<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OALibJ</journal-id><journal-title-group><journal-title>Open Access Library Journal</journal-title></journal-title-group><issn pub-type="epub">2333-9705</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oalib.1101490</article-id><article-id pub-id-type="publisher-id">OALibJ-68355</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Business&amp;Economics</subject><subject> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Engineering</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject><subject> Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prevalence of Hepatitis B Virus Infection and Associated Factors among HIV Positive Adults Attending ART Clinic at Hawassa Referral Hospital, SNNPR, Ethiopia
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Fanuel</surname><given-names>Belayneh</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>School of Public Health, Department of Epidemiology, Wolaita Sodo University, Sodo, Ethiopia</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>fanuelbelayneh@gmail.com</email></corresp></author-notes><pub-date pub-type="epub"><day>29</day><month>05</month><year>2015</year></pub-date><volume>02</volume><issue>05</issue><fpage>1</fpage><lpage>7</lpage><history><date date-type="received"><day>13</day>	<month>April</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>28</month>	<year>April</year>	</date><date date-type="accepted"><day>4</day>	<month>May</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   
   Background: Hepatitis B and HIV infections are serious global public health problems. Among the estimated 40 million persons infected with HIV worldwide, an estimated 2 - 4 million (5% - 15%) have chronic hepatitis B virus. This co-infection is common due to shared transmission routes of the agents. In Ethiopia, even though, HBV infection is more common in HIV infected individuals, only little is known about the distribution as well as factors associated with the infection. Objective: To assess the prevalence of hepatitis B infection and associated factors among HIV positive adults attending ART clinic at Hawassa University Referral Hospital, Hawassa, Southern Ethiopia. Methods: Hospital based cross-sectional study was conducted from May 2 to July 2, 2014 in Hawassa University Referral Hospital. Samples were taken consecutively to get the calculated sample size of 348 adults living with HIV. Pretested interviewer administered structured questionnaire was implemented. Statistical Package for Social Sciences (SPSS) Version 20 was used for statistical analysis. Result: Among the sample of 348 HIV positive adults, 128 (36.8%) were males and 220 (63.2%) were females with mean (&#177;SD) age of 33.2 (&#177;9.1) years old. Hepatitis B surface antigen was detected in 24 (6.9%) of individuals. The prevalence of HBV infection was 17 (7.7%) among females and 7 (5.5%) among males. About 66% of study participants have poor knowledge regarding Hepatitis B. History of surgical procedure [AOR = 4.6: 95% CI, 1.8 - 11.6] and previous opportunistic infection [AOR = 5.2: 95% CI, 1.1 - 23.2] were significantly associated with the presence of HBsAg. Conclusion: The prevalence of HBsAg was found to be intermediate in HIV positive adults and majority of them had poor knowledge about the disease. We recommend provision of routine screening and vaccination service together with accurate information on risk factors such as opportunistic infection and surgical procedure for transmission of HBV. 
  
 
</p></abstract><kwd-group><kwd>Hepatitis B Surface Antigen (HBsAg)</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Viral hepatitis is a disease characterized by inflammation of liver and in many cases permanent damage to liver tissue [<xref ref-type="bibr" rid="scirp.68355-ref1">1</xref>] . Common types of hepatitis virus are hepatitis A, B, C, D, E and G. Hepatitis B is the most serious type of viral hepatitis, which can lead to chronic liver disease and put people at high risk of death from cirrhosis of the liver and liver cancer. It is a DNA virus replicates in hepatocytes and damages the liver by immune response to the virus [<xref ref-type="bibr" rid="scirp.68355-ref2">2</xref>] .</p><p>Hepatitis B virus shares similar transmission route with human immunodeficiency virus (HIV); thus, co-in- fection with these two viruses is common and both are serious global public health problems. An estimated two billion people around the globe have been contaminated with hepatitis B virus. Persons with HIV infections are disproportionately affected by viral hepatitis. Among the estimated 40 million persons infected with HIV worldwide, an estimated 2 - 4 million (5% - 15%) have chronic HBV [<xref ref-type="bibr" rid="scirp.68355-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref4">4</xref>] .</p><p>Viral hepatitis progresses faster among persons with HIV and persons who are infected with viruses experience greater liver related health problems than those who do not have HIV infection [<xref ref-type="bibr" rid="scirp.68355-ref1">1</xref>] .</p><p>Evidences indicated that HIV positive individuals are more likely to be chronic carrier and have a higher HBV replication rate than HIV negative individuals. In addition, it is evident that immuno-suppression brought by HIV infection may cause re-activation or re-infection in those previously exposed to HBV [<xref ref-type="bibr" rid="scirp.68355-ref4">4</xref>] . Furthermore, HIV infection exacerbates liver disease in HBV/HIV co-infected individuals and there is an even greater risk of liver disease when HIV and HBV co-infected patients are treated with HAART [<xref ref-type="bibr" rid="scirp.68355-ref5">5</xref>] . It has been observed that HBV/HIV co-infection leads to increased morbidity and mortality as compared to HIV or HBV mono-infections [<xref ref-type="bibr" rid="scirp.68355-ref6">6</xref>] .</p><p>Many of the countries with high HIV burden are also affected by high prevalence of hepatitis B infection; leading to frequent HIV/HBV co-infection. The co-infection was reported as high as 10% - 20% in countries where HBV infection is either endemic or intermediate to high HBV cases [<xref ref-type="bibr" rid="scirp.68355-ref6">6</xref>] .</p><p>Even though, HBV and HIV have common routes of transmission and endemic areas, HBV is about 50-100 times more infectious than HIV. Consequently, in some settings up to two thirds of all HIV-infected people have blood markers of past or present HBV infection [<xref ref-type="bibr" rid="scirp.68355-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref8">8</xref>] .</p><p>A community based sero-epidemiological survey of Addis Ababa, Ethiopia has shown a 7% sero-prevalence for HBsAg [<xref ref-type="bibr" rid="scirp.68355-ref9">9</xref>] . Other hospital-based studies in the country conducted at St Paul’s General Specialized Hospital and Shashemene General Hospital documented a 3.9% to 14% of HBsAg prevalence among HIV positive individuals consecutively [<xref ref-type="bibr" rid="scirp.68355-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref11">11</xref>] .</p><p>Hepatitis B is avoidable with a readily available and efficacious vaccine [<xref ref-type="bibr" rid="scirp.68355-ref2">2</xref>] . Among the groups for whom CDC recommends vaccination against hepatitis B are persons who have or are at risk for HIV infection, including men having sex with men (MSM); persons who inject drugs; susceptible sex partners of infected persons; persons with multiple sex partners; anyone with a sexually transmitted infection (STI); and health care and public safety workers exposed to blood on the job [<xref ref-type="bibr" rid="scirp.68355-ref1">1</xref>] .</p><p>Ethiopia is being one of the countries that most hit by HIV infection (prevalence of 2.1%) and is also found in a region classified as high endemic area for HBV; the likelihood of HBV/HIV co infection is highly anticipated [<xref ref-type="bibr" rid="scirp.68355-ref12">12</xref>] .</p><p>However, in Africa in general and in Ethiopia in particular, information on the magnitude of HBV positivity at different risk groups including people living with HIV/AIDS is scarce.</p><p>Because of the significant burden and clinical impact of HBV in HIV-infected individuals, understanding the epidemiologic trends, exposure proportions and associated risk factors have paramount importance to undertake effective prevention measures [<xref ref-type="bibr" rid="scirp.68355-ref13">13</xref>] .</p></sec><sec id="s2"><title>2. Methods</title><sec id="s2_1"><title>2.1. Study Setting and Study Population</title><p>Hospital based cross-sectional study was conducted from May 2 to July 2, 2014 at Hawassa University Referral Hospital. All adults living with HIV, who visited the hospital during the study period and fulfilled the inclusion criteria, were included in the study using consecutive sampling technique. An interview with pretested structured questionnaire having open and closed ended questions adapted from similar survey reviews that have been carried out inside and outside the country was used for data collection. Three milliliters of venues blood was collected from each patient with standard operational procedure. Serum was separated by centrifugation at 3000 rpm for 5 minutes after the blood has been clotted. The serum was tested for HBsAg by Wondfo one step HBsAg test strip according to the manufacturer’s instruction. This test strip had sensitivity and specificity of 96.2% and 99.3% respectively.</p><p>The study variables were selected after reviewing relevant literatures according to the objective of the study. The dependent variables were Hepatitis B virus infection status. The independent variables were categorized under socio-demographic characteristics, behavioral, clinical and knowledge related factors.</p></sec><sec id="s2_2"><title>2.2. Data Processing and Analysis</title><p>Data was entered into Epi Data version 3.1 then exported to SPSS version 20 for analysis. Summary statistics such as frequencies and percentages were computed. Bivariate analysis was conducted primarily to check association of each variable with the dependent variable. To control for possible effect of confounding, variables found to have association with the dependent variable at P-value of 0.2 were entered into multivariate logistic regression. The variables which had significant association with P-value less than 0.05 in the multivariate logistic regression were considered to be independent factors. The model was diagnosed by Hosmer and Lemeshow goodness of fit tests.</p></sec><sec id="s2_3"><title>2.3. Ethical Consideration</title><p>Ethical clearance was obtained from Jimma University, College of Public Health and Medical Sciences. Letter of cooperation was taken from the Department of Epidemiology and Biostatics and from Hawassa University Referral Hospital. Each respondent was informed about the objective of the study and a written consent was obtained. Confidentiality was kept at each step of data collection and processing. In addition, positive HBsAg test results of the study participants were communicated with their physician for farther investigation and better management of the patients.</p></sec></sec><sec id="s3"><title>3. Result</title><p>From 358 HIV positive adults contacted, 348 of them were included in the analysis with a response rate of 97.2%.</p><p>Majority, 220 (63.2%) of the respondents were females, age ranged 25 - 34 years old (52.9%) with mean (&#177;SD) age of 33.2 (9.1) years old. About 92% of them were urban residents (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>The prevalence of HBsAg was found to be 24 (6.9%); of whom 17(7.7%) were females and 7 (5.5%) were males. With respect to age, the prevalence of HBsAg was 3 (7.5%) in age category of 18-24, 15 (8.2%) in age category of 25 - 34 and 6 (4.8%) for above 34 years old. All of the participants with HBsAg positive results live in urban areas.</p><p>Concerning to their marital status, the prevalence of HBsAg was 12.3% among singles, 7.2% among married, 2.0% among divorced and 6.2% among widowed participants. Illiterate had a prevalence of 12.8%; while among those with primary and secondary schools the rate was 5.7% and 9.6% respectively (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Bivariate logistic regression analysis was done using enter method to identify factors for the multiple logistic regression. In the analysis, average family income, WHO stage classification of HIV/AIDS, surgical history, previous history of opportunistic infection and sharing of sharp instruments were selected for the multiple logistic regression analysis based on their P-value of &lt;0.2.</p><p>Multivariate analysis revealed that those who have previous history of surgical procedure were 4.6 times more likely to be contaminated with HBV than who did not [AOR = 4.6: 95% CI, 1.8 - 11.6] and those with previous opportunistic infection were about 5 times more likely to show HBV surface antigen marker than who did not [AOR = 5.2: 95% CI, 1.1 - 23.2] (<xref ref-type="table" rid="table3">Table 3</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>In this study, the prevalence of HBsAg was 6.9%. This result is in line with HBsAg prevalence documented</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Socio-demographic and economic characteristics of respondents attending ART clinic at Hawassa University Referral Hospital, Hawassa, South Ethiopia, 2014</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristics</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Present (%)</th></tr></thead><tr><td align="center" valign="middle" >Sex</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >220</td><td align="center" valign="middle" >63.2</td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >128</td><td align="center" valign="middle" >36.8</td></tr><tr><td align="center" valign="middle" >Age (Years Old)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >18 - 24</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >11.5</td></tr><tr><td align="center" valign="middle" >25 - 34</td><td align="center" valign="middle" >184</td><td align="center" valign="middle" >52.9</td></tr><tr><td align="center" valign="middle" >35 - 44</td><td align="center" valign="middle" >92</td><td align="center" valign="middle" >26.4</td></tr><tr><td align="center" valign="middle" >≥45</td><td align="center" valign="middle" >32</td><td align="center" valign="middle" >9.2</td></tr><tr><td align="center" valign="middle" >Place of Residence</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Urban</td><td align="center" valign="middle" >322</td><td align="center" valign="middle" >92.5</td></tr><tr><td align="center" valign="middle" >Rural</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >7.5</td></tr><tr><td align="center" valign="middle" >Educational Level</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Illiterate</td><td align="center" valign="middle" >45</td><td align="center" valign="middle" >12.9</td></tr><tr><td align="center" valign="middle" >Elementary (≤8 grade)</td><td align="center" valign="middle" >122</td><td align="center" valign="middle" >35.1</td></tr><tr><td align="center" valign="middle" >Secondary (9 - 12 grade)</td><td align="center" valign="middle" >115</td><td align="center" valign="middle" >33</td></tr><tr><td align="center" valign="middle" >Higher education</td><td align="center" valign="middle" >36</td><td align="center" valign="middle" >10.3</td></tr><tr><td align="center" valign="middle" >Universities</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >8.6</td></tr><tr><td align="center" valign="middle" >Marital Status</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Single</td><td align="center" valign="middle" >56</td><td align="center" valign="middle" >16.1</td></tr><tr><td align="center" valign="middle" >Married</td><td align="center" valign="middle" >165</td><td align="center" valign="middle" >47.4</td></tr><tr><td align="center" valign="middle" >Separated &amp; Divorced</td><td align="center" valign="middle" >63</td><td align="center" valign="middle" >18.1</td></tr><tr><td align="center" valign="middle" >Widowed</td><td align="center" valign="middle" >64</td><td align="center" valign="middle" >18.4</td></tr><tr><td align="center" valign="middle" >Average Monthly Income(ETB)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >≤500</td><td align="center" valign="middle" >76</td><td align="center" valign="middle" >21.8</td></tr><tr><td align="center" valign="middle" >501 - 999</td><td align="center" valign="middle" >63</td><td align="center" valign="middle" >18.1</td></tr><tr><td align="center" valign="middle" >≥1000</td><td align="center" valign="middle" >209</td><td align="center" valign="middle" >60.1</td></tr></tbody></table></table-wrap><table-wrap-group id="2"><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Prevalence of hepatitis B surface antigen among the study participants attending ART clinic at Hawassa University Referral Hospital, Hawassa, South Ethiopia, 2014</title></caption><table-wrap id="2_1"><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Variables</th><th align="center" valign="middle"  colspan="2"  >HBsAg Screening Result</th></tr></thead><tr><td align="center" valign="middle" >Negative (%)</td><td align="center" valign="middle" >Positive (%)</td></tr><tr><td align="center" valign="middle" >Sex Male Female</td><td align="center" valign="middle" >121 (94.5) 203 (93.3</td><td align="center" valign="middle" >7 (5.5) 17 (7.7)</td></tr><tr><td align="center" valign="middle" >Age Interval 18 - 24 25 - 34 &gt;35</td><td align="center" valign="middle" >37 (92.5) 169 (91.8) 118 (95.2)</td><td align="center" valign="middle" >3 (7.5) 15 (8.2) 6 (4.8)</td></tr></tbody></table></table-wrap><table-wrap id="2_2"><table><tbody><thead><tr><th align="center" valign="middle" >Educational Level Illiterate Elementary School (&lt;8 grade) Secondary and above</th><th align="center" valign="middle" >41 (91.1) 115 (94.3) 168 (92.8)</th><th align="center" valign="middle" >4 (6.7) 7 (5.7) 13 (7.2)</th></tr></thead><tr><td align="center" valign="middle" >Marital Status Single Married Widowed Separated &amp; Divorced</td><td align="center" valign="middle" >50 (89.3) 155 (93.9) 60 (93.8) 59 (93.7)</td><td align="center" valign="middle" >6 (10.7) 10 (6.1) 4 (6.2) 4 (6.3)</td></tr><tr><td align="center" valign="middle" >Avg Monthly Income &lt;500 501 - 999 &gt;1000</td><td align="center" valign="middle" >74 (97.4) 57 (90.5) 193 (92.3</td><td align="center" valign="middle" >2 (2.6) 6 (9.5) 16 (7.7)</td></tr></tbody></table></table-wrap></table-wrap-group><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Risk factors associated with Hepatitis B surface antigen from the multiple logistic regression analysis, among HIV positive adults attending ART clinic at Hawassa University Referral Hospital, 2014</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Variables</th><th align="center" valign="middle"  colspan="2"  >HBsAg Screening Result</th><th align="center" valign="middle"  rowspan="2"  >COR (95%CI)</th><th align="center" valign="middle"  rowspan="2"  >AOR (95%CI)</th></tr></thead><tr><td align="center" valign="middle" >Negative No (%)</td><td align="center" valign="middle" >Positive No (%)</td></tr><tr><td align="center" valign="middle" >Avg Monthly Income (ETB) &lt;500 501 - 999 &gt;1000</td><td align="center" valign="middle" >74 (97.4) 57 (90.5) 193 (92.3</td><td align="center" valign="middle" >2 (2.6) 6 (9.5) 16 (7.7)</td><td align="center" valign="middle" >1 3.9 (0.75 - 20.02) 3.0 (0.68 - 13.66)</td><td align="center" valign="middle" >1 3.0 (0.5 - 16.4) 2.8 (0.6 - 13.1)</td></tr><tr><td align="center" valign="middle" >Surgical History Yes No</td><td align="center" valign="middle" >40 (81.6) 284 (95.0)</td><td align="center" valign="middle" >9 (18.4) 15 (5.0)</td><td align="center" valign="middle" >4.2 (1.7 - 10.3) 1</td><td align="center" valign="middle" >4.6 (1.8 - 11.6)<sup>*</sup> 1</td></tr><tr><td align="center" valign="middle" >Opportunistic Infection Yes No</td><td align="center" valign="middle" >227 (91.2) 97 (98.0)</td><td align="center" valign="middle" >22 (8.8) 2 (2.0)</td><td align="center" valign="middle" >4.7 (1.08 - 20.38) 1</td><td align="center" valign="middle" >5.2 (1.1 - 23.2)<sup>*</sup> 1</td></tr><tr><td align="center" valign="middle" >Sharing Sharp Instruments Yes No</td><td align="center" valign="middle" >153 (91.1) 171 (95.0)</td><td align="center" valign="middle" >15 (9.9) 9 (5.0)</td><td align="center" valign="middle" >1.8 (0.79 - 4.37) 1</td><td align="center" valign="middle" >1.6 (0.7 - 4.1) 1</td></tr></tbody></table></table-wrap><p>NB: <sup>*</sup> = Significant at P-value 0.05, Hosmer and Lemeshow goodness of fit test = 0.9.</p><p>from the study conducted in India (6.3%). Other similar studies among HIV positive individuals showed that HBV/HIV co-infection prevalence of 5.6% in Malawi, 4.9% in Rwanda and 6% in Kenya which was consistent with the findings of this study [<xref ref-type="bibr" rid="scirp.68355-ref14">14</xref>] - [<xref ref-type="bibr" rid="scirp.68355-ref17">17</xref>] .</p><p>HBsAg prevalence from this study is also in agreement with previous studies conducted among HIV positive adults in Ethiopia. Studies at Debretabor Hospital and at Gondar University Teaching Hospital showed 6.1% and 5.6% HBV/HIV co-infection respectively [<xref ref-type="bibr" rid="scirp.68355-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref19">19</xref>] .</p><p>However, the prevalence of HBsAg was found lower compared to HBV/HIV co-infection prevalence of 13.4% in Tehran, Iran, 11.4% among Nigerian HIV-infected individuals and 12.2% among similar population in Gambia [<xref ref-type="bibr" rid="scirp.68355-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref21">21</xref>] .</p><p>Similarly, it is also lower than the 14.0% reported in Shashemene, 20% among HIV positive immigrants of Israel from Ethiopia and 10.9% at Gondar [<xref ref-type="bibr" rid="scirp.68355-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref23">23</xref>] . The discrepancy might be due to the difference in the diagnostic methods followed in which these studies used ELISA technique, whereas in our study serological test was applied.</p><p>In contrast, the prevalence of HBV in this study was higher when compared to the 2.4% and 4.1% prevalence reported from Uganda and Rwanda respectively as well as 3.9% HBsAg prevalence in Addis Ababa [<xref ref-type="bibr" rid="scirp.68355-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.68355-ref24">24</xref>] .</p><p>This difference might be due to accessibility of information about mode of transmission and prevention as it can be seen from proportion of participants with poor knowledge score in this study.</p><p>In this study previous history of surgical procedure showed significant association with HBV infection. This result is in line with the results of the studies conducted in Ethiopia at Debretabor [<xref ref-type="bibr" rid="scirp.68355-ref18">18</xref>] .</p><p>Those with previous history of opportunistic infection were about 5 times more likely to be positive for HBV surface antigen marker than who did not. This result is also in agreement with the previous study at Debretabor Hospital [<xref ref-type="bibr" rid="scirp.68355-ref18">18</xref>] . The association might be due to the fact that HIV/HBV co-infected individuals have weak immunity than those with HIV mono-infected individuals which will make them more prone to opportunistic infection. In addition wounds due to opportunistic infections may increase the chance of infection [<xref ref-type="bibr" rid="scirp.68355-ref25">25</xref>] .</p></sec><sec id="s5"><title>5. Conclusion and Recommendation</title><p>The prevalence of HBsAg was found to be intermediate in HIV positive adults at Hawassa University Referral Hospital. Previous history of opportunistic infection and history of surgical procedures have statistically significant association with hepatitis B infection.</p><p>Thus, we recommend provision of routine screening and vaccination service together with accurate information on risk factors such as opportunistic infection and surgical procedure for transmission of HBV.</p></sec><sec id="s6"><title>6. Limitations of the Study</title><p>In this study HBV DNA was not detected by polymerase chain reaction due to unavailability of resources, which may increase the prevalence of HBV in this study as it would allow early diagnosis of these infections before surface antigen of HBV were detectable in serum.</p></sec><sec id="s7"><title>Cite this paper</title><p>Fanuel Belayneh, (2015) Prevalence of Hepatitis B Virus Infection and Associated Factors among HIV Positive Adults Attending ART Clinic at Hawassa Referral Hospital, SNNPR, Ethiopia. Open Access Library Journal,02,1-7. doi: 10.4236/oalib.1101490</p></sec></body><back><ref-list><title>References</title><ref id="scirp.68355-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Hoffmann, C.J., Dayal, D., Cheyip, M., McIntyre, J.A., Gray, G.E., Conway, S. and Martinson, N.A. (2012) Prevalence and Associations with Hepatitis B and Hepatitis C Infection amongst HIV-Infected Adults in South Africa. International Journal of STD &amp; AIDS, 23, e10-e13. http://dx.doi.org/10.1258/ijsa.2009.009340</mixed-citation></ref><ref id="scirp.68355-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Yami, A., Alemseged, F. and Hassen, A. (2011) Hepatitis B and C Viruses Infections and Their Association with Human Immunodeficiency Virus: A Cross-Sectional Study among Blood Donors in Ethiopia. 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