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Dehydrate dementia patients to death to save money: British Medical Journal editorial
LifeSiteNews ^ | 07/16/12 | Hilary White

Posted on 07/16/2012 6:10:54 PM PDT by Brian Kopp DPM

Dehydrate dementia patients to death to save money: British Medical Journal editorial

by Hilary White, Rome CorrespondentMon Jul 16, 2012 15:38 EST

July 16, 2012 (LifeSiteNews.com) – The courts should not interfere with doctors who want to dehydrate to death incapacitated patients who are a drain on scarce financial resources, according to an editorial in this week’s edition of the prestigious British Medical Journal.

Raanan Gillon, emeritus professor of medical ethics and former chairman of the Institute of Medical Ethics governing body, wrote that a ruling last year by the High Court against dehydrating an incapacitated patient to death was “profoundly disturbing” because it took the life and death decision-making power out of the hands of doctors and required that the principle of the “sanctity of life” take precedence over other considerations.

The judgment, he said, “threaten[s] to skew the delivery of severely resource-limited healthcare services towards providing non-beneficial or minimally beneficial life prolonging treatments including artificial nutrition and hydration to thousands of severely demented patients whose families and friends believe they would not have wanted such treatment”.

He complained that the ruling required that, under the “stringent” Mental Capacity Act, in order to remove “life prolonging treatment” like a feeding and hydration tube, the patient himself must have left a legally binding “advance decision” in writing, and that previous casual or unrecorded statements to relatives were not sufficient grounds. 

The editorial, titled, “Sanctity of life law has gone too far,” said that unless it is overturned, the court ruling “will gradually and detrimentally distort healthcare provision, healthcare values, and common sense.”

Its logical implication, Gillon wrote, is that “doctors should no longer decide, in consultation with those who know their incapacitated patients, whether life prolonging treatment including artificial nutrition and hydration will be in their patients’ best interests.”

Furthermore, he said, the ruling logically means that those patients in “a higher than minimal state of consciousness must be similarly protected”.

The court ruling in question was that in the M Case, in which the family of a 52-year-old woman who was found to be in a “minimally conscious state” and who was “otherwise clinically stable,” were petitioning the court to have her feeding and hydration tube removed. The Court of Protection ruled that all patients in such a state must be referred individually to the Court of Protection if “life prolonging treatment” by artificial nutrition and hydration is to be withheld or withdrawn.

Mr. Justice Baker said in the September 2011 decision, “The factor which does carry substantial weight, in my judgment, is the preservation of life. Although not an absolute rule, the law regards the preservation of life as a fundamental principle.”

Justice Baker wrote that the courts should not “attach significant weight” to the patient’s previous statements unless they had been expressed in a way that could stand up to legal scrutiny. As in the case of Terri Schiavo in the U.S., M’s family had argued that her alleged previous statements indicated that she would not want to be dependent on such care.

Baker responded to this by ruling, “[Given] the importance of the sanctity of life, and the fatal consequences of withdrawing treatment, and the absence of an advance decision that complied with the requirements previously specified by the common law and now under statute, it would in my judgment be wrong to attach significant weight to those statements made prior to her collapse.”

Anthony Ozimic, communications manager for the Society for the Protection of Unborn Children, said that the ideology being espoused by Gillon and the British Medical Journal is indistinguishable from the materialist utilitarian ethic that led to the elimination of the “unfit” by eugenicists in the early 20th century, including in pre-World War II Germany. 

“What is particularly disturbing about Professor Gillon’s opinions is that he is judging certain disabled people as having lives unworthy of life, balancing those lives against the needs of other patients and seeking to justify killing the disabled on the grounds of rationing,” Ozimic told LifeSiteNews.com.

“Such a utilitarian calculus is in substance no difference to the calculus made during World War II by the German authorities: that the disabled should die so that wounded soldiers could live. In any case, assisted food and fluids are basic nursing care, not futile medical treatments.”

As shocking as such pronouncements are to the general public, the idea that disabled patients should be euthanized, either directly or by the removal of food and hydration, is actually a mainstream of thought among many of the western world’s medical ethicists. Gillon himself is a major voice in the field as a former editor of the Journal of Medical Ethics and the author of the 1985 book “Philosophical Medical Ethics”.

Classical medical ethics, that held as paramount the principle “Do no harm,” has in large part been set aside in favor of the new utilitarian-based Bioethics, a formal or “normative” branch of ethical philosophy that seeks “the greatest good for the greatest number” according to the “principles” of “justice, beneficence and autonomy”.



TOPICS: Extended News; Front Page News; News/Current Events; Politics/Elections
KEYWORDS: cultureofcorruption; deathcare; deathpanels; deathpanels4all; euthanasia; healthcare; hillarycare; moralabsolutes; nazism; obamacare; prolife; romneycare; romneydeathpanels; socializedmedicine; terrischiavo; zot
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Friday, 13 July 2012

People with severe dementia should be starved and dehydrated to death to save money says BMJ editorial

There is an editorial in the British Medical Journal this week by a retired professor of philosophy titled ‘Sanctity of life law has gone too far’.

Raanan Gillon (pictured) reviews the case of M, a woman in minimally conscious state, who was the subject of a court of protection ruling last year.

I have written about the case before on this site, both before and after the judgement, and spoke to the Telegraph about it earlier today so I won’t repeat all the details again here.

Essentially the judge decided that M’s feeding tube should not be removed as she did not have a valid and applicable advance directive in place. Instead he gave priority to preserving her life.

Gillon didn’t like the judgement for two reasons.

First he felt that the judge ‘did not accord “significant weight” to the patient’s previously expressed values, wishes, and views’. But in fact these were not sufficiently clear and in the absence of a clear statement of the patient’s wishes, Justice Baker was simply giving precedence to the preservation of life over uncertain autonomy.

Second, Gillon was unhappy that decisions about starting or stopping life prolonging treatment, including the withholding or withdrawal of artificial nutrition and hydration, for all incapacitated patients should be brought to the Court of Protection. But in so doing the judge was simply acting in accordance with precedent laid down in the Tony Bland case (involving a man in persistent vegetative state) and outlined in the Mental Capacity Act 2005.

Gillon’s real problem is that he doesn’t like the current law and considers that the lives of some seriously brain-damaged people are not worth living. He thinks that giving nutrition and hydration to people with severe brain damage or dementia is not beneficial and that they should have this basic care withdrawn and allowed to die.

His real reasons come out later in the editorial:

‘The logical implications of this judgment threaten to skew the delivery of severely resource limited healthcare services towards providing non-beneficial or minimally beneficial life prolonging treatments including artificial nutrition and hydration to thousands of severely demented patients whose families and friends believe they would not have wanted such treatment. The opportunity cost will probably be reduced provision of indisputably beneficial treatments to people who do want them.’

Now this statement is very interesting indeed as M was not actually demented, just seriously brain damaged. In addition she had some degree of residual brain function.

It is noteworthy that Gillon is very selective in his reporting of these facts and conveniently does not mention that M had some awareness of herself and her environment, some understanding of language, occasionally spoke, appeared to be able to appreciate some things that were said to her and responded to music. Although she regularly experienced pain, this was not constant or extreme, and her condition was stable. And unlike dementia patients, who are terminally ill, she had a non-progressive condition.

Gillon's suggestion, that severely demented and brain-damaged people should be sedated, starved and dehydrated to death on the basis of their friends and relatives vague and contradictory recollections of 'what they would have wanted' would create a most dangerous precedent and place us on a very slippery slope indeed.

His implication that we should be withholding nutrition and hydration from such people so that we can spend the money elsewhere is chilling and demonstrates precisely why we don't give doctors, politicians and most importantly philosophers (like Gillon!) the power and authority to make such decisions on utilitarian grounds.

People who are severely brain-damaged or suffering from dementia, but not imminently dying, should be given nutrition, hydration, symptom relief and warm human interaction until the day that they die peacefully and naturally.

We don’t kill them either by giving them lethal injections or dehydrating them to death and we ensure that there is adequate legal protection in place so that no one who has an interest in their deaths, whether financial or emotional or to get rid of an unwelcome care burden, should be able to exploit or harm them in any way.

The law is there primarily to protect vulnerable individuals from exploitation and abuse and as such it needs the strength to deter individuals and institutions who have something to gain, financially or otherwise, from another person's death.

It does not need changing and the involvement of the Court of Protection in difficult cases is a necessary and effective safeguard.

1 posted on 07/16/2012 6:11:03 PM PDT by Brian Kopp DPM
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To: Dr. Brian Kopp

Lives not worth living = not worth anything to him.
Allowed to die when they are not even dying = killed.


2 posted on 07/16/2012 6:18:12 PM PDT by Lady Lucky (If you believe what you're saying, quit making taxable income.)
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To: wagglebee
Coming to an ObamaCare Independent Payment Advisory Board (IPAB = Death Panel) near you soon!

NATIONAL REVIEW ONLINE

IPAB, Obamacare’s Super-Legislature

By Michael F. Cannon & Diane Cohen

June 15, 2012 4:00 A.M.

EXCERPT:

The individual mandate isn’t Obamacare’s only unconstitutional provision, or even its most unconstitutional provision. That distinction belongs to the Independent Payment Advisory Board. A heretofore unreported feature of this super-legislature makes it even more authoritarian and dangerous than anyone knew.

IPAB consists of up to 15 unelected government “experts.” Its stated purpose is to restrain Medicare spending. If projected spending exceeds certain targets, Obamacare requires IPAB to issue “legislative proposals” to reduce future spending. Those proposals could include drastic cuts that jeopardize seniors’ access to care, leading some critics to label IPAB a “death panel.”

But the really dangerous part is that these are not mere “proposals.” Obamacare requires the secretary of Health and Human Services to implement them — which means they become law automatically — unless Congress takes certain steps to head them off. Congress may replace the Board’s proposal with its own cuts, at least initially. But Obamacare requires a three-fifths vote in the Senate to pass any replacement that spends more than the Board’s proposal. In other words, to override IPAB’s proposal completely, opponents must assemble a simple majority in the House and a three-fifths majority in the Senate and the president’s signature.

That makes IPAB more than an advisory board. It’s a super-legislature whose members are more powerful than members of Congress. If eight members of Congress propose a bill, all that’s necessary to block it is a majority of either chamber, or one-third of either chamber plus the president.

Worse, Obamacare forbids Congress to repeal IPAB outside of a brief window in the year 2017 — and even then requires a three-fifths supermajority in both chambers plus a presidential signature. Under Obamacare, after 2017 Congress could repeal Medicare, but not the board it created to run Medicare. Congress and the states could repeal the Bill of Rights — but not IPAB.

What kind of laws will these super-legislators impose? Obamacare supposedly prohibits these super-legislators from raising taxes or rationing care. Yet those restrictions are unenforceable and meaningless. For instance, the statute lets IPAB define “rationing” and protects that definition — along with the secretary’s implementation of IPAB’s edicts — from administrative or judicial review. The prohibition on raising taxes is likewise toothless. IPAB can raise taxes as surely as it can cut Medicare spending.

In effect, Obamacare gives IPAB the power to raise taxes, spend money, place conditions on federal grants to states, and exercise other powers the Constitution reserves solely to Congress. If the Supreme Court upholds Obamacare’s mandated Medicaid expansion, states may soon see IPAB imposing similar mandates on states. And if President Obama fails to appoint any IPAB members, all these powers fall to Secretary of Health and Human Services Kathleen Sebelius...


3 posted on 07/16/2012 6:19:07 PM PDT by Brian Kopp DPM
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To: Dr. Brian Kopp

Coming soon to a hospital near you.

I’m sure I don’t need to tell you that dehydration is a painful thing—very painful.....


4 posted on 07/16/2012 6:19:11 PM PDT by basil (Second Amendment Sisters.org)
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To: Dr. Brian Kopp
Raanan Gillon should be among the first to personally undergo this treatment to demonstrate the efficacy of this policy ~ as soon as possible.

Time is being wasted.

5 posted on 07/16/2012 6:19:48 PM PDT by muawiyah
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To: Dr. Brian Kopp

To even have this discussion shows how disgusting and vile humanity has become.


6 posted on 07/16/2012 6:20:35 PM PDT by eak3
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To: Dr. Brian Kopp

Why not just stab ‘em to death? Why make them suffer? Afraid you will spend too much washing the sheets?

D!ckhead...hope its you one day.....


7 posted on 07/16/2012 6:22:33 PM PDT by Adder (Da bro has GOT to go!)
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To: All


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8 posted on 07/16/2012 6:24:59 PM PDT by musicman (Until I see the REAL Long Form Vault BC, he's just "PRES__ENT" Obama = Without "ID")
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To: basil
Coming soon to a hospital near you.

If you don't have money or insurance, you should die. Who is willing to pay for the deadbeats?

9 posted on 07/16/2012 6:27:43 PM PDT by Doe Eyes
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To: basil

Why in hell did the Brits try to defend themselves in WW2?
The Nazis would have provided the same standard of “medical care” for them....


10 posted on 07/16/2012 6:28:46 PM PDT by faithhopecharity
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To: basil
When my mother-in-law was dying of cancer last summer, a nurse with the local hospice thrust a sheet of paper into my wife's hands with the following text (because we insisted on continuing a simply IV for comfort measures, as my mother-in-law was frequently complaining of thirst in her last two weeks of life and had lost the ability to swallow):

Changing Pattern of Feeding and Hydration Needs in Terminal Care

[snip]

Dehydration is nature at work and can bring relief from distressing symptoms such as
Hiccough
Abdominal Bloating
Vomiting from increased stomach secretions
Pressure from the tumor causing pain
Shortness of breath
Lung congestion
Rattling secretions
Impaired consciousness

There are certain circumstances where some of these statements may be true, but to use this across the board to discourage or refuse simple IV hydration among all cancer patients is wrong.

I won't even go into the details of the battle we had to fight just to get her the IV in the first place.

11 posted on 07/16/2012 6:31:41 PM PDT by Brian Kopp DPM
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To: Dr. Brian Kopp

All you need is a fast and loose definition of dementia.

Look up how Yuri Andropov utilized the “psychiatric hospitals”.


12 posted on 07/16/2012 6:32:03 PM PDT by Fred Hayek (The Democratic Party is the operational wing of CPUSA.)
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To: Doe Eyes
If you don't have money or insurance, you should die. Who is willing to pay for the deadbeats?

Food and water are basic human rights, not medical treatments that can arbitrarily be withdrawn at whim. Denying folks water and food is murder.

By the way, this is a pro-Life forum.

13 posted on 07/16/2012 6:36:03 PM PDT by Brian Kopp DPM
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To: Dr. Brian Kopp

The NAZIs began with terminating the patients they thought were a drain on society and then expanded that program to gypsies, Jews, and further expanded it to troublemakers and those who refused to go along with the program.

The Weather Underground figured they would need to kill 25 million Americans who would refuse to be “re-educated”.


14 posted on 07/16/2012 6:38:58 PM PDT by a fool in paradise (Eric Holder's NAACP rally against the voter ID laws required the press to bring govt issue photo ID.)
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To: Dr. Brian Kopp
Dehydrate dementia patients to death to save money: British Medical Journal editorial

Demons.

15 posted on 07/16/2012 6:39:02 PM PDT by Talisker (One who commands, must obey.)
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To: Fred Hayek
Indeed.

Under ObamaCare, voting for the wrong party might eventually be interpreted as a sign of dementia...

Why any retiree or anyone nearing retirement would vote for Obama is beyond comprehension.


16 posted on 07/16/2012 6:40:22 PM PDT by Brian Kopp DPM
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To: Doe Eyes
If you don't have money or insurance, you should die. Who is willing to pay for the deadbeats?

Shut up, scumbag.

17 posted on 07/16/2012 6:43:08 PM PDT by Talisker (One who commands, must obey.)
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To: Dr. Brian Kopp

To offer government healthcare, then to use that system to kill patients negates any justification for it in the first place.

At this point, religions need to enter the situation as “no kill” caregivers, who, while not offering technological dehumanization, either, will only tolerate natural death.

The only thing the government has to do is to offer people a choice. It does not want to do this, because now it has an effective monopoly over life and death. And it invariably chooses death.


18 posted on 07/16/2012 6:44:43 PM PDT by yefragetuwrabrumuy
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To: Dr. Brian Kopp

Hmmm. At the other end of the default process, we could dehydrate the more educated members of the political sturgeon class.


19 posted on 07/16/2012 6:46:05 PM PDT by familyop ("Wanna cigarette? You're never too young to start." --Deacon, "Waterworld")
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To: Dr. Brian Kopp

Dementia patient don’t actually require much “medical care” — they just need plain old care from nurses’ aides and plain old caregivers. So, the whole premise is buncomb.


20 posted on 07/16/2012 6:46:17 PM PDT by WashingtonSource
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