Surgeon General Backpedals on Flawed Tylenol Study. Because of ACSH

Surgeon General Backpedals on Flawed Tylenol Study. Because of ACSH.

https://www.acsh.org/news/2019/07/15/surgeon-general-backpedals-flawed-tylenol-study-because-acsh-14153

Fireworks can be an awful lot of fun on July 4th, but not so much if they blow up in your face. Unfortunately for Surgeon General Dr. Jerome Adams, his face was in the wrong place on Independence Day because of a ridiculous paper in a ridiculous journal called Emergency (Tehran). 

“Comparison of the Analgesic Effect of Intravenous Acetaminophen and Morphine Sulfate in Rib Fracture; a Randomized Double-Blind Clinical Trial” concludes that IV Tylenol works better (or as well) as morphine for patients who go to emergency departments for broken ribs – a notoriously painful injury. 

Here are Dr. Adams’ Tweets from July 3rd and 4th. Pay special attention to the one from July 4th on the right. Dr. Adams tells us that he unquestioningly believes the study results and offers no doubt about its accuracy.

It appears that Dr. Adams didn’t bother to read the paper from which this conclusion was drawn. So I did. And it was a colossal mess, something I explained on July 8th (See Need General Surgery? Ignore The Surgeon General). The study was so bad that it was impossible to tell whether Tylenol worked better than morphine, morphine worked better than Tylenol, or either drug worked at all.

A few days later ACSH friend, Dr. Aric Hausknect, a New York neurologist and pain management expert, who has both written for and been interviewed by us) must have read the paper as well because his July 12th letter made what I had to say seem rather tame by comparison (See Dr. Aric Hausknecht Responds To SG Jerome Adams’ Tylenol Recommendation).

Apparently, we hit the mark because in subsequent Tweets Dr. Adams was backpedaling like the bicycle scene from The Wizard of Oz played backward. Here are a few from July 13th…

Finally, there’s this…

What Dr. Adams did is no different than what PROP, certain members of the CDC, politicians, academic zealots, and various other self-serving individuals and groups have been doing for almost a decade –  making up a story and backing it up with faulty (or non-existent) research to “prove” a point. 

We just happened to catch him. 

(Illegal) fentanyl is now the leading cause of fatal drug overdoses claiming 49,000 lives in 2017

Chinese fentynal dealer busted by the DEA

https://foxsanantonio.com/news/local/chinese-fentynal-dealer-busted-by-the-dea

Chinese fentynal dealer busted by the DEA as he shipped thousands of dollars worth of fentynal into South Texas.

The DEA tells Fox San Antonio how the Chinese government help to bust the dealer in this week’s On the Frontlines with the DEA.

It’s a case that was years in the making, but now a major fentynal dealer from China has been taken down after the DEA identified him as the person shipping fentynal to Texas. The tiniest amount of this drug has proven to be deadly all over the country. In fact according to the DEA, fentanyl is now the leading cause of fatal drug overdoses claiming 49,000 lives in 2017. So when a man in China was identified shipping a kilo of fentynal into Texas the DEA was quick to move.

“At that time a parcel was seized of a bout a kilogram of what is known as molly MDMA. An investigation was done and what started as a kilogram turned into a lot more. We found out that this company was sending this product all over the country and actually all over the world,” said Dante Sorianello, the assistant special agent in charge of the San Antonio district.

The seller was in China and he would coordinate the movement of MDMA, steroids and fentynal all over the world including to a buyer right here in Texas.

“We found out that this lone individual had received over the past several years over 52 kg of MDMA that makes a lot of stimulant getting out on the streets and that’s just one individual,” said Sorianello.

But this case could not have been closed according to the DEA without the help of the Chinese government who help find a hidden lab in operating in China.

“Ultimately with our Chinese partners the Chinese government was able to identify that laboratory, seize it, dispose of the laboratory and arrest that individual,” said Sorianello.

Is it illegal to ship via. Is it illegal to ship via the us postal service and is it also illegal via a private company like UPS or Fedex?” Yami asked. “You’re dealing with a controlled substance, so yes it’s all illegal,” said Sorianello.

The DEA says that if you are caught shipping drugs via the us postal service vs a private company there are laws that allow them file more charges against you.

In your neighborhoods, on the streets, Fox San Antonio and the DEA will keep you informed and safe.

Insulin In Canada cost 10% of the USA price… Insurance/PBM industry is the reason but the Pharma industry gets the blame

Family says 21-year-old son died rationing insulin

https://www.khou.com/article/news/local/breaking-the-news/family-says-21-year-old-son-died-rationing-insulin/89-d451a01b-9170-4341-9010-155cb87edccc

The price of insulin is costing some people who can’t afford it their lives.

RAMSEY, Minn. — Advocates say it is a sign of the growing problem of rising prescription costs in America.

Friday, friends and family said 21-year-old Jesimya David Scherer-Radcliff died as a result of rationing his insulin.

His father, David Radcliff Jr. III, said everyone called his son Jesy.

“The cost of insulin is ridiculous. It is hard for me to even go in there and look at his casket. He is gone now. I can’t say, ‘hey let’s go here,’” he said. ‘I just think this country is backwards and I am a veteran. I have seen other countries and how they operate.”

Jesy was 21. A service celebrating his life was held at the Lord of Life Church in Ramsey.

Friday, Jesy’s mom, Cindy, and other members of the family wore red and black.

Nicole Smith-Holt, an advocate for affordable insulin, stopped by to show her support.

Nicole’s son Alec was 26. He died trying to ration his insulin one month after losing healthcare coverage. Nicole was among the caravan of Minnesotans who traveled to Canada in search of insulin which is ten times cheaper there than it is in the U-S.

“We lost another Type 1 diabetic due to insulin rationing. This is something you know we hoped would never happen again,” she said. “After losing my 26- year-old son to the same situation and fighting so hard at the legislative level to pass the Alec Smith emergency insulin act and it going nowhere and telling them if they did not implement this law we were going to lose more lives this just goes to show we were right.”

But this is a time she wishes she wasn’t right.

“My son and Jesy, they were murdered. They were killed by big Pharma. The cause of death should actually be on their death certificates, corporate greed,” she said. “I want justice for all of their deaths.”

Jesy’s godfather, Ianin St. James holds memories in his heart and hands. He said Jesy would transport him to and from the Mayo Clinic when he was undergoing chemotherapy treatments.

As he shared memories about the 21-year-old, he held a thank you note he received from Jesy soon after his high school graduation.

“One of the last things he wrote was, ‘I love you and everything about you.’ Don’t ever stop being you,” he said. “He accepted everybody and everything. That is all he ever did he just gave of himself.”

Earlier this month I made this post  When POLITICIANS don’t know their “APPLES” from their “ORANGES”

Where I think that I clearly explained why there is a difference in prices of prescriptions and it is all due to GREED…but they have been pointing the fingers at the wrong industry and the industry that is really to blame…. it is apparently very happy with everyone blaming the wrong industry.

I expect to see the PBM industry to attempt to confiscate as much money out of community pharmacies until the bureaucrats finally get their act together and stop being influenced on the HUGE PILE OF MONEY that the PBM industry has to lobby Congress.   Collectively, the entire Lobbying industry spend 9+ million/day to influence members of Congress.  The above story is just how LETHAL the GREED of the insurance/PBM industry can be to some people who can’t afford to pay “rack rate price” of some/many life sustaining medications.

Our society discourages proper treatment of pain and mental health… which disease state is next ?

How Did We Come to Abandon America’s Pain Patients?

https://filtermag.org/2019/07/15/abandon-americas-pain-patients/amp/

Overdosesnot those involving prescription opioids, but of heroin and illicit fentanyl, often combined with benzodiazepinescontinue to go up. But opioid prescribing continues to go down. Pain patients are untreated and suffering. Pharmaceutical companies are being sued and settling. Law enforcement is cracking down on providers. And many physicians, caught in the middle, have stopped prescribing because they don’t want to get in trouble and possibly lose their livelihood.

This situation is continuing despite the Centers for Disease Control and Prevention (CDC) emphasizing in a commentary published this spring that their guideline on prescribing for chronic pain, released in 2017, is being misapplied.

The CDC authors wrote in April:

Clinicians might universally stop prescribing opioids, even in situations in which the benefits might outweigh their risks. Such actions disregard messages emphasized in the guideline that clinicians should not dismiss patients from care, which can adversely affect patient safety, could represent patient abandonment, and can result in missed opportunities to provide potentially lifesaving information and treatment.

So what has gone so terribly wrong? Because it has.

The Victims

Ian Lewis, who lives in Ohio, having grown up in Tennessee, is 37 years old. He had his most recent surgery on July 8.

His pain started in middle school. He began suffering in seventh grade, but nobody believed that he was in pain. His serious congenital spine problems were discovered when he was 12 years old. He had two blown-out discs, 16 fractures, and a cut durum bleeding into the spinal cord.

Ian’s mother, Terri Lewis, PhD, who teaches for the Rehabilitation Institute at Southern Illinois University in Carbondale, has been his caretaker throughout.

“Up to this point everybody had denied the pain that he was expressing,” said Lewis. He then got excellent care at Vanderbilt in Tennessee, she said, but in 2003 his pain increased. He had two more surgeries, but never healed. For 10 years, he got along on opioids, a “combination of legal and street,” said Lewis. “Cannabis was also pretty helpful, he discovered.”

The problem was the opioid crackdown. After it happened, medical providers  “went all around the block to try not to label this as chronic pain, to call it trouble sleeping, or anxiety, but what he was givenantipsychoticsdidn’t help,” said Lewis. “Why didn’t they label it as chronic pain?”

Ian had received nothing at all as a child, when nobody believed that he was in pain. “I can speculate it’s because we don’t recognize pain in kids,” said his mother.

The images below show the fractured Harrington rods that were removed from Ian’s back during his latest surgery, and his back after the operation.

 

 

 

 

 

 

Photos courtesy of Terri Lewis

According to the National Institutes of Health, nearly 50 million American adults suffer chronic pain. They typically face onerous and invasive requirements to obtain repeat opioid prescriptions, and live with the constant threat of being cut off—if they can get them in the first place.

Unfortunately, there is no way to assess the number of patients who have been subject to opioid dose reduction of an informal nature, said Stefan Kertesz, MD, professor of medicine and addiction scientist at the University of Alabama at Birmingham School of Medicine. “Neither is there a there a formal survey to assess the number of patients who have been discontinued, either voluntarily or against their will.”

The situation is difficult because nobody can tell how large the problem is if no data is collected, and because a major policy chance is being enacted with no entities reporting outcomes, Kertesz told Filter. (This study came close in terms of looking at outcomes, but not overall prevalence.)

The suffering caused by denial of opioids sometimes becomes unbearable, and numerous suicides for this reason have been reported.

Gail Groves Scott, an opioid use disorder policy researcher,and doctoral student in health policy, told Filter about a relative of hers who killed herself. The relative had been a urologist, but had switched to prescribing buprenorphine. She developed a pain disorder and probably a substance use disorder as well, and was most likely going to lose her license.

“She was ashamed,” said Scott. “She didn’t have staff, and was probably really struggling financially.” She put fentanyl patches all over her body and died that way.

As for her patients on buprenorphine, “They had nowhere to go, but luckily there were fewer than 20.” She was in Tennessee, where registration requirements deterred new clinics and resulted in a reduction of patient slots.

In general, “Doctors are really nervous about taking a new patient who is on a controlled substance,” said Scott. Asked why, she listed concern about substance use disorder, concern about whether a patient’s previous doctor had been prescribing appropriately, and fear of oversight and potential sanctions.

Why Is the CDC Being Misinterpreted?

Deborah Dowell, MD, MPH, chief medical officer at the CDC’s Injury Center, told Filter that the 2017 guideline was meant to help “primary care clinicians work with their patients to consider all safe and effective treatment options for pain management,” and that “CDC encourages clinicians to continue to use their clinical judgment, base treatment on what they know about their patients, maximize use of safe and effective non-opioid treatments, and consider the use of opioids only if their benefits are likely to outweigh their risks.”

Dowell also referred to the recent CDC commentary, noting that it highlighted “the misapplication of the CDC guideline” and raised “awareness about issues that could put patients at risk.”

Dowell went on to say that the guideline did not apply to anyone but primary care clinicians treating chronic pain for patients 18 and older. It was not intended, she said, for patients in cancer treatment, for example, patients with post-surgical pain, or patients with acute sickle cell crises.

Yet the guideline has been appliedor misappliedto all of these groups.

What’s more, Dowell said, there was nothing in the guideline’s dosage recommendation that should have resulted in hard limits for cutting off opioids. The guideline states: “When opioids are started, clinicians should prescribe the lowest effective dosage. Clinicians should… avoid increasing dosage to ≤90 MME/day or carefully justify a decision to titrate dosage to >90 MME/day.”

Yet this is what is happening. “High dose prescriptions, which overwhelmingly accrue to long-term recipients, have fallen 61 percent according to [pharmaceutical consulting company] IQVIA,” said Kertesz.

The details of the CDC guideline are not objectionable. Yet neither is it particularly encouraging to doctors who prescribe opioids needed for pain.

Dowell noted that that 2017 guideline also does not support abrupt tapering or sudden discontinuation of opioids, which can result in severe withdrawal symptoms, leading some patients to “seek other sources of opioids.” In addition, she said, “policies that mandate hard limits conflict with the guideline’s emphasis on individualized assessment of the benefits and risks of opioids given the specific circumstances and unique needs of each patient.”

Yet these policies are abundant, even prevalent. Abrupt tapering and discontinuation is happening, far too often.

Dowell also noted that patients receiving medication-assisted treatment (with methadone or buprenorphine, both opioids) for opioid use disorder (OUD) do not fall under the guideline, which concerns only chronic pain, not OUD. In fact, the guideline recommends offering these medications to patients with OUD.

The details of the CDC guideline are not objectionable. Yet neither is it particularly encouraging to doctors who prescribe opioids needed for pain. And the guideline’s widespread misinterpretation gives reason to question whether it puts too little emphasis on the importance of opioid prescribing to relieve sufferingand too much on the possibility of opioid prescriptions leading to OUD.

The CDC acknowledges the rarity of this latter scenario. When I asked Dowell how many patients who take opioids as prescribed actually develop OUD (as opposed to becoming physically dependent, which every long-term opioid user does), she replied in an email:

“One [2014] study* found that, among patients prescribed opioids for pain, rates of opioid use disorder diagnosis ranged from 0.7% with lower-dose (≤36 MME) chronic therapy to 1.3% for medium dose chronic therapy to 6.1% with higher-dose (≥120 MME) chronic therapy (versus 0.004% with no opioids prescribed).”

So for addiction rates of 0.7 -6.1 percent across all doses, virtually all pain patients are now either suffering in untreated pain or under threat of it? How did this happen?

“The guideline has been institutionalized to forcibly change patients’ care.”

By issuing the recent comment, the CDC basically admitted that misapplication of its guideline has had a chilling effect on prescribing. But it’s also important to acknowledge the limits of the CDC’s influence.

The CDC doesn’t regulate doctors. After the guideline was released, many in the addiction field did not think doctors would reduce prescribing, as there was no enforcement behind it.

It turned out, they were wrong. Still, scaremongering politicians’ pronouncements, law enforcement crackdowns, Pharma lawsuits and relentless media “opioid epidemic” coverage have all played their part.

Kertesz supported the initial CDC guideline, but became concerned about its interpretation. “Over the last three years, I have seen patients harmed,” he told Filter. “I have written repeatedly about the fact that the CDC’s guideline was good but was misapplied. Broadly speaking, it was a reasonable document, but it has been institutionalized to forcibly change patients’ care.”

This March, he, along with other experts and Human Rights Watch, submitted a letter making this point to the CDC. It caused distress at the agency, which did not believe it had caused the denial of pain medication.

“I asked them how difficult would it be for the CDC to issue a defense of the guideline, with a little clarification?” Kertesz said. That day, a CDC official told him it was very difficult. But on April 24, in the New England Journal of Medicine, that clarification came.

“That’s courage in action,” said Kertesz, who is somewhat of a hero to pain patients across the country.

Why Physicians Are Frightened

Regardless of what the CDC says, it’s doctors who do the prescribingand they’re the ones who don’t want to do it any more.

Scott, now an opioid use disorder policy researcher, previously worked as a pharmaceutical representative, selling many drugs for addiction and pain. Even thenwell before the CDC guidelineshe saw doctors’ hesitancy to prescribe.

“Doctors were becoming more aware,” she said. “We know that there was overprescribing. There was also an increase in electronic health records and prescription drug monitoring programs, which made everyone more aware of who was an outlier. This impacted physicians’ comfort level in prescribing opioids.

“They say that they want to know who has addiction and who doesn’t, but the real reason is they are terrified, of administrative and legal problems.”

“Nobody saw what was going to happen,” Mark A. Weiner, MD, representing the American Society of Addiction Medicine, told Filter. “Pain doctors are coming to me and my colleagues to answer the question of who’s who”meaning which patients on opioids for pain have pain, and which are addicted.

This has been going on for years, according to Weiner. “They say that they want to know who has addiction and who doesn’t, but the real reason is they are terrified, of administrative and legal problems.” Weiner supports law enforcement, but “do they think everybody’s an addict?” He believes that prescription drug monitoring programs can helpbut only if they are used properly. Used improperly, they just contribute to the problem.

Like many, Weiner cites the “pendulum”one of his presentation slides has a moving pendulum in it. “On one side is 1985-2000, where people said we need to treat all the pain we can,” he said. “Then the pendulum started moving, through the middle partthe rational approach.”

But now, it’s swung too far to the other side. Weiner helps move it back toward the middle by reassuring physicians who provide palliative care for cancer and hospice that “it’s okay” to prescribe opioids. “I’m an addiction doctor, not a pain doctor, so I they listen,” he said. “But I often hear they’re not happy with it.” That’s because it’s their livelihoods on the line.

“The focus on prescribing is not unimportant,” said Richard Saitz, MD, professor at Boston University Schools of Medicine and Public Health. “Yes, exposure to opioids is a factor in developing opioid addiction, but it isn’t the sole factor, and focusing on prescribing of opioids is a bit like looking for the keys under the lamppost because that is where the light is.”

Rather, he told Filter, it’s important to focus on appropriate prescribing for the individual. Of course, nobody would argue with that medically. “But instead, PDMPs and insurance regulations focus on what is easily countable and set population goals to reduce and eliminate. As a result clinicians want less and less to do with opioid prescribing, even for acute pain.”

What the CDC guideline did, said Saitz, was give clinicians who were already uncomfortable prescribing opioids back-up to just taper or not prescribe.

Pharma Lawsuits’ Chilling Effects on Prescribing

A string of high-profile lawsuits against opioid manufacturersthe first in Chicago in 2016, the most recent in Oklahomahave further impacted prescribing by adding to physicians’ discomfort, although the chill started before then. State medical boards and the American Medical Association, too, seem more concerned about overprescribing than patient abandonment.

The lawsuits definitely had a chilling effect on Pharma itself, and on the organizations Pharma supported. As for cancer and other conditions, pain patient advocacy often comes from the treatment field.

Loss of Pharma funding for pain advocacy groups has been significant. Lawsuits have alleged that Pharma used organizations like the American Pain Society, which is now disbanding, to promote their products.

In 2016, about the same time that Pharma companies started getting sued, they cut off the American Pain Society and others, said Bob Twillman, PhD, former executive director of the Academy of Integrative Pain Management and current clinical associate professor at the Department of Psychiatry, University of Kansas Medical Center. They no longer took booths at conferences. And they started reserving their cash for settlements. “Pain is still a valid specialty, but now, everybody’s too scared to prescribe.”

They were suing companies for dishonestly marketing products that relieved pain, so it wasn’t convenient to acknowledge the value of these products.

A combination of finance and politics motivates the lawsuits, Twillman told Filter. “There’s money there.” There is the money that Oklahoma, for example, will receive—but also a motive for prosecutors who may want to get elected to higher office.

But Kertesz said that the prosecutors are doing their job. “They have one goal, which is to secure as much money as possible, not to worry about people who aren’t getting pain medication,” he said. “That’s not their department.”

And Kertesz, like Scott, is skeptical of all Pharma marketing. “I view it as a public menace,” he said. “I don’t think it’s wrong to get money out of the pharmaceutical companies.” But he does think the money should go to treating people. “I have a concern about significant portions of the settlement money going to pay scholars,” he said, referring to academic appointments.

“The other thing that concerned me about the attorneys general,” Kertesz said, “is they seem to want to preserve a pristine, simple, one-directional narrative, and anything that acknowledged the value of pain care was a threat to the lawsuit.”

So they left that part out. They were suing companies for dishonestly marketing products that relieved pain, so it wasn’t convenient to acknowledge the value of these products. And that directly hurt pain patients.

None of this is black-and-white. But the attempt to make it so has demonized pharmaceutical companies, prescribers and patients.

“Callous paternalism will be a poor substitute for care, resulting in promoting harm, suffering and a contempt for the healthcare delivery system.”

“There is no question that prescription opioids have been mis-prescribed and over prescribed,” H. Westley Clark, MD, JD, dean’s executive professor with Santa Clara University, told Filter. “There is no question that a few opioid prescribers devolved into being quasi-drug dealers. There is also no question that some patients have developed opioid use disorders as a result of imprudent opioid prescriptions.”

“However, in our zeal to curtail the excessive prescribing of opioids for the treatment of pain, we have trampled on the clinical needs of those individuals who have benefited from the use of opioids for the treatment of pain, said Clark, a former director of the Center for Substance Abuse Treatment at the federal Substance Abuse and Mental Health Services Administration.

“Those living with chronic non-cancer pain need to be heard,” he continued. “Their opinions need to a part of the dialogue for treatment. Those experiencing intractable pain are stakeholders in the discussion about the appropriate treatment of pain, but their opinions have been dismissed and their input trivialized. It is time to return to a rational approach to pain management, an approach that takes into consideration of input of those who suffer from pain, making sure that they are a part of the treatment team.”

“Otherwise,” he concluded, “callous paternalism will be a poor substitute for care, resulting in promoting harm, suffering and a contempt for the healthcare delivery system.”

Moving the Pendulum

“I certainly see liberal prescribing as playing a role,” said Kate Nicholson, a civil rights attorney who advocates for pain patients, of the overdose crisis. “I think people can become addicted, of course.”

Nicholson, who has a pain history of her own, and does most of her advocacy work for free, cites the National Institute on Drug Abuse/CDC incidence range of 0.7 to 6.1 percent.

Andrew Kolodny, MD, is co-director of Opioid Policy Research at the Heller School for Social Policy and Management at Brandeis University and a leading advocate for much stricter controls on opioid prescribing. He did not want to be quoted in this article but his testimony was instrumental in the Oklahoma lawsuit.

Rather than the NIDA-CDC figures, Kolodny instead uses a cross-sectional OUD prevalence figure, which includes people who had a history of misuse and in general were not well-screened before being prescribed opioids, said Nicholson. One article Kolodny cites gives figures of 3.5 percent for severe OUD symptoms and 58.7 percent for “no or few symptoms.”

“What I find difficult is that the treatment of pain is being framed as responsible for spawning a crisis.”

“We know that most who misuse did not receive medications directly from a doctor and already had a developed history of using other strong substances,” Nicholson said. “But, sure, some people undoubtedly got hurt from liberal prescribing. What we need is a return to nuance. What I find difficult is that the treatment of pain is being framed as responsible for spawning a crisis—and so patients in pain are beleaguered and disregarded.”

Amid the suffering, there have been rays of hope. The CDC’s April comment was one of them. And in New Hampshire this month, one physician was reprimanded for cutting back on a patient’s painkillers.

Pain patientsfor all the stigma, lack of funding and other obstacles they faceare continuing to speak out. If we want the pendulum to swing back to somewhere rational, we have to hear them.


* Edlund MJ, Martin BC, Russo JE, DeVries A, Braden JB, Sullivan MD. The role of opioid prescription in incident opioid abuse and dependence among individuals with chronic noncancer pain: the role of opioid prescription. Clin J Pain 2014;30:557–64.

Top photo by Ryan Park on Unsplash

The author wishes to dedicate this piece to “all of the physicians who bravely treat pain patients with opioids, and to the patients who have been suffering through this nightmare.”

Retail Pharmacist Beware

DEATH on the Battlefield is Preferable

DEATH on the Battlefield is Preferable

Trump WH Seeks To Monitor The Disabled To Ensure They Aren’t “Too” Happy

Trump WH Seeks To Monitor The Disabled To Ensure They Aren’t “Too” Happy

https://mavenroundtable.io/theintellectualist/news/trump-wh-seeks-to-monitor-the-disabled-to-ensure-they-aren-t-too-happy-1GE1YTfza0KHKw1oGIOrYA/

A new policy proposal by the Trump administration calls for the surveillance of disabled people’s social media profiles to determine the necessity of their disability benefits. The proposal, which reportedly aims to cut down on the number of fraudulent disability claims would, monitor the profiles of disabled people and flag content that shows them doing physical activities. When it comes down to it, the policy dictates that disabled people shouldn’t be seen living their lives for fear of losing vital financial aid and, possibly, medical care.

The administration has been working closely with the Social Security Administration in an effort to reduce false claims believing that social media holds a cache of information regarding eligibility of Social Security Disability Benefits. They believe that by monitoring the social media accounts of disability benefit recipients, they can root out false claims and reduce the overall amount of money spent on the programs.

The proposal, like many of its policies regarding disabled people, shows a fundamental misunderstanding of disability and takes advantage of how social media operates in order to cut them off from the support they need. Disabled people don’t all function in the same way, and disability is not a set of stereotypes like taking selfies staring longingly at the world. They live lives while managing their energy for the activities they can handle and trying to make those they cannot more accessible.

Additionally, studies have shown that a majority of social media users show only the good in their lives, not the hardships or difficulties. Disabled people should be allowed to share the full scope of their existence without fear they’ll be accused of lying—and even fraud—by the United States Government which will likely reason that if a disabled person is seen going to the mall or taking time to swim or jog, they can be working.

The truth about disability is that it isn’t a series of down moments but both highs and lows that comprise the lives of the disabled. Simply because disabled people are seen exercising, dancing or shooting hoops does not mean that they have the ability to sustain that level of energy all day. This type of policy also plays upon the assumption that people with disabilities all function and move about in the world in the same way, which is entirely untrue. There are wheelchair users who can walk, people with cerebral palsy that can run and amputees that are bionic. It is just as dangerous to assume that disabled people should have to “overcome” their disabilities to do what they love as it is to assume there is nothing they want to do. One person’s body should never be considered a prescription for another.

Another thing that the general public does not understand about disability and the internet is that attention to disability issues often operates within an economy of “Inspiration Porn.” Abled people often film, post, share and circulate photos and videos of disabled people doing extraordinary things as a litmus test to how “poor” life could be with a disability and how disabled people achieve “in spite of” their disabilities (quite often, this type of posting occurs without the disabled person’s permission). And, while many disability advocates disdain this type of media representation and are vocally calling for an end to inspiration porn, there’s a not-so-often talked about number of disabled people who play upon these stereotypes for their advocacy and to further their own quest for disability rights.

Quite often, in order for disabled people to be seen as needing help, nondisabled people need to see them as pitiful, helpless and ripe for a nondisabled person to swoop in and play hero. Without the ability to do so, a great many nondisabled people would not pay attention to disability issues. Disabled people know that, and it would appear the U.S. Government does as well. Public sympathies rarely side with disabled people who appear confident and comfortable in their own bodies. Therefore, there will be little outrage for cuts to disability benefits for active disabled people.

Aside from the cruelty it takes to cut necessary funds from a disabled person’s life because of a moment of activity, it seems willfully ignorant. Many in society already see disabled as “fakers” trying to take money from unsuspecting people, and this policy would only raise those tensions among the public. Disabled people are people, and as such, lead complex lives with ups and downs like the rest of the population. Relying upon a reductive narrative of disability is dangerous and will cost lives. Due to this, the administration should look inward and learn how to #BeBest.

CDC did not follow the Federal Advisory Committee Act in developing opiate dosing guidelines

CDC’s new opioid guidelines will be used by plaintiffs bar, WLF says

https://legalnewsline.com/stories/510704148-cdc-s-new-opioid-guidelines-will-be-used-by-plaintiffs-bar-wlf-says#.XSopWi6hyUg.facebook

WASHINGTON (Legal Newsline) – A Washington, D.C.-based public-interest law firm that has been outspoken about the Centers for Disease Control and Prevention’s handling of an opioid guideline development team argues the agency’s new guidelines, which were issued this month, will “no doubt” have an effect on future litigation.

Richard Samp, chief counsel for the Washington Legal Foundation, argues plaintiffs law firms, including Cohen Milstein Sellers & Toll PLLC, will use the CDC’s approval and release of the guidelines to their advantage.

“Will the plaintiffs bar use these guidelines in their pending litigation? I have no doubt that, yes, they will,” Samp told Legal Newsline.

The CDC released its new guidelines regarding prescriptions for opioid painkillers, such as Vicodin and OxyContin, March 15. The guidelines, which are voluntary, recommend primary care physicians:

* Use non-opioid therapy for chronic pain management, outside of active cancer, palliative and end-of-life care;

* Prescribe the lowest possible dosage when opioids are needed; and

* Always exercise caution when prescribing opioids, monitoring patients closely.

“Overprescribing opioids — largely for chronic pain — is a key driver of America’s drug-overdose epidemic,” CDC Director Tom Frieden said in a statement. “The guidelines will give physicians and patients the information they need to make more informed decisions about treatment.”

Samp says WLF takes no issue with the guidelines themselves, but the agency’s procedures used to develop the guidelines.

“We’re not medical experts,” he said. “We take no issue on whether guidelines should be issued, or what they should say.

“But we do recognize there is a broad spectrum of views as to what could be done, and the process used by the CDC did not provide a fair opportunity for everyone to participate.”

For one, Samp argues the CDC did not follow the Federal Advisory Committee Act.

FACA, which became law in 1972, governs the behavior of federal advisory committees.

Under the law, an advisory committee is defined as “any committee, board, commission, council, conference, panel, task force, or other similar group” that dispenses “advice or recommendations” to an agency or government official.

Committees composed of full-time officers or employees of the federal government do not count as advisory committees under FACA.

The CDC has argued that its Core Expert Group, or CEG, didn’t qualify as an advisory committee under the federal law.

WLF, in a 13-page letter sent to Frieden in November, countered that the CEG indeed fell under the definition and was required to comply with each of the law’s “numerous obligations,” including opening all meetings to the public; publicly releasing all documents that the CDC made available to the CEG; and preparing and publicly releasing minutes of all CEG meetings.

Instead, the CDC complied with none of the requirements, Samp and General Counsel Mark Chenoweth wrote in their letter for WLF.

“(The CDC) nominated this advisory group to help come up with these guidelines, but the group met totally in secret,” Samp said.

“Only after the initial draft guidelines were released did they say who was on the advisory group.”

A complete list of the Core Expert Group members and other internal documents surrounding the prescribing guidelines surfaced in September.

The names on the list included Jane Ballantyne, a paid consultant for Cohen Milstein.

Ballantyne, a retired professor of anesthesiology and pain medicine at the University of Washington, is a member of the International Association for the Study of Pain, or IASP, and in 2014 was named president of the Physicians for Responsible Opioid Prescribing, or PROP. PROP’s mission, according to its website, is to “reduce opioid-related morbidity and mortality by promoting cautious and responsible prescribing practices.”

WLF, in its letter, pointed out that Ballantyne was one of “numerous” members of the CEG who were on record — well before joining the committee — as “strongly supporting the need to tighten opioid prescribing standards.”

“Conspicuously absent from the CEG, however, were physicians and others with experience in treating patients suffering from chronic pain,” Samp and Chenoweth wrote.

The foundation called Ballantyne’s inclusion the “most egregious.”

Ballantyne disclosed her services as a paid consultant for Cohen Milstein to the CDC, but didn’t recuse herself. The plaintiffs law firm is known for its class action lawsuits and has been hired by a number of state attorneys general in recent years, including some of those to whom it donated.

The firm currently is helping to represent the City of Chicago in a lawsuit filed against a group of pharmaceutical companies over the marketing of opioid painkillers, and another by the California counties of Orange and Santa Clara.

It also is trying to assist the New Hampshire Attorney General’s Office in a similar investigation over drug makers’ marketing of the powerful prescriptions. However, a state judge recently struck down the contingency fee agreement between the attorney general and Cohen Milstein.

“Clearly, if the CDC issues guidelines that essentially urge states to change prescribers’ practices and to implicitly criticize past prescribing practices, that’s something you would expect Cohen Milstein in its lawsuits around the country against drug companies to tout,” Samp explained. “It’s in the direct financial interest of plaintiffs lawyers to have these CDC guidelines adopted.

“That’s why we think it was a terrible mistake to include people like Jane Ballantyne on its advisory group, when she clearly has an interest in the outcome.”

Andrew Kolodny, a senior scientist at the Heller School for Social Policy and Management at Brandeis University and PROP’s executive director and co-founder, has countered that Ballantyne is “one of the most respected pain specialists in the country,” which is why the CDC asked her to join its expert group.

No doubt in response to the public outcry over the development of its guidelines, the CDC announced in December it planned to publicly post the guidelines and seek comment.

“We received feedback from our partners that a formal public comment period would be helpful, and we are augmenting our process to incorporate a 30-day public comment period into our guideline development,” the agency said in a statement.

The public comment period ended Jan. 13, pushing back the agency’s original release date. The CDC had hoped to release the opioid guidelines in January.

Also in December, the CDC said it would convene the National Center for Injury Prevention and Control’s Board of Scientific Counselors, a federal advisory committee, to review the draft guidelines.

“I would like to think that the CDC’s decision in December to slow things down might have been based, in part, on our complaints,” Samp said. “But they never really corrected the problem.

“It again displays their misunderstanding of what is required by FACA.”

From Legal Newsline: Reach Jessica Karmasek by email at jessica@legalnewsline.com.

Senators Manchin and Braun Are Attempting to Practice Medicine Without a License—And Fighting the Wrong War

https://www.cato.org/blog/senators-manchin-braun-are-attempting-practice-medicine-without-license-fighting-wrong-war

Senator Joe Manchin (D-WV) and Mike Braun (R-IN) are still trying to address the fentanyl and heroin overdose crisis—soon to be joined by a methamphetamine and cocaine overdose crisis—by denying chronic pain patients access to pain relief. They have just introduced a bill they call The FDA Opioid Labeling Accuracy Act, which would “prohibit the Food and Drug Administration (FDA) from allowing opioids to be labeled for intended use of ‘around-the-clock, long-term opioid treatment’ until a study can be completed on the long-term use of opioids.”

Set aside the fact that most pain specialists agree that, in some cases, long-term opioid therapy is all that works for some chronic pain patients. The 2016 guidelines on opioid prescribing put forth by the Centers for Disease Control and Prevention have already been misinterpreted and misapplied by legislators and regulators, leading to forced and rapid tapering off of opioids in many chronic pain patients, causing many to resume lives immobilized by pain, and in many cases, seek relief in the black market or by suicide. It has gotten so bad that the CDC recently issued a “clarification” in April, reminding regulators that the guidelines were only meant to be suggestive, not prescriptive, and did not in any way mean to encourage the rapid tapering of patients on chronic opioids for pain management. Johns Hopkins bioethicist Travis Rieder, PhD delves deeply into this subject and relates his own experiences in his book, In Pain.

What the senators fail to recognize is that patients are not one-size-fits-all. Different patients respond to pain and to pain management differently. Their proposed legislation, if passed, will only serve to exacerbate the unnecessary suffering of patients in pain that the CDC is trying to undue with its guideline clarification.

Meanwhile, they should take a look at the government’s own numbers. The data show there is no correlation between the number of prescriptions written and the incidence of non-medical use of prescription opioids or prescription pain reliever use disorder. And less than 10 percent of opioid-related overdose deaths in 2017 involved prescription pain relievers unaccompanied by other drugs such as cocaine, heroin, alcohol, or fentanyl.

The continued war on patients by politicians and regulators will not get one IV heroin user to take the needle out of their arm. Senators Manchin and Braun need to recognize that the overdose crisis has been on a steady, exponential increase since the 1970s and shows no signs of stopping—and that its ultimate cause is drug prohibition

If they want to get serious about addressing the problem, they should switch their focus to harm reduction. A good way to start would be to repeal the “Crack House” statutes that prevent cities and states from establishing overdose prevention sites called “safe injection facilities.”

Opioid Labeling Bill Drawing Fire from Chronic Pain Advocates

Opioid Labeling Bill Drawing Fire from Chronic Pain Advocates

www.nationalpainreport.com/opioid-labeling-bill-drawing-fire-from-chronic-pain-advocates-8840456.html

A bill introduced by West Virginia Democratic Senator and Indiana Republican Senator is drawing fire from chronic pain patient advocates.

The bill they call The FDA Opioid Labeling Accuracy Act would “prohibit the Food and Drug Administration (FDA) from allowing opioids to be labeled for intended use of ‘around-the-clock, long-term opioid treatment’ until a study can be completed on the long-term use of opioids.”

Jeffrey Singer writing for the Libertarian Cato Institute said, “Senator Joe Manchin (D-WV) and Mike Braun (R-IN) are still trying to address the fentanyl and heroin overdose crisis—soon to be joined by a methamphetamine and cocaine overdose crisis—by denying chronic pain patients access to pain relief.

Meanwhile, he continued, “they should take a look at the government’s own numbers. The data show there is no correlation between the number of prescriptions written and the incidence of non-medical use of prescription opioids or prescription pain reliever use disorder. And less than 10 percent of opioid-related overdose deaths in 2017 involved prescription pain relievers unaccompanied by other drugs such as cocaine, heroin, alcohol, or fentanyl.”

Richard “Red” Lawhern Ph.D. left Senator Manchin’s office an email that in part said.

“Get your head out of a very dark place and withdraw the bill which would deny effective pain relief to patients already in agony. You are trying to ‘solve’ the wrong ‘crisis’ by restricting availability of the only class of therapy that works for the majority of those who suffer severe pain. And you are doing so despite conclusive proof that physicians prescribing to their patients did not cause and are not now sustaining our public health crisis.”

Manchin said in a press release: “I have introduced this bill today with Senator Braun to address how the FDA approves opioid prescriptions for treating different types of pain. Addressing the opioid epidemic has always been my top priority and I will continue to fight for legislation that helps West Virginians and our country fight this epidemic and I look forward to working with my colleagues on both sides of the aisle to pass.”

Read Jeffrey Singer’s entire blog on Cato Institute.

According to Senator Manchin, “The FDA Opioid Labeling Accuracy Act would prohibit opioids from being labeled for intended use to treat long-term chronic pain, except for cancer pain, end-of-life care or when a prescriber has determined that all non-opioid treatments are inadequate or inappropriate.”

Here’s the text of the bill.