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1.
J Law Med Ethics ; 51(4): 735-747, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38477284

RESUMEN

Across the country, legal and health care professionals who understand that health outcomes are most influenced by social and environmental conditions have improved patient health by adopting the interdisciplinary MLP health care delivery model. However, the MLP field cannot advance population health, let alone long-term health equity, until it addresses the structural determinants of health inequity that are rooted in discrimination, segregation, and other forms of racial and ethnic subordination.


Asunto(s)
Equidad en Salud , Racismo , Humanos , Inequidades en Salud , Grupos Raciales
2.
Ethn Dis ; 29(Suppl 3): 629-640, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31889768

RESUMEN

In January 2015, President Barack Obama unveiled the "Precision Medicine Initiative," a nationwide research effort to help bring an effective, preventive, and therapeutic approach to medicine. The purpose of the initiative is to bring a precise understanding of the genetic and environmental determinants of disease into clinical settings across the United States.1 The announcement was coupled with $216 million provided in the President's proposed budget for a million-person national research cohort including public and private partnerships with academic medical centers, researchers, foundations, privacy experts, medical ethicists, and medical product innovators. The Initiative promises to expand the use of precision medicine in cancer research and modernize regulatory approval processes for genome sequencing technologies. In response, Congress passed the 21st Century Cures Act in December 2016, authorizing a total of $1.5 billion over 10 years for the program.2 Although the Precision Medicine Initiative heralds great promise for the future of disease treatment and eradication, its implementation and development must be carefully guided to ensure that the millions of federal dollars expended will be spent equitably. This commentary discusses two key threats to the Precision Medicine Initiative's ability to proceed in a manner consistent with the United States Constitutional requirement that the federal government shall not "deny to any person . . . the equal protection of the laws."3 In short, this commentary sounds two cautionary notes, in order to advance precision medicine equity. First, achieving precision medicine equity will require scientists and clinicians to fulfill their intellectual, moral, and indeed legal duty to work against abusive uses of precision medicine science to advance distorted views of racial group variation. Precision medicine scientists must decisively denounce and distinguish this Initiative from the pseudo-science of eugenics - the immoral and deadly pseudo-science that gave racist and nationalist ideologies what Troy Duster called a "halo of legitimacy" during the first half of the 20th century.4 Second, to combat the social threat to precision medicine, scientists must incorporate a comprehensive, ecological understanding of the fundamental social and environmental determinants of health outcomes in all research. Only then will the Precision Medicine Initiative live up to its potential to improve and indeed transform health care delivery for all patients, regardless of race, color, or national origin.


Asunto(s)
Eugenesia , Genómica , Programas Nacionales de Salud , Medicina de Precisión , Racismo/prevención & control , Genómica/ética , Genómica/organización & administración , Regulación Gubernamental , Equidad en Salud/ética , Equidad en Salud/legislación & jurisprudencia , Humanos , Programas Nacionales de Salud/economía , Programas Nacionales de Salud/ética , Programas Nacionales de Salud/legislación & jurisprudencia , Medicina de Precisión/economía , Medicina de Precisión/ética , Medicina de Precisión/métodos , Medicina de Precisión/tendencias , Estados Unidos
3.
J Law Med Ethics ; 46(3): 588-594, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-30336092

RESUMEN

"Medicalization" has been a contentious notion since its introduction centuries ago. While some scholars lamented a medical overreach into social domains, others hailed its promise for social justice advocacy. Against the backdrop of a growing commitment to health equity across the nation, this article reviews historical interpretations of medicalization, offers an application of the term to non-biologic risk factors for disease, and presents the case of housing the demonstrate the great potential of medicalizing poverty.


Asunto(s)
Vivienda/economía , Medicalización , Pobreza , Determinantes Sociales de la Salud , Humanos , Factores de Riesgo , Estados Unidos
4.
J Law Med Ethics ; 36(1): 150-73, 4, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18315768

RESUMEN

That minority patients have not figured at all in the literature about informed consent is an egregious omission which this article begins to repair. Moreover, the article demonstrates that by addressing identifiable harms which informed consent law now causes to racial, religious, and ethnic minority patients, the law may also better address many of the concerns legal commentators have been discussing for years with only majority patients in mind. Ironically, the solution to the discrimination felt by the excluded members of society may turn out to provide the remedy for the informed consent doctrine as a whole.


Asunto(s)
Consentimiento Informado/ética , Consentimiento Informado/legislación & jurisprudencia , Grupos Minoritarios/legislación & jurisprudencia , Religión y Medicina , Derechos Civiles/legislación & jurisprudencia , Humanos , Mala Praxis/legislación & jurisprudencia , Autonomía Personal , Relaciones Médico-Paciente/ética , Ciencias Sociales , Estados Unidos
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