Patient, Heal Thyself How The "New Medicine" Puts The Patient in Charge PDF
Patient, Heal Thyself How The "New Medicine" Puts The Patient in Charge PDF
Patient in Charge
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1 2009
1
Oxford University Press, Inc., publishes works that further
Oxford University’s objective of excellence
in research, scholarship, and education.
9 8 7 6 5 4 3 2 1
Printed in the United States of America
on acid-free paper
For
Willard Gaylin
Andre E. Hellegers (1926-1979)
Edmund D. Pellegrino
Victor W. Sidel
physicians who have mastered the art of respecting patients
and given them the freedom to heal
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preface
viii | p r e f a c e
This volume is the culmination of this career-long journey toward what
I call a new or postmodern medicine. It is a medicine that had its begin-
nings in the exciting days of the 1970s when patients first began demand-
ing their right to make medical choices based on their own values. It is a
medicine now irreversibly launched as the replacement for what is now old-
fashioned modern medicine. It is a medicine that is radically different from
modern medicine in the role the layperson must play in medical decision
making.
In this volume I bring together my thoughts over the past decades. I
make a case that a new medicine is well on its way to emerging and that it
is destined to replace modern medicine. It is a medicine that will rely on
professional medical expertise as much or more than before for more techni-
cal matters of diagnosis, prognosis, and treatment options, but will require
a much more active patient in charge of choosing which options are best
for his or her own medical decisions. It is a world in which physicians and
health professionals will become assistants of patient who will have to take
charge and heal themselves.
This manuscript has been in preparation for several years. Some of the
ideas have germinated, often in only partially developed form, in articles I
have written over the years:
Portions of chapters 3–6 incorporate some parts of “Doctor Does Not
Know Best: Why in the New Century Physicians Must Stop Trying
to Benefit Patients,” Journal of Medicine and Philosophy 25, no. 6 (De-
cember 2000):701–721, by permission of Oxford University Press.
Portions of chapters 11 and 12 are adapted from “Abandoning Informed
Consent,” Hastings Center Report 25, no. 2 (March–April 1995):5–12,
© The Hastings Center. Reprinted with permission.
Portions of chapters 16 and 17 are adapted from “Single Payers and Multi-
ple Lists: Must Everyone Get the Same Coverage in a Universal Health
Plan?” Kennedy Institute of Ethics Journal 7, no. 2 (1997): 153–169.
Portions of chapters 20 and 21 draw on “Indifference of Subjects: An Al-
ternative to Equipoise in Randomized Clinical Trials,” in Bioethics,
ed. Ellen Frankel Paul, Fred D. Miller, Jr., and Jeffrey Paul, 295–323
(Cambridge: Cambridge University Press, 2002). Reprinted with the
permission of Cambridge University Press.
Portions of chapters 23–24 incorporate “Technology Assessment: Inevi-
tably a Value Judgment,” in Getting Doctors to Listen: Ethics and Out-
comes Data in Context, ed. Philip J. Boyle, 180–195 (Washington,
DC: Georgetown University Press, 1998) © 1998 by Georgetown
p r e f a c e | ix
University Press, reprinted with permission; and “Consensus of Ex-
pertise: The Role of Consensus of Experts in Formulating Public Pol-
icy and Estimating Facts,” The Journal of Medicine and Philosophy 16
(1991):427–445, by permission of Oxford University Press.
In all of these chapters new material is included and material from articles
has been revised and integrated into a coherent account of what I am calling
the new medicine.
x | p r e f a c e
acknowledgments
I have over the years given prominent attention to the individual case. In
collaboration with others, I have written six different collections of case
studies, some of which have gone through multiple editions. I incorporate
some cases in this volume to illustrate the themes I develop. A few of the
cases are stories I have told before, particularly in the new edition of Case
Studies in Medical Ethics, which is also published by Oxford University Press,
but all reflect some real-life event that shows how values from outside med-
icine must shape medical decisions.
I had help from many people in developing the ideas and text for this
manuscript. My colleagues at the Kennedy Institute of Ethics have been a
continual stimulus for decades. They will recognize some of their input in this
volume. The professional librarians of the National Reference Center for Bio-
ethics Literature, the Kennedy Institute’s library, are a rich resource that any
academic researcher would treasure. Their knowledge of the field and its lit-
erature has been enormously helpful, as has been the support of Linda Powell,
Moheba Hanif, and Sally Schofield. Alexander Curtis and Traviss Cassidy have
read large portions of the manuscript and offered many helpful suggestions.
My wife, Ann, has heard many of these ideas so often that she can antici-
pate my thinking. She has tolerated these unusual interests and research
projects in a graceful and supporting way, for which I am grateful.
At Oxford University Press, Peter Ohlin has shepherded this project
with professional skill and talent. This is my fifth volume with Oxford. It is
a press of great quality for which I express my appreciation.
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contents
List of Cases xv
xiv | c o n t e n t s
list of cases