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Viewing: Blog Posts Tagged with: organ donation, Most Recent at Top [Help]
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1. Pieces of Me: Amber Kizer

Book: Pieces of Me
Author: Amber Kizer
Pages: 304
Age Range: 12 and up

I very much enjoyed Amber Kizer's post-apocalyptic survival story A Matter of Days. In Pieces of Me she takes on a very different topic. Pieces of Me is about a high school girl named Jessica who finds her life connected with those of four other teenagers, after a terrible accident. 

Stop here if you prefer to know nothing about a book, because I can't discuss this book without telling you what it's about. The truth is strongly hinted at by the title and jacket copy, and becomes clear quite early in the book anyway. 

So what happens is that Jessica, who always felt more or less invisible in high school, ends up brain dead in a car crash. Her various organs are donated and transplanted into the bodies of four other teens, three of them local and one from another state. Jessica's consciousness remains tied to these four teens, and in alternating chapters we hear her thoughts on their continued experiences (though she is not able to communicate with them). Eventually, the threads of Jessica that connect these teens bring them together. 

I found this to be an interesting premise. The alternating chapters lend a certain suspense to the story, and seeing the characters (eventually) as they see one another helps to give a clear view. There's a fairly overt pro-organ donation message to this book, which is addressed directly in an author's note at the end. There's also a fair bit of detail about what it's like to have a chronic, life-threatening illness such as cystic fibrosis. This is a book that I do think will expand readers' perspectives, giving them a look into the lives of people whose problems may be bigger than their own. 

However, as a reader, I personally had trouble with the viewpoint. Each chapter is kind of a mix of Jessica's viewpoint and that of whichever other kid she is inhabiting (or however you would put it). These sections are in limited third person perspective, from each teen's viewpoint, but then Jessica's thoughts are there, too, sometimes. This is probably deliberate, showing how Jessica's consciousness is becoming intertwined with her organ recipients. But I had trouble wrapping my head around it, and tell what thoughts were from Jessica and what were from Samuel, Vivian, Leif, and Misty. Like this:

"The more time we spent here, the more I felt the humble and special appeal it held for Misty. There was peace here. Answers.... Dropping her backpack on the ground, she slid into a massive leather armchair that was surprisingly comfortable." (Page 61, at the library). 

Does Jessica know that Misty is comfortable, and she's telling us? Or is it Misty telling us? Probably this is nit-picking, but thinking things like this kept taking me out of the book. There are also some IM exchanges between the (living) kids, full of abbreviations, that I found hard going, though the target teen audience will probably enjoy them.  

I did find the end of the book moving, and Pieces of Me definitely made me think. I probably would have found the premise irresistible when I was a teenager, and I do think that teens today will enjoy it, too. The protagonists are all sympathetic, and quite varied, giving a wide range of readers someone to root for. There's a modern feel to the text, too, with message boards, blogs, and of course hospitals. All in all, I think that Piece of Me is well worth a look by librarians who serve teens, even though it didn't quite work for me personally. 

Publisher: Delacorte Press (@RandomHouseKids
Publication Date: February 11, 2014
Source of Book: Review copy from the publisher

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© 2014 by Jennifer Robinson of Jen Robinson's Book Page. All rights reserved. You can also follow me @JensBookPage or at my Growing Bookworms page on Facebook

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2. Organ donor shortage versus transplant rates

By David Talbot

The article in this week’s Times with the commentary written by Chris Watson illustrates the significant changes that have happened in transplantation over the last two years. In 2008, the Organ Donor Taskforce (ODTF) came up with 14 recommendations to address the problem of donor shortage, and then UK Transplant (which then changed to Blood Transplant) acted upon these.

In addition to these changes, organ donation surgery became restricted to six zones whereas before the ODTF recommendations, all 26 transplant units in the country contributed to cadaveric organ donation. Also, the national sharing of organs (which had been voluntary, in so far as we aimed to serve our own community primarily and additional organs were shared only in certain cases) became enforced. This essentially was because there was a postcode imbalance, and some kidney failure patients waited six years for their transplant whereas in the northeast, patients generally waited only for 18 months.

The reasons for this imbalance were complex and were partly influenced by certain ethnic minority populations who didn’t support cadaveric donation while simultaneously making up a significant percentage of the number of patients who needed a transplant.

Additionally, different transplant unit structures had varying degrees of enthusiasm for donation. The work force obviously recognized these problems and tried to unify the approach and also ensure equality of access.

On a personal level, I was reluctant to throw my lot in with these national developments because our transplant population had a good deal! Indeed, with the national sharing mechanism, our local transplant rates initially fell, resulting in an increased waiting time.

The ODTF 14 point plan was, to me, an experiment which should be abandoned if it didn’t work. However, its effect was to promote donation by embedding Transplant Coordinators in most hospitals, thereby insuring that potential organ donors are not overlooked. In addition, numbers of Non-Heart-beating donors (aka donor after cardiac death), thanks to our pioneering work, have really taken off, accounting for 37% of cadaveric kidney transplants nationally. So although from a local level the national sharing scheme was a bad idea at the time, because of the promotion of donors through the enactment of the ODTF plan, the transplant numbers have now increased nationally, so my concerns for the future have proved wrong.

For example, I was on call for the week between Christmas and New Year and we did six kidneys and two liver transplants. Last week, I was again on call, and we did a liver, a kidney/pancreas, three live donor kidneys, two double kidney transplants, and an islet transplant! On the background of this our unit did 135 cadaveric donors last year.

Our next pressing problem is surgical exhaustion!

David Talbot is a Consultant Transplant Surgeon at Newcastle Hospitals NHS Trust and co-author of Organ Donation and Transplantation After Cardiac Death.

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3. Redefining Death — Again

medical-mondays

Frederick Grinnell is Professor of Cell Biology and founder of the Program in Ethics in Science and Medicine at the University of Texas Southwestern Medical Center, Dallas. His newest book, Everyday Practice of Science: Where Intuition and Passion Meet Objectivity and Logic offers an insider’s view of real-life scientific practice. Grinnell demystifies the textbook model of a linear “scientific method,” suggesting instead a contextual understanding of science. Scientists do not work in objective isolation, he argues, but are motivated by interest and passions.  In the article below he looks at a recent article in Nature about defining death.  Read previous posts by Grinnell here and visit his website here.

An editorial in Nature (1 October, 2009) entitled “Delimiting death” supports the proposal to reconsider the legal definition of death. “Ideally,” writes the Nature editor, “the law should be changed to describe more 9780195064575accurately and honestly the way that death is determined in clinical practice.” The current definition uses the criteria: (1) irreversible cessation of circulatory and respiratory functions, or (2) irreversible cessation of all functions of the entire brain, including the brain stem. However, assessing ‘irreversible’, ‘all functions’ and ‘entire brain’ becomes to some degree a matter of physician judgment. In cases involving organ procurement for transplantation, the physician is under pressure to obtain donor organs that are as fresh as possible. The situation becomes conflicted. “Physicians know that when they declare that someone on life support is dead, they are usually obeying the spirit, but not the letter, of this law. And many are feeling increasingly uncomfortable about it.”

The Nature piece might be dismissed as adding nothing new to the discussion except for the provocative, two part, conceptual definition of death that the editor proposes: (1) “the person is no longer there” and (2) “can never be made to return.” The first part of this definition helps makes clear the symmetry between the most contentious issues of modern bioethics – endings and beginnings of life. The person is no longer there; we can harvest the body for organs. The person is not yet there; we can harvest the body (embryo) for stem cells.

Franz Rosenzweig’s metaphorical description of death — “His I would be only an It if it were to die.” –no longer is just a metaphor. The meaning of human death emerges according to the organization of human life. For a newly formed embryo, death means loss of viability of a single cell. After several cell divisions, loss of viability of a single cell no longer equals death. Rather, death becomes equivalent to development arrest. After 3-4 months of gestation, once the cardiovascular system develops, it becomes reasonable to speak of cardiovascular death. After 6-7 months, once the central nervous system develops, it becomes reasonable to speak of brain death. After development of modern life support systems, once machines can replace heart and brain functions, it becomes reasonable to speak of the person and the body as separated entities. Modern medical technology has succeeded in separating the I from the “living” It. Modern social thinking remains conflicted about accepting this separation.

Using Nature’s conceptual definition of death as a point of departure is unlikely to produce a more easily implemented legal definition of death for two reasons. First, nobody knows the answer to the question “Where is the person?” Indeed, trying to answer this question has become the central focus of cognitive neuroscience research with no consensus in sight except that – which would return us to the current definition of death — the person will be gone after cessation of brain function. Those who support using human embryos for research up to 14 days of embryo life select 14 days not because they know when the person has arrived but rather because they agree that before day 14 the person could not yet have arrived. Second, both from technical and practical points of view, the statement “can never be made to return” will add the word ‘never’ to the ambiguous list of other terms, i.e., irreversible, all functions and entire brain, about which the Nature editor complains. Therefore, given the inherent ambiguity, trying to decide the moment of an organ donor’s death with certainty will continue to have the potential to create a conflicted (or so it might feel) situation of choosing to sacrifice one life to save another. Clinical judgment still will be required as always is the case in the practice of clinical medicine.

If changing the legal definition of death cannot solve the practical problem, is there an alternative? One approach might be to change the informed consent process so as to involve organ donors more explicitly in the choosing process. Some donors will want to gift their organs only after certainty of death. Their wishes oblige physicians to act cautiously in declaring death, even if it means potentially reducing the value of the organs. However, other donors might view themselves as more involved participants whose advanced directives encourage their physicians to act to maintain the value of their organs, even if doing so means instructing the physician to obey the spirit and not necessarily the letter of the law. Instead of deriving a new definition of life’s end as proposed by the Nature editorial, we should aim for better public understanding of how modern medical technology has made defining life’s end so difficult.

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