Joseph R. Volpicelli

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Joseph R. Volpicelli
Joseph volpicelli headshot.jpg
BornJune 25, 1953
Norristown, Pennsylvania
Alma materUniversity of Pennsylvania
Known forFirst to show naltrexone was effective in treating alcohol use disorder
Websitewww.volpicellicenter.com www.instituteaddictionmedicine.org

Joseph R. Volpicelli (born June 25, 1953) is an American psychiatrist, research scientist, medical academic, and expert in the treatment of addictive disorders. He is Professor Emeritus, Perelman School of Medicine at the University of Pennsylvania. [1] He is board certified in neurology, psychiatry and addiction psychiatry. He currently is Medical Director at Volpicelli Center, [2] an out-patient addiction treatment facility in Plymouth Meeting, Pennsylvania, as well as the Executive Director at Institute of Addiction Medicine, a non-profit research entity also in Plymouth Meeting, Pennsylvania.

Contents

Education

Volpicelli attended Dickinson College for his undergraduate education where he double majored in biology and psychology. He earned his MD and PhD degrees from Perelman School of Medicine at the University of Pennsylvania in 1981. [3] Following this, he went on to complete a psychiatry residency at Hospital of the University of Pennsylvania from 1982-1985. In 1986, Volpicelli completed a fellowship program in neuropsychopharmacology, also at the University of Pennsylvania.

Career

Volpicelli worked at the Perelman School of Medicine until 2008. [1] Throughout his tenure, he served in several capacities including research scientist and associate professor for the department of psychiatry and psychology.

He studied topics including, but not limited to, the use of naltrexone within the context of PTSD, the relationship between stress and alcohol drinking, and most notably, the use of naltrexone to treat alcohol dependence. [4]

During this time, he also designed a treatment modality called the BRENDA Approach. [5] Each letter in the acronym BRENDA represents a step in the process. B(biopsychosocial evaluation), R(report findings to patient), E(empathize), N(what are the Needs of the patient), D(direct advice), A(assess patient's response to advice).

Additionally, he created clinical assessments such as the Penn Alcohol Craving Scale (PACS) to be used in research as well as clinical practice. The PACS assessment continues to be widely used today. [6]

Notable contribution to science

Based on his early experimental research with an animal model of alcohol drinking, [4] he designed and conducted the first clinical trial of naltrexone in the treatment of alcohol dependence. With the support of his mentor, Charles P. O'Brien, and funding from the U.S. Veterans Administration Substance Abuse Center in Philadelphia, Volpicelli found that naltrexone significantly reduced alcohol relapse in recently detoxified alcohol-dependent subjects. [4] While all subjects received alcohol addiction counseling, compared to the group that received placebo medication, the naltrexone-treated subjects reported significantly reduced alcohol craving and less high or euphoria associated with drinking alcohol on occasions when they drank alcohol.

This study was published in the Archives of General Psychiatry in 1992, by Volpicelli with his colleagues Al Alterman, Motoi Hayashida, and Charles P. O'Brien. Based on the results of this and another study conducted at Yale by Stephanie O'Mally, in 1994, the FDA approved the use of naltrexone to treat alcohol dependence; it was the first new medication to be FDA approved for this condition in nearly 50 years. [7]

Publications

As of May 2023, Volpicelli has authored two books and over 100 peer-reviewed research publications. In April 2000, Volpicelli's first book, Recovery Options: The Complete Guide, [8] with Maia Szalavitz, was released. Later, March 2001, Volpicelli and co-authors Helen Pettinati, A.Thomas McLellan and Charles P. O'Brien released Combining Medication and Psychosocial Treatments for Addictions: The BRENDA Approach [9] .

Awards and honors

Related Research Articles

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Alcoholism is the continued drinking of alcohol despite it causing problems. Some definitions require evidence of dependence and withdrawal. Problematic use of alcohol has been mentioned in the earliest historical records, the World Health Organization (WHO) estimated there were 283 million people with alcohol use disorders worldwide as of 2016. The term alcoholism was first coined in 1852, but alcoholism and alcoholic are stigmatizing and discourage seeking treatment, so clinical diagnostic terms such as alcohol use disorder or alcohol dependence are used instead.

<span class="mw-page-title-main">Alcohol abuse</span> Substance abuse of alcoholic beverages

Alcohol abuse encompasses a spectrum of alcohol-related substance abuse, ranging from the consumption of more than 2 drinks per day on average for men, or more than 1 drink per day on average for women, to binge drinking or alcohol use disorder.

Drug rehabilitation is the process of medical or psychotherapeutic treatment for dependency on psychoactive substances such as alcohol, prescription drugs, and street drugs such as cannabis, cocaine, heroin or amphetamines. The general intent is to enable the patient to confront substance dependence, if present, and stop substance misuse to avoid the psychological, legal, financial, social, and physical consequences that can be caused.

<span class="mw-page-title-main">Opioid use disorder</span> Medical condition

Opioid use disorder (OUD) is a substance use disorder characterized by cravings for opioids, continued use despite physical and/or psychological deterioration, increased tolerance with use, and withdrawal symptoms after discontinuing opioids. Opioid withdrawal symptoms include nausea, muscle aches, diarrhea, trouble sleeping, agitation, and a low mood. Addiction and dependence are important components of opioid use disorder.

<span class="mw-page-title-main">Baclofen</span> Medication for muscle movement disorders

Baclofen, sold under the brand name Lioresal among others, is a medication used to treat muscle spasticity such as from a spinal cord injury or multiple sclerosis. It may also be used for hiccups and muscle spasms near the end of life, and off-label to treat alcohol use disorder or opioid withdrawal symptoms. It is taken orally or by intrathecal pump. It is also sometimes used transdermally in combination with gabapentin and clonidine prepared at a compounding pharmacy.

<span class="mw-page-title-main">Naltrexone</span> Medication

Naltrexone, sold under the brand name Revia among others, is a medication primarily used to manage alcohol use or opioid use disorder by reducing cravings and feelings of euphoria associated with substance use disorder. It has also been found effective in the treatment of other addictions and may be used for them off-label. An opioid-dependent person should not receive naltrexone before detoxification. It is taken by mouth or by injection into a muscle. Effects begin within 30 minutes, though a decreased desire for opioids may take a few weeks to occur. Side effects may include trouble sleeping, anxiety, nausea, and headaches. In those still on opioids, opioid withdrawal may occur. Use is not recommended in people with liver failure. It is unclear if use is safe during pregnancy. Naltrexone is an opioid antagonist and works by blocking the effects of opioids, including both opioid drugs as well as opioids naturally produced in the brain.

<span class="mw-page-title-main">Acamprosate</span> Medication

Acamprosate, sold under the brand name Campral, is a medication which reduces alcoholism cravings. It is thought to stabilize chemical signaling in the brain that would otherwise be disrupted by alcohol withdrawal. When used alone, acamprosate is not an effective therapy for alcohol use disorder in most individuals, as it only addresses withdrawal symptoms and not psychological dependence. It facilitates a reduction in alcohol consumption as well as full abstinence when used in combination with psychosocial support or other drugs that address the addictive behavior.

Cue reactivity is a type of learned response which is observed in individuals with an addiction and involves significant physiological and psychological reactions to presentations of drug-related stimuli. The central tenet of cue reactivity is that cues previously predicting receipt of drug reward under certain conditions can evoke stimulus associated responses such as urges to use drugs. In other words, learned cues can signal drug reward, in that cues previously associated with drug use can elicit cue-reactivity such as arousal, anticipation, and changes in behavioral motivation. Responses to a drug cue can be physiological, behavioral, or symbolic expressive. The clinical utility of cue reactivity is based on the conceptualization that drug cues elicit craving which is a critical factor in the maintenance and relapse to drug use. Additionally, cue reactivity allows for the development of testable hypotheses grounded in established theories of human behavior. Therefore, researchers have leveraged the cue reactivity paradigm to study addiction, antecedents of relapse, craving, translate pre-clinical findings to clinical samples, and contribute to the development of new treatment methods. Testing cue reactivity in human samples involves exposing individuals with a substance use disorder to drug-related cues and drug neutral cues, and then measuring their reactions by assessing changes in self-reported drug craving and physiological responses.

The modern disease theory of alcoholism states that problem drinking is sometimes caused by a disease of the brain, characterized by altered brain structure and function. Today, alcohol use disorder (AUD) is used as a more scientific and suitable approach to alcohol dependence and alcohol-related problems.

<span class="mw-page-title-main">Nalmefene</span> Opioid antagonist

Nalmefene is a medication that is used in the treatment of opioid overdose and alcohol dependence. Nalmefene belongs to the class of opioid antagonists and can be taken by mouth, administered by injection, or delivered through nasal administration.

<span class="mw-page-title-main">George Koob</span> American academic

George F. Koob is a Professor and former Chair of the Committee on the Neurobiology of Addictive Disorders at the Scripps Research Institute and Adjunct Professor of Psychology, Psychiatry, and Skaggs School of Pharmacy and Pharmaceutical Sciences at the University of California, San Diego. In 2014 he became the director of the National Institute on Alcohol Abuse and Alcoholism.

SMART Recovery is an international community of peer support groups that help people recover from addictive and problematic behaviors, using a self-empowering and evidence-informed program. SMART stands for Self-Management and Recovery Training. The SMART approach is secular and research-based. SMART has a global reach, with a presence established in more than 30 countries. SMART Recovery is effective with a range of addictive and problematic behaviors

Drug detoxification is variously construed or interpreted as a type of "medical" intervention or technique in regards to a physical dependence mediated by a drug; as well as the process and experience of a withdrawal syndrome or any of the treatments for acute drug overdose (toxidrome). The first definition however, in relation to substance dependence and its treatment is arguably a misnomer and even directly contradictory since withdrawal is neither contingent upon nor alleviated through biological excretion or clearance of the drug. In fact, excretion of a given drug from the body is one of the very processes that leads to withdrawal since the syndrome arises largely due to the cessation itself and the drug being absent from the body; especially the blood plasma, not from ‘leftover toxins’ or traces of the drug still being in the system.

<span class="mw-page-title-main">Polysubstance dependence</span> A type of substance use disorder

Polysubstance dependence refers to a type of substance use disorder in which an individual uses at least three different classes of substances indiscriminately and does not have a favorite substance that qualifies for dependence on its own. Although any combination of three substances can be used, studies have shown that alcohol is commonly used with another substance. This is supported by one study on polysubstance use that separated participants who used multiple substances into groups based on their preferred substance. The results of a longitudinal study on substance use led the researchers to observe that excessively using or relying on one substance increased the probability of excessively using or relying on another substance.

Bankole A. Johnson, DSc, MD, MPhil, FRCPsych is a Nigerian psychiatrist. He served as Alumni Professor and Chairman of the Department of Psychiatry and Neurobehavioral Sciences at the University of Virginia and is known for his research into addiction.

Olivier Ameisen was a French-American cardiologist who wrote a best-selling book about curing alcoholism using the drug baclofen.

The Severity of Alcohol Dependence Questionnaire is a 20 item clinical screening tool designed to measure the presence and level of alcohol dependence.

<span class="mw-page-title-main">Charles P. O'Brien</span> American research scientist, medical educator (born 1939)

Charles P. O'Brien is a research scientist, medical educator and a leading expert in the science and treatment of addiction. He is board certified in neurology, psychiatry and addiction psychiatry. He is currently the Kenneth E. Appel Professor of Psychiatry, and vice chair of psychiatry, in the Perelman School of Medicine at the University of Pennsylvania.

Subjective response to alcohol (SR) refers to an individual's unique experience of the pharmacological effects of alcohol and is a putative risk factor for the development of alcoholism. Subjective effects include both stimulating experiences typically occurring during the beginning of a drinking episode as breath alcohol content (BAC) rises and sedative effects, which are more prevalent later in a drinking episode as BAC wanes. The combined influence of hedonic and aversive subjective experiences over the course of a drinking session are strong predictors of alcohol consumption and drinking consequences. There is also mounting evidence for consideration of SR as an endophenotype with some studies suggesting that it accounts for a significant proportion of genetic risk for the development of alcohol use disorder.

John David Sinclair was an American scientist and researcher best known for discovering the Alcohol Deprivation Effect (ADE) and targeted pharmacological extinction, otherwise known as the Sinclair Method, as a medication treatment for Alcohol Use Disorder (AUD).

References

  1. 1 2 "Joseph R Volpicelli | Faculty | About Us | Perelman School of Medicine | Perelman School of Medicine at the University of Pennsylvania". www.med.upenn.edu. Retrieved 2023-06-05.
  2. "About the Volpicelli Center for Addiction Treatment - Meet the Team". Volpicelli Center Rehab in Pennsylvania – Outpatient, Suboxone, Vivitrol, Addiction Treatment. Retrieved 2023-06-05.
  3. "Joseph Volpicelli". orcid.org. Retrieved 2023-06-05.
  4. 1 2 3 Bain, L. J. (2001). The science of addiction. Penn Medicine, Summer(2001), 6–14.
  5. Gluck, S. (2007, August 1). Medical Treatment of Alcoholism Online Conference Transcript, HealthyPlace. Retrieved on 2023, June 14 from https://www.healthyplace.com/addictions/transcripts/medical-treatment-of-alcoholism-online-conference-transcript
  6. Hartwell, Emily E.; Bujarski, Spencer; Green, ReJoyce; Ray, Lara A. (2019-12-01). "Convergence between the Penn Alcohol Craving Scale and diagnostic interview for the assessment of alcohol craving". Addictive Behaviors Reports. 10: 100198. doi:10.1016/j.abrep.2019.100198. ISSN   2352-8532. PMC   6599943 .
  7. "Medications Development Program | National Institute on Alcohol Abuse and Alcoholism (NIAAA)". www.niaaa.nih.gov. Retrieved 2023-05-26.
  8. Volpicelli, Joseph; Szalavitz, Maia (2000). Recovery Options: The Complete Guide. Wiley.
  9. Volpicelli, Joseph; Pettinati, Helen; McLellan, A. Thomas; O'Brien, Charles P. (2001). Combining Medication and Psychosocial Treatments for Addictions: The BRENDA Approach. The Guilford Press.