Zomo33 said:
What do you guys think, and how would you answer these interview questions:
How I would deal with the following situation: a 4 y/o patient with severe cerebral palsy was brought in with pneumonia unresponsive to antibiotics and the parents asked me not to treat their child aggressively.
One way or another, I'm going to treat the kid. The thing that will be tough about this one is trying to work with the parents to help them feel ok about this action. I would start by trying to understand why they don't want aggressive treatment, listening carefully, and attempting to address their concerns. By the end of our conversation, however, I would have let them know that for this particular situation, agressive treatment is the standard of care, for their kid as for any other. I would go to court to get an order to treat the child if it came to that, by I would do my utmost to get the parents' consent first--before even bringing up the possibility of legal intervention.
If the kid ultimately lives, before it leaves the hospital or leaves my care, I would want to try to hook the parents up with more resources for dealing with a severely disabled child, either personally or by giving them a social work referral. I would take that action because I believe there's a good chance parents not wanting aggressive treatment for a kid with a severe but nonfatal disability are struggling with one or both of a) not enough help or b) a too-gloomy sense of what is possible for their child. These resources might include online or in-person parent support groups, books, respite care programs, early childhood ed programs, and especially ways to meet adults with severe CP who are living successfully in the community.
Zomo33 said:
A patient of yours has metastatic cancer and is tired of treatment. She asks you to help her die...what do you do?
This would somewhat depend on her prognosis. If it seems possible or likely to me that she can continue to live with reasonable pain control for some time more, I would explore whether she is depressed, help connect her to some social supports, and generally try to boost her hopefulness while acknowledging her weariness. If the side effects of her treatments are what's making her life unlivable, I would consider any available alternatives. I would ask her to hang in there for a while to see whether we can't help her feel better and improve her quality of life together. I would also ask her for suggestions about what we could do to help accomplish this.
If she is dying already or in intractable pain, I would acknowledge her weariness and help connect her to the hospice system in her community. I wouldn't personally help her die, for legal and ethical reasons, but I would make sure that she was connected to people who could help her make end-of-life choices for herself.
Zomo33 said:
If a man comes to you who's father has Huntingtons Disease, a dominant genetic disorder, how do you advise him?
I would start by finding out how he's doing with his sick father, and providing referrals to supports if it seems like a good idea. I would move on to finding out what he knows about his own chances of getting the disease and about the disease itself. If appropriate, I would provide him with information about these things. Ultimately the big question for him at this stage is going to be whether or not he wants to get tested. I would talk to him about that, assure him about confidentiality and that it's his decision, and either offer him the test or refer him to a genetic counselor who can do it. If I have the test done, I would make sure to be on hand to give him the results personally and address any concerns he has at that time.