Will recommendations from Choosing Wisely ever be followed?

Choosing Wisely is the new campaign advocated by the ABIM Foundation to help physicians “be better stewards of finite health care resources.” The recommendations in the campaign have been published in Consumer Reports and has been distributed to AARP members.

At first glance, the campaign seems to make sense. Limit unnecessary testing and decrease costs. However, I predict that the Choosing Wisely campaign will also have many less desirable effects. I picked out a few random examples of current Choosing Wisely recommendations to illustrate some of the problems that I perceive will occur.

The American College of Physicians recommended that we, ”Don’t obtain imaging studies in patients with non-specific low back pain.” Notice how the ACP didn’t describe how to classify back pain as non-specific prior to testing? Third party payors will be citing this recommendation routinely. Any back pain imaging that shows no pathology is likely to be retrospectively labeled as unnecessary because the back pain was non-specific. What if a patient has urinary retention with his acute back pain? Would anyone argue that an urgent MRI wasn’t indicated? However, the MRI shows nothing but an enlarged prostate and the urinary retention was probably just caused by the opiates the patient was taking for the pain. Retrospective diagnosis: Unnecessary test. Doctor should have known better. Patient gets stuck with bill.

The American Society for Clinical Oncology recommended that we, ”Don’t perform surveillance testing (biomarkers) or imaging (PET, CT, and radionuclide bone scans) for asymptomatic individuals who have been treated for breast cancer with curative intent.”

Isn’t the idea of cancer survival to catch things early? By the time we wait for an asymptomatic metastasis to become symptomatic so that testing is appropriate, the cancer will most likely be too late to treat. Using this recommendation, third party payors will refuse to pay for follow up screens because they are unnecessary. Patients won’t get the testing, and more patients will die from cancer recurrence.

Are most surveillance tests normal? Of course. But instead of having a group of stewards act as barriers to testing, patients should be presented with data regarding the effectiveness of the testing and then make an informed decision as to whether they want to have the testing performed. If ASCO truly believes that surveillance testing is inappropriate, it should check its own web site. The recommendation against surveillance testing isn’t even one of its own clinical practice guidelines for breast cancer. And if you look at ASCO’s recommendations for use of tumor markers in breast cancer, the Society does recommend use of some tumor markers which seems to contradict their own Choosing Wisely recommendation (“The following categories showed evidence of clinical utility and were recommended for use in practice: CA 15-3, CA 27.29, carcinoembryonic antigen, estrogen receptor, progesterone receptor … “).

The American College of Radiology recommended that we, “Don’t image for suspected [pulmonary embolism] without moderate or high pre-test probability of [pulmonary embolism].” The actual incidence of pulmonary embolism in patients with a low pre-test probability of pulmonary embolism is between 4% and 15%. Adhering to ACR recommendations, doctors would miss up to 1 in 7 cases of pulmonary embolism. About one in three patients with untreated pulmonary embolism die, meaning that up to 5% of patients with low pre-test probability of a pulmonary embolism would die using the ACR recommendations. Even if we obtain a normal D-dimer assay in patients with a low pre-test probability of pulmonary embolism, the incidence of pulmonary embolism in patients is still 0.7% to 2.0%. There is no test that detects pulmonary embolism 100% of the time, but shouldn’t patients be making an informed decision whether or not they wish to have testing performed to help decrease the likelihood of this potentially deadly disease?

To push the steward envelope in decreasing the number of imaging tests being ordered, the American College of Radiology has even created its own Image Wisely campaign. However, radiologists aren’t the ones who get sued for failing to order imaging tests — they’re only liable for failing to properly interpret tests that other doctors order. By telling other physicians not to order that testing, the radiologists look like great stewards, but have no skin in the game. If the American College of Radiology wanted to have an impact upon the amount of radiologic testing being ordered, it would have created an Interpret Wisely or a Report Wisely campaign to deter its members from recommending low yield follow up studies on questionable x-ray abnormalities.

While there are many appropriate entries on Choosing Wisely’s list (we don’t need antibiotics in acute sinusitis, folks), many of the Choosing Wisely recommendations either have little applicability or are just too vague. Even recommendations that make good clinical sense don’t appreciably affect the project’s stated goals. How much of our country’s finite resources will be saved by refusing that unnecessary $4 amoxicillin prescription for sinusitis, anyway? Many of the recommendations in this project will give bean counters extra ammunition to use against us in determining our worth as physicians, in determining whether we are appropriately compensated for our services, and in shaping a negative public opinion about how uncaring physicians perform unnecessary and wasteful testing and treatments.

In addition, many of the tests that Choosing Wisely recommends withholding from patients have some element of physician judgment involved in deciding whether the test is indicated. See catch phrases such as “low-risk”, “asymptomatic” and “non-specific” within the current Choosing Wisely recommendations. These judgment calls limit the applicability of the recommendations, but don’t we see where this is headed? Like the non-specific back pain example above, once a test has been interpreted as being normal, third parties are going to retrospectively second guess the physician’s judgment in order to avoid paying for the test: “The doctor misclassified the patient as ‘intermediate-risk’ when the patient was really ‘low-risk’ and therefore [insert name of negative test] was not indicated.”

Insurance companies will have an incentive to use this discretionary language to refuse pre-authorization for expensive testing or treatments and to deny payment for tests that were performed.

Before any tests or treatments make the Choosing Wisely list, there should be proof that the involved activities are truly unnecessary and that no harm to patients will come from excluding those tests. If, instead, the tests are deemed low yield or discretionary an evidence-based assessment of the risks and benefits of the testing or treatment, including a summary with projected cost savings and projected morbidity and mortality, should be published along with the recommendation and the public should be allowed to comment on the summaries and recommendations. Using this information, patients could then decide whether or not they are willing to forego the testing and/or treatment based on their own assessment of the risks and benefits of the testing or treatment. Doctors need to focus upon informed consent, not upon paternalism.

Choosing Wisely also needs to emphasize that many low-yield tests are performed due to a fear of lawsuits and that those discretionary tests might not be necessary if physicians were not held liable for failing to diagnose highly unlikely diseases or for failing to prolong the lives of terminally ill patients by a few months.

The Choosing Wisely campaign has good intentions, but isn’t a good idea. There isn’t a Suing Wisely campaign for attorneys and there isn’t a Legislating Wisely campaign for Congress. The amount of discretionary medical testing performed in this country is undoubtedly excessive, but in order to diminish the amount of discretionary testing, we shouldn’t erect barriers to performing those tests. Instead, we should help our patients understand that medicine will never be perfect and that sometimes doing everything or getting every test isn’t in a patient’s best interests. Until we impart this wisdom upon our patients, it is unlikely that any recommendations from a Choosing Wisely campaign will be routinely followed.

William Sullivan is an emergency physician and an attorney and who blogs at Dr. William Sullivan’s Med Law Chronicles.

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  • http://onhealthtech.blogspot.com Margalit Gur-Arie

    I’m afraid the conclusion in the last paragraph is not supported by the preceding arguments in this article. Once insurers incorporate these “guidelines” into reimbursement policies, and effectively “choose wisely” on behalf of both physicians and patients, there will be no need for anyone else to make hard choices and the recommendations will be widely followed (except for wealthy people), and it will cost us less to have a few more people die sooner. This is just another example of the new and improved “patient centered” care philosophy.

  • http://www.facebook.com/people/Steven-Reznick/100000549195050 Steven Reznick

    In the eyes of the economists, driving todays health care reform engine, it is acceptable for more people to become gravely ill and die if it saves money. Missing a few diagnoses early in the disease process reduces the dollars spent per study performed to save or extend a life. This is good for employers, this is good for insurers it just isn’t acceptable if it is you or your loved one.

    It is not fair to put a $45 K per year family with a reasonable deductible in the position of having to decide if they should have a study that will break their budget even if the risks and benefits and pros and cons have been explained to them. What is an acceptable risk? What is a reasonable suspicion leading to ordering a test? Once you put the insurers in charge of anything let alone medical decision making, the decision made is the one that is best for their investors and shareholders not what is best for the individual patient.

    The individual physician is still supposed to be the patients advocate working with the patient to explore the pros and cons of a particular evaluation and why their individual and unique situation is appropriate for taking a particular test. If we start at the medical school level by indoctrinating future physicians with programs like Choose Wisely and then extend it through internship and residency , the new physicians will have no idea that they should even question these recommendations. I much prefer the program i had as a house officer at the University of Miami Affiliated Hospitals Jackson Memorial program , where we received an itemized bill for each test we ordered so that we knew what each test cost. During teaching rounds and residents report we were often asked to justify why we ordered a particular test and if we could have gotten to the same conclusion with a different or more efficient approach. It was non threatening and left a strong impression of what things cost. It additionally forced us to think and reason why we chose one test over another. I prefer this approach to insurers making the decision

  • Kathleen Ogle

    “Isn’t the idea of cancer survival to catch things early? By the time we wait for an asymptomatic metastasis to become symptomatic so that testing is appropriate, the cancer will most likely be too late to treat.”
    This is nonsense. Metastatic cancer in the vast majority of adult cancers is incurable, no matter when the mets are found. Incurable doesn’t mean “too late to treat” unless the patient has waited to seek medical care until they are near death. Numerous studies have shown no difference in survival or even quality of life in patients whose mets were found when they showed up with symptoms vs those who were rigorously screened for asymptomatic mets. The idea that early detection improves survival is only applicable to the primary diagnosis of cancer, not to the diagnosis of mets, with rare exceptions (testis cancer in young men, some lymphomas, etc).

  • James Sinclair

    ASCO’s “minimal” intervention for breast cancer follow up guidelines published 10 years ago suggested routine imaging was not indicated. I presented this to a breast cancer support group with the scientific explanation. They were politely silent after the talk but a week later my patient who was there said they all got together and said the hated what I had to say and would still ask for these scans. We have plenty of unreimbursed education to do before we have to see an increased death rate from economizing on healthcare.

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