All patients will soon become e-patients

by Daphne Swancutt

I’m having a weird, visceral reaction to all of the recent brouhaha surrounding the term “e-patient.”

For some reason, semantically speaking, the term is slipping in to derogatorium. Up there with “cyberchondriac,” which definitely is derogatory. It’s kind of like research—one day, omigod, it’s Mecca; the next day, it’s the scab on a rotting wound.

Whatever.

I have a chronic condition—I’m not dying, it’s not fatal, I don’t have cancer. Not yet, anyway. But it is absolutely a condition that affects my quality of life. What I also have is the will and the tools to learn more because, unfortunately, my providers simply don’t have all the answers. And they sure don’t have the time to find them.

If I’m a “regular” patient, I simply nod my head, take the next prescription, get a pat on the back, make the next appointment and hope (and even pray) that it’ll work.

This time.

When it doesn’t, I think: This is my fate. Or worse, maybe I’m imagining it (hail to the SSRIs).

But, I’m not a regular patient. I’m pissed and I want answers. Getting those answers is where all those “e’s” come in. I’m proud of those e’s. Proud to have stepped beyond a place of relative ignorance over the years in to something that is…yup, you got it: Empowered. Educated. Enlightened. E-cubed. E-patient.

So, don’t call me a patient. And, don’t just group me in with the rest of the “people.”

I’m a frigging e-patient armed with information that not even my doctors have 90 percent (yes, 90 percent) of the time. Appalling, but true.

One day, we’ll get to a point when all patients are e-patients. Perhaps then, we go back to the future and begin anew with “patient,” which will implicitly suggest e-patient. But, we’re not there, yet. Not today. Not tomorrow. Likely not next year.

Although the Pew study referred to in linked post above tells us that 61 percent of American adults are looking for health information online, that still leaves nearly 40 percent out there who aren’t.

And, for those e-patients who are, they’re going to have to get even more savvy, discriminating and analytical as the volume of health information online continues to expand.

So, toss “e-patient” out to the netherworld? I don’t think so. And, by the way, don’t tell me what I’m supposed to call myself. I decide that.

For now, providers—and others—beware, and be prepared. This e-patient ain’t no regular patient.

Oh, and because I’m bound by my role to tie this back to healthcare marketing and communications, here’s a tip to all of the healthcare marketers and communicators out there: Get familiar with what e-patient means and advocate for the accurate, timely and comprehensive resources we crave. And then some.

Daphne Swancutt is Director, Healthcare Strategy at IMRE, and blogs at HealthIntel.

Submit a guest post and be heard.

email

  • http://33charts.com DrV

    My concern is that the the definition and concept of e-patient is being shaped within the social health bubble.

    Every patient should be empowered – that means thinking and acting as they wish not as they think they should act. Let’s ask people how they would like to be addressed.

  • Michael F. Mirochna, MD

    I can’t rationalize the juxtaposition of Ms. Swancutt scathing “them” (e-patient haters) for not liking e-patients, but then is derogatory right back. It suggests that she doesn’t want a symbiotic relationship with her primary care provider, rather just the scripts/tests/orders she wants written.

    I am in my last year of residency. I know there is a lot that I still don’t know. I read a ton, to the point where it interferes with my relationships, and I still don’t “know it all.” I used to be afraid of patients knowing more about their condition than I do. I came to the realization that its impossible to know everything and with the internet, information is widely available. It will be patients like Ms. Swancutt that will reinvigorate that fear and embarassment.

    Medicine is so diverse now, so many things we can do, so many things to offer. And all of this has to be done in less and less time.

    • HJ

      “I used to be afraid of patients knowing more about their condition than I do. … It will be patients like Ms. Swancutt that will reinvigorate that fear and embarassment.”

      I find the best doctors are the ones that admit they don’t know and are honest about it. The worst ones are those who hide behind their fear and embarrasement with a misdiagnosis. I had several doctors misdiagnose me with a condition that had been eliminated by another doctor. I would have preferred, “I don’t know.”

      “It suggests that she doesn’t want a symbiotic relationship with her primary care provider, rather just the scripts/tests/orders she wants written.”

      I became an e-patient because my PCP failed to provide the care I needed. Unable to find a replacement during a medical crisis, I navigated the health care system on my own. I don’t walk into my current PCP’s office with a list of demands as you suggest. I go to my PCP when my symptoms indicate that a presciption, test or examination is needed.

  • http://secondbasedispatch.com Jackie Fox

    Just my .02– I don’t think of myself as an e-patient. I used the internet for research when I was diagnosed with ductal carcinoma in situ, but I am not accessing online records or exchanging e-mails or anything like that. I mean, I e-mail and text my husband all the time–am I an e-wife? I still think of myself as a patient, even if I start using more communication vehicles. I know the other part of the “e” often refers to empowerment and I totally get that we should take more responsibility for our health and advocate for ourselves. I’m sure that’s even more important if you have a chronic condition. I’m just beginning to wonder why we’re all spending so much time on semantics.

    This was a great post, and I hope the discussion continues. Daphne, I can’t wait to see your thoughts on these issues going forward.

  • stargirl65

    I have no problem with patients being informed and participating in their health care. My concern is that many patients read information from unreliable sites or choose information that does not relate to their problem. (One patient came in with pages on hyperthyroidism and wanted to know why I wasn’t doing any of the testing mentioned. They had hyperPARAthyroidism which sounds similar but is entirely different.) They are then angry when I dismiss their information. OTOH there are patients that have brought me information that I have found very useful. I try to keep up on current treatments and ideas. I read online information daily from medical sites and I read journals weekly as well to keep up to date. Of course, this is all building on my previous base of information. I welcome patients bringing in information but only a small amount of it is new, correct, or relevant.

  • Empowered physician

    ” I’m pissed and I want answers.”
    “So, don’t call me a patient”
    “I’m a frigging e-patient armed with information that not even my doctors have 90 percent (yes, 90 percent) of the time. Appalling, but true.”

    “For now, providers—and others—beware”

    These statements are not conducive to the doctor patient relationship. It is not supposed to be a power struggle. Because I am also “empowered”, I would remove myself from this patients care.

    Taking care of patients who

  • 3rd year med student

    “I’m a frigging e-patient armed with information that not even my doctors have 90 percent (yes, 90 percent) of the time. Appalling, but true.”

    Maybe I misinterpret this post, but it strikes me as pretty aggressive. The above quote struck me as representative of this impossibility that patients like Ms. Swancutt expect/demand. An impossibility because the science is too overwhelming for a single person to accumulate. Sure a patient can get through the recent literature and have a good understanding of it. That’s taking an active role in your care, and it’s commendable. But for an internist to keep up with all the literature for all the diseases they routinely treat would literally take more hours than there are in a day. Not to mention actually putting it in practice and see patients.

    That’s the whole problem with the “health care is a right” mentality, and it’s made worse by attitudes like that in this article. Sure it’s a right; you have the right to take care of your own health. But to demand that people to serve you, at a price set by disinterested parties, expect it to be done quickly and cheaply, and be fully informed of all the latest studies or else have comments like “beware, and be prepared”. Geez, who would want to do that if they were a good student and had better options available?

    So you have students like me, who are good students and love the idea of brilliant internists, pediatricians, and family practitioners who can get to know people when they are healthy so that they can better help them when they are sick. We love the idea of cutting health care spending by doing more ourselves and not referring to expensive specialists. But attitudes sway me. This person’s attitude sways me.

    Maybe if I were a specialist, I could carve out my own little niche, and wouldn’t have to deal with people who are “appalled” that my ability to help most people reduces my ability to help her specific problems; that 7 years of training wont make me as expert in your particular circumstances as you. But that attitude would just contribute to less trained people having to do more.

    What we have is a problem of unrealistic expectations. Open hostility from “e-patients” will not inspire physicians to help them. But maybe by working together, and by remembering that there are 30 other equally important people that need to be seen that day, we can do our best.

    • HJ

      ” But for an internist to keep up with all the literature for all the diseases they routinely treat would literally take more hours than there are in a day. Not to mention actually putting it in practice and see patients.”

      So what’s the value of seeing a doctor that doesn’t have the background or knowledge to deal with a problem. Do I get my money back if you don’t know how to treat my condition?

      • DB

        Yes. you get your money back. If that is what it takes to remove a militant patient from my panel, then yes. Best $60 I ever spent. Enough with the doctor hating.

        • HJ

          So you are happy that I act like a consumer?

    • another med student

      Great comment, although just because persons believe that health care is a right, does not make them into a terrible patient you describe.

      Look into the direct-pay practice or ideal medical practice model. Persons like Gordon Moore and Brian Forrest have implemented such practices with success. Also, I think these models address many of the concerns you have.

      Best of luck

  • http://www.pacificpsych.com/ pacificpsych

    I’m not a provider, thankfully, but she said “others” [beware], so I’m kinda scared…in case ‘others’ refers to M.D.s, and is not a clever reference to ‘Lost’.

    Sounds threatening. I don’t do threatening. I certainly won’t be calling you ‘patient’! Or anyone else, for that matter, who thinks threatening and talkin’ trash to doctors is OK. Not in outpatient, ever, and rarely in inpatient. You are MORE than welcome to seek help elsewhere. Nobody’s stopping you. —–> Door.

  • http://www.twitter.com/daphneleigh Daphne Swancutt

    Thanks for everyone’s comments here. We all have our own story; this is mine, this is where I stand, these are my thoughts, opinions, and personal insights. But, I’m not alone.

    Does it come across aggressive? Yes, because part of the concept of being an “e-patient” is assertive and persistent personal advocacy. No one has more at stake in me than me. The collaborative physicians out there get this and work with it.

    Do I want healthcare that is performed quickly and cheaply at the risk of quality and comprehensive care? No, and am quite sure I did not suggest this at all in my post.

    For those physicians who would “remove themselves from my care,” I would likely beat you to the punch. I absolutely recognize that I can seek help elsewhere, and have done so for myself and for my family.

    For the record, I have an awesome primary care doctor who is neither threatened by me nor thinking of showing me the door. She is neither fearful nor embarrassed, and I don’t walk in to her office ever with a “list of demands.” Specialists are another story.

    Truly, at the heart of my post is a disagreement that the term “e-patient,” and what it means to me and others per above, is somehow becoming obsolete. Plenty of patients out there are just beginning to empower themselves, and I do believe physicians need to respect and be prepared for this.

    Thanks, again-
    Daphne

  • 3rd year med student

    There’s background, and then there’s literature. They are not interchangeable and should not be mistaken. Internists have background. It’s what you pick up in 7 grueling years of training and tens of thousands of hours of clinical experience. Literature is composed of studies. It’s what is picked up on the internet and in journals. They are nice, and improve care, but 99% of the time an individual study is unnecessary, and most physicians read the 1% of “high impact studies” that are. That the author finds some information somewhere that her physicians are unaware of is hardly appalling. They were most likely too busy seeing patients to keep up with every

    “Do I get my money back if you don’t know how to treat my condition?”
    Do you get your money back from a mechanic if he can’t fix your car? No, because it takes a tremendous amount of time and energy until you can finally say that you don’t know how to treat something. Your health is not a gimme; for those that think it is, please see my comment on impossible and unrealistic expectations. We do the best we can, and aggressive attitudes towards those of us who exhaust ourselves trying to help is not beneficial to anyone.

    • HJ

      “Do you get your money back from a mechanic if he can’t fix your car? ”

      Yeah. I have never gotten charged for something when someone promises a result and then fails to deliver…except medicine.

      “Your health is not a gimme;”

      Being agree at someone because they are empowered and educated about their health was the reason for my comment. If I can find it on the internet, so can my doctor. But attitudes sway me. Your attitude sways me.

  • DrA

    Like I said in a recent previous post, The sacred doctor patient relationship appears dead in this country. KevinMD has morphed into blog where once high quality discourse on medical current events and thought provoking discussions took place. Now it’s patients yelling at the medical care providers.

  • IndiepsychNP

    The process of reviewing history, doing an assessment including interview, labs, scans as needed is called ruling out diagnoses by way of what is in the universe of possible diagnoses, also called differential diagnosis. If your internist has slogged through the sometimes long list of possible diagnoses and has not found a diagnosis that fits 1) you have gotten more than your share of his or her time and you should count yourself lucky and 2) you would be unwise not to pursue the referral you are given. HJ, you referred to antidepressants as “junk” in your comments on the STAR*D psychiatric study. If you are unhappy with allopathic medicine, there is always naturopathy for you. It might give you grounds for comparison.

    • HJ

      “HJ, you referred to antidepressants as ‘junk’”

      That was pacificpsych that used the word “junk.” I questioned the quality of research of antidepressants and their prevalance with such shaky evidence.

  • http://theYogadr.com Kathleen

    I applaud patients who take an active interest in their care and who choose to be proactive about finding and implementing new information in our world of medical information overload. Doesn’t matter what you call them. “E-patients” is fine. Personal responsibility is an attribute. A doctor-patient relationship is about team-work. It’s a partnership of care and concern, support and trust and advice. Physicians have the back-ground big picture and training to put new ideas and new studies into perspective, and they have the wisdom that comes from experience of treating many different patients with the same concerns and also very different concerns that may provide reflection. Patients have the time and drive to do exhaustive information searches and then to bring the results to their trusted adviser and partner for discussion. They also are the ones who must implement treatment, and must be fully on board with a treatment plan for it to be effective. Medicine not an adversarial power struggle or a “cookbook” project. It’s a complicated field with many unknowns in which we must all work to together to get the best results. Let’s drop the ego-centered fear and get on with the love.

  • http://secondbasedispatch.com Jackie Fox

    I have to do something here I’ve never done before, and hope never to do again. I want to take back a comment I made here. Not take it back exactly, but I have to confess to being guilty of pandering. When I first read Daphne’s original blog posting, my response on her blog was more true to who I am. I had tackled a similar issue on kevinmd, comparing patients to consumers, in which I came down pretty squarely on the side of doctors. I mentioned in my reply to her then that the word “patient” seems to have become synonymous with subservient.

    After that original post, Daphne posted a nice reply to my comment and started following me on Twitter. And I think it went to my head. So you may have seen my earlier comment here saying “Great post! Can’t wait to hear what else you have to say!” Because I’ve gotten some positive attention from Daphne, I wanted to be positive in return, but I fear it made me sound more “Power to the people!” than I really am. It’s still true that I want to hear what else Daphne has to say about these issues. But if I had it to do over again, I would have said, “Thought provoking post” instead of “great” because “great” implies I agree with everything, and I don’t. I really do believe too many of us are beginning to view doctors as the hired help. I also believe that is wrong and erodes trust, as I said in my patient/consumer kevinmd post.

    I see a lot of anger on both sides, and that bothers me. Daphne is catching some flak from doctors, and I caught a pretty massive amount of flak from patients on my consumer post. And I can handle that. But I can’t handle myself being so two-faced. My apologies.

  • http://www.twitter.com/daphneleigh Daphne Swancutt

    Jackie: I love your clarification and completely respect where you stand; no need to apologize to me.

    Regarding any flak here, I’m tough and can take it ;-)

    Best-
    Daphne

  • IndiepsychNP

    I would like to mention 2 specific thankfully small subsets of patients who present for care having done so much research that they are terrified of all pharmaceuticals. With the caveat that I practice independent outpatient psychiatry and do not give out brand new medications and instead wait for the post marketing to settle out, these two groups of patients are maddening to treat (but you do have to let people choose…).
    The first group are those who smoke marijuana multiple times per day and are philosophically against pharmaceutical drugs of any kind. Upon inquiry, they disclose that their marijuana is not organic and they do not know who or how it is grown. They are not disturbed by the proven effects it has been shown to have on the body as they consider this to be government propaganda. That the marijuana could be feeding the crippling anxiety for which they seek treatment pales in comparison to what they have read about the FDA conspiracies to collude with Big Pharma to cover up problems with drug trials. These patients are not paranoid schizophrenics.
    The other group is between 50 and 65 and is deeply suspicious of all Western medicine because of all that web research and because “I know my body better than a doctor does”. I should hope so. However, they think nothing of paying $300 out of pocket for Chinese herbs and acupuncture treatments though they can not begin to explain how these treatments work or how to gauge if they work. This is the Seattle e-patient Boomer-style. Gotta love it.

  • Alina

    Daphne, I loved your post! There are some good doctors, but sometimes trying to find them is like treasure hunting.

    For all you guys who were insulted by the article you should know that usually businesses embrace feedback from their customers (and not just the positive kind). They use this information to make changes to their products and or services and ultimately improve their business. There are companies that pay quite a pretty penny for this type of information, where you get it for free.

  • http://www.twitter.com/daphneleigh Daphne Swancutt

    Alina: You make a most excellent point. Listening before reacting — it’s a good skill, difficult to master.

    Back up to Kathleen, I second your wise call to action, particularly where dropping ego-centered fear is concerned. Also, a difficult skill to master.

    The good ones out there do it, though, and everyone is in a better place for it.

    Daphne

  • http://bizsavvytherapist.com Susan Giurleo

    The comments here are more interesting than the article itself (with all due respect, Daphne).

    The truth is the concept of the doctor-patient relationship is shifting. In the past docs were the “experts.” Patients had to just believe what they said and do as told.

    Now times are different and some docs understand this and accept it, some understand and resent it and others just don’t get it.

    Every one has a right to be empowered. Everyone has a right to their feelings. And everyone has the right to find a doctor-patient relationship that is comfortable for them. (and I mean doctors and patients) Being angry at Daphne for being angry is doesn’t change that the world of health care is changing all around us. If you don’t want someone like her as your patient, I’m sure there are others out there who are a better fit.

    • Empowered physician

      Well said, Susan. And just to be clear, my removing myself from a patient’s care is not about anger or feeling threatened. It is done when I realize I cannot help that patient. Empowerment or e-patient, whatever you want to call it, is a good thing. This article, however, has a hostile tone. It’s not a scary thing, it’s just unpleasant to deal with, and a physician has a right to not have to work in a hostile environment. Ask yourself about your own job, and if you had someone coming in pissed off at you and not trusting you before they ever met you and demanding you help them the way they insist on being helped. It’s emotionally taxing. It’s far more constructive to start out with a little trust.

      For Alina, regarding feedback. Yes feedback is good and appreciated. But feedback delivered in scathing comments tends to put people on the defensive. Walking into your doctor’s office and telling them in a mean spirited way how aweful doctors are is not conducive to you getting what you want from your doctor, if what you want is care and help.

      And HJ, I think it is clear how you feel. I got nothing for you.

      Every doctor has patients that are leery of medicine. Most of the time, that guard is let down when they see that you really care. That is actually a very rewarding part of my job. I hope that I have conveyed that yes, we care and we want to help, but it’s easier for us to help when we are not getting chewed out.

      • Alina

        “Walking into your doctor’s office and telling them in a mean spirited way how awful doctors are is not conducive to you getting what you want from your doctor, if what you want is care and help.” What patients would do this and for what reason?

        Let’s face it, physicians that comment on this blog can’t take any constructive criticism. You guys complain about the slightest comments, complain about patients, about each other – one specialty against another, complain about fees, and so on…There always seem to be an excuse and a blame placed on anyone else except on self. If people are not even open to acknowledge the problem, how can we ever fix it?

        As Susan put it, either you like it or not things are changing. I mentioned before there are some great doctors out there, but there are also others that are simply not.

        It’s extremely frustrating to have to take time off work so you can have the pleasure of waiting in your doctor’s office for 40+ minutes only to have a 10 minutes appointment and get nothing out of it. I posted a comment a couple of weeks ago or so for another article about a visit to a specialist (first time visit). The wait time was exactly over 40 minutes – and no, it wasn’t because the doctor had some emergency appointment that ran over. No, it was simply because he booked 5 patients during the same time. I find that appalling! Then he said that we need it a plan to keep the disease under control, after which he left the office. Came back…no plan. We asked how long the patient had to continue with the medication and told the doctor there were 3 more refills. Doctor said that it’s not necessary to continue once the refills expire. Asked about the disease because the patient doesn’t have the typical risk factors. Nothing. And mind you this is not some orphan disease. Quite contrary. Anyhow, we stopped by the check out desk at which point the doctor comes by with the Rx for the same medication that we just discussed it wasn’t need it. So you want to tell me that this was somehow our fault?

        Unfortunately this is what many patients experience during an office visit. You know many of you guys underestimate the patients because they have not gone to school for the extra years. First of all, you are making an assumption before even knowing anything about that patient. Even though we may not have that medical education we can still spot the physicians who are competent. We pay a lot of money for this “care” and we want some value in return. Is this too much to ask for?

      • HJ

        “And HJ, I think it is clear how you feel.”

        I was told that if I act like a consumer, all our problems would go away. You have no idea how I feel.

  • http://theYogadr.com Kathleen

    “Let’s face it, physicians that comment on this blog can’t take any constructive criticism.”

    Maybe you missed my recent comment.

    Doctors are people. We have good days and bad days, and with the state of the health care environment today, many have more bad days than good. The system is broken. Let’s work together to fix it. Let’s be partners, not finger-pointing adversaries.

  • IndiepsychNP

    Ms. Swancutt has continually been referred to by others posting responses as an “epatient”. Certaintly, she is someone’s patient. However, I think we have generally lost sight of the fact that she works for IMRE, a healthcare consulting corporation in their marketting division which focuses on telling hospitals and major facilities and groups what patients want in their consumer healthcare experience. What I think is objectionable about Ms. Swancutt’s post is that instead of posting as a marketing expert informing with statistics from marketing studies on what patients want or presenting more information on who researches which subjects on the internet, she instead presents herself as an angry wronged patient with only the internet available for information because medical providers won’t spend enough time educating her.  As a “vendor” or “non-MD” guest post it was truly unusual post, unlike anything else I have seen on KevinMD.com.
    Being in the medical support industry, she knows why her physician cannot spend a tremendous amount of time explaing her condition to her: E&M codes are generally not being covered by insurance anymore. But instead, she initially used
    vitriol and then flattery latter in the response
    section. I think this was a great way to market
    herself. My web designer told me that posting on the blogs of your target market is actually a
    marketing technique. I am used to academic, professional, and sometimes scrappy political
    discourse, not marketing ploys which anger a lot of exhausted hard working, stressed out medical providers.

    • Alina

      You’re implying that Daphne is trying to create a need for her services, which shows that you lack awareness of how patients feel. nowadays You’re welcome to do your own study and I bet your findings will be very similar to this article.

      “….because medical providers won’t spend enough time educating her.” This is pretty much the trend nowadays in a good majority of cases, so it’s not just “her.” Let me ask you something, shouldn’t educating the patient be part of the whole office visit? If not, what exactly is the physician’s job? Surely it can’t just be coming in that room for 5 minutes: “hi, bye and next.”

  • http://www.twitter.com/daphneleigh Daphne Swancutt

    IndiepsychNP: I’m proud of my professional role, as I’m sure you’re proud of yours. While there are certainly healthcare marketers out there whose motives are questionable, we are not all in the category of the unwashed and unwanted (just as not all physicians are paternalistic and condescending). I’ve been quite transparent, and the fact that I’m a marketer does not make me any less an “e-patient” or a human being, nor does it prohibit me from having an opinion (just as being a medical professional does not prohibit you from expressing your disagreement).

    We obviously need more people speaking out for patients, and if that’s considered a “ploy,” then so be it.

    Thanks for your comment and your perspective-
    Daphne

  • IndiepsychNP

    What drives this lack of time? Innattentive, uncaring medical providers or the profit drive insurance companies reimbursement structures which will not pay enough for staff, living expenses and student loans. Insurance companies no longer pay for time spent to talk to patients,the E&M codes I referred to before. It is the patient’s insurance they are usingto pay for the visit so, ultimately, they are simply not paying for enough time with their provider. That is the grim reality of the economics of the patient/ medical provider relationship. We are not parentsal figures who will or can spend time with patients without getting reimbursed unless it is an emergent situation. We have families and lives and have to pay our bills.

    • HJ

      “It is the patient’s insurance they are usingto pay for the visit so, ultimately, they are simply not paying for enough time with their provider. That is the grim reality of the economics of the patient/ medical provider relationship.”

      So we become e-patients. Why are you so offended by that? Would you prefer that I not get the care I need? Why do you blame patients for their insurance situation? Are you offended because e-patients question your prescibing habits?

    • Alina

      Interesting that you somehow blame the patients because “their” insurance doesn’t cover whatever fee you have in mind. I can only guess what that fee is as you have not given us any numbers. Why do you take these insurance plans if you find that it interferes with your ability of doing your job? And you still have not told us what is the responsibility of a practitioner, in your opinion.

      About the student loans…Yes, I think that school in the US is outrageously expensive and that’s wrong. But again how is this the patient’s fault? Why don’t you get the schools to lower their fees? We’re already subsidizing the residency program. Or one could go to Texas for medical school and pay only a fraction of the East/West coast fees.

      Also, for many physicians the fees are not as dismal as you’re trying to imply here. Insurance companies have been sending EOBs to patients for many years and we can see how much they pay for the services.

  • IndiepsychNP

    I am a psychiatric nurse practitioner trying to shed some perspective for those who are disgruntled with primary care doctors and also explain some of the financial pressures on younger practitioners of all types which have lead to this current situation. Let’s use my situation as a teaching moment to examine the reality of insurance fees, students single handedly changing fees at teaching institutions or picking less expensive schools.
    First, nurse practitioners do not receive any Medicare funding for their training. There is an estimated shortage of 45,000 psychiatrists at present. Primary care complains about reimbursement, but they should check out psychiatry. Likely due to the downward pressure on reimbursement over the last 30 years, the bulk of psychiatrists are baby boomers whose mean and median ages are 60 and 62 according to AMA survey data. I have completely independent practice in my state and am paid $5-15 less per time based billing code than psychiatrists. We can not, nor would I, short shrift patients on the amount of time I spend with them. We can not bill based on the severity of the illness or on any of the coordination of care or how elaborate the history taking is or how much time we actually spend. However, due to Congress’ lowering of the payment formula by Medicare once in the 80′s and once disastrously in 1996 reimbursement for psychiatry is far below that of any other medical specialty.

    The result is that long before the current threatened cuts to Medicare rates by 21%, it is nearly impossible to find a Medicare provider unless the patient is disabled due to chronically mental illness and gets care AND has as state Medicaid coupon as well as Medicare. This leaves the elderly, even with Medigap, in most place without access to psychiatry particularly if they are in a rehabilitation facility. Medicare patients are the most time consuming and require the most coordination with other medical providers and with their family. This is what happens if providers only take insurance they are comfortable with. It took me 4 years in private practice to finally swallow my ethics and drop Medicare. If the government doesn’t value what I do, I can’t fight them on it.
    For that matter, I could not fight the ivy league university I trained at over their fees. Located in New York City, it is closely affiliated with one of the preeminent psychoanalytic institutes where I trained. I’ve lived in Texas as a child (where nurse practitioners can’t prescribe independently). I wouldn’t go back on a bet. But more to the point, not everyone can go to state institutions for medical or nursing or PA school. It is a straw man argument when it comes to the problem of student loans. There are a lot of complicated reasons why the price of all higher education has skyrocketed in the last 30 years just as wages in the US has stagnated. I am not going to into it here with you.
    As for providers’ fees, I wonder if you understand all of the incredibly obfuscated columns on the EOBs you are reading. Providers can charge whatever we want, but we are paid whatever the contracted rate is. This rate which in my state at least can be changed without notice by the insurance company. So I could tell you what I charge for a certain code, but it would be meaningless, because each any every plan under each and every insurance company pays me a different amount. The difference between the two is called a “contractual write off”. I give a discount to those who pay in full on the day of service because they are uninsured or have security clearances such that they do not want to use mental health benefits. As I cannot afford office staff (and even if I could) I will always give a break to the uninsured and would do anything to avoid billing.

    And, yes, since we are all patients and voters in a what you feel is an influence-able democracy, contacting your representative about how much the training of health care providers costs is your responsibility because we all pay for it in the end.

    As for what my responsibility as a health care provider is regarding your health care insurance? Absolutely none. However, last year I had many long term patients losing their jobs at the rate of one to two per week for weeks on end and therefore losing health insurance. I continued to see most of those patients for the cost of their co-pays while my stay-at-home husband and 2 children scrimped by on all of our savings. I signed them up for programs with drug companies for free medications. However, when they found employment again just enough of those same patients were unwilling to inconvenience themselves if the commute were longer to my office or they had to pay $25 more per visit because I was out of network with their new insurance, etc. that I re-examined what my responsibility to my patients is versus my responsibility to myself. I don’t at all regret giving away the care. But it made me think that since I am the one doing the caring regardless of whether I get paid I should try to get paid more fairly more of the time by companies and patients. Especially when most psychiatrists in this city do not take insurance at all.

    But, yes, your insurance is yours and you have to get your employer to get you better coverage if you do not have good coverage. That should be easier than influencing tuition rates at a university. But as I said, insurance companies have followed Medicare’s lead and will no longer pay medical providers to provide E&M which means “education and management” which means explaining things to patients. Physicians can’t afford to hire RNs who understand disease processes to do this for them. That is why you are getting such brief visits. I am not reducing medical providers to technicians, but this metaphor for the payment structure might help you understand the situation. Imagine you are paying for a tune up on a Japanese car. There is an hourly fee for labor. You ask to have the whys and wherefores of the tune up explained to you. If you want to pay for the time to have it explained, it will cost you. The greed of insurance companies set up this absurd situation.

    Being a medical provider is not like being a monk, priest, or nun. Our savings accounts run dry at some point.

    • HJ

      If you wish to give away your services, how is that my fault?

      My insurance pays my providers well. I still get the driveby treatment.

      So which type of health care system do you want me to vote for? The one that raises taxes? The one the burdens business with premiums?

    • Alina

      “There are a lot of complicated reasons why the price of all higher education has skyrocketed in the last 30 years just as wages in the US has stagnated.” No other country on earth has this type of fees for education and it’s wrong. It just happends that some of us have a lot more knowledge than probably you do on this matter and let me tell you there is absolutely NO reason to have such fees.

      “…I wonder if you understand all of the incredibly obfuscated columns on the EOBs you are reading. Providers can charge whatever we want, but we are paid whatever the contracted rate is.” There is nothing complicated in the EOBs. When you have a column with charge submitted by the doctor (rack rate), negotiated price (contracted price), copay (paid by patient) which comes out of the contracted price, then remainder paid by the insurance company. You’re making a lot of assumptions about people you don’t know at all.

  • http://www.consentcare.com Martin Young

    My suggestion is that the best antidote for the unpleasant aspects of the ePatient-doctor relationship is for the doctor to become an eDoctor as well, using the same resources as the ePatient.

    The sooner that arrives the better we will all be, with a truly equal and empowered relationship from both sides.

  • http://www.twitter.com/daphneleigh Daphne Swancutt

    Nice point, Martin. Thanks for chiming in here.

    Daphne

  • IndiepsychNP

    I use lots of e-tools: full electronic electronic health record, hand held online device with multiple medication and diagnostic referenced and my billing software streams electronically from my health records. I am as e-savvy as they come. I know exactly how to use my time effectively on behalf of my patients and myself. But as all of
    these posts from patients demonstrate, patients want to feel cared for as singular human beings, as people. Perhaps that is why 5 minute visits make them mad.
    I suggest the only thing standing in the way of patient empowerment and provider empowerment are those getting rich off of medicine: health insurance companies. This doesn’t mean government control is the solution, but since health insurance companies lead to neither better outcomes OR decreased costs we have to ask: what are they doing for us? Making patients and medical providers really unhappy with substandard very expensive healthcare……

Trending