Getting the ethics right regarding research in the emergency setting: lessons from the PolyHeme study.

PubWeight™: 0.82‹?›

🔗 View Article (PMID 18018997)

Published in Kennedy Inst Ethics J on June 01, 2007

Authors

Neal W Dickert1, Jeremy Sugarman

Author Affiliations

1: Osler Medicine Residency Program, Johns Hopkins Hospital, Baltimore, MD, USA.

Articles by these authors

(truncated to the top 100)

The limitations of "vulnerability" as a protection for human research participants. Am J Bioeth (2004) 14.06

Patients' views on identifiability of samples and informed consent for genetic research. Am J Bioeth (2008) 5.73

Dealing with the long-term social implications of research. Am J Bioeth (2011) 5.41

Research ethics recommendations for whole-genome research: consensus statement. PLoS Biol (2008) 5.24

Ethics and best practice guidelines for training experiences in global health. Am J Trop Med Hyg (2010) 5.05

Medical and nursing students' television viewing habits: potential implications for bioethics. Am J Bioeth (2008) 4.94

A national survey of provisions in clinical-trial agreements between medical schools and industry sponsors. N Engl J Med (2002) 4.42

Oversight of human participants research: identifying problems to evaluate reform proposals. Ann Intern Med (2004) 3.58

Ethical goals of community consultation in research. Am J Public Health (2005) 3.46

The cost of institutional review boards in academic medical centers. N Engl J Med (2005) 3.06

Bioethics consultation in the private sector. Hastings Cent Rep (2002) 3.01

The inescapable relevance of bioethics for the practicing clinician. Chest (2006) 2.70

New ISSCR guidelines underscore major principles for responsible translational stem cell research. Cell Stem Cell (2008) 2.61

Protecting research subjects under the waiver of informed consent for emergency research: experiences with efforts to inform the community. Ann Emerg Med (2003) 2.56

Ethical considerations for short-term experiences by trainees in global health. JAMA (2008) 2.48

The Presidential Bioethics Commission's database of human subjects research. IRB (2013) 1.98

Universal antiretroviral therapy for HIV infection: should US treatment guidelines be applied to resource-limited settings? Clin Infect Dis (2013) 1.92

Informed consent in a clinical trial of a novel treatment for rheumatoid arthritis. Arthritis Rheum (2003) 1.86

The OHRP and SUPPORT. N Engl J Med (2013) 1.78

Ethics in human subjects research: do incentives matter? J Med Philos (2004) 1.70

Measuring trust in medical researchers. Med Care (2006) 1.69

Study of the media's potential influence on prospective research participants' understanding of and motivations for participation in a high-profile phase I trial. J Clin Oncol (2002) 1.64

What patients say about medical research. IRB (1999) 1.63

Views of potential research participants on financial conflicts of interest: barriers and opportunities for effective disclosure. J Gen Intern Med (2006) 1.63

Back to the rough ground: working in international HIV prevention as ethical debates continue. IRB (2003) 1.62

Do patients treated with dignity report higher satisfaction, adherence, and receipt of preventive care? Ann Fam Med (2005) 1.62

Permission and assent for clinical research in pediatric anesthesia. Anesth Analg (2002) 1.56

Ethical and practical issues associated with aggregating databases. PLoS Med (2008) 1.53

Community hospital oversight of clinical investigators' financial relationships. IRB (2009) 1.51

Patient reactions to confidentiality, liability, and financial aspects of informed consent in cardiology research. Circ Cardiovasc Qual Outcomes (2010) 1.50

Applying justice in clinical trials for diverse populations. Clin Trials (2007) 1.46

Policies of academic medical centers for disclosing financial conflicts of interest to potential research participants. Acad Med (2006) 1.43

Untying the Gordian knot: policies, practices, and ethical issues related to banking of umbilical cord blood. J Clin Invest (2005) 1.43

Implications of universal screening for HIV infection. BMJ (2013) 1.37

The Bio-PIN: a concept to improve biobanking. Nat Rev Cancer (2011) 1.32

Beyond "compliance": the role of institutional culture in promoting research integrity. Acad Med (2010) 1.30

Fertility patients' views about frozen embryo disposition: results of a multi-institutional U.S. survey. Fertil Steril (2008) 1.30

Preventive misconception: its nature, presence, and ethical implications for research. Am J Prev Med (2007) 1.30

Regulatory challenges for the resuscitation outcomes consortium. Circulation (2008) 1.26

Variability in the costs of institutional review board oversight. Acad Med (2006) 1.25

Toward protecting the safety of participants in clinical trials. Control Clin Trials (2003) 1.23

Effects of disclosing financial interests on attitudes toward clinical research. J Gen Intern Med (2008) 1.23

Improving informed consent: the medium is not the message. IRB (2004) 1.23

Controversy and quality improvement: lingering questions about ethics, oversight, and patient safety research. Jt Comm J Qual Patient Saf (2008) 1.22

Ethical issues in identifying and recruiting participants for familial genetic research. Am J Med Genet A (2004) 1.20

Disclosing conflicts of interest in clinical research: views of institutional review boards, conflict of interest committees, and investigators. J Law Med Ethics (2006) 1.19

An intervention to improve cancer patients' understanding of early-phase clinical trials. IRB (2009) 1.18

Disclosure of cancer diagnosis and prognosis in Northern Tanzania. Soc Sci Med (2003) 1.17

Developing ethics guidance for HIV prevention research: the HIV Prevention Trials Network approach. J Med Ethics (2010) 1.15

Conducting empirical research on informed consent: challenges and questions. IRB (2004) 1.14

Challenges to effective research in acute trauma resuscitation: consent and endpoints. Shock (2011) 1.13

Establishing HIV treatment as prevention in the HIV Prevention Trials Network 052 randomized trial: an ethical odyssey. Clin Trials (2012) 1.11

Reflecting on short-term international service-learning trips. Acad Med (2013) 1.08

Purpose and benefits of early phase cancer trials: what do oncologists say? What do patients hear? J Empir Res Hum Res Ethics (2008) 1.08

Principles, organization, and operation of a DNA bank for clinical trials: a Department of Veterans Affairs cooperative study. Control Clin Trials (2002) 1.08

Factors that affect infertility patients' decisions about disposition of frozen embryos. Fertil Steril (2006) 1.07

Disclosure of financial relationships to participants in clinical research. N Engl J Med (2009) 1.06

Hematopoietic growth factors--use in normal blood and stem cell donors: clinical and ethical issues. Transfusion (2008) 1.06

Ethics, oversight and quality improvement initiatives. Qual Saf Health Care (2010) 1.04

Impact of percutaneous coronary intervention performance reporting on cardiac resuscitation centers: a scientific statement from the American Heart Association. Circulation (2013) 1.04

Pre-counseling education materials for BRCA testing: does tailoring make a difference? Genet Test (2002) 1.04

Developing model language for disclosing financial interests to potential clinical research participants. IRB (2007) 1.03

Comparison of conflict of interest policies and reported practices in academic medical centers in the United States. Account Res (2007) 1.03

Ethics guidance for HIV prevention trials. BMJ (2003) 1.03

Position statement on the provision and procurement of human eggs for stem cell research. Cell Stem Cell (2013) 1.02

India's new policy to protect research participants. BMJ (2013) 1.01

Ethical considerations in determining standard of prevention packages for HIV prevention trials: examining PrEP. Dev World Bioeth (2013) 0.96

Who refuses enrollment in cardiac clinical trials? Clin Trials (2007) 0.96

Ethical challenges in international HIV prevention research. Account Res (2004) 0.94

Determining the costs of Institutional Review Boards. IRB (2007) 0.94

Consulting communities when patients cannot consent: a multicenter study of community consultation for research in emergency settings. Crit Care Med (2014) 0.94

Bioethics and professionalism in popular television medical dramas. J Med Ethics (2010) 0.94

The importance of cultural considerations in the promotion of ethical research with human biologic material. J Lab Clin Med (2005) 0.93

"Special scrutiny": a targeted form of research protocol review. Ann Intern Med (2004) 0.92

Confirming comprehension of informed consent as a protection of human subjects. J Gen Intern Med (2006) 0.92

An ethics curriculum for short-term global health trainees. Global Health (2013) 0.91

Effects of disclosing financial interests on participation in medical research: a randomized vignette trial. Am Heart J (2008) 0.90

Oversight of financial conflicts of interest in commercially sponsored research in academic and nonacademic settings. J Gen Intern Med (2010) 0.89

Empirical research on informed consent with the cognitively impaired. IRB (2004) 0.89

Forecast for the Physician Payment Sunshine Act: partly to mostly cloudy? Ann Intern Med (2014) 0.89

Quality assurance questionnaire for professionals fails to improve the quality of informed consent. Clin Trials (2007) 0.87

Ethics in population-based genetic research. Account Res (2004) 0.87

Perspectives of clinical research coordinators on disclosing financial conflicts of interest to potential research participants. Clin Trials (2007) 0.86

The role of animal models in evaluating reasonable safety and efficacy for human trials of cell-based interventions for neurologic conditions. J Cereb Blood Flow Metab (2008) 0.86

Missing the informed in consent. Anesth Analg (2003) 0.86

Educational approaches to the responsible conduct of clinical research: an exploratory study. Acad Med (2007) 0.85

Seeking assent and respecting dissent in dementia research. Am J Geriatr Psychiatry (2010) 0.85

Commentary: Per capita payments in clinical trials: reasonable costs versus bounty hunting. Acad Med (2010) 0.85

Ethical issues in evidence-based surgery. Surg Clin North Am (2006) 0.85

Are research subjects adequately protected? A review and discussion of studies conducted by the Advisory Committee on Human Radiation Experiments. Kennedy Inst Ethics J (1996) 0.84

Reviewing HIV-Related Research in Emerging Economies: The Role of Government Reviewing Agencies. Dev World Bioeth (2014) 0.83

Determining the appropriateness of including children in clinical research: how thick is the ice? JAMA (2004) 0.83

The ethical review of health care quality improvement initiatives: findings from the field. Issue Brief (Commonw Fund) (2010) 0.81

Enhancing communication among data monitoring committees and institutional review boards. Clin Trials (2008) 0.80

The influence of HIV serostatus on physicians' clinical decisions. AIDS Public Policy J (1994) 0.80

Community consultation for prehospital research: experiences of study coordinators and principal investigators. Prehosp Emerg Care (2014) 0.80

Ethics in behavioral genetics research. Account Res (2004) 0.80

Realizing HOPE: The Ethics of Organ Transplantation From HIV-Positive Donors. Ann Intern Med (2016) 0.79

Community consultation: not the problem--an important part of the solution. Am J Bioeth (2006) 0.79

Bioethical considerations in developing a biorepository for the Pneumonia Etiology Research for Child Health project. Clin Infect Dis (2012) 0.79