The book that I’m currently reading is titled, Twelve
Patients: Life and Death at Bellevue Hospital
by Dr. Eric Manheimer. Dr. Manheimer was the medical director at the hospital
for 14 years and is currently a professor at NYU School of Medicine. In this book
he gives the reader a glimpse not only into this notable hospital but also into
the health care system, both its successes and failures.
Bellevue Hospital is 275 years old, making it the oldest
hospital in the country. Bellevue has been a leader since the beginning having
many firsts: maternity ward, pediatric ward, and C-section to name a few. Over
the next few posts I’ll look at few of the more profound comments that have
stuck with me.
An area of medicine that is growing at an enormous rate is
that of palliative care. The fundamental basis of palliative care is death and
the rights that should be afforded to the patient in this process. Quoted from
Dr. Manheimer:
How people die and
how we participate in their deaths is as much about us as about them. Our own
humanity is at stake. In a society that is increasingly mesmerized by
efficiency, measurement by numbers and a bottom-line mentality that extols
profit and wealth over any other human value, the risk is clear to everyone I
work with. When health care is now measured by a “medical loss ratio,” and the
percentage of spending on health care is considered a “loss,” then we are
really lost.
This comment was prompted by a story he told about a young
man with terminal cancer that had lost both his legs and was literally falling
apart at every point. He wished to return to his native country, Mexico, to
die. Obviously this is not something insurance would pay for nor was it
something that anyone would recommend. We are constantly pushed to use every
available treatment to keep someone alive despite his or her quality of life.
Just because we have the technology to keep someone alive doesn’t mean it is
always the right thing to do.
When discussing this very situation in a class I took this
fall, a comment was made in our text that often the family needs to see the
suffering in order to make it feel real. If they are unable to see their loved
one suffering they are unable to process their death. This harkens back to the
comment of making death about us. When or why should it ever be about us?
Wouldn’t the most respectful thing be to help the dying fulfill their wishes
even if that’s not what medicine would tell us to do?
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