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1.
Vaccine ; 39(1): 85-120, 2021 01 03.
Artigo em Inglês | MEDLINE | ID: mdl-31060949

RESUMO

Zika virus, influenza, and Ebola have called attention to the ways in which infectious disease outbreaks can severely - and at times uniquely - affect the health interests of pregnant women and their offspring. These examples also highlight the critical need to proactively consider pregnant women and their offspring in vaccine research and response efforts to combat emerging and re-emerging infectious diseases. Historically, pregnant women and their offspring have been largely excluded from research agendas and investment strategies for vaccines against epidemic threats, which in turn can lead to exclusion from future vaccine campaigns amidst outbreaks. This state of affairs is profoundly unjust to pregnant women and their offspring, and deeply problematic from the standpoint of public health. To ensure that the needs of pregnant women and their offspring are fairly addressed, new approaches to public health preparedness, vaccine research and development, and vaccine delivery are required. This Guidance offers 22 concrete recommendations that provide a roadmap for the ethically responsible, socially just, and respectful inclusion of the interests of pregnant women in the development and deployment of vaccines against emerging pathogens. The Guidance was developed by the Pregnancy Research Ethics for Vaccines, Epidemics, and New Technologies (PREVENT) Working Group - a multidisciplinary, international team of 17 experts specializing in bioethics, maternal immunization, maternal-fetal medicine, obstetrics, pediatrics, philosophy, public health, and vaccine research and policy - in consultation with a variety of external experts and stakeholders.


Assuntos
Epidemias , Doença pelo Vírus Ebola , Vacinas contra Influenza , Vacinas , Infecção por Zika virus , Zika virus , Criança , Feminino , Humanos , Gravidez , Gestantes , Vacinação , Infecção por Zika virus/epidemiologia , Infecção por Zika virus/prevenção & controle
2.
Am J Public Health ; 101(10): 1857-67, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21852635

RESUMO

Despite the recognition of its importance, guidance on community engagement practices for researchers remains underdeveloped, and there is little empirical evidence of what makes community engagement effective in biomedical research. We chose to study the Navrongo Health Research Centre in northern Ghana because of its well-established community engagement practices and because of the opportunity it afforded to examine community engagement in a traditional African setting. Our findings suggest that specific preexisting features of the community have greatly facilitated community engagement and that using traditional community engagement mechanisms limits the social disruption associated with research conducted by outsiders. Finally, even in seemingly ideal, small, and homogeneous communities, cultural issues exist, such as gender inequities, that may not be effectively addressed by traditional practices alone.


Assuntos
Pesquisa Biomédica/organização & administração , Participação da Comunidade , Grupos Focais , Gana , Humanos , Governo Local , Estudos de Casos Organizacionais , Governo Estadual
3.
BMC Med Ethics ; 8: 11, 2007 Oct 26.
Artigo em Inglês | MEDLINE | ID: mdl-17963497

RESUMO

BACKGROUND: Health research is increasingly being conducted on a global scale, particularly in the developing world to address leading causes of morbidity and mortality. While research interest has increased, building scientific capacity in the developing world has not kept pace. This often leads to the export of human tissue (defined broadly) from the developing to the developed world for analysis. These practices raise a number of important ethical issues that require attention. DISCUSSION: In the developed world, there is great heterogeneity of regulatory practices regarding human tissues. In this paper, we outline the salient ethical issues raised by tissue exportation, review the current ethical guidelines and norms, review the literature on what is known empirically about perceptions and practices with respect to tissue exportation from the developing to the developed world, set out what needs to be known in terms of a research agenda, and outline what needs to be done immediately in terms of setting best practices. We argue that the current status of tissue exportation is ambiguous and requires clarification lest problems that have plagued the developed world occur in the context of global heath research with attendant worsening of inequities. Central to solutions to current ethical concerns entail moving beyond concern with individual level consent and embracing a robust interaction with communities engaged in research. CONCLUSION: Greater attention to community engagement is required to understand the diverse issues associated with tissue exportation.


Assuntos
Pesquisa Biomédica/ética , Países Desenvolvidos , Países em Desenvolvimento , Ética em Pesquisa , Propriedade/ética , Coleta de Tecidos e Órgãos/ética , Mercantilização , Países Desenvolvidos/economia , Países em Desenvolvimento/economia , Comitês de Ética em Pesquisa , Saúde Global , Humanos , Índia , Cooperação Internacional , Patentes como Assunto , Pesquisadores , Sujeitos da Pesquisa , Justiça Social , Tonga , Uganda , Populações Vulneráveis
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