Anatomical public engagement has the potential to enhance anatomical literacy and patient-provider communication. However, the lack of consensus on effective practices, ethical considerations, and cultural sensitivities poses challenges for anatomists conducting outreach events. This study aimed to explore these issues by examining the international landscape of anatomical public engagement. A multi-language, online survey was distributed to anatomists worldwide with the help of the International Federation of Associations of Anatomists (IFAA), asking open-ended questions about their experiences and perspectives on good and bad public engagement practices, appropriate resources, cultural and accessibility considerations, and training needs. Responses from 50 participants across various continents were analyzed using inductive semantic thematic analysis. Eight major themes were identified, revealing problematic practices, considerations for designing effective outreach, and the importance of adapting outreach to audiences-all of which were underpinned by a need for more guidance. Respondents emphasized the importance of respectful and educational demonstrations, expressed varied opinions on the use of human and animal tissues, and highlighted the need to consider cultural norms and accessibility. Interactive, hands-on experiences were favored over didactic engagement methods. The findings highlight the need for establishing defined standards, ethical frameworks, and training programs to support anatomists in delivering inclusive and culturally aware outreach activities. Future research should explore public perspectives on effective anatomy engagement and address the identified gaps in training and resources. This study provides valuable insights for developing such guidelines and training programs to promote effective and ethical public engagement in anatomy.
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J Prof Nurs
March 2025
University at Buffalo School of Nursing, 3435 Main St. (Wende Hall), Buffalo, NY 14214, United States of America; Farmingdale State College Department of Nursing, 2350 Broadhollow Rd. (Gleeson Hall), Farmingdale, NY 11735, United States of America. Electronic address:
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Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Melbourne, Victoria, Australia.
Introduction: Early childhood education and intervention programmes can improve the developmental outcomes for priority groups of children. However, in Australia, a culturally responsive developmental outcome measure that has been validated for use with Aboriginal and Torres Strait Islander children is required to effectively evaluate impact.The Ages and Stages Questionnaire-Steps for Measuring Aboriginal Child Development (ASQ-STEPS) has been developed to fill this gap.
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Genome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), Singapore
Objectives: To explore husbands' views on breast cancer screening, risk-based screening and their role in influencing their wives' health-seeking behaviours.
Design: Qualitative focus group discussion (FGD) supplemented by quantitative data from a cohort study using a structured questionnaire.
Setting: This study was conducted in a community-based setting, with participants recruited online through non-profit organisations via social media and email.
BMJ Open
March 2025
Institute for Health Research, University of Bedfordshire Faculty of Health and Social Sciences, Luton, UK.
Objectives: To explore the barriers to conversations about deceased organ donation among adults living in the UK.
Design: Systematic review with narrative synthesis.
Data Sources: PubMed, MEDline via OVID, APA PsycInfo via EBSCO, Web of Science via Clarivate and Scopus via Elsevier, covering studies that were published between January 2006 and December 2023.
BMJ Open
March 2025
Division of Paediatric Medicine and Paediatric Outcomes Research Team (PORT), The Hospital for Sick Children, Toronto, Ontario, Canada.
Objectives: Authentic patient and family engagement in child health research is defined as researchers working in partnership with patients and families on all aspects of the research process, including refining the research question, tailoring the intervention, devising study procedures and disseminating study findings. While there is good evidence of a positive impact of patient engagement on the research process, on research teams and on patient partners, there are few empirical data on the impact of patient and family engagement on research quality and dissemination. We conducted a systematic review to compare research quality and dissemination metrics for paediatric randomised controlled trials (RCTs) that engaged patients and families in the research process with trials that did not.
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