In the Netherlands, where euthanasia is legal, reports circulate regularly about elderly people refusing to go to the hospital for fear that a physician will deem their life unworthy. The “right to die” quite easily becomes the “obligation to die” once physicians start becoming judge and executor.
James A. Avery, MD, The Daily Progress.
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READER'S VIEWS: Physician-assisted suicide is a bad idea
Posted: Thursday, January 29, 2015 12:00 am READER'S VIEWS: Physician-assisted suicide is a bad idea James A. Avery, MD The Daily Progress
In the dark ages of medicine, physicians routinely ended the life of their patients. However, since the time of Hippocrates 2500 years ago, physicians have promised their patients that they will not intentionally terminate a life.
When, as he wrote in the Decorum, “patients become overmastered by their disease,” physicians agreed to not hasten or prolong death. “Cure sometimes, treat often, comfort always” was the basic strategy. Of course, since that earlier time and, up to today, physicians have always been tempted to help desperate and despondent patients kill themselves. Time and time again, euthanasia and physician-assisted suicide causes were championed – only to be ultimately rejected by the medical profession and almost all cultures.
G. K. Chesterton once said, “Don't ever take a fence down until you know why it was put up.” Since the time of Hippocrates, medicine has made huge advances in our ability to control and manage pain. So, I ask, why has there been a recent effort to take down this fence?
Certainly, the recent highly publicized case of Brittany Maynard, a winsome and attractive 29 year-old newlywed, has renewed the old tiresome arguments. Diagnosed with a brain tumor, Brittany moved from California, where she was born and raised, to Oregon where right-to-die laws are legal. On November 1, 2014, physicians prescribed a massive dose of life-ending barbiturates so Brittany could kill herself before many of the symptoms she feared and imagined could develop. It’s a sad and tragic story but the conclusion that suicide was the compassionate solution was even sadder.
As a board-certified hospice physician, I have personally taken care of many young people with brain tumors. I have found that once the hospice team addresses their suffering in all dimensions – physical, emotional, social, and spiritual – and reassures them about the future, anxieties are reduced and a peaceful death is the norm.
There are many reasons why I oppose physician-assisted suicide but let me focus on one of them here: it will change the medical profession in a dramatic and negative way. I don’t believe it is commonly known by most people that physicians in almost all countries are forbidden from participating in capital punishment. And, when physicians are inducted into the military, they do not bear arms. There are fundamental reasons for this and these go to the heart and soul of medicine: physicians heal and comfort – they do not kill.
In the Netherlands, where euthanasia is legal, reports circulate regularly about elderly people refusing to go to the hospital for fear that a physician will deem their life unworthy. The “right to die” quite easily becomes the “obligation to die” once physicians start becoming judge and executor.
Patients want their physicians to care for them without pondering and considering whether “they are worth the effort”. Taking care of seriously ill and dying patients is hard work - just ask any physician who does hospice or palliative medicine. “Assisted suicide is the easy way out for doctors,” said Johns Hopkins physician, Paul McHugh, “physician-assisted suicide tears down the time-honored barrier protecting patients from physician mischief.” Patients want a caring physician who tries his best to cure, comfort always, reassure them when they are despondent, honor reasonable wishes, and labor for their good.
So … back to our original question: was poisoning Brittany the best response a physician can offer a sad, desperate, and frightened young girl? I, like almost all physicians for the last 2500 years, emphatically say “no.”
Thirty-seven years ago, I entered medical school with the goal of reducing human suffering; the years have taught me that the physician-assisted suicide is not the answer for compassionate end of life care. The answer, in my view, is skilled compassionate hospice care.
James A. Avery, MD is the CEO of Hospice of the Piedmont.
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9 comments:
Ann
I am real sorry to read about this dying of Kate Kelly's mother; I am NOT saying this is a clear case pro euthanasia. I am saying Kelly's mother has been given very bad, insufficient palliative care, where the caregivers used morphine in the wrong way (calculating on the double effect??), causing side effects which resulted in this unwanted outcome: a terrible death!
I am not a fervent supporter of VSED, certainly not in all cases. The person must to begin with have the serious wish him/herself knowing the consequences; (s)he must be nearly moribound, barely be eating and drinking already, before starting the process of VSED at all. And... most important: good professional and competent guidance with optimal palliative care should have been arranged and available day and night.
It is a pity that Alex is using this story as a proof for the dangerous developments in the end-of-life decisions (a n=1 study) and not as a signal that Palliative Care failed in this case and thus that also providers of Palliative Care need education and transparancy.
I know cases (more then one for that) of VSED with late Alzheimer's where the patient received professional Palliative Care with VSED and died quietly and humanely; in a country where through (or at least since) legalisation of euthanasia, Palliative Care has been developed to a very high ranking (both in availablity and in quality) in the world, and where thus all end-of-life decisions (from "let nature take its role" via "palliative care/sedation" to "euthanasia or physician assisted suicide") are mostly seen as an issue to be talked about when appropriate.
Rob reduces the pain of Kate's mothers death to poor palliative care. He is only partly right.
The fact is that to kill someone, who is not otherwise dying by dehydration is euthanasia, does cause an horrific death and should be referred to as elder abuse.
To say that - if we only used the proper amount of morphine everything would be fine - negates the fact that this is not a good death because it requires large amounts of morphine to mask the pain.
This is totally different in a situation where someone is dying and is nearing death, whether it be through cancer or other causes that has led to organ failure.
In those circumstances the body is naturally shutting down and the body has stopped requiring or being able to circulate or absorb the hydration. In this circumstance the natural process of death requires, at some point, that fluids be withdrawn in order to prevent suffering.
Kate Kelly's mother had a mild stroke, she was not otherwise dying, she was not experiencing organ failure, but rather a decision was made, by others, that her life was not worth living.
This also occurs in the Netherlands.
It is with tears and heartache that I read your story. I am so sad and sorry that your mother and you were treated so horribly in the hospital. You see your story is so similar in so many ways to that of our dear dad and our family. I tell our story to anyone who will listen and most times others relate their own eerily similar and tragic story of a loved one. We knew what had happened to our dad and our family was not a unique story, but I had no idea just how often this is happening. So many tragic accounts that I have even considered documenting them.
There is something so corrupt happening and the corruption is resulting in unnecessary death.
My father was labelled with Alzheimers. Although, upon more detailed research, after the fact, we believe he was inaccurately labelled. He had some cognitive impairment. With much time and effort from our family (tireless efforts from my brother) he was actually able to re learn many things. And just months before he had the misfortune of ending up in the hospital he sat in the living room with us and stated “I am just happy to be sitting here with my family”. He was a happy and positive man and loved to connect with people. Quality of life for sure. Quality of life that was stolen from him and our family. He trusted us to take care of him the best we could and we did. But we were not prepared for the onslaught at the hospital and seemed powerless to help him there.
My dad’s story in the hospital is quite lengthy and involved so will not go into detail here.
We firmly believe that they withheld the proper medical care because of his Alzheimer label. That was confirmed to us even more so, once we obtained a copy of his medical file from the hospital. The medical file consisting of pages of notes from doctors and nurses -, purposeful and prejudicial entries with no foundation in truth and also purposeful omissions. Much time spent making notes. Much time… He was denied medical care because of his disability - and as such it would appear he was denied his basic human rights – at least his human rights as they are described in Canada. It is most unlikely that the majority of Alzheimer patients who end up in the hospital for another health issue actually die of Alzheimer’s. And yet it is most likely listed as the cause of death on the death certificate.
There appears to be a serious human rights violation occurring as it relates to disabled Canadians – whether Alzheimer or any other disability. I am not aware of any legislation that allows the removal of those human rights when one enters the hospital.
Kate -Please continue to tell your story about your mom and we will continue to tell ours about our dad. And if we can help even one family from torturous treatment in the hospital and help their loved one to return to their home and be cared for by those who know them best and love them, then we have succeeded – in memory and to the honour of all of those who didn’t make it home.