Kent Bottles: Is Good Patient Care About Choice or Collaboration?

August 31, 2009 at 10:27 am 9 comments

My July 23, 2009 blog on the ideal relationship between patients and doctors elicited more comments than most of my postings.  ePatient Dave was interested enough to repost that blog on his site, which elicited even more comments. One comment from Anne Marie Cunningham suggested that I read The Logic of Care:  Health and the Problem of Patient Choice by Annemarie Mol, the Socrates Professor of Political Philosophy at the University of Twente, the Netherlands.

Even though this slender paperback cost more than $40 on Amazon, I’m glad I bought and read it.  Mol has thought long and hard about how framing the doctor/patient relationship around the question of choice and who has more power misses much of what is important and meaningful in the interaction between professional and patient.

By studying what really happens to patients, nurses, doctors, and others in a diabetes clinic in Holland, Mol concludes that it is more useful to think of the doctor/patient relationship as a “logic of care” rather than a “logic of choice.” This book has profoundly changed the way I think about this central theme in health care reform.  Mol’s logic is a way to understand the “rationale of the practices I am studying.” “I will make words for, and out of, practices.  And I will do so comparatively, using contrast as a way of gaining insight.  This book articulates the logic of care through a detailed comparison with the logic of choice.”

The logic of choice summarized in my July 23 blog is well known: supply should follow demand, and care should be guided by what patients want.  Many advocate that the term “patient” is too passive and should be replaced by “customer,” a term that emphasizes action and empowerment.  Mol objects to this on the grounds that what she observes in the consulting room between physician and diabetes patient is not a commercial transaction defined with a beginning and an end.  Instead, Mol sees an interaction that is open-ended, non-linear, and involved with many different actors.  Mol also notes that the market model of choice involves target groups and selling; if the target group is too small then the company ignores that segment of the market.  In the examining room, the physician and nurse do not give up on anyone.

“The art of care is to figure out how various actors (professionals, medication, machines, the person with a disease and others concerned) might best collaborate in order to improve, or stabilize, a person’s situation.  What to do and how to share the doing? In the logic of care, patients are not a target group, but crucial members of the care team.”

Mol also explores the “gap between well-ordered theories that tell them how to handle science and technology and the far messier practices in their consulting rooms.”  Within the logic of choice, scientific knowledge is a growing collection of acts that gradually increase in certainty.  Physicians should provide their patients with accurate information so the patient can determine the value of possible courses of action (tight or mild regulation of blood sugars, a pen or a pump, etc.).

While the logic of choice separates facts from values, Mol’s logic of care attends to them jointly as the doctor, nurse, patient, family, and others try to achieve a balance between what evidence-based medicine dictates and what is possible for this individual patient.  For example, Mol describes a patient who must choose between tight control and being able to drive his car without fear of hypoglycemia because he has to drive to keep his job.  “Good professionals need to ask patients about their experiences and attend carefully to what they are told, even if there is nothing about it in the clinical trial literature.”  According to Mol, “the crucial question in relation to doctoring is not who is in charge, but whether or not the various activities involved are well attuned to one another.”

When Mol examines the question of patient guilt, she believes the logic of care better serves sick patients than the logic of choice.  “In the logic of choice, having a choice implies that one is responsible for what follows.”  “Does your insulin pump not live up to its promises? Bad luck. You wanted it.”  In the logic of care, when things go wrong you do not have to blame yourself or feel guilty.  “The logic of care does not impose guilt, but calls for tenacity.  For a sticky combination of adaptability and perseverance.”  Mol also describes the criticisms of the logic of choice centering on some patients with coma, depression, and/or high fever not being able to make good decisions and the research that establishes that all Homo sapiens have some trouble with making sound decisions.

The value of this book for me is that it made me think deeper about my reservations about the patient as customer always being right in their demands of providers.  Mol argues that good care is not all about making thought out individual care choices; rather she believes good care grows out of collaboration and ongoing attempts to balance knowledge and technologies with diseased bodies and complex lives.

The final word goes to Dr.Victor Montori, a shared decision-making expert at the Mayo Clinic in Rochester, Minnesota.  In a comment to the July blog about the doctor/patient relationship, Victor wrote, “Care, empathy, guidance, choice, expertise, evidence, context, values and preferences – all matter.  What is the right combination?  Ahhh…the right combination is the one that furthers the goals of the patient.”

Entry filed under: Evidence-Based Medicine, Patient Engagement. Tags: .

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9 Comments

  • 1. Jane Sarasohn-Kahn  |  August 31, 2009 at 12:37 pm

    Bravo! Great food for thought, consideration, and policy making. I’ve been thinking a lot about moving care beyond the institution in the context of a ‘connected’ patient. This requires the patient-health citizen to be activated. At the same time, that tree may fall in the forest, but if care providers don’t hear the patient, the connection isn’t made, and as Dr. Montori writes, the goals of the patient and outcomes aren’t fully realized. This will require going beyond “the visit,” which is currently constrained by the CPT code. That’s a huge sticking point in health reform tactical discussions right now: how to reallocate resources toward the benefit of the patient-health citizen — which will, inevitably, result in certain stakeholder groups with fewer resources. Thanks for talking about Mol’s great book.

  • 2. Janice McCallum  |  August 31, 2009 at 4:01 pm

    Kent,
    I agree that the “choice” model that compares health care consumption choices to consumer product purchases is inappropriate in health care. Currently, most patients don’t have enough information to make informed choices, implications of choices extend beyond a single transaction, and the decision process is very complex with health outcomes and financial impacts for each patient.

    Collaborative care makes perfect sense to me, but it requires changes in the fragmented system of providers that we currently have. I’m seeing some signs of movement toward a more collaborative model in some hospitals, and it helps if collaborative care is positioned as being more efficient and cost-effective, but we have a long way to go — and there will be bumps in the road on the way to more progress. I’m concerned that implementation of evidence-based medicine order sets without sufficient collaborative care and considerable progress in patient education will make some things worse before they get better.

    In brief, I believe patients should be the ultimate decision-makers (ideally in consultation with their caregivers), but we have a lot of work to do to make more information available to patients and we have a lot of work to do to improve the current state of evidence-based medicine.

    It isn’t easy to write brief comments to your post, since it touches on virtually every aspect of health care and the health care industry. But thank you for your very thoughtful post. I hope it leads to much more discussion.

  • 3. Trisha Torrey  |  August 31, 2009 at 4:39 pm

    Interesting exploration, Kent – but I get lost in the analysis sometimes because to me it seems so much simpler, yet vastly more complex, than all this.

    Patients are human beings, and no two are alike. Physicians and other providers are also human beings and no two of you are alike either.

    Doing the math, then, it seems that there are as many combinations of care (times) choice as there are patients (times) providers. And one size just does not fit all.

    Victor Montori came the closest to the “right” answer – and that is, that there is no, one, right answer for all patient and physician combinations. For each new relationship requires a new “fit” of what will work better — care or choice — or both — or neither.

    I often tell patients that they must choose their doctors as they would choose a lifelong partner or spouse because it may need to be a lifelong, and intimate, relationship. And we all know how difficult that can be!

  • 4. Gregg Masters  |  August 31, 2009 at 7:48 pm

    Hi Kent:

    Might this be a ‘faux” choice since elements of both must factor into the health care value proposition?

    Maybe I’m missing the key premise of Mol’s argument, but it seems that the logic of care and the logic of choice are simply different sides of the same question.

    The more commercial or market based “logic of choice,” which no doubt underlies the risk push back to patients via “consumer-directed health plans,” and simultaneously serves as Holy Grail motivation for many health 2.0 companies, may never succeed in equitably leveling the playing field between the consumer and the multi-focal health care delivery system. It’s just too complex, peppered with inexplicable variation, with too many moving parts to create a peer-to-peer (aka collaborative) engagement in treatment choices. I don’t think we”ll ever see such a CPT code to bridge that divide!

    While the “logic of care” seems more open to “shaman” or healing (physician) energies, attesting to the underlying nature of medicine as art, embedding it in a decision tree of collaboration vs. choice, still strikes me as in service to the choice question.

    What am I missing? I’ll admit, this one may be above my pay grade!

    I absolutely love and agree with the statement: “The art of care is to figure out how various actors (professionals, medication, machines, the person with a disease and others concerned) might best collaborate in order to improve, or stabilize, a person’s situation.”

    As Deming says: “If you can’t describe what you are doing as a process, you don’t know what you’re doing.”

    Unfortunately too much of our delivery system can neither describe, let alone enforce even regional variations in desired clinical practice patterns. Why not start there?

  • 5. Bonnie Kavanagh RN, Geriatric Care Manager  |  September 1, 2009 at 7:51 am

    After reading this blog I was able to get a sample copy of the book referenced on my Kindle. In comparison to the U.S.’s health care, people’s ability and rights in health care choices to what a small countries view is quite frankly, unfair. In further contemplation of this thin book, I sought out, and could not find the credentialing of the author, Annemarie Mol. I find it hard to imagine she herself has sat with patients/clients and helped them review their health care choices.

    What of the diabetic patient/client used as an example in the referenced book? Granted, I have merely been exposed to the “sample version of the book” so, I may have missed an important point to the argument of choice versus collaboration.
    Well, I have, within my client contacts come across a newly diagnosed diabetic young adult. For the sake of discussion, I imagine myself a physician. Do I simply go with standard protocol and best practice in “telling her and her family” that she should go on the traditional diet management taught by dietary and combined oral and insulin diabetic management? Do I let her and her family go with the thought this is in her best interest? Do I expose her to the cutting edge research and trialed information of insulin pumps in controlling blood sugars and limiting the tissue damage of high blood sugars? The later choice is more expensive and still not the first line of treatment for a newly diagnosed diabetic.

    If this patient/client is only exposed to the first choice, than this would be a travesty in the making. What of the inevitable obesity (because of the yo-yo of oral hypoglycemic’s in weight gain). For this young adult, to have limited choices, inevitable self-esteem issues because of obesity, and be rendered powerless because she was not encouraged and allowed the right to choice in health care decisions is not what this country is about. Surely, we assume, the physician would be presenting this but what if not? I can tell you, on a regular basis, I participate with my clients in empowering them to exercise their right to choice health care decisions.

    As much as I would like to intellectually assume the right decisions are going on behind closed doors with and for patient/client care, I must continue to disagree. I disagree because I am in the trenches and helping my clients with those choices, often with the collaboration of physicians and the team members. Quite frankly, sometimes, I must stand alone with my patients and family members, in disputes and advocacy for medical decisions, in discussions with the health care team. Fortunately, I have a knack for winning (and I always do my research).

  • 6. Albert  |  September 2, 2009 at 6:12 am

    Ah we Americans love to keep things simple don’t we? I mean, choice, there it is, you have it. Oh yes information is what you need, here’s plenty, “Joe back up that truck load of digital health stuff and dump it right here.”

    Now cost, hmmm that’s a bit trickier, let’s see, did you plan on having this cancer a few years ago when you purchased your insurance or when you were in between jobs to take care of your dying, Alzheimer’s ridden mother? Oh geez, that’s a bummer.

    Choice is perfect for a homogeneous, well-educated, society that has an integrated medical system. We aren’t there yet. Choice is a political buzz word just like universal care is–there is no such thing. But we are simple and we like to glaze over complexity with nice neat packages, preferably ones that keep the blame to one place.

    Now some would say that because of free will, the blame, credit, and responsibility is always with the patient. In the vacuum of your health, that decision seems easy. We don’t live in vacuums. We fail in this little discussion of patient care to highlight the external forces that play on daily choices, some purely capitalistic by companies focused on shareholder value, some well intentioned, and some necessary adventures into the unknown for the benefit of future patients. That’s called risk, innovation, and/or last resorts, but they help us learn how to improve the quality of life for others.

    I believe our lexicon about the patient decision-making process stinks. Our culture’s habits, our agricultural and food marketing system’s inherent conflicts, and the overall math of “health care” all make this discussion of patient choice or care much more complex.

    Although, perhaps it is simple. Just say no. No to smoke, no to drink, no to riding a motorcycle. You know the list, we all do. The insurance companies do. This is the second best ultimate bet, life insurance is the first you know.

    This relationship is more than patient and physician. It requires a longer term view of life that in many situations is at odds with our external culture (there are signs the externals are changing primarily do to the economics, but slowly). In addition to the patient, the more knowledgeable side of this equation, the physician care team, needs to have more time to educate or describe the alternatives. I don’t mean go to some website and shop around. I mean, Doc, nurse, researcher, what does this treatment plan mean to me. Perhaps the system is moving in that direction by making patients have greater access to regular maintenance shall we say, which then frees up time for physicians to deal with higher priority and urgent patients. We’ll see.

    I’m not one to think we have a broken health care system, my experience has been fine. It is expensive, but we do have a choice on what to spend our money on, yes?

  • 7. Bill Yates  |  September 2, 2009 at 2:03 pm

    Wow! I am impressed by the post and the thoughtful comments of the readers in this blog.

    I agree with Trish’s comment about the complexity of this issue. In thinking of medical care I tend to picture a middle-aged white physician interacting with a middle-aged white female patient in an outpatient setting. But what a complex health care system we live in.

    What about the comatose teenager in the ICU who may be facing significant lifelong brain rehabilitation with impairment in decision making capability?

    What about the undocumented Hispanic immigrant in the emergency room who doesn’t speak English and the health care team with marginal Spanish speaking skills and no knowledge of Hispanic culture?

    What about the physician who is involved in a frivolous malpractice suit that is taking significant time, energy, emotional reserves and money?

    How do the issues of choice and care play out in the above scenarios? I think whatever framework we support, there is a need to provide for flexibility and customization.

  • 8. Victor Montori  |  September 4, 2009 at 5:36 pm

    Hi Kent
    Thanks a million for quoting me. I have read this book and at moments I loved and at moments I disliked it. Why the response? I think that in an effort to create a contrast, what may have been missed is what you quote me saying – that there is a perfect combination of care and choice that every patient needs and wants and that neither the logic of care alone or the logic of choice alone will work well. Of the two, I would take the logic of care any day, but unfortunately without my participation I wonder whether my care providers will find treatments that fit me or whether they would try to make them fit and look good from a performance/quality metric standpoint. Very complex. Thanks again!

  • 9. e-Patient Dave  |  September 5, 2009 at 10:43 pm

    Boy, what a post. This is not your garden variety blogmumble about healthcare.

    The excellent Trisha and I differ in our perspective on this, I think, due probably to her being more sensible and my unstoppable urge to wonder what’s going on under the hood. I certainly agree that in the end it all comes down to the need to adjust to everyone’s differences.

    But I always wanna know the next question: what can we understand about THAT? Is there no useful pondering we can do to bolster our understanding of encounters past and future? And in the messiest, most ambiguous situations, what’s our guidepost?

    Two lines stick out to me:

    “The logic of care does not impose guilt, but calls for tenacity. For a sticky combination of adaptability and perseverance.”

    “Ahhh…the right combination is the one that furthers the goals of the patient.”

    I know first-hand about the adaptability and perseverance thing; it’s what I faced and many kidney cancer patients face: “This didn’t work? Okay, next we try this.”

    What I see newly in all this – and missing, I think, from the comments – is the participatory perspective, the balance of responsibility. It ain’t just docs who are responsible for this shift; we the people need to ramp up our sense that WE have something to do with it.

    Perhaps the single most lasting new meme I’ve found in these 19 months is Stanley Feld’s “Physician as coach, patient as player.” I returned from my first e-Patient Working Group meeting (Feb 08) with a nascent sense that we didn’t just need a patients’ bill of rights, we needed a bill of rights and responsibilities. That’s evolved now into this whole idea of a mutually empowered partnership – collaboration.

    When I wrote about Feld last December I mentioned it, but the real juice hit a week later when I read about Robert Veatch’s Patient, Heal Thyself. That SOB :) has the gall to say that patients alone are in charge, and they have no choice but to assume that active role – because it is the patient who does or does not do what the physician says.

    Well, maybe: it’s all academic if the patient’s skull hasn’t been infiltrated with the participatory meme.

    It’s not just that we patients have a right to do some doc stuff – it’s that we should no kidding be engaged, pulling together, like two people carrying a big box up the stairs, side by side. Or maybe a useful image is the railroad handcart. http://is.gd/2WpdZ

    Except in the box-carrying and handcart images the people have equivalent roles. Anybody got a metaphor that’s one step better?


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