The prescription opioid epidemic in a nutshell

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http://www.sun-sentinel.com/local/p...stifies-painkillers-trial-20151109-story.html

She also said Schultz treatment method wasn't generally accepted and the majority of doctors agreed that higher dosages were not appropriate for pain treatment.

"You have to admit that there are other doctors, very prestigious doctors, who disagree with that opinion," she said.

Prosecutors said earlier in the trial that Schultz also ran an in-house pharmacy — something prosecutors said Schultz was doing for profit.

Schultz, however, told jurors he started his in-house pharmacy after a prescription pill shortage at larger pharmacies nationwide, and because his patients were embarrassed about receiving pain medication.

Schultz was arrested after one of his former patients tried to fill a 30-day supply of oxycodone totaling 1,590 pills with a dosage of 30 milligrams at a Lake Worth pharmacy.

Ken Jerkins, a retired pharmacist who ran the Tru-Valu Drug store, testified earlier in the trial that the prescription raised alarms for him.

"I've never seen a prescription for that large a quantity of any drug," Jerkins said.

He told jurors that typically 1,590 pills would last a patient nine months, not 30 days.
 
Quiet desperation in graphical format.
 

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Intensity of Chronic Pain — The Wrong Metric?
Jane C. Ballantyne, M.D., and Mark D. Sullivan, M.D., Ph.D.

N Engl J Med 2015; 373:2098-2099November 26, 2015DOI: 10.1056/NEJMp1507136

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Pain causes widespread suffering, disability, social displacement, and expense. Whether the issue is viewed from a moral, political, or public health perspective, pain that can be relieved should be relieved. Yet the most rapidly effective drugs for relieving pain — opioids — are caught up in a morass of concerns about addiction. Achieving a balance between the benefits and potential harms of opioids has become a matter of national importance.

The United States recently established a national plan to address pain, as Canada, Australia, Portugal, and Malaysia have previously done.1 This National Pain Strategy grew out of recognition by the Institute of Medicine (now the National Academy of Medicine) of the enormous burden of chronic pain in the United States. For three decades, there has been hope that more liberal use of opioids would help reduce the number of Americans with unrelieved chronic pain. Instead, it produced what has been termed an epidemic of prescription-opioid abuse, overdoses, and deaths — and no demonstrable reduction in the burden of chronic pain.2

Although the chronic-pain crisis can be attributed in part to the aging of the population, improved survival from disease and trauma, changes in disability policy, and multiple factors such as obesity that contribute to chronic ill health, the suggestion that chronic pain can and should be eliminated by opioids hasn't helped. The National Pain Strategy concludes that current reimbursement policies, provider attitudes and training, and “myths, misunderstandings, stereotypes, and stigma” in the health care system have denied Americans the benefit of evidence-based multimodal approaches to managing chronic pain, in favor of costly interventions that don't produce long-term benefit. Opioids are a case in point: they have good short-term efficacy, but there is little evidence supporting their long-term benefit. The National Pain Strategy emphasizes the importance of self-management and interdisciplinary treatments and recognizes that drug treatment alone has limited utility when it comes to managing chronic pain.

During the late 1980s and early 1990s, it was argued, largely on moral grounds, that opioids should be available for treating chronic pain, and physicians were persuaded that addiction to opioid treatment would be rare. Both the idea that chronic pain could be effectively and safely managed with opioids and the principles of opioid pain management were based on the successful use of these drugs to treat acute and end-of-life pain. That success was based on the “titrate to effect” principle: the correct dose of an opioid was whatever dose provided pain relief, as measured by a pain-intensity scale. The dissemination of the World Health Organization's stepladder approach to managing cancer pain was the beginning of widespread adoption of reduction of pain intensity as the goal of drug treatment. When the Joint Commission for the Accreditation of Healthcare Organizations (now the Joint Commission) introduced a mandate that pain be recognized and treated, numerical ratings of pain intensity were chosen as the chief metric. The promotion of pain as the “fifth vital sign” was a response to that mandate.

But is a reduction in pain intensity the right goal for the treatment of chronic pain? We have watched as opioids have been used with increasing frequency and in escalating doses in an attempt to drive down pain scores — all the while increasing rates of toxic drug effects, exposing vulnerable populations to risk, and failing to relieve the burden of chronic pain at the population level. For many patients, especially those who have become dependent on opioids, maintaining low pain scores requires continuous or escalating doses of opioids at the expense of worsening function and quality of life. And for many other people, especially adolescents and young adults, increased access to opioids has led to abuse, addiction, and death.

Pain-intensity ratings aren't necessarily a reflection of tissue damage or sensation intensity in patients with chronic pain. The intensity of chronic pain can't be reliably predicted from the extent or severity of tissue damage, since chronic pain is not determined primarily by nociception. Functional neuroimaging studies and other prospective clinical studies have shown that what feels like the same pain is initially associated with the classic sensory “pain matrix” brain regions but is later associated with brain regions involved in emotion and reward. Thus, over time, pain intensity becomes linked less with nociception and more with emotional and psychosocial factors.3

Suffering may be related as much to the meaning of pain as to its intensity. Short-lived pain may be excruciating, but it is better tolerated and causes less suffering because it's finite and may be necessary to attain a valuable goal, such as childbirth, healing, or athletic achievement. Persistent helplessness and hopelessness may be the root causes of suffering for patients with chronic pain yet be reflected in a report of high pain intensity. Strong support for such a relationship between the meaning of pain and the degree of suffering can be found in the relief that occurs because anxiety is reduced when the source of pain is understood, pain is no longer a threat, or effective treatment is known to be at hand.4

Many of the interdisciplinary and multimodal treatments recommended in the National Pain Strategy use coping and acceptance strategies that primarily reduce the suffering associated with pain and only secondarily reduce pain intensity. Willingness to accept pain, and engagement in valued life activities despite pain, may reduce suffering and disability without necessarily reducing pain intensity. Patients who report the greatest intensity of chronic pain are often overwhelmed, are burdened by coexisting substance use or other mental health conditions, and need the type of comprehensive psychosocial support offered by multimodal treatment approaches. Reliance on pain-intensity ratings tends to result in the use of opioid treatment for patients with mental health or substance abuse problems who are least likely to benefit from opioid treatment and most likely to be harmed by it — a phenomenon we have termed “adverse selection.”5 These patients are more likely than others to be treated long-term with opioids and sedatives, to misuse their medications, and to experience adverse drug effects leading to emergency department visits, hospitalizations, and death.

The National Pain Strategy outlines a number of initiatives to help achieve the “cultural transformation” needed to ease the burden of chronic pain in the United States. Many of these initiatives recognize that chronic pain differs from short-lived pain in its causes, psychopathology, and social meaning. Borrowing treatment principles from acute and end-of-life pain care, particularly a focus on pain-intensity scores, has had unfortunate and harmful consequences. The titrate-to-effect principle fails when pain is chronic, because our best chronic-pain treatments don't produce an immediate or substantial change in pain intensity. Multimodal therapy encompasses behavioral, physical, and integrated medical approaches. It is not titrated to pain intensity but has a primary goal of reducing pain-related distress, disability, and suffering. When it does that successfully, a reduction in pain intensity might follow — or acceptance might make the intensity of pain less important to a person's functioning and quality of life.

We propose that pain intensity is not the best measure of the success of chronic-pain treatment.When pain is chronic, its intensity isn't a simple measure of something that can be easily fixed. Multiple measures of the complex causes and consequences of pain are needed to elucidate a person's pain and inform multimodal treatment. But no quantitative summary of these measures will adequately capture the burden or the meaning of chronic pain for a particular patient. For this purpose, nothing is more revealing or therapeutic than a conversation between a patient and a clinician, which allows the patient to be heard and the clinician to appreciate the patient's experiences and offer empathy, encouragement, mentorship, and hope.


Dr. Ballantyne reports receiving grants from Pfizer and being president of Physicians for Responsible Opioid Prescribing. Dr. Sullivan reports receiving grants from opioid REMS program companies and personal fees from Janssen and Relievant.
 
It's a real shame we don't have a specialty organization (cough AAPMed) that can outline some decent guidelines.
 
Odds ratio of an ODD by Opioid Dose.
 

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Central sensitization explained...

http://www.hngn.com/articles/162475...covered-that-is-remodeled-by-chronic-pain.htm
"The study shows you can think of chronic pain as the brain getting addicted to pain," said A. Vania Apkarian, co-author of the study. "The brain circuit that has to do with addiction has gotten involved in the pain process itself."

http://www.nature.com/neuro/journal/vaop/ncurrent/full/nn.4199.html
The indirect pathway of the nucleus accumbens shell amplifies neuropathic pain
 
Central sensitization explained...

http://www.hngn.com/articles/162475...covered-that-is-remodeled-by-chronic-pain.htm
"The study shows you can think of chronic pain as the brain getting addicted to pain," said A. Vania Apkarian, co-author of the study. "The brain circuit that has to do with addiction has gotten involved in the pain process itself."

http://www.nature.com/neuro/journal/vaop/ncurrent/full/nn.4199.html
The indirect pathway of the nucleus accumbens shell amplifies neuropathic pain

Doubt that the policymakers will buy it. Sounds like something expensive to treat. Easier to understand and adjudicate chronic pain as a character deficit.
 
Lee Fang
Dec. 23 2015, 7:08 a.m.


The pharmaceutical companies that manufacture and market OxyContin, Vicodin, and other highly addictive opioid painkillers — drugs that have fueled the epidemic of overdoses and heroin addiction — are funding nonprofit groups fighting furiously against efforts to reform how these drugs are prescribed.

While the Centers for Disease Control and Prevention was close to finalizing voluntary prescribing guidelines for opioid painkillers next month, it abruptly changed course. According to a report from theAssociated Press, the CDC was forced to “abandoned its January target date, instead opening the guidelines to public” comment after a number of “industry-funded groups like the U.S. Pain Foundation and the American Academy of Pain Management warn[ed] that the CDC guidelines could block patient access to medications.”

The new guidelines would encourage doctors to prescribe opioids as a last choice for chronic pain, a sharp departure from the status quo, in which many doctors, under pressure from pharmaceutical sales representatives, often prescribe painkillers for mild back pain or a toothache. As expertsnote, many painkiller and heroin addicts start abusing opioids after receiving a legitimate prescription for pain-related medical issues.

An investigation by The Intercept has found that the pharmaceutical companies that dominate the $9 billion a year opioid painkiller market have funded organizations attacking reform of the prescribing guidelines:

  • The Washington Legal Foundation, a nonprofit that litigates to defend “free-market principles,” threatened the CDC with legal action if the agency moved forward with the proposed opioid guidelines. The WLG claimed the CDC’s advisory panel for the guidelines lacked “fair ideological balance,” because it included a doctor who is part of an advocacy effort against opioid addiction. The WLG does not disclose donor information, but has filed friend of the court briefs on behalf of Purdue Pharma, the makers of OxyContin. In a recent article with Pain News Network, a spokesperson for Purdue Pharma conceded: “We’re long-standing supporters of WLF, in addition to several other business and legal organizations. We’ve provided them with unrestricted grants.”
  • The Pain Care Forum organized opposition to the CDC prescribing guidelines, mobilizing regular meetings among stakeholders opposed to the idea, according to an investigation by AP reporter Matthew Perrone. A recently re-filed complaint by the City of Chicago found that Burt Rosen, the chief in-house lobbyist for Purdue Pharma, controls the Pain Care Forum. A former drug company employee allegedly told investigators that Rosen tells the Pain Care Forum “what to do and how we do it.” The Pain Care Forum is funded through contributions by Purdue Pharma, as well as major opioid manufacturers Cephalon, Endo, and Janssen, a subsidiary of Johnson & Johnson.
  • The Power of Pain Foundation, a group funded by Purdue Pharma,asked supporters to contact the CDC in opposition to the guidelines, claiming that, “taking away pain medication and making providers afraid to prescribe due to your guidelines is only going to make more abusers, increase suicides, and tear apart the lives of millions.”
  • The U.S. Chamber of Commerce, a corporate lobbying group that represents opioid manufacturers, including Johnson & Johnson, issued apress release masquerading as a news story criticizing the CDC guidelines (The U.S. Chamber operates a public relations effort dressed up as as a bonafide media outlet called Legal Newsline, which it uses todisseminate stories that support the political priorities of its member companies.)
The over-prescription of opioid products has made the United States the center of the painkiller abuse epidemic. Americans consume about 81 percent of the global supply of oxycodone products (the active ingredient in OxyContin) and almost 100 percent of hydrocodone (the active ingredient used in brands such as Vicodin). More than 16,000 people die from opioid painkiller overdose every year.

The skyrocketing use of opioids in America is also closely linked to the rising heroin crisis, which reached new heights this year. Prescription opioids, which provide a high that is very similar to heroin, are often a gateway drug. As many as four out of five heroin users get started with opioid painkillers.
 
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Pain intensity is codified into some state law, regulations, and most guidelines. It is here to stay, as imperfect as it is. There are many things at play here: a lot of hype about opioids that are not directly connected to addiction or overdose such as the stats on hydrocodone use being almost exclusively used by the US. Hydrocodone has not been directly related to significant addiction nor death since very few deaths are associated with hydrocodone. There are few studies showing ineffectiveness of high dose opioids. On the other hand, the deaths cannot be denied, although the specific causes are not quite so clear. When one evaluates T codes (sub groups of opioids), it is found most coroners are unwilling to specify an opioid as the major cause of death- rather they use a broad based code that relates to polypharmacy. Most CDC stats quote 18,000+ deaths associated with opioids, but this means they had opioids in their system, not that the opioids caused the death. In most cases, coroners simply don't know the cause of death and the CDC misrepresents the data for their own purposes. Yet, people are dying of something in larger numbers and even if polypharmacy, it is difficult to determine the exact cause, but clearly opioids are in their system. We need to constrain opioid prescribing regardless of all the arguments for and against.
 
It's as if we as a specialty don't even exist. Can you imagine another field where this would happen?
 
"He started to accept Medicaid patients because, with more patients coming in, he could afford to take the lower reimbursement rates. But he’s gambling on the president’s plans, which haven’t gone into effect yet. “That’s the only thing that stresses him out,” his wife, Allison, says. “He has to figure out what he wants to do long-term. I think he’s getting impatient.”

In late fall, McCoy took a second job as medical director of a county jail. He’s about to start a third job running a medical detox unit at a newly opened psychiatric hospital. He plans on working at the hospital in the mornings and seeing his clinic patients in the afternoons and evenings. He needs the extra money to help support his four children and to keep the clinic going."


Under-resourced work. I wonder why health plans won't pay appropriately for it?
 

PROP says that racial stereotypes are protecting blacks from opioid overdoses? Who's in charge of the PR machine over there?

That certainly wasn't true in the late 70's in Detroit, NYC, and other urban areas. Who remembers hearing African American activists speculate in the 70's that heroin was a government conspiracy to ruin black communities?
 
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PROP says that racial stereotypes are protecting blacks from opioid overdoses? Who's in charge of the PR machine over there?

That certainly wasn't true in the late 70's in Detroit, NYC, and other urban areas. Who remembers hearing African American activists speculate in the 70's that heroin was a government conspiracy to ruin black communities?
Almost as bad as the reporter who asked the new head of the AMA (43 yo retired ER doc) why there are so many older white male physicians.
 
He's merely pointing out - correctly - the commonly held belief that racial discrimination is
protective against adverse risk selection.
 
Perspective

Opioid Prescribing for Chronic Pain — Achieving the Right Balance through Education
Daniel P. Alford, M.D., M.P.H.

N Engl J Med 2016; 374:301-303January 28, 2016DOI: 10.1056/NEJMp1512932

Comments open through February 3, 2016

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Interview with Dr. Daniel Alford on how prescriber education can help address the epidemic of prescription-opioid misuse. (12:39)

In recent decades, the United States has seen a dramatic increase in opioid prescribing for chronic pain. That growth has been associated with increasing misuse of prescription opioids1and has led to increases in deaths due to unintentional opioid overdose and in the number of people seeking treatment for opioid-misuse disorders. There’s probably 100% agreement that we, as a profession and society, have become overly opioid-centric in our management of chronic pain. Far more controversial are the role of long-term opioid therapy in managing chronic pain and the best strategy for ending the epidemic of prescription-opioid misuse.

Groups lobbying against prescribing opioids for chronic pain remind us that the effectiveness of long-term opioid therapy has been inadequately studied.2I believe that this is a case of absence of evidence rather than evidence of absence. As we await scientific evidence, questions remain regarding how best to address the epidemic of prescription-opioid misuse now. Groups advocating quick fixes believe that regulations that limit opioid availability are the best plan. This strategy is well intentioned and will certainly reduce opioid prescribing, but such blunt approaches will also limit access to opioids for patients who are benefiting or may potentially benefit from them.


Such an objection is not about protecting clinicians’ autonomy, but rather about protecting access to opioids for our patients who are in severe pain. These regulations will lead some clinicians to refuse to prescribe opioids even when they’re indicated, seeing it as too risky or too much work. They also create a climate of mistrust between patients and their health care teams. Clinicians are accused of both undertreating pain and overprescribing opioids, and patients with chronic pain who take opioids are viewed with suspicion. In addition, we don’t know what impact indiscriminate reductions in access to prescription opioids will have on long-term clinical outcomes.


Prescriber education is a more finely tuned approach to addressing the opioid-misuse epidemic, allowing us to individualize care on the basis of a patient’s needs after a careful benefit–risk assessment. That, after all, is the way we manage all chronic diseases. Education can empower clinicians to make appropriate, well-informed decisions about whether to initiate, continue, modify, or discontinue opioid treatment for each individual patient at each clinical encounter. Education has the potential to both reduce overprescribing and ensure that patients in need retain access to opioids.


In July 2012, a national voluntary prescriber-education initiative was begun. The Food and Drug Administration (FDA) approved a single shared Risk Evaluation and Mitigation Strategy (REMS) requiring manufacturers of extended-release and long-acting opioid analgesics to fund accredited education on safe opioid prescribing based on an FDA curricular blueprint. Although this program has not yet trained the targeted number of prescribers, a recent evaluation suggests that REMS education can shift clinicians’ self-reported practice toward safer, guideline-concordant care.3Comprehensive training in safe opioid prescribing is needed at all stages of medical education (undergraduate, graduate, and continuing), since training in this area has historically been lacking. This education must go beyond opioid prescribing to include comprehensive, multimodal pain management,4and it can be designed for the entire health care team: our nursing, pharmacy, and behavioral health colleagues have also been inadequately trained. This education can be coupled with enhanced clinical systems that support these new practices, including decision-support tools in electronic medical records.


Managing chronic pain is complex. Chronic pain is subjective and can present without objective evidence of tissue injury, which results in diagnostic uncertainties despite our most thorough assessments. Patients with chronic pain are desperately seeking immediate relief from their suffering; they tend to have unrealistic expectations regarding the potential benefits of opioids and not to fully appreciate the degree of risk conferred by escalating their own doses in a desperate (yet futile) attempt to obtain pain relief.


Clinicians have limited tools at their disposal to help these patients. Our reimbursement system favors the use of medications alone, despite evidence supporting multimodal care. Clinicians often have no easy access to nonpharmacologic therapies and cannot obtain pain consultations because there are too few pain specialists offering comprehensive pain care. Moreover, whereas clinicians can use objective measures to guide their management of other chronic diseases, here they must rely solely on the patient’s (or family’s) reports of benefits (such as improved function) and harms (such as loss of control). Clinicians are thus left basing treatment decisions on a brief subjective assessment of whether there’s enough benefit to justify continued opioid therapy or enough harm to justify discontinuing it.


Many guidelines for safe opioid prescribing exist, and all include similar recommendations, including use of assessments of risk of opioid misuse, signed agreements that include informed consent, and monitoring strategies such as drug testing, pill counts, and prescription-drug–monitoring programs. But it’s also essential for safe-opioid-prescribing education to include teaching of effective communication skills. How does one explain to a patient who’s desperate for help that an opioid treatment must be discontinued despite the lack of alternative treatments? How does one deal with a new patient who is already taking high-dose opioids and insists that it’s the only treatment that helps?


It’s important for clinicians to judge the opioid treatment rather than the patient.5When opioid therapy is deemed too risky or inadequately beneficial, discontinuing it means abandoning not the patient but merely an inappropriate treatment. When a clinician changes the treatment approach with a patient who tests positive for an illicit drug, that response is not about punishing the patient, but about changing the treatment plan on the basis of a new risk and addressing a newly identified problem.


When a clinician determines that discontinuing opioid treatment is appropriate, the patient may disagree and express anger. Is such frustration attributable to an appropriate desire for pain relief, inappropriate drug seeking, or a combination of the two? Though a patient-centered approach is always preferred, there are times in managing opioid therapy for patients with chronic pain when the clinician’s approach must be at odds with the patient’s request but intended to keep the patient safe. Such an approach may be perceived as paternalistic and may threaten the therapeutic alliance. Although transparent communication leading to a patient-centered approach is important, it goes only so far when a patient with chronic pain also shows signs of opioid misuse (e.g., unsanctioned dose escalation), necessitating discontinuation of opioid treatment.


Addressing the crisis of prescription-opioid misuse has become a national priority. To judge from the progress of the REMS program for extended-release and long-acting opioids, voluntary prescriber education may be insufficient to address this problem. Mandatory education may be required. If so, it will be important to link mandated education to medical licensure to avoid having clinicians opt out — since that could lead to reduced treatment access, as well as burnout among the clinicians who opt in. Alternatively and ideally, we could mandate proof of clinical competence, allowing clinicians who are already well trained to test out of an education requirement. Unfortunately, it may be impossible to measure such skill-based competence on a national scale.


I believe that the medical profession is compassionate enough and bright enough to learn how to prescribe opioids, when they are indicated, in ways that maximize benefit and minimize harm. Though managing chronic pain is complicated and time consuming and carries risk, we owe it to our patients to ensure access to comprehensive pain management, including the medically appropriate use of opioids.
 
J Pain. 2016 Jan 29. pii: S1526-5900(16)00499-5. doi: 10.1016/j.jpain.2015.12.018. [Epub ahead of print]
Trends in Opioid Dosing Among of Washington State Medicaid Patients Before and After Opioid Dosing Guideline Implementation.
Sullivan MD1, Bauer AM2, Fulton-Kehoe D3, Garg RK4, Turner JA5, Wickizer T6, Franklin GM7.
Author information

Abstract
By 2007, opioid-related mortality in Washington State (WA) was 50% higher than the national average, with Medicaid patients showing nearly 6 times the mortality of commercially-insured patients. In 2007, the WA Interagency Guideline on Opioid Dosing for Chronic Non-cancer Pain was released, which recommended caution in prescribing >120mg morphine-equivalent dose (MED) per day for patients not showing clinically meaningful improvement in pain and function. We report here on opioid dosing in the WA Medicaid fee-for-service population for 273,200 adults with a paid claim for an opioid prescription between 4-1-2006 and 12-31-2010. Linear regression was used to test for trends in dosing over that time period, with quarter-year as the independent variable and median daily dose as the dependent variable. Prescription opioid use among WA Medicaid adults peaked in 2009, as evidenced by the unique number of opioid users (105,232), the total number of prescriptions (556,712), and the total person-years of prescription opioid use (29,442). Median opioid dose was unchanged from 2006-2010 at 37.5mg MED, but doses at the 75th, 90th, 95th, and 99thpercentiles declined significantly (p<.001). These results suggest that opioid treatment guidelines with dosing guidance may be able to reduce high-dose opioid use without affecting the median dose used.

PERSPECTIVE:
Some fear that opioid dosing guidelines might restrict access to opioid therapy for patients who could benefit. However, there is evidence that high-dose opioid therapy entails significant risks without demonstrated benefit. These findings indicate that high-dose opioid therapy can be reduced without altering median opioid dose in a Medicaid population.

Copyright © 2016 American Pain Society. Published by Elsevier Inc. All rights reserved.
 
I think the FDA is the correct agency. At least they have statisticians that have a clue how prospective studies work unlike the CDC that extrapolates to the bounds of the universe based on a few case reports. Also, the FDA does have the power to regulate our medical licenses through the use of the courts and promulgation of regulations (having the force of law). The CDC on the other hand, can mere make suggestions, using their own definition of a "guideline" without systematic reviews or analysis. The DEA can regulate prescribing for a "legitimate medical purpose" but backed away from defining exactly what that meant after publishing their own consensus based remarks on the subject on their website, then retracting them. They have not ventured forth any new definitions in nearly a decade now, and it appears none are forthcoming, leaving physicians in a nebulous state of potential peril. Now if they will actually put together numbers and meaningful limits rather than speaking in vague generalities, we will all be better served.
 
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Well that sucks- the FDA has decided to support a secretly developed document with a shadow organization of namely doctors that remain accountable to no one, using undefined metrics, and who have somehow arrived at the conclusion that limiting primary care physicians from high dose prescribing will stop the problem. If that is the case, then there is no credible federal agency that is capable of functioning as a means of rational regulation development. Perhaps we should just develop a majority vote approved document from this forum, brand it the "STANDARD OF CARE FOR OPIOID PRESCRIBING", publish it anywhere and everywhere, and send it to the FDA and CDC directors telling them they can now disband their redundant efforts.
 
The document was written by three people, one of which was a non-physician that had an inherent conflict of interest since that person was an employee of the agency that directed its creation. We all know exactly the history of Chou, but Dowell was a relatively unknown. She published zero studies regarding opioids in the clinical literature (pubmed) until May 2015 when a non-peer reviewed MMWR report she helped author demonstrated a 29% drop in Statin Island Opioid deaths through a 5 prong effort. The "stakeholders" input into the document was either substantial (advisory) or was minimal (observational). It is probable that the latter was the case, thus the preservation of their name secrecy. In that case, there were only two physician authors, one with no prior clinical publication experience in opioids (other than what appears to be a joint letter to the editor in JAMA), and the other Dr. Chou, to determine the fate of the country. Most "guidelines" of this nature have scores of authors attached, but not the CDC guideline, therefore it was literally authored by only two physicians without substantial input by any "stakeholder" representative. So, are we to trust the judgment of only two physicians in such an important matter? And should the FDA? CDC comment periods are frequently like those of the FDA, that are just that- a mechanism for people to voice concerns and displeasure, but frequently do not alter the fundamental precepts of the created document, not the conclusions.
 
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Well that sucks- the FDA has decided to support a secretly developed document with a shadow organization of namely doctors that remain accountable to no one, using undefined metrics, and who have somehow arrived at the conclusion that limiting primary care physicians from high dose prescribing will stop the problem.

It probably will.

But with some negative consequences and collateral damage.

Isn't that the same approach the government usually takes whenever they make massive cuts to abused CPT codes?
 
Aaron Colodney is a pain medication expert? News to me. To quote Dr. Bogduk, "I always feel like I need a shower after attending a meeting with Dr. Colodney".

He is one of the docs in Tyler who have a physician owned hospital. Colodney was so cavalier, he would let the nurses rotate the canulas and do the second burn on rf's, while he would start his next procedure in adjacent room. Efficient, yes. Safe? Not so much.


I think you have the wrong Colodney

http://www.phoenixhouse.org/team/andrew-kolodny/
 
In the words of Rosanne Rosanadana, nevermind.

Sent from my SAMSUNG-SM-G920A using SDN mobile
 
Angus Deaton on the rising tide of ODD's in poor white America (Start Time 10:45)

http://www.cfr.org/economics/angus-deaton-foreign-aid-inequality/p37546

What's missing in this analysis is the role that Unions and Organized Labor played in essentially forcing companies to move manufacturing overseas. No company can be competitive if its labor costs at home are 15 times the labor costs in China and India. Money wasted on failing Obama-care policies should have been used for job creation, education, and vocational retraining...
 
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