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Clinical course and perinatal transmission of chronic hepatitis B during pregnancy: A real-world prospective cohort study.
Chen, Zhi-Xian; Gu, Gui-Fang; Bian, Zhao-Lian; Cai, Wei-Hua; Shen, Yi; Hao, Yan-Li; Zhang, Sheng; Shao, Jian-Guo; Qin, Gang.
Affiliation
  • Chen ZX; Department of Clinical Pharmacy, Nantong Health College of Jiangsu Province, China. Electronic address: ntchenzhixian@hotmail.com.
  • Gu GF; Department of Obstetrics and Gynaecology, Nantong Third People's Hospital, Nantong University, Jiangsu, China. Electronic address: jj6668@126.com.
  • Bian ZL; Center for Liver Diseases, Nantong Third People's Hospital, Nantong University, Jiangsu, China. Electronic address: bianzhaolian1998@ntu.edu.cn.
  • Cai WH; Center for Liver Diseases, Nantong Third People's Hospital, Nantong University, Jiangsu, China. Electronic address: ntcty@sina.com.
  • Shen Y; Department of Epidemiology and Biostatistics, School of Public Health, Nantong University, Jiangsu, China. Electronic address: sunny@ntu.edu.cn.
  • Hao YL; Center for Liver Diseases, Nantong Third People's Hospital, Nantong University, Jiangsu, China. Electronic address: 863157552@qq.com.
  • Zhang S; Department of Epidemiology and Biostatistics, School of Public Health, Nantong University, Jiangsu, China. Electronic address: 1372170612@qq.com.
  • Shao JG; Center for Liver Diseases, Nantong Third People's Hospital, Nantong University, Jiangsu, China. Electronic address: shaojianguo4144@ntu.edu.cn.
  • Qin G; Center for Liver Diseases, Nantong Third People's Hospital, Nantong University, Jiangsu, China; Department of Epidemiology and Biostatistics, School of Public Health, Nantong University, Jiangsu, China. Electronic address: tonygqin@ntu.edu.cn.
J Infect ; 75(2): 146-154, 2017 08.
Article in En | MEDLINE | ID: mdl-28551372
ABSTRACT

OBJECTIVE:

To determine the clinical course and perinatal transmission of chronic hepatitis B during pregnancy in a real life setting.

METHODS:

A total of 221 singleton pregnant women with detectable HBV-DNA levels (≥103 copies/mL) were enrolled during January 2011 to June 2015. Forty-three high viraemic patients (≥106 copies/mL) received telbivudine in the 2nd or 3rd trimester according to their intention, while 89 high viraemic and 79 low viraemic (≥103 and <106 copies/mL) patients were the control cohorts. Primary endpoint was the pregnancy outcomes and secondary endpoint the perinatal transmission including intrauterine infection, immunoprophylaxis failure and occult infection.

RESULTS:

In all, 209 patients completed pregnancy with 209 infants, while 2 in telbivudine-treated cohort had unexplained late stillbirths. Twenty-nine (70.7%) of telbivudine-treated patients and 3 (3.4%) of untreated high viraemic controls achieved undetectable HBV-DNA levels prior delivery. At 7 months postpartum, immunoprophylaxis failure was significantly lower (2.4%) in telbivudine-treated cohort, compared with 16.9% and 10.1% in untreated high and low viraemic cohorts, respectively.

CONCLUSIONS:

Low viraemic patients may also need antiviral therapy since they bear moderate risk for perinatal transmission of HBV. However, more multicenter, large-scale studies are required before antepartum antiviral therapy is routinely recommended in patients with detectable viral loads.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Complications, Infectious / Pregnancy Outcome / Infectious Disease Transmission, Vertical / Hepatitis B, Chronic Type of study: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: J Infect Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Complications, Infectious / Pregnancy Outcome / Infectious Disease Transmission, Vertical / Hepatitis B, Chronic Type of study: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: J Infect Year: 2017 Document type: Article