How AI and a mobile phone app could help you quit smoking

Newswise — A stop smoking mobile app that senses where and when you might be triggered to light up could help people quit – according to University of East Anglia research.

Quit Sense is the world’s first Artificial Intelligence (AI) stop smoking app which detects when people are entering a location they used to smoke in. It then provides support to help manage people’s specific smoking triggers in that location.

Funding for the Quit Sense app has come from the National Institute for Health and Care Research (NIHR) and the Medical Research Council.

A study published today shows how the new app helped more smokers to quit than people who were only offered online NHS support.

The team hope that by helping people manage trigger situations, the new app will help more smokers to quit.

Lead researcher Prof Felix Naughton, from UEA’s School of Health Sciences, said: “We know that quit attempts often fail because urges to smoke are triggered by spending time in places where people used to smoke. This might be while at the pub or at work, for example.

“Other than using medication, there are no existing ways of providing support to help smokers manage these types of situations and urges as they happen.

Dr Chloë Siegele-Brown, from the University of Cambridge and who built the app, said: “Quit Sense is an AI smartphone app that learns about the times, locations and triggers of previous smoking events to decide when and what messages to display to the users to help them manage urges to smoke in real time.

Prof Naughton added: “Helping people attempting to quit smoking to learn about and manage these situations is a new way of increasing a smoker’s chances of quitting successfully.”

The research team carried out a randomised controlled trial involving 209 smokers who were recruited via social media.

They were sent links by text message to access their allocated treatment – all participants received a link to NHS online stop smoking support but only half received the Quit Sense app in addition.

Six months later, the participants were asked to complete follow-up measures online and those reporting to have quit smoking were asked to post back a saliva sample to verify their abstinence.

Prof Naughton said: “We found that when smokers were offered the Quit Sense app, three-quarters installed it and those who started a quit attempt with the app used it for around one month on average.

“We also found that four times more people who were offered the app quit smoking six months later compared to those only offered online NHS support.”

The research team note that one limitation of this relatively small scale study was that less than half of the people who reported quitting smoking returned a saliva sample to verify that they had quit smoking. And more research is needed to provide a better estimate of the effectiveness of the app.

Health Minister Neil O’Brien said: “Technology and smartphones have a role to play in driving down smoking rates, which is why I’ve set out our plans to explore the use of QR codes in cigarette pack inserts to take people to stop-smoking support.

“Making better use of technology – alongside the world’s first national ‘swap to stop’ scheme and financial incentives for pregnant women alongside behavioural support – will help us to meet our smokefree ambition by 2030, reduce the number of smoking-illnesses needing to be treated, and cut NHS waiting times.”

This study was led by the University of East Anglia in collaboration with researchers from the University of Cambridge, the Norwich Clinical Trials Unit, the University of Nottingham, King’s College London, University College London, and Imperial College London.

‘An automated, online feasibility randomised controlled trial of a Just-In-Time Adaptive Intervention for smoking cessation (Quit Sense)’ is published in the journal Nicotine and Tobacco Research.

ENDS

Rutgers Expert Available to Discuss Biden-⁠Harris Administration Designation of Fentanyl Combined with Xylazine (“Tranq”) as an Emerging Threat

Lewis Nelson, an expert in overdose and addiction management and Chair of Emergency Medicine at Rutgers New Jersey Medical School, is available to discuss the White House’s official designation of fentanyl adulterated or associated with xylazine — a non-opioid tranquilizer also known as “tranq” approved by the Food and Drug Administration for veterinary use but not human use — as an emerging threat to the United States.

The following quote is available for pick up. If you are covering this issue and would like to interview Dr. Nelson, please let me know.

“Although xylazine has been in the illicit heroin and fentanyl supply for several years, it is finally receiving attention from federal authorities. Despite the concerns expressed in the recent release, the data to support the dangers of xylazine adulteration on overdose risk, withdrawal severity, treatment complexity and skin wounds are limited, and we should be cautious not to let the rhetoric get ahead of the science,” Nelson says.

The brain's cannabinoid system protects against addiction following childhood maltreatment

Newswise — High levels of the body’s own cannabinoid substances protect against developing addiction in individuals previously exposed to childhood maltreatment, according to a new study from Linköping University in Sweden. The brains of those who had not developed an addiction following childhood maltreatment seem to process emotion-related social signals better.

Childhood maltreatment has long been suspected to increase the risk of developing a drug or alcohol addiction later in life. Researchers at Linköping University have previously shown that this risk is three times higher if you have been exposed to childhood maltreatment compared with if you have not, even when accounting for confounds from genetics and other familial factors.

“There’s been a lot of focus on addiction as a disease driven by a search for pleasure effects and euphoria, but for many it has more to do with the drugs’ ability to suppress negative feelings, stress sensitivity, anxiety and low mood. Based on this, we and other researchers have had a theory that if affected in childhood, the function of the brain’s distress systems is altered, and that this may contribute to addiction risk in adulthood,” says Markus Heilig, professor and director of the Center for Social and Affective Neuroscience, CSAN, at Linköping University and consultant at the Psychiatric Clinic of the University Hospital in Linköping.

Endocannabinoids, i.e. the body’s own cannabis-like substances, are an interesting player in this context. The endocannabinoid system plays an important part in regulating reactions to stress and discomfort. Recent research suggests that this endogenous system may function as a stress buffer.

The researchers behind the study, published in Molecular Psychiatry, aimed to investigate possible mechanisms behind susceptibility or resilience to developing substance use disorder later in life after exposure to childhood maltreatment. One difficulty in research is that people who develop problems later in life tend to overreport negative life experiences when questioned about earlier events. The researchers therefore used psychiatric care registers of children and young people having been treated for traumatic childhood experiences to find study participants with objectively and prospectively documented exposure. The study included about 100 young adults divided into four equal sized groups: individuals that had been exposed to childhood maltreatment and had developed an addiction, individuals that had been exposed but had not, individuals that had not been exposed but had developed an addiction, and individuals who had neither been exposed nor developed an addiction. The researchers measured endocannabinoid levels in participants’ blood and carried out several experiments to test stress reactions. The participants’ brains were also scanned using magnetic resonance imaging, MRI, while their reactions to social stimuli were tested.

It turned out that one group stood out compared to the other three: the group that had experienced childhood maltreatment but had not later developed an addiction. The researchers refer to this group as ‛resilient’. In comparison with the other groups, this group showed increased function of the endocannabinoid system as well as different brain activity. Surprisingly, the resilient group differed most from the control group, which had not been exposed to childhood maltreatment, nor had any addictions.

 Faced with emotional social stimuli, the resilient group showed higher activity in three areas of the brain. Two of these areas are part of a brain network that focuses attention and cognitive abilities on what is important at the moment and modifies individuals’ behaviour according to the situation at hand. The third area of the brain is in the frontal lobe and is associated with regulating emotions. This area communicates extensively with other areas in the brain that process emotions. In comparison with other animals, humans have a well-developed frontal lobe that regulates impulses and emotions, for instance by suppressing fear impulses in situations where fear is not relevant.

­“Increased activity in certain areas of the brain in the resilient group, which had not developed an addiction despite childhood maltreatment, may be linked to a more adaptive way of reacting to emotional social information. We can see that also in a resting state they show increased communication between the frontal lobes and other parts of the brain, which could indicate that this group has better emotional regulation,” says Irene Perini, staff scientist at CSAN at Linköping University.

A question this discovery raises is whether the resilient group had a high endocannabinoid system function from the outset, or whether they were better able to activate the system in response to stress, thereby avoiding long-term consequences of childhood maltreatment. Because of its cross-section nature, this is not possible to determine from the present study.

The study was funded by, among others, the Swedish Research Council, Knut and Alice Wallenberg Foundation, Region Östergötland, Linköping University, Systembolaget’s Alcohol Research Council and the Brain & Behaviour Research Foundation NARSAD Young Investigator Grant. It was carried out by Markus Heilig’s research group at CSAN. Irene Perini is the lead author together with Leah Mayo, previously with CSAN at LiU, and currently professor at the University of Calgary in Canada.

Open-label placebo improved outcomes for people in treatment for opioid use disorder

BYLINE: Jacqueline Mitchell

Newswise — BOSTON – There were more than 100,000 reported deaths from opioid overdoses in 2021, according to the Centers for Disease Control and Prevention. Methadone treatment remains one of the most reliable means of treating opioid use disorder, with success rates reportedly ranging from 60 to 90 percent for patients who stick with the long-term regimen. Adherence, though, remains a challenge.

In a novel randomized clinical trial published in JAMA Network Open, senior author Ted J. Kaptchuk at Beth Israel Deaconess Medical Center (BIDMC), lead author Annabelle Belcher, PhD, of the University of Maryland School of Medicine, and colleagues tested whether using open-label placebo could increase the efficacy of methadone treatment for people undergoing care for opioid use disorder. The researchers found that participants who knowingly received placebo pills in addition to standard-of-care methadone treatment were significantly more likely to remain in treatment than participants who received methadone treatment alone. Participants who received placebo pills also reported better sleep quality.

“The clinical implications of our intervention have great potential impact, as retention in treatment is a serious challenge for the field of addiction medicine,” said Belcher. “We’ve demonstrated it’s feasible to administer a placebo in addition to standard-of-care methadone in a community-based opioid treatment setting without adding a significant burden to clinic procedures, and the low-cost, low-risk nature of this intervention could provide an appealing strategy to target early methadone treatment adherence.”

It has long been assumed that deception or concealment is necessary for placebo effects – i.e. “tricking” a patient to believe an inert pill contains active medication. But, a growing body of evidence in randomized controlled trials with irritable bowel syndrome, chronic low back pain, cancer-related fatigue, migraine and other conditions has demonstrated no such deception is necessary for placebo treatment to alleviate symptoms. Additionally, conditioning study participants to placebos by having them pair the placebo with an active medication – thereby potentially associating the placebo with a relief in symptoms that may be caused by the active drug – has also been shown to treat symptoms of insomnia, ADHD, post-surgical pain, and more.

For this two-arm, open-label, single-blind randomized controlled trial, 131 newly enrolled adult patients seeking treatment for moderate-to-severe opioid use disorder (OUD) at an academically affiliated community opioid treatment program were recruited. All participants were informed of the possible benefits of open-label placebo and conditioning. The research team also described the neurobiological and psychological mechanisms of placebo effects and conditioning in lay terms and in a routine, supportive setting. Then, participants were randomized either to receive treatment-as-usual or treatment-as-usual plus conditioned open-label placebo (microcrystalline cellulose pills).

While the participants were aware that they were taking a placebo pill, the clinical addiction care team was unaware as to which participants were in the treatment-as-usual or treatment-plus-placebo groups and the trial altogether to avoid any unconscious differential treatment. All participants were seen at weeks two, four, eight, and 12 after the initial enrollment and underwent the same outcome assessments. Those in the placebo group were not provided with any additional information about placebos or the rationale of the study beyond what was provided at the baseline meeting.

Researchers assessed patients’ 90-day methadone dose, treatment retention, self-reported drug use, withdrawal, craving, quality of life, and sleep quality. Contrary to the researchers’ expectations, the conditioned open-label placebo had no impact on the 90-day methadone dose. However, participants treated with open-label placebo were significantly more likely to remain in treatment; 78 percent of the placebo-treated group stayed with the program compared to 61 percent of the methadone-only group. The placebo group also reported better sleep quality. No statistically significant differences were found in any other outcome measures.

“Implementing a unique combination of two methods to harness the placebo effect – open-label placebo and pharmacological conditioning – we found a significant difference in the group’s 90-day retention rates, demonstrating that placebo treatment can provide valuable benefits and still adhere to ethical norms of informed consent,” said Kaptchuk, director of the Program in Placebo Studies and the Therapeutic Encounter at BIDMC and professor of medicine at Harvard Medical School. “Previous assumptions that placebo treatment needs concealment or deception to ‘work’ are not true. Additionally, there is growing evidence that open-label placebo demonstrates similar neurotransmitter engagement to double-blind and deceptive placebos. It is important to note that a patient-clinician relationship is an important component of open-label placebo.”

Co-authors included Thomas O. Cole, MA, Emerson M. Wickwire, PhD, Aaron D. Greenblatt, MD, William Wooten, MS, and Lawrence Magder, PhD, and Eric Weintraub, MD, of University of Maryland, School of Medicine; Ebonie Massey, MA, Amy S. Billing, MSSA, Michael Wagner, PhD, and Eric D. Wish, PhD, of Center for Substance Abuse Research (CESAR), University of Maryland; David H. Epstein, PhD, of Real-world Assessment, Prediction, and Treatment Unit, National Institute on Drug Abuse Intramural Research Program (NIDA-IRP/NIH); Stephen W. Hoag, PhD, of University of Maryland, School of Pharmacy; Luana Colloca, MD, of University of Maryland School of Nursing; and John Rotrosen, MD, of NYU Grossman School of Medicine.

This work was supported by the Foundation for the Science of the Therapeutic Encounter; the University of Maryland MPowering the State Opioid Use Disorders Initiative; the University of Maryland, Baltimore, Institute, for Clinical & Translational Research (ICTR); the National Center for Advancing Translational Sciences (NCATS) Clinical Translational Science Award (CTSA) (grant number 1UL1TR003098.)

Please see the publication online for a complete list of disclosures.

About Beth Israel Deaconess Medical Center

Beth Israel Deaconess Medical Center is a leading academic medical center, where extraordinary care is supported by high-quality education and research. BIDMC is a teaching affiliate of Harvard Medical School, and consistently ranks as a national leader among independent hospitals in National Institutes of Health funding. BIDMC is the official hospital of the Boston Red Sox.

Beth Israel Deaconess Medical Center is a part of Beth Israel Lahey Health, a health care system that brings together academic medical centers and teaching hospitals, community and specialty hospitals, more than 4,800 physicians and 36,000 employees in a shared mission to expand access to great care and advance the science and practice of medicine through groundbreaking research and education.

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IU researchers receive $8.6M NIH grant renewal to study alcohol use, binge drinking

Newswise — INDIANAPOLIS—A multi-disciplinary team of Indiana University researchers is focusing their efforts on a growing public health concern: binge and “high-intensity” drinking—extreme drinking behaviors that are increasingly prevalent among college-age adults.

The researchers, who are part of the Indiana Alcohol Research Center, recently received a five-year, $8.65 million grant renewal from the National Institute on Alcohol Abuse and Alcoholism to support this work.

Established in 1987, the Indiana Alcohol Research Center (IARC) is housed at IU School of Medicine and led by director David Kareken, PhD, a professor of neurology at the school. The center’s broad mission is to study the behavioral and neurobiological risks for alcohol use disorder.

“The IARC begins its eighth consecutive funding cycle by continuing its long tradition of multi-disciplinary collaboration across animals and humans to better understand the neurobiological and behavioral risks for developing alcohol use disorder,” Kareken said. “We believe that our combined diverse methods and perspectives are best suited to studying a problem of both great importance and complexity.”

Cristine Czachowski, PhD, a professor of psychology at the School of Science at IUPUI, and Christopher Lapish, PhD, a professor of anatomy, cell biology and physiology at IU School of Medicine, serve as the center’s deputy director and scientific director, respectively.

“The center provides researchers like me—those studying rodent models of behavior—valuable interactions with colleagues (and friends) who work on the clinical side,” Czachowski said. “The crosstalk between disciplines, and across many departments, keeps us at the top of our game with regard to the latest findings and focused on the human experience of alcohol use disorder.”

Working as a team across basic and clinical research, center faculty will work to determine how inherited and acquired behavioral and neurobiological vulnerabilities predispose people to more intense patterns of drinking, with a particular emphasis on factors that lead to faster initial rates of drinking and a proclivity for sustained high intake.

“Our ability to measure how brain function is altered in alcohol use disorder is rapidly improving,” Lapish said. “This is true for humans and rodent models of the disorder. Our hope is that we can find similarities across the species, which, in turn, will facilitate new treatments.”

The researchers will also work with the community, schools, health care providers and state policy makers in providing education about the science, prevention, and treatment of alcohol use disorder.

This funding renewal is the Indiana Alcohol Research Center’s eighth consecutive five-year grant from the National Institute of Alcohol Abuse and Alcoholism since its founding. Over the past three decades, center researchers and their collaborators have played key roles in studying alcohol use disorder heritability—showing differing genetic and environmental influences across the disorder’s developmental timeline.

Their animal and human research models are also used worldwide in alcohol-related research. Center researchers conceived, and continue to refine, the “Computer-assisted Alcohol Infusion System,” an intravenous alcohol administration research method that permits exquisite experimental control over an individual’s level of alcohol exposure—a technique employed in human research laboratories around the world. The center’s animals—rats and mice selectively bred by the IARC to prefer alcohol—are similarly used throughout the world to help understand inherited risk.

Other Indiana Alcohol Research Center project and core resource leaders include IU School of Medicine’s Martin Plawecki, MD, PhD; Frederic (Woody) Hopf, PhD; Tamika Zapolski, PhD; and Karmen Yoder, PhD; and the IUPUI School of Science’s Marian Logrip, PhD; Nicholas Grahame, PhD; Melissa Cyders, PhD; and Stephen Boehm, PhD. Collaborating scientists include researchers at IU School of Medicine, the School of Science at IUPUI, the IU School of Public Health-Bloomington, and Purdue University.

About IU School of Medicine

IU School of Medicine is the largest medical school in the U.S. and is annually ranked among the top medical schools in the nation by U.S. News & World Report. The school offers high-quality medical education, access to leading medical research and rich campus life in nine Indiana cities, including rural and urban locations consistently recognized for livability.

NIH Awards $8 Million to Wake Forest University School of Medicine's Translational Alcohol Research Center

Newswise — WINSTON-SALEM, N.C. – April 4, 2023 – The National Institute on Alcohol Abuse and Alcoholism (NIAAA), part of the National Institutes of Health (NIH), has awarded Wake Forest University School of Medicine a renewal grant of $8 million over five years for research on alcohol use disorder.

With the support of the grant, the Wake Forest Translational Alcohol Research Center will build upon a highly productive translational alcohol research program that was established with prior support from the NIH.

According to the NIAAA, more than 140,000 people die from alcohol-related causes each year in the U.S., and an estimated 15 million people have alcohol use disorder.

“Our center’s primary research focus is understanding what makes people vulnerable to alcohol use disorder,” said Jeffrey L. Weiner, Ph.D., professor of physiology and pharmacology at Wake Forest University School of Medicine and the center’s director.

The center seeks to identify behavioral adaptations and brain mechanisms that contribute to vulnerability and resilience to alcohol use disorder. For example, one ongoing study seeks to understand how abstinence alters craving and brain network connectivity in risky drinkers. And a recent study, published in the Journal of Neurosurgery, analyzed chemical fluctuations in the brain in patients with alcohol use disorder.

Researchers are also examining brain network dynamics associated with hazardous drinking by analyzing a dataset from the National Consortium on Alcohol and Neurodevelopment in Adolescence, a longitudinal study that is collecting brain imaging and alcohol consumption history from adolescents over eight years. 

“There’s a lot of research on the role of genetics in alcohol addiction, but we’re learning more about how environmental factors such as early-life adversity, poverty and childhood stress have a huge influence on the brain and its susceptibility to neuropsychiatric disorders including alcohol use disorder,” Weiner said. “Our hope is that our research will lead to evidence-based therapies for those who are most at risk.” 

'UC Quits' project helps patients stop smoking

Newswise — A new University of California study shows long-term success when health care providers make electronic referrals (e-referrals) for their patients to California’s tobacco quitline. The paper was published today in the journal Nicotine & Tobacco Research.

Quitlines offer free help to stop tobacco use. They typically double the chances that a person stays quit for good.

Tobacco is the leading cause of preventable disease, disability and death in the United States. Quitting significantly reduces these risks. However, until this study was conducted, there had been little research about the real-world implementation, maintenance, and outcomes of e-referrals to quitlines. The study is the first collaboration of its kind to be conducted by all five University of California health systems.

“Even though the five UC health systems are under the umbrella of UC Health, they each are independent, which is why the implementation benefited from a whole-systems approach, taking into account the different IT systems and clinical workflows,” said Elisa Tong, lead author of the study and UC Davis co-leader of CA Quits.

Tong is also an internist and medical director of the Stop Tobacco Program at UC Davis Health. She said that including both outpatient and inpatient settings is important for offering and sustaining e-referrals to patients. The study showed that patients referred by providers had similar quit rates as people who called the quitline seeking help.

Method and results

In 2013, UC Davis Health was the first health system to implement an e-referral to the California quitline, now known as Kick it California. Beginning in 2014, the UC-wide project UC Quits worked with inpatient, outpatient, and nursing champions to scale up quitline e-referrals from one to five UC health systems. This also included UC San Francisco, UC Irvine, UC Los Angeles, and UC San Diego.

Data on e-referred patients and quitline callers were collected April 2014-March 2021. Analysis of referral trends and cessation outcomes was conducted in 2021-2022.

Of the more than 20,000 patients referred, the quitline contacted 47.1%; 20.6% of those completed the intake process. Data collected showed 15.2% requested counseling and 10.9% received the cessation help. In a sample randomly selected for follow-up, patients e-referred by their UC providers were as likely as general quitline callers to attempt quitting (68.5% vs. 71.4%), quit for 30 days (28.3% vs. 26.9%) and quit for six months (13.6% vs. 13.9%).

The study supports the broad implementation of tobacco quitline e-referrals across health care settings and finds that modifying electronic health records systems and clinical workflows will enable and encourage e-referrals.

If implemented and maintained appropriately, the study showed that e-referrals will improve patient care, make it easier for clinicians to support patients in quitting, and increase the number of patients using evidence-based treatment.

“More health systems can use electronic referral systems to link with the quitline and collaborate on systems changes,” said Shu-Hong Zhu, UC San Diego co-leader of CA Quits and co-author. “Establishing and maintaining electronic referrals is an important way to ensure patients who are trying to stop smoking are set up for success.”

Acknowledgements

Other authors included Shu-Hong Zhu, Christopher M. Anderson, Mark V. Avdalovic, Alpesh N. Amin, Allison L. Diamant, Timothy W. Fong, Brian Clay, Robert El-Kareh, Sujatha Sankaran, Catherine Bonniot, Carrie A. Kirby, Antonio Mayoral, and Linda Sarna.

Funding was supported by the UC Center for Health Quality and Innovation, with additional support secured from Tong from the Tobacco-Related Disease Research Program (#28CP-0039HS). Kick It California is funded by the California Department of Public Health, First 5 California and the Centers for Disease Control and Prevention.

From the doctor's office to the operating room: Keep up with the latest in healthcare here

Whether you are keeping up with your vaccinations at a community healthcare center or prepping for surgery in a major hospital, like it or not, we all have to deal with our modern healthcare system. According to Revcycle Intelligence, U.S. healthcare spending rose by 4.6 percent compared to last year, while healthcare employment growth was driven by hospitals, which added 19,400 jobs in February 2023. With rising insurance premiums, and the politics of future funding of Medicare, healthcare affects our wallets as well as our well-being.

Keep up with this ever-growing, changing sector. Below are some of the latest stories on healthcare on Newswise.

Naloxone Prescriptions Increased at U.S. Hospitals Between 2012 and 2019

Significant Disparities in Breast Cancer Care Persist, But Surgeons Can Drive Change

Patients with septic shock benefit from a combination of hydrocortisone-fludrocortisone therapy

New program shows promise in reducing financial burden of cancer care

Average privately insured family spends $1,300 for child’s hospitalization

Women with higher out-of-pocket costs receive fewer follow-up procedures to screening mammograms

Clinical Trial Participation Associated with Improved Overall Survival in Ovarian Cancer Patients

‘Smart’ bandages monitor wounds and provide targeted treatment

How one state beat national surgery opioid trends

Largest US state-by-state analysis of COVID-19 impact reveals the driving forces behind variations in health

Mental distress among female individuals of reproductive age after overturning of Roe v Wade

2022 heatwave struck off surgery in fifth of UK hospitals

Investigators Find Disparities in Mesothelioma Survival Due to Social Determinants, Limited Access

Survey finds patients value immediate access to test results

Cataract surgery reimbursements may not be enough for some patients

Seniors’ use of urinary-tract infection antibiotics halved

Machine learning programs predict risk of death based on results from routine hospital tests

 

Legal cannabis markets linked to increased motor vehicle deaths

Newswise — A new study from the University of Illinois Chicago used death certificate data to compare mortality rates in states that legalized recreational cannabis dispensaries with states that only provided access to medical cannabis.

The UIC researchers found that there was a substantial increase in crash fatalities in four of the seven states used in the study with legalized recreational markets and that, on average, recreational markets were associated with a 10% increase in motor vehicle accident deaths.  

Study first author Samantha Marinello said the findings suggest that it may be beneficial for states with legal recreational cannabis to invest in policies and public health initiatives to mitigate this potential harm and build awareness of the dangers of driving under the influence.  

“To see a 10% increase in motor vehicle accident deaths associated with recreational markets is concerning. Previous studies have found cannabis impairs driving ability and that driving while high is fairly common among regular cannabis users,” said Marinello, a postdoctoral research associate with the division of health policy and administration at the UIC School of Public Health. 

For the analysis, Marinello and Lisa Powell, UIC distinguished professor and director of the division, focused on seven states that implemented legal recreational cannabis markets: Alaska, California, Colorado, Massachusetts, Nevada, Oregon and Washington. They collected data from death certificates from 2009-2019 on deaths in three areas that have previously been linked to cannabis use but are still poorly understood: motor vehicle accidents, suicide and opioid overdose.  

For each cause of death, the researchers compared trends in deaths in states with legal markets with those in states that had comprehensive medical cannabis programs and similar trends in death rates prior to implementing markets.

“We didn’t want to compare states with very different mortality trends or social ideology, so we looked at each state and outcome and identified comparison states with existing medical cannabis programs and with similar pre-trends to conduct our analysis,” Marinello said.  

The data revealed significant increases in crash fatalities in Colorado (16%), Oregon (22%), Alaska (20%) and California (14%).

“The results suggest that a potential unintended consequence of recreational markets is increased cannabis-intoxicated driving and crash deaths, and, hence, a potential need for policies focused on reducing driving under the influence of cannabis,” the authors write.

The researchers found no evidence that recreational markets impacted suicides, which is notable because cannabis use is associated with the development of depressive disorders and suicidality.

For opioid overdose deaths, recreational markets were associated with an 11% reduction in fatalities, on average. Across all seven states, the reduction ranged from 3% to 28%.  

Marinello said that the reduction in opioid overdose fatalities is another potential area of impact that should be a factor in states considering legalization.  

“This study provides evidence of both potential benefits and harms that policymakers should consider when legalizing recreational cannabis markets,” Marinello said. 

The impact of recreational cannabis markets on motor vehicle accident, suicide, and opioid overdose fatalities” is published in the journal Social Science & Medicine.

Where there's smoke, there's thiocyanate: McMaster researchers find tobacco users in Canada are exposed to higher levels of cyanide than other regions

Newswise — HAMILTON, ON – Mar 24, 2024 Tobacco users in Canada are exposed to higher levels of cyanide than smokers in lower-income nations, according to a large-scale population health study from McMaster University.

Scientists made the discovery while investigating the molecule thiocyanate – a detoxified metabolite excreted by the body after cyanide inhalation. It was measured as a urinary biomarker of tobacco use in a study of self-reported smokers and non-smokers from 14 countries of varying socioeconomic status. 

“We expected the urinary thiocyanate levels would be similar across regions and reflect primarily smoking intensity. However, we noticed significant elevation of thiocyanate in smokers from high-income countries even after adjusting for differences in the number of cigarettes smoked per day,” says Philip Britz-McKibbin, co-author of the study and a professor of chemistry and chemical biology at McMaster.

Tobacco-related illness remains the leading cause of preventable illness and premature death in Canada, contributing to approximately 48,000 deaths annually. According to researchers, the findings could be caused by the type of cigarettes smoked in high-income countries like Canada.

“The cigarettes commonly consumed in Canada are highly engineered products with lower tar and nicotine content to imply they’re less harmful. Heavy smokers with nicotine dependence compensate by smoking more aggressively with more frequent and deeper inhalations that may elicit more harm, such as greater exposure to the respiratory and cardiotoxin, cyanide.”

Smoking rates in Canada have declined from 26 per cent in 2001 to 13 per cent in 2020. But participation in smoking cessation programs has declined during the COVID-19 pandemic, leading to concern about a potential uptick in smoking rates, including cannabis use and a plethora of vaping of products popular among young adults.

Researchers say urinary thiocyanate can serve as a robust biomarker of the harms of tobacco smoke that will aid future research on the global tobacco picture, since most smokers now reside in developing countries. As smoking rates have decreased here in Canada, at-risk groups like youth and pregnant women have been prone to underreport their tobacco use when surveyed, making a reliable biomarker more valuable.

“Historically assessing tobacco behaviors have relied on questionnaires that are prone to bias, especially when comparing different countries and local cultures. The idea is to find robust methods that can quantify recent tobacco smoke exposure more reliably and objectively, which may better predict disease risk and prioritize interventions for smoking cessation.” says Britz-Mckibbin.

The study was published in the latest issue of Nicotine and Tobacco Research and received funding from the Natural Sciences and Engineering Research Council of Canada, Genome Canada, the Canada Foundation for Innovation, Hamilton Health Sciences New Investigator Fund, and an internal grant from the Population Health Research Institute.

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For more information please contact:

Photos of Philip Britz-McKibbin can be found here

Credit: McMaster University