Week 1 Introduction Flashcards

1
Q
  • Ethics is a rather generic term covering
A

different ways of
examining and interpreting the moral life.

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2
Q
  • Some approaches to ethics are normative, others nonnormative.
  • Normative ethics seeks to respond to:
A

Normative ethics seeks to respond to:
* Which general moral norms should we use to guide and evaluate conduct,
and why?
* Ethical theories seek to identify and justify these norms, which are often
referred to as principles, rules, rights, or virtues

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3
Q

Ethics seeks to answer normative inquiries, such as

A
  • Is there a difference between right and wrong?
  • How can we judge which actions are right and which are wrong?
  • Are values/principles absolute or relative?
  • What rights, do we have? Are they absolute? What infringements are
    allowable?
  • What duties and responsibilities do we have? What should we do when we
    have competing duties or responsibilities?
  • What is the “good life”? What is happiness?
  • How can I be a responsible and supportive member of my community? What
    is equity?
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4
Q
  • The International Association of Bioethics
    defines bioethics as:
A
  • “The critical examination of ethical issues in health and biological
    sciences.”
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5
Q

Two parts in BIOETHICS

A
  • Bios: Life
  • Ethos: Manners, conduct of life
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6
Q

Bioethics:
The critical examination of ethical issues
in health and biological sciences. (examples)

A

-Research with
human subjects
+ Consent.
-Allocation of
scarce resources
-Should health
decisions be
individually or
collectively
done?
-Decisions to
withhold or
withdraw
treatment
-What’s privacy
in digital
medicine?
-What’s about
biases and
discrimination in
health research
and healthcare
delivery?

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7
Q

Birth of bioethics

A
  • Van Rensselaer Potter’s book Bioethics: Bridge to the Future (1970) (concerned about nuclear weapons + future)
  • Kennedy Institute of Ethics at Georgetown University (1971) (respect for person, benevolence, nonmaleficence, autonomy, came after bad research/experimental practices)
  • May also be in 1927 by Fritz Jahr who published an article entitled: “Bio-Ethics: A Review of the Ethical Relationships of Humans to Animals and Plants”
  • Jahr proposed a “Bioethical Imperative,” extending Kant’s moral imperative to all
    forms of life.
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8
Q

Difference between law and ethics

A

-law is not the same as ethics
-both have consequences e.g. medical professionals not following ethics and losing license as a result, social ethics
-Google: “Ethics are a set of moral values an individual establishes for one’s self and your own personal behavior. Laws are structured rules utilized to govern all of society.”

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9
Q

Trolley problem

A

-2 skytrain/trolley tracks, 1 with 5 people, other with 1 person
-deontological pov: don’t do anything, it’s not my responsibility to decide who lives/dies
-utilitarian pov: choose to save 5 (more people)
-in a dilemma, both perspective’s can’t exist at the same time

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10
Q

In all cases, bioethics is

A
  • A social and cultural happening
  • A rather complex enterprise
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11
Q

Why does bioethics matter?

A
  • The scope of bioethics
  • affects every person, throughout life individually and as a society locally and
    globally
  • Fields of study and practice
  • e.g., clinical, research, public health, health policy
  • Specific fields of interest
  • e.g., beginning and end of life, non communicable diseases, pandemics, AI,
    health data, -omics
  • Tools and methods
  • e.g., conceptual/normative analysis, legal analysis, empirical studies
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12
Q

The Henrietta
Lacks Case
(1951)

A

-In 1951, a young African American woman named Henrietta Lacks
sought treatment at Johns Hopkins Hospital for an aggressive form of
cervical cancer. Without her knowledge or consent, doctors took
samples of her cancer cells during treatment and discovered something
unprecedented: her cells were immortal, meaning they could replicate
indefinitely outside the human body. These cells, named HeLa cells,
became one of the most important tools in medical research.
-For decades, HeLa cells were used in countless scientific breakthroughs,
from the development of the polio vaccine to advancements in cancer
research, virology, and even space biology. Despite their enormous
contribution to science, neither Lacks nor her family were aware of the
use of her cells until years after her death. The unconsented harvesting
and use of her cells raised significant ethical questions, especially
regarding informed consent and the exploitation of vulnerable
populations, particularly African Americans, in medical research.

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13
Q

The Henrietta
Lacks Case
(1951) Key Ethical Issues

A

-Informed consent: Lacks was never informed that
her cells would be used for research, raising
questions about autonomy and respect for persons.
-Exploitation: The commercialization of HeLa cells
generated significant profit, but neither Lacks nor
her family were compensated.
-Privacy and genetic data: The publication of Lacks’
genetic information without family consent poses
modern concerns over genetic privacy and
ownership of biological materials.

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14
Q

The Daigle v.
Tremblay Case
(1989)

A

-The Daigle v. Tremblay case was a landmark legal battle in Canada
involving the rights of a woman to access an abortion and the opposing
rights of the biological father. The case arose when Chantal Daigle, a
pregnant woman in Quebec, decided to have an abortion after
separating from her partner, Jean-Guy Tremblay.
-Tremblay, opposed to the abortion, sought and obtained a court
injunction to prevent Daigle from terminating the pregnancy, arguing
that the fetus had a right to life and that he, as the father, had the right
to protect his unborn child.
-The Quebec courts initially ruled in favor of Tremblay, issuing an
injunction that prohibited Daigle from obtaining an abortion. The case
quickly escalated to the Supreme Court of Canada, which had to
consider whether a biological father had the legal right to prevent an
abortion and whether a fetus had constitutional rights under Canadian
law

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15
Q

The Daigle v.
Tremblay Case
(1989) Key Ethical Issues

A

-Bodily autonomy: Central to the case was Daigle’s right to control her
own body and make decisions regarding her reproductive health. The
case tested the extent to which a woman’s right to bodily autonomy
could be overridden by the interests of the biological father or the fetus.
-Fetal rights vs. maternal rights: Tremblay argued that the fetus had a
right to life, and by extension, he had a right to protect it as the father.
The court had to consider whether a fetus had legal standing and
whether it had rights that could be defended by the father, pitting the
rights of the mother against those of the fetus and the father.
-Gender equality and reproductive rights: The case raised broader
questions about gender equality, particularly around reproductive rights.
If men were granted the legal authority to block abortions, it could be
seen as undermining women’s ability to make autonomous choices
about their bodies and their lives.

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16
Q

The Icelandic
Health Sector
Database Act
(1998) &
deCODE
Genetics

A

-In 1998, Iceland’s Parliament passed the Icelandic Health Sector
Database Act, allowing the creation of a centralized database that
combined the health records, genetic information, and genealogical
data of nearly the entire Icelandic population.
-The database was intended to facilitate genomic research, with the goal
of uncovering genetic links to diseases and conditions that could lead to
medical breakthroughs. The company deCODE Genetics was granted
exclusive rights to manage and exploit the data for research and
commercial purposes.
-The initiative was controversial from the start, as it positioned Iceland,
with its small, genetically homogenous population, as an ideal location
for large-scale genomic research. Proponents argued that the database
would enable scientists to uncover connections between genes and
diseases, ultimately leading to new treatments and precision medicine
tailored to genetic profiles.

17
Q

The Icelandic
Health Sector
Database Act
(1998) &
deCODE
Genetics Key Ethical Issues

A

-Informed consent: The Act allowed individuals’ data to be included
in the database without explicit informed consent, relying instead
on presumed consent with an opt-out option. This sparked debates
over whether presumed consent respects individual autonomy.
-Privacy and data security: The potential for misuse or unauthorized
access to sensitive genetic and health data raised concerns about
privacy and data security, especially as the database contained
extensive personal and familial information.
-Commercialization of genetic data: The partnership with deCODE
Genetics, a for-profit company, raised ethical concerns about
corporate control over public health data and the potential for
exploitation of Iceland’s genetic heritage for profit.
-Discrimination and stigmatization: Genetic data could potentially
be used to discriminate against individuals or groups, particularly in
contexts like insurance, employment, or social services, based on
genetic predispositions to certain diseases

18
Q

Allocation of
Ventilators
during COVID19 (2020)

A

The global COVID-19 pandemic
caused a critical shortage of
ventilators, particularly in
overwhelmed healthcare systems.
Hospitals were forced to develop
triage protocols to allocate limited
resources, raising difficult ethical
questions.

19
Q

Allocation of
Ventilators
during COVID19 (2020) Key Ethical Issues

A

-Triage and resource allocation: When resources are scarce, how do
healthcare providers decide who receives life-saving treatment?
Decisions were often based on factors like the likelihood of survival,
age, or pre-existing conditions.
-Equality vs. equity: Should ventilators be distributed equally (firstcome, first-served) or equitably (prioritizing those with the highest
chances of survival or social utility)? This raised concerns about
discrimination against marginalized groups.
-Public trust and transparency: Transparent decision-making was
crucial to maintain public trust in the healthcare system, as secretive
or inconsistent protocols could lead to perceptions of unfairness or
bias.
-Moral distress for healthcare workers: Doctors and nurses faced
severe emotional strain in making life-or-death decisions, leading to
widespread moral distress and burnout.

20
Q

Doctors Using
ChatGPT and
Violating Privacy
Laws (2023)

A

-With the rise of AI tools like ChatGPT in
healthcare, some doctors have begun using
these tools for tasks like patient
documentation, treatment recommendations,
and drafting notes.
-However, concerns have emerged that doctors
may be unknowingly violating Privacy Laws
(such as HIPAA, US Health Insurance Portability
and Accountability Act) by inputting patient
data into ChatGPT without proper safeguards.

21
Q

Doctors Using
ChatGPT and
Violating Privacy
Laws (2023) Key Ethical Issues

A

-Patient confidentiality: Privacy Laws (such as HIPAA in the US) requires healthcare
providers to safeguard patient information, ensuring that it is not shared or
accessed inappropriately. Inputting identifiable patient data into an AI tool like
ChatGPT may violate this principle if the data is exposed or misused.
-Lack of transparency: Many doctors may not fully understand how ChatGPT
processes, stores, or shares the data it receives. Without clear guidelines, there’s a
risk of accidental data breaches or misuse of sensitive patient information.
-Informed consent: Patients are often unaware that their data is being processed by
AI tools, raising concerns about informed consent and whether patients should be
informed when their information is used in AI-driven platforms.
-Accountability in AI: If HIPAA violations occur, it is unclear who is responsible—the
doctors, the developers of AI platforms, or healthcare institutions? The use of AI in
medicine introduces new challenges in determining legal and ethical accountability.