We found that the proportion of men did not differ between the group of patients with virological response and the group without virological response (p 0.05) (Table 3.25). This result is similar to some authors in the world [161]. Univariate logistic regression analysis did not show any association between men and virological response, biochemical response and HBeAg serological response after 12 months of ETV or TDF treatment with p 0.05 (Table 3.29, Table 3.31 and Table 3.33). However, in multivariate logistic regression analysis, there was an association between men and virological response after 12 months of ETV or TDF treatment with OR=3.7; 95%CI: 1.3-10.9 and p=0.02 (Table 3.29).
The mean age of patients with virological response was 42.7 ± 12.7 years, higher than that of patients without virological response was 38.4 ± 13.6 years with p=0.046 (Table 3.25). The study by author Wong GLH (2013) found that the age of patients with virological response after 12 months of ETV treatment was higher than that of patients without virological response, respectively 52 ± 11 (years) compared to 49 ± 12 (years) with p=0.02 [161] and the study by Chon YE (2011) also found that the age of patients with virological response after 12 months of ETV treatment was higher than that of patients without virological response (p=0.865) and the proportion of men was also not different (p=0.973) [41]. Univariate analysis showed that age was not associated with virological response, biochemical response and HBeAg seroconversion after 12 months of treatment with p 0.05 (Table 3.29, Table 3.31 and Table 3.33). This result is similar to that of Lee MH (Korea - 2011), Lee JM (Korea - 2011), Luo J (China - 2013) and Wong GLH (Hong Kong - 2013) who found that in univariate analysis, age and male sex were not associated with virological response [90],[91],[106],[161] and HBeAg seroconversion after 12 months of ETV treatment (p 0.05) [91].
4.4. Limitations of the topic
Maybe you are interested!
-
Epidemiological, molecular biological, clinical, paraclinical characteristics and factors affecting the effectiveness of treatment of chronic hepatitis B virus with antiviral drugs - 21 -
Accounting determines business performance at Thanh Son Company Limited and factors affecting the effectiveness of this accounting work - 21 -
Factors Affecting Listening Effectiveness -
Factors affecting the effectiveness of internal control system in social insurance collection at Binh Duong Provincial Social Insurance - 19 -
Internal control factors affecting the effectiveness of business operations at commercial banks in Vinh Long province - 4
The research topic on 202 patients diagnosed with chronic hepatitis B virus and treated with antiviral drugs at the Department of Infectious Diseases - Bach Mai Hospital has met the 3 research objectives of the topic. However, the topic was conducted at the final hospital of the Northern region, so when coming to the hospital, the majority of patients were seriously ill from other levels or patients from provinces and cities around Hanoi or patients with conditions from provinces and cities coming for examination and treatment, so the data on epidemiological characteristics are only meaningful in the research population, not meaningful in the community and not representative of the community.

CONCLUDE
Studying 202 patients diagnosed with chronic hepatitis B and treated with antiviral drugs at the Department of Infectious Diseases - Bach Mai Hospital from August 2010 to February 2014, we have the following conclusions:
1. Epidemiological and molecular biological characteristics
Patients were distributed in many ages with different occupations, the average age was 39.6 ± 13.9 years old, male accounted for 63.8%. The time from the time of detection of HBV infection to medical examination was mostly within 5 years (74.3%), of which 43.6% of patients detected from 6 - 12 months. The vast majority (98.5%) of patients detected HBV infection when they were over 16 years old. A significant proportion of epidemiological factors of HBV infection in the family were detected (mother was 30.9% and siblings were 53.5%).
Two main genotypes were detected, genotype B and genotype C, of which genotype B accounted for the majority (73.6%). HBV strains with mutations in the PC/BCP region accounted for a high proportion (69.5%) with PC G1896A, BCP A1762T, BCP G1764A mutations accounting for 29.8%; 47.9% and 44.6%, respectively. PC G1896A mutations were higher in genotype B than in genotype C, whereas BCP A1762T, BCP G1764A mutations were higher in genotype C than in genotype B. There was a positive correlation between PC/BCP mutations and age and HBeAg-negative status. The study results did not detect drug-resistant mutations M204I/V, I169T, V173L, L180M, A181T/V, T184G, S202I/G, N236T and M250V in
natural HBV strains as well as HBV strains after 12 months of ETV or TDF treatment. The mean HBV-DNA load of patients was 6.4 ± 1.5 log 10 IU/ml, mainly at 5 - <8 log 10 IU/ml (64.4%).
2. Clinical and paraclinical characteristics
Most patients do not have typical clinical symptoms, in which specific symptoms for hepatitis account for a very low percentage (jaundice, yellow eyes: 10.4%; enlarged liver: 2%; yellow urine: 35.7%). Clinical symptoms do not correspond to the severity.
ALT and HBV-DNA load increased, 22.8% of patients had biochemical flare with ALT increased above 5 ULN.
There was no difference in clinical and paraclinical symptoms (biochemistry, hematology, HBeAg and anti-HBe) between genotypes B and C. The level of increased ALT, positive HBeAg and HBV-DNA was higher in the younger age group.
3. Some factors affecting the effectiveness of antiviral drugs.
Factors that influence the treatment effectiveness in terms of virological response after 12 months include: low HBV-DNA load, negative HBeAg and positive anti-HBe before treatment. No factors affecting the treatment effectiveness in terms of serological response were detected in patients with positive HBeAg. Factors affecting the increase in biochemical response were low HBV-DNA load before treatment.
RECOMMENDATION
1. There needs to be a plan to detect people infected with HBV early so that they can be managed, cared for, treated and monitored periodically.
2. It is necessary to check the HBV infection status of the patient's family members to detect early other family members infected with HBV for timely management, monitoring and treatment.
3. Patients with chronic hepatitis B treated with NA antiviral drugs (ETV or TDF) need to have their HBV-DNA load tested and when there is a viral outbreak, drug resistance mutations with the antiviral drugs being used need to be identified to adjust the appropriate drugs.
LIST OF PUBLISHED RESEARCH WORKS RELATED TO THE THESIS TOPIC
1. Nguyen Van Dung, Bui Thi Lan Anh, Nguyen Thuy Linh, Trinh Thi Ngoc, Nguyen Thi Lan Anh (2013), "Study on mutations in the precore/core gene region of HBV virus in patients with chronic hepatitis B virus at Bach Mai hospital", Journal of Preventive Medicine , Volume XXIII, No. 7 (143), pages 19 - 25.
2. Nguyen Van Dung, Bui Thi Lan Anh, Nguyen Thuy Linh, Do Thi Diem Trinh, Do Huy Duong, Trinh Thi Ngoc, Nguyen Thi Lan Anh (2014), "Clinical and paraclinical epidemiological characteristics of patients with chronic hepatitis B treated at Bach Mai hospital", Preventive Medicine Journal , Volume XXIV, No. 8(153), pages 134 - 142.
REFERENCES
VIETNAMESE
1. Dong Thi Hoai An and Pham Hoang Phiet (2003), "Technique for determining hepatitis B virus genotype by Multiplex PCR in patients with chronic hepatitis B virus infection " , Ho Chi Minh City Medicine . 7, pp. 145-150.
2. Nguyen Dat Anh and Nguyen Thi Huong (2013), Routine tests applied in clinical practice , Medical Publishing House.
3. Mai Hong Bang and Le Huu Song (2008), "Comparative study of the effectiveness of entecavir and lamivudine in the treatment of chronic hepatitis B " , Vietnam Journal of Hepatobiliary Medicine . 8, pp. 6-12.
4. Ministry of Health (2009), "Guidelines for diagnosis and treatment of HIV/AIDS, issued with Decision No. 3003/QD-BYT dated August 19, 2009 of the Minister of Health " .
5. Nguyen Manh Duc (2008), Clinical and paraclinical characteristics and initial comments on the effects of entecavir in the treatment of patients with chronic hepatitis B , Master's thesis in medicine, Hanoi Medical University.
6. Pham Thi Le Hoa, Huynh Trung Hieu and Nguyen Thi Cam Hung (2010), "Precore and core promoter mutations in patients with chronic hepatitis B at Ho Chi Minh City Tropical Hospital " , Ho Chi Minh City Medicine . 14(1), pp. 440-446.
7. Bui Huu Hoang and Pham Hoang Phiet (2003), "Genotype of hepatitis B virus in patients with cirrhosis and primary liver cancer " , Ho Chi Minh City Medicine . 7(1), pp. 145-150.
8. Dinh Da Ly Huong (2007), "Results of 1 year of entecavir treatment for patients with HBeAg negative chronic hepatitis B " , Vietnam Journal of Hepatology . 2, pp. 26-29.
9. Nguyen Cong Long (2007), Study on the relationship between HBV-DNA concentration in blood with genotype and HBeAg in healthy people and chronic liver disease patients HBsAg (+) , Master of Medicine, Hanoi Medical University.
10. Trinh Thi Ngoc and Nguyen Van Dung (2011), "Initial assessment of the effectiveness of tenofovir in the treatment of patients with chronic hepatitis B " , Journal of Practical Medicine . 781, pp. 14-18.
11. Luong Thi Hong Nhung (2009), Determination of genotype, mutations in the pre-core/core promoter gene region and relationship with HBeAg of some HBV strains in patients with chronic hepatitis at the National Institute of Infectious and Tropical Diseases , Master of Medicine, Hanoi Medical University.
12. Phan Thi Phi Phi, Tran Thi Chinh and Truong Mong Long (1993), "Contribution to the study of primary hepatocellular carcinoma in Vietnam. Frequency of HBsAg in serum of healthy people and people with hepatocellular carcinoma " , Vietnamese Medicine . 1(171), pp. 26-30.
13. Tran Ngoc Que (2003), Study on HIV, HBV, HCV infection in blood donors at the Institute of Hematology and Blood Transfusion , Master's thesis in Medicine, Hanoi Medical University.
14. Nguyen Truong Son (2005), Study on the proportion of hepatitis B virus genotypes in some healthy virus carriers and people with chronic liver disease , Master's thesis in Medicine, Hanoi Medical University.
15. Nguyen Truong Son et al. (2006), "Study on the proportion of hepatitis B virus genotypes in some healthy virus carriers and people with chronic liver disease in Northern Vietnam " , Clinical Medicine . 2, pp. 139-142.
ENGLISH
16. Ahn SS et al. (2014), "Tenofovir disoproxil fumarate monotherapy for nucleos(t)ide-naive chronic hepatitis B patients in Korea: data from the clinical practice setting in a single-center cohort " , Clin Mol Hepatol . 20(3), pages 261-6.
17. Alfaresi M. et al. (2010), "Hepatitis B virus genotypes and precore and core mutants in UAE patients " , Virol J. 7, page 160.
18. Alter MJ et al. (1990), "The changing epidemiology of hepatitis B in the United States. Need for alternative vaccination strategies " , JAMA . 263(9), pages 1218-22.
19. Alter MJ and Margolis HS (1990), "The emergence of hepatitis B as a sexually transmitted disease " , Med Clin North Am . 74(6), pages 1529-41.
20. Aung MN et al. (2013), "Chronic hepatitis B prognostic markers other than pre-treatment viral load predict composite treatment outcome " , J Infect Dev Ctries . 7(7), pages 541-9.
21. Baran B. et al. (2013), "Efficacy of tenofovir in patients with Lamivudine failure is not different from that in nucleoside/nucleotide analogue-naive patients with chronic hepatitis B " , Antimicrob Agents Chemother . 57(4), pages 1790-6.
22. Berg T. et al. (2010), "Tenofovir is effective alone or with emtricitabine in adefovir-treated patients with chronic-hepatitis B virus infection " , Gastroenterology . 139(4), pages 1207-17.
23. Blumberg BS, Alter HJ and Visnich S. (1965), "A "New" Antigen in leukemia sera " , JAMA . 191, pages 541-6.
24. Bonino F. et al. (2007), "Predicting response to peginterferon alpha-2a, lamivudine and the two combined for HBeAg-negative chronic hepatitis B " , Gut . 56(5), pages 699-705.





