Ifreann wrote:Nui-ta wrote:All this having been said: he should also have gone home. If he's on hospice, he should be home. If his parents decide to seek additional treatment, that's their right as parents. Healthcare professionals have to do the best they can to ensure the best treatment and care given to those under their charge, but unless the parents were being abusive they cannot deny the wishes of the parents to seek more care, even if it wasn't medically sound. Ethics in a care-giving setting are such that sometimes, you just have to let the POA do what they think is right.
I would be interested to see an investigation of the hospital's handling of the discussion between parent and clinician. I'm not saying that doctors shouldn't have their opinions respected (they did go through years of medical school), but there is still a level of choice that must be given to parents when taking care of terminally ill children.
Run by me why doctors need to put the the feelings of the parents of their patient ahead of the interests of their patient himself.
Ideally they shouldn’t. But when you’re dealing with a person in a vegetative state that can’t communicate with you, medical ethics gives the power of choice and interest to the POA.
In this case: his parents.
This is especially true in the case of children. There’s entire classes that you have to take on medical ethics to work in healthcare that dictate the if’s and when’s of when a patient is incapacited to the point of being unable to make their own medical decisions —- and the answer of who you go to when this is the case is ALWAYS the POA unless the POA is being abusive or if there isn’t a POA to begin with.
Do I think the decision to keep Alfie alive is in his best interest? No.
But are his parents being abusive in their handling of him? Also no.
Their right as POA stands. This is the way the law is set up (at least in the States, but as far as In aware in Britain it’s supposed to be about the same).