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Dimensions
of Dying
Yale
doctors are helping their patients talk about death -- and are hearing
a lot they didn't learn in medical school.
October
1994
by Bruce Fellman
The last
time Mary Kathleen Figaro talked to Noel (not her real name), a
cancer patient at Yale-New Haven Hospital, the woman was close to
death. And yet,
said Figaro, who this fall entered her third year at the School
of Medicine, although the end was clearly in sight, Noel, an emigrant
from Barbados who was in her early 30s, was not brooding about the
past. "She kept on talking about going to immigration -- she was
looking directly at the future," explained Figaro. "It
was obvious she wasn't going to make it, and she knew that, I guess,
but against all odds, she was dreaming of a future. She taught me
that you could have hope even in a hopeless situation."
Noel died only weeks
after her first conversation with Figaro, but not before providing
the future physician with numerous other insights about the nature
of the doctor-patient relationship at the end of, as well as throughout,
life. But this "mentorship" was not simply the result
of a happenstance meeting in a cancer ward. The women came to know
each other because of an innovative and, according to a recent survey
of 111 U.S. medical schools that appeared in the journal Academic
Medicine, a unique approach to the once-taboo topic of death
and dying.
The "Seminar on
the Seriously Ill Patient," developed in 1986 by Medical School
chaplain Alan C. Mermann '79MDiv, is an elective course, usually
taken in the first year, that pairs each student in the class with
someone who is dying. As a result of frequent conversations between
acolyte and mentor -- often several times a week over the course of
a semester -- along with readings, weekly discussions with peers, and
plenty of private soul-searching, a doctor-to-be develops an understanding
of what to say, what not to say, and when to say nothing at all.
"This is learnable
information," says Mermann, who is also a pediatrician. "But
first, you have to have some direct, personal experience."
A sizable number of
students come to the course having had no experience whatsoever
with death. "I'd never even been to a funeral," notes
Michael Fischer, who is going into his second year as a medical
student.
Fischer's teacher was
a women in her mid-30s who was battling recurrent cervical cancer,
and he recalls sitting with her while she underwent chemotherapy.
"Her treatment was pretty routine and uncomplicated, but for
her, it was everything," he explains, adding that he can now
see how easy it would be to lose sight of a patient's perspective.
"I just tried to be there for her to talk to, and I came away
from our conversations with an understanding of what it's like to
be dealing with pain, extended disability, the stigma of having
cancer, and mortality. I hope I can keep that knowledge on file."
At most
medical schools, these lessons in listening are hard to come by
because the curriculum
generally calls for little more than a few formal lectures on various
aspects of end-stage diseases and a talk by a terminally ill patient
or two about what it's like to be dying. And while Mermann feels
that this modest approach is infinitely better than the way the
subject was treated when he was in school in the 1950s -- typically,
it was ignored -- he argues that students and, ultimately, society
will be better served by providing physicians-to-be with direct
contact with patients whose care can bring out the best -- and worst -- in
the medical establishment. "One hopes this experience will
make them better doctors," says Mermann, who is quick to add
that he hasn't done any follow-up studies.
Annie Egan '92MD doesn't
need statistics to know how crucial the Yale course was for her.
Now a senior resident in pediatrics at the Children's Hospital of
Pittsburgh, Egan took the seminar in 1988 and was mentored by a
woman in her early 30s who was dying of advanced lymphoma. "There's
a saying around medicine that you learn the most from the sickest
patients, and though her experience as an adult was very different
from what I deal with in pediatrics, there was at least one lesson
I've carried with me," Egan explains. "I learned that
the most important thing in the relationship was honesty."
There was another critical
lesson. In telling her life's story, Egan's teacher talked about
how her boyfriend had left her as soon as her cancer was diagnosed
and how she'd had to move in with her mother. "I'd had a fair
amount of experience with death in my own family," says Egan,
explaining that in her case, the family came closer together each
time one of its own died. In her teacher's case, however, the family
disintegrated.
One night while Egan
was on call at the Children's Hospital, an 8-year-old was brought
in with blood in his urine. The mother was in tears, the pediatrician
recalls, complaining that no one, including her child's doctor,
would give her a straight answer about what was wrong. An X-ray
showed an ominous mass, probably a bladder tumor, and it fell to
Egan to deliver the news.
There are doctors who
would do so and then disappear, but Egan faced the family members
directly. "I told them, `Your life has now profoundly changed,
and it's time to reach out for help.' My teacher made me acutely
aware of the fragility of family structure in a medical crisis,
and how you have to treat the family, not just the patient. I wouldn't
have thought of that before taking the course."
Too often in what one
physician has dubbed the "high-tech wasteland" of modern
medicine, the essential twin skills of empathy and listening get
lost, says Mermann. There are many reasons.
Chief
among them is what professors at the Medical School frequently call
the "third-year syndrome."
Mermann explains that students, most of whom entered medicine with
the altruistic motive of caring for the sick, often "run smack
into disillusionment" in the third year of schooling when they
begin the clinical portion of their education and have to shift
their focus to technique. "They see patients winding up as
little more than numbers, even called disparaging names like 'scum
bag' and 'dirt ball,' and this leaves students startled and upset,"
says Mermann.
Of course, a certain
amount of detachment is essential, both for sound medical judgment
and for psychological survival, but there is an ever-present danger
that detachment will become what is technically known as alexithymia,
the inability to feel emotion. Worse still, in the ever-faster-paced
world of the hospital where most doctors learn the trade, there
is, increasingly, too little time to develop any kind of relationship
with someone who will eventually be well, let alone someone who
is dying.
"A hospital like
Yale-New Haven is simply a very difficult place to carry out the
care of a terminally ill patient," says Gerard Burrow, dean
of the Medical School. "The whole place is set up to run on
a 24-hour-a-day, battle-station type arrangement." Still, those
doctors who avoid becoming shell-shocked and continue to have the
"healer's touch" tend to be lionized by those who are
in their care. Horror stories abound about the physician who walks
in, looks at the chart, and doesn't even ask a patient's name. "Compare
this," says Mermann, "to the doctor who sits down on your
bed, takes your hand, and asks, 'How are you this morning?' The
amount of time the physician is in the room is exactly the same -- you're
still getting 37 seconds -- but to the patient, the difference between
the two doctors is phenomenal."
Never is the difference
more noticeable than when someone is dying, and yet at that time,
a physician's response is frequently to pull back, even vanish.
Medical students, notes Mermann, are understandably anxious about
confronting death, but this timor mortis -- "the fear
of death" -- often persists among the doctors who are training
them. And since, as Dean Burrow notes, students in their clinical
training learn primarily by example, it is not surprising that they
too come to avoid this painful subject.
Another barrier to dealing
with the dying is that many physicians see death as a sign that
they've failed. That syndrome is outlined in detail in the recent
bestselling book, How
We Die: Reflections on Life's Final Chapter (Alfred A. Knopf,
1994). Written by Sherwin B. Nuland
'55MD, an associate clinical professor of surgery at Yale, it explains
that while doctors are exhaustively trained to solve what the author
terms "the riddle" of disease, admitting defeat in the
face of the inevitable and providing care without cure are rarely
part of the modern physician's education -- or inclination.
Mermann's popular course,
which last year was taken by nearly half of the Medical School's
first-year students, is designed to create a cadre of doctors who,
having seen the effects of a terminal illness through the eyes of
a patient, are less likely to break, however inadvertently, a central
tenet of the physician's creed: First, do no harm.
And harm
can indeed result from what amounts to a fundamental failure to
communicate. Nuland,
who has more than 30 years of surgical experience, recounts numerous
instances of "heroic" lifesaving interventions, not all
of which turned out to be, from the patient's point of view, wise
or even desirable. "Doctors really believe in their own beneficence,
and they think that whatever recommendation they make is the right
one for their patient," notes Nuland. "But that's an enormous
obstacle to reality because it means that physicians approach the
patient's problem with a whole different set of values than those
of the patient."
As an illustration,
Nuland relates the case of a 92-year-old woman he calls "Hazel
Welch," who arrived at YNHH unconscious, a victim of a perforated
digestive tract. Already afflicted with severe arthritis, gangrene,
and arteriosclerosis -- her leukemia was in remission -- Miss Welch, when
she regained consciousness after treatment in the hospital's emergency
room, refused surgery. "In a broad Yankee inflection, she told
me that she had been on this planet 'quite long enough, young man'
and didn't wish to go on," Nuland writes.
The doctor heard what
the patient was saying, but didn't absorb its importance. "How
can you let someone die when you think you can save her? It made
no sense," Nuland explains. So, deliberately minimizing the
post-operative difficulties his patient would face, he talked her
into agreeing to the surgery, which she survived, only to die from
a stroke, probably brought on by the procedure, two weeks later.
From his current vantage
point as a retired, 63-year-old surgeon, Nuland views his intervention
in the case of Hazel Welch as clearly inappropriate. "Had I
the chance to relive this episode, or some others like it in my
career, I would listen more to the patient and ask her less to listen
to me," he says.
Nevertheless, he would
have operated. "The accepted code of my specialty demanded
it," he says. "My treatment in this case was based not
on her goal but on mine. I pursued a form of futility that deprived
her of the particular kind of hope she had longed for -- the hope that
she could leave this world without interference when an opportunity
arose."
Doctors who don't know
their patients -- a common circumstance in the tertiary-care hospitals
where most people now come to die -- are particularly likely to pursue
what ironically is a hopeless path. "We take away their clothes,
and, as Eric Cassell, a practicing internist, has said, we take
away their personhood -- we don't see patients in their setting,"
Nuland says. "But you make one house call, and your viewpoint
of a patient changes so much. You see a crucifix, look at certain
kinds of books, hear bits of conversation, walk up three flights
of steps, and you understand things you never understood. Only a
doctor who knows that house, and knows the person who lived there -- and
not a doctor who met the patient on the day the kidneys began to
fail -- can help that person make decisions about life and death."
Nuland,
and many others who are embroiled in the debate over the direction
of health care in the U.S., argues for the creation of a new breed
of family practice doctor:
a cradle-to-grave physician who is trained to radiate the empathy
embodied in a Norman Rockwell portrait as well as to deal with most
health problems in his or her own office, while acting as a broker
when there is a need for specialists. However, current trends in
medicine-like the push toward health maintenance organizations with
their constantly changing cast of caregivers -- and the mobility of
the American public, make the return of the family doctor more of
a fantasy than a realistic prospect. Says gastroenterologist Howard
Spiro, professor of medicine and director of the Medical School's
Program for Humanities in Medicine: "We're all strangers taking
care of strangers. Everyone ought to have some family physician
or nurse practitioner out there who does know you, but the notion
that you'll always know your doctor is hopelessly romantic."
All of which -- the reluctance
to confront death, the need to keep fighting it, and the conflict
of interests -- can conspire to place terminally ill patients and their
families in a nightmarish limbo, a lonely place from which the likes
of Jack Kevorkian and his suicide machine sometimes seem to offer
the only hope of easy escape.
But some 20 years ago,
Morris Wessel, clinical professor of pediatrics, Florence Wald,
former dean of the School of Nursing, and a number of colleagues
created an alternative when they started the first hospice in this
country. Modeled after the nursing-intensive approach to dying that
was pioneered in England by Cicely Saunders in the 1960s, the hospice
was developed to offer, either in a specially designed facility
or, when possible, in the home, a kind of care that was radically
different from what existed in hospitals.
There comes a point
when nothing more -- no additional testing, surgery, or any of the
myriad other procedures in the medical arsenal -- can be done to reverse
the inevitable. "At a hospice, we help patients and families
deal with the end," says Robert Donaldson, a Yale professor
of medicine and a doctor at Connecticut Hospice, Inc., which is
located in Branford. "We provide support, relief from symptoms,
particularly pain, and the assurance that we're here, no matter
what," says Donaldson. "If you don't do that, you haven't
finished your job as physician."
Death can be hideous,
cruel, and utterly capricious, but when the pace of life's final
journey is somewhat stately, even predictable, the hospice -- there
are now more than 2,000 in this country -- offers what many consider
the closest thing to a "good death" on this planet. "The
surroundings are pleasant, and the rules are loose -- if you want to
have a beer, so be it," says Donaldson, noting that right until
the end, patients retain their personhood. "And they're so
relieved to get out of the stream of diagnostic technology, where
they're punctured and invaded all the time."
Less treatment and more
caring may be just what the doctor ordered -- or should order, says
Donaldson. "The patients are grateful, because I can provide
what they need. I find that very enriching."
To every
thing there is a season.
So notes the Old Testament
book of Ecclesiastes, and in the modern debate over how to best
care for the dying, that ancient declaration provides worthwhile
advice, says Richard Selzer, a retired New Haven surgeon and former
Yale professor whose most recent book, Raising the Dead, offers
an intimate look at the author's own harrowing and near-fatal brush
with Legionnaire's disease. "We don't accept death as a natural
phenomenon -- this is wrong," says Selzer, acknowledging the irony
in his statement. For had the 67-year-old physician's doctors been
more accepting, he wouldn't be around to tell his tale.
While there is a time
to die, says the author of Ecclesiastes, precisely when is now a
matter that modern medicine has taken largely out of the hands of
God and nature. But just as the women's movement helped reclaim
birth from the medical establishment, patients are asserting their
formerly God-given right to a decent end. At Yale, doctors-to-be
are gradually learning to listen.
Peter Bernstein '86,
'91MD, took Mermann's course in 1987 as a kind of test. "I
was afraid that I couldn't deal with sick or dying people,"
says Bernstein, now chief resident in obstetrics and gynecology
at YNHH. So he was terrified when he met "Bob," a man
in his 40s who was losing his fight with a long-term illness. Over
the course of a semester, the student sat with his teacher through
CAT scans, transfusions, and the interminable waits for appointments.
"Seeing Bob go through all this opened me up to the idea that
explaining things and just sitting with a patient is really important,"
notes Bernstein, recalling his grandfather, a pediatrician who practiced
medicine in the days before antibiotics when often the best thing
a doctor could do was hold a patient's hand. "I'm still learning
as a doctor, but my real education began with Bob."
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