My last post discussed the wide gulf between health care and the rest of the world in the area of customer service.  To sum up what took over 1,000 words to express: Customer service in health care totally sucks because the system promotes that suckiness and does nothing to penalize docs who make people wait, ignore what they say, rush through visits, and over-charge for their care.  We get what we pay for.

But shouldn’t we judge the system for what it was build for: the quality of the care we give?  Sure, the service is overwhelmed with serious suckitude, but that can be forgiven if we give good quality care for people, right?

Even if that was the case, there is no excuse for the lousy service people get from our system.  The lack of respect we, as medical “professionals” show to our patients undermines the trust our profession requires. Why should people believe we care about their health when we don’t care about them as people?  Why should they respect us when we routinely disrespect them?   No, the incredibly poor service we have all come to expect from hospitals and doctors is, and never should be overlooked or forgiven.

Now I want to cover the actual care we give, and how it too has moved away from the needs of the people it is supposedly for.  The people question how much providers care (verb) mainly based on the (lousy) service they get.  The care (noun) we give is all about the quality of the product purchased by whoever pays for that (be they third-party or the patients themselves).  The real question I am asking here is not if this care is good or bad (the answer to that is, yes, it is good and bad), but whether it is patient-centered.

This should be a silly question, like asking if car repair is car-centered.  But it is clear that much of the high cost of care in our country is due to the huge number of unnecessary procedures, medications, hospitalizations, and services given to/done on people. Unnecessary care is, almost always, not patient-centered.

There are many reasons for unnecessary care, including:

Defensive care, where the provider knowingly does unnecessary things to protect themselves from perceived legal threat.  For example, a baby in the ER with a fever will often get a chest x-ray and lab tests drawn.  In my office, babies with fevers get a good history and physical.  Labs and x-rays are only done when I am still not certain after the H&P.

Protocol-driven care, where care is ordered because the provider is under the impression that they are being measured for a certain item of care.  While this is sometimes appropriate, it is often either a bad guideline (such as checking cholesterol in low-risk populations, or doing PSA testing in men over 65), or a misinterpretation of the guidelines (such as doing mammography or colonoscopy in the elderly).

Profit-driven care, where the provider simply orders something because they can rationalize it and it is paid for.  Once, in my previous practice, we got part ownership in some x-ray equipment.  Very soon after getting this, we noticed that far more people with coughs were getting chest x-rays and far more people with knee pain were getting (you guessed it) knee films.  Our care didn’t improve; it simply got more expensive (and profitable).  Other examples of this are the annual lab profiles many physicians order when their office owns lab equipment (despite a lack of evidence that they improve care).

Add to this the high percentage of office visits that are not necessary but are done because they are the physicians’ only means of payment for care (about 75 percent when I last counted), and you get a glimpse of just how much care done in the U.S. is not necessary.

This is the antithesis of patient-centered care.

• It is costly.
• It exposes the patient to risk from the procedures.
• It exposes them to the risk of over-diagnosis.
• It does nothing to actually help the patient.

So again I turn to my experience over the past three years in a practice where I am financially obligated to give the best care possible.  What does good care look like?  More specifically, is good care the same thing as patient-centered care?

I think the answer to the second is “mostly yes.”  Most of the time the care I give looks toward what is best for people and not at other things.  I say “mostly” because there are some circumstances in which the patient as a customer works against good care, and I feel significant pressure to keep the customer happy by giving lower-quality care. The main time this happens is when people demand antibiotics for conditions in which antibiotics don’t help.  Sinusitis, bronchitis, and most pharyngitis gets better without any medication, and giving antibiotics just raises risk of adverse reactions or drug-resistant bacteria.  But people still believe antibiotics are wonder drugs and are often impatient to get well.  So where do I give in to them for the sake of keeping their business?  It does happen.  It always will happen to some degree.  But I will state categorically that it happens much less in my current practice than it did in my old one, as I have much more time to educate people, and they don’t feel nearly the pressure to walk out of my office with “something to show for it” (since access to me is easy).

So what is true patient-centered care?  I think there are two main things that define patient-centeredness in care:

1. It is focused on decreasing the risk of problems.  The first question I ask when someone comes to my office with a complaint or problem is: “What are the most important things to rule out?”  Someone with chest pain, for example, needs to be ruled out for heart problems.  This is usually done by listening to the story, but sometimes requires further testing.

The same criteria can be used for any testing or treatment.  Does giving the medication decrease the person’s risk, or does it increase it.  Giving a statin drug to a 60-year-old diabetic who smokes is probably something that will lower their risk of death from heart attack or stroke. Giving that same drug to a 30 year old who has no other risk factors (but has the exact same cholesterol profile) is likely to increase their risk of problems.  All care needs to be ordered and explained from this perspective.  I recommend flu shots to high-risk people, explaining that it makes it more likely they will be around in a year (to which one of my patients responded: “What if I only want 6 months?”  Smartass).

2. It is focused on improving quality of life. Once bad stuff is ruled out, the focus turns to the other reason people seek care: they want to feel better.  Many times I’ve heard of people with knee pain who get an x-ray and are simply told it is “normal,” without any treatment for the pain itself (perhaps the doc thinks the x-ray is therapeutic?).  I’ve heard other exasperated people tell of times they’ve been told that, despite significant distress, “nothing’s wrong.”  While I think often the doc is simply being clueless or socially inept, it raises an implied accusation that the person is making things up or wildly exaggerating.  This is often taken as what it is: an insult.

Again, all testing and treatment needs to be oriented toward this question as well. Does the testing increase the ability to improve a person’s quality of life?  If it identifies risk or avenues of treatment, then it shouldn’t be done.  If a medication doesn’t make a person feel better or, conversely, if it has significant side-effects, it shouldn’t be given (unless it substantially reduces risk).

One of the main problems with the care given by many providers is that, even if these issues are considered they aren’t discussed with the patient.  This is a way in which my current situation greatly favors patient-centered care in that I have time to explain why we might want to use a medication with potential side-effects (or even risks) if it improves risk or quality of life enough.  People are far more open to taking medications that they understand, but it is our job to explain this.

Rob Lamberts is an internal medicine-pediatrics physician who blogs at Musings of a Distractible Mind.

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