“The moral test of a government is how it treats those who are at the dawn of life, the children; those who are in the twilight of life, the aged; and those who are in the shadow of life, the sick and the needy, and the handicapped.” – Hubert Humphrey
passionate pachyderms
Pharmacist Steve steve@steveariens.com 502.938.2414
Some professionals claim to be “experts”; however, few are experts in the entire scope of their chosen field of study. Most likely they will end up being “specialists” in certain subsets of their profession. Either because they have become interested in one or more subsets, or that is where there is a need to provide services.
Has anyone noticed that there are seemingly endless array of personal injury attorneys appearing on TV, offering to sue someone because someone has gotten injured or died?
Most seem to focus on trucking/vehicles accidents, nursing home neglect, and other areas where there is some entity with a “deep pocket” to sue.
I have heard or read from countless chronic pain patients, about them contacting an attorney to sue over patient abuse/neglect/discrimination – and all have been turned down.
They are being turned down because in our legal system, the “value of life” of a person who is handicapped/disabled, elderly, unemployable, retired, is about the same as the value of the family pet… nearly ZERO. Likewise, if a law firm did take such a case, most states have a rather low cap on settlements… To a point where there is no financial upside for the law firm for winning the case.
But the “the times they are a changing”… An increasing number of various healthcare entities are seemingly taking it upon themselves to practice medicine. Some of those entities are insurance companies, PBM’s, large hospital corporations, chain pharmacies and other such entities.
They are creating edicts that their employed prescribers, pharmacists and others are to limit/restrict controlled medications – regardless of what the patient’s personal prescriber deems necessary.
Beside attempting practicing medicine without a license, they are discriminating against a protected class of people under the Americans with Disability Act, Civil Rights Act and numerous other legal issues.
What do these healthcare businesses have in common with the entities that these personal injury attorney normally sue? DEEP POCKETS!!!
Now is the time for chronic pain patients to start contacting law firms and point out to them – EDUCATE THEM… all the patient abuse, neglect and discrimination that is going on at the hands of these corporate entities that are called “healthcare companies” – and individually these companies are harming hundreds, thousands or tens of thousands of chronic pain patients.
With 20 to 30 million intractable chronic pain patients in our country, the total number of patients being affected is really not known. All we know is that whatever the number is today, it is GROWING.
OR… you can keeping contacting President Trump, members of Congress, signing petitions and creating hundreds of Facebook pages… and how has that been working for you?
WASHINGTON D.C. –The Drug Enforcement Agency (DEA) on May 22 issued an internal directive that apparently acknowledges some cannabis products are not currently prohibited under the Controlled Substances Act (CSA) and that specific parts of cannabis plants are not prohibited for use under current policy.
According to the directive, the DEA’s enforcement policy is consistent with a 2004 decision handed down by the U.S. Ninth Circuit Court of Appeals, in Hemp Industries Association v. DEA.
The directive stated:
“Products and materials that are made from the cannabis plant and which fall outside the CSA definition of marijuana (such as sterilized seeds, oil or cake made from the seeds, and mature stalks) are not controlled under the CSA. Such products may accordingly be sold and otherwise distributed throughout the United States without restriction under the CSA or its implementing regulations. The mere presence of cannabinoids is not itself dispositive as to whether a substance is within the scope of the CSA; the dispositive question is whether the substance falls within the CSA definition of marijuana.”
The directive also said that the policy directive did not change the DEA’s current policy toward cannabis extracts and resin.
Cannabis law firms reacted to the directive, which in effect, potentially clears the way through the dense legal grey area for CBD or hemp-based products, and could signal a boon to cannabis/hemp growers and product manufacturers.
Canna Law Blog™ refined the definition of parts of cannabis plants that the DEA has said are exempt for use in product manufacturer. They include:
Mature stalks
Fiber produced from mature stalks
Oil or cake made from seeds
Seeds incapable of germination
The DEA directive also said that “any other compound, manufacture, salt, derivative, mixture, or preparation” created from named plant parts were also not prohibited, though Canna Law pointed out any extracted resin is still considered “marijuana” by the DEA and would be prohibited under the CSA.
The DEA directive went on to essentially say products produced from non-prohibited ingredients were okay for sale in the United States. Products containing THC, the psychoactive compound in cannabis, and products otherwise designated as marijuana by the DEA were still federally prohibited. Non-THC products, however, would not be prohibited. The directive did not directly address hemp or hemp-based products.
“Such products may accordingly be sold and otherwise distributed throughout the United States without restriction under the CSA or its implementing regulations. The mere presence of cannabinoids is not itself dispositive as to whether a substance is within the scope of the CSA; the dispositive question is whether the substance falls within the CSA definition of marijuana,” the directive said.
Lane & Powell’s The Pipeline Blog said, “… The logical and scientific inconsistency puts the DEA and purveyors of CBD goods in a precarious position: how will they determine which CBD products are subject to the CSA and will people really be prosecuted for trafficking a Schedule I controlled substance where the substance is chemically indistinguishable from one that is not prohibited by the CSA?
“We anticipate that at least one outcome will be buyers insisting on statements or warrantees from sellers, and buyer quality control due diligence, that their CBD products contain only excepted marihuana (sic) oil,” Pipeline blog authors Justin E. Hobson & Lewis M. Horowitz added.
Fentanyl manufactured in foreign countries and smuggled into the U.S. poses the greater risk compared to the medication illegally diverted by patients and doctors, according to the Drug Enforcement Administration.
The synthetic opioid is up to 50 times more potent than heroin and 100 times that of morphine, the DEA says. It’s increasingly cut into heroin or sold on its own, sometimes to unsuspecting users.
Fentanyl surpassed heroin as the leading opioid detected in fatal drug overdose cases in Pennsylvania two years ago and continues to rise in prevalence.
The Philadelphia Division of the DEA reports 79 percent of overdose deaths in 2017 involved fentanyl, either included in mixed-drug toxicity fatalities or the outright cause. That’s up from 52 percent in 2016.
In the 12 months through October 2017, no state in the country counted more overdose deaths than Pennsylvania’s 5,535, according to the latest provisional data from the Centers for Disease Control and Prevention. An estimated 68,400 fatal overdoses occurred nationally during the same period. Both estimates are on the rise.
“The supply of fentanyl, as determined by law enforcement seizures and intelligence, continues to rise. Fentanyl production is cheaper than heroin production and Transnational Criminal Organizations are increasing their profit by supplying fentanyl over other drugs,” said Laura Hendrick, field intelligence manager for the DEA’s Philadelphia division.
The DEA reports counterfeit opioids mostly manufactured in China and Mexico, and distributed through an illegal supply chain in the U.S., Canada and Mexico as well as the internet’s dark web. Agents in New York, New Jersey and Pennsylvania seized 200,359 grams of fentanyl in 2017, up from 58,102 grams the year before.
Northumberland County set a new record for overdose deaths in 2017: 30. Of those cases, 18 involved fentanyl in some way. Fentanyl was present in seven of 18 drug deaths occurring in Union County since 2016.
Two defendants in Northumberland and Snyder counties, respectively, have criminal cases pending for the alleged sale of fentanyl in unrelated fatal overdose cases.
“It’s much cheaper and they’re using it as a replacement for heroin. People think they’re buying heroin and they’re buying pure fentanyl,” said Todd Owens, a retired police chief and current Northumberland County deputy sheriff who heads the Northumberland-Montour Drug Task Force.
First responders should be more cautious now — surgical masks, thicker exam gloves — as fentanyl and even deadlier derivatives circulate among users, Owens said. There’ve been several confirmed reports of law enforcement or ambulance personnel overdosing themselves on contact with synthetic opioids dusting an overdose patient’s clothing or skin.
Bob Hare, general manager of Sunbury’s Americus Hose Co., said the company’s responders are on high alert for risks involved with all narcotics, not just fentanyl.
“I think our responders are in danger. People are more violent when on these drugs; needles, you got HIV, hepatitis — all things that play into the fact that make it more dangerous today than it has ever been,” Hare said.
Police continue to make arrests in the Valley for heroin, methamphetamine and the like, particularly in Northumberland County’s coal region. Owens admits the seemingly neverending cycle can wear on law enforcement.
“We arrest one person and two more pop up,” Owens said “It sometimes feels like we’re not winning. It’s frustrating.”
Imagine the terror of being diagnosed with cancer.
Your doctor writes a prescription that you pray will save your life. You go to the hospital or oncology clinic’s in-house pharmacy. The medicine is right there on the shelf, but you’re told the only way your insurance will cover your medication, which might cost $10,000 or more per month, is if you get it through the mail.
So, you go home empty-handed and wait. If you’re lucky, the medicine will arrive in just a couple of days. But it could be up to a month before delivery of the drugs.
Uncounted numbers of Ohio cancer patients don’t have to imagine this dilemma. They have experienced it because health insurers and the pharmacy benefit managers hired by insurers dictate it.
They require that prescriptions be filled at mail-order pharmacies. These are often owned by the pharmacy benefit managers rather than allowing patients to get the drugs immediately by going down the hall at the James Cancer Hospital at Ohio State University, Cleveland Clinic, Mount Carmel Health System or Nationwide Children’s Hospital.
“Rather than filling a prescription I have on the shelf, I have to tell the patient they have to go home and wait for a phone call from the pharmacy and arrange having this medicine sent to you,” said Christine Pfaff, pharmacist for the Zangmeister Center, a Columbus cancer-treatment facility. “I can’t give it to you today. Your insurance won’t allow it.”
Health-care providers say the goal is to start treatment as soon as possible, because delays can be detrimental to their patients’ health.
“New diagnosis, with medications as good as we have today, speed to therapy is important. Even a few days can make a difference,” said Curt Passafume, vice president of pharmacy services for Ohio Health.
Josh Cox says that CVS will go pretty far in trying to wrest the lucrative business of filling cancer prescriptions away from oncology clinics.
The company, which operates a retail pharmacy chain and manages prescription-drug payments for millions of Americans, has long sent unsolicited faxes to cancer doctors, using confidential patient information, in an attempt to steer business to its own pharmacies, said Cox, pharmacy director for the Dayton Physicians Network.
CVS says that it does not engage in deceptive practices.
But two weeks ago, Cox said, the company took things to a whole new level when a representative called and told Cox that he would be breaking the law if he didn’t transfer a particular patient’s prescription to CVS’s mail-order pharmacy. Cox said that claim was false.
And he would know. In addition to being pharmacy operations director for a large oncology practice, Cox sits on the Ohio State Board of Pharmacy.
“I was told it was against the law for our pharmacy to fill the prescription, which was very disturbing to me, because not only is that certainly untrue — there are no federal or state of local laws that dictate where a patient can get their prescription — but it took the whole trolling of prescriptions to a whole new level,” Cox said.
CVS has been accused by some pharmacists and lawmakers of using its dominance as Ohio Medicaid’s leading pharmacy-benefit manger to cut reimbursements to competing retail pharmacies and send letters offering to buy them out.
Pharmacy benefit managers are hired by insurers or employers to negotiate prices and rebates with drug makers, decide which medications are covered, and set rates paid to pharmacies.
Ohio pharmacists also say that CVS uses its access to Medicare patients’ information to steer them to its own mail-order and retail pharmacies. Now it and the other dominant PBMs also are being accused by patients and hospital administrators of forcing cancer patients into the PBM’s own mail-order pharmacies, leading to confusion and delays in getting expensive, life-saving drugs, critics say.
On Friday, CVS defended its outreach and its other business practices.
“It is not our policy or practice to mislead or intimidate patients or providers,” spokesman Mike DeAngelis said in an email. “It is common for CVS Caremark to fax prior authorizations and refill requests to providers. A patient’s specialty prescriptions may be moved to CVS Specialty if a client has switched to a preferred or exclusive network when making a change to their plan design. Patients are notified in advance if their plan sponsor chooses to make such a change.”
Cox found the company’s behavior to be unacceptable.
“It was deeply disappointing to me that the process of trying to acquire business, so to speak, had devolved into intimidation tactics among pharmacies,” Cox said.
This video is not only about the appalling coverage by CBS News but all major news outlets. I could just as easily of named Fox News, the Washington Post or even Andrea McCarren of WUSA Channel 9, Washington DC (another CBS affiliate) who has now blocked me on Tweeter for requesting her assistance in exposing these genocidal policies. Sadly they all REFUSE to contact me even after hundreds of emails, Tweets & even phone calls. America needs to know the truth. President Trump needs to know before he can help. Who among you are willing to spread the horror stories from coast to coast? Remember; just one second! One accident. One diagnosis. In just one second any of you can join us as the 100 million forgotten Americans left to suffer cruel and inhumane torture daily. Robert D. Rose Jr. BSW, MEd. USMC Semper Fidelis
A long-awaited report from the President’s Commission on Combating Drug Addiction and the Opioid Crisis, with strategies to combat it, was just issued by The White House. The document is over 130 pages long and consists of 56 recommendations designed to get a handle on what should more accurately be called “the fentanyl crisis.”
Some of the recommendations are no-brainers, such as better training of emergency personnel in the use of Narcan (Naloxone) to block the effects of opioids, expansion of electronic record keeping, and fast-tracking technological alternatives that would treat pain without the downside of opioids.
But some of the recommendations are controversial; some are good and others are terrible. Let’s grade a few of the recommendations that may have the greatest impact – good or bad – on pain patients and addicts, the groups with the most to gain or lose. If you have read it as well, you can add your own in the comments section.
RECOMMENDATION # 7 – ONE-SIZE-FITS-NONE
“The Commission recommends that HHS coordinate the development of a national curriculum and standard of care for opioid prescribers. An updated set of guidelines for prescription pain medications should be established by an expert committee composed of various specialty practices to supplement the CDC guideline that is specifically targeted to primary care physicians.”
As I have written before, it is impossible to establish standards of care that will apply to the general population, especially with regard to opioid drugs. Standardized doses will fail because they do not account for two critical variables. One is the large variation in patient weight. A 100-pound woman will have a very different response to set opioid dose than that of a 350-pound man, based on size alone. But size is only one variable. Metabolism is another. This already-impossible job of determining a standard drug dose or regimen for the public becomes even “more impossible” when the difference in opioid metabolism is included.
Some people, independent of weight, are much more efficient in metabolizing opioids because of their liver oxidase enzymes. Can government identify a “standard dose” that provides the same pharmacological response in a 350-pound man who is a slow metabolizer, as it does in a 100-pound woman who is fast metabolizer? No, it can’t because the differences in metabolism between two people can be as large as 15-times.
When both these factors are taken together it becomes obvious why a fixed-dose approach to a diverse will fail. It may be easy for the government to establish a maximum dose of a drug, but this number is not only a guess but a poor one at that.
Grade: F
RECOMMENDATION # 10- EDUCATING DOCTORS WHO DON’T NEED TO BE EDUCATED
“Recommends the Administration work with Congress to amend the Controlled Substances Act to allow the DEA to require that all prescribers desiring to be relicensed to prescribe opioids show participation in an approved continuing medical education program on opioid prescribing.”
On the surface, this may seem like a fine idea, but it is really a mixed bag. While a few physicians may benefit from more training in opioid prescribing, this recommendation suggests that doctors were to blame for today’s crisis and that “educating” them (1) will help reverse the harm done. This is false. Although there are pill mill doctors who did enormous damage, the overwhelming majority of doctors have not. The fact that pain patients become addicted only a very small percentage of the time (about 1%) clearly demonstrates that physicians who were caring for their patients ethically and responsibly were helping patients, not harming them.
There is a “blame the doctor” mentality built into this recommendation, which is unfair. Ethical doctors did not create today’s fentanyl epidemic. A few unethical doctors, and people who use opioids to get high did.
GRADE: C
RECOMMENDATION # 11- PHARMACISTS CAN OVERRULE DOCTORS
“The Commission recommends that HHS, DOJ/DEA, ONDCP, and pharmacy associations train pharmacists on best practices to evaluate the legitimacy of opioid prescriptions, and not penalize pharmacists for denying inappropriate prescriptions.”
Recently, CVS took a “bold,” but atrocious step of establishing restrictions that limit the dose, number of days of the prescription, and even the type of drug (time release vs immediate release). (See: CVS’s Transparent Opioid PR Stunt). This will mean that the pharmacist will have the power to overrule a physician.
This is wrong on many levels. Pharmacists should (and do) consult with physicians when there is a question about a drug or its dose, or when it might be dangerous when taken with another drug, but pharmacists cannot be permitted to unilaterally overrule the wishes of the physician. It is not their job to do so.
Grade: F
RECOMMENDATION # 17- DISPOSING OF UNUSED OPIOIDS
“The Commission recommends community-based stakeholders utilize Take Back Day to inform the public about drug screening and treatment services. The Commission encourages more hospitals/clinics and retail pharmacies to become year-round authorized collectors and explore the use of drug deactivation bags.”
In a perfect world (even sane) world, disposing of unused opioids would be entirely appropriate. Whenever excess pills are kept around there is always a chance that children or (more likely teens) will get their hands on them, so it is better not to have them lying around.
GRADE (in a perfect world): A
But, we are not in a perfect world; we are in the middle of a war on pain medications, which is really a war on pain patients. If you are counting on getting some Vicodin when you really need it, for example, a toothache or a migraine headache, you will probably be seriously disappointed. The opioid jihad, which is aimed at persecuting pain patients will touch all of us at some point in our lives. It is inevitable.
My personal opinion: You have to be out of your mind to give back a single pill. Instead store them safely, because at some point they will come in mighty handy. (See the article that my colleague Alex Berezow and I wrote for the Boston Globe website STAT: “Why we are hoarding our opioid pills.”) You may be less likely to return them.
GRADE (in the real world): D
RECOMMENDATION # 23- ENHANCED CRIMINAL PENALTIES FOR FENTANYL TRAFFICKING AND SALE
The harsh enforcement of drug laws, (e.g.’ The Rockefeller Laws’) which have resulted in absurdly lengthy prison sentences for people who were caught selling marijuana and other illegal drugs, has now been recognized as an abject failure. Prisons are full of non-violent offenders, while the flow of drugs continued unabated.
Except it is different this time. Fentanyl is both a drug and a murder weapon; there has never been a drug like it. As it continues to replace heroin (2), it is almost inevitable that “heroin” addicts will eventually die from an accidental fentanyl overdose. It is perfectly reasonable to apply severe penalties to people who knowingly are involved in trafficking fentanyl.
That said, it is unlikely that even the most fervent prosecution of dealers or traffickers will stop the deaths from overdoses. At best it will slow them.
GRADE: B
RECOMMENDATION # 19: FINANCIAL INCENTIVES TO DISCOURAGE PROPER MEDICAL CARE
“The Commission recommends CMS review and modify rate-setting policies that discourage the use of non-opioid treatments for pain, such as certain bundled payments that make alternative treatment options cost prohibitive for hospitals and doctors, particularly those options for treating immediate post-surgical pain.”
Of the 56 recommendations, this one may be the worst. If doctors and hospitals are incentivized to avoid giving patients the opioid pain medications that they need after surgery, be prepared for a world of suffering. This is not to say that viable alternatives are not sometimes available, such as nerve blocks or the use of long-acting local anesthetics in repaired wounds. (See: Surviving Post-Op Pain Without Opioids, Thanks To Chemistry). But the assumption that a few days of morphine or Percocet for post-surgical pain will lead to addiction is ludicrous. If hospitals will make more money giving post-op patients Tylenol (which doesn’t even work, See: Tylenol Isn’t So Safe, But At Least It Works, Right?) instead of something stronger, surgical wards are going to become very noisy places. From patients screaming in pain because the Tylenol did nothing.
GRADE: F-
RECOMMENDATION: KEEP FENTANYL OUT OF THE US
“Fentanyl defies detection at our borders, as the small quantities involved for psychoactivity of fentanyl and fentanyl analogs challenge Customs and Border Protection, USPS, and express consignment carriers’ ability to detect and interdict. We are miserably losing this fight to prevent fentanyl from entering our country and killing our citizens. We are losing this fight predominately through China. This must become a top-tier diplomatic issue with the Chinese.”
Of all the recommendations in the Commission’s report, this may be the most important, but it won’t be easy. By being less than vigilant about illegal fentanyl manufacturing, the Chinese government has been, in effect, waging a pharmacological war against the US. But there are signs that this may be changing. As I wrote last month, two large fentanyl factories in China were shut down and the owners indicted. (See: How Chinese Organic Chemists Get Away With Murder – Literally). The Chinese must understand that it is in their best interest to put a stop to this one-sided war.
GRADE: A
CONCLUSION:
The Commission’s report is a mixed bag. Many of the recommendations deal with funding initiatives, a topic I have not included. Many are common sense and noncontroversial. But the recommendations I have covered are controversial and will have a great impact on pain patients. Some are harmful in that they reinforce the false narrative about pain patients becoming addicted, further inserting government into the already-growing gap between patients and physicians, and creating financial incentives that will result in bad medicine and more suffering. On the other hand, the report does show a glimmer of understanding about what the real problem is (and has always been)—heroin and fentanyl—and concrete steps have been proposed to address this. Because without identifying the real problem, all “solutions” will be misguided and ultimately harmful. This is a good start.
NOTES:
(1) Why is the Orwellian-sounding “re-education” limited to doctors who prescribe opioids? Why not antidepressants, antibiotics, ADHD drugs, or sedatives?
(2) There is no longer any doubt what is killing Americans. It’s fentanyl, not pills. A recent DEA report revealed that of the drugs seized and analyzed by the agency, fentanyl was identified 65% of the time and furanyl fentanyl (even worse) 9% of the time.
Yes, three-quarters of the drugs accounted for by the agency were deadly poisons, yet we worry about how many days of pain medication can be prescribed to surgical patients. Insane.
HARRISBURG, Pa. (WHTM) – Susquehanna Township EMS responds to a handful of medical calls every day.
First responders are often responding to pain related issues, which has become a difficult condition to treat because of the opioid crisis. Now they have a new pain reliever that’s less harmful than opioids.
“What we’re used to using is an opioid, a morphine or fentanyl. What that does is it helps reduce the messages for pain sent to the brain. And what this drug is going to do is actually treat at the site of the pain,” Capt. Daniel Tempel said.
The drug is called ketorolac, also known as Toradol. The state Department of Health recently approved EMS agencies to carry the non-addictive pain drug.
First responders say ketorolac is the better option for responding to certain types of pain; it’s more effective with fewer side effects.
“It gives us the option to provide someone that does have an opioid addiction some type of pain management. It also prevents getting someone started on that opioid,” Tempel said.
EMTs across the state can begin using ketorolac on July 1.
Ketorolac is classified as a NSAID.. .like Aspirin, Aleve, Motrin…BUT… has a VERY LARGE FDA BLACK BOX WARNING attached to this medication… and now they are allowing EMT to administer this medication to people in which they have a very limited medical background and the most they know about the pt is that they are in PAIN. This may end up being a situation where the CURE IS WORSE THAN THE DISEASE.
Politicians and journalists often tell a story about greedy pharmaceutical companies that turned doctors into dealers and patients into addicts. And now, we’re told, tens of thousands of Americans are dying of overdoses every year because of government inaction.
If this is truly an epidemic, the diagnosis is wrong in a few major ways. And the cure prescribed by the government is making the disease worse.
Pain and Suffering
Dr. Forest Tennant is one of the last doctors in America willing to treat pain patients using high doses of opioid painkillers. He operates out of a strip mall in West Covina, California. And he’s contacted by patients from all over the country on a daily basis, pleading with him to treat them because nobody else will.
But in a matter of months, thanks in part to increased pressure in the government’s war on opioids, he may be closing his clinic’s doors, which have been open since 1975.
When Reason did a story on Tennant’s clinic in 2017, his patients spoke of how government restrictions on opioid use were causing legitimate pain patients to suffer needlessly. Four months after we ran that story, the DEA raided Tennant’s clinic and home. The search warrant accused him of overprescribing medication and accepting payoffs from the pharmaceutical company INSYS. Tennant has earned speaking fees from the company as recently as 2015, which he says is standard practice. And his nonprofit clinic regularly operates at a loss, according to financial statements submitted to the Department of Justice.
“I think the government is trying to kill me and every one of [Tennant’s] patients,” said Gary Snook, a resident of Montana, when asked about the raid on Tennant’s clinic. Snook, who suffers from chronic pain resulting from back surgery complications, turned to Tennant when he couldn’t find adequate pain treatment from a local physician.
“We have no place to run,” says Snook.
Last year, the Centers for Disease Control recommended new opioid prescription guidelines, with a maximum dosage of 90 morphine-milligram equivalents (MME) a day. Although the guidelines were supposed to be voluntary, Tennant says most physicians have begun to treat them as mandatory. Several states have adopted legislation that mirrors the federal recommendations.
“I do not know of physicians who will be willing to prescribe high-dose opioids anymore,” says Tennant.
This situation has put a target on the back of doctors who don’t follow the guidelines, and Tennant says the pressure that the guidelines have put on him are a major reason that he’s decided to wind down his practice and focus on tapering his patients down below 90 MME so that they can find other doctors to treat them once he retires.
But he maintains that some patients exhibit genetic variations that require them to take unusually high doses of opioids to achieve pain relief.
“I don’t know how those people are going to get down to 90,” says Tennant. “There has been propaganda—and it’s pure propaganda—that you can just stop opioids. No need to taper them. Just stop. And we’re going to have some patients commit suicide.”
Prohibition, Then and Now
Government officials like Attorney General Jeff Sessions and former New Jersey governor Chris Christie, who heads the President’s Commission on Combating Drug Addiction and the Opioid Crisis, have repeatedly blamed the problem on doctors overprescribing opioids to their patients and turning them into addicts.
“It’s not starting on our street corners. It’s starting in our doctors’ offices and hospitals,” Christie told CNN’s Jake Tapper in July 2017.
But the story isn’t quite so straightforward. Several studies, including a recent one out of Harvard, pegs opioid abuse among postsurgical patients at less than one percent. Estimates about abuse among chronic pain patients vary, with the high end being a little less than eight percent.
“Most policy makers have bought into this idea that we doctors prescribe opioids to our patients, who then rapidly become drug addicts,” says Jeffrey Singer, a Phoenix-based general surgeon and policy analyst (and a donor to Reason Foundation, the nonprofit that publishes this website). “All of the evidence suggests that this is not the case.
Singer says it’s a myth that most nonmedical users start on pills prescribed to them by a doctor. Instead, they more often borrow, buy, or take them from a friend or family member with leftover pills. The DEA calls it “diversion.” A 2014 analysis of data from the National Survey on Drug Use and Health (NSDUH) confirms that most nonmedical pain pill users obtain their pills via diversion, not directly from a physician.
In many ways, the story of the opioid overdose crisis begins with the introduction of OxyContin to the US market in 1995. It promptly became the pill of choice for nonmedical street users of opioids.
Purdue Pharma, the manufacturer of OxyContin, was aware of its popularity as a street drug, which it allegedly worked to conceal. Yet the company also created abuse-resistant formulations (ADFs), which are uncrushable and can’t be liquefied. By doing so, the company was able to extend the drug’s patent. With encouragement from the Food and Drug Administration, Purdue soon made all OxyContin pills uncrushable. Singer says policies of this sort have profound unintended consequences.
“The only thing [ADFs] have done is to make nonmedical users switch over to something other than [pain pills], and most of the time it’s been heroin,” says Singer.
Singer compares ADFs to attempts by the federal government to control alcohol consumption during Prohibition. The government ordered the “denaturing” of industrial alcohol through the addition of unpalatable chemicals. But it’s hard to stop determined consumers from getting what they want, and people kept drinking the denatured alcohol. So the government went a step further by adding poison to the alcohol, a move that likely resulted in thousands of deaths.
Seymour Lowman, the assistant U.S. treasury secretary partially responsible for overseeing alcohol prohibition, even said that if drunks were “dying off fast from poison ‘hooch'” then “a good job will have been done” if it meant a more sober America. Singer doesn’t think that modern government officials have the same attitude but argues that the effects are quite similar.
“If [policy makers] step back and think about what they’re doing by promoting abuse-deterrent formulations of opioids, they’re in effect doing to same thing that alcohol prohibition people did. They’re driving people to much more deadly, dangerous substances,” says Singer.
A June 2017 National Bureau of Economic Research paper found that “there appears to have been one-for-one substitution of heroin deaths for opioid deaths. Thus it appears that the intent behind the abuse-deterrent reformulation of OxyContin was completely undone by changes in consumer behavior.”
The Nature of Addiction
“The focus on prescription pain killers is especially misguided now that the vast majority of opioid-related deaths actually involve illegally produced drugs,” says Reason’s Jacob Sullum.
Sullum been writing about the suffering caused by restricting access to pain medication for 21 years. His April cover feature for Reason magazine examines the myths underlying the government’s response to the opioid overdose problem. He says the misguided focus on the supply of opioids is a proven failure but that politicians continue to do it because it’s much simpler than dealing with the complicated nature of addiction.
Jillian Monda is an Ohio-based bartender and photographer who struggled with and overcame an addiction to heroin several years ago. She says her boyfriend introduced her to heroin and that she took to it because it allowed her to turn off her mind and forget about a recent sexual assault she experienced and keep her obsessive-compulsive disorder under control.
“Heroin is really good at making you not feel anything at all,” says Monda. “The big unifying factor [among users I knew] was that everyone had some kind of mental problem or thing they were trying to avoid…and rather than getting proper psychiatric care for that, they were doing heroin.”
Victims of trauma like Monda, or people with mental illnesses who are self-medicating, are far more likely to develop an opioid addiction than are pain patients. To deal with these complex psychological and social problems, Sullum says a more nuanced approach than supply-side prohibition is needed.
Harm Reduction
Cities like San Francisco and Oakland, California are at the forefront of what’s called the “harm reduction” movement in America.
“Harm reduction is, at its core, a pragmatic way of looking at all risk-taking behavior,” says Eliza Wheeler of the Harm Reduction Coalition, a policy organization that advocates for harm reduction measures such as needle exchanges, many of which operate in the Bay Area. These exchanges allow heroin users to turn in dirty needles and obtain clean ones to prevent the spread of diseases. They also offer medications like naloxone, which can save lives by reversing the effects of an opioid overdose.
And now San Francisco’s Department of Public Health is preparing to convert some needle exchanges into “safe consumption sites,” where drug users can shoot up, snort, or smoke their drugs under supervision.
San Francisco would be the first American city to allow safe consumption sites, but Vancouver has already allowed the practice for years and the U.S. Surgeon General recently announced support for the idea in the United States.
“The problem with implementation [of harm reduction measures] is not lack of evidence that it works,” says Wheeler. “What we’re battling is a moral discomfort.”
There’s an even more radical approach than harm reduction. In response to its own overdose crisis, Portugal decriminalized all drugs in 2001. The country saw rates of overdose deaths, disease transmission, and overall use fall. Portugal’s drug overdose rates are now approximately six deaths per million people. In the U.S., it’s 312 per million.
Meanwhile, the DEA investigation of Dr. Tennant is still ongoing. He hopes to find another doctor to take over his clinic. If not, he’ll close its doors by the end of June, and his patients—already turned away by their hometown doctors—will need to find someone else to care for them.
“When people get hopeless is when they think about suicide,” says Tennant. “And so we need to give people some hope. If nothing else, let them know that somebody cares.”
Sullum says that if the government doesn’t change its approach to opioids soon, we can expect more of the same results.
“The strategy the government seems to be pursuing is one of harm maximization,” says Sullum. “If it continues to do that, at the expense of harm reduction policies, you’re not going to see a decrease in opioid-related deaths—and in fact, they may continue to go up.”
CORRECTION: This story originally stated that the Harm Reduction Coalition “funds and oversees” needle exchanges. Though the Harm Reduction Coalition does provide support in the form of coordinating the distribution of naloxone, it is a policy organization and doesn’t directly fund or oversee the operation of exchanges. The text has been edited to correct the error.
Doctors have reduced their prescribing of opioid painkillers for the fifth year in a row, the nation’s largest physician group announced.
The American Medical Association found that between 2013 and 2017, the number of opioid prescriptions fell by more than 55 million, a 22.2 percent decrease.
Doctors also became more likely to use a state database that tracks when patients previously have been prescribed opioids, called the prescription drug monitoring program. The database allows doctors to make sure that their patients aren’t getting multiple prescriptions from different doctors to sell or abuse them and to decline the prescription when they suspect abuse.
The findings were detailed in a report from the AMA, showing that in 2017 doctors and other medical providers used the databases more than 300.4 million times, a 121 percent increase from 2016.
More than 42,000 people died of opioid overdoses in 2016. That includes prescription painkillers, but more often the overdoses are the result of cheaper and more easily available alternatives such as heroin and fentanyl. Many of the addictions to illegal opioids begin after an initial doctor prescription to painkillers such as OxyContin or Vicodin.
The new report also shows that doctor involvement in drug treatment and overdose reversals increased as well.
Doctors increased their prescriptions of naloxone, a drug used to reverse an opioid overdose, from 3,500 to 8,000 a week. The upward trend appears to be continuing in 2018, with weekly prescriptions at 11,600. A growing number of states require doctors to prescribe naloxone if their patients have a history of drug abuse or if they provide patients with a high amount of prescription painkillers.
More than 50,000 doctors as of May 2018 have become certified to prescribe buprenorphine, a drug that helps reduce withdrawal symptoms for people with addictions. That marks a 42.4 percent increase from a year ago.
Doctors need a special certification by law because the drug can also be abused, though lawmakers and advocacy groups hope to loosen restrictions so that more healthcare providers will be able to give the drug to patients. The AMA made the recommendation as a way to continue progress against the opioid crisis.
“What is needed now is a concerted effort to greatly expand access to high-quality care for pain and for substance use disorders,”
said Dr. Patrice Harris, chairwoman of the AMA’s Opioid Task Force. “Unless and until we do that, this epidemic will not end.”
