The Belmont Report at 40: Reckoning With Time

Am J Public Health. 2018 Oct;108(10):1345-1348. doi: 10.2105/AJPH.2018.304580. Epub 2018 Aug 23.

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.

MeSH terms

  • Alabama
  • Biomedical Research / ethics*
  • Black or African American
  • Ethics, Research*
  • Female
  • Human Experimentation / ethics*
  • Humans
  • Informed Consent / ethics
  • Male
  • Patient Selection / ethics
  • Personal Autonomy
  • Research Subjects
  • Social Justice / ethics*
  • Syphilis / epidemiology
  • United States
  • Volunteers