Skip to main content

Articles

Page 8 of 17

  1. Biobanks are considered to be key infrastructures for research development and have generated a lot of debate about their ethical, legal and social implications (ELSI). While the focus has been on human genomi...

    Authors: Kim H. Chuong, David M. Hwang, D. Elizabeth Tullis, Valerie J. Waters, Yvonne C. W. Yau, David S. Guttman and Kieran C. O’Doherty

    Citation: BMC Medical Ethics 2017 18:1

    Content type: Debate

    Published on:

  2. Norway has extensive and detailed legal requirements and guidelines concerning involvement of next of kin (NOK) during involuntary hospital treatment of seriously mentally ill patients. However, we have little...

    Authors: Reidun Førde, Reidun Norvoll, Marit Helene Hem and Reidar Pedersen

    Citation: BMC Medical Ethics 2016 17:76

    Content type: Research article

    Published on:

  3. Recent rapid technological and medical advance has more than ever before brought to the fore a spectrum of problems broadly categorized under the umbrella of ‘ethics of human enhancement’. Some of the most con...

    Authors: Ognjen Arandjelović

    Citation: BMC Medical Ethics 2016 17:75

    Content type: Correspondence

    Published on:

  4. New technologies are transforming and reconfiguring the boundaries between patients, research participants and consumers, between research and clinical practice, and between public and private domains. From pe...

    Authors: Michael Morrison, Donna Dickenson and Sandra Soo-Jin Lee

    Citation: BMC Medical Ethics 2016 17:74

    Content type: Editorial

    Published on:

  5. The past 10 years have witnessed a significant growth in sharing of health data for secondary uses. Alongside this there has been growing interest in the public acceptability of data sharing and data linkage p...

    Authors: Mhairi Aitken, Jenna de St. Jorre, Claudia Pagliari, Ruth Jepson and Sarah Cunningham-Burley

    Citation: BMC Medical Ethics 2016 17:73

    Content type: Research article

    Published on:

  6. As part of the research project “End-of-life Communication in Nursing Homes. Patient Preferences and Participation”, we have studied how Advance Care Planning (ACP) is carried out in eight Norwegian nursing ho...

    Authors: Lisbeth Thoresen and Lillian Lillemoen

    Citation: BMC Medical Ethics 2016 17:72

    Content type: Research article

    Published on:

  7. Internationally, clinical ethics support has yet to be implemented systematically in community health and care services. A large-scale Norwegian project (2007–2015) attempted to increase ethical competence in ...

    Authors: Morten Magelssen, Elisabeth Gjerberg, Reidar Pedersen, Reidun Førde and Lillian Lillemoen

    Citation: BMC Medical Ethics 2016 17:70

    Content type: Research article

    Published on:

  8. Resuscitation and treatment of critically ill newborn infants is associated with relatively high mortality, morbidity and cost. Guidelines relating to resuscitation have traditionally focused on the best inter...

    Authors: C. Arora, J. Savulescu, H. Maslen, M. Selgelid and D. Wilkinson

    Citation: BMC Medical Ethics 2016 17:69

    Content type: Research article

    Published on:

  9. Healthcare ethics is neglected in clinical practice in LMICs (Low and Middle Income Countries) such as Nepal. The main objective of this study was to assess the current status of knowledge, attitude and practi...

    Authors: Samaj Adhikari, Kumar Paudel, Arja R. Aro, Tara Ballav Adhikari, Bipin Adhikari and Shiva Raj Mishra

    Citation: BMC Medical Ethics 2016 17:68

    Content type: Research article

    Published on:

  10. A child is a developing person with evolving capacities that include autonomy, mental (decisional) capacity and capacity to assume responsibility. Hence, children are entitled to participatory (autonomy) right...

    Authors: Wandile Ganya, Sharon Kling and Keymanthri Moodley

    Citation: BMC Medical Ethics 2016 17:66

    Content type: Debate

    Published on:

  11. When conducting research with Indigenous populations consent should be sought from both individual participants and the local community. We aimed to search and summarise the literature about methods for seekin...

    Authors: Emily F. M. Fitzpatrick, Alexandra L. C. Martiniuk, Heather D’Antoine, June Oscar, Maureen Carter and Elizabeth J. Elliott

    Citation: BMC Medical Ethics 2016 17:65

    Content type: Research article

    Published on:

  12. Ethical and regulatory guidance on the collection and use of human biospecimens (HBS) for research forms an essential component of national health systems in Sub-Saharan Africa (SSA), where rapid advances in g...

    Authors: Francis Barchi and Madison T. Little

    Citation: BMC Medical Ethics 2016 17:64

    Content type: Research article

    Published on:

  13. The focus on translational research in clinical trials has the potential to generate clinically relevant genetic data that could have importance to patients. This raises challenging questions about communicati...

    Authors: David J. Pulford, Philipp Harter, Anne Floquet, Catherine Barrett, Dong Hoon Suh, Michael Friedlander, José Angel Arranz, Kosei Hasegawa, Hiroomi Tada, Peter Vuylsteke, Mansoor R. Mirza, Nicoletta Donadello, Giovanni Scambia, Toby Johnson, Charles Cox, John K. Chan…

    Citation: BMC Medical Ethics 2016 17:63

    Content type: Research article

    Published on:

  14. Conducting research during or in the aftermath of disasters poses many specific practical and ethical challenges. This is particularly the case with research involving human subjects. The extraordinary circums...

    Authors: Signe Mezinska, Péter Kakuk, Goran Mijaljica, Marcin Waligóra and Dónal P. O’Mathúna

    Citation: BMC Medical Ethics 2016 17:62

    Content type: Research article

    Published on:

  15. Advance care planning is a voluntary process whereby individual preferences, values and beliefs are used to aid a person in planning for end-of-life care. Currently, there is no local instrument to assess an i...

    Authors: Pauline Siew Mei Lai, Salinah Mohd Mudri, Karuthan Chinna and Sajaratulnisah Othman

    Citation: BMC Medical Ethics 2016 17:61

    Content type: Research article

    Published on:

  16. Pediatric biobanking is considered important for generating biomedical knowledge and improving (pediatric) health care. However, the inclusion of children’s samples in biobanks involves specific ethical issues...

    Authors: Noor A. A. Giesbertz, Karen Melham, Jane Kaye, Johannes J. M. van Delden and Annelien L. Bredenoord

    Citation: BMC Medical Ethics 2016 17:59

    Content type: Debate

    Published on:

  17. Returning neuroimaging incidental findings (IF) may create a challenge to research participants’ health literacy skills as they must interpret and make appropriate healthcare decisions based on complex radiolo...

    Authors: Caitlin E. Rancher, Jody M. Shoemaker, Linda E. Petree, Mark Holdsworth, John P. Phillips and Deborah L. Helitzer

    Citation: BMC Medical Ethics 2016 17:58

    Content type: Research article

    Published on:

  18. Biobanks are precariously situated at the intersection of science, genetics, genomics, society, ethics, the law and politics. This multi-disciplinarity has given rise to a new discourse in health research invo...

    Authors: Keymanthri Moodley and Shenuka Singh

    Citation: BMC Medical Ethics 2016 17:57

    Content type: Research article

    Published on:

  19. Cervical cancer disproportionately burdens disadvantaged women. Organised cervical screening aims to make cancer prevention available to all women in a population, yet screening uptake and cancer incidence and...

    Authors: Jane H. Williams and Stacy M. Carter

    Citation: BMC Medical Ethics 2016 17:56

    Content type: Research article

    Published on:

  20. Health research increasingly relies on organized collections of health data and biological samples. There are many types of sample and data collections that are used for health research, though these are colle...

    Authors: Kieran C. O’Doherty, Emily Christofides, Jeffery Yen, Heidi Beate Bentzen, Wylie Burke, Nina Hallowell, Barbara A. Koenig and Donald J. Willison

    Citation: BMC Medical Ethics 2016 17:54

    Content type: Review

    Published on:

  21. Avon Longitudinal Study of Parents and Children (ALSPAC) is a birth cohort study within which the Project to Enhance ALSPAC through Record Linkage (PEARL) was established to enrich the ALSPAC resource through ...

    Authors: Suzanne Audrey, Lindsey Brown, Rona Campbell, Andy Boyd and John Macleod

    Citation: BMC Medical Ethics 2016 17:53

    Content type: Research article

    Published on:

  22. Respect for confidentiality is important to safeguard the well-being of patients and ensure the confidence of society in the doctor-patient relationship. The aim of our study is to examine real situations in w...

    Authors: Cristina M. Beltran-Aroca, Eloy Girela-Lopez, Eliseo Collazo-Chao, Manuel Montero-Pérez-Barquero and Maria C. Muñoz-Villanueva

    Citation: BMC Medical Ethics 2016 17:52

    Content type: Research article

    Published on:

  23. As in other countries, the traditional doctor-patient relationship in the Japanese healthcare system has often been characterised as being of a paternalistic nature. However, in recent years there has been a g...

    Authors: Victoria Coathup, Harriet J. A. Teare, Jusaku Minari, Go Yoshizawa, Jane Kaye, Masanori P. Takahashi and Kazuto Kato

    Citation: BMC Medical Ethics 2016 17:51

    Content type: Research article

    Published on:

  24. Experience with open disclosure and its study are restricted to certain western countries. In addition, there are concerns that open disclosure may be less suitable in non-western countries. The present study ...

    Authors: Minsu Ock, Hyun Joo Kim, Min-Woo Jo and Sang-il Lee

    Citation: BMC Medical Ethics 2016 17:50

    Content type: Research article

    Published on:

  25. Few studies have identified the willingness rate of developing countries population to be enrolled in clinical trials.

    Authors: Wahid Bouida, Mohamed Habib Grissa, Asma Zorgati, Kaouthar Beltaief, Hamdi Boubaker, Asma Sriha, Riadh Boukef and Semir Nouira

    Citation: BMC Medical Ethics 2016 17:47

    Content type: Research article

    Published on:

  26. In most Anglophone nations, policy and law increasingly foster an autonomy-based model, raising issues for large numbers of people who fail to fit the paradigm, and indicating problems in translating practical...

    Authors: Giles Birchley, Kerry Jones, Richard Huxtable, Jeremy Dixon, Jenny Kitzinger and Linda Clare

    Citation: BMC Medical Ethics 2016 17:46

    Content type: Research article

    Published on:

  27. Moral Case Deliberation is a specific form of bioethics education fostering professionals’ moral competence in order to deal with their moral questions. So far, few studies focus in detail on Moral Case Delibe...

    Authors: Margreet Stolper, Bert Molewijk and Guy Widdershoven

    Citation: BMC Medical Ethics 2016 17:45

    Content type: Research article

    Published on:

  28. Maximizing comprehension is a major challenge for informed consent processes in low-literacy and resource-limited settings. Application of rapid qualitative assessments to improve the informed consent process ...

    Authors: Adamu Addissie, Serebe Abay, Yeweyenhareg Feleke, Melanie Newport, Bobbie Farsides and Gail Davey

    Citation: BMC Medical Ethics 2016 17:40

    Content type: Research article

    Published on:

  29. Biobanks have been heralded as essential tools for translating biomedical research into practice, driving precision medicine to improve pathways for global healthcare treatment and services. Many nations have ...

    Authors: Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V. Campbell, Calvin W. L. Ho, Kazuto Kato, Jusaku Minari, Chih-hsing Ho, Colin Mitchell, Fruzsina Molnár-Gábor, Margaret Otlowski, Daniel Thiel, Stephanie M. Fullerton and Tess Whitton

    Citation: BMC Medical Ethics 2016 17:39

    Content type: Review

    Published on:

  30. In the Netherlands, consent from relatives is obligatory for post mortal donation. This study explored the perspectives of relatives regarding the request for consent for donation in cases without donor regist...

    Authors: Jack de Groot, Maria van Hoek, Cornelia Hoedemaekers, Andries Hoitsma, Hans Schilderman, Wim Smeets, Myrra Vernooij-Dassen and Evert van Leeuwen

    Citation: BMC Medical Ethics 2016 17:38

    Content type: Research article

    Published on:

  31. Over the past 25 years, there has been growing recognition of the importance of studying the Ethical, Legal and Social Implications (ELSI) of genetic and genomic research. A large investment into ELSI research...

    Authors: Jessica Bell, Mirko Ancillotti, Victoria Coathup, Sarah Coy, Tessel Rigter, Travis Tatum, Jasjote Grewal, Faruk Berat Akcesme, Jovana Brkić, Anida Causevic-Ramosevac, Goran Milovanovic, Marianna Nobile, Cristiana Pavlidis, Teresa Finlay and Jane Kaye

    Citation: BMC Medical Ethics 2016 17:37

    Content type: Debate

    Published on:

  32. Continuous deep sedation at the end of life is a practice that has been the topic of considerable ethical debate, for example surrounding its perceived similarity or dissimilarity with physician-assisted dying...

    Authors: Kasper Raus, Kenneth Chambaere and Sigrid Sterckx

    Citation: BMC Medical Ethics 2016 17:36

    Content type: Debate

    Published on:

  33. While evaluation of ethical aspects in health technology assessment (HTA) has gained much attention during the past years, the integration of ethics in HTA practice still presents many challenges. In response ...

    Authors: Nazila Assasi, Jean-Eric Tarride, Daria O’Reilly and Lisa Schwartz

    Citation: BMC Medical Ethics 2016 17:34

    Content type: Research article

    Published on:

  34. The language of “participant-driven research,” “crowdsourcing” and “citizen science” is increasingly being used to encourage the public to become involved in research ventures as both subjects and scientists. ...

    Authors: J. Patrick Woolley, Michelle L. McGowan, Harriet J. A. Teare, Victoria Coathup, Jennifer R. Fishman, Richard A. Settersten Jr., Sigrid Sterckx, Jane Kaye and Eric T. Juengst

    Citation: BMC Medical Ethics 2016 17:33

    Content type: Debate

    Published on:

  35. Moral case deliberation (MCD) as a form of clinical ethics support is usually implemented in health care institutions and educational programs. While there is no previous research on the use of clinical ethics...

    Authors: Wike Seekles, Guy Widdershoven, Paul Robben, Gonny van Dalfsen and Bert Molewijk

    Citation: BMC Medical Ethics 2016 17:31

    Content type: Research article

    Published on:

  36. We have examined healthcare staff attitudes of toward a blogging cancer patient who publishes critical posts about her treatment and their possible effect on patient-staff relationships and treatment decisions.

    Authors: Niels Lynøe, Sara NattochDag, Magnus Lindskog and Niklas Juth

    Citation: BMC Medical Ethics 2016 17:30

    Content type: Research article

    Published on:

  37. Research ethics review is a critical aspect of the research governance framework for human subjects research. This usually requires that research protocols be submitted to a research ethics committee (REC) for...

    Authors: Odile Ouwe Missi Oukem-Boyer, Nchangwi Syntia Munung and Godfrey B. Tangwa

    Citation: BMC Medical Ethics 2016 17:27

    Content type: Research article

    Published on:

2019 Journal Metrics

  • Citation Impact
    2.451 - 2-year Impact Factor
    2.88 - 5-year Impact Factor
    1.705 - Source Normalized Impact per Paper (SNIP)
    1.15 - SCImago Journal Rank (SJR)
     

    Usage 
    715,939 downloads
     

    Social Media Impact
    3554 mentions