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The document discusses the ethical dilemmas faced in modern medicine, covering topics such as patient confidentiality, informed consent, and the implications of advanced medical technologies. It is structured into six parts, exploring issues related to medical practice, body parts, reproduction, societal good, practical matters, and end-of-life decisions. The author aims to stimulate discussion and reflection on these complex moral challenges within healthcare settings.
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100% found this document useful (12 votes)
744 views14 pages

Who Says You're Dead? Medical & Ethical Dilemmas For The Curious & Concerned Scribd PDF Download

The document discusses the ethical dilemmas faced in modern medicine, covering topics such as patient confidentiality, informed consent, and the implications of advanced medical technologies. It is structured into six parts, exploring issues related to medical practice, body parts, reproduction, societal good, practical matters, and end-of-life decisions. The author aims to stimulate discussion and reflection on these complex moral challenges within healthcare settings.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Who Says You're Dead?

Medical & Ethical Dilemmas for the


Curious & Concerned

Visit the link below to download the full version of this book:

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-for-the-curious-concerned-full-pdf-download

Click Download Now


In memory of Professor Edward Beiser,
who asked all the hard questions,
and for Rosalie, who helps me find the answers
CONTENTS

Introduction

Part One: Inside the Mind of a Doctor


1. “You’re Not My Real Dad”
Reflection: False Paternity
2. “How Many of Your Patients Survive?”
Reflection: Informed Consent
3. “Please Don’t Tell Anyone about My Crime”
Reflection: Doctor-Patient Confidentiality
4. “Please Don’t Put It in My Chart”
Reflection: Privacy and Medical Records
5. When the President Has a Secret
Reflection: Public Disclosure
6. “The Worst Patient Ever”
Reflection: Patient Conduct
7. “I’d Never Actually Do It, But …”
Reflection: A Doctor’s Duty to Report
8. Sleeping with the Doctor
Reflection: Doctor-Patient Attraction
9. A Physician with a Dark Past
Reflection: Professional Standards
10. Turning a Blind Eye to Torture
Reflection: Enhanced Interrogation
11. When Medical Secrets Are Business Secrets
Reflection: CEO Responsibility
12. A Doctor’s Buried History
Reflection: Evolving Ethical Norms

Part Two: Body Parts


13. “Take My Foot, Please”
Reflection: Elective Limb Amputation
14. Should She Stop Growing?
Reflection: Growth-Attenuation Therapy
15. “She Must Be Marriageable”
Reflection: Female Genital Cutting
16. “Give Her My Liver”
Reflection: Live Organ Donation
17. “Am I My Brother’s Donor?”
Reflection: The Unwilling Donor
18. Organs for Celebrities
Reflection: Favoritism
19. Ads for Organs
Reflection: The Free Market of Medicine
20. Transplantation on Death Row
Reflection: Prisoners’ Rights
21. A Chimp Heart
Reflection: Xenotransplantation
22. A Head Case
Reflection: Experimental Transplants
23. Reducing Sexual Urges
Reflection: Voluntary Castration
24. “Give Me a Horn”
Reflection: Body Modifications
25. Conjoined Twins at Odds
Reflection: Quality of Life / Sanctity of Life

Part Three: Making Babies


26. A Child with a Purpose
Reflection: Savior Siblings
27. “We Want a Deaf Baby”
Reflection: Reproductive Technologies and Disability
28. Who Owns That Embryo?
Reflection: Embryo Custody
29. Privacy Invasion or Child Protection?
Reflection: Punishing Prenatal Conduct
30. “We’re Waiting for a Sign from God”
Reflection: Preemptive Detention
31. “That Woman Stole My Sperm”
Reflection: Forced Abortion
32. “I Won’t Have a C-Section”
Reflection: Involuntary Cesareans
33. “Whose Fetus Is This?”
Reflection: Surrogacy after a Homicide
34. When Sterilization Is Forced
Reflection: Eugenics in History
35. Paying for Girls
Reflection: Sex Selection
36. Tube-Tied
Reflection: Wrongful Birth
37. When Human Cloning Becomes Possible
Reflection: Human Cloning
38. Bringing Up (Neanderthal) Baby
Reflection: Animal Cloning
39. Fertility and Fundamentalism
Reflection: LGBTQ Rights

Part Four: The Good of the Many


40. Paid to Not Have Kids
Reflection: The Rights of Substance Abusers
41. “They Tried to Make Me Go to Rehab”
Reflection: Drug Court
42. A Modern Typhoid Mary
Reflection: Mandatory Quarantines
43. Beyond 23andMe
Reflection: DNA Dragnets
44. Requiring a DNA Test
Reflection: Mandatory Genetic Screening
45. “I’d Rather Die Than Abandon My Hunger Strike”
Reflection: Force-Feeding Prisoners
46. Nonvaccinators in the Waiting Room
Reflection: Parental Dissent
47. The Evidence Is in His Leg
Reflection: Searches and Seizures
48. Echoes of Tuskegee
Reflection: Research Standards
49. “It Will Help Others, Not You”
Reflection: Research or Treatment?
50. Lithium in the Water
Reflection: Preventing Suicide
51. “Why Didn’t You Warn Me I Was at Risk?”
Reflection: Inherited Diseases and Privacy
52. The Boundaries between Mice and Men
Reflection: Human-Animal Hybrids
53. Doctoring a Dictator
Reflection: Human Rights and Treatment

Part Five: Practical Matters


54. Screening Future Employees
Reflection: Genetic Discrimination
55. “I Want a White Surgeon”
Reflection: Patient Prejudice
56. “We Don’t Tell Our Elders They Have Cancer”
Reflection: Autonomy and Culture
57. “The Best Treatment Is Prayer”
Reflection: Cognitive Capacity
58. Well-Intentioned Fraud
Reflection: Health Insurance
59. A Most Expensive Patient
Reflection: Visible and Invisible Victims
60. When Doctors Choose Who Lives
Reflection: Ventilator Allocation
61. A Cheaper Knockoff
Reflection: Intellectual Property
62. No Black Sperm Donors Need Apply
Reflection: The Business of Reproduction
63. “She Can Share a Room with a Man”
Reflection: Gender-Blind Hospital Rooms
64. Healthy Workers Only
Reflection: Employee Rights
65. Will I Get Alzheimer’s?
Reflection: Genetic Testing and Privacy
66. “I Want to Live to Meet My Child”
Reflection: Healthcare Rationing
67. Pills for Peak Performance
Reflection: Cognitive Enhancement
68. “I’d Rather Be Psychotic Than Stupid”
Reflection: Psychiatric Advance Directives
69. Hazardous Hobbies
Reflection: The Cost of Risk
70. Sex in the Nursing Home
Reflection: Dementia and Consent

Part Six: End-of-Life Issues


71. Who Says You’re Dead?
Reflection: Defining Death
72. Easing Suffering, Hastening Death
Reflection: Pediatric Euthanasia
73. Death and Taxes
Reflection: Inheritance
74. “Did He Have AIDS?”
Reflection: Posthumous Privacy
75. Stranded on a Ventilator
Reflection: Physician-Assisted Suicide
76. “Give Me My Late Fiancé’s Sperm”
Reflection: Posthumous Sperm Retrieval
77. Waiting for Reincarnation
Reflection: Death-Defying Decisions
78. Cadaver Confusion
Reflection: Therapeutic Privilege
79. “He’d Rather Die Than Live Like This”
Reflection: Withdrawing Life Support

Sources and Further Reading


About the Author
INTRODUCTION

Today’s hospitals and clinics are the settings of some of the most
challenging and controversial ethical dilemmas our society confronts. Every
day, it seems, a pioneering researcher or clinician announces a new
breakthrough: hand transplants, cloned sheep, targeted biological cancer
therapies, cognitive enhancers, preimplantation genetic screening,
transgenic mice—the list of scientific “miracles” seems endless. With these
technologies, of course, arise far more complex moral challenges. How to
allocate scarce donor hearts and kidneys among potential recipients, for
example, is not an issue unless the immunosuppressive drugs that prevent
our bodies from rejecting those organs exist. Now they do.
Two recent technological developments offer windows into the
strikingly different sorts of ethical challenges that such advances pose. One
of these innovations is three-parent conception. As readers may or may not
recall from high school biology, most of our DNA is housed in the nuclei of
our cells, but some of our genetic blueprint is contained in small organelles
outside the nucleus called mitochondria. Both types of DNA are necessary
to produce a healthy baby. Under rare circumstances, the DNA in the
mitochondria becomes defective through mutations; as a result, babies are
born with debilitating genetic diseases. These conditions often run in
families. To prevent these diseases, doctors can now take the nucleus of an
egg cell from a potential mother who comes from such a family and
combine it with the mitochondrial DNA of a second, unrelated woman. This
process is known as “cytoplasmic transfer.” If this combined egg is then
fertilized by a sperm, the result will be a baby with DNA from three distinct
biological parents—what the media has dubbed a “three-parent baby.” On
the one hand, this is a great breakthrough: women once faced with the
choice of conceiving a sick child or no child at all can now give birth to
healthy offspring who live long, meaningful lives. On the other hand, such a
process raises novel questions: Should two mothers be listed on this child’s
birth certificate? What happens if the woman who contributed mitochondria
demands partial custody? Visitation rights? An inheritance? Alternatively,
does the child ever have a right to learn the identity of the mitochondrial
donor? Or the donor’s medical history? And in the age of surrogate
motherhood, if the embryo is implanted inside a third woman’s uterus, what
are the ethical and legal implications for a “four-parent baby”? While more
than a dozen babies have been born over the past two decades through
cytoplasmic transfer, many of these questions remain unresolved.
At the opposite end of the technological spectrum stands an advance far
more familiar to the average healthcare consumer: the rise of the electronic
medical record (EMR). These days, anyone who visits a doctor’s office or
hospital emergency room has likely encountered the ubiquitous appearance
of the computerized chart. Experts tell us that these EMRs will decrease
medical errors and speed the transfer of health information. The ultimate
goal, for many, is a so-called “intraoperative system,” where a patient can
walk into any hospital or physician’s office in the nation, and the staff will
immediately be able to access the patient’s medical history, current
medications, and regular healthcare providers’ contact information. This
technology might prove particularly valuable in emergencies or when a
patient has lost consciousness.
At the same time, it is fraught with the potential for lost privacy.
Millions of healthcare professionals would require access to such a system
for it to function well. But some patients may not want their records
available in this manner. They may object to their podiatrist knowing that
they suffer from a mental illness or their dentist learning what method of
contraception they use. The potential for abuse also remains glaring: How
will the system know if a pharmacist from Wyoming accesses the medical
records of his soon-to-be son-in-law in Florida in order to discover whether
his daughter will be marrying a man with a history of drug addiction? And
if he does breach the system in this way, how should we punish him? Firing
the victim’s future father-in-law may actually exacerbate the injured man’s
misfortune and will certainly not put the genie back in the bottle. And then,
of course, there is the possibility that hackers will break into the system and
post the medical records of everyone on the internet. Certainly, these pitfalls
require a careful balancing between privacy rights and access to top-notch
care.
As a practicing psychiatrist and bioethicist, I explore these exciting and
often daunting ethical dilemmas every day. Over the course of nearly two
decades teaching at Brown University, Columbia University, New York
University, and the Icahn School of Medicine at Mount Sinai, I have written
a trove of these difficult conundrums to stimulate discussion among medical
students and residents. Some are drawn from the headlines, others loosely
modeled on cases reported in professional journals. A few, painstakingly
disguised, come from my own clinical encounters. Whether you are
planning a career in healthcare or you are a layperson intrigued by the
ethical issues you often witness all too briefly on popular television shows,
the dilemmas that follow are designed to let you investigate your own
values, engage with difficult “real-world” issues, and argue (in good cheer)
with friends and family across the dinner table.
The commentary provided after each conundrum is not intended to sway
your opinions. Rather, these are reflections that offer some of the real ways
in which established bioethicists, clinicians, and policy makers have tackled
similar moral quandaries. Some of these quandaries may arise in your own
life, and there is value in having thought about the issues in advance. The
hope is that you will examine these questions from multiple vantage points,
whatever your ultimate feelings, and will recognize that intelligent people
of goodwill may arrive at different conclusions.
In the hospital or in the legislature, addressing these highly fraught
subjects can prove emotionally grueling. Fortunately, discussing them
hypothetically, in your own living room, should be precisely the opposite:
invigorating and inspiring. Above all, the goal of this volume is to convey
the intellectual pleasure of engaging with complex ethical questions—to let
you do what professional bioethicists do every day. So I do hope you enjoy!
JACOB M. APPEL, MD, JD, MPHIL, MPH, MFA
Director of Ethics Education in Psychiatry
Assistant Professor of Psychiatry and Medical Education
Icahn School of Medicine at Mount Sinai
PART ONE

Inside the Mind of a Doctor

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