical transmission.

Interestingly, pregnant women who had shared their tooth brushes almost 4.5 times (AOR 4.5, 95% CI 1.1–18) more likely at risk of getting HBV infection compared to their counterparts. This might be due to during tooth brushing there may be gum bleeding and may transmit HBV from an infected person to a susceptible person. HBV is highly contagious and a hundred times more infectious than HIV and waits more time outside the blood than HIV. It is a tricky enveloped virus transmitted even on surfaces and acts as a non-enveloped virus during transmission [6].

In this study, only 20 (1.8%) pregnant women were vaccinated for HBV prevention. This figure is less than the vaccination status of pregnant women in Gambia 41.3% [35]. This is due to HBV vaccination in Ethiopia is started lately in 2007 [51]. This is an indication that more efforts were required to vaccinate adults born before 2007 in Ethiopia. Since 1991, the WHO recommended universal HBV vaccination of children and high-risk groups to reduce new infections and prevent progression to cirrhosis and hepatocellular carcinoma [52]. Universal vaccination is exemplary in Taiwan, together with catch-up vaccination and maternal screening, which decreases the prevalence of HBsAg from 9.8% in 1984 to 0.3% in 2009 in children younger than 15 years [53]. Likewise, in 2009, the WHO recommended a birth dose vaccine for infants within 24 h of birth [10]. However, studies have shown that birth dose vaccination may not prevent those infants born from HBeAg-positive pregnant women and have a high viral load of HBV DNA [8, 27]. Combined treatment with HBV immunoglobulin and birth dose vaccine highly recommended and prevents 85–95% vertical transmission [52]. However, hepatitis B hyperimmune globulin is expensive and not readily available at most health institutions in Ethiopia. The authors recommended that giving birth dose vaccines within 24 h of the birth of infants is essential to prevent MTCT and integrate into HIV PMTCT in Ethiopia. Yet it is not a routine practice of provision of the birth dose vaccines in Ethiopian health institutions.

Therefore, the findings of this study will provide insights for policy makers to implement routine practice of screening of HBV and HCV in pregnant women and immunization of infants for HBV and integration into PMTCT of HIV. However, this study has some limitations. The molecular DNA test is better for diagnosing occult hepatitis has not done in this study, which may underestimate the prevalence of HBV among pregnant women.

HBV and HCV infections are intermediate among pregnant women in the Amhara region. This finding suggests that 4.6% and 1.6 of infants born to HBV and HCV-infected pregnant women are more likely at risk of contracting infection vertically from their mothers in the Amhara region. We advocate that the integration of HBV and HCV-infected pregnant women into PMTCT is important in Ethiopia. Factors such as being HIV-positive, history of multiple sexual partners, blood transfusion, tattooing, family history of hepatitis, and sharing of tooth brushes were significant predictors of HBV infection. Therefore, providing health education on HBV and HCV transmission, risk behaviors, vaccination, screening of all pregnant women, and provision of a birth dose vaccine for newly born infants within 24 hours is recommended to prevent MTCT. Moreover, further longitudinal MTCT and molecular studies will be recommended on HBV and HCV in Ethiopia.

Acknowledgement

We are very grateful for the University of Gondar for funding this research. We also acknowledge data collectors for their great support. Finally, we would like to extend our gratitude to the study participants.

Funding

University of Gondar funding this study.

Availability of data and materials

Data are available upon reasonable request from the corresponding author.

Authors’ contribution

MD, conceptions of research proposal, data collection, laboratory work, conducted data analysis and interpreted the results and drafted the manuscript. MT, FM and MA were assisted in interpreting the results, and reviewing the initial and final drafts of the manuscript. YM, SE, MG GY, and LA were involved in data collection, data analysis, reviewing the initial and final drafts of manuscripts. All authors have read and approved the final manuscript.

Competing interest

We declare that we have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Ethical approval for the study was obtained from the Institutional Review Board (IRB) of the University of Gondar. Written informed consent was obtained from each pregnant woman before enrolling in this study. Study participants anonymity was maintained throughout the study. Study participants were identified only by their code numbers. Confidentiality of information was maintained by locking the information using a computer password. Those patients positive for HBsAg and anti-HCV antibody were referred for better management

Competing interest

We declare that we have no competing interests.

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Table1. Sociodemographic characteristics of pregnant women attending in the Amhara region referral hospitals from May1,2018 to September 30,2019.

Characteristics	Category	Number (%)
Age in year	17-25	464(39.6)
Age in year	26-45	657(60.4)
Marital status	Single	17(1.5)
	Married	1094(97.6)
	Windowed	1(0.1)
	Divorced	9(0.8)
Residence	Urban	895(79.8)
Residence	Rural	226(20.2)
Religion	Orthodox	1064(94.9)
	Muslim	49(4.4)
	Protestant	7(0.6)
	Catholic	1(0.1)
Income	<1000	159(14.2)
	1000-4000	799(71.3)
	>4000	163(14.5)
Educational status	No education	254(22.7)
	Read and write	61(54)
	Primary	173(15.4)
	High school	302(26.9)
	College& above	331(29.5)
Occupation	Housewife	732(65.3)
	Employed	191(17)
	Daily laborers	92(8.2)
	Student	33(2.9)
	Others	73(6.5)
Gravida	Primigravida	409 (36.5)
Gravida	multigravida	712(63.5)
Parity	Nullipara	545(48.6)
Parity	Multipara	576(51.4)
Vaccination history	Yes	20(1.8)
Vaccination history	No	1101(98.2)
Study site	UOGCSH	593(52.9)
	FHCSH	447(39.9)
	DMH	81(7.2)

Table 2. Bivariate analysis of sociodemographic characteristics in relation with HBV infection among pregnant women in the Amhara region hospitals from May1,2018 to September 30,2019.

Characteristics	Category	Number (%)	HBV status		Crude odds ratio (COR)(95%CI)
Characteristics	Category	Number (%)	Pos	Neg	Crude odds ratio (COR)(95%CI)
Religion	Orthodox	987(95.0)	44(4.5)	943(95.5)	1
Religion	Others	52(5)	4 (7.7)	48(92.3)	1.98(.67-5.8)
Residence	Urban	895(79.8)	38(4.2)	857(95.8)	1
Residence	Rural	226(20.2)	14(6.2)	212(93.8	1.5(.79-2.8)
Marital status	Married	1017(97.8)	43(4.2)	974(95.8)	1
Marital status	Unmarried	23(2.2)	5(21.7)	18(78.3)	3.9(1.5-9.6)*
Age	17-25	464(39.6)	30(6.5)	434(93.5)	2(1.1-3.5)
Age	26-45	657(60.4.)	22(3.3)	635(96.7)	1
Income	<1000	159(14.2)	15(9.4)	144(90.6)	.37(0.2-0.7.0)
	1000-4000	799(71.3)	30(3.8)	769(96.2)	1
	>4000	163(14.5)	7(4.3)	156(95.7)
Education	No education	254(22.7)	14(5.5)	240(94.5)	1.77(.68-4.5)
	Primary + RW	234(20.9)	11(4.7)	223(95.3)	1.64(.58-4.6)
	High school & above	633(56.5.4)	27(4.3)	606(95.7)	1.07(.39-2.9)
Occupation	Housewife	522(62.4)	23(4.4)	499(95.8)	1.49(.51-4.4)
	Employed	140(16.8)	5(3.6)	135(96.4)	1
	Others	174 (20.8)	9(5.2)	165(94.8)	1.9(.56-6.15)
Gravida	Primigravida	409(36.5)	24(5.9)	385(94.1)	1.2(.62-2.4)
Gravida	multigravida	712(63.5)	28(3.9)	684(961)	1
Parity	Nullipara	545(48.6)	33(6.1)	512(93.9)	1.85(.92-3.7)
Parity	Multipara	576(51.4)	19(3.5)	557(96.7)	1

Others- muslim, protestant and catholic, RW=Write and Read ** =P<0.001, *=P<0.5

Table 3. Bivariate and multivariate analysis of factors associated with HBV infection among pregnant women in the Amhara region hospitals from May1,2018 to September 30,2019.

Variable	Category	Number	HBV status		COR	Adjusted Odds ratio AOR (95%CI)
Variable	Category	Number	Pos Neg		COR	Adjusted Odds ratio AOR (95%CI)
Age	17-25	464(39.6)	30(6.5)	434(93.5)	2(1.1-3.5)	2.5(1.3-4.5)*
	26-45	657(60.4)	22(3.3)	635(96.7)	1
Marital status	Married	1017(97.8)	43(4.2)	974(95.8)	1
	Unmarried	23(2.2)	5(21.7)	18(78.3)	4.5(1.9-10.6)
Tattoo	Yes	351(31.3)	23(6.6)	328(93.4)	1.8(1.0-3.1)* 1	2(1-3.8)*
Tattoo	No	770(68.7)	29(3.8)	741(96.2)	1.8(1.0-3.1)* 1	2(1-3.8)*
Dental extraction	Yes	156(13.9)	6(3.8)	150(96.2)	1.3(.53-3) 1
Dental extraction	No	965(86.1)	46(4.8)	919(95.2)	1.3(.53-3) 1
Blood transfusion	Yes	34(3)	7(20.6)	27(79.4)	6(2.5-15)*** 1	7.6(2.9-16.9)**
Blood transfusion	No	1087(97)	45(4.1)	1042(95.9.)	6(2.5-15)*** 1	7.6(2.9-16.9)**
Surgery	Yes	78(8.3)	3(3.8)	75(96.2)	.8(.24-2.7) 1
Surgery	No	1043(91.7)	49(4.7)	994(95.3)	.8(.24-2.7) 1
Sexual trans. Dis.	Yes	138(12.3)	9(6.5)	129(93.5)	.65(.31-1.3) 1
Sexual trans. Dis.	No	983(87.7)	43(4.4)	940(95.6)	.65(.31-1.3) 1
HIV	Yes	113(10.1)	10(8.8)	103(91.2)	2.2(1.09-4.6) 1	2.5(1-5.9)^*
HIV	No	1008(89.9)	42(4.2)	966(95.8)	2.2(1.09-4.6) 1	2.5(1-5.9)^*
Abortion	Yes	203(16)	9(4.4)	194(95.6)	1.1(0.5-2.2) 1
Abortion	No	918(81.9)	43(4.7)	875(95.3)	1.1(0.5-2.2) 1
Unprotected sex	Yes	84(7.5)	6(7.1)	78(92.9)	1.6(.68-4.0)
Unprotected sex	No	1037(92.5)	46(4.4)	991(95.6)	1
Multiple sexual partner	Yes	61(5.4)	7(11.5)	54(88.5%)	3.9 (1.8-8.4) 1	3.2(1.3-7.6) 1
Multiple sexual partner	No	1060(94.6)	45(4.2)	1015(95.8)	3.9 (1.8-8.4) 1	3.2(1.3-7.6) 1
Ear pricing	Yes	248(22.1)	18(7.3)	230(92.7)	1.9(1-3.5)* 1
Ear pricing	No	873(77.9)	34(3.9)	839(96.1)	1.9(1-3.5)* 1
Nose piercing	Yes	50(4.5%)	6(12%)	44(88%)	3(1.2-7.5)* 1	0.145
Nose piercing	No	1071(95.5)	46(4.3%)	1025(95.7%)	3(1.2-7.5)* 1	0.145
Diabetes	Yes	25(2.2)	3(12)	22(88)	2.9(.84-10 1	2.8(0.7-11)
Diabetes	No	1096(98.2)	49(4.5)	1047(95.5)	2.9(.84-10 1	2.8(0.7-11)
Hospitalization .	Yes	144(12.8)	6(4.2)	138(95.8)	0.88(.36-2) 1
Hospitalization .	No	977(87.2)	46(4.7)	931(95.3)	0.88(.36-2) 1
Family history of HBV	Yes	99(8.8)	11(11.1)	88(88.9)	3(1.5-6)	3.5(1.7-7.6)^**
Family history of HBV	No	981(91.2)	41(4)	981(96)	1
Sharing tooth brush	Yes	18(1.6)	3(16.7)	15(83.3)	4.3(1.2-15)	4.5(1.1-18)*
Sharing tooth brush	No	1103(98.4)	49(4.4)	1054(95.6)	1
Sharing sharp material	Yes	62(4.5)	3(4.8)	59(95.2)	1.0(.28-4.3)
Sharing sharp material	No	1059(94.5)	49(4.6)	1010 (95.4)	1

** =p<0.001, *=p<0.5

Hepatitis B and C viruses’ infection and associated factors among pregnant women in the Amhara region, Ethiopia: implications for prevention of vertical transmission.

Status:

Version 1

Abstract

Background

Methods

Results

Conclusions

Background

Materials And Methods

Study area, design, and period

Study population, sample size, and sampling technique

Data collection

Sample collection, transportation, and processing

Data quality

Data Analysis

Results

Sociodemographic characteristics

Seroprevalence of HBV and HCV

Factors associated with HBV infection in pregnant women

Discussion

Conclusion and recommendations

Declarations

references

tables

Status:

Version 1