Literature DB >> 30138058

The Belmont Report at 40: Reckoning With Time.

Eli Y Adashi1, LeRoy B Walters1, Jerry A Menikoff1.   

Abstract

It was the summer of 1972 when a stunned nation first learned of the infamous Tuskegee Syphilis Study, during which hundreds of poor, disease-stricken black men from Macon County Alabama, had been deliberately left untreated for 40 years. Coming on the heels of multiple, earlier examples of unethical human experimentation, the Tuskegee Syphilis Study made it plain that the moral foundation of human subject research was in desperate need of repair. Blind reliance on the Nuremberg Code and the Declaration of Helsinki was no longer going to suffice. It was against this backdrop that Congress resolved to act. Numerous hearings and multiple spirited discussions later, an agreement was struck to constitute the "Commission." The outgrowth of a retreat held at the Smithsonian Institution's Belmont Conference Center, the Belmont Report lays out a principled analytical framework to "guide the resolution of ethical problems arising from research involving human subjects." Durable and ever-present, the Belmont Report, which is the foundational document that reset the ethics of human subject research, must now reckon with all-important novel issues of the day that could not have been foreseen by its drafters.

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Year:  2018        PMID: 30138058     DOI: 10.2105/AJPH.2018.304580

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  9 in total

1.  Determinants of Trustworthiness to Conduct Medical Research: Findings from Focus Groups Conducted with Racially and Ethnically Diverse Adults.

Authors:  Derek M Griffith; Emily Cornish Jaeger; Erin M Bergner; Sarah Stallings; Consuelo H Wilkins
Journal:  J Gen Intern Med       Date:  2020-06-03       Impact factor: 5.128

Review 2.  The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE.

Authors:  Stephanie A Bien; Genevieve L Wojcik; Chani J Hodonsky; Christopher R Gignoux; Iona Cheng; Tara C Matise; Ulrike Peters; Eimear E Kenny; Kari E North
Journal:  Annu Rev Genomics Hum Genet       Date:  2019-04-12       Impact factor: 8.929

3.  Precision Medicine Approaches to Health Disparities Research.

Authors:  Derek M Griffith
Journal:  Ethn Dis       Date:  2020-04-02       Impact factor: 1.847

4.  Perspective on the "African American participation in Alzheimer disease research: Effective strategies" workshop, 2018.

Authors:  Andrea Denny; Marissa Streitz; Kristin Stock; Joyce E Balls-Berry; Lisa L Barnes; Goldie S Byrd; Raina Croff; Sujuan Gao; Crystal M Glover; Hugh C Hendrie; William T Hu; Jennifer J Manly; Krista L Moulder; Susan Stark; Stephen B Thomas; Rachel Whitmer; Roger Wong; John C Morris; Jennifer H Lingler
Journal:  Alzheimers Dement       Date:  2020-08-17       Impact factor: 21.566

Review 5.  Ethical and regulatory oversight of clinical research: The role of the Institutional Review Board.

Authors:  Lindsay McNair
Journal:  Exp Biol Med (Maywood)       Date:  2022-02-16

6.  An Idealized Clinicogenomic Registry to Engage Underrepresented Populations Using Innovative Technology.

Authors:  Patrick Silva; Deborah Vollmer Dahlke; Matthew Lee Smith; Wendy Charles; Jorge Gomez; Marcia G Ory; Kenneth S Ramos
Journal:  J Pers Med       Date:  2022-04-29

7.  The Meaning of Informed Consent: Genome Editing Clinical Trials for Sickle Cell Disease.

Authors:  Stacy Desine; Brittany M Hollister; Khadijah E Abdallah; Anitra Persaud; Sara Chandros Hull; Vence L Bonham
Journal:  AJOB Empir Bioeth       Date:  2020-10-12

8.  Genes do not operate in a vacuum, and neither should our research.

Authors:  Daphne Oluwaseun Martschenko; Markia Smith
Journal:  Nat Genet       Date:  2021-03       Impact factor: 38.330

9.  Urban American Indian and Alaska Native Data Sovereignty: Ethical Issues.

Authors:  Emily A Haozous; Juliet Lee; Claradina Soto
Journal:  Am Indian Alsk Native Ment Health Res       Date:  2021
  9 in total

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