Wednesday, April 08, 2009

Altruistic Desires Are Not the End All and Be All in Organ Donation

A very sad case in Canada is testing the ethics of organ donation at a Canadian hospital. A terminally ill baby was going to be allowed to die naturally and then after cardiac arrest, be an organ donor under the "Non Heart Beating Cadaver Donor Protocol." But the baby didn't die as planned and the donation has been called off, about which the parents are not happy. From the story:

Two-month-old Kaylee has a fatal brain condition called Joubert Syndrome, which has caused a malformation of her brain, leaving her unable to breathe without a machine when she sleeps. With no way to save their child's life and not wanting to see her suffer any longer, Kaylee's parents, Jason Wallace and Crystal Vitelli, wanted to take her off life support and donate her heart to another baby in need.

They thought Tuesday would be their last day with their daughter. Wallace said that Kaylee was expected to fall asleep in the operating room Tuesday evening and then be taken off life support. If she died within two hours, her heart would be removed for a transplant. But doctors called off the surgery when she did not fall asleep as thought.

Wallace said he wants doctors to try again. "If she's going to die, we got to keep trying," he said. "I want my child to pass on because she can't survive, and to save that child." Dr. Jim Wright, chief of surgery at the Hospital for Sick Children, told reporters late Tuesday that Kaylee is no longer a candidate for a heart transplant at this time. He said that is subject to change, however.
We can all sympathize with the parents' anguish and desire that some good come out of their family's tragedy. But more is at stake here than this baby and the hoped-for recipient. If the baby's time has not really yet come, it hasn't yet come. More to the point, the ethics of the entire system must be maintained or the whole system could fall into chaos.

The parents, for example, want their baby's heart to go to a particular child at the same hospital. But it isn't--and shouldn't be--their say. The donation is not to a particular person but to the system, which of necessity utilizes triage, the dispassionate and fair management of which is vital to managing the system and maintaining public confidence:

Wallace and Vitelli have already decided who they would like to receive their baby's heart. Her name is Lillian O'Connor and she is in the neonatal unit in the floor below Kaylee at SickKids...But SickKids says there is no guarantee the heart will go to Lillian. Deciding who will receive the heart depends on who is at the top of the transplant waiting list, based on their urgent medical need...

Medical ethicist Kerry Bowman of Mount Sinai hospital in Toronto told CTV Newsnet that hospital officials are following both legal and ethical protocols. "Obviously they are going to great length to respect protocol," he said Tuesday. "They are respecting two lives here."
We too often hear about hospitals that seem to cut corners in organ transplantation. Now, one is acting ethically and it's is being, in my view, implicitly criticized in this story for not doing what the parents want. But if the emotions of the moment came to control actions in these matters, the entire system would collapse and who received organs would depend on who one knew or being in the right place at the right time--rather than the orderly, if frustrating, current system that strives to provide equal access to treatment. Good for hospital administrators keeping their heads and following the rules--even when it hurt their hearts.

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10 Comments:

At April 08, 2009 , Blogger Unknown said...

I don't like organ transplantation. When body parts are fungible life becomes considered fungible too. Cf. embryo selection, "futile care theory," etc. It's not right. All a body's parts are for that particular body. So we're able to do it; so what. Doesn't mean we should.

 
At April 08, 2009 , Blogger Unknown said...

When body parts are fungible life becomes considered fungible, too. Cp. embryo selection, "futile care" theory, etc. A body's parts are made for that body. Stop messing with nature -- messing with nature=the culture of death.

 
At April 08, 2009 , Blogger SAFEpres said...

I don't understand the connection between this baby's disability and not being able to survive. If she can breath without a machine as long as she is awake, doesn't that mean that all she would need to live a normal life would be a respirator while she is asleep, allowing her to lead a normal life the rest of the time?

 
At April 08, 2009 , Blogger kimba said...

According to NDY the baby's parents may not want her to live.

 
At April 09, 2009 , Blogger Unknown said...

If that's the case I wonder if that was their idea to start with, or did the hospital put a flea in their ear and now is acting all righteous -- but not righteous enough to have done whatever could stand up for the baby's life in terms of protecting the kid from the parents. A transplant like this is good big publicity for a hospital. I think I saw this on the network evening news last night, unless it was another situation pretty much on all fours with it.b

 
At April 09, 2009 , Blogger Not Dead Yet said...

Wesley,

I did some research yesterday on issues related to this situation.

It's highly doubtful that Kaylee is "dying" or "terminally ill" by any definition you would accept as valid.

The hospital, parents and press have all worked together to build an impression that this is a situation of saving a "dying" child from a prolonged death. It really looks to be a "quality of life" judgment.

 
At April 09, 2009 , Blogger Broad Meadow said...

OMG!! I'll raise that baby! What is wrong with this world?!!!

 
At April 10, 2009 , Blogger ngojakidogo said...

So, it's the same as if you knew your baby wouldn't survive unless you fed it, not feeding would be murder. And if you knew your child couldn't breathe while sleeping and you don't help her when she's sleeping, isn't that murder? Think of all the hours of joy she has to share with people who love her! We're awake more than we sleep once we get to a certain age, and who's to say the brain won't find a way to compensate as she grows an another part would take over that function?

 
At April 10, 2009 , Blogger angel said...

NDY: you are quite right, IMO.
And it appears that the parents are making a quality of life judgement here. I hate to judge them by their statements but that's all we have to go on and the father did express the concern that their dreams had been shattered. The tone of the newspaper article I read was essentially one of disappointment in the lack of a perfect baby. While no parent wants to see their child suffer, ultimately, it is up to us parents to protect and nurture the life of the child God gave us, to the best of our abilities. And that doesn't mean writing them off so quickly. Children with disabilities need their parents to be advocates. Otherwise, who will?

 
At April 15, 2009 , Blogger Unknown said...

US

 

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