Jun 16, 2010 9:43 AM
Should people be paid to take medication?
-
Like (0)
A recent New York Times article profiles monetary incentive programs designed to increase prescription medication adherence. Methods range from electronic lotteries, discounted copayments and monthly adherence payments for patients, through to paying pharmacists to help patients with adherence and paying doctors to prescribe medications. There is evidence that high levels of medication adherence can reduce hospitalization and lower all-cause medical costs - but is paying people to take their medication the right way to go?
On first blush, I find the notion of paying people to take their medication disconcerting, almost patronizing. However, given the correlation between prescription use and reductions in overall medical costs, as seen in the Medical Care article, it makes sense to look at every possible way to incentivize compliance. The New York Times article presents different patient models with the common benefit of providing small to moderate financial performance incentives. Mid-point in the article it digresses to discuss paying doctor’s to get their patients to take their medications – resulting in a financial incentive of between 3% - 5% of the physician practice’s base income, not insufficient by any means. This latter point, I did find confusing to the point of the article.
I have two thoughts. First, the New York Times article states that one-fourth of patients don't fill their prescriptions which, obviously, results in their inability to take their medications. Of course, it’s a leap to assume that people don't fill prescriptions solely because they are non-compliant. I would suspect that it has more to do with financial barriers (e.g., cost of co-pays and deductibles, lack of prescription coverage). Second, it doesn't appear that these examples of paying patients have enough longevity. I would be interested to see if long-term financial incentives continues to result in patience medication compliance.
There are several considerations in trying to answer the question:
1. Is the patient in agreement with the provider on necessity of taking the medication?
2. Does the patient have the insurance backing and or financial resources to pay for the medication?
3. If the answer to 1 and 2 are yes, then I feel that a patient has both rights and responsibilities with respect to compliance with therapeutic recommendations. Taking the medication becomes the patient's responsibility. By not taking the medication, despite agreeing with the provider that it is the "right thing to do", then patient is exercising a right, even if somewhat perverse.
If by not taking the medication or following other therapeutic suggestions, the patient incurs a deterioration of health status, then who is exactly responsible?
By not being compliant and incurring medical consequences, should the patient be required to pay for medical care directly related to non compliance? I feel that for completely competent patients this is worth considering..
It may be useful to reward medication compliance for chronic conditions at certain long term intervals. The reward could be reduced prescription cost, reduced co-pay for follow-up provider visits or some other token economic benefit.
All of the above are great ideas, however it adds more bureaucracy to the equation, and who is going to pay for that? Individual doctors, insurance companies, hospitals? PCPs are already overworked, who is going to be respnsible for information from specialists. Nope this is not a good idea.
Earlier today I came across this article that linked cash to safer sex/reduced sexual risk taking. Although these are different, I think the similarities should be given some serious consideration. If cash payments have the potential to encourage a desired behavior or discourage an undesired behavior, could the same be said for medication compliance? If lack of money is the reason for failure to comply with doctor's orders - rather, with that the doctor and patient discussed and decided together - then it logically follows that providing cash for the purpose of purchasing medication may increase compliance. We shouldn't rule this out on the basis of patient responsibility. When we get into talking about who's responsible and who's not is when we lose sight of the real-life situations that people are dealing with People struggle with having to choose between food, rent, and medicine. If we can help them cover their medicine and reduce subsequent burdens on the health care system, then why not.
Over a 15 year period of delivering primary care in eastern Omaha, people progressively ran out of funding earlier and earlier in the month. The reasons that took months or years to find out, were things such as illnesses in the family, son lost a job, disabilities, legal actions involving family, programs screwed up, mentally ill people (or their family members) did not fill out complicated paperwork that any of us would find to onerous or difficult to fill out. For some patients this resulted in even a $2 co-pay being too much. Of course even with people paid to take medication, they could take the funding and not take the medication. On the other hand going to a pharmacy now is very different from 10 years ago, especially for government Medicaid and Medicare patients. Far too many go expecting the prescription to be filled, but there are delays - including essential medicines like seizure medicine for my grandchild. A reasonable policy would seem to be to remove any and all barriers to medications, particularly for patients with complexities. Complexities include difficulties negotiating the barriers which can be mental health or just complex lives that so many lead. I would focus on removing the barriers such that we go back to go to the provider, get therapy prescribed, go to prescribed therapy and get therapy without hassles, don't increase the cost to patients or pharmacies or providers by complicated low yield barriers.
I have had the same bitter experience in having benefits for my son with cystic fibrosis. He obtained most of his medns via California Children Services and/or medi-cal. It would be a nightmare every month as to how to bill properly so that the computer would spit out the approval. His bills run 5000 dollars/month when he is well. We became uninsurable as a family having burned through our maximum coverage....and believe it or not I am a physician (now retired)). There was always difficulty to have CCS fighting with medi-cal as to who was supposed to pay the bill. Mandates do not mean payment....Politicians will promise almost anything to stay in office. Common sense has also left the building with giant pharmacy corporations. They will not dispense vital medications (they used to, when the pharmacies were Mom and Pop or a neighborhood Pharmacy knew your family.) Perhaps I am old fashioned and definitely a dinosaur, but not a luddite. These problems are not unique to medicine, but reflect the greater melt down of our American society.
While we ponder on monetary incentives to promote medication adherence, do we have the technology in place to track medicatuion adherence. Thisis a classic case that reinforces the need to have a true National Health Information Network. While similar initiative across the pond (in U.K) have run into cust overruns, at the end of the day had the PCP been on the same network and had the looked at a unified medication record via an integrated network the oversight of potential side effects would not have happened.
Weaving medication adherence into larger wellness tracking might be another way to look at this issue. Instead of cash incentives, non-cash incentives like a points system wherein the patient accumulates a certain number of 'wellness miles' and adherence gives an accelerator effect to these, which could overtime be used to defray co-pays/ pay for preventative screening among others.
Having a unified national health information network does not mean we have socialized medicine. Each of these problems are unique and are not solvable by one unified solution.
I agree with Roy's points 1-3. That said, if affordability is not an issue and the patient agrees with the physician's prescription, then the first question should be "why don't people fill and take medication?" The approach of the lottery mentioned in the Times article does appear effective, however, I have two thoughts: 1) there are other incentives to exhaust before we start throwing money at the situation, and 2) if done for the long term, eventually the novelty wears off and the incentive turns to an entitlement.
Sunstein and Thaler write about libertarian paternalism in their book Nudge. I think the authors would agree this situation is ideal for helping people to make good decisions (i.e., filling and taking their medication). So, I like the idea of incentives, but not financial ones. I agree with another response that discusses barriers... a perfect nudge would make the process of filling and taking the medication barrier-free and seamless.
I knew of one company in Colorado Springs that had a stand-alone team of nurses that provided ongoing maintenance of a large group of diabetic patients, and there results were stunning. Unfortunately, their funding ran out and the maintenance stopped. I wonder with the current research that shows the cost-effectiveness of consistent medication for chronic conditions would encourage the upcoming ACO's or insurance companies to do more consistent monitoring. A nudge of a phone call reminder might incent someone to do their part of their care.
Studies that never appear in print
Cleveland Clinic pathologist giving a talk in Indiana - He noted a pilot study done by a female cardiologist on amyloid heart, with a 4 - 6 month prognosis. Intervention - thalidomide. Results - 14 - 17 month survival. But the cardiologist and her office departed. The study was replicated by 4 or 5 offices - no difference shown. Problem - the patients in the non-dedicated offices did not get the same nursing and counseling to get them through the considerable side effects of this "chemotherapy" His diagnosis - patients were essentially left to their own devices and did not stay with the therapy.
Studies confirm poor results in high side effect meds in disadvantaged populations. A good source is pediatric cancer therapy where over 85% of patients are studied.
Those of us in health care, particularly young and on few medications and not on the complex regimens of today, fail to comprehend this.
Took me three years to learn how to take Lactaid right and what I could do to make it work, and the kinds of foods and situations where it would not work.
Also one of the biggest factors involves confidence in the provider and in the medication. When patients have low confidency in providers and low confidence in medicine (specific or generic), there are huge problems with adherence.
Most puzzling case - major diabetic patient with early renal and other side effects essentially not taking medication at all (even without a co-pay or barriers) - eventually he had to have an aortic aneurism repaired. For a year he had no sign of diabetes at all although eventually "relapsing" Still wonder what possibly resulted in this major change (Immune, change in healing process?) I have had patients in the early phase of treatment get a honeymoon, but not the late phase people.
Also Medicaid is already doing lotteries. The co-pay and barriers to medications resulted in certain patients with medication failures. In the case of a man with previous duodenal ulcer, the result was near death and over $50,000 cost and lost productivity costs, etc. This lottery cost the hospital, the physicians, the patient, Medicaid, and all of us. Few studies demonstrate the overall consequences of co-pays for medications, reducing from 7 to 3 prescriptions, barriers to certain drugs, etc. But primary care folks see the consequences, take the time to explain to bureaucrats that duodenal ulcer may not be on their list, but is a lifelong indication, etc.
Bob Bowman
The key to adherence with medications and treatment plans is providing the patient with the knowledge and skills (improving self-efficacy) needed to manage their health. The degree of responsibility for each individual will vary but the goal should be to assist every person in achieving to her or his individual ability/capability. Paying people to take medication is not the answer. Training an adequate number of health professionals with different skill sets working in teams is required.
As a provider for safety net clinic patients I would not recommend paying patients to take medication. I agree with many of you about the need for the patient to understand the purpose and effect of medications. Also I do believe that having the pharmacist actively involved in patient care helps. I do wonder if the patient would be more compliant if the provider knew through technology (escrpts or an emr) if the patient actually refills medications and when. We do have a pharmacy as part of our clinic and patients are required to get medications only through our pharmacy. We know if the medications are properly refilled and we call the patients on it if they are not refilling in a timely manner. Also the pharmacist spends time designing labels for the patient who cannot read. I have not seen any research on the Ready Fill programs that many retail pharmacies are not offering, but it appears that the program must increase compliance because it takes one step out of the patient reordering process
Wow, paying people to take medication -- while I can related to some of the comments of support for this -- it just seems like going way to far.
No only is that basic premise that a 'carrot' is needed to help people help themselves disconcerting, the HUGE problem of actual verification and payment logistics would sink it!
There are soooooo many other things to work on and solve. This idea would just bring more problems to the table.
| Privacy/Terms of Use | | | Community Guidelines | | | Support | | | ![]() | Download Acrobat Reader |
