The Tracey Ullman Patient Compliance Videos

04-15-2008 | Categories:

Patient Education Goes Bollyhood




Once again, AlignMap takes patient education from the sad and drab ghetto of mainstream materials to the fab world of entertainment.

Check out Tracey Ullman’s conceptualization of patient counseling performed by the pharmacist.





Related Posts:

Yep, The AlignMap In The Slate Article Is This AlignMap

03-25-2008 | Categories:


slate-alignmap-story


AlignMap readers will, I suspect, find little new in “Doctors Without Orders,” an article about medication noncompliance by Jessica Wagner at Slate.com.

In fact, the material may seem very familiar to those readers of AlignMap posts because much of the article is indeed based on an interview with me and data drawn from the AlignMap site.

Even the material dredged from these archives, however, seems altogether more impressive when Ms Wagner writes it under the Slate aegis.

Jessica Wagner’s Slate.com essay on medication noncompliance can be found at





Related Posts:

Medication Adherence Reminders and Doctor-Patient Communication In The Wall Street Journal



Two Wall Street Journal articles that are especially pertinent to patient compliance were published on 20 November 2006 during the AlignMap blog’s holiday hiatus.


Cell Phones Provide Medication Information and Reminders

don’t 4get ur pills: Text Messaging for Health1 by Rachel Zimmerman explores the use of text messaging on nearly ubiquitous mobile phones as a real time means of conveying information about medical treatment, responding to healthcare queries, and, most significantly for patient compliance, sending reminders about medication doses to patients.

While I have been critical of marketing that promotes reminders of various sorts2 to be the complete solution to medication noncompliance or suggests that reminders always result in downright miraculous improvements in adherence rates, I am taken with the notion of cell phone text messaging as a useful tool for patients who have difficulty taking the right medications at the right time (a category in which I frequently find myself when a new medication, such as an antibiotic, is added to my ongoing medication schedule for a one or two week period) and for exchanging information precisely because it requires, for most of us, no new or specialized equipment and fits into our daily routines.

Because I already use an analogous service to text messages to myself about everything from taking out the trash early Monday mornings for the weekly pickup and buying specific items currently on sale at my local grocery to adapting a business presentation in time for a meeting next week, I can see how medication reminders could also integrate into rather than impinge upon ones behavioral patterns. I can also imagine younger individuals, such as my 18 and 21 year old sons who would promptly toss a reminder device that attracted attention to themselves under a passing truck, being comfortable with this type of reminder.

Readers may recognize one service provider mentioned in the article, Intelecare Compliance Solutions, as the group represented by Knight, the author of the Medication Noncompliance Blog:

Intelecare Compliance Solutions Inc., based in New Haven, Conn., sells a service — which companies can then provide to their employees or customers — that sends text, email or voice-mail messages reminding users to take their pills, refill prescriptions, get to appointments or check vital signs. Drug companies, insurers and large employers hoping to improve efficiency and decrease absenteeism are Intelecare’s main customers,


Patients, Doctors, Dollars, and Communication

Your Doctor’s Business Is Your Business by David Armstrong discusses how patients might best deal with the possibility that their doctor has a potential conflict of interest (e.g., a physician with a financial interest in an orthopedic device he developed might be tempted to prescribe it unnecessarily or a doctor might advise patients to undergo a CT scan at a given facility which he owned). While I certainly see the value of open disclosure on the part of clinicians re special financial considerations they might receive from prescribing a specific treatment, I’m less convinced of the practicality of the course of action promoted by this article. In a framed box entitled “WHAT EXPERTS RECOMMEND,” the recommendations are

1. Ask if your doctor has any financial connection to the recommended treatment.
2. If the answer is yes, seek a second opinion.
3. If unwilling to ask the doctor, do research on the Web. …

Even though I’m a physician myself, I would find it awkward to ask each of my doctors every time they prescribe a medication, operation, physical therapy, etc, if they will personally benefit from that transaction. Using as an example, the treatment I received for my recent hip fracture as an example, I should, according to a straightforward reading of the article, have asked about conflicts of interest when

  • My personal physician ordered a diagnostic x-ray from a facility located in a different office of the same medical building as his office
  • My personal physician had his nurse obtain blood samples for the hospital admission work-up
  • My personal physician referred me to a specific hospital for reparative surgery
  • My personal physician referred me to a specific orthopedic group for further diagnosis and treatment
  • The orthopedic surgeon recommended a hip pinning rather than other options
  • The orthopedic surgeon referred me to a inpatient physical therapist for purchase of an assistive walking device and training in its use as a condition of discharge
  • The orthopedic surgeon ordered pain medication for my post-operative use as needed
  • The orthopedic surgeon ordered follow-up x-rays of the hip to be done in his office before every follow-up appointment
  • The orthopedic surgeon recommended outpatient physical therapy at a specific facility

It seems to me that the real question readers are being prompted to consider is “Is my doctor ripping me off?” And, I think that is a legitimate enough concern; the problem is that if such fiscal treachery is afoot, one would hardly expect the perpetrator to automatically fess up when confronted with a simple question. How useful would it be to ask a car salesman, “By the way, my good man, are you charging me an excessive amount for this automobile and pushing the special undercoating only to build up your own commission?”3

The author of the article, perhaps recognizing this issue, advocates a second opinion if any potential conflict of interest is found. I’ve always pushed my own patients to obtain second opinions to pacify any qualms about my diagnoses or treatment recommendations, but second opinions are themselves often expensive (especially if not covered by insurance) and take time to arrange. Moreover, an expert in the appropriate field whose reputation is blemish-free and who is absolutely independent of potential conflicts may be hard to find on short notice. And, if the course of action recommended in the second opinion differs from the first treatment suggested, does the patient get a third opinion to break the tie? What if it turns out that the doctor providing the second opinion has his or her own financial arrangements that compete with those of the first doctor?

Finally, how significant and how specific to a given treatment does that financial involvement have to be to warrant notifying patients? Should the doctor who sells and dispenses mediations within the office list his profit margins for those medications? Does the prescriber who owns stock in a pharmaceutical company have a different obligation to inform clients than the prescriber who helped developed a medication and receives a royalty for every pill sold? Do doctors working for an HMO who receive an incentive for prescribing generic rather than brand drugs disclose that to every patient? Does a doctor who sends patients to a facility that uses a certain type of CT machine on which holds a patent have a different responsibility to disclose his financial arrangement than a doctor who orders CT scans on his patients done in the office with the CT machine his group practice owns and operates?

If the following statements were true, should I have told patients, “I’m prescribing Prozac for your depression, but you should be aware that Eli Lily, the company that manufactures Prozac, …

    … pays me a royalty for every Prozac capsule sold because I helped get FDA approval”
    … sells these capsules to our pharmacy wholesale and our pharmacy, which our practice owns, charges you a 200% markup when we sell you your medicine I’m prescribing”
    … sends a salesman here every month who takes me to lunch where he tells me why I should prescribe Prozac instead of another medication”
    … may be in the portfolio of some of the stock funds in which I’ve invested so their profit would benefit me”
    … offered second year medical students at many medical schools in 1973 a free, medium quality stethoscope that I accepted”

I suspect few would think that admitting that I accepted a stethoscope from Lily is either necessary or useful, but defining how much financial involvement by a physician merits or requires disclosure is not a trivial task.

My discomfort with this piece, in fact, is not that the problem of a physician’s conflict of interest doesn’t exist but that the simple fixes the article described belies that complexity of the problem.

Additionally, such questions put to doctors are not always benign and may yield negative results, a concern noted in this excerpt:

Patient advocate Trisha Torrey isn’t so sure it is a topic worth bringing up. The doctor-patient relationship is already stressed, and questioning a doctor about financial connections “can create more harm,” she says. That doesn’t mean patients should be unconcerned about financial relationships. She says patients should do their own research and seek second opinions if they suspect their doctor could profit from a certain treatment recommendation.

Readers may also recognize Trisha Torrey as the author of Every Patient’s Advocate, a blog which occasionally appears here at AlignMap.

_________________________________


Disclosure Statement

Ahem, I have not accepted any financial remuneration from The Wall Street Journal, Every Patient’s Advocate, Medication Noncompliance, their authors, or their associated companies for mentioning them in this post.

One possible reason, in addition to my stalwart Midwestern upbringing, my seven years of perfect attendance at Sunday School, the two semesters I spent at Oklahoma Christian College, and my preternaturally staunch moral fiber, for my incredibly righteous stance in this regard is that none of those entities has (yet) offered me any such remuneration. I mean, if someone were to go to the trouble of, say, placing a manila envelope filled with a significant chunk of cash in small, unmarked bills in a locker at the bus station and sending me the locker key, it would be rude not to at least consider taking the money. Or if Mr Murdoch, who could certainly afford it, saw fit to comp me a daily copy of the WSJ, to which I subscribe at the exorbitant, full-price online subscription rate, I would feel obligated to live up to the standards of politeness instilled in me by my mother and to accept that offer as a no-strings goodwill gesture from a fellow publisher.

I freely admit that both of the individual blog authors mentioned do occasionally email me, typically to tell me or ask me about something going on in the wide world of patient compliance or exchange a tidbit or two about our personal lives. Trisha, for example, moved recently, and we briefly discussed the stresses such endeavors may inflict on households. I am only a teen-tiny bit jealous that their businesses were mentioned in WSJ articles and mine wasn’t. Both bloggers have written positive comments about AlignMap or me in previous posts, which is always nice.



Footnotes


  1. If this article falls in the “subscriber-only” section of the WSJ, readers without such a subscription may be able to access this article by first going to the Digg Connection to this piece and then clicking on that link [back]
  2. ”Reminders” include wrist watches that signal the time for medication, dispensers with flashing lights, recorded messages, and overtly noxious sounds, telephone calls, orbs that glow at the appropriate time, and a variety of Rube Goldberg contraptions [back]
  3. While a villainous doctor might be more forthcoming and the questioning process more amusing and gratifying if one employed more vigorous interrogation methodology such as that used on TV police procedurals or in the Spanish Inquisition, those techniques could prove off-putting to some healthcare professionals and could tend to taint the relationship between physician and patient. [back]



Related Posts:

The New York Times On Lipitor Vs Simvastatin Study

11-04-2007 | Categories:


Follow-up To AlignMap Post On Study Claiming Switch From Lipitor To Generic Is Dangerous

Rather than sacrifice blogging’s inherent advantage of timeliness, I’m deferring the promised conclusion and summary post on the Personal Medication Record to link to and comment on this 3 November 2007 New York Times article, Maker of Lipitor Digs In to Fight Generic Rival, by Stephanie Saul And Alex Berenson, which addresses the Pfizer-sponsored statin research project study that was the focus of the 8 September 2007 AlignMap post, Lipitor Would Rather Fight Than (Have Patients) Switch



The article from the Times recapitulates much of argument I made in the earlier blog entry sans my lengthy exposition of some of the study’s problematic methodological issues. The crux of the New York Times essay is congruent with the final line of my post:

The most useful lesson from this study may well be the reminder that certain medical research projects may have as much to do with market share as with morbidity and mortality.

I’ve included a short excerpt of the opening of the article but the full piece is available without charge at ~ Maker of Lipitor Digs In to Fight Generic Rival ~


__________________________


It is shaping up to be the biggest shift yet to a generic drug, potentially saving the nation $2 billion a year or more in prescription costs. And scientists and doctors say that for most of the 16 million people in America who take drugs to reduce cholesterol, the low-priced alternative will work as well as the name-brand medicine — Lipitor, which is made by Pfizer and is the nation’s most widely prescribed drug. While Lipitor itself is not available as a generic, a very similar drug made by Merck, Zocor, lost its patent protection last year. The generic version of Zocor, simvastatin, is now much cheaper than Lipitor, leading insurers to press doctors and patients to switch.
But Pfizer is not letting its flagship drug go down without a fight. The company has mounted a campaign that includes advertisements, lobbying efforts and a paid speaking tour by a former secretary of the federal Department of Health and Human Services. Pfizer is also promoting a study — whose findings many experts are questioning — that concluded that British patients who switched to simvastatin had more heart attacks and deaths than those who remained on Lipitor.





Related Posts:

John Edwards On Patient Compliance

And Bloggers On John Edwards



Were one to draw the Venn diagram of patient compliance and presidential campaigns, one would anticipate the intersecting portion would be minuscule if it existed at all. Further restricting that intersection to an overlap patient compliance, presidential campaigns, and public controversy certainly, one would think, doom that result to the ignominy of the null set.

Well, as of 2 September 2007, one would be wrong.

That day, presidential candidate, John Edwards elaborated on his healthcare plan to the folks in Tipton Iowa in a speech described in Edwards Backs Mandatory Preventive Care, the AP news story by Amy Lorentzen:

“It requires that everybody be covered. It requires that everybody get preventive care,” he told a crowd sitting in lawn chairs in front of the Cedar County Courthouse. “If you are going to be in the system, you can’t choose not to go to the doctor for 20 years. You have to go in and be checked and make sure that you are OK.” He noted, for example, that women would be required to have regular mammograms in an effort to find and treat “the first trace of problem.” Edwards and his wife, Elizabeth, announced earlier this year that her breast cancer had returned and spread. Edwards said his mandatory health care plan would cover preventive, chronic and long-term health care. The plan would include mental health care as well as dental and vision coverage for all Americans.

From the lighting of that fuse to explosions of outrage in the conservative blogosphere required only a few hours.

Consider, for example, a Newsalert post published at 7:52 PM the same day the speech was given:

John Edwards Plans to Force You to Go to the Doctor

The AP reports on Comrade Edwards:
… [An excerpt from the AP story referenced above follows] …
Comrade Edwards is going to force you to go to the doctor whether you like it or not.You will not be free because Comrade Edwards wants a monopoly on your health care.

And, just in case the reader doesn’t pick up on the subtle political connotations of “Comrade Edwards,” the post is headed by the following emblem:


_________________________



How about a few other examples, just for grins?

From the post with my favorite title, Healthcare Part VIII - Drop that Twinkie or I’ll Shoot! at Angry Bear,

… Presidential candidate John Edwards says that under his universal health care program everyone WILL see the doctor for preventive care. Women WILL have mammograms. No word on the enforcement mechanism.
In the UK, a panel of Conservative MPs have a recommendation that Brits who live an unhealthy lifestyle should not receive certain types of care. The healthy lifestyle initiative would also be tied to health care service reforms and various social initiatives including housing and schooling reforms. Brits who live healthy lifestyles would be rewarded by receving (suc) points to be used for vegetables and gym memberships.
Is this the future of health care? Slightly Orwellian?

No word if Edwards will give us veggies.

_________________________


And from John Edwards: “you can’t choose not to go to the doctor for 20 years” posted at Althouse, come these passages:

Edwards’ universal health care proposal ignores individual autonomy
So, the mental health check is mandatory too? Why does he not even realize how bad that sounds? He’s so warmed up about the generous benefits he’s promising that he doesn’t even hear the repressiveness in his own statements. I’m sure he won’t be able to deliver on these promises. I’m just wondering about a person with so little sensitivity toward personal freedom.
_________________________


Daystar51 goes beyond lambasting Edwards for promoting “mandatory preventive health care” to speculating on the possible origins of this notion buried in the candidate’s psyche:

Is John Edwards trying to pay back all the doctors he sued, or what?

Mandatory preventive health care? Come on, no one could think that.

But Edwards says he does. He says if you’re going to be in the system, “you have to go in and be checked and make sure that you are OK.” Only he doesn’t happen to mention any way to opt out of the system. His plan “requires that everybody be covered. It requires that everybody get preventive care.” Not only that, but mental health is part of Edwards’s plan. I can only take this to mean that annual check-ins with a psychiatrist would be required, cradle to grave.

I wonder whether Edwards’s plan is designed to fund pill police to make sure you choke down all the good things Doctor gives you.

Interestingly, medical malpractice litigation was Edwards’s specialty when he practiced law. He tried more than 60 med-mal cases, more than half of which brought verdicts exceeding $1 million. He reported an AGI of $11.4 million in 1997. Tidy.

Perhaps Edwards is now enthralled with doctors because his wife has breast cancer. Perhaps his compulsory exam plan is a token of his appreciation, a way of paying doctors back.

_________________________


An blog/article, dated September 5, 2007, in US News & World Report wields the British healthy practices incentives plan as a blunt instrument to batter the obligatory preventive care Edwards espouses:

U.K. Offers Insight Into the Edwards Healthcare Plan

The dream of universal healthcare, as outlined so far in the Democratic presidential race, looks like this to me: Every American (says John Edwards) gets health insurance or at least most people (says Barack Obama). Will it mean higher government spending? Probably. But it can be paid for via higher taxes on wealthy Americans (Edwards). But who knows, maybe through greater use of technology, cost savings will be enough to avoid a tax increase (Hillary Clinton).

But as the various plans get looked over, explained, and debated, it seems very likely that all sorts of unanticipated aspects to them will pop up, such as this recent piece of insight from Edwards regarding his plan, via an AP story:

“It requires that everybody be covered. It requires that everybody get preventive care,” he told a crowd sitting in lawn chairs in front of the Cedar County Courthouse. “If you are going to be in the system, you can’t choose not to go to the doctor for 20 years. You have to go in and be checked and make sure that you are OK.”

Certainly at first glance, Edwards seems to be advocating a system where you get health insurance only if you follow certain government-prescribed healthcare routines, like regular doctor visits. Now after re-examining the Edwards plan, liberal blogger Ezra Klein concludes that patients “will have incentives to avail themselves of preventive options. But there won’t be any mandate for X doctor’s visits every Y years.” Maybe he’s right. But then again, maybe Edwards was accidentally describing the future of any government-directed healthcare system. Just look at Great Britain. That nation’s national health system already demands that obese patients lose weight before receiving hip replacements. But the out-of-power Tory Party wants to go further, according to London’s Evening Standard (via the Drudge Report):

Failing to follow a healthy lifestyle could lead to free NHS treatment being denied under the Tory plans. Patients would be handed “NHS Health Miles Cards” allowing them to earn reward points for losing weight, giving up smoking, receiving immunisations or attending regular health screenings…. But heavy smokers, the obese and binge drinkers who were a drain on the NHS could be denied some routine treatments such as hip replacements until they cleaned up their act…. Those who abused the system—by calling an ambulance when a trip to the GP would be sufficient, or telephoning out of hours with needless queries—could also be penalized…. Yet while the Health Miles Card would award points for giving up smoking and losing weight, it could penalise those who are already fit and well because they would receive no benefits under the scheme.

_________________________


Weird Is Relative, writing in What’s the punishment for noncompliance? Endless jury duty?, implies that the Tipton Iowa speech may be fatal to the Edwards candidacy:

John Edwards’ has a Howard Dean moment: He’s to rehashing a talking point from the Kerry/Edwards 2004 campaign: [Quotes from that same AP story follow] …
Forcing people to go to the doctor is not the equivalent of a national healthcare plan. But thanks for the soft paternalism.
_________________________


It would be difficult to misunderstand the perspective of Not Larry Sabato, who exclaims in John Edwards on Health Care,

You have to see this to believe it. John Edwards says his health care plan would REQUIRE Americans to go to the doctor for checkups.

This kind of crap is exactly what allows politicians like George Allen to talk about the “nanny state” and collect votes. I totally support universal health care so every American has coverage- but if some people choose not to use that coverage they are given- that is their decision. How is Edwards going to enforce this - will he send the police out to get people who miss their scheduled preventative doctor’s appointments?

_________________________


In fairness, not every blogger or commenter was bashing Edwards, but pro-Edwards postings are difficult to find. Plunderchat is a one of those few who straightforwardly support the mandatory preventive care, declaring in John Edwards Looking Good on Health Care that

he’s [Edwards is] pushing a health care plan that meets the two big criteria for success.

First: “It requires that everybody be covered.”

To make health care affordable for everyone, you need to spread the cost out across the entire population. Twenty-year-olds will often opt out of healthcare because they rarely need it while seventy-year-olds require constant medical- especially if they’ve had little or poor health care while they were younger. If you can keep the twenty-year-olds in the health care pool- then the cost goes down for everyone else.

Second: “It requires that everybody get preventive care.”

It is MUCH cheaper to prevent major medical problems than it is to treat them once they hit. Under the Edwards Plan “If you are going to be in the system, you can’t choose not to go to the doctor for 20 years. You have to go in and be checked and make sure that you are OK.”

If he keeps up like this, I might actually be able to look past his accent. Maybe.

_________________________


Commentary

1. It turns out that the complete healthcare plan Edwards supports apparently allows folks to opt out of the program if they wish to manage their own healthcare without government mandates. This discovery disappoints me; when I read about the Tipton speech, I envisioned a post about Edwards declaring Patient Compliance “Mission Accomplished.” Then, I would go on to sardonically observe that “the answer to noncompliance was right in front of us - just issue a presidential proclamation that compliance was obligatory. And so on. If folks have the alternative of leaving the system, the obligatory preventive care lacks the extremity of arrogance that would otherwise render this notion an appealing target.

2. Few bloggers noted that we already have a batch of healthcare mandates on the books, including reporting and quarantine of various infectious diseases, undergoing certain vaccinations, obligating parents to follow doctor’s orders re their sick children, lest they be made wards of the state, and, more recently, restrictions on smoking and intake of some foods.

3. I have to wonder if Mr. Edwards and his advisers have considered the difficulty of monitoring, let alone enforcing patient compliance. While checking attendance records to determine who kept and didn’t keep a doctor’s appointment seems simple enough (although distinguishing between appointments missed because of traffic, scheduling snafus, and family emergencies from those missed through noncompliance may require compliance interrogations abetted by bright lights, good copy-bad cop tactics, and polygraphs), medication compliance, for example, is notoriously difficult to determine, and adherence to diet, exercise, and similar non-medication prescriptions is rarely even attempted. Enforcement methods, short of the Pill Police, are relatively easy to come by; e.g., dropping healthcare coverage for noncompliant patients or tying official authorizations such as driver’s licenses to certificates of healthcare compliance would be simple enough, but even a compliance-pusher like me recognizes that this would be a major shift in the patient-clinician relationship as well as in the role of government in this country.




Related Posts:

The pills were a leash

06-01-2007 | Categories:

Patient Compliance Used To Develop A Character In A Crime Novel



From A Darkness More Than Night by Michael Connelly

McCaleb took two tall glasses from the cabinet and put them on the counter. He filled the first with bottled water and the second with orange juice. He then began ingesting the twenty-seven pills he had lined up on the counter, intermittently taking swallows of water and orange juice to help them go down. Eating the pills - twice a day - was his ritual and he hated it. Not because of the taste - he was long past that after three years. But because the ritual was a reminder of how dependent he was on exterior concerns for his life. The pills were a leash. He could not live long without them. Much of his world now was built around ensuring he would always have them. He planned around them. He hoarded them. Sometimes he even dreamed about taking pills.



Related Posts:

The Scrubs Patient Compliance Subplot - Part II

05-24-2007 | Categories:

Empathic Young Doctor Empowers Patient



Source: Scrubs: My Big Move. Episode: 90 Season: 4 First Aired: April 12, 2005
[This post is the continuation of The Scrubs Patient Compliance Subplot - Part I]



Elliot, although less skilled clinically than Dr. Cox, has insight into the patient that he lacks because of her own experiences.



Because of Elliot’s empathy (key point: teenaged girls have no control over their own lives), the patient reveals she is “so tired of people telling [her] what to do, when to be home, what to wear, when to take [her] medicine, …” and declares she can handle her own treatment.



Elliot builds rapport [note her forward leaning to signify interest in the patient] and then empowers patient by putting control of her medication in her hands. (Prescription will go to patient instead of parents; she will be in charge of getting and taking her Dilantin.)



Patient says “Thank you” to Elliot [and, one suspects, becomes 100% compliant and lives happily ever after]. Dr. Cox learns a valuable lesson from Elliot.



Upcoming: Commentary On The Scrubs Patient Compliance Subplot




Related Posts:

Wall Street Journal Offers Practical Compliance Tactics

05-23-2007 | Categories:



Taking The Right Pills At The Right Time

In yesterday’s Wall Street Journal Health Journal column, Take Your Medicine: Strategies for Sticking to a Drug Regimen, Tara Parker-Pope takes on the practical problems of medication compliance, focusing on pill organizers, reminders, and a few of the strategies previously discussed in this blog: Picture-cards, Alerting Devices, The Asheville Pharmacist-driven Project, and Pharma-sponsored Compliance Programs.


Commentary

My criticism of this article is - well, that it’s not the article I would have written.1 The time and space restrictions on a columnist are not issues I face posting here. If I skip a day, someone might complain, but I won’t be fired. And, if I am rant-oriented, I can write as many pages if I wish. Ms Parker-Pope does not enjoy such luxuries.

That said, I still believe the columnist’s criteria for usefulness when it comes to compliance methodologies is a tad lax. As the Dodo declares after a race in Alice’s Adventures in Wonderland, “Everybody has won, and all must have prizes.” While one may be able to find instances in which each of the techniques listed made a difference for a given individual or group of individuals, but convincing evidence of overall efficacy is lacking for most.

Interventions to Enhance Medication Adherence in Chronic Medical Conditions: A Systematic Review by Kripalani and colleagues,2 an article referenced in the column, concludes its abstract with a sobering line, “Several types of interventions are effective in improving medication adherence in chronic medical conditions, but few significantly affected clinical outcomes.” I would contend that the column should have emphasized both clauses of that statement rather than focus exclusively on the first.



Footnotes


  1. If I were to write a single piece for a periodical like the WSJ, I would want to delve into the research, the conceptual basis of compliance, the political and economic implications, … , creating a tome which would displace all other news, columns, and features for weeks. Consequently, the risk to readers is, I suspect, slight. [back]
  2. Sunil Kripalani, MD, MSc; Xiaomei Yao, MD; R. Brian Haynes, MD, PhD. Interventions to Enhance Medication Adherence in Chronic Medical Conditions: A Systematic Review. Arch Intern Med. 2007;167:540-549 [back]



Related Posts:

The Scrubs Patient Compliance Subplot - Part I

05-22-2007 | Categories:

Pompous Doctor Unable to Deal With Noncompliance




Source: Scrubs: My Big Move. Episode 90, Season 4, First Aired: April 12, 2005

The Story

Dr. Cox confronts his 16 year old patient, with whom he mistakenly feels he has good rapport, on her nonadherence to her anti-epileptic medication regimen, informing her that she will die if she doesn’t take the medication appropriately. Elliot [AKA "Blond Haired Doctor"], is appalled.



The patient meekly agrees to take her medication, but [gasp] doesn’t do so.



Guilty to discover that shouting at his patient caused her to cry, Dr. Cox awkwardly tries to establish communication with his patient by talking about issues he, again mistakenly, thinks teenaged girls would find interesting.



Dr. Cox, despite hours of effort, fails to forge a working relationship with his patient.


Stay tuned for Part II of The Scrubs Patient Compliance Subplot



Updated: The Scrubs Patient Compliance Subplot - Part II




Related Posts:

Medication Noncompliance As Plot Device

04-23-2007 | Categories:



The Scene

During the fourth season of Seinfeld, Dr. Reston, Elaine’s manipulative psychiatrist, has whisked her to Europe. He breaks an embrace with her on a balcony in Paris and assumes a thoughtful, concerned stance. Elaine asks “What is it?”

The psychiatrist replies, “I was just thinking about this patient of mine, … just wondering if he’s taking his medication.”

As it turns out, the patient, “Crazy Joe Davola,” has not taken his medication and becomes psychotic. Wikipedia recounts his course following his unilateral termination of medication.

Davola is noted for stalking Jerry. The incident started in “The Pitch” where they meet him at NBC offices (Davola, a writer, is dropping off a script.) It continues in “The Ticket”, where Jerry and George hid from him in a restaurant. Throughout the fourth season (the season which focused on Jerry’s failed television pilot), Davola appears frequently, including both parts to “The Pilot, Part 1″ and “The Pilot, Part 2″. In the first part, both Jerry and George attempt to hide, but are seen by him when they were leaving for NBC. In the final part, he is noted for saying “Sic semper tyrannis!” (incorrectly translated by Jerry as, “Death to tyrants”) and then jumping off the stands into the set in an attempt to attack Jerry. Davola’s action is reminiscent of John Wilkes Booth, the assassin of Abraham Lincoln.

Elaine once dated Davola’s doctor; also she inadvertently dated Davola while trying to break up with the doctor. When Elaine finds out that Davola is the same “Crazy Joe Davola” that Kramer and Jerry are running from, she also becomes a target.

Davola blames all of his problems on Jerry (even simple inconveniences like a stray hair on his mouth) and even attacked Kramer, who didn’t invite him to a party he was having. Kramer survived a kick to the head because he was wearing Newman’s helmet. The helmet was acquired by Kramer in a trade in which Newman received Kramer’s radar detector (which turned out to be broken).

Davola is also in exceptional shape. He keeps himself fit by lifting weights (while crying) and in one scene uses martial arts to defend himself from hooligans in the park.


["Crazy Joe Davola" disguised as opera clown to stalk Jerry and Kramer]


The Moral

Once you’ve seduced one of your patients and taken her to Paris, it’s too late to worry about another patient’s medication compliance.


Reference
Seinfeld. Season 4; Episode 3. “The Pitch”
First Aired: September 16, 1992




Related Posts:

Health Literacy: A Clear Problem Without A Clear Solution

02-23-2007 | Categories:



Interest In Health Literacy Grows

Two major newspaper stories in the past month addressed health literacy, one of the major causes of patient-clinician miscommunication, which in turn often leads to inadequate treatment plan execution, a phenomenon typically included under the aegis of patient compliance.

Sources:

‘Doctor-ese’ often stumps patients Jane E. Brody New York Times 4 Feb 2007

A Silent Epidemic Sandra G. Boodman Washington Post 20 Feb 2007


The Points Made In These Articles Are Straightforward

1. Impaired Health literacy is a national healthcare problem of huge proportions. According to the Institute of Medicine, more than 90 million Americans of all ages, races, and income and education levels, are unable to adequately understand basic health information.1

2. Poor health literacy results in poor adherence to prescription instructions, infrequent use of preventive medical services, increased hospitalizations and visits to the emergency room, and worse control of chronic diseases. The consequences are poorer health and greater medical costs.

3. Doctors fail to speak to patients in plain English (or Spanish or Chinese or any other language) and fail to make sure that patients understand what they are told and what they are supposed to do and why.

Studies of health literacy have found that a surprisingly large number of adults were perplexed by the meaning of the term “orally,” didn’t know the difference between a teaspoon and tablespoon and were unable to calculate the proper dose of medicine.
A study published in the Journal of the American Medical Association in 1995 found that more than 80 percent of patients treated at two of the nation’s largest public hospitals could not understand instructions written at the fourth-grade level for the preparation of gastrointestinal X-rays known as an upper GI series. A 1999 study of more than 3,200 Medicare recipients found that one in three native-born patients could not answer a question about normal blood sugar readings even after being given a paper to read that listed the correct answer.

The disconnect between the offerings from healthcare and the capacity of patients is noted in a 1999 report by the American Medical Association which found that consent forms and medical information are typically written at the graduate school level while the average American adult reads at the eighth-grade level. Worse, a 2003 survey completed by the U.S. Department of Education found that over 40% percent of adults read at a fifth-grade level or lower, and 5 percent are not literate in English (in some cases because it is not their first language). Math skills are similarly lacking.


The Impact Of Low Health Literacy Is Equally Clear-Cut

These excerpts are characteristic:

In a study published in the Journal of Internal Medicine, conducted among 2,512 elderly men and women living on their own in Memphis and Pittsburgh, those with limited health literacy were nearly twice as likely to die in a five-year period as were those with adequate health literacy. That held true even when age, race, socioeconomic factors, current health conditions, health care access and health-related behaviors were taken into account.

Another study in the Journal among 175 adult asthma patients treated by Cornell University doctors found that “less health literacy was associated with worse quality of life, worse physical function and more emergency department utilization for asthma over two years.”

Among the many problems resulting from limited health literacy are misinterpretations of warning labels on prescription drugs. For example, among 251 adults attending a primary care clinic in Shreveport, La., those with low literacy were three times more likely to misunderstand warnings than the more literate.

Despite major reports on the need to improve health literacy issued in the last decade by organizations including the American Medical Association and the National Academy’s Institute of Medicine, little improvement has been noted in how much patients understand and remember about encounters with health care practitioners.

Primary Problems

A main obstacle has been the decreased time patients can spend with their doctors, dictated largely by managed care and other medical reimbursement plans.

A second hurdle is the embarrassment that patients with limited health literacy experience when they do not understand what the doctor has said. And, of course, asking for clarification is seriously impeded by the imbalance in power between the white-coated physician and the paper-wrapped patient. Even when conversations are conducted in the doctor’s office with a fully clothed patient, patients are often reluctant to ask questions.


Fixes

These newspaper reports included several specific recommendations for clinicians as well as patients to improve communications, many of which come with the imprimatur of the Joint Commission which recently presented 35 recommendations to address this problem, along with the implication that such suggestions might become future Joint Commission requirements for healthcare facility accreditation. Examples follow:

Doctors should assess the patient’s baseline understanding before providing extensive information: “Before we go on, could you tell me what you already know about high blood pressure?”

Doctors should use plain language, not medical jargon, vague terms and words that may have different meanings to a lay person. They should say “chest pain” instead of “angina,” “hamburger” instead of “red meat” and “You don’t have HIV” instead of “Your HIV test was negative.”

Experts on health literacy also encourage doctors to assess patients’ health literacy by asking them to read aloud a list of 66 medical terms, each within five seconds. Patients are scored on how many words they pronounce correctly.

The advice for the patients is clear – be proactive or risk poor healthcare.

Do not wait until doctors become better at communicating. If you want the best medical care, you have to take the initiative. If the doctor says something you do not understand, ask that it be repeated in simpler language. If you are given a new set of instructions, repeat them back to the doctor to confirm your understanding. If you are given a new device to use, demonstrate how you think you are to use it.

Insist that conversations about serious medical matters take place when you are dressed and in the doctor’s office. Take notes or take along an advocate who can take notes for you. Better yet, tape-record the conversation to replay it at home for you and your family or another doctor.

Also mentioned is a Pfizer-sponsored program called Ask Me 3 that was designed by the Partnership for Clear Health Communication, a coalition of national health and literacy groups. The program encourages patients to ask three simple questions and to be sure they understand the answers: What is my main problem? What do I need to do? Why is that important?


Commentary

I’ve summarized and excerpted material from these articles at length to point out (1) the importance of the problem, (2) the growing urgency demonstrated in the press, professional organizations, and regulatory agencies for a solution, and (3) the solution being promoted.

While the severity of the problem and the mounting pressure for a solution are, it seems to me, clear cut, the only solutions offered are incomplete.

Doctors, for example, are unlikely to find that “none of this [i.e., the suggested improvements in communication techniques] should take more than a few minutes,” as the experts quoted approvingly in the New York Times article declare, to be reassuring. By simple arithmetic, “a few minutes” added onto each appointment in a busy day, assuming the estimate is accurate, accumulates into “a few hours” added every week.

Even more problematic is the contention that every patient has, within himself or herself, the capacities to be a “patient expert” on his or her disorders and a self- advocate with the interpersonal skills to assure that the right information (whatever that might be) is provided and understood without being so confrontational that the relationship with the clinician is jeopardized. Neither clinical experience or personality studies would seem to support this hypothesis.

What is to be done for those individuals who cannot, especially in the sick role, assume this proactive stance?

The current Patient Literacy campaigns do not seem to take this issue into consideration, let alone provide pragmatic answers. I believe, however, that there are potentially useful responses, some of which I will be addressing in forthcoming posts.



Footnotes


  1. The Journal of General Internal Medicine August 2006 [back]



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ADD Medication Adherence: Cultural Changes & Individual Attitudinal Shifts

12-19-2006 | Categories:

Many of the ‘ADD generation’ say no to meds; Newly minted grown-ups are carrying out a massive natural experiment by choosing to do without the drugs that profoundly affected their experience of childhood. By Melissa Healy, Las Angeles Times December 18, 20061


This article focuses primarily on a number of young adults who, diagnosed with and treated with medication for Attention Deficit Disorder in childhood, have chosen to discontinue those stimulants.

Commentary

This article exemplifies one of the most problematic aspects of the lay press reporting on healthcare issues by promoting a point of view that could influence readers.

There is no indication that any aspect of the story is inaccurate or intentionally misleading. On the other hand, each of the individuals who decided to stop taking their ADD medications is reported to have done well. Further, support for the discontinuation of medication is presented uncritically while doubt is cast upon theories and studies favoring the ongoing use of these medications.

And, consider the tone of these excerpts:

But as the 23-year-old navigates his way into adulthood, he’s managed to pay the roadside distractions a little less attention. And he’s learned a thing or two about getting himself from one destination to the next without taking major detours.
Looking back, he acknowledges that Ritalin did help him academically. But he also felt that it blunted his natural sociability, made it “hard to feel passionate about anything.” And the same intensity of focus that helped him in class, he believes, impaired his instincts on the soccer field — a troublesome side effect for a rising soccer star. He quit Ritalin as a freshman in high school. Off the drug, he says: “I felt more like a happier person. I just felt more like myself,” voicing an observation heard again and again among young adults who abandoned their ADD medication.
They [young adults who have taken stimulants for ADD] want, overwhelmingly, to feel normal, Fischer says — to be like other kids who can make it through a school day without being chided for daydreaming or sent to the nurse for a midday pill. Many, she says, are keen to try life without the medications to prove something: “to feel that your success, your accomplishments, your failures are truly your own and not the product of medication.”
In a nod to his ADD, Barclay says he accomplishes many of his grown-up tasks in pinball fashion, bouncing haphazardly from paying a bill to tending the home he owns to walking his dog. “I get things accomplished. It’s probably not as efficiently or as quickly as other people, but it happens in my own way,” he says.

The penultimate portion of the article is devoted to Dr. Lawrence Diller, the author of “The Last Normal Child,” in which he “raises concerns about the effect on society and children when parents, schools and the medical establishment reach too easily for such medication [for ADD].”

Diller calls it “unduly pessimistic” to believe that two-thirds of kids with ADD will continue to suffer symptoms negative enough to require medication as adults. By a young adult’s mid-20s or so, he believes that many who were diagnosed with ADD as children have developed strategies, as Devin Barclay has, to work around their weaknesses. And they are better equipped to answer the question — to medicate or not? — with a clear sense of their adult selves. Diller feels that those diagnosed with ADD — as well as their parents and counselors — should revisit “the bargain” that many made with Ritalin and other such drugs as children as they meander through their early adult years. In return for the often-reported side effects of the medication — sleep difficulties, appetite suppression, a “not quite me” feeling — children and their parents expected ADD medication to help them succeed in school at a time when sitting still and compliance with rules was highly valued. But in the adult world, young people with ADD have far wider choices, and they should make them with an awareness of their strengths and their weaknesses, Diller says — not what others expect of them. Using medication “to take octagonal kids and fit them into square holes” may be acceptable in grade school, he says. But “they will be patients for the rest of their lives,” he adds, if they pursue fields that require enormous attention to detail or intense concentration on matters that do not fire their interest.

The issues raised, whether ADHD medications should be taken indefinitely and, if not, how the decision to continue or discontinue the medication is determined, is both legitimate and important. A reporter’s responsibilities in presenting the story are less clear. In this case, a newspaper story that features reports of interesting individuals who seem to have made the right decision going off a medication, breezy summaries of research and ideas about the disease, and a clear air of approbation for independence-minded young adults who defy their parents and doctors by discontinuing their medications is, it would seem, more likely to influence those facing this decision than pages of grey print reporting findings of scientific studies.


Footnotes


  1. Also see Related Stories “in their own words” [back]



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