Stakeholders' engagement with Ebola therapy research in resource limited settings

被引:12
作者
Folayan, Morenike Oluwatoyin [1 ,2 ]
Brown, Brandon [3 ]
Haire, Bridget [4 ]
Yakubu, Aminu [5 ]
Peterson, Kristin [6 ]
Tegli, Jemee [7 ]
机构
[1] Obafemi Awolowo Univ, Inst Publ Hlth, Ife, Nigeria
[2] Obafemi Awolowo Univ, Dept Child Dent Hlth, Ife, Nigeria
[3] UCR Sch Med, Ctr Hlth Communities, Div Clin Sci, Riverside, CA 92521 USA
[4] UNSW, Kirby Inst, Sydney, NSW, Australia
[5] Fed Secretariat, Fed Minist Hlth, Natl Hlth Res Eth Comm, Abuja, Nigeria
[6] Univ Calif Irvine, Dept Anthropol, Irvine, CA USA
[7] Univ Liberia, UL PIRE Africa Ctr, Monrovia 100010, Liberia
来源
BMC INFECTIOUS DISEASES | 2015年 / 15卷
基金
美国国家科学基金会;
关键词
Ebola; Government; IRB; Communities; Engagement; Research;
D O I
10.1186/s12879-015-0950-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: The current Ebola Virus Disease (EVD) outbreak in West Africa is the largest in history. As of February 18th 2015, 23,258 cases of EVD have been cumulatively reported from Nigeria, Senegal, Guinea, Liberia, Mali, Sierra Leone, Spain, the United Kingdom and the United States of America resulting in more than 9,000 deaths. It is therefore exigent to develop prevention and treatment therapies for EVD. Discussion: Several new EVD treatments are in clinical development at this time. Based on lessons learned, four critical processes need to be implemented before clinical trials begin. First, all global EVD research need to be coordinated to promote data sharing and synergistic overlap, while reducing unnecessary duplication of efforts. The World Health Organization is well-placed to undertake such an endeavor. Second, governments of affected nations where trials are being proposed need to lead discussions regarding immediate access to any proven medications for epidemics. Also, governments need to leverage international resources to support and expand existing national expertise to jointly conduct high-caliber clinical research; and resources must be used to enhance local technical skills and expand existing personnel. Third, ethics committees must review protocols, monitor the research process, and work closely with research scientists to insure the ethical integrity of research throughout the trials. Fourth, community advisory boards (CAB) need to be formed, linked with existing community leadership structures and organized in conjunction with trial implementation. These community structures should work together with ethics committees to facilitate the study design, informed consent process, and study implementation. Summary: We must facilitate communication and mutual understanding between trial communities and research teams, and promote positive collaborations between all stakeholders engaged in EVD research. The community engagement process for EVD research is crucial to address myths and misconceptions, and to promote study volunteers' understanding of the research details. The collaboration between all stakeholders is crucial for continued long term partnership to address EVD outbreak and none of the stakeholders should be left behind in ongoing efforts to develop EVD therapies.
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页数:5
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