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NIDAMED has just updated its webpage, streamlining the content into categories such as, For Your Practice, Health Professions Education, and Patient Resources.
Content incudes resources on:
Please encourage your members to visit the updated webpage and browse for resources to help them fight drug abuse and addiction—and ultimately improve individual, community, and public health.
If you have suggestions for improvements to the NIDAMED webpage, please contact the NIDAMED coordinator, Michelle Corbin: firstname.lastname@example.org.
As a partner working to fight opioid and heroin abuse, Senator Baldwin wanted to make sure you were aware of new federal grant funding for critical treatment initiatives to help address this epidemic:
Improving Access to Overdose Treatment
The Substance Abuse and Mental Health Services Administration (SAMHSA), Center for Substance Abuse Prevention (CSAP), is accepting applications for fiscal year (FY) 2017 Improving Access to Overdose Treatment (Short Title: OD Treatment Access). SAMHSA will award OD Treatment Access funds to a Federally Qualified Health Center (FQHC), Opioid Treatment Program, or practitioner who has a waiver to prescribe buprenorphine to expand access to Food and Drug Administration (FDA)-approved drugs or devices for emergency treatment of known or suspected opioid overdose. The grantee will partner with other prescribers at the community level to develop best practices for prescribing and co-prescribing FDA-approved overdose reversal drugs. Click here for more information regarding OD Treatment Access grants and note applications are due by July 31, 2017.
Rural Health Opioid Program
The Health Resources and Services Administration is currently accepting applications for the Rural Health Opioid Program (RHOP), which seeks to promote rural health care services outreach by expanding the delivery of opioid related health care services to rural communities. The program will reduce the morbidity and mortality related to opioid overdoses in rural communities through the development of broad community consortiums to prepare individuals with opioid-use disorder (OUD) to start treatment, implement care coordination practices to organize patient care activities, and support individuals in recovery through the enhancement of behavioral counselling and peer support activities. The program supports three years of funding. Click here for more information regarding the Rural Health Opioid Program and note applications are due by July 21, 2017.
First Responders – Comprehensive Addiction and Recovery Act Cooperative Agreement
The Substance Abuse and Mental Health Services Administration (SAMHSA), Center for Substance Abuse Prevention (CSAP), is now accepting applications for fiscal year (FY) 2017 First Responders-Comprehensive Addiction and Recovery Act (FR-CARA) Cooperative Agreements. The purpose of this program is to allow first responders and members of other key community sectors to administer a drug or device approved or cleared under the Federal Food, Drug, and Cosmetic Act for emergency treatment of known or suspected opioid overdose. Click here for more information regarding FR-CARA grants and note applications are due by July 31, 2017.
If you would like to request a letter of support from Senator Baldwin to include with your application(s), please contact Grants & Special Projects staff in the Senator’s Madison office. You can also visit Senator Baldwin’s website to learn more about additional federal resources and funding opportunities that may be available to your community.
Sincerely, The Office of US Senator Tammy Baldwin
The Rhode Island health insurance commissioner says the state's four major health insurers will end a practice that has been criticized for delaying treatment for patients with opioid dependency disorders.
Read full article here.
Communities in northeast Ohio are affected daily by the rising incidence of opioid overdoses. The Cuyahoga Medical Examiner’s Office reported at least 61 heroin- or fentanyl-related deaths in a single month earlier this year. The alarming death rate brings the gravity of the situation home to physicians in the area.
“There’s no more playing around with this,” said Jason Jerry, MD, until recently an addiction psychiatrist at the Cleveland Clinic’s Alcohol and Drug Recovery Center. Dr. Jerry, now with FirstHealth Moore Regional Hospital in Pinehurst, N.C., is a recognized leader in efforts to curb opioid abuse and misuse, and he and his colleagues use medication-assisted treatment (MAT) to help patients with substance-use disorders through recovery. They have cared for patients with opioid substance issues since the mid-1990s.
Dr. Jerry told AMA Wire® that it is important for medical students and residents to think about the state of the opioid crisis and consider joining the specialty of addiction medicine “because there is no end in sight. ... We’re trying to teach the next wave so they can have an impact going forward.”
To that end, Dr. Jerry and other physicians at the center were joined on their rounds by medical residents, who rotate on the center’s inpatient detox unit. He served as a mentor to one resident each year, in addition to teaching medical students interested in addiction medicine.
Dr. Jerry offers this advice based on what he taught those who rounded with him every day in the detox unit. It includes:
“I think we need to get away from writing blanket prescriptions for one-month supplies because what’s happening is people are abusing them, or we’re having supplies of opioids that are sitting idle in patient’s medicine cabinets at home that are getting swiped by loved ones or by people that visit their houses,” Dr. Jerry said. “It’s a big source of diversion so I think that’s one of the major steps that we can make in terms of moving in the right direction.”
Before they leave the Cleveland Clinic, many patients also benefit from Project DAWN, an opioid overdose education and naloxone-distribution program that was founded by Cleveland emergency physician Joan Papp, MD, an assistant professor at Case Western Reserve University’s medical school.
“Many have already enrolled in DAWN and so they have their naloxone kits,” Dr. Jerry said. “They’re readily available if you’re around the Cleveland area.”
The AMA Opioid Task Force has been working for several years to increase access to naloxone, the life-saving opioid overdose antidote, increase access to MAT for patients struggling with substance-use disorder, encourage physicians to register for and use prescription drug monitoring programs (PDMP), reduce the stigma of substance-use disorder and educate patients and physicians on the matter.
Two new educational modules on what every physician needs to know and on chronic pain management are available in the AMA Education Center. They can help physicians in their efforts to battle against opioid abuse and misuse in their practices.
The American Board of Preventive Medicine now offers physicians who are certified by a member board of the American Board of Medical Specialties the opportunity to become certified in the subspecialty of addiction medicine. During the next five years following the date of the first exam, physicians are eligible to become board certified in addiction medicine without completing an addiction-medicine fellowship.
Physicians interested in taking the exam and becoming certified in addiction medicine need to complete the application on the ABPM website by June 30. The exam takes place in several locations Oct. 16–28. Learn more.
Journal of Addiction Medicine - Read more
Objectives: We sought to determine sex-specific associations between experiences of physical pain, pain management, and frequency of nonmedical prescription opioid (NMPO) use among young adults.
Methods: Among participants enrolled in the Rhode Island Young Adult Prescription Drug Study, we identified associations between physical pain in the past 6 months, pain history, pain management, polysubstance use, and weekly NMPO use. In sex-specific models, independent correlates of weekly NMPO use were identified via modified stepwise Poisson regression.
Results: Of 199 participants, the mean age was 24.6, and 65.3% were male. The racial composition was 16.6% black, 60.8% white, and 22.1% mixed or other race. A total of 119 (59.8%) participants reported weekly or greater NMPO use. The majority of male (86.2%) and female (84.1%) participants reported ever experiencing severe pain. A majority of males (72.3%) and females (81.2%) reported that they engaged in NMPO use to treat their physical pain, and one-quarter (26.9%) of males and one-third (36.2%) of females had been denied a prescription from a doctor to treat severe pain. Among males, frequent NMPO use was independently associated with white race (P < 0.001) and reporting greater physical pain (P = 0.002). Among females, older age (P = 0.002) and monthly or greater nonmedical benzodiazepine use (P = 0.001) were independently associated with weekly NMPO use.
Conclusions: Among young men in Rhode Island, physical pain may be related to frequent NMPO use. More research is needed to identify sex-specific, pain-related factors that are linked with NMPO use to improve harm reduction and pain management interventions.
(C) 2017 American Society of Addiction Medicine
WI Health News
The Controlled Substances Board modified rules regarding the use of the Prescription Drug Monitoring Program to align with a recently approved change to the state budget, but rejected other proposals from health systems and doctors.
The proposed rule and emergency rule involve the implementation of laws that recently went into effect, including a requirement that prescribers review patient records before prescribing a controlled substance.
The board approved changes Friday clarifying that prescribers can delegate review of a patient's record and that the board would only refer prescribers to an appropriate law enforcement agency if it determines a criminal violation occurred.
Both changes square with a motion approved by the Legislature's Joint Finance Committee last week. They were also requested by the Wisconsin Medical Society and Wisconsin Hospital Association at the public hearing.
"There's always room for improvement," Mark Grapentine, the society's vice president of government relations, told board members.
But the board pushed back against recommendations to provide more specifics on what has to be contained in a record to satisfy the review requirement.
Matthew Stanford, the hospital association's general counsel, said they've heard from members who are concerned there isn't a list of information that is required to be in a record that has to be reviewed.
"It's both an issue of regulatory clarity but then where that ultimately becomes a bigger issue is when you start thinking about integrations and options for integration," he said. Having more clarity could help electronic health record vendors connect with the program, he said.
Board member Dr. Tim Westlake said that, as a prescriber, he didn't want "a checklist of all this."
"I could see this as becoming burdensome," he said. The board decided not to change its current definition of review.
Other speakers at the public hearing raised concerns about the integration of electronic health records with the program.
Wisconsin Statewide Health Information Network CEO Joe Kachelski said the process to connect with the updated Prescription Drug Monitoring Program, which was launched in January, has been "a little bit bumpy."
"Our validation processes have revealed some substantial data quality completeness issues," he said. "Although we have worked through many of them, some of them do remain."
The board requested the Department of Safety and Professional Services work on ways to better facilitate health system and user adoption of the new version of the program.
May 12, Wisconsin Health News
The state added an additional opioid-addiction treatment to its preferred list for Medicaid patients Wednesday, after law enforcement and legislators raised concerns about a current preferred drug that they say is being smuggled into jails.
The Medicaid Pharmacy Prior Authorization Advisory Committee classified the medication Zubsolv, which comes in a tablet, as a preferred drug for treating opioids. The committee also kept Suboxone, a film strip that dissolves under the tongue, on its preferred list.
In April, two associations representing sheriffs in Wisconsin wrote Medicaid Director Michael Heifetz that the "thin and malleable" strips have become "leading contraband" in jail, as inmates can abuse the drug. The associations suspected Medicaid-eligible families were "partially responsible" given jail demographics.
Rachel Currans-Henry, director of the Bureau of Benefits Management in the department's Division of Medicaid Services, said Wednesday that adding Zubsolv gives providers and members another option.
"There is an increased cost of this for the department," she said. "But in the interest of ensuring that we are addressing a public health epidemic in the state and the country, we believe that the benefits outweigh the costs."
Heifetz said they have "to balance all these things."
"We cannot just look through one lens," he said. "We have to look through a number of lenses, the taxpayer lens, the clinical lens and in this situation the law enforcement lens as well, which is a rarity for us."
Marquette County Sheriff Kim Gaffney, president of the Badger State Sheriffs' Association, hoped the decision would make a difference.
"On behalf of sheriffs across the state, we are hopeful that more opioid treatment options in the Medicaid program will reduce the prevalence of film strips and them being smuggled into jails," he said in a statement.
At a public hearing before the committee took its vote, Assembly Committee on Corrections Chair Mike Schraa, R-Oshkosh, demonstrated how the strip could be concealed under a stamp.
The strip is easier to "sneak into" jails than pills, cigarettes and other contraband, sometimes coming in through children's artwork or Bibles, he said.
"There's no good reason for the government to fuel the black market with this product," he said.
He was also concerned because Wisconsin Attorney General Brad Schimel has joined more than 40 other states to sue Indivior, the maker of Suboxone, alleging that the company switched from a tablet to a film to ensure patent protection and discourage the development of generics.
William Mullen, managed care clinical advisor for medical affairs at Indivior, encouraged the committee to "open the formulary for all" medication-assisted treatments approved by the Food and Drug Administration for opioid addiction.
That would allow doctors to choose what works best for their patients, he said. But Mullen cautioned that all drugs that contain buprenorphine, like Suboxone and Zubsolv, have a potential for abuse, misuse and diversion.
"The company will continue work with the FDA to address misuse, abuse and diversion," he said.
Lawmakers approve bills targeting opioid addiction
The Senate and Assembly passed a number of bills that are part of Gov. Scott Walker's special session targeting opioid addiction Tuesday.
The proposals originated from a preliminary report issued in January by a task force co-chaired by Rep. John Nygren, R-Marinette, and Lt. Gov. Rebecca Kleefisch.
"With the nine special session bills advanced today, the Senate has taken several great strides towards helping to combat our state's ongoing opioid crisis," Senate Majority Leader Scott Fitzgerald, R-Juneau, said in a statement.
But Democrats questioned whether the bills go far enough.
"After years of struggles, we're taking baby steps when we should be making major strides to improve outcomes and strengthen community safety," Senate Democratic Leader Jennifer Shilling, D-La Crosse, said in a statement.
The Senate approved proposals that would:
The Assembly approved the bills last month, so they now head to Walker's desk for his approval.
The chamber also approved two additional bills Tuesday that are part of the package but haven't been taken up by the Senate. Those measures would:
The Senate Committee on Education approved two bills Monday that are part of a special session ordered by Gov. Scott Walker to tackle the opioid epidemic.
A bill that would provide $50,000 to help establish a recovery charter school, which would serve 15 high school students in recovery from substance use disorder, passed out of committee 6-1. Sen. Steve Nass, R-Whitewater, voted against it.
An additional proposal providing $200,000 a year to expand the use of a substance abuse screening by the Department of Public Instruction passed 7-0. The Assembly has already approved both measures.
April 26, 2017
Today, Inspirion Delivery Sciences LLC announced that RoxyBond (oxycodone hydrochloride) tablets CII have been approved by the FDA for oral use to manage severe pain requiring an opioid analgesic and for which alternative treatments are insufficient, according to a press release.
“Inspirion is pleased to receive FDA approval for our second abuse-deterrent product, RoxyBond, which is intended to address the long-standing unmet need for immediate-release abuse-deterrent opioids,” Stefan Aigner, MD, CEO of Inspirion, said in the release. “There are nearly 18 million prescriptions for immediate-release oxycodone hydrochloride annually in the U.S. alone.”
RoxyBond uses physical and chemical barriers without aversive agents or opioid antagonists to deter abuse even when subjected to manipulation or extraction, and it is the first and only immediate-release opioid analgesic approved with abuse-deterrent label claims, according to the release. The drug is approved in dosages of 5 mg, 15 mg and 30 mg. According to the release, inactive ingredients in RoxyBond make misuse and abuse more difficult, and in head-to-head trials with another approved oxycodone immediate-release tablet, RoxyBond had higher resistance to cutting, crushing, grinding or breaking, as well as passage through a needle. Furthermore, RoxyBond indicated resistance to extraction in selected household and laboratory solvents under various conditions, whether intact or manipulated. The tablet also makes developing solutions for IV injection difficult. However, it is still possible for abuse to occur via the intranasal, oral and IV route, according to the release.
Researchers performed a clinical abuse potential study.
“As reflected in the prescribing information, the data from the clinical study, along with support from in vitro data, also indicate that RoxyBond has physicochemical properties that are expected to reduce abuse by the intranasal route of administration,” Lynn R. Webster, MD, principal investigator from PRA Health Sciences, said in the release.
The FDA’s Anesthetic and Analgesic Drug Products Advisory Committee and Drug Safety and Risk Management Advisory Committee voted 19 to 0, with one abstention, to recommend approval of RoxyBond on April 5, 2017, according to the release.
“Oxycodone immediate-release opioid tablets are widely abused and the development of RoxyBond will offer clinicians a new approach for treating patients in pain while also fighting against the potential for abuse,” Jeffrey Gudin, MD, department director of the Pain Management Center Englewood Hospital and Medical Center, said in the release.
Curbing opioid abuse has been a focus over the last several months for the FDA, which earlier this year approved several pain relief agents that are specifically manufactured to make them more difficult to abuse.
Citing the “epidemic of overdose deaths,” the CDC issued guidelines for primary care physicians and other medical professionals for opioid prescriptions last year.
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