在非洲接种出生剂量乙型肝炎疫苗:5 个国家的评估结果。

Journal of immunological sciences Pub Date : 2018-08-02 Epub Date: 2018-07-02
Edna Moturi, Carole Tevi-Benissan, José E Hagan, Stephanie Shendale, David Mayenga, Daniel Murokora, Minal Patel, Karen Hennessey, Richard Mihigo
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引用次数: 0

摘要

导言:尽管世界卫生组织(WHO)建议接种乙肝疫苗(HepB-BD),但很少有非洲国家在出生时接种乙肝疫苗。出生后 24 小时内接种乙肝疫苗,随后至少接种两剂,对预防围产期乙肝病毒传播的有效率达 90%。本文介绍了为记录五个非洲国家的医护人员在实施乙肝疫苗方面的知识、态度和实践而进行的评估结果:2015年8月至2016年11月期间,在博茨瓦纳、冈比亚、纳米比亚、尼日利亚以及圣多美和普林西比(STP)的公立和私立医疗机构进行了一系列知识、态度和实践评估。免疫接种和产科工作人员通过由访谈者主持的调查问卷收集数据,重点是乙肝疫苗接种的知识、实践和障碍,包括与在家分娩有关的障碍。计算了每个受访医疗机构的乙肝疫苗接种覆盖率:共访问了 78 家医疗机构:结果:共访问了 78 家医疗机构:圣多美和普林西比 5 家(6%)、尼日利亚 23 家(29%)、冈比亚 9 家(12%)、博茨瓦纳 16 家(21%)和纳米比亚 25 家(32%)。冈比亚医疗机构的总覆盖率高达 84%(范围:60-100%),但及时估计值较低,为 7%(16-28%),接受乙肝疫苗治疗的中位天数为 11 天(IQR:6-16 天)。尼日利亚的 HepB-BD 总估计值(23% [范围:12-40%])和及时估计值(13% [范围:2-21%])均较低。博茨瓦纳医疗机构的 HepB-BD 总覆盖率(94% [范围:80-100%])和及时覆盖率(74% [范围:57-88%])较高。由于产妇乙肝病毒 (HBV) 感染情况未记录在分娩登记册中,因此未计算 STP 的覆盖率。纳米比亚的研究不包括覆盖率评估部分。及时进行乙肝疫苗接种的障碍包括:缺乏标准操作程序来界定负责乙肝疫苗接种的工作人员、未将乙肝疫苗接种纳入新生儿基本疫苗包、在产妇出院时接种乙肝疫苗、缺乏日常疫苗接种服务、工作人员对乙肝疫苗接种禁忌症和年龄限制的了解不够充分、缺乏外联计划来帮助设施外出生的婴儿,以及报告工具无法记录乙肝疫苗接种剂量的及时性:这些评估结果表明,工作人员的观念和缺乏外联计划以帮助在医疗机构外出生的婴儿获得基本服务,是及时接种乙肝疫苗的障碍。应对这些挑战可加快乙肝疫苗在非洲的实施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Implementing a Birth Dose of Hepatitis B Vaccine in Africa: Findings from Assessments in 5 Countries.

Implementing a Birth Dose of Hepatitis B Vaccine in Africa: Findings from Assessments in 5 Countries.

Implementing a Birth Dose of Hepatitis B Vaccine in Africa: Findings from Assessments in 5 Countries.

Introduction: Few African countries have introduced a birth dose of hepatitis B vaccine (HepB-BD) despite a World Health Organization (WHO) recommendation. HepB-BD given within 24 hours of birth, followed by at least two subsequent doses, is 90% effective in preventing perinatal transmission of hepatitis B virus. This article describes findings from assessments conducted to document the knowledge, attitudes, and practices surrounding HepB-BD implementation among healthcare workers in five African countries.

Methods: Between August 2015 and November 2016, a series of knowledge, attitude and practices assessments were conducted in a convenience sample of public and private health facilities in Botswana, the Gambia, Namibia, Nigeria, and São Tomé and Príncipe (STP). Data were collected from immunization and maternity staff through interviewer-administered questionnaires focusing on HepB-BD vaccination knowledge, practices and barriers, including those related to home births. HepB-BD coverage was calculated for each visited facility.

Results: A total of 78 health facilities were visited: STP 5 (6%), Nigeria 23 (29%), Gambia 9 (12%), Botswana 16 (21%), and Namibia 25 (32%). Facilities in the Gambia attained high total coverage of 84% (range: 60-100%) but low timely estimates 7% (16-28%) with the median days to receiving HepB-BD of 11 days (IQR: 6-16 days). Nigeria had low total (23% [range: 12-40%]), and timely (13% [range: 2-21%]) HepB-BD estimates. Facilities in Botswana had high total (94% [range: 80-100%]), and timely (74% [range: 57-88%]) HepB-BD coverage. Coverage rates were not calculated for STP because the maternal Hepatitis B virus (HBV) status was not recorded in the delivery registers. The study in Namibia did not include a coverage assessment component. Barriers to timely HepB-BD included absence of standard operating procedures delineating staff responsible for HepB-BD, not integrating HepB-BD into essential newborn packages, administering HepB-BD at the point of maternal discharge from facilities, lack of daily vaccination services, sub-optimal staff knowledge about HepB-BD contraindications and age-limits, lack of outreach programs to reach babies born outside facilities, and reporting tools that did not allow for recording the timeliness of HepB-BD doses.

Discussion: These assessments demonstrate how staff perceptions and lack of outreach programs to reach babies born outside health facilities with essential services are barriers for implementing timely delivery of HepB-BD vaccine. Addressing these challenges may accelerate HepB-BD implementation in Africa.

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