Tag: end of life

Blog Posts (65)

April 25, 2015

The Importance of Advance Directives and Power of Attorneys

This week I had the privilege of job shadowing in the clinical ethics department at a hospital here in Illinois. In clinical ethics, it is impossible to know exactly what your days will look like in advance, since your schedule depends on the varying needs of others in your workplace. There may be several days in a row where no requests for consults come in,... // Read More »
April 3, 2015

Some Responses Regarding PAS

I’ve posted several times on physician-assisted suicide (PAS) over the last 3+ years, including this past January 15, January 22, January 29, February 5, February 12, and March 27. Whew!  I hadn’t realized until I created that list how focused I’d been on the topic this year.  Of course, my thoughts are neither new nor my interest unique; others on this blog, for starters, have... // Read More »
March 28, 2015

Call to Action: Quality of Life

Earlier this month BBC News reported on Chris Graham, a 39-year-old man with early onset Alzheimer’s disease, an extremely rare gene mutation, which killed Chris’ father at 42-years-old. Graham, has a newborn son, to whom he may have passed on the gene mutation, but Graham remains hopeful, saying, “If we can put a man on the Moon then surely we can find a cure for... // Read More »
March 27, 2015

California PAS Bill Passes State Senate Committee

That’s the page 1 story in my local paper this morning (Thursday, March 26).  The California State Senate Health Committee passed SB 128 by a 6-2 margin.  The debate was accompanied by the usual testimonials, including one videotaped by Brittany Maynard before her suicide. Opponents raised appropriate arguments against the bill.  Perhaps the key statement was made by Dr. Warren Fong, president of the Medical... // Read More »
March 23, 2015

Will Ariadne Lead Us Through the Maze of End-of-Life Healthcare?

Note: The Bioethics Program blog will be moving to its new home on April 1, 2015. Be sure to change your bookmarks to http://bioethics.uniongraduatecollege.edu/blog/   by Richard Koo, Bioethics Program Alum (MSBioethics 2011) and Adjunct Faculty About four years ago, Susan D. Block, M.D. posted a blog on Harvard Business Review’s website as part of a series of […]
February 25, 2015

The Man Who Mistook His Life For A Hat

by Jacob Dahlke, Bioethics Program Alum (MSBioethics 2012) Our society tends to put on pedestals the celebrities among us, particular upon their deaths. For author Oliver Sacks, it is no different except that he is not yet dead. He did, however, recently announce in the New York Times that metastasized tumors were found in his body. […]
February 12, 2015

Which Doctor Should Carry Out the End of Life Conversation?

Yesterday, Steve Phillips echoed my support for Dr. Atul Gawande’s book, Being Mortal.  One of Dr. Gawande’s key points is how difficult it can be for doctors to talk with their patients about care at the end of life, when the doctor cannot “fix” the problem.  Steve also raised the difficulty of these discussions in his January 28 post on this blog. This past Tuesday,... // Read More »
February 12, 2015

How to Die in Canada

by Sean Philpott-Jones, Director of the Center for Bioethics and Clinical Leadership Last week, our neighbors to the north took a huge step towards legalizing physician aid-in-dying. On Friday, the Supreme Court of Canada unanimously struck down that country’s ban on the practice, suspending two sections of the Criminal Code that outlawed assisted suicide and […]
February 11, 2015

Debate on Physician Assisted Suicide

Here's a debate on Physician Assisted Suicide at higher than the normal level of discourse. Enjoy!
February 11, 2015

Something to live for

I just finished reading Atul Gawande’s book Being Mortal and would recommend it to anyone interested in the issues surrounding death and dying. In the book Gawande comes across as both a caring physician and an engaging author. He weaves together the things he has learned about how we die and stories of the lives of a number of people as the live out the... // Read More »

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Published Articles (3)

American Journal of Bioethics: Volume 11 Issue 7 - Jul 2011

A Philosophical Obituary: Dr. Jack Kevorkian Dead at 83 Leaving End of Life Debate in the US Forever Changed

American Journal of Bioethics: Volume 11 Issue 2 - Feb 2011

Book Review of D. Micah Hester, End of Life Care and Pragmatic Decision Making

American Journal of Bioethics: Volume 7 Issue 10 - Oct 2007

"Show Me" Bioethics and Politics

News (46)

October 23, 2012 6:01 pm

Watch your Words! The Challenges of Law Around the End of Life (Oxford Uinversity Blog)

[I]n South Australia last week, a bill has been proposed to clarify the legal status of advance directives. One very small part of that bill involves a modification to an older palliative care act. The modification corrects an ambiguity in wording in the earlier act. The ambiguity is subtle. However, that choice of words has had major consequences for seriously ill children and adults in South Australia and for health practitioners. It is a salutary reminder of how hard it is to enact good laws in the area of end of life, and how easily such laws can make things worse rather than better.

September 21, 2012 8:12 pm

After Death, Helping to Prolong Life (The New Tork Times)

EDINA, Minn. — Just down the hallway, in Room 356, Curtis Kelly’s body lay covered to the chest by a white blanket, his torso rising and falling with the help of a ventilator. A neurologist at Fairview Southdale Hospital had declared him brain-dead nearly six hours earlier.  Mr. Kelly’s far-flung family — a son, three siblings, a sister-in-law, his girlfriend and the daughter of a former girlfriend — had gathered in a narrow conference room in the intensive care unit so that John P. LeMay could ask permission to recover his tissue and organs.

 

August 14, 2012 7:47 pm

End-of-Life Care for Kids Raises Ethics Issues (MedPage Today)

Healthcare providers should have rapid access to legal remedies for end-of-life disputes involving children whose parents resist withdrawal of aggressive therapy on the basis of religious beliefs, authors of a review concluded.  Over a 3-year period, 17 of 203 cases could not be resolved after lengthy discussions with parents. Subsequently, most of the cases were resolved, but five remained undecided, each because of the parents’ belief in a miracle for their children, according to an article published online in the Journal of Medical Ethics.

August 14, 2012 7:45 pm

Deeply Religious Parents Often Reluctant to Cease Medical Care (ABC News)

Arthur Caplan, the head of the division of medical ethics at NYU Langone Medical Center, recalls a case of a man who had beaten his six-month-old child to death. It was a horror the mother simply could not accept.  A deeply religious woman, she pushed the doctors to do more, telling them that God would intervene and allow her daughter to make a miraculous recovery. For several hours there was a tense standoff between caregivers and parent.

August 7, 2012 9:35 pm

At the End of Life, Talk Helps Bridge a Racial Divide (The New York Times)

Living or dying is not at issue. The question this family confronts is how the patient will die: a little sooner, with adequate morphine, surrounded by loved ones in the hospice unit, or a little later, in a never dark or quiet patch of the I.C.U., ribs broken by failed, if well-intentioned, CPR.  Add to this the following: The patient and family are black. And while race should not be relevant at this moment, research tells us otherwise.

July 27, 2012 5:57 pm

Are Doctors More Likely to Refuse CPR? (The Atlantic)

Are doctors more likely to refuse revival in the event of cardiac arrest? In the Hopkins study, 90 percent of doctors said they’d rather die by cardiac arrest than be resuscitated. Only a quarter of the public feels the same way.  Do doctors know something we don’t about the miracles of CPR? In one Japanese study of 95,000 CPR cases, just eight percent of patients survived for longer than a month after being revived.

July 26, 2012 4:25 pm

King: U.S. lifestyles to blame for high health costs (Houston Chronicle)

Another challenge for the U.S. with respect to overall health care costs is our cultural approach to end of life care. Medicare now estimates that 27 percent of its budget goes for care provided in the last year of life, and a big chunk of that is spent in the last few weeks of a person’s life. The Lien Foundation did a study on end of life care in 40 developed countries. While the U.S. ranked high on the availability and quality of end-of-life care, its cost of care was one of the highest.

July 11, 2012 6:41 pm

Legal Euthanasia Didn’t Raise Death Rate, Researchers Say (Bussinessweek)

“Countries differ greatly in demography, culture and organization of medical care,” Lo, who is also director of the medical ethics program at the University of California, San Francisco, wrote in a comment accompanying the study. More in- depth information is needed to better understand how patients and physicians reach their decisions, he said.

July 10, 2012 4:23 pm

Doctor accused of ending patients' lives prematurely (ABC Online)

There are calls for a Queensland doctor to be stripped of his right to practice medicine and investigated over allegations he prematurely ended the lives of patients under his care.  Former Queensland Medical Board investigator Jo Barber says the doctor’s actions are so dangerous he could have been charged with manslaughter or murder.  Ms Barber says there are a number of deaths linked to the doctor, who, after fronting the state’s medical board, was allowed to continue practising as long as he was not working in intensive care.

July 9, 2012 9:12 pm

Ensuring a good death: a public health priority (Oxford University Press Blog)

Protecting the health and wellbeing of the population directly or indirectly involved with death and dying is a huge public health challenge. Currently, high quality end of life care is not yet available in most parts of the world, and in those countries where it is available it is not accessible or not initiated timely for all in need, independent of their disease, age, gender, socioeconomic, or ethnic background. Largely as a result of that, a large majority receives overly aggressive treatment until death or shortly before death, has undertreated psychological and physical symptoms at the end of life, and is not able to die in a place or manner that accords with their personal preferences.

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