Skip to main content

ORIGINAL RESEARCH article

Front. Glob. Womens Health, 27 April 2023
Sec. Infectious Diseases in Women
This article is part of the Research Topic Insights in Infectious Diseases in Women: 2022/2023 View all 5 articles

Prevalence of hepatitis B infection and its associated factors among pregnant mothers attending antenatal care at public hospitals at Hararghe, Eastern Ethiopia

\r\nAbbas UmerAbbas Umer1Zelalem TeklemariamZelalem Teklemariam2Firayad Ayele
Firayad Ayele2*Melkamu Merid Mengesha,&#x;\r\nMelkamu Merid Mengesha3,†
  • 1West Hararghe Zone Health Office, Chiro, Ethiopia
  • 2School of Medical Laboratory Sciences, Haramaya University College of Health and Medical Sciences, Harar, Ethiopia
  • 3School of Public Health, College of Medicine and Health Sciences, Arba Minch University, Arba Minch, Ethiopia

Background: Hepatitis B infection is one of the world's most serious public health problems, causing significant morbidity and mortality. More than 2 billion individuals around the world have been infected with the hepatitis B virus (HBV), and approximately 400 million people are chronically infected with the virus, with more than a million dying each year from hepatitis B virus-related liver disease. A newborn infant whose mother is positive for both HBsAg and HBeAg has a 90% chance of developing chronic infection by the age of 6. Its infectivity is a 100 times that of the human immunodeficiency virus, but it receives little attention in public health. Therefore, this study was conducted to assess the prevalence of hepatitis B infection and its associated factors among pregnant mothers attending antenatal care at public hospitals in west Hararghe, eastern Ethiopia 2020.

Method: This institution-based cross-sectional study was conducted on 300 pregnant mothers selected by systematic random sampling from September to December 2020. Data were collected by face-to-face interview using a pretested structured questionnaire. A blood sample was collected and tested for hepatitis B surface antigen using the enzyme-linked immunosorbent assay test method. Data were entered into EpiData version 3.1 and exported to Statistical Package for the Social Science version 22 for analysis. Bivariate and multivariable logistic regressions were used to assess the association between outcome and predictor variables. P-value <0.05 was considered to be statistically significant.

Results: The overall seroprevalence of hepatitis B virus infection was 8% [95% confidence interval (CI): 5.3–11.0] among pregnant mothers. History of tonsillectomy [adjusted odd ratio (AOR) = 5.7; 95% CI: 1.3–23.9], tattoo (AOR = 4.3; 95% CI: 1.1, 17.0), having multiple sexual partners (AOR = 10.8; 95% CI: 2.5, 45.9), and history of contact with jaundiced patients (AOR = 5.6; 95% CI: 1.2, 25.7) were factors associated with the seroprevalence of hepatitis B virus infection among pregnant mothers.

Conclusion: The hepatitis B virus was highly prevalent. A history of tonsillectomy, tattooing, having multiple partners, and contact with jaundiced patients were factors associated with hepatitis B virus infection. To reduce HBV transmissions, the government should increase HBV vaccination coverage. All newborns should receive the hepatitis B vaccine as soon as possible after birth. It is also recommended that all pregnant women have HBsAg testing and antiviral prophylaxis to reduce the risk of transmission from mother to child. Hospitals, districts, regional health bureaus, and medical professionals should also educate pregnant women about hepatitis B virus transmission and prevention, both in the hospital and in the community, with a focus on modifiable risk factors.

Introduction

Hepatitis B virus (HBV) is one among the prominent public health problems globally (1). The disease is caused by the hepatotropic deoxyribonucleic acid (DNA) virus and happens over the immune-mediated killing of diseased liver chambers (2, 3). Hepatitis B virus is a potentially life-threatening pathological virus of the liver that leads to critical or prolonged hepatitis (3). In childhood, less than 5% of infections result in chronic hepatitis (4).

Hepatitis B virus can cause coagulation defects, postpartum hemorrhage, organ failure, and high maternal mortality, as well as poor newborn outcomes such as stillbirth, neonatal deaths, severe, and prolonged liver disease. Early intervention and prevention of these illnesses is now a priority, with universal screening in antenatal care (ANC) and as part of reproductive health programs (3). It has an average incubation period of 75 days and can be detected in the blood within 30–60 days (3). In light of this, the virus is more contagious and powerful than the human immunodeficiency virus (HIV) virus (5, 6).

The World Health Organization (WHO) estimates that approximately 296 million people had chronic hepatitis B infection in 2019, with 1.5 million new infections occurring each year. In 2015, 2.7 million people were HIV coinfected (7) with a total of 68% of infected people in Africa and Western Pacific Asia (8). Furthermore, 5%–15% of populations in developing and poor-income countries are chronic carriers of hepatitis B infection (9). Furthermore, the World Health Organization reported that hepatitis is responsible for 1.34 million deaths, which is equivalent to deaths due to tuberculosis but higher than deaths due to HIV in 2015 (3). In addition, 1.8 million children less than 5 years are living with hepatitis B virus infection (10). Due to the high price of the vaccine, private access is less likely (11).

As a part of the sub-Saharan region, Ethiopia ranked medium to high endemicity for HBV infection (12). In Ethiopia, even if there is a lack of data representing the spread of HBV infection nationally, according to the findings of some individual studies, the country is regarded as having a high burden of the disease (12). Systematic reviews and meta-analyses revealed that the prevalence of HBV in the general population ranged from 6% to 7.4% (13) whereas 5%–7% of pregnant mothers were a major source of disease for newborns (14).

Despite the fact that the disease is endemic in all populations and/or pregnant mothers in the country, there has been no research done in west Hararghe, eastern Ethiopia, where the prevalence and factors associated with HBV infection among pregnant mothers are unknown. Furthermore, evidence-based information on the prevalence and risk factors for HBV infection in pregnant women enables effective HBV prevention and management. Therefore, the present study is aimed to estimate the seroprevalence and to identify factors associated with hepatitis B virus infection among pregnant mothers attending public hospitals in west Hararghe, Ethiopia.

Materials and methods

Study area and study period

The study was conducted in the west Hararghe zone of the Oromia region from September to December 2020. West Hararghe is one of the 21 administrative zones in the Oromia regional state. Chiro town, which is 317 km to the east of Addis Ababa, serves as the zone's capital. Based on information from the 2007 Ethiopian CSA census, it is estimated that there are 2,667,000 people living in the west Hararghe zone. There are 17 woredas and 496 kebeles that make up the administrative division of the zone, of which 39 are urban and 457 are rural. In the zone, there are currently 4 public hospitals, 85 health centers, and 465 health posts. During the months of September to December 2020, the study was carried out at the public hospitals in Gelemso and Chiro (Source: 2019–2020 document profile from the West Hararghe Zonal Health Office).

Study design and population

A cross-sectional study design was conducted among pregnant mothers attending ANC clinics at public hospitals in west Hararghe. All confirmed pregnant mothers who were chosen through a systematic random sampling method and gave their written consent to take part in the study during the study period were included. Those who were mentally unconscious or who made a second ANC visit during the data collection period were excluded.

Sample size, sampling technique, and procedure

The sample size of the study was determined using a single population proportion formula by considering the prevalence of HBV infection in pregnant mothers at the Deder hospital in eastern Ethiopia (15), with a prevalence of 6.9%, a 95% confidence level (CI), and a margin of allowable error of 3%. To minimize the errors arising from the likelihood of noncompliance, 10% of the sample size was added. The final sample size was 302. Systematic random sampling was used until the required sample was reached.

A total of 1,358 pregnant mothers were expected to attend ANC clinics in two hospitals in the west Hararghe zone (460 pregnant mothers at the Chiro General Hospital and 898 pregnant mothers at the Gelemso General Hospital) for routine ANC from a previous registered annual number of clients served. A total of 302 study participants were selected proportionally from each hospital. A systematic random sampling technique was applied to select study participants. We took 3 months' average sampled population from the registration books, which were done in ANC clinic, where 460 (source population) pregnant mothers were divided for a sample size of 102 for the Chiro zonal hospital and 898 (source population) pregnant mothers were divided for a sample size of 200 for the Gelemso general hospital to get sample interval (kth value), which became 4 for both sites. Then, the first pregnant mother was randomly selected by the lottery method. Therefore, every 4th mother attending the clinics was enrolled in the study until the calculated sample size was achieved within 3 months of data collection. A total of 302 study participants were included in the study during the study period (Figure 1). Participants' identification number was used to avoid repetition.

FIGURE 1
www.frontiersin.org

Figure 1. Schematic presentation of the sampling procedure and sampling technique for including in the study pregnant mothers attending routine antenatal clinics in west Hararghe public hospitals, 2020.

Data collection methods

A pretested and structured questionnaire adapted from the WHO checklist for the assessment of hepatitis B infection in antenatal patients (16) was used to collect information on sociodemographic information, circumcision, history of blood transfusion, risky sexual behavior, history of hospital admission and surgery, history of abortion, contact with HBV-infected individuals, and other factors. Data were collected by three trained midwives through a face-to-face interview. Data collectors introduced themselves and informed the participants of the purpose of the study. After the participants agreed to participate, they were asked to give written consent and were assigned a study identification number; then, the interview was held in a private room in the hospitals using a structured questionnaire.

Blood sample collection and laboratory examination

At the time of arrival to the laboratory, all study participants' arms was cleaned with 70% denatured alcohol, and then approximately 3 ml of venous blood was collected using blood collection tubes following the standard operating procedure (SOP) by a trained laboratory technologist at the hospital laboratory. Blood collected by venipuncture was allowed to clot naturally. Serum was separated from whole blood cells and transferred to CryoTube and stored at −20°C. The serum sample was then transported to the Chiro Blood Bank Center Laboratory using a triple packing system with a vaccine carrier, where it was tested for HBsAg using an antibody sandwich enzyme-linked immunosorbent assay (ELISA) test kit (Human type, Germany) in accordance with the manufacturer's instructions. The test has a 99.9% specificity and 100% sensitivity. With monoclonal antibodies tailored to HBsAg, polystyrene microwell strips are used in the sandwich ELISA technique. A second antibody that was conjugated with horseradish peroxidase (HRP) and formed in the event that HBsAg was present in the sample, which is captured on the solid phase, was added to the microwells along with a patient sample. Since the color's intensity correlated with the antigen content of the sample, it was measured. Using a second AiDTM HBsAg ELISA, all reactive and some nonreactive results were confirmed.

Operational definitions

The following operational definitions were used in this study:

Prevalence: Percentage of pregnant mothers that were affected with HBsAg during this study period at this study place.

Abortion: Spontaneous or deliberate ending of pregnancy before the fetus could be expected to survive.

Female circumcision: Comprises all procedures that involve partial or total removal of the external female genitalia traditionally.

Piercing: This is a type of body beautification where a sharp material punctures a hole in the body ears or nose parts where jewelry had been inserted.

Tattoo: Is any form of body art that is created when ink is inserted, using a needle or other sharp materials into the dermis layer of the skin.

Tonsillectomy: Traditional tonsillectomy: Complete or partial removal of tonsils traditionally.

Chronic HBV infection: Defined by the continued presence of HBsAg in the blood for longer than 6 months.

Knowledge: In this case, participants who scored 50% and above from all asked questions were labeled as have good knowledge and those who scored less than 50% were labeled as having poor knowledge on HBV infection and transmission (17).

Quality assurance

The questionnaires were prepared in English and translated into Afaan Oromo language by an independent translator that could be understood by the study participants. Finally, the questionnaires were translated back to English to ensure their consistency with the previous initial version. Data collectors along with supervisors were trained on data collection procedures. The questionnaires were pretested on 15 pregnant mothers attending ANC clinics in the Chiro hospital to check their appropriateness and understandability by study participants before the actual data collection process to correct questionnaires. Supervisors and principal investigators checked the collected data for consistency and completeness. Codes were given to completed questionnaires. Oriented laboratory professionals collected blood specimens. Standardized procedures were followed during blood sample collection, storage, transportation, and analytical process. The ELISA test was performed by experienced laboratory personnel who were trained by Hema diagnosis laboratory with a Huma reader and Washer (Human, Germany). Quality control of serological tests, known positive and negative controls, was run in parallel with test samples. All laboratory procedures were carried out following SOP according to the manual instructions. The results were recorded with the patient's identification number, to avoid errors in the results of the test, and repeatedly checked before reporting.

Data processing and analysis

Data were checked for completeness and consistency of the collected information, coded and entered into Epi-data version 3.1, and exported to Statistical Package for the Social Science (SPSS) version 22.0 software package for analysis. Descriptive statistical analysis was done using frequency tables, and proportions were used to summarize the data. Bivariate logistic regression analysis was carried out using cross-tabulation to see the association between HBsAg serostatus and independent variables while controlling for colinearity. Variables having a P-value less than 0.25 were included in the multiple logistic regression analysis at a 95% confidence interval. Then, multivariate logistic regression was done to control for possible confounders and identify the true effect of the selected predictor variables. The model adequacy was checked using the Hosmer–Lemeshow test to show the goodness of fitness. Finally, the strength of association between the outcome and predictor variables was assessed using an adjusted odd ratio (AOR) with a 95% confidence interval, and the significance of the association was declared at a P-value of less than 0.05.

Ethical consideration

Ethical clearance was obtained from the Institutional Health Research Ethics Review Committee (IHRERC) of the Haramaya University College of Health and Medical Science. The ethical letter was submitted to the West Hararghe Zonal Health office and official permission was sought from the West Hararghe Zonal Health Office and Gelemso and Chiro public hospitals’ administration; then, support letter was obtained from hospitals’ administration. Written informed voluntary consent was obtained after informing the purpose and importance of the study to each participant. To ensure the confidentiality of the participant's information, a code was used instead of the name of the participant. Participants were interviewed alone to maintain privacy. Individual test results were communicated with the attending physician for further care as national protocol and health education were given to clients on preventive measures to be taken as well as to protect others.

Results

Sociodemographic characteristics of the study participants

A total of 300 pregnant mothers were included in this study with an overall response rate of 99%. The mean age of the study participants was 28.6 (SD ± 6.88) years and it ranged from 18 to 47 years. More than half of the participants (65.3%) were urban residents, and 79.3% were pregnant between 6 and 9 months. Nearly all of the participants, 298 (99.3%), were married and out of which 28 (9.3%) were polygamous. A total of 86 (28.7%) and 148 (49.3%) participants were not able to read and write and were merchants, respectively (Table 1).

TABLE 1
www.frontiersin.org

Table 1. Sociodemographic characteristics of pregnant mothers attending ANC clinics in public hospitals in west Hararghe, eastern Ethiopia, from September to December 2020.

Pregnancy-related, cultural, and clinical characteristics

The majority of study participants (81.7%) had more than three children, had a history of body piercing (87%), and had previously undergone an abortion at a health facility [53 (74%)] and at home [19 (26%)], of which 5 (31%) at home and 11 (69%) in a health facility were HBsAg positive. More than half of the study participants had a history of female genital mutilation (FGM) (60.3%). Of the participants, 65% did not practice home delivery, and 56% had a history of health facility admission. A total of A total of 111 (37%), 50 (17%), 64 (21%), 68 (22.7%), and 125 (41.7%) had an experience of a tattoo, blood transfusion, surgical procedures, dental procedures, and tonsillectomy, respectively. About 49 (16.7%) study participants had multiple sexual partners (Table 2).

TABLE 2
www.frontiersin.org

Table 2. Pregnancy, cultural and clinical related characteristics of pregnant mothers attending ANC clinics in public hospitals in west Hararghe, Eastern Ethiopia, from September to December 2020.

Knowledge about HBV

Out of the 300 study participants, 239 (79.7%) had poor knowledge. Of the participants, 35% and 38% had heard of a disease termed hepatitis B as a viral disease and affected liver function, respectively. Only 25% knew nausea, vomiting, and loss of appetite are common symptoms of hepatitis B. About 26%, 16%, and 33% of the study participants said there is no symptom of hepatitis B virus infection, HBV transmission can occur from mother to child during pregnancy, and HBV has a vaccine, respectively (Table 3).

TABLE 3
www.frontiersin.org

Table 3. Knowledge about HBV among pregnant mothers attending routine ANC clinics in public hospitals in west Hararghe, eastern Ethiopia, from September to December 2020.

Seroprevalence of hepatitis B virus infection

The overall prevalence of HBV among pregnant mothers was 8% (24/300) (95% CI: 5.3–11.0). Among those HBV-seropositive pregnant mothers, 15 (62.5%) and 9 (37.5%) were from the Gelemso and Chiro Hospitals, respectively. The proportion of HBV was 9% among the 31–49 year age groups. Additionally, as one's level of education increases, the prevalence of HBV decreases.

Factors associated with hepatitis B virus infection

In bivariate analysis, age, residence, educational status, history of home delivery, FGM, parity, history of abortion, tattooing, history of admission to the health facility, history of blood transfusion, history of surgical procedure, history of dental extraction, history of tonsillectomy, history of cesarean section, history of sexually transmitted diseases, history of multiple sexual partners, history of jaundice, history of contact with liver disease patient, and knowledge about HBV were candidate variables for multivariate analysis (Table 4).

TABLE 4
www.frontiersin.org

Table 4. Bivariate analysis of factors associated with hepatitis B virus infection among pregnant mothers attending ANC clinics in public hospitals in west Hararghe, eastern Ethiopia, from September to December 2020.

In multivariable analysis, those pregnant mothers who had a tattoo, history of tonsillectomy, history of multiple sexual partners, and previous contact with liver disease patients were identified to have factors associated with HBV infection.

Pregnant mothers who had a tattoo had 4.3 times the odds of being HBsAg positive compared to those who did not have tattoos (adjusted odds ratio = 4.3; 95% CI: 1.1–17.0). Similarly, pregnant mothers who had a history of tonsillectomy had 5.7 times the odds of being HBsAg positive compared those who did not have a history of tonsillectomy (adjusted odds ratio = 5.7, 95% CI: 1.3–23.9). Mothers who had a history of contact with liver disease patients had 5.6 times the odds of being HBsAg positive compared to their counterparts (adjusted odds ratio = 5.6; 95% CI: 1.2–25.7). Pregnant mothers who had a history of multiple sexual partners had 10 times the odds of being HBsAg positive compared to those who did not have history of multiple sexual partners (adjusted odds ratio = 10.8; 95% CI: 2.5–45.9) (Table 5).

TABLE 5
www.frontiersin.org

Table 5. Multivariable logistic regression analysis for factors associated with hepatitis B virus infection among pregnant mothers attending ANC clinics in public hospitals in west Hararghe, eastern Ethiopia, from September to December 2020.

Discussion

The overall prevalence of hepatitis B virus among pregnant mothers attending routine ANC clinics was 8% (95% CI: 5.3–11.0); this finding was classified as high according to the WHO classification. History of a tattoo, history of tonsillectomy, experiencing multiple sexual partners, and history of contact with HBV-infected patients were factors found to be associated with hepatitis B virus infection among pregnant mothers.

The current study's findings were in agreement with those of a study carried out in various countries (Table 6).

TABLE 6
www.frontiersin.org

Table 6. Prevalence of Hepatitis B infection among pregnant mothers conducted in different countries.

However, the current study finding is higher than the study conducted at the Arba Minch Hospital in southern Ethiopia (4.3%0 (28), Gandhi hospital in Addis Ababa (2.3%) (29), Dawuro hospital in southern Ethiopia (3.5%) (30), and Felegehiwot hospital in Bahir Dar (4.7%) (31), as well as in Kenya (3.8%) (12), Tanzania (3.9%) (32), Rwanda (3.7%) (33), and Turkey (2.1%) (34). This variation might be due to differences in the sociodemographic characteristics of study participants, geographical area, health policy implemented on hepatitis prevention strategies, differences in cultural practices of community, sexual behaviors as well as differences in sampling method, small sample size, and laboratory test methods employed to detect HBsAg. Additionally, it could be due to poor adherence with the national immunization program, known as the expanded program on immunization (EPI) in Ethiopia (35).

According to this study, pregnant mothers who had tattoos on any part of their bodies were more likely to acquire hepatitis B infection than their counterparts. This finding is comparable to research done in Ethiopia, Bahir Dar (27), southwestern Bench-Maji (36), and Debra-Tabor (37), and in Antioch of Turkey (34) and China (38). This could be attributed to the fact that tattoos are performed using non-sterile equipment. This suggests that the spread of HBV in the study area may be facilitated by the sharing of hazardous materials for customary practice. Tonsillectomy and tattooing are traditional practices in this study area. Hepatitis B virus can remain alive and infectious on surfaces of contaminated materials for at least 7 days, such as blood (5).

Pregnant mothers who had a history of tonsillectomy were at higher risk of HBV infection compared to those who did not. A similar finding was reported in a study conducted in Dawuro in southern Ethiopia (28), Uganda (39), and Nigeria (40). This finding may be explained as most of the time tonsillectomy was practiced with a traditional practitioner possibly by using repeatedly unsterilized instruments, which might increase the probability of transmission of HBV infection in the community.

Hepatitis B virus infection is a sexually transmitted disease and the transmission increases with the duration of sexual activity and the number of sexual partners exposed (4). In the current study, pregnant mothers having a history of multiple partners were more likely to be infected with HBV. This is in agreement with the findings from other parts of Deder (15), Dessie (41), Dawuro in southern Ethiopia (40), Yirgalem (26), Arba Minch (28), Bishoftu (42), Felegehiwot in Bahir Dar (42), and Congo (43) and southern Uganda (44).

Moreover, our study revealed that pregnant mothers who had a history of contact with a jaundiced patient had a higher chance of acquiring hepatitis B infection. This finding is supported by the study conducted at the Attat hospital in southern Ethiopia (45) and Mizan-Tepi (46). In addition to the difference in behavioral and cultural practice, exposure to the chronic carrier has a wide chance of contact with body fluids. Our findings are in accordance with other studies reported, which indicate that the risk of HBV transmission is high in people who are in contact with chronically infected HBV participants (47).

Residence, abortion, and blood transfusion did not show a significant association with HBV infection. The residence of participants and educational status were in agreement with study findings in Hawassa (20) and Arba Minch (28), which is opposite to a study in Dessie (48). History of having an abortion failed to indicate a significant association among pregnant mothers as it is in line with other studies conducted in Bahir Dar (27), contrary to studies in Deder (15) and Gambella (49). History of blood and blood product transfusion failed to show any evidence of association of virus transmission, which was in agreement with studies of HBV infection in pregnant mothers in Nairobi, Kenya (32), Kinshasa, Tanzania (32), and Mulago hospital in Uganda(50), but it contradicted other studies that indicated evidence of blood transfusion was significantly associated with virus transmission in Bishoftu in Ethiopia (24), and Arba Minch in southern Ethiopia (28). The possible explanation may be the variation in study area and period, sample size, safety precaution being taken, and proper screening for virus in a regularly carried out manner currently before blood donation in the study area.

Pregnant mothers with a history of surgical procedures failed to show hepatitis B infection association with virus transmission supported by studies conducted in Hawassa (20), Gambella hospital (50), Dawuro in southern Ethiopia (20, 30). and Arba Minch (28), in contrary to study findings in Addis Ababa (42) and Harar in Ethiopia (51), Deder in eastern Ethiopia (15), and Bahir Dar in northwest Ethiopia (27). The difference may be attributed to variation, the use of standard procedures, and disinfected instruments by a health professional.

The current study showed that about 78% of study participants had poor knowledge (scored less than 50%) regarding HBV infection, mode of transmission, and other. Only about 84 (28%), 43 (14%), and 73 (24%) study participants responded positively about HBV infection, transmission, and prevention-related knowledge, respectively. It has been documented that community awareness of the transmission of hepatitis B is low in Ethiopia (52). A similar low knowledge was observed in a study conducted in Cameron (53). This may be related to the type of occupation due to nonadherence to guidelines on infection control, the use of non-disposable or reusable equipment, and the lack of adequate sterilization techniques as it is mostly with those who have knowledge better than those who want to get service.

Strengths and limitations of study

One of the strengths of this study was the use of the ELISA method for laboratory examination, which is uncommon in Ethiopia to test for HBV. Another strength was the identification of potential associated risk factors using quality-assured data obtained by trained personnel using the pretested structured questionnaire. However; laboratory tests for serological markers such as hepatitis B core antibody, hepatitis B surface antibody, total hepatitis B core antibody, and IgM antibody to hepatitis B core antigen, which were necessary to diagnose HBV infection and to identify the stage of infection, were not performed due to resource limitation. Additionally, due to the lack of resources, HBsAg-positive pregnant women were not tested for HBeAg or viral load, making it impossible for this study to determine the extent of perinatal transmission of HBV. The study was also conducted in antenatal clinics, which can limit results representative of the entire population, and information obtained from mothers could be subjected to responder bias.

Conclusion and recommendations

The prevalence of HBV infection among pregnant mothers attending antenatal care clinics in west Hararghe public hospitals was high according to the WHO classification, suggesting that HBV is an important public health issue in the study area. History of having a tonsillectomy, tattooing, having multiple sexual partners, and having contact with jaundiced patients were identified as factors associated with hepatitis B virus infection.

In order to reduce transmissions, it is recommended that the government should start HBV vaccination campaigns, begin with mass vaccination, and implement a national immunization program. As soon as possible after birth, ideally within 24 h, all newborns should receive hepatitis B vaccines. Additionally, to reduce the risk of transmission from mother to child, all pregnant women with HBV infection should receive HBsAg testing and take antiviral prophylaxis. The health bureau and medical professionals should also educate expectant mothers more about preventing and controlling HBV infection.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving human participants were reviewed and approved by Institutional Health Research Ethics Review Committee (IHRERC) of Haramaya University College of Health and Medical Science. The patients/participants provided their written informed consent to participate in this study.

Author contributions

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis, and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Acknowledgments

We acknowledge the Haramaya University Colleges of Health and Medical Sciences Institutional Health Research Ethical Review Committee for giving ethical clearance. We also thank the study participants and all individuals who have in one way or another contributed to the completion of this research.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Liu J, Liang W, Jing W, Liu M. Countdown to 2030: eliminating hepatitis B disease, China. Bull World Health Organ. (2019) 97:230–8. doi: 10.2471/BLT.18.219469

PubMed Abstract | CrossRef Full Text | Google Scholar

2. World Health Organization. Global health sector strategy on viral hepatitis 2016-2021. Towards ending viral hepatitis (2016). https://apps.who.int/iris/handle/10665/246177 (Accessed October 20, 2020).

3. World Health Organization. Hepatitis B fact sheet (2016). https://www.who.int/news-room/fact-sheets/detail/hepatitis-b (Accessed July 29, 2020).

4. Inoue T, Tanaka Y. Hepatitis B virus and its sexually transmitted infection - an update. Microb Cell. (2016) 3:420–37. doi: 10.15698/mic2016.09.527

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Bond W, Favero M, Petersen N, Gravelle C, Ebert J, Maynard J. Survival of hepatitis B virus after drying and storage for one week. Lancet. (1981) 1:550–1. doi: 10.1016/s0140-6736(81)92877-4

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Aberg JA, Kaplan JE, Libman H, Emmanuel P, Anderson JR, Stone VE, et al. Primary care guidelines for the management of persons infected with human immunodeficiency virus: 2009 update by the HIV medicine Association of the Infectious Diseases Society of America. Clin Infect Dis. (2009) 49:651–81. doi: 10.1086/605292

PubMed Abstract | CrossRef Full Text | Google Scholar

7. WHO. (2022). Hepatitis B. Available at: https://www.who.int/news-room/fact-sheets/detail/hepatitis-b. (Accessed July 10, 2020).

8. World Health Organization. Global hepatitis report 2017: web annex A: estimations of worldwide prevalence of chronic hepatitis B virus infection: a systematic review of data published between 1965 and 2017 (2018). https://apps.who.int/iris/handle/10665/277004 (Accessed June 3, 2020).

9. Abbas Z, Siddiqui AR. Management of hepatitis B in developing countries. World J Hepatol. (2011) 3:292–9. doi: 10.4254/wjh.v3.i12.292

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Razavi H. Global epidemiology of viral hepatitis. Gastroenterol Clin North Am. (2020) 49:179–89. doi: 10.1016/j.gtc.2020.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Akibu T. (2018) Formative research for enhancing interventions to prevent violence against women: men’s perceptions in Diepsloot, South Africa. [doctoral dissertation]. [Johannesburg]: University of Witwatersrand. https://hdl.handle.net/10539/25369 (Accessed October 11, 2020).

12. Negero A, Sisay Z, Medhin G. Prevalence of hepatitis B surface antigen (HBsAg) among visitors of Shashemene General Hospital voluntary counseling and testing center. BMC Res Notes. (2011) 4:35. doi: 10.1186/1756-0500-4-35

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Belyhun Y, Maier M, Mulu A, Diro E, Liebert UG. Hepatitis viruses in Ethiopia: a systematic review and meta-analysis. BMC Infect Dis. (2016) 16:761. doi: 10.1186/s12879-016-2090-1

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Yazie TD, Tebeje MG. An updated systematic review and meta-analysis of the prevalence of hepatitis B virus in Ethiopia. BMC Infect Dis. (2019) 19:1–3. doi: 10.1186/s12879-019-4486-1

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Umare A, Seyoum B, Gobena T, Mariyam TH. Hepatitis B virus infections and associated factors among pregnant women attending antenatal care clinic at Deder hospital, Eastern Ethiopia. PLoS One. (2016) 11:e0166936. doi: 10.1371/journal.pone.0166936

PubMed Abstract | CrossRef Full Text | Google Scholar

16. World Health Organization. Expanded Programme on Immunization. Protocol for assessing prevalence of hepatitis B infection in antenatal patients (1990). https://apps.who.int/iris/handle/10665/61617 (Accessed September 13, 2020).

17. Frambo AA, Atashili J, Fon P, Ndumbe P. Prevalence of HBsAg and knowledge about hepatitis B in pregnancy in the Buea health district, Cameroon: a cross-sectional study. BMC Res Notes. (2014) 7:394. doi: 10.1186/1756-0500-7-394

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Mekonnen R, Admasu D, Belete M. Sero-prevalence of hepatitis B virus and associated factors among pregnant mothers attending antenatal care in public health facilities, Dire Dawa. J Med Microb Diagn. (2018) 7:281. doi: 10.4172/2161-0703.1000281

CrossRef Full Text | Google Scholar

19. Bayo P, Ochola E, Oleo C, Mwaka AD. High prevalence of hepatitis B virus infection among pregnant women attending antenatal care: a cross-sectional study in two hospitals in northern Uganda. BMJ Open. (2014) 4:e005889. doi: 10.1136/bmjopen-2014-005889

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Metaferia Y, Dessie W, Ali I, Amsalu A. Seroprevalence and associated risk factors of hepatitis B virus among pregnant women in southern Ethiopia: a hospital-based cross-sectional study. Epidemiol Health. (2016) 38. doi: 10.4178/epih.e2016027

PubMed Abstract | CrossRef Full Text | Google Scholar

21. 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) 13:1–5. doi: 10.1186/1471-2393-13-127

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Tegegne D, Desta K, Tegbaru B, Tilahun T. Seroprevalence and transmission of hepatitis B virus among delivering women and their new born in selected health facilities, Addis Ababa, Ethiopia: a cross sectional study. BMC Res Notes. (2014) 7:1–7. doi: 10.1186/1756-0500-7-239

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Atilola G, Tomisin O, Randle M, Isaac KO, Odutolu G, Olomu J, et al. Epidemiology of HBV in pregnant women, south west Nigeria. J Epidemiol Glob Health. (2018) 8:115. doi: 10.1016/j.jegh.2018.09.002

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Desalegn Z, Mihret A, Beyene H, Yilma M, Seid Y, Tamiru W, et al. Survey of hepatitis B virus infection and risk factors among pregnant women at public hospital in Ethiopia. Int J Biomed Res. (2016) 7:450–6. doi: 10.7439/ijbr

CrossRef Full Text | Google Scholar

25. MacLachlan JH, Cowie BC. Hepatitis B virus epidemiology. Cold Spring Harb Perspect Med. (2015) 5:a021410. doi: 10.1101/cshperspect.a021410

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Amsalu A, Ferede G, Eshetie S, Tadewos A, Assegu D. Prevalence, infectivity, and associated risk factors of hepatitis B virus among pregnant women in Yirgalem hospital, Ethiopia: implication of screening to control mother-to-child transmission. J Pregnancy. (2018) 2018. doi: 10.1155/2018/8435910

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Zenebe Y, Mulu W, Yimer M, Abera B. Sero-prevalence and risk factors of hepatitis C virus infection among pregnant women in Bahir Dar city, northwest Ethiopia: cross sectional study. Pan Afr Med J. (2015) 22(1). doi: 10.11604/pamj.2015.21.158.6367

CrossRef Full Text | Google Scholar

28. Yohanes T, Zerdo Z, Chufamo N. Seroprevalence and predictors of hepatitis B virus infection among pregnant women attending routine antenatal care in Arba Minch hospital, south Ethiopia. Hepat Res Treat. (2016) 2016. doi: 10.1155/2016/9290163

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Abera ZN, Getahun DD. Seroprevalence of hepatitis B surface antigen and associated risk factors among pregnant women in Gandhi memorial hospital, Addis Ababa. J Public Health Epidemiol. (2019) 11:123–9. doi: 10.5897/JPHE2019.1153

CrossRef Full Text | Google Scholar

30. Chernet A, Yesuf A, Alagaw A. Seroprevalence of hepatitis B virus surface antigen and factors associated among pregnant women in Dawuro zone, SNNPR, southwest Ethiopia: a cross sectional study. BMC Res Notes. (2017) 10:418. doi: 10.1186/s13104-017-2702-x

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Gedefaw G, Waltengus F, Akililu A, Gelaye K. Risk factors associated with hepatitis B virus infection among pregnant women attending antenatal clinic at Felegehiwot referral hospital, Northwest Ethiopia, 2018: an institution based cross sectional study. BMC Res Notes. (2019) 12(1):509. doi: doi: 10.1186/s13104-019-4561-0.31416477

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Rashid S, Kilewo C, Aboud S. Seroprevalence of hepatitis B virus infection among antenatal clinic attendees at a tertiary hospital in Dar es Salaam, Tanzania. Tanzan J Health Res. (2014) 16(1):9–15. doi: 10.4314/thrb.v16i1.2

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Mutagoma M, Balisanga H, Malamba SS, Sebuhoro D, Remera E, Riedel DJ, et al. Hepatitis B virus and HIV co-infection among pregnant women in Rwanda. BMC Infect Dis. (2017) 17:618. doi: 10.1186/s12879-017-2714-0

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Cetin S, Cetin M, Turhan E, Dolapcioglu K. Seroprevalence of hepatitis B surface antigen and associated risk factors among pregnant women. J Infect Dev Ctries. (2018) 12:904–9. doi: 10.3855/jidc.10018

PubMed Abstract | CrossRef Full Text | Google Scholar

35. World Health Organization. Expanded program on immunization (EPI) (2018). https://www.afro.who.int/publications/2018-epi-annual-report-who-ethiopia (Accessed November 14, 2020).

36. Belyhun Y, Maier M, Mulu A, Diro E, Liebert UG. Hepatitis viruses in Ethiopia: a systematic review and meta-analysis. BMC Infect Dis. (2016) 16:761. doi: 10.1186/s12879-016-2090-1

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Walle F, Asrat D, Alem A, Tadesse E, Desta K. Prevalence of hepatitis B surface antigen among pregnant women attending antenatal care service at Debre-Tabor hospital, northwest Ethiopia. Ethiop J Health Sci. (2007) 17:13–21.

Google Scholar

38. Zhang Y, Fang W, Fan L, Gao X, Guo Y, Huang W, et al. Hepatitis B surface antigen prevalence among 12 393 rural women of childbearing age in Hainan province, China: a cross-sectional study. Virol J. (2013) 10:1–8. doi: 10.1186/1743-422X-10-1

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Hillary A, Julius M, Joseph N, Musa K, Ronald M, Hamson K, et al. Prevalence and factors associated with hepatitis B surface antigen positivity among women receiving antenatal care at Mbarara regional referral hospital. J Trop Dis. (2019) 7:321. doi: 10.35248/2329-891X.19.7.321

CrossRef Full Text | Google Scholar

40. Okoye JI, Eze-Steven PE. Study on the Prevalence of Hepatitis B Virys among Blood Donors. INOSR Scientific Research. (2020) 6(1):57-60. http://www.inosr.net/wp-content/uploads/2020/10/INOSR-SR-61-57-60-2020.pdf (Accessed November 25, 2020).

Google Scholar

41. Seid M, Gelaw B, Assefa A. Sero-prevalence of HBV and HCV infections among pregnant women attending antenatal care clinic at Dessie Referral Hospital, Ethiopia. Adv Life Sci Health. (2014) 1(2):109–20. doi: 10.1186/s12879-019-4220-z

42. Desalegn Z, Wassie L, Beyene HB, Mihret A, Ebstie YA. Hepatitis B and human immunodeficiency virus co-infection among pregnant women in resource-limited high endemic setting, Addis Ababa, Ethiopia: implications for prevention and control measures. Eur J Med Res. (2016) 21:16. doi: 10.1186/s40001-016-0211-3

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Nlombi CM, Natuhoyila AN, Tudiakuilayi M, Luendu M. Evaluation of seroprevalence and factors associated with the portage of HBsAg in pregnant women in Rural Vanga and Semi-Urban Maluku. Int J Health Sci Res (2019) 9:1–9.

Google Scholar

44. Fouelifack FY, Fouedjio JH, Fouogue JT, Fouelifa LD. Seroprevalences and correlates of hepatitis B and C among Cameroonian pregnant women. Clin Med Insights Reprod Health. (2018) 12:1179558118770671. doi: 10.1177/1179558118770671

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Bafa TA, Egata AD. Seroepidemiological patterns and predictors of hepatitis B, C and HIV viruses among pregnant women attending antenatal care clinic of Atat hospital, southern Ethiopia. SAGE Open Med. (2020) 8:2050312119900870. doi: 10.1177/2050312119900870

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Asaye Z, Aferu T, Asefa A, Feyissa D, Regasa T, Kebede O, et al. Prevalence of hepatitis B virus among pregnant women on antenatal care follow-up at Mizan-Tepi university teaching hospital and Mizan Health Center, southwest Ethiopia. Int J Gen Med. (2021) 14:195. doi: 10.2147/IJGM.S292070

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Fomulu NJ, Morfaw FL, Torimiro JN, Nana P, Koh MV, William T. Prevalence, correlates and pattern of hepatitis B among antenatal clinic attenders in Yaounde-Cameroon: is perinatal transmission of HBV neglected in Cameroon? BMC Pregnancy Childbirth. (2013) 13:1–10. doi: 10.1186/1471-2393-13-158

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Seid M, Gelaw B, Assefa A. Sero-prevalence of HBV and HCV infections among pregnant women attending antenatal care clinic at Dessie referral hospital, Ethiopia. Adv Life Sci Health. (2014) 1:109–20.

Google Scholar

49. Tanga AT, Teshome MA, Hiko D, Fikru C, Jilo GK. Sero-prevalence of hepatitis B virus and associated factors among pregnant women in Gambella Hospital, south western Ethiopia: facility based cross-sectional study. BMC Infect Dis. (2019) 19:602. doi: 10.1186/s12879-019-4220-z

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Allen N, Bashir M, Taremwa I. Prevalence and associated factors of hepatitis B virus infection among pregnant women attending antenatal care clinic at Mulago National Referral Hospital, Uganda. Int Blood Res Rev. (2017) 7:1–10. doi: 10.9734/IBRR/2017/36972

CrossRef Full Text | Google Scholar

51. Tiruye G, Shiferaw K, Tadesse F. Seroprevalence of hepatitis B virus infection and associated factors among pregnant women attended antenatal care services in Harar city, Eastern Ethiopia. J Womens Health Care. (2018) 7(3):3–10. doi: 10.4172/2167-0420.1000436

CrossRef Full Text | Google Scholar

52. Shiferaw F, Letebo M, Bane A. Chronic viral hepatitis: policy, regulation, and strategies for its control and elimination in Ethiopia. BMC Public Health. (2016) 16:769. doi: 10.1186/s12889-016-3459-1

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Frambo AAB, Atashili J, Fon PN, Ndumbe PM. Prevalence of HBsAg and knowledge about hepatitis B in pregnancy in the Buea health district, Cameroon: a cross-sectional study. BMC Res Notes. (2014) 7:394. doi: 10.1186/1756-0500-7-394

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: hepatitis B virus infection, prevalence, pregnant mothers, antenatal care, western Hararghe, eastern Ethiopia

Citation: Umer A, Teklemariam Z, Ayele F and Mengesha MM (2023) Prevalence of hepatitis B infection and its associated factors among pregnant mothers attending antenatal care at public hospitals at Hararghe, Eastern Ethiopia. Front. Glob. Womens Health 4:1056488. doi: 10.3389/fgwh.2023.1056488

Received: 28 September 2022; Accepted: 29 March 2023;
Published: 27 April 2023.

Edited by:

Rebecca F. Grais, Epicentre, France

Reviewed by:

Ze Xiang, Zhejiang University, China
Peyton Thompson, University of North Carolina Hospitals, United States
John Franzone University of North Carolina Chapel Hill, United States, in collaboration with reviewer PT

© 2023 Umer, Teklemariam, Ayele and Merid. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Firayad Ayele firayadayele@gmail.com

ORCID Melkamu Merid Mengesha orcid.org/0000-0003-4312-0136

Specialty Section: This article was submitted to Infectious Diseases in Women, a section of the journal Frontiers in Global Women's Health

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.