LizzyM: I just wanted to say publicly I really enjoy reading your posts. If only the med school and residency applicants I interview demonstrated half your zeal and patient advocacy skills. I definitely thought the discussion in this board was a lot more interesting to read than the one over at the residency board.
Folks please remember that, while there is no question that there are a lot of business aspects to the practice of medicine, it is still viewed as "the noblest of professions" and ultimately held to a higher standard, in all regards. So yes, at times the law demands us to "suck it up" and eat the costs. there is no shortage of patients and over time these things balance out. unfunded mandate? sure. sucks? yes it does. but morally and ethically, it's the right thing to do. the ama of which I am a member, is a pretty useless organization...well, at least useless for patients. it's sole purpose is to lobby against anything that can prevent doctors from getting paid -- at least, that's their public image. And for those that say health is a human right, the United States has not explicitly adopted that viewpoint. If it did, then we would have changed our health system a long time ago.
At the core of it all, this case went as far as it did because the physician didn't listen to his patient. he blew her off and had the audacity to say he couldn't afford to accomodate her, instead relying on a similarly deaf partner, a 9 year old kid, and notes on the "butcher paper" on the exam table. the patient was not a native english speaker and I'm guessing from a cultural perspective she felt initially obligated to stick with this physician because this is who her primary care doc sent her to. whether or not the care he provided was adequate is irrelevant. she was discriminated against.
had this doc taken time out to actually communicate with his patient, or listen to the call from an interpreter service, or negotiate up front re frequency of interpreter use, or heck -- contact someone in his state medical society for guidance, he never would have been in this predicament. he would not have had to pay 200 bucks every time this patient came in because they would have agreed up front re: when it would be a good idea to bring in an interpreter (i.e. significant procedure or change in management) and when they could get by with family and paper (medication refill). And I also highly doubt he was only getting paid $49/visit from Medicare. There's other ways the subspecialists pad the bill when seeing medicare patients by doing additional procedures, as well as he could've billed for extended visit codes.
interestingly enough there's no mention of any action against her primary care doc. nor is there any mention of any action against the rheumatologist who took over her care.
while the award will likely be reduced on appeal, I kinda hope it isn't.