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Navigating the Ethical Maze: Dr. Arthur Caplan on Bioethics in Modern Medicine
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Manage episode 397586425 series 3535889
Dr. Arthur Caplan, a distinguished bioethicist, discusses various topics related to bioethics. He highlights the importance of bioethics in areas such as organ transplantation, genetic testing, artificial intelligence, and personalized medicine.
Dr. Caplan emphasizes the need for informed consent in research ethics and the importance of providing research participants with the results of studies. He also addresses the ethical considerations in organ transplantation, including the allocation of scarce resources and the role of living donors. Additionally, he discusses the ethical implications of expensive treatments and the allocation of limited resources in healthcare. The conversation explores the disparity in healthcare attention given to rare diseases compared to chronic conditions. It highlights the need for organized advocacy and lobbying for conditions that lack representation.
The discussion also delves into the balance between investing in genetic therapies for rare diseases and preventive measures for chronic conditions. The ethical considerations of gene editing using CRISPR technology are examined, including the need for monitoring and surveillance of adverse effects. The potential for societal inequalities in access to gene editing is discussed, raising concerns about eugenics and the widening gap between those who can afford the technology and those who cannot.
Chapters
00:00 Introduction to Dr. Arthur Caplan
01:35 The Importance of Bioethics in Various Areas
09:25 Informed Consent in Research Ethics
17:29 Balancing Scientific Progress and Ethical Considerations in Human Subject Research
33:41 Ethical Considerations in Organ Transplantation
47:22 Healthcare Resource Utilization and Pricing
48:25 Disparity in Healthcare Attention
51:18 Balancing Rare Diseases and Chronic Conditions
53:36 Genetics vs. Environmental Intervention
58:26 CRISPR and Bioethical Concerns
01:05:13 Societal Inequalities in Access to Gene Editing
01:06:03 Inspiration from Ben Franklin
Resources
- Dr. Arthur Caplan
- Succumbing to AI with a whimper, not a bang
- Working Group on Compassionate Use and Preapproval Access (CUPA)
- Vaccine Working Group on Ethics and Policy
- Working Group on Pediatric Gene Therapy & Medical Ethics
- Transplant Ethics and Policy
- If you donate DNA, what should scientists give in return? A ‘pathbreaking’ new model
- Treating the dead; how far ought medicine go to obtain transplantable organs?
- Consideration and Disclosure of Group Risks in Genomics and Other Data-Centric Research: Does the Common Rule Need Revision?
- Research involving the recently deceased: ethics questions that must be answered
- Regaining Trust in Public Health and Biomedical Science following Covid: The Role of Scientists
- Protect newborn screening programs
- Why the Gene Was (Mis)Placed at the Center of American Health Policy
25 episoder
Fetch error
Hmmm there seems to be a problem fetching this series right now. Last successful fetch was on November 18, 2024 13:18 ()
What now? This series will be checked again in the next day. If you believe it should be working, please verify the publisher's feed link below is valid and includes actual episode links. You can contact support to request the feed be immediately fetched.
Manage episode 397586425 series 3535889
Dr. Arthur Caplan, a distinguished bioethicist, discusses various topics related to bioethics. He highlights the importance of bioethics in areas such as organ transplantation, genetic testing, artificial intelligence, and personalized medicine.
Dr. Caplan emphasizes the need for informed consent in research ethics and the importance of providing research participants with the results of studies. He also addresses the ethical considerations in organ transplantation, including the allocation of scarce resources and the role of living donors. Additionally, he discusses the ethical implications of expensive treatments and the allocation of limited resources in healthcare. The conversation explores the disparity in healthcare attention given to rare diseases compared to chronic conditions. It highlights the need for organized advocacy and lobbying for conditions that lack representation.
The discussion also delves into the balance between investing in genetic therapies for rare diseases and preventive measures for chronic conditions. The ethical considerations of gene editing using CRISPR technology are examined, including the need for monitoring and surveillance of adverse effects. The potential for societal inequalities in access to gene editing is discussed, raising concerns about eugenics and the widening gap between those who can afford the technology and those who cannot.
Chapters
00:00 Introduction to Dr. Arthur Caplan
01:35 The Importance of Bioethics in Various Areas
09:25 Informed Consent in Research Ethics
17:29 Balancing Scientific Progress and Ethical Considerations in Human Subject Research
33:41 Ethical Considerations in Organ Transplantation
47:22 Healthcare Resource Utilization and Pricing
48:25 Disparity in Healthcare Attention
51:18 Balancing Rare Diseases and Chronic Conditions
53:36 Genetics vs. Environmental Intervention
58:26 CRISPR and Bioethical Concerns
01:05:13 Societal Inequalities in Access to Gene Editing
01:06:03 Inspiration from Ben Franklin
Resources
- Dr. Arthur Caplan
- Succumbing to AI with a whimper, not a bang
- Working Group on Compassionate Use and Preapproval Access (CUPA)
- Vaccine Working Group on Ethics and Policy
- Working Group on Pediatric Gene Therapy & Medical Ethics
- Transplant Ethics and Policy
- If you donate DNA, what should scientists give in return? A ‘pathbreaking’ new model
- Treating the dead; how far ought medicine go to obtain transplantable organs?
- Consideration and Disclosure of Group Risks in Genomics and Other Data-Centric Research: Does the Common Rule Need Revision?
- Research involving the recently deceased: ethics questions that must be answered
- Regaining Trust in Public Health and Biomedical Science following Covid: The Role of Scientists
- Protect newborn screening programs
- Why the Gene Was (Mis)Placed at the Center of American Health Policy
25 episoder
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