Each year $100 billion is spent on care for the 75 million persons in the U.S. with acute or chronic pain; yet, businesses still lose $60 billion annually from lost productivity due to ineffective and suboptimal pain care delivery, mainly for chronic pain conditions. AAPMedicine President, Rollin M. Gallagher, MD MPH, says the population-based approach in their new plan includes four steps designed to deliver timely access to levels of care that are needed to prevent chronic pain from beginning, or when pain persists, minimizing morbidity through effective care:
- Step One: Prevention of disease or injury with the use of evidence-based self-care, such as diet, exercise, ergonomics (alteration of work activities), or cessation of smoking and other drug abuse to reduce the risk of injury or disease.
- Step Two: If self-care is not working, the patient will then visit their primary care physicians for evaluation and management using evidence-based algorithms.
- Step Three: If disabling pain persists, the patient will be referred to a pain medicine specialist [called “algiatrist”] who will collaborate with a team of providers, including, nurse case managers, psychologists, and physical therapists.
- Step Four: If the patient remains in disabling pain [called “maldynia” at this point], he/she will be referred to a pain medicine specialist within a subspecialty of care.
Commentary: The Academy’s Position Paper offers an excellent review of the state of pain medicine today; so, it is recommended reading for everyone in the field [PDF available here]. However, the Paper also is somewhat disturbing and it is disheartening, to say the least, that when it comes to managing a condition so ubiquitous in our society as pain the healthcare delivery system appears to be in a state of such disarray and deficiency. As things stand today, the AAPMedicine’s four-step plan outlined above breaks down at Step Three; they acknowledge that, “Currently there are not enough pain medicine specialists to treat back pain and other pain conditions, and the system for training physicians in the discipline of pain medicine remains insufficient”; and, the number of pain specialists is actually declining. The Academy's solution calls for better residency training programs in pain medicine, which will lead to better and more cost-effective pain care. They further believe that recognizing pain medicine as a primary medical specialty also would increase federal funding for pain research and improve healthcare coverage for pain care by insurance companies (which often refuse to cover many pain-relieving treatments today).
However, according to conditions described in this Position Paper, it appears that it could take years, possibly decades, before pain care achieves an acceptable level of performance in America. Furthermore, it should be understood that the so-called “Healthcare Reform Program” still being debated in the U.S. Congress is actually an “access to healthcare insurance reform program.” The outcome may well be that more Americans will have insurance coverage to receive healthcare that, in the case of pain management, is still in limited supply and inadequate. If you have opinions, add a comment.
Reference: Dubois MY, Gallagher RM, Lippe PH, eds. Pain Medicine Position Paper. Pain Med. 2009;10(6):972-1000 [Click here to view the document PDF].








3 comments:
Read the paper, the Academy's laudable acknowledgements and efforts are useless if doctors are afraid to treat for fear of prosecution on drug trafficking charges.
Why should any doc risk his life and livelyhood to treat pain when the DEA decides what is acceptable medical care?
I find it disheartening and disturbing that this aspect of the 'pain crisis' goes without mention from the academics as well as the mainstream pain advocacy groups.
Americans in pain are dicscriminated against because of the nature of the medicines they need to live. Thank God for Siobhan Reynolds and her political activist work on behalf of Americans in pain and the docs who treat us.
I have to say a Big and resounding AMEN to Tami above.
Shortages of doctors or doctors that are willing to treat pain is not the problem I have found. I have a failed spinal fusion of L4,L5 S1 and a list of secondary problems caused by the pain that would take a half a page to write.
No problem finding a doctor to treat me but when it comes to seeing eye to eye about how the treatment will be done most of the time there is a big problem. The big money is for them to stick me full of needles like a voodoo doll but I've been that route for way to many years about 10 to be exact. The first few were well placed and did help for a while. Then came the 12 to 15 misplaced injections that started a land slide of additional problems. So I'm not saying a few, mind you I say few, well placed injections may help, if the first 3 don't my advice is to stop they are not going to help you they will do more damage than good and I tell you this from experience. But be advised these injections do not come cheap don't think well this will probably won't cost me over 100 bucks well closer to 300 to 400 each would be a better guess. Then if they are giving you medications along with the injections some will start dangling the script in front of your nose like a carrot to a mule and if you take the injections they'll give you your meds. This has happened to me on 3 ocassions I speak nothing but the truth here, so there is some policing of the pain industry that needs done but not by the DEA. What amazes me is Medicare and the Insurance companies are apparently clueless to this and they will approve the injection before they will approve a cheaper medication that does a better job controling the pain. The truly sad part is our insurance premiums and the whole Sha-Bang is being paid by us on both ends so you get a double shaft because of the premiums and the co-pays.
They will use every excuse in the world to start with but after suffering with this problem for 35 years I know my way around the hoops pretty well.
Untill we get government doing propper studies and pain research also in doing this reining in the DEA and putting them in ther propper place. The local police can catch the pill pushing doctor easier than the DEA by the lines outside their office door for peats sake. Then the FDA and the Pharma companies come up with some realistic guidelines for their wonder drugs and what I mean by that is rate them correctly.
How many of you pain patients out there have actually found that their 12 hour pain pill last anything close to 12 hours and God forbid a doctor want to give me a 24 hour pain pill I have never let a doctor prescribe me a 24 hour pain pill and the only way I can use the pain patch is if it is changed every 48 hours because is does not last 72 hours, call me crazy but during all these years this is what I have found.
Thank God for finally sending me to a young doctor eager to Learn, Listen and not be so quick to pass judgement my pain is better controled than it has been in 15 years. Praise God is all I can say because I was to the point that I was going to stop the pain for good. Please if there are any of you out there like that don't give up if the doctor doesn't show any sign of helping you and comes at you at every turn with a needle after 6 or 7 months and is still doing you no good find a new one because the one you got is not going to help you. Sorry if I stepped on some of you needle happy doctors toes out there but I went that route for over 10 years and I won't go in to ALL the problems it is causing as I age and I'm a whopping 50 years old. Good Luck and God Bless.
Your problems are worse than mine, but you have the 'game' described to a T. Jump thru the hoops that you know have to in order to get what you need. And the meds never last as long as they claim - especially if they're generic. I'm (now) 53 and feel as if the docs see me as a teenager scamming for drugs.
I've developed the usual tolerance to the doses that I was at 2 years ago. Every year, at my annual check in visit, I've said that the meds don't works as well as they first did but that I'll deal with it. Instead of trying to work with me & increase or change them, he nods his head & writes me the same scripts.
It took me a couple of years to finally get the strong meds I needed. My fear of being cut off for appearing pushy (or whatever) stops me from making strongly worded statements that 'It's not enough.' So, I live with more pain than I think I should so that I can (at least) get the modicum of relief that the current dose supplies.
We shouldn't have to play such games, but i know no other way to avoid being labeled some sort of problem & (potentially) losing the relief that I do get.
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