Saturday, March 31, 2012
Patients and Doctors
How Patients Think
I have really enjoyed reading Groopman’s book. I really related to some of the points he made in the book and many of his stories brought up my own life experiences. Reading the quote:
“A wealth of research shows that patients thought to have a psychological disorder get short shrift from internists and surgeons and gynecologists. As a result, their physical maladies are often never diagnoses or the diagnosis is delayed.” (39)
Made me think of a number of cases I am familiar with. One such case is of a friend of mine and although not directly a case of a psychological disorder, it still follows the same principle. When she was younger, her parents were going through a divorce and it was very difficult on everyone. She began to suffer from excruciating (lower) back pain and would complain about it. They took her to be checked out more than once. The doctors repeatedly (without doing a full MRI) decided that it was psychosomatic pain and/or she was faking it for attention. She had a tumor the size of a grapefruit in her spine which they finally discovered when she became paralyzed from the waist down. Pain, especially vague symptoms of pain are often taken less seriously than visible symptoms. The only symptom is patient reported and they cannot verify that symptom. So unless they find the cause, they cannot verify whether or not it is psychosomatic.
Groopman late states:
“These days, when we are not getting better, most of us return to see the doctor with ideas about what might be wrong. Our notions sometimes come from knowing a friend or relative with a similar symptom, or ideas may have been sparked by looking on the Internet. Our thoughts about our unrelieved symptoms often focus on the worst-case scenario.” (261)
Just like this quote of Groopman’s, when I began experiencing excruciating lower back pain this past summer I kept in mind the case of my friend. In my case, it began with leg pain/numbness and other symptoms, but then spread to unbearable lower back pain. Lower back pain is a fairly common symptom and is often due to “”strain” or “sprain” in the lumbar region” (226) and “90 percent improve within two to seven weeks without specific therapy”(226). However, my mind jumped to the “worst-case scenario”(261) of what if it didn’t go away on its own. What if it were like the case of my friend and it only got worse? I tried to wait it out and see if it would get better. Instead, it got slowly (and then more rapidly) worse. I scheduled an appointment to see my doctor*.
I found it interesting that Groopman learned that, “doctors desperately need patients and their families and friends to help them think. Without their help, physicians are denied key clues to what is really wrong. I learned this not as a doctor but when I was sick, when I was the patient.” (7-8). The idea that you can learn more as a patient than as a doctor I find interesting. The amount of information that my doctors would miss if I didn’t understand my medical history as well as I do is baffling. Without my mother’s probing questions at a consult for a tonsillectomy, I wouldn’t have been sent for a hematology work-up. My ENT refused to operate on me without it, which is good, because I could have bled out during the surgery without the proper medication beforehand. Being a smart patient and having smart medical minded parents has saved my organs and probably my life more than once.
(*If anyone is interested in what happened when I saw the doctor for my back, feel free to ask me via email or in class. I wound up having to have neurosurgery on my spinal cord and I have found the entire experience highly educational and fascinating. I do not mind discussing my medical oddities with people who plan to pursue medicine and might learn something from them.)
How Do You Determine If a Doctor Is Competent?
Dr. Jerome Groopman provides an interesting insight into the world of doctors in his book “How Doctors Think.” Dr. Groopman comments on questions that I believe many people who have ever been to see a doctor have had. The most interesting subject I believe he brings up is how do you know if a doctor is truly competent or not. Dr. Groopman brings forth the fact that a doctor can be very nice, full of concern, and his patients will love him for that, However, these great attributes have little to do with his competence as a doctor. Dr. Groopman provides the example in the beginning of his book of a lady who went to multiple doctors in the course of fifteen years and was misdiagnosed or not diagnosed at all until finally one doctor discovered that she had celiac disease. He relates back to his time as a physician and recounts times where he met doctors that he didn’t believe to be best fit to be practicing doctors.
The main question is, and subject of much of our conversations during the lectures, is how can someone determine if their doctor is diagnosing them correctly or not. Of course there is not one magical technique that can help you determine this. A doctor is someone who you should trust and believe has your best medical interests in mind and constantly doubting them will not solve your issues. However, as Groopman states, no doctor is perfect and they make mistakes as well. I believe that Groopman gives great advice for patients in his epilogue to help avoid these problems of misdiagnoses, especially when you feel something is wrong and you aren’t getting the adequate amount of help to cure it. When seeking medical attention from doctors, it should be a two-way conversation. You should tell your doctor everything you know, feel, and are worried about with your ailment instead of depending on your doctor alone to discover what is wrong with you. I especially like Dr. Groopman’s advice to retell the story from the beginning. There are many things about medicine that are confusing and there aren’t always obvious correlations between what hurts and what is actually wrong with your body. By telling the whole story, it gives your doctor a better chance at picking out what could be wrong with your health and provide proper diagnoses to cure what is wrong. If you don’t feel that your doctor is providing you with the proper care after this, you should always seek a second opinion to make sure that you are getting the best care possible .
Uncertainty in How Doctors Think
In his discussion of the availability heuristic (enabling a person to discover or learn something for themselves), or the "hands on" approach, Groopman explains that in making a diagnosis, many doctors are partial to the cases they see most often. This is dangerous, since categorizing disease on a macroscopic level (using general symptoms) and using that diagnosis to decide which treatments to provide can lead to adverse, even fatal, effects on the microscopic level. This is why patients are advised to seek attention from various doctors in order to avoid misdiagnosis and get treatment for a condition that they do not have.
As someone who wants to be a doctor, I found Groopman's book to be very interesting and helpful. As a doctor, it is inevitable that, on a constant basis, you will be put in situations where you are uncertain. However, it is your duty to deal with that anxiety, make decisions that you believe will be best for your patients, and when those decisions prove to be the wrong ones, you will have to find coping mechanisms to deal with that. Now, from a patient's perspective, you will obviously not be happy when a doctor does not diagnose you or somebody that you love in the right way. But, this is an unfortunate reality that happens, even when dealing with the most credible of physicians. Both patients and doctors must consider the fact of uncertainty when receiving and providing treatment.
Monday, March 26, 2012
The truth is quite disturbing
Sunday, March 25, 2012
Uncertainty / Different perspectives
Saturday, March 24, 2012
Are Drug Companies Alone?
Marcia Angell does a good job at addressing my question in the reading by stating: "If prescription drugs were like ordinary consumer goods, all this might not matter very much. But drugs are different. People depend on them for their health and even their lives". I found this quote to be quite interesting, it is true that American consumers spend over $200 billion annually on prescription drugs. But what about the food industry? According to The Food Industry Plunkett Research, Americans spend over $1 trillion a year on food and just like drugs, we need food to survive. This may be a foolish comparison, however, similar to drug companies, the food industry is not known for their honest policies and will also commit unethical acts to make a profit.
The truth about drug companies
Drug Companies Influence of Medical Education
Football and Impotence
One thing about watching football is that while you are getting nearly four hours of quality entertainment (if you like football), you are also getting an obscene amount of ads. As a result, I have become pretty adept at seeing right through commercials that try to appeal to a football "audience" more than others, using masculine music, titles, or celebrities appearing in the commercials.
But one commercial was a little different, it came out in 2003, and it's this ad for Levitra, which Angell specifically mentions in her book. I have probably seen this commercial 200 times in my life, but when it first was on the air, I was twelve. I specifically remember asking my dad "What the hell was that?" I think to just avoid an awkward moment he said he didn't know either. But watching it now, the not-so-subliminal messages are hard to miss, particularly with that ball going through the tire. However, I find it difficult to see how else an ad for this product could be done, and it is exactly that characteristic of the ad, and of drug companies in general that I find so frustrating: they are so good at what they do.
Not only do they understand what it takes to make you think you need something (not want, need), but they are also so good at hiding from you what that thing you need actually costs you. I vaguely remember Mike Ditka's TV spot for Levitra, but more important than actually seeing it is realizing what the drug companies have done by picking Ditka, who is a football celebrity that men not only generally like, but also have come to trust in his long career as a broadcaster after hanging up his whistle.
Convincing men to do anything with respect to their own health is hard, getting them to admit that they have a problem in their sex life is even harder, but with respect to drug companies, it's difficult to not respect how they manage to exploit the weaknesses of the human condition, to constantly seek full satisfaction instead of dealing with our idiosyncrasies.
Biased Scientific Research
http://www.theatlantic.com/magazine/print/2010/11/lies-damned-lies-and-medical-science/8269/
A Different Kind of Industry
Again on a different topic, I recently watched Michael Moore's documentary Sicko, which criticizes the healthcare system in the United States. Though, like all of Moore's films, it has been heavily criticized, I would recommend watching it as it delves into many of the things that we have been discussing in class, the pharmaceutical industry included.
Deception and Action
In her book, Angell describes in detail the deception and expansion of Big Pharma and associated pharmaceutical research. While the deception remains constant and undeterred, she gives us the inspiration to do something about it. First off the bat, I would like to commend Angell for her unyielding and thoroughly analytical writing. Her two decades at the New England Journal of Medicine have obviously given her a sharp edge with which she makes a compelling arguement. So much so that it is easy for the reader to get caught up in the writing and not bring in their own comparisons and experience. She is propaganda-ish and exceedingly easy to trust, similar to way Survival of the Sickest seemed. Regardless, one cannot dismiss her experience with the industry and her crude yet informative investigative style.
In light of this writing style, I came to agree with the points Angell made. The slide towards the commercialization and corruption of clinical research has led to a full on privately run business that is producing over $200 billion a year. Commercialization has led to investigations into the control research sponsors at these private firms can exert on the analysis and design of clinical trials. The evident distortion of outcomes and the issues of non-reporting/biased reporting are points made which would make any honest American citizen suspicious of the drugs they take. Furthermore, the increasing association between the big industry and the facilities of universities allows the private firms to buy into the best minds of the pharmaceutical industry. I was very shocked by Angell's example of the exorbitant consulting fees paid out to individual faculty members and selected scientists. More broadly however, the effects of commercialization spread out to the commercialization of universities, medical schools and to individual doctors around the nation. How can we support the integration of these companies into our very health-care system and not be knowledgeable about the scandal. These firms are taking up more power resources then they deserve from the American public. We have a name for when the cells in our body take more then they deserve: cancer.
And so I rather entirely agree with Angell. We need to change the way we manage the research, development and distribution of new drugs through public education and political action. Angell also seemed to stress that small actions will not help us. One pill isn't going to cure your cancer. However, an intensive treatment with the full power of the public would easily stop the nonsense that is forming. In effect, we need everyone knowing and ready to act if we are to cure ourselves. Not only is the health care system and the health of the individual at risk, but also the entire scale of the medical system including universities and governments. The thought of leaving the decisions of health to the American marketplace is an appalling and frightening thought.
Socialize the Drug Companies
In the final chapter of her book, Angell goes through a variety of reforms that would most definitely limit the power of drug companies. She writes that we should strengthen the FDA, create more oversight, regulation and transparency, and so forth. All of these reforms are great, and I think they would be an improvement to the current situation. However, Angell doesn’t get to the root of the problem. Drug companies are for-profit private institutions. Therefore, their main goal will always be to make the most amount of profit possible. They will fight regulations tooth and nail and seek any sort of loophole to increase the prices of drugs. As long as they remain a for-profit entity, drug companies will care about profits more then people.
In my opinion, drug companies should be socialized. Angell says that the reforms she suggests would “lead to better drugs at lower prices (259).” But why should these drugs cost any money at all? It seems to me that health is a human right. Health care should not be run like a business. Every individual deserves free access to the drugs they need. This is why I believe we should transfer drug companies to the public sector and implement a public healthcare system. That is the ultimate reform.
The Truth About...How to fix what you can't change
Lower the Prices
The Truth About Drug Companies by Marcia Angell plants an unsettling image of the drug companies and then I realized how little I knew about the influence of these drug companies. Every time I watch the television, I see these ads and slowly they unconsciously influence me to turn to look towards name brand medicine like Claritin when someone has allergies. I had no clue how much our budget goes towards these drug companies. I never gave them a second thought, naively believing that they actually are trying to create new innovated medicine to help people. It was not until I saw commercials for new medicine, an example Clarinex, that sounded exactly like they treated you like the old drugs, continuing the example Claritin, that I was began to second guess my view of the drug companies. I started hearing grumbles about the rising cost of drugs and how there are too many "me too" drugs are out there. I realized that they are businessmen and instead of trying to help those they are ill, they are using their revenue to make themselves richer. Just last week my suite mate came into my room and complained that since her insurance did not cover the eyedrops prescribed to her, she had to pay eighty dollars out of pocket. I thought that was ridiculous that she had to pay so much for a tiny bottle but after talking to a friend who is an ophthalmologist, she claimed that is the normal price for that kind of eyedrops. I understand why it will be hard to generate change in the system but I feel that price regulation is necessary. Angell mentions that the price of Norvasc is $715 but diuretics, a pill that that is found to work better than the other drugs for hypertension, is less than forty dollars. Unfortunately, the commercials drill it into our minds that we need these name brand drugs when generics do the trick and it is much cheaper. Change must be brought forth that limit the control of the big drug companies, especially since most of the money they claim goes into R&D seem to go into marketing the drug more. Since these drugs are a necessity to us, should they not also be affordable by those who need it the most?
Saturday, March 17, 2012
Why (not) medicalize?
I appreciated the "bracketing whether a phenomenon is "really" a medical problem" (10) point that Conrad made. He mentions it various times throughout the book. The first time he says:
We can examine the medicalization of human problems and bracket the question of whether they are "real" medical problems. What constitutes a real medical problem may be largely in the eyes of the beholder or in the realm of those who have the authority to define a problem as medical (3-4).
Often, when I have been exposed to the medicalization discussion/debate it often veers towards inadvertently undiagnosing people. Essentially stating that certain diagnoses are not real or over-diagnosed and therefore (at least most of) the people receiving that diagnosis don’t really have anything wrong with them. This has always been very problematic to me and I’ll come back to that point later. Also, he makes the important point that “Having a biological basis does not make something ipso facto a medical problem." (146). Often when research points to a biological cause for a phenomenon we immediately label it as a medical problem based on that evidence.
I also wanted to touch upon the effect of health insurance on medicalization. I felt that this point was eventually made towards the end of the book but seemed to be downplayed throughout. He explains that, "the fact that insurance companies won't pay for treatment of certain medical diagnoses limits its medicalization but does not necessarily undermine it, so long as medical categories are accepted and applied to problems" (11). He also mentions the bizarre situation caused by the fact that psychotherapy is not usually covered but psychiatric medications are. This places the focus more squarely on medicalization, since psychiatric drugs must be prescribed by someone with an MD. Often, doctors (such as internists or pediatricians) prescribe psychiatric medication to their patients without the patient ever seeing a mental health professional. Other times, people do see a mental health professional but cannot afford to remain in therapy on a long-term basis. Therefore behavioral or mood problems that cannot be fixed easily and quickly by psychotherapy are often treated with medication instead. Conrad towards the end of the book says:
It is worth restating that one reason for medicalization in our society is related to the way in which we finance human services. The only way individuals can get the services they want or need to be paid for is to define them as medical problems. Thus, there is an incentive to define problems as medical so that their treatment can be reimbursed by health insurance. This obviously encourages medicalization (160).
This is an incredibly important point. However, he waits until the last five pages of the book to make it. When discussing the various forces that influence medicalization, this seems an extremely important one. He mentions patient advocacy as a factor in medicalization, but seems to gloss over the bank breaking difference in whether or not they receive a medical diagnosis or not.