As an oncologist, I have witnessed patients go home and
heard later how they died at home, surrounded by family and friends. I have
witnessed others die in a hospital room, comforted by the care of the inpatient
team even as they depart this earth. These are the ones that stick with me and
what I think about when I hear the term a “good death”. It’s what I would want
for myself—dignity, serenity, and comfort.
The reality of the end of life, however, is that not
everyone shares my view of what constitutes a good death, and I’ve come to
realize that when a patient has a very different view of the end of life from
mine, it can be very difficult to do what’s right.
Such was the case with Jean. I met her during my time as an
inpatient attending. She was only 32 years old and only ten months prior had
been diagnosed with stage IV lung cancer. When we met she had been hospitalized
for pain control. Review of her treatment history showed that multiple trials
of chemotherapy had not been successful, that her cancer was widely metastatic,
including involvement of her bones and brain. Still, she did not accept
hospice, nor would she talk of end of life. She wanted more treatment, wanted
to know what else could be done. Yet, she had also begun to cycle through
inpatient stays due to her cancer: two weeks prior, it was brain metastases
that had caused seizures, this time it was a pathologic fracture of her hip.
All the while she had become weaker, bed bound, and unable to perform the
simplest of tasks, like getting dressed on her own.
When I met her, I tried to get a sense of her goals and
preferences. She understood her cancer was advanced, but she was not going to
stop fighting. She wanted to do “everything,” no matter how aggressive. It
turns out, even her own oncologist had tried to talk with her about prognosis,
but was rebuffed. Jean, despite how sick she was, refused to hear bad news and
talk of “end-stage” anything. She even resisted a palliative care evaluation.
However, this admission would be the one where it all became
critical. Very quickly during this stay, Jean began to decompensate. Her oxygen
levels were unstable and in hours she went from not requiring oxygen to
requiring a non-rebreather. We had wanted to get imaging, but she proved too
unstable. We suddenly faced a potentially terminal situation.
“Jean, you’ve become very sick,” I told her. “We need to
transfer you to the Intensive Care Unit, perhaps even put you on a breathing
machine.”
She looked panic stricken. “Will I make it off the machine?”
she asked.
“I am not sure,” I told her, “but I am afraid you’ll die in
the unit.” I had hoped she would refuse the ICU transfer, let us care for her
and ease her pain and suffering, allowing her to recover with standard care, or
else, to die with dignity.
“Okay then.” That was her only response. The inpatient team
was resigned to having her move to the ICU. They had known her better than me,
and they had witnessed how quickly she had deteriorated. I sensed that they had
wanted to help her find peace, acknowledge that she was at the end of her life.
I also sensed they saw the move to the ICU as inappropriate, especially given
how quickly and how significantly her cancer had advanced.
Still, with that, she was taken to the ICU and later that
evening, intubated. It turned out she had had several acute pulmonary emboli
that had caused a strain to her right heart. She soon became hemodynamically
unstable requiring pressors to support her blood pressure. Despite doing all
that they could do, Jean died in the ICU—intubated, sedated, and alone.
I asked myself if I could have done anything differently, as
has her own oncologist since. But, ultimately, we only have one life to live,
and one death to experience. I suppose as much as I know how I want to die, I
cannot assume that others will feel the same way. I have had patients embrace
the term, “death with dignity” but it has not been universal. There are others
who hear that phrase and shudder—because there is no dignity in death, there is
only death.
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