1. Introduction
Hepatitis B—a liver infection caused by the hepatitis B virus (HBV)—has long been considered a threat to global health due to its high prevalence and mortality rate [1]. According to the World Health Organization, the number of people with positive HBV surface antigen (HBsAg) was as high as 257 million in 2015, while fatality records were estimated to be 887,000 in 2015 alone [2]. Hepatitis B has been particularly prevalent in Asian countries, especially in those of Southeast Asia—classified as a high endemic region with over 8% of the population being diagnosed with positive HBsAg [3].
Hepatitis B virus infection has a distinct course of progression, of which a significant step is the transition of an acute episode to a chronic condition [4]. Studies have found that the initiation of HBV chronicity is generally associated with the condition of the immune system and host factors [5,6]. Although the rate of developing chronic HBV is highest among infants (90%), adults with a competent immune system can also develop HBV chronicity at a 5–10% rate [7]. Meanwhile, chronic HBV has been considered the main cause of hepatocellular carcinoma (HCC) or primary liver cancer—the second leading cause of cancer mortality, with an annual death count of 745,000 [8]. A Global Burden of Disease Study in 2010 indicated that chronic HBV accounted for almost 45% of HCC cases investigated globally [9]. Understanding the risky behaviors of chronic HBV patients, especially in relation to HCC development, is essential to reduce HBV-related deaths and the burden of diseases. Risky behaviors are defined as behaviors that expose people to harm and negatively affect physical, economic, or psycho-social well-being [10]. Prevailing literature has identified risky sexual behavior as one of the main risk factors for the transmission of HBV [11,12], while recent research has reported associations of alcohol consumption [13] and cigarette smoking with a risk of liver cancer in those infected with chronic HBV [14].
The prevalence of chronic HBV in Vietnam is substantial—HbsAg positive infection was found to be in the range of 9 to 14% of the population in the two largest cities of Vietnam [15], with a projection of total chronic HBV cases reaching 8 million by 2025 [16]. However, there is little literature that contributes to identifying the risk behaviors of Vietnamese chronic HBV patients. Thus, this study aimed to explore these risk behaviors (in particular drinking, smoking, and risky sexual behavior) among a cohort of people with chronic HBV in a Vietnamese urban setting, as well as investigating potential associated factors, with the hope of identifying appropriate clinical and policy-level implications.
2. Materials and Methods 2.1. Study Setting and Sampling Method
In this study, we collected data from a cross-sectional study, which was performed in October 2018 in the Chronic Hepatitis Clinic in the Viet-Tiep Hospital, Hai Phong, Vietnam. The inclusion criteria for selecting patients included being diagnosed with chronic hepatitis B (CHB), being aged 18 years old and above, agreeing to participate in the study and having the ability to communicate with the interviewers. Participants were excluded from the study if they suffered from severe health conditions which may have affected their ability to answer the questionnaire. The convenient sampling method was used to recruit patients, and a total of 298 participants agreed to be involved in the study.
2.2. Data Measurement
The 20 mininute face-to-face interviews were performed. Health staff in the clinic, who had undergone intensive training, were trained to interview the participants in order to secure the quality of the data. The confidentiality of the participants was ensured and written informed consent was obtained from the participants.
2.2.1. Socioeconomic and Health Status
Data on socioeconomic characteristics including gender, age, education, marital status, occupation, and monthly income were collected. Health status was self-reported based on the EuroQol -visual analog scale (EQ-VAS), rating from 0 (the worst health condition that you can imagine) to 100 (the best health condition that you can imagine).
2.2.2. Substance Use
In order to assess alcohol use disorder, we used the Alcohol Use Disorders Identification Test-Consumption (AUDIT-C). Participants were asked about their frequency of alcohol drinking, standard alcohol drinking in a typical day, and the frequency of having six or more drinks with the total score ranging from 0 to 12. An AUDIT-C positive result was defined as male participants having a score of 4 or more and female participants having a score of 3 or more. Binge drinking was defined as participants having six or more drinks on one occasion. The current smoking status of patients was also explored by asking them to report their smoking status in the previous 30 days. The number of cigarettes per day was also examined. In this study, the information on cigarettes only focused on tobacco smoking.
2.2.3. Sexual Practices
Participants were asked to report the number of sex partners in the last 12 months; the type of sex partners, including casual sexual partners (defined as sexual partners having sexual behavior outside of a committed/romantic relationship [17]), one-night stands (a single sexual encounter without further relations between the sexual participants [18]), and sex workers (people who receive money or goods in exchange for sexual services [19]); and whether they had used condoms in the last sexual intercourse within the last 12 months.
2.3. Statistical Analysis
Data analysis was conducted using STATA version 15.0 (Stata Corp. LP, College Station, TX, USA). Descriptive statistics were used to present the socioeconomic characteristics variables, alcohol and tobacco use, and the sexual practices among the participants. A chi-squared test was performed to compare gender differences. A multivariate logistic regression model was used to identify factors associated with risk behaviors, including monthly alcohol use or more, current smoker, and having multiple sex partners in the previous 12 months. The independent variables included socioeconomic characteristics (age, gender, marital status, educational level, occupation, and income level) and current smoking status. To explore a parsimonious regression model, we used stepwise backward selection strategies with the threshold of 0.2 for selecting variables. Statistical significance was acknowledged at a p-value of less than 0.05.
2.4. Ethical Approval
The protocol of this study was reviewed and approved by the Institutional Review Board of Hai Phong University of Medicine and Pharmacy.
3. Results
Table 1 illustrates the information regarding the socioeconomic characteristics and self-rated health status of participants. Half of the participants were male (54.5%), and 82.8% of participants were aged above 30. The majority of patients had a high school education and above (81%) and lived with a spouse/partner (89.2%). Of the participants, 36.6% were freelancers, which was followed by farmer/blue-collar workers and accounted for 34.1%. The mean EQ-VAS score was 74.5 (SD = 13.1).
Table 2 shows the alcohol and tobacco use among CHB patients. It shows that 82.5% of participants reported never using alcohol. Abstaining from alcohol was significantly and statistically higher among women than that of men (97% and 70.4%, respectively). The majority of patients drank from 0 to 2 cups of alcohol in a typical day (95.3%) and participants who drank 3–4 cups or 5–6 cups per day were only males (4.7%). Of the participants, 90.2% reported that they never had six or more drinks, and 11.7% of male participants drank six or more drinks less than monthly. No female patients had an AUDIT-C positive result while the percentage among male patients was 7.4%. Of the participants, 14.5% were current smokers, and the percentage of smoking among males (25.9%) was statistically and significantly higher than that of females (0.7%). The mean number of cigarettes per day was 7.4 (SD = 3.4).
The information regarding sexual practices among CHB patients is presented in Table 3. It shows that 77.2% of participants had sexual intercourse in the last 12 months. About half of the participants had one sex partner in the last 12 months, and 35.4% of male patients had sex with two or more sex partners. The percentage of male participants having sex with casual partners/one-night stands and sex workers was statistically and significantly higher than that of female patients. Approximately one-fifth of participants used condoms when having sex with their spouse/main partner (20.8%), and 66.7% and 74.1% of participants used condoms when having sex with casual partners/one-night stands and sex workers, respectively.
The reduced regression model is presented in Table 4. Female participants were less likely to use alcohol monthly (OR = 0.08; 95%CI = 0.02–0.25), be a current smoker (OR = 0.03; 95%CI = 0.00–0.22), or have multiple sex partners in the last 12 months (OR = 0.04; 95%CI = 0.01–0.13), compared to male participants. White-collar workers were also less likely to have more than one sex partner within the last 12 months (OR = 0.1; 95%CI = 0.01–0.88). Higher monthly individual income was associated with having multiple sex partners within the last 12 months (OR = 9.55; 95%CI = 2.66–34.35). Using alcohol monthly was positively related to being a current smoker (OR = 3.19; 95%CI = 1.3–7.83), and in contrast being a current smoker was also positively associated with monthly alcohol use or more (OR = 3.16; 95%CI = 1.3–7.68).
4. Discussion
The findings of this study contribute to the literature by adding information regarding smoking and drinking status and sexual practices among chronic hepatitis B patients. The participants who were female were less likely to have risky behavior in any dimension (monthly alcohol use, current smoker, or having multiple sex partners in the last 12 months). In terms of sexual practices, white-collar workers had a lower risk of having multiple sex partners in the last 12 months compared to participants who were unemployed, while people who had a higher individual income level were more likely to have multiple sex partners in the last 12 months. Monthly alcohol use was positively associated with being a current smoker, and in contrast, being a current smoker was also related to monthly alcohol use.
The percentage of current smokers in our study was relatively low and lower than the prevalence of smoking among Vietnamese males in the general population [20], as well as in previous studies which were conducted among the HBV population in China and Korea [21,22]. The disproportionate rates of cigarette smoking among CHB patients in other settings can be explained by the differences in socioeconomic status [23], the concurrence of other substance use disorders [13], as well as chronic smoking-related comorbidities [24] since the treatment duration of CHB patients is prolonged. This percentage was also lower than the proportion of smokers among HIV/AIDS patients in the previous study [25]. This higher proportion can be explained by the fact that among people infected with HIV/AIDS, especially those who are drug users, smoking and drug use are complementary by sharing similar cues and withdrawal symptoms [26]. Moreover, given the close relationship between smoking and chronic liver disease for instant hepatocellular carcinoma, smoking screening and support for smoking cessation should be integrated into the HBV treatment program in Vietnam. In another study among rural immigrants in Hanoi, Vietnam, there was a significantly higher likelihood of engaging in smoking and drinking behavior compared to our study [27].
In our study, percentage of people abusing alcohol was relatively lower than what has been reported in previous studies [28,29], which shows the result of the relationship between alcohol consumption and hepatitis B. In comparison with people infected with HIV/AIDS in Vietnam, our result also depicted a lower proportion of drinking alcohol than males receiving antiretroviral therapy treatment [30]. Alcohol is considered as the only cause for alcoholic liver disease, especially chronic viral hepatitis [31]. The progression of chronic liver disease to cirrhosis and hepatocellular carcinoma is significantly impacted by heavy alcohol consumption [13]. Moreover, alcohol use disorder may impair the response to medications when treating chronic hepatitis B [13]. Furthermore, smoking and being male were also considered as risk factors for drinking alcohol on a monthly basis, which is similar to a previous study [28]. People who smoke are more likely to drink alcohol, and by contrast, drinkers tend to smoke more heavily [32]. The co-use of alcohol and cigarette smoking increase the synergistic carcinogenic effects [33].
In this study, we highlighted that the percentage of participants having multiple sex partners was relatively low. However, the proportion of individuals using condoms when having sexual intercourse with casual sex partners or sex workers was low, which is consistent with a previous study of HIV/AIDS patients [34]. HBV can be easily transmitted by having sexual contact with an infected person, and it is also considered as one of the prevalent sexually transmitted infectious diseases, particularly among people who have multiple sex partners [35]. In our study, those working white-collar jobs were less likely to have multiple sex partners in the last 12 months, compared to those who were unemployed. Unemployment can be considered as a risk factor for multiple partners due to a deprived social background and excess free time, which in turn can induce more frequent casual sexual events [36,37].
Several public health suggestions can be drawn from this study. First, along with medical treatment care, more effort should be put in place to thoroughly address smoking and drinking among CHB patients. Since alcohol and smoking abstinence are recommended to slow the progression of chronic liver disease, counseling sessions should be promptly recommended and incorporated into treatment clinics. Education on safe sexual behavior, as well as sufficient distribution of condoms, should be integrated into healthcare services during hepatitis B treatment so that the risk behaviors and virus transmission can be reduced. In addition, safe-sex education should be focused on unemployed CHB patients, as they are more likely to have more than one sex partner.
There were several limitations to our study. Participants answered the questionnaire based on their recall ability regarding the number of cigarettes, alcohol consumption, and the number of sex partners in the last 12 months, which can cause recall bias. Secondly, the sampling method in this study was convenience sampling, which could possibly have decreased the generalizability of our findings. Thirdly, a cross-sectional study design cannot establish the causal relationship between risk factors and outcomes. Therefore, further research and longitudinal data are more appropriate to gain deeper knowledge and provide adequate explanations for the results. Several variables regarding risk factors should be included in future studies, such as injection drug users (IDU); data on the history of tobacco use disorder; type of intercourse—anal, vaginal, or oral; and orientation—heterosexual, bisexual, or homosexual.
5. Conclusions
This study highlights a low level of cigarette smoking and alcohol consumption but a high proportion of participants having sexual intercourse with casual sex partners or sex workers without using a condom. In order to decrease the risk of smoking and alcohol abuse among CHB patients, counseling sessions should be promptly recommended and incorporated into treatment clinics. To reduce virus transmission, education about safe sexual behaviors, along with sufficient condom distribution, should be integrated into healthcare services during CHB treatment.
Characteristics | Male | Female | Total | p-Value | |||
---|---|---|---|---|---|---|---|
n | % | n | % | n | % | ||
Total | 162 | 54.5 | 135 | 45.5 | 297 | 100.0 | |
Age group | |||||||
≤30 years old | 21 | 13 | 30 | 22.2 | 51 | 17.2 | 0.17 |
31–45 years old | 37 | 22.8 | 32 | 23.7 | 69 | 23.2 | |
46–60 years old | 52 | 32.1 | 38 | 28.1 | 90 | 30.3 | |
>60 years old | 52 | 32.1 | 35 | 25.9 | 87 | 29.3 | |
Education | |||||||
<High school | 22 | 13.7 | 34 | 25.4 | 56 | 19 | <0.01 |
High school | 82 | 50.9 | 43 | 32.1 | 125 | 42.4 | |
>High school | 57 | 35.4 | 57 | 42.5 | 114 | 38.6 | |
Marital status | |||||||
Single | 17 | 10.6 | 6 | 4.4 | 23 | 7.8 | 0.07 |
Having spouse/partner | 141 | 87.6 | 123 | 91.1 | 264 | 89.2 | |
Divorce/Widow | 3 | 1.9 | 6 | 4.4 | 9 | 3.0 | |
Occupation | |||||||
Unemployed | 5 | 3.2 | 7 | 5.2 | 12 | 4.1 | 0.52 |
Freelancer | 60 | 38.5 | 46 | 34.3 | 106 | 36.6 | |
White-collar workers | 30 | 19.2 | 29 | 21.6 | 59 | 20.3 | |
Farmer/Blue-collar workers | 51 | 32.7 | 48 | 35.8 | 99 | 34.1 | |
Others | 10 | 6.4 | 4 | 3 | 14 | 4.8 | |
Mean | SD | Mean | SD | Mean | SD | ||
Age | 50.6 | 15.8 | 47.5 | 16.2 | 49.2 | 16.0 | 0.11 |
Monthly personal income (mil VND) | 7.1 | 3.3 | 5.9 | 2.3 | 6.6 | 3.0 | <0.01 |
Self-rate health (0–100) | 73.5 | 14.1 | 75.6 | 11.8 | 74.5 | 13.1 | 0.34 |
Characteristics | Male | Female | Total | p-Value | |||
---|---|---|---|---|---|---|---|
n | % | n | % | n | % | ||
Frequency of alcohol drinking | |||||||
Never | 114 | 70.4 | 131 | 97 | 245 | 82.5 | <0.01 |
Monthly or less | 29 | 17.9 | 4 | 3 | 33 | 11.1 | |
2–4 times a month | 9 | 5.6 | 0 | 0 | 9 | 3 | |
2–3 times a week | 6 | 3.7 | 0 | 0 | 6 | 2 | |
≥four times per week | 4 | 2.5 | 0 | 0 | 4 | 1.3 | |
Standard alcohol drinking in a typical day | |||||||
0–2 cups | 148 | 91.4 | 135 | 100 | 283 | 95.3 | <0.01 |
3–4 cups | 6 | 3.7 | 0 | 0 | 6 | 2 | |
5–6 cups | 8 | 4.9 | 0 | 0 | 8 | 2.7 | |
Frequency of having six or more drinks | |||||||
Never | 134 | 82.7 | 134 | 99.3 | 268 | 90.2 | <0.01 |
Less than monthly | 19 | 11.7 | 1 | 0.7 | 20 | 6.7 | |
Monthly | 5 | 3.1 | 0 | 0 | 5 | 1.7 | |
Weekly | 3 | 1.9 | 0 | 0 | 3 | 1 | |
Daily or almost daily | 1 | 0.6 | 0 | 0 | 1 | 0.3 | |
AUDIT-C positive | 12 | 7.4 | 0 | 0 | 12 | 4.0 | <0.01 |
Current smoking | 42 | 25.9 | 1 | 0.7 | 43 | 14.5 | <0.01 |
Mean | SD | Mean | SD | Mean | SD | ||
AUDIT-C score | 0.9 | 1.7 | 0.0 | 0.2 | 0.5 | 1.4 | <0.01 |
Number of cigarettes per day (n = 43) | 7.4 | 3.4 | 6 | 0.0 | 7.4 | 3.4 | 0.76 |
Characteristics | Male | Female | Total | p-Value | |||
---|---|---|---|---|---|---|---|
n | % | n | % | n | % | ||
Having sexual intercourse in the last 12 months | 132 | 82 | 95 | 71.4 | 227 | 77.2 | 0.03 |
Number of sex partners in the last 12 months | |||||||
0 | 29 | 18.0 | 38 | 28.6 | 67 | 22.8 | <0.01 |
1 | 75 | 46.6 | 90 | 67.7 | 165 | 56.1 | |
≥2 | 57 | 35.4 | 5 | 3.8 | 62 | 21.1 | |
Types of sex partner in the last 12 months | |||||||
Spouse/main partner (n = 227) | 131 | 99.2 | 95 | 100 | 226 | 99.6 | 0.40 |
Casual partner/One-night stand (n = 227) | 29 | 22.0 | 1 | 1.1 | 30 | 13.2 | <0.01 |
Sex worker (n = 226) | 27 | 20.5 | 0 | 0.0 | 27 | 11.9 | <0.01 |
Condom use in the last sexual intercourse within the last 12 months | |||||||
Spouse/main partner (n = 226) | 33 | 25.2 | 14 | 14.7 | 47 | 20.8 | 0.06 |
Casual partner/One-night stand (n = 30) | 19 | 65.5 | 1 | 100 | 20 | 66.7 | 0.47 |
Sex worker (n = 27) | 20 | 74.1 | 0 | 0 | 20 | 74.1 |
Characteristics | Monthly Alcohol Use or More | Current Smoker | Having Multiple Sex Partners in the Last 12 Months | |||
---|---|---|---|---|---|---|
OR | 95%CI | OR | 95%CI | OR | 95%CI | |
Age | 0.96 ** | 0.93; 1.00 | 0.99 | 0.96; 1.03 | 0.92 *** | 0.89; 0.96 |
Gender | ||||||
Male | ||||||
Female | 0.08 *** | 0.02; 0.25 | 0.03 *** | 0.00; 0.22 | 0.04 *** | 0.01; 0.13 |
Education | ||||||
<High school | ||||||
High school | 1.03 | 0.31; 3.47 | 0.68 | 0.21; 2.18 | 2.03 | 0.51; 8.13 |
>High school | 1.81 | 0.46; 7.08 | 0.48 | 0.11; 2.03 | 1.45 | 0.30; 7.06 |
Marital status | ||||||
Single | ||||||
Having spouse/partner | 0.79 | 0.22; 2.86 | 2.02 | 0.44; 9.36 | 0.43 | 0.09; 2.10 |
Divorce/Widow | 0.90 | 0.04; 18.97 | 13.94 * | 0.83; 234.49 | 1.15 | 0.05; 28.53 |
Occupation | ||||||
Unemployed | ||||||
Freelancer | 0.67 | 0.05; 8.72 | 0.18 | 0.02; 1.94 | 0.18 * | 0.03; 1.17 |
White-collar workers | 0.35 | 0.02; 5.07 | 0.11 * | 0.01; 1.39 | 0.10 ** | 0.01; 0.88 |
Farmer/Blue-collar workers | 0.21 | 0.02; 2.85 | 0.09 * | 0.01; 1.06 | 0.30 | 0.04; 2.00 |
Others | 0.23 | 0.01; 7.66 | 0.07 * | 0.00; 1.60 | - | - |
Log monthly individual income | 2.10 | 0.71; 6.19 | 1.58 | 0.50; 4.95 | 9.55 *** | 2.66; 34.35 |
Monthly alcohol use or more | ||||||
No | ||||||
Yes | 3.19 ** | 1.30; 7.83 | 0.72 | 0.27; 1.93 | ||
Current smoker | ||||||
No | ||||||
Yes | 3.16 ** | 1.30; 7.68 |
*** p < 0.01, ** p < 0.05, * p < 0.1. OR: Odd ratio; 95%CI: Confidence Interval.
Author Contributions
Conceptualization, T.T.M.V., T.V.L., A.K.D., G.T.V., L.H.N., B.C.N., B.X.T., C.A.L., C.S.H.H., and R.C.M.H.; formal analysis, A.K.D., G.T.V., L.H.N., B.X.T., C.A.L., C.S.H.H., and R.C.M.H.; investigation, T.T.M.V., T.V.L., and B.C.N.; methodology, A.K.D., B.X.T., C.A.L., C.S.H.H., and R.C.M.H.; project administration, G.T.V., L.H.N., and R.C.M.H.; writing-original draft, T.T.M.V., T.V.L., A.K.D., G.T.V., L.H.N., B.C.N., and B.X.T.; writing-review and editing, A.K.D., G.T.V., L.H.N., T.H.T., B.X.T., C.A.L., C.S.H.H., and R.C.M.H.
Funding
No funding was received for this study.
Conflicts of Interest
The authors declare that they have no conflict of interest.
© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
1. World Health Organization. Global Hepatitis Report 2017; World Health Organization: Geneva, Switzerland, 2017.
2. World Health Organization. Hepatitis B-Factsheet. Available online: http://www.who.int/news-room/fact-sheets/detail/hepatitis-b (accessed on 1 December 2018).
3. Janahi, E.M. Prevalence and risk factors of hepatitis B virus infection in Bahrain, 2000 through 2010. PLoS ONE 2014, 9, e87599.
4. Zhang, H.W.; Yin, J.H.; Li, Y.T.; Li, C.Z.; Ren, H.; Gu, C.Y.; Wu, H.Y.; Liang, X.S.; Zhang, P.; Zhao, J.F.; et al. Risk factors for acute hepatitis B and its progression to chronic hepatitis in Shanghai, China. Gut 2008, 57, 1713-1720. [Green Version]
5. Deng, G.; Zhou, G.; Zhai, Y.; Li, S.; Li, X.; Li, Y.; Zhang, R.; Yao, Z.; Shen, Y.; Qiang, B.; et al. Association of estrogen receptor alpha polymorphisms with susceptibility to chronic hepatitis B virus infection. Hepatology 2004, 40, 318-326.
6. Thio, C.L.; Thomas, D.L.; Karacki, P.; Gao, X.; Marti, D.; Kaslow, R.A.; Goedert, J.J.; Hilgartner, M.; Strathdee, S.A.; Duggal, P.; et al. Comprehensive analysis of class I and class II HLA antigens and chronic hepatitis B virus infection. J. Virol. 2003, 77, 12083-12087.
7. Lavanchy, D. Worldwide epidemiology of HBV infection, disease burden, and vaccine prevention. J. Clin. Virol. 2005, 34 (Suppl. 1), S1-S3.
8. Ferlay, J.; Soerjomataram, I.; Dikshit, R.; Eser, S.; Mathers, C.; Rebelo, M.; Parkin, D.M.; Forman, D.; Bray, F. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int. J. Cancer 2015, 136, E359-E386.
9. Lozano, R.; Naghavi, M.; Foreman, K.; Lim, S.; Shibuya, K.; Aboyans, V.; Abraham, J.; Adair, T.; Aggarwal, R.; Ahn, S.Y.; et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: A systematic analysis for the Global Burden of Disease Study 2010. Lancet 2012, 380, 2095-2128.
10. Killianova, T. Risky Behavior. In Encyclopedia of Behavioral Medicine; Gellman, M.D., Turner, J.R., Eds.; Springer: New York, NY, USA, 2013; pp. 1692-1693.
11. Lavanchy, D.; Kane, M. Global Epidemiology of Hepatitis B Virus Infection; Hepatitis B Virus in Human Diseases. Molecular and Translational Medicine; Humana Press: Cham, Switzerland, 2016; pp. 187-203.
12. Kwon, S.Y.; Lee, C.H. Epidemiology and prevention of hepatitis B virus infection. Korean J. Hepatol. 2011, 17, 87-95.
13. Iida-Ueno, A.; Enomoto, M.; Tamori, A.; Kawada, N. Hepatitis B virus infection and alcohol consumption. World J. Gastroenterol. 2017, 23, 2651-2659.
14. Chuang, S.C.; Lee, Y.C.; Hashibe, M.; Dai, M.; Zheng, T.; Boffetta, P. Interaction between cigarette smoking and hepatitis B and C virus infection on the risk of liver cancer: A meta-analysis. Cancer Epidemiol. Biomarkers Prev. 2010, 19, 1261-1268.
15. Tu, H.A.; Woerdenbag, H.; Riewpaiboon, A.; Kane, S.; Le, D.; Postma, M.; Li, S.C. Cost of Illness of Chronic Hepatitis B Infection in Vietnam. Value in Health Regional Issues 2012, 1, 23-28. [Green Version]
16. Bui, T.T.T.; Tran, T.T.; Nghiem, M.N.; Rahman, P.; Tran, T.T.T.; Dinh, M.N.H.; Le, M.H.; Nguyen, V.V.C.; Thwaites, G.; Rahman, M. Molecular characterization of hepatitis B virus in Vietnam. BMC Infect. Dis. 2017, 17, 601. [Green Version]
17. Lyons, H.A. Subjective adult identity and casual sexual behavior. Adv. Life Course Res. 2015.
18. Wentland, J.; Reissing, E. Casual Sexual Relationships: Identifying Definitions for One Night Stands, Booty Calls, Fuck Buddies, and Friends with Benefits. Can. J. Hum. Sex. 2014, 23, 167-177.
19. World Health Organization. Sex Workers; World Health Organization: Geneva, Switzerland, 2018.
20. Van Minh, H.; Giang, K.B.; Ngoc, N.B.; Hai, P.T.; Huyen, D.T.; Khue, L.N.; Lam, N.T.; Nga, P.T.; Quan, N.T.; Xuyen, N.T. Prevalence of tobacco smoking in Vietnam: Findings from the Global Adult Tobacco Survey 2015. Int. J. Public Health 2017, 62, 121-129.
21. Liu, X.; Baecker, A.; Wu, M.; Zhou, J.Y.; Yang, J.; Han, R.Q.; Wang, P.H.; Jin, Z.Y.; Liu, A.M.; Gu, X.; et al. Interaction between tobacco smoking and hepatitis B virus infection on the risk of liver cancer in a Chinese population. Int. J. Cancer 2018, 142, 1560-1567.
22. Jee, S.H.; Ohrr, H.; Sull, J.W.; Samet, J.M. Cigarette smoking, alcohol drinking, hepatitis B, and risk for hepatocellular carcinoma in Korea. J. Natl. Cancer Inst. 2004, 96, 1851-1856.
23. Tosun, S.; Aygun, O.; Ozdemir, H.O.; Korkmaz, E.; Ozdemir, D. The impact of economic and social factors on the prevalence of hepatitis B in Turkey. BMC Public Health 2018, 18, 649.
24. Altamirano, J.; Bataller, R. Cigarette smoking and chronic liver diseases. Gut 2010, 59, 1159-1162.
25. Nguyen, N.P.; Tran, B.X.; Hwang, L.Y.; Markham, C.M.; Swartz, M.D.; Phan, H.T.; Nong, V.M.; Nguyen, C.T.; Nguyen, A.H.; Latkin, C.A.; et al. Prevalence of cigarette smoking and associated factors in a large sample of HIV-positive patients receiving antiretroviral therapy in Vietnam. PLoS ONE 2015, 10, e0118185.
26. McCool, R.M.; Paschall Richter, K. Why do so many drug users smoke? J. Subst. Abuse Treat. 2003, 25, 43-49.
27. Nguyen, L.T.; Rahman, Z.; Emerson, M.R.; Nguyen, M.H.; Zabin, L.S. Cigarette smoking and drinking behavior of migrant adolescents and young adults in Hanoi, Vietnam. J. Adolesc. Health 2012, 50, S61-S67.
28. Park, B.; Jung, K.W.; Oh, C.M.; Choi, K.S.; Suh, M.; Jun, J.K. Factors associated with alcohol consumption in hepatitis B carriers: A nationwide study in the Republic of Korea. PLoS ONE 2014, 9, e110144.
29. Chevillotte, G.; Durbec, J.P.; Gerolami, A.; Berthezene, P.; Bidart, J.M.; Camatte, R. Interaction between hepatitis b virus and alcohol consumption in liver cirrhosis. An epidemiologic study. Gastroenterology 1983, 85, 141-145.
30. Tran, B.X.; Nguyen, L.T.; Do, C.D.; Nguyen, Q.L.; Maher, R.M. Associations between alcohol use disorders and adherence to antiretroviral treatment and quality of life amongst people living with HIV/AIDS. BMC Public Health 2014, 14, 27.
31. Balasubramanian, S.; Kowdley, K.V. Effect of Alcohol on Viral Hepatitis and Other Forms of Liver Dysfunction. Clin. Liver Dis. 2005, 9, 83-101.
32. Cook, J.W.; Fucito, L.M.; Piasecki, T.M.; Piper, M.E.; Schlam, T.R.; Berg, K.M.; Baker, T.B. Relations of alcohol consumption with smoking cessation milestones and tobacco dependence. J. Consult. Clin. Psychol. 2012, 80, 1075-1085.
33. Pelucchi, C.; Gallus, S.; Garavello, W.; Bosetti, C.; La Vecchia, C. Cancer risk associated with alcohol and tobacco use: Focus on upper aero-digestive tract and liver. Alcohol Res. Health 2006, 29, 193-198.
34. Vu, T.M.T.; Boggiano, V.L.; Tran, B.X.; Nguyen, L.H.; Tran, T.T.; Latkin, C.A.; Ho, C.S.H.; Ho, R.C.M. Sexual Risk Behaviors of Patients with HIV/AIDS over the Course of Antiretroviral Treatment in Northern Vietnam. Int. J. Environ. Res. Public Health 2018, 15, 1106.
35. Inoue, T.; Tanaka, Y. Hepatitis B virus and its sexually transmitted infection-An update. Microb. Cell 2016, 3, 420-437.
36. Caballero-Hoyos, R.; Villasenor-Sierra, A.; Millan-Guerrero, R.; Trujillo-Hernandez, B.; Monarrez-Espino, J. Sexual risk behavior and type of sexual partners in transnational indigenous migrant workers. AIDS Behav. 2013, 17, 1895-1905.
37. Hammarstrom, A.; Janlert, U. Unemployment and sexual risk-taking among adolescents. Scand. J. Soc. Med. 1997, 25, 266-270.
1 Viet-Tiep Friendship Hospital, Hai Phong 180000, Vietnam
2 Hanoi Medical University, Hanoi 100000, Vietnam
3 Institute for Global Health Innovations, Duy Tan University, Da Nang 550000, Vietnam
4 Center of Excellence in Evidence-based Medicine, Nguyen Tat Thanh University, Ho Chi Minh City 700000, Vietnam
5 Center of Excellence in Behavioral Medicine, Nguyen Tat Thanh University, Ho Chi Minh City 700000, Vietnam
6 Institute of Orthopaedic and Trauma Surgery, Vietnam—Germany Hospital, Hanoi 100000 Vietnam
7 Institute for Preventive Medicine and Public Health, Hanoi Medical University, Hanoi 100000 Vietnam
8 Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA
9 Department of Psychological Medicine, National University Hospital, Singapore 119074, Singapore
10 Department of Psychological Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore
* Correspondence: [email protected]; Tel.: +84-982-228-662
† The authors contributed equally.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
According to the World Health Organization, the number of people with positive HBV surface antigen (HBsAg) was as high as 257 million in 2015, while fatality records were estimated to be 887,000 in 2015 alone [2]. [...]there is little literature that contributes to identifying the risk behaviors of Vietnamese chronic HBV patients. [...]this study aimed to explore these risk behaviors (in particular drinking, smoking, and risky sexual behavior) among a cohort of people with chronic HBV in a Vietnamese urban setting, as well as investigating potential associated factors, with the hope of identifying appropriate clinical and policy-level implications. 2. Sexual Practices Participants were asked to report the number of sex partners in the last 12 months; the type of sex partners, including casual sexual partners (defined as sexual partners having sexual behavior outside of a committed/romantic relationship [17]), one-night stands (a single sexual encounter without further relations between the sexual participants [18]), and sex workers (people who receive money or goods in exchange for sexual services [19]); and whether they had used condoms in the last sexual intercourse within the last 12 months. 2.3. A multivariate logistic regression model was used to identify factors associated with risk behaviors, including monthly alcohol use or more, current smoker, and having multiple sex partners in the previous 12 months.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer