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埃及急性乙型和丙型肝炎病毒感染相对风险持续降低的证据,以及甲型肝炎病毒感染负担的增加:2001-2017 年哨点急性病毒性肝炎监测结果比较。

Evidence of sustained reductions in the relative risk of acute hepatitis B and C virus infections, and the increasing burden of hepatitis a virus infection in Egypt: comparison of sentinel acute viral hepatitis surveillance results, 2001-17.

机构信息

Division of Global Health Protection, Center for Global Health, U.S. Centers for Disease Control and Prevention, Cairo, Egypt.

U.S. Naval Medical Research Unit No. 3, Cairo, Egypt.

出版信息

BMC Infect Dis. 2019 Feb 14;19(1):159. doi: 10.1186/s12879-019-3806-9.

DOI:10.1186/s12879-019-3806-9
PMID:30764780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6376689/
Abstract

BACKGROUND

Egypt ranks fifth for the burden of viral hepatitis worldwide. As part of Egypt's renewed national strategy for the elimination of viral hepatitis, surveillance for acute viral hepatitis (AVH) was re-established during 2014-2017 to describe the current epidemiology and associated risk factors, and changes from surveillance conducted during 2001-2004.

METHODS

Patients with suspected AVH were enrolled, completed a questionnaire, and provided blood for testing for hepatitis viruses A (HAV), B (HBV), C (HCV), D, and E (HEV) infections by enzyme-linked immunosorbent assay. Odds ratios and Chi were used to detect differences between hepatitis types by patient characteristics and exposures. Newcombe-Wilson method was used to compare results between surveillance periods 2001-2004 and 2014-2017.

RESULTS

Between 2014 and 2017, among 9321 patients enrolled, 8362 (89.7%) had one or more markers of AVH including 7806 (93.4%) HAV, 252 (3.0%) HCV, 238 (2.8%) HBV, and 31 (0.4%) HEV infection. HAV infection occurred most commonly among children < 16 years age, while HBV infection occurred among ages 16-35 years and HCV infection in ages greater than 45 years. Healthcare-associated exposures were significantly associated with HBV and HCV infections compared to HAV infection including receiving therapeutic injections, surgery, wound suture, or urinary catheter and IV line insertions, while significant lifestyle exposures included exposure to blood outside the healthcare system, IV drug use, or incarceration. Exposures significantly associated with HAV infection were attending nursery or pre-school, contact with person attending nursery or pre-school, having meals outside the home, or contact with HAV case. Compared with AVH surveillance during 2001-2004, there was a significant increase in the proportion of HAV infections from 40.2 to 89.7% (RR = 2.3) with corresponding reductions in the proportions of HBV and HCV infections from 30.0 to 2.8% (RR = 0.1) and 29.8 to 3.0% (RR = 0.1), respectively.

CONCLUSIONS

Healthcare-associated exposures were significantly association with and remain the greatest risk for HBV and HCV infections in Egypt. Additional studies to evaluate factors associated with the reductions in HBV and HCV infections, and cost effectiveness of routine HAV immunization might help Egypt guide and evaluate control measures.

摘要

背景

埃及在全球病毒性肝炎负担中排名第五。作为埃及新的病毒性肝炎消除国家战略的一部分,2014-2017 年重新建立了急性病毒性肝炎(AVH)监测,以描述当前的流行病学和相关危险因素,并与 2001-2004 年监测结果进行比较。

方法

对疑似 AVH 患者进行登记,填写问卷,并采集血液进行酶联免疫吸附试验检测甲型肝炎病毒(HAV)、乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)、丁型肝炎病毒(HDV)和戊型肝炎病毒(HEV)感染。采用比值比和卡方检验检测患者特征和暴露因素与肝炎类型之间的差异。采用 Newcombe-Wilson 方法比较 2001-2004 年和 2014-2017 年监测期间的结果。

结果

2014 年至 2017 年间,在登记的 9321 例患者中,8362 例(89.7%)有 1 种或多种 AVH 标志物,包括 7806 例(93.4%)HAV 感染、252 例(3.0%)HCV 感染、238 例(2.8%)HBV 感染和 31 例(0.4%)HEV 感染。HAV 感染最常见于<16 岁儿童,HBV 感染见于 16-35 岁人群,HCV 感染见于>45 岁人群。与 HAV 感染相比,医疗保健相关暴露,包括接受治疗性注射、手术、伤口缝合或导尿以及静脉置管,与 HBV 和 HCV 感染显著相关,而显著的生活方式暴露包括接触医疗系统以外的血液、静脉吸毒或监禁。与 HAV 感染显著相关的暴露包括入托或上幼儿园、与入托或上幼儿园的人接触、外出就餐或与 HAV 病例接触。与 2001-2004 年 AVH 监测相比,HAV 感染的比例从 40.2%显著增加到 89.7%(RR=2.3),HBV 和 HCV 感染的比例分别从 30.0%降至 2.8%(RR=0.1)和 29.8%降至 3.0%(RR=0.1)。

结论

医疗保健相关暴露与埃及 HBV 和 HCV 感染显著相关,仍是其最大风险因素。进一步研究评估 HBV 和 HCV 感染减少的相关因素以及常规 HAV 免疫接种的成本效益,可能有助于埃及指导和评估控制措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/0b61ed869aef/12879_2019_3806_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/afce45d210b6/12879_2019_3806_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/7416baef10c3/12879_2019_3806_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/314502e427f7/12879_2019_3806_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/0b61ed869aef/12879_2019_3806_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/afce45d210b6/12879_2019_3806_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/7416baef10c3/12879_2019_3806_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/314502e427f7/12879_2019_3806_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b922/6376689/0b61ed869aef/12879_2019_3806_Fig4_HTML.jpg

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