Lay persons' perception of the requirements for research in emergency obstetric and newborn care [0.03%]
非医务人员对紧急妇幼保健研究需求的认知
Dan Kabonge Kaye
Dan Kabonge Kaye
Background: Factors that could potentially act as facilitators and barriers to successful recruitment strategies in perinatal clinical trials are not well documented. The objective was to assess lay persons' understanding...
Barriers in implementing the dying patient law: the Israeli experience - a qualitative study [0.03%]
实施安乐死的障碍——以以色列为例：一项定性研究
Avi Zigdon,Rachel Nissanholtz-Gannot
Avi Zigdon
Background: Coping with end-of-life issues is a major challenge for governments and health systems. Despite progress in legislation, many barriers exist to its full implementation. This study is aimed at identifying these...
Communication patterns in the doctor-patient relationship: evaluating determinants associated with low paternalism in Mexico [0.03%]
墨西哥医患关系中的交流模式：评估低父权主义的相关因素
Eduardo Lazcano-Ponce,Angelica Angeles-Llerenas,Rocío Rodríguez-Valentín et al.
Eduardo Lazcano-Ponce et al.
Background: Paternalism/overprotection limits communication between healthcare professionals and patients and does not promote shared therapeutic decision-making. In the global north, communication patterns have been regu...
Qualitative study of comprehension of heritability in genomics studies among the Yoruba in Nigeria [0.03%]
尼日利亚约鲁巴人对基因组学研究中遗传性的理解的定性研究
Rasheed O Taiwo,John Ipadeola,Temilola Yusuf et al.
Rasheed O Taiwo et al.
Background: With growth of genomics research in Africa, concern has arisen about comprehension and adequacy of informed consent given the highly technical terms used in this field. We therefore decided to study whether th...
Mario Tarzi,Malke Asaad,Joudi Tarabishi et al.
Mario Tarzi et al.
Background: The perception of organ donation and brain death among Syrian population has not been previously explored. The goal of this study is to evaluate the attitude and knowledge of organ donation among Syrians and t...
Moral structuring of children during the process of obtaining informed consent in clinical and research settings [0.03%]
临床和研究环境中知情同意获取过程中儿童的伦理建构
Anderson Díaz-Pérez,Elkin Navarro Quiroz,Dilia Esther Aparicio Marenco
Anderson Díaz-Pérez
Background: Informed consent is an important factor in a child's moral structure from which different types of doctor-patient relationships arise. Children's autonomy is currently under discussion in terms of their decent...
Physicians' attitudes in relation to end-of-life decisions in Neonatal Intensive Care Units: a national multicenter survey [0.03%]
新生儿重症监护病房医师有关生命终结期决策态度的全国多中心调查
Ilias Chatziioannidis,Zoi Iliodromiti,Theodora Boutsikou et al.
Ilias Chatziioannidis et al.
Background: End-of-life decisions for neonates with adverse prognosis are controversial and raise ethical and legal issues. In Greece, data on physicians' profiles, motivation, values and attitudes underlying such decisio...
Multicenter Study
BMC medical ethics. 2020 Nov 23;21(1):121. DOI:10.1186/s12910-020-00555-6 2020
Correction to: South Africa's new standard material transfer agreement: proposals for improvement and pointers for implementation [0.03%]
Correction to：南非新的标准材料转让协议：改进建议和实施指南
Donrich W Thaldar,Marietjie Botes,Annelize Nienaber
Donrich W Thaldar
An amendment to this paper has been published and can be accessed via the original article.
Published Erratum
BMC medical ethics. 2020 Nov 20;21(1):120. DOI:10.1186/s12910-020-00547-6 2020
Intensive and pharmacological care in times of COVID-19: A "special ethics" for emergency? [0.03%]
新冠肺炎时期的强化护理与药物治疗：紧急状态下的“特别伦理学”？
Enrico Marinelli,Francesco Paolo Busardò,Simona Zaami
Enrico Marinelli
Background: The Authors have laid out an analysis of Italian COVID-19 confirmed data and fatality rates, pointing out how a dearth of health care resources in northern regions has resulted in hard, ethically challenging d...
Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia [0.03%]
关于在澳大利亚昆士兰开展临床基因组学数据管理的公众期望的调查：与研究人员分享临床检验的基因组数据
Miranda E Vidgen,Sid Kaladharan,Eva Malacova et al.
Miranda E Vidgen et al.
Background: There has been considerable investment and strategic planning to introduce genomic testing into Australia's public health system. As more patients' genomic data is being held by the public health system, there...