There is a great blog that I stumbled across as I began reading various blogs. I ran across a blog by an Oncologist named CancerDoc (Link), about a budding Oncologist trying to make sense of the world. I asked him to give me insight into my blog especially entries like “Why Don’t They Stop Chemo?”, I decided to post his comment as an entry because I think it’s worth reading and I really appreciated his honest insight. I also wrote a response in return. It’s long but I think well worth the read.
I think your insights are excellent. I can’t speak for others, but as an oncologist, I’m often confronted by other docs and allied health professionals who wonder “why we don’t stop chemo?” or “why we are even doing this to begin with?”
I think that it is complex and individualized in many cases, but there are probably some common themes, whether oncology docs will admit it or not.
One, as you alluded to, there IS a financial incentive to do more for patients. I know, this is dreadful. But, as is being discussed in our current health care “debate” in this country, the incentives in the US are for “doing”, not “talking” or “preventing” or “comforting”. Why do we do so many cardiac catherizations or MRI scans or arthroscopies. There is a medical-industrial reason for this. Oncology is no different. Okay, enough about that.
Two, the patients want it. In this culture in the US, where we are resistant to talking about death and dying, where people want taut skin and sexual potency and to “feel good” well past the point where it is likely biologically, there is a resistance to death. Just witness the whole donnybrook over the Sarah Palin “death panel” thing. People are so used to having whatever they want or at least having the perception that they can have what they want indefinitely at any age for low cost that the death panel idea was revolting. So, for an oncologist, there is often subtle pressure from patients and families, buoyed by the 10K runs for breast cancer and the story of Lance Armstrong, to do as much as possible. The oncologist is often put in a position of doing it, because if you say no sometimes, the patient will just leave to seek another avenue.
Three, oncologists in general are often biased by they’re success stories. We’ve all had patients on death’s door, severely ill and with poor performance status from their cancers, who, when treated, respond like Lazarus. Many of these people are never seen by other docs or other people because INPATIENT oncologic care is generally end-stage and the bulk of care occurs as an outpatient. So, there is a little selection bias amongst hospitalists and other inpatient specialists who see terminal onc patients in-house and think we are just drubbing them. When they pull through and “make it”, they are only seen by us as outpatients. When, they are flogged to death in the hospital, all the inpatient staff thinks is “here we go again.” All onc docs have had tremendous saves in their practices who were written off by other physicians. We want to believe that this is possible for all patients.
This is another thing where the good of the individual is taking precedence over the whole of the population. From a cost-benefit standpoint, it probably is NOT cost-effective to “save” that one person our of 20 or a 100, but rather to not pour resources into that person and let them die. And do divert those resources to other, treatable illnesses. But, this is precisely the kind of discussion, this kind of “rationing” or zero-sum analysis that Americans are unable to tackle.
Somehow, we cannot accept that we already ration care and that for every 80 year old with lung cancer that I treat and give an extra year of life to, there are countless other people that I give very expensive chemo to who derive little benefit. Until society as a whole comes to grip with the enormous resources that are poured into peoples lives in the final 1-3 years of their life, we will never get the cost of care under control.
Response from HospicePhysician
Thank-you for your great and insightful reply. I really appreciate your honesty. There are many things in your post that I could relate to.
1. The more we do the more we reimburse. It is unfair to just pick on oncologists. I’ve known many a gastroenterologist who put feeding tubes into End Stage Dementia patients even though they didn’t necessarily agree with this. I think the attitude is “I’m the specialist, I’m called in to do a job and I will do what’s asked of me or they will stop consulting me.” I spoke with a young GI doc that has just started and he stated “I hate putting G-tubes into the old dementia patients.” Well one would ask why would you then? Well he not only has pressure from family, referring physicians but also from his group of senior doctors. Imagine if he would refuse, what would happen to his career? Myself, I have been consulted by a physician because he thought he was doing me a financial favor. Luckily he did, because the patient and family benefited with the involvement of palliative care, but his intent was to fatten my pocketbook first and foremost.
2. Part of doing more, which we haven’t touched on, is also liability. Doctors just don’t want to get sued and if they have to do 1,000’s MRI’s so they don’t miss that one that can bite them in the butt, they will do it! We only have ourselves (society) to blame for this since we are a sue happy society. They taught me in residency that even if everything was done appropriately, in an emergent situation, but the patient dies, expect litigation.
3. Patients do want chemo and almost don’t give the oncologist a choice. I’ve witnessed this for myself. There was a young 49 y/o patient with metastatic breast cancer that didn’t want to hear that her cancer was in the terminal stages and chemo was only palliative. She wanted to believe that she would live another 30 years because she had a young 6 y/o son, that she wanted to live for. I even told her that her treatment was palliative. Well, she didn’t want to hear it and she kept going back to her oncologist for more treatment and he also mentioned that her chemo was palliative. Then when she really declined and had to be admitted, both her and her husband were angry with the oncologist because he wasn’t straight forward with them and “lied” to them. I was pretty amazed at how much she pushed for chemo, was in denial and then easily turned around to blame the oncologist.
4. I have witnessed this “bringing someone back from the dead with salvage chemo” in the hospital with an oncologist that is notorious for giving patients chemo who are actively dying. I’m sure that for every patient he is thinking, “this could be the one I save” as you have eluded to. Unfortunately, as you stated, this is rare and the question is whether this should take place or not. Maybe, instead of asking the financial question, the question should be; should many patients be put through more pain and suffering to save the one? I’m not sure what the answer is but I guess I’m biased in that I want to make everyone comfortable and not suffer.
5. If I could find an oncologist such as yourself, I would send patients to them since I do get patients that want second opinions etc. Also, if I worked with someone like you, I would feel like I’m giving honest answers to patients when I ask the oncologist what the prognosis for this patient is as part of my information gathering before a family meeting. I would feel that for once Oncology and Palliative Care could work more as partners rather than as opponents.
Thanks again for your post CancerDoc!