Clinical Guidance: Stimulant Use

July 17, 2024

Purpose of This Guidance

Date of current publication: July 17, 2024
Lead authors: Judith Griffin, MD; William Supplee, MD
Writing group: Susan D. Whitley, MD; Timothy J. Wiegand, MD, FACMT, FAACT, DFASAM; Sharon L. Stancliff, MD; Brianna Norton, DO, MPH; Christopher J. Hoffmann, MD, MPH, MSc; Charles J. Gonzalez, MD
Committee: Substance Use Guidelines Committee
Date of original publication: July 3, 2023

The New York State Department of Health AIDS Institute (NYSDOH AI) developed this guidance for primary care and other clinicians with patients who use stimulants to:

  • Inform clinicians about different types of stimulants and current terminology for describing stimulants and their use.
  • Provide strategies for talking with patients about stimulant use and the associated risks, including opioid overdose due to concomitant use of opioids and stimulants or to contamination of illicitly manufactured stimulants with synthetic opioids.
  • Summarize the treatment options for stimulant use disorder.

The guidance focuses on nonprescription stimulant substances, including cocaine and crack; methamphetamine, 3,4-methylenedioxy-methamphetamine (MDMA; hallucinogen with stimulant effects); and synthetic cathinone (bath salts).

Rising use and mortality: The results of the U.S. 2021 National Survey on Drug Use and Health indicate that among people aged ≥12 years, 4.8 million had used cocaine, 2.5 million had used methamphetamines, 2.2 million had used MDMA, and 107,000 had used synthetic stimulants (including cathinone) in the previous year SAMHSA 2023. Misuse or chronic use of stimulants can cause or worsen neuropsychiatric, cardiovascular, and other conditions SAMHSA 2021, and stimulant injection has been associated with an increased incidence of HIV and hepatitis C virus Cepeda, et al. 2020Farrell, et al. 2019.

In addition, in the United States, drug overdose deaths involving methamphetamine increased from 547 in 1999 to 23,837 in 2020, and drug overdose deaths involving cocaine increased from 5,419 in 2014 to 19,447 in 2020 NIDA 2024. In New York State from 2018 to 2022, drug overdose deaths involving synthetic stimulants increased from 180 to 664, and those involving cocaine increased from 1,276 to 2,880 OASAS 2024. For more information, see the Office of Addiction Services and Supports Addiction Data Bulletin Stimulant Use and Stimulant Use Disorder In New York State. These dramatic increases in cocaine- and methamphetamine-related mortality have been characterized as a fourth wave of the U.S. overdose crisis Ciccarone and Shoptaw 2022Fischer, et al. 2021.

Much of the recent increase in mortality is attributed to concomitant use of fentanyl and stimulants. In 2021 in the United States, approximately 66% of overdose deaths were attributed to concomitant use of fentanyl and cocaine (16.6% of overdose deaths), fentanyl and methamphetamine (10.7%), and other opioids with stimulants (39.9%) CDC 2024. The presence of fentanyl as an adulterant in the supply of illicitly manufactured stimulants is correlated with this increase in mortality, although the extent of adulteration is unclear Wagner, et al. 2023.

KEY POINTS

Commonly Used Stimulants: Characteristics and Adverse Effects

“Stimulants” is the general term used to describe the many synthetic or naturally occurring substances that elevate mood and increase alertness, attention, and energy. These substances increase catecholamines, including dopamine, norepinephrine, and serotonin, to varying degrees, generally through either inhibition of reuptake (e.g., cocaine) or through a combination of reuptake inhibition and increased release (e.g., methamphetamine). Some stimulants are also inhibitors of monoamine oxidase (MAOIs). Table 1, below, summarizes the types and characteristics of commonly used stimulants.

Abbreviations: ADHD, attention-deficit hyperactivity disorder; MDMA, 3,4-methylenedioxy-methamphetamine.

Notes:

  1. Common names and slang for stimulants vary widely and evolve constantly.
  2. Cathinones are not routinely included in toxicology testing.
  3. Often purchased online; purchasers may not get pharmaceutically produced products.
  4. Concerta is indicated for ADHD treatment, not narcolepsy. Lisdexamfetamine (Vyvanse) is also indicated for the treatment of moderate to severe binge eating disorders in adults.
  5. Methylphenidate (e.g., Ritalin, Concerta, generics) is not an amphetamine. It is metabolized to ritalinic acid and will not be identified by laboratory testing for amphetamines.
Table 1: Characteristics of Commonly Used Stimulants
Characteristics Patient-Reported Reasons for Use and Slang [a]
Cathinone, Synthetic [b]
  • Source and forms: Synthetic substance chemically similar to natural cathinone (khat plant); available as a white or brown crystal-like powder; less expensive substitute for cocaine and amphetamines
  • Administration: Intravenous, oral, intranasal insufflation, smoking
  • Onset of action: 30 to 60 minutes (oral)
  • Half-life: 3 to 6 hours
  • Reasons for use: Produces euphoria and alertness; designed to imitate the effects of other stimulants such as cocaine, MDMA, and methamphetamines (see below)
  • Street names: Bath salts, Molly
Cocaine
  • Source and forms: Hydrochloride salt derived from the coca plant; available as a powder. Freebase cocaine (crack) is a form of cocaine boiled with another substance, usually baking soda; available as a powder or rock.
  • Cocaine administration: Intravenous, intranasal insufflation, vaginal or rectal as a solution
  • Freebase cocaine (crack) administration: Can be smoked as a powder or rock; injectable if dissolved in acid solutions such as vinegar (acetic acid) or citric acid
  • Onset of action: Immediate
  • Half-life: 40 to 90 minutes
  • Reasons for use: Sexual enhancement, attenuate sedation from other substances (heroin, fentanyl, alcohol), mood enhancement, work enhancement, withdrawal avoidance, euphoria
  • Street names: Blow, bump, C, candy, coke, girl, Perico, Piedra, Scotty, rock
MDMA
  • Source and forms: Synthetic; available as tablets, capsules, crystals, powder
  • Administration: Oral, intranasal insufflation, rectal (“boofing”)
  • Onset of action: 20 to 60 minutes
  • Half-life: 8 to 9 hours
  • Reasons for use: Sexual enhancement, improving depression (including in low doses), interpersonal relationship enhancement (empathogenic effects), co-use or collective use
  • Street names: Ecstasy, Molly, XTC, E, X, Miley Cyrus
  • Slang for use: Raving, rolling, ate up (for long-term use)
Methamphetamine
  • Source and forms: Synthetic; available as a white or clear odorless substance (powder, crystals, or pressed pills) that dissolves easily in water or alcohol
  • Administration: Intravenous, intranasal insufflation, smoked, oral ingestion, vaginal or rectal as a solution
  • Onset of action: Immediate
  • Half-life: 10 hours
  • Reasons for use: Sexual enhancement, increased work duration and stamina, wakefulness, weight loss, improving depression, withdrawal avoidance, enhancement of other drug effects, improved function and self-image, sensory enhancement
  • Street names: Meth, crank, crystal, ice, Tina, speed, water
  • Slang for use: Tweaking, amping, spun, booty bumping (rectal administration)
Prescribed: Amphetamines, Amphetamine Derivatives, Methylphenidate, and Other Stimulants [c]
  • Source and forms: Synthetic medications that may be prescribed for treatment of ADHD or narcolepsy [d]. Includes: Dextroamphetamine-amphetamine (e.g., Adderall, generics), dextroamphetamine sulfate (e.g., Dexedrine, generics), lisdexamfetamine (e.g., Vyvanse), methylphenidate hydrochloride (e.g., Ritalin, Concerta, generics) [e]
  • Administration: Oral, intravenous, intranasal insufflation
  • Onset of action: 20 to 60 minutes
  • Half-life: 6 to 13 hours (depending on formulation)
  • Reasons for use: Performance enhancement, weight loss, improving depression, reductions in use of other amphetamines
  • Street names: Addies, bennies, dexies, crank, pep pills, ice, speed, uppers, Superman, vitamin R
  • Slang for use: Speeding, tweaking, spun, amping

Download Table 1: Characteristics of Commonly Used Stimulants Printable PDF

Common adverse effects: Common adverse effects of stimulant intoxication and chronic use are listed below SAMHSA 2021. See guideline section Withdrawal for stimulant withdrawal symptoms. For adverse effects associated with stimulant use in pregnant individuals, see Stimulant Use in Pregnancy: An Under-Recognized Epidemic Among Pregnant Women Smid, et al. 2019.

Stimulant intoxication:

  • Neuropsychiatric: Grandiosity/egocentricity, hypervigilance, paranoia or psychotic symptoms (associated with higher doses), agitation/anxiety, choreoathetosis (abnormal body movements), insomnia, appetite suppression, mydriasis (dilated pupils), tremors, psychomotor agitation (excessive or animated rapid movements)
  • Cardiovascular: Tachycardia, hypertension, chest pain, palpitations
  • Constitutional: Hyperthermia, weight loss

Chronic stimulant use:

  • Neuropsychiatric: Extreme fatigue and disrupted sleep, formication (sensation of bugs crawling on skin), paranoia or psychosis, depression, anhedonia, anxiety/panic attacks, choreoathetosis (abnormal body movements), headache, seizures
  • Cardiovascular: Heart attack, arrhythmia, myocarditis, hypertensive crisis, heart failure, stroke (ischemic and hemorrhagic), renal infarction, ischemic bowel
  • Constitutional: Malnutrition, cachexia, extreme weight loss, refeeding syndrome
  • Respiratory: Chronic obstructive pulmonary disease, pneumonitis (especially with inhalation)
  • Dermatologic: Secondary skin infections, excoriations (e.g., due to formication)
  • Dental: Dental carries, teeth loss, gum disease, gingivitis, aphthous ulcers

The term “overamping” may be used by patients to describe the negative effects of overusing stimulants. Symptoms associated with overamping vary between individuals and include anxiety, paranoia, psychosis, seizure, palpitations, hypertension, hyperthermia, and cardiac and cerebrovascular events Ciccarone and Shoptaw 2022Harding, et al. 2022. Overamping may not be an acute or discrete event, and different patients may define and experience it differently. Treatment for overamping includes symptom management (e.g., hypertension) and supportive care. Individuals experiencing these symptoms should be advised to hydrate, replenish electrolytes, and remain in a calm environment.

Screening, Assessment, and Counseling

Screening and Assessment

The NYSDOH AI evidence-based guideline Substance Use Screening, Risk Assessment, and Use Disorder Diagnosis in Adults recommends annual substance use screening for all adult patients. A positive screening result for stimulant use or a history of stimulant use disorder or overdose should prompt an assessment of the patient’s level of risk. Stimulant use disorder is defined as the continued use of amphetamine-type substances, cocaine, or other stimulants leading to clinically significant impairment or distress; diagnosis is based on the Diagnostic and Statistical Manual of Mental Disorders (DSM-5-TR) criteria. See the following tables in the NYSDOH AI guideline Substance Use Screening, Risk Assessment, and Use Disorder Diagnosis in Adults:

KEY POINTS
  • Stigma among clinicians against people who use substances has been well documented Stone, et al. 2021Tsai, et al. 2019van Boekel, et al. 2013 and may prevent individuals from seeking or receiving medical care, substance use treatment, and harm reduction services.
  • The NYSDOH AI evidence-based guideline Substance Use Harm Reduction in Medical Care recommends that clinicians:
    • Actively examine their assumptions and decisions for personal bias that may adversely affect their ability to provide effective care for individuals who use substances.
    • Use nonjudgmental language that respects individuals’ dignity and avoid language that perpetuates stigma.

Patients may be concerned that substance use disclosure will bias their clinicians and have a negative effect on their care, or they may have previous experience with healthcare bias and legal ramifications. Before screening, assure patients that the detailed questions are intended to help the care provider offer appropriate treatment and services. Remind patients that responses are voluntary but will be documented in the medical record and available to the healthcare team. Medical records will not be released without the patient’s signed consent, except when subpoenaed by a court.

The experience of trauma is common among people with a substance use disorder Bartholow and Huffman 2021Karsberg, et al. 2021Zarse, et al. 2019, and a trauma-informed approach is advised. See NYSDOH AI guideline Substance Use Harm Reduction in Medical Care > Trauma-Informed Care.

Box 1, below, describes an approach to talking with patients about substance use during the screening and assessment processes and ongoing conversations that may help to build trust in the clinician-patient relationship.

Box 1: Talking With Patients About Substance Use [a]
  • Normalize discussions of substance use by linking them to discussions of tobacco and alcohol use in a nonjudgmental manner.
  • Ask permission to talk about substance use, e.g., Would it be okay if we discussed this today or during your next visit? I want to be sure to offer you every treatment or service that might be beneficial, help keep you out of harm’s way, and improve your health and well-being.
  • Proactively destigmatize and normalize conversations about substance use with patients, e.g., Have you ever felt discriminated against because of your drug use? If you experience anything that feels like discrimination here, please let me know.
  • Avoid making assumptions, ask open-ended and clarifying follow-up questions, as needed, and ask only for information relevant to a patient’s current medical care. Discussing history related to substance use may be difficult for patients and should be asked about once rapport and trust are well established.
  • Substance use language and terminology change often, and one term may refer to different substances, e.g., “dope” may refer to cannabis or heroin. Ask patients to define any unfamiliar terms and to correct any misuse of terms (see Table 1: Characteristics of Commonly Used Stimulants).
  • Some modes of use carry stigma and patients may be reluctant to mention them. If clinicians ask specifically, it may encourage conversation, e.g., How do you use (drug of choice)? Are you injecting, snorting, or smoking? Mode(s) of use inform harm reduction strategies.
  • The use of substances with sex may increase a patient’s risk of acquiring HIV, hepatitis C virus, and other STIs. Clinicians may ask, e.g., Do you use drugs with sex? Are there any drugs that you use only with sex? How do you use (drug of choice) with sex? Some methods, such as rectal use of methamphetamine or cocaine, are associated with abrasions that increase the risk of exposure to HIV and other STIs during condomless sex.

Abbreviation: STI, sexually transmitted infection.

Counseling and Medical Care for Patients Who Use Stimulants

Based on the clinical expertise of the authors and this committee, the strategies below can help clinicians engage patients in a discussion of their stimulant use, harm reduction, and recommended medical care.

Effects of stimulant use: Ask patients who use stimulants about how the substance affects them positively and negatively, e.g., How does meth make you feel? Are there negative effects? Understanding patients’ drug use experience can inform harm reduction and treatment goals.

Explore the effect of stimulant use on underlying medical and mental health conditions or symptoms in an objective, nonjudgmental manner. For example, stimulant use may cause or worsen cardiovascular conditions Reddy, et al. 2020Kevil, et al. 2019Darke, et al. 2017. Asking patients about symptoms associated with stimulant use (e.g., chest pain, shortness of breath, or headache) may help clinicians engage patients in a conversation focused on harm reduction or prevention.

Stimulant use may worsen pre-existing anxiety and depression and may cause or worsen other symptoms including mania, paranoia, and delusions McKetin, et al. 2019McKetin, et al. 2013Darke, et al. 2008Zweben, et al. 2004. A clinician might say, “I’m concerned that meth might be increasing your anxiety,” or ask, “Some people who use ICE can have paranoia or believe things that aren’t real. Has that happened to you?”

In assessing the effects of stimulant use, avoid prematurely attributing symptoms to a patient’s substance use and perform indicated routine and symptom-related clinical evaluation. Treatment for conditions such as hypertension should not be withheld or delayed in patients who continue to use stimulants.

Withdrawal: Stimulant withdrawal symptoms may include fatigue, irritability, insomnia, poor concentration, anxiety, depression, and decreased ability to perform daily activities Ciccarone and Shoptaw 2022. Although stimulant withdrawal is not itself life-threatening, symptoms may persist for days or weeks in individuals who have a history of chronic use. Of note, there is also an increased risk of self-harm and suicide due to symptoms of depression and dysphoria related to stimulant withdrawal SAMHSA 2021Lerner and Klein 2019.

Sexualized stimulant use: Specific psychoactive drugs, such as methamphetamine, gamma-hydroxybutyrate (GHB), gamma butyrolactone (GBL), and mephedrone, may be used to enhance sex, most commonly by men who have sex with men (MSM). “Chemsex” or “party and play” often refers to sexualized stimulant use during sex with anonymous partners or group sex, over an extended period, that is arranged using digital apps Harm Reduction International 2021. “Slam sex” refers to the use of injected stimulants during sex Schreck, et al. 2021. In MSM, sexualized stimulant use has been associated with condomless sex, sex with multiple partners, and injection drug use, all of which increase the risk of exposure to or transmission of HIV and other sexually transmitted infections Strong, et al. 2022Curtis, et al. 2020Guerra, et al. 2020Tomkins, et al. 2019. For patient education resources, see ChemSex Harm Reduction: Safer Chemsex & Safer Sex Guides and Tweaker: Crystal Meth.

Harm reduction: In counseling patients, clinicians should take a nonjudgmental and supportive approach to the potential risks of stimulant use and strategies. For example, people who use stimulants are at high risk of dental problems, including caries, abscesses, and poor dentition ASAM 2023, and harm reduction can include encouraging regular dental care and referrals to dental care when required.

KEY POINT
  • All patients who inject stimulants or other substances should be counseled about safer use of drug equipment. Licensed pharmacies, healthcare facilities, and healthcare providers may sell or furnish hypodermic needles or syringes to individuals age ≥18 years without a patient-specific prescription; drug equipment is also available at New York State Authorized Syringe Exchange Sites.

All patients who use stimulants should be encouraged to make an overdose prevention plan. Individuals who use stimulants, even if only occasionally or episodically, may underestimate their opioid overdose risk.

Overdose prevention strategies: Counsel patients to:

  • Assume all illicitly manufactured opioids will contain fentanyl or other high-potency synthetic opioids and that stimulants and counterfeit pills may contain these agents.
  • When possible, test drugs with fentanyl test strips or other drug-checking strategies. Online sources include MATTERS (for New York State residents and programs, no charge), DanceSafe, and BTNX. Some New York State Authorized Syringe Exchange Sites may provide fentanyl test strips and other drug-checking strategies.
  • Try to avoid using drugs alone, and if they have to use alone, arrange for someone to check in or use phone- and web-based apps (e.g., Never Use Alone Inc. at 800-484-3731).
  • Start with a small amount (low dose) when using any drug.
  • Carry naloxone (NLX), learn how to use it to reverse an opioid overdose, and encourage friends and contacts to do the same. The 4 mg NLX nasal spray formulation is available at pharmacies, at NYSDOH-Registered Opioid Overdose Prevention Programs (no charge), and through online resources such as NEXT Distro. NLX is covered by New York State Medicaid and most private insurers.

See the NYSDOH AI guideline Substance Use Harm Reduction in Medical Care > Box 1: Harm Reduction Resources in New York State (September 2023).

Treatment

Stimulant use disorder (StUD): If a patient is diagnosed with StUD, discuss harm reduction strategies, assess readiness to change behavior, and advise on available evidence-based behavioral and pharmacologic treatments. A collaborative approach will help identify the treatment options best suited to a patient’s life circumstances and preferences. Also helpful are discussions about barriers to care (e.g., housing, transportation, competing priorities) and positive supports and experiences that may facilitate treatment success.

Goals of treatment: Abstinence from stimulants may not be achievable in the short term, and more feasible treatment goals can lead to substantial improvements in the health and lives of patients who use stimulants. With a harm reduction approach, treatment goals may include staying in care; treating co-occurring medical conditions; reducing use; reducing risky behaviors; improving mental health; and improving quality of life and other social indicators, such as employment, stable housing, and reduced risk of incarceration. Develop a plan in collaboration with the patient using the principles of shared decision-making and schedule a follow-up appointment to reassess progress. A patient’s treatment goals may change over time and should be reassessed periodically.

Concomitant opioid use disorder (OUD) treatment: Stimulant use or StUD has been associated with lower rates of OUD treatment initiation and retention in care Frost, et al. 2021. Continue medication for OUD treatment in patients who also use stimulants. If a StUD is adversely affecting OUD treatment, have a nonjudgmental discussion with the patient, reassess their treatment and harm reduction goals and strategies, counsel them to continue OUD treatment, and consider treatment for StUD.

Behavioral treatment options: Evidence supports contingency management (CM) as the primary component of a behavioral treatment plan for patients with StUD, in conjunction with a community reinforcement approach, cognitive behavioral therapy (CBT), and the Matrix Model ASAM 2023. Systematic reviews and meta-analyses indicate that CM is more effective than other treatments for cocaine use disorder Bentzley, et al. 2021 and more effective than CBT, 12-step groups, and other behavioral strategies for StUD De Crescenzo, et al. 2018. The goal of CM is to increase desired behavior (i.e., reducing substance use) by providing immediate reinforcing incentives, such as cash or vouchers when the target behavior occurs. However, providing a CM intervention in a real-world setting can be difficult; barriers include regulatory obstacles, cost, stakeholder buy-in, and program resources ASAM 2023SAMHSA 2021.

For a detailed discussion of behavioral treatment for StUD, including online or mobile applications, see the ASAM/AAAP Clinical Practice Guideline on the Management of Stimulant Use Disorder.

KEY POINTS

For patients with StUD, clinicians who are not specialists in substance use treatment are encouraged to:

  • Discuss harm reduction strategies, including overdose prevention.
  • Evaluate patient’s readiness to engage in treatment; if ready, collaborate with patient on treatment goals.
  • Refer patient for behavioral therapy based on availability and patient preference. Evidence indicates that, overall, CM and other behavioral approaches are more effective than pharmacologic treatment for StUD ASAM 2023.
  • Consult with or refer patient to a substance use treatment specialist for pharmacologic treatment.

Pharmacologic treatment options: The U.S. Food and Drug Administration has not approved any medications for the treatment of StUD. In randomized, placebo-controlled clinical trials, several treatment regimens have been associated with reductions in stimulant use in some individuals with cocaine or methamphetamine use disorder Brandt, et al. 2021Trivedi, et al. 2021Coffin, et al. 2020Levin, et al. 2020Nuijten, et al. 2016Shoptaw, et al. 2008. Treatment response rates are generally low, and results are complicated by multiple factors, including low adherence, high dropout rates, comorbid substance use disorders, and the use of abstinence as a primary outcome Brandt, et al. 2021.

Table 2, below, lists medications that may benefit some patients with StUD with factors from the ASAM/AAAP Clinical Practice Guideline on the Management of Stimulant Use Disorder to consider when reviewing pharmacologic treatment options. There is little evidence to guide clinicians; consultation with or referral to a substance use treatment specialist is strongly encouraged. Treatment with psychostimulants such as methylphenidate and sustained-release dextroamphetamine to treat StUD is controversial. Although not prohibited by federal law, state laws governing their use vary ASAM 2023.

Abbreviations: ADHD, attention-deficit hyperactivity disorder; AUD, alcohol use disorder; ASAM/AAAP, American Society of Addiction Medicine/American Academy of Addiction Psychiatry; CBT, cognitive behavioral therapy; FDA, U.S. Food and Drug Administration; MSM, men who have sex with men; RCT, randomized clinical trial; XR, extended-release.

Notes:

  1. For treatment considerations in pregnant patients, see ASAM/AAAP Clinical Practice Guideline on the Management of Stimulant Use Disorder > Population-Specific Considerations > Pregnant and Postpartum Patients.
  2. Bupropion is a cathinone and can cause a false positive result for amphetamines/methamphetamines FDA 2017.
  3. The use of psychostimulants to treat stimulant use disorder is controversial and has regulatory considerations.
Table 2: Medications and Factors to Consider for Stimulant Use Disorder Treatment in Nonpregnant Adults From the ASAM/AAAP Clinical Practice Guideline on the Management of Stimulant Use Disorder [a]
Note: No medications are approved by the FDA for the treatment of stimulant use disorder.
Medication(s)/Key Citations Considerations ASAM 2023
Amphetamine or Methamphetamine Use Disorder
Mirtazapine
Coffin, et al. 2020Colfax, et al. 2011
  • May also treat co-occurring depressive disorders
  • May reduce stimulant-associated sexual risk behaviors in MSM; may reduce insomnia
  • Adverse effects include weight gain and drowsiness
Injectable XR naltrexone plus XR oral bupropion [b]
Trivedi, et al. 2021Mooney, et al. 2016
  • May also treat co-occurring AUD, tobacco use, and depression
  • Injectable XR naltrexone is contraindicated in patients taking opioids or experiencing opioid withdrawal symptoms. For all contraindications, see prescribing information.
Bupropion [b]
Siefried, et al. 2020Chan(b), et al. 2019
  • Consider for treatment of patients with <18 days use per month; may also treat co-occurring tobacco use or depression
  • More effective for treatment of cocaine use disorder than amphetamine use disorder
Methylphenidate (MPH) [c]
Siefried, et al. 2020Lee, et al. 2018
  • Refer patient to an addiction specialist to consider use
  • Consider for treatment of patients who use ≥10 days per month; may also treat co-occurring ADHD
  • May require dosing at or above the maximum FDA-approved dose for ADHD treatment
Topiramate
Siefried, et al. 2020Lee, et al. 2018Elkashef, et al. 2012
  • May also treat co-occurring AUD
  • Adverse effects (brain fog, appetite suppression) limit efficacy
Cocaine Use Disorder
XR mixed amphetamine salts [c] and topiramate
Levin, et al. 2020Tardelli, et al. 2020
  • Refer patient to an addiction specialist to consider use
  • May also treat co-occurring AUD or ADHD
Sustained-release dextroamphetamine [c]
Nuijten, et al. 2016
  • Refer patient to an addiction specialist to consider use
  • May also treat co-occurring ADHD and may require dosing at or above the maximum FDA-approved dose for ADHD treatment
Modafinil [c]
Sangroula, et al. 2017Castells, et al. 2016
  • Refer patient to an addiction specialist to consider use
  • Avoid in patients with co-occurring AUD or history of pre-existing or substance-induced psychosis
  • May be particularly helpful in helping a patient achieve abstinence early in treatment or for highly motivated and treatment-adherent patients with frequent use upon treatment initiation
Bupropion [b]
Shoptaw, et al. 2008Poling, et al. 2006
  • May also treat co-occurring AUD or tobacco use
  • In 2 RCTs, bupropion combined with CBT or contingency management was superior to placebo for sustained abstinence.
Topiramate
Pearl, et al. 2023Chan(a), et al. 2019Baldaçara, et al. 2016Johnson, et al. 2013
  • May also treat co-occurring AUD
  • Adverse effects (brain fog, appetite suppression) limit efficacy
RESOURCES

Shared Decision-Making

Download Printable PDF of Shared Decision-Making Statement

Date of current publication: August 8, 2023
Lead authors:
Jessica Rodrigues, MS; Jessica M. Atrio, MD, MSc; and Johanna L. Gribble, MA
Writing group: Steven M. Fine, MD, PhD; Rona M. Vail, MD; Samuel T. Merrick, MD; Asa E. Radix, MD, MPH, PhD; Christopher J. Hoffmann, MD, MPH; Charles J. Gonzalez, MD
Committee: Medical Care Criteria Committee
Date of original publication: August 8, 2023

Rationale

Throughout its guidelines, the New York State Department of Health (NYSDOH) AIDS Institute (AI) Clinical Guidelines Program recommends “shared decision-making,” an individualized process central to patient-centered care. With shared decision-making, clinicians and patients engage in meaningful dialogue to arrive at an informed, collaborative decision about a patient’s health, care, and treatment planning. The approach to shared decision-making described here applies to recommendations included in all program guidelines. The included elements are drawn from a comprehensive review of multiple sources and similar  attempts to define shared decision-making, including the Institute of Medicine’s original description [Institute of Medicine 2001]. For more information, a variety of informative resources and suggested readings are included at the end of the discussion.

Benefits

The benefits to patients that have been associated with a shared decision-making approach include:

  • Decreased anxiety [Niburski, et al. 2020; Stalnikowicz and Brezis 2020]
  • Increased trust in clinicians [Acree, et al. 2020; Groot, et al. 2020; Stalnikowicz and Brezis 2020]
  • Improved engagement in preventive care [McNulty, et al. 2022; Scalia, et al. 2022; Bertakis and Azari 2011]
  • Improved treatment adherence, clinical outcomes, and satisfaction with care [Crawford, et al. 2021; Bertakis and Azari 2011; Robinson, et al. 2008]
  • Increased knowledge, confidence, empowerment, and self-efficacy [Chen, et al. 2021; Coronado-Vázquez, et al. 2020; Niburski, et al. 2020]

Approach

Collaborative care: Shared decision-making is an approach to healthcare delivery that respects a patient’s autonomy in responding to a clinician’s recommendations and facilitates dynamic, personalized, and collaborative care. Through this process, a clinician engages a patient in an open and respectful dialogue to elicit the patient’s knowledge, experience, healthcare goals, daily routine, lifestyle, support system, cultural and personal identity, and attitudes toward behavior, treatment, and risk. With this information and the clinician’s clinical expertise, the patient and clinician can collaborate to identify, evaluate, and choose from among available healthcare options [Coulter and Collins 2011]. This process emphasizes the importance of a patient’s values, preferences, needs, social context, and lived experience in evaluating the known benefits, risks, and limitations of a clinician’s recommendations for screening, prevention, treatment, and follow-up. As a result, shared decision-making also respects a patient’s autonomy, agency, and capacity in defining and managing their healthcare goals. Building a clinician-patient relationship rooted in shared decision-making can help clinicians engage in productive discussions with patients whose decisions may not align with optimal health outcomes. Fostering open and honest dialogue to understand a patient’s motivations while suspending judgment to reduce harm and explore alternatives is particularly vital when a patient chooses to engage in practices that may exacerbate or complicate health conditions [Halperin, et al. 2007].

Options: Implicit in the shared decision-making process is the recognition that the “right” healthcare decisions are those made by informed patients and clinicians working toward patient-centered and defined healthcare goals. When multiple options are available, shared decision-making encourages thoughtful discussion of the potential benefits and potential harms of all options, which may include doing nothing or waiting. This approach also acknowledges that efficacy may not be the most important factor in a patient’s preferences and choices [Sewell, et al. 2021].

Clinician awareness: The collaborative process of shared decision-making is enhanced by a clinician’s ability to demonstrate empathic interest in the patient, avoid stigmatizing language, employ cultural humility, recognize systemic barriers to equitable outcomes, and practice strategies of self-awareness and mitigation against implicit personal biases [Parish, et al. 2019].

Caveats: It is important for clinicians to recognize and be sensitive to the inherent power and influence they maintain throughout their interactions with patients. A clinician’s identity and community affiliations may influence their ability to navigate the shared decision-making process and develop a therapeutic alliance with the patient and may affect the treatment plan [KFF 2023; Greenwood, et al. 2020]. Furthermore, institutional policy and regional legislation, such as requirements for parental consent for gender-affirming care for transgender people or insurance coverage for sexual health care, may infringe upon a patient’s ability to access preventive- or treatment-related care [Sewell, et al. 2021].

Figure 1: Elements of Shared Decision-Making

Figure 1: Elements of Shared Decision-Making

Download figure: Elements of Shared Decision-Making

Health equity: Adapting a shared decision-making approach that supports diverse populations is necessary to achieve more equitable and inclusive health outcomes [Castaneda-Guarderas, et al. 2016]. For instance, clinicians may need to incorporate cultural- and community-specific considerations into discussions with women, gender-diverse individuals, and young people concerning their sexual behaviors, fertility intentions, and pregnancy or lactation status. Shared decision-making offers an opportunity to build trust among marginalized and disenfranchised communities by validating their symptoms, values, and lived experience. Furthermore, it can allow for improved consistency in patient screening and assessment of prevention options and treatment plans, which can reduce the influence of social constructs and implicit bias [Castaneda-Guarderas, et al. 2016].

Clinician bias has been associated with health disparities and can have profoundly negative effects [FitzGerald and Hurst 2017; Hall, et al. 2015]. It is often challenging for clinicians to recognize and set aside personal biases and to address biases with peers and colleagues. Consciously or unconsciously, negative or stigmatizing assumptions are often made about patient characteristics, such as race, ethnicity, gender, sexual orientation, mental health, and substance use [Avery, et al. 2019; van Boekel, et al. 2013; Livingston, et al. 2012]. With its emphasis on eliciting patient information, a shared decision-making approach encourages clinicians to inquire about patients’ lived experiences rather than making assumptions and to recognize the influence of that experience in healthcare decision-making.

Stigma: Stigma may prevent individuals from seeking or receiving treatment and harm reduction services [Tsai, et al. 2019]. Among people with HIV, stigma and medical mistrust remain significant barriers to healthcare utilization, HIV diagnosis, and medication adherence and can affect disease outcomes [Turan, et al. 2017; Chambers, et al. 2015], and stigma among clinicians against people who use substances has been well-documented [Stone, et al. 2021; Tsai, et al. 2019; van Boekel, et al. 2013]. Sexual and reproductive health, including strategies to prevent HIV transmission, acquisition, and progression, may be subject to stigma, bias, social influence, and violence.

SHARED DECISION-MAKING IN HIV CARE
  • As prevention and treatment modalities in HIV care expand (i.e., vaccines, barriers, injectables, implants, on-demand therapies), it is important for clinicians to ask patients about their goals for prevention and treatment rather than assume that efficacy is the primary factor in patient preference [Sewell, et al. 2021].
  • The shared decision-making approach to clinical care enhances patient knowledge and uptake of new technologies and behavioral practices that align with the patient’s unique preferences and identity [Sewell, et al. 2021], ensures that the selection of a care plan is mutually agreed upon, and considers the patient’s ability to effectively use and adhere to the selected course of prevention or treatment.

Resources and Suggested Reading

In addition to the references cited below, the following resources and suggested reading may be useful to clinicians.

RESOURCES
References

Acree ME, McNulty M, Blocker O, et al. Shared decision-making around anal cancer screening among black bisexual and gay men in the USA. Cult Health Sex 2020;22(2):201-16. [PMID: 30931831]

Avery JD, Taylor KE, Kast KA, et al. Attitudes toward individuals with mental illness and substance use disorders among resident physicians. Prim Care Companion CNS Disord 2019;21(1):18m02382. [PMID: 30620451]

Bertakis KD, Azari R. Patient-centered care is associated with decreased health care utilization. J Am Board Fam Med 2011;24(3):229-39. [PMID: 21551394]

Castaneda-Guarderas A, Glassberg J, Grudzen CR, et al. Shared decision making with vulnerable populations in the emergency department. Acad Emerg Med 2016;23(12):1410-16. [PMID: 27860022]

Chambers LA, Rueda S, Baker DN, et al. Stigma, HIV and health: a qualitative synthesis. BMC Public Health 2015;15:848. [PMID: 26334626]

Chen CH, Kang YN, Chiu PY, et al. Effectiveness of shared decision-making intervention in patients with lumbar degenerative diseases: a randomized controlled trial. Patient Educ Couns 2021;104(10):2498-2504. [PMID: 33741234]

Coronado-Vázquez V, Canet-Fajas C, Delgado-Marroquín MT, et al. Interventions to facilitate shared decision-making using decision aids with patients in primary health care: a systematic review. Medicine (Baltimore) 2020;99(32):e21389. [PMID: 32769870]

Coulter A, Collins A. Making shared decision-making a reality: no decision about me, without me. 2011. https://www.kingsfund.org.uk/sites/default/files/Making-shared-decision-making-a-reality-paper-Angela-Coulter-Alf-Collins-July-2011_0.pdf

Crawford J, Petrie K, Harvey SB. Shared decision-making and the implementation of treatment recommendations for depression. Patient Educ Couns 2021;104(8):2119-21. [PMID: 33563500]

FitzGerald C, Hurst S. Implicit bias in healthcare professionals: a systematic review. BMC Med Ethics 2017;18(1):19. [PMID: 28249596]

Greenwood BN, Hardeman RR, Huang L, et al. Physician-patient racial concordance and disparities in birthing mortality for newborns. Proc Natl Acad Sci U S A 2020;117(35):21194-21200. [PMID: 32817561]

Groot G, Waldron T, Barreno L, et al. Trust and world view in shared decision making with indigenous patients: a realist synthesis. J Eval Clin Pract 2020;26(2):503-14. [PMID: 31750600]

Hall WJ, Chapman MV, Lee KM, et al. Implicit racial/ethnic bias among health care professionals and its influence on health care outcomes: a systematic review. Am J Public Health 2015;105(12):e60-76. [PMID: 26469668]

Halperin B, Melnychuk R, Downie J, et al. When is it permissible to dismiss a family who refuses vaccines? Legal, ethical and public health perspectives. Paediatr Child Health 2007;12(10):843-45. [PMID: 19043497]

Institute of Medicine. Crossing the quality chasm: a new health system for the 21st century. 2001. https://www.ncbi.nlm.nih.gov/books/NBK222274/

KFF. Key data on health and health care by race and ethnicity. 2023 Mar 15. https://www.kff.org/racial-equity-and-health-policy/report/key-data-on-health-and-health-care-by-race-and-ethnicity/ [accessed 2023 May 19]

Livingston JD, Milne T, Fang ML, et al. The effectiveness of interventions for reducing stigma related to substance use disorders: a systematic review. Addiction 2012;107(1):39-50. [PMID: 21815959]

McNulty MC, Acree ME, Kerman J, et al. Shared decision making for HIV pre-exposure prophylaxis (PrEP) with black transgender women. Cult Health Sex 2022;24(8):1033-46. [PMID: 33983866]

Niburski K, Guadagno E, Abbasgholizadeh-Rahimi S, et al. Shared decision making in surgery: a meta-analysis of existing literature. Patient 2020;13(6):667-81. [PMID: 32880820]

Parish SJ, Hahn SR, Goldstein SW, et al. The International Society for the Study of Women’s Sexual Health process of care for the identification of sexual concerns and problems in women. Mayo Clin Proc 2019;94(5):842-56. [PMID: 30954288]

Robinson JH, Callister LC, Berry JA, et al. Patient-centered care and adherence: definitions and applications to improve outcomes. J Am Acad Nurse Pract 2008;20(12):600-607. [PMID: 19120591]

Scalia P, Durand MA, Elwyn G. Shared decision-making interventions: an overview and a meta-analysis of their impact on vaccine uptake. J Intern Med 2022;291(4):408-25. [PMID: 34700363]

Sewell WC, Solleveld P, Seidman D, et al. Patient-led decision-making for HIV preexposure prophylaxis. Curr HIV/AIDS Rep 2021;18(1):48-56. [PMID: 33417201]

Stalnikowicz R, Brezis M. Meaningful shared decision-making: complex process demanding cognitive and emotional skills. J Eval Clin Pract 2020;26(2):431-38. [PMID: 31989727]

Stone EM, Kennedy-Hendricks A, Barry CL, et al. The role of stigma in U.S. primary care physicians’ treatment of opioid use disorder. Drug Alcohol Depend 2021;221:108627. [PMID: 33621805]

Tsai AC, Kiang MV, Barnett ML, et al. Stigma as a fundamental hindrance to the United States opioid overdose crisis response. PLoS Med 2019;16(11):e1002969. [PMID: 31770387]

Turan B, Budhwani H, Fazeli PL, et al. How does stigma affect people living with HIV? The mediating roles of internalized and anticipated HIV stigma in the effects of perceived community stigma on health and psychosocial outcomes. AIDS Behav 2017;21(1):283-91. [PMID: 27272742]

van Boekel LC, Brouwers EP, van Weeghel J, et al. Stigma among health professionals towards patients with substance use disorders and its consequences for healthcare delivery: systematic review. Drug Alcohol Depend 2013;131(1-2):23-35. [PMID: 23490450]

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Updates, Authorship, and Related Guidelines

Updates, Authorship, and Related Guidelines
Date of original publication July 03, 2023
Date of current publication July 17, 2024
Highlights of changes, additions, and updates in the July 17, 2024 edition

Intended users New York State clinicians
Lead author(s)

Judith Griffin, MD; William Supplee, MD

Writing group

Susan D. Whitley, MD; Timothy J. Wiegand, MD, FACMT, FAACT, DFASAM; Sharon L. Stancliff, MD; Brianna Norton, DO, MPH; Christopher J. Hoffmann, MD, MPH, MSc; Charles J. Gonzalez, MD

Author and writing group conflict of interest disclosures There are no author or writing group conflict of interest disclosures.
Committee

Substance Use Guidelines Committee

Developer and funder

New York State Department of Health AIDS Institute (NYSDOH AI)

Development process

See Guideline Development and Recommendation Ratings Scheme, below.

Related NYSDOH AI guidelines

Guideline Development and Recommendation Ratings

Guideline Development: New York State Department of Health AIDS Institute Clinical Guidelines Program
Program manager Clinical Guidelines Program, Johns Hopkins University School of Medicine, Division of Infectious Diseases. See Program Leadership and Staff.
Mission To produce and disseminate evidence-based, state-of-the-art clinical practice guidelines that establish uniform standards of care for practitioners who provide prevention or treatment of HIV, viral hepatitis, other sexually transmitted infections, and substance use disorders for adults throughout New York State in the wide array of settings in which those services are delivered.
Expert committees The NYSDOH AI Medical Director invites and appoints committees of clinical and public health experts from throughout New York State to ensure that the guidelines are practical, immediately applicable, and meet the needs of care providers and stakeholders in all major regions of New York State, all relevant clinical practice settings, key New York State agencies, and community service organizations.
Committee structure
  • Leadership: AI-appointed chair, vice chair(s), chair emeritus, clinical specialist(s), JHU Guidelines Program Director, AI Medical Director, AI Clinical Consultant, AVAC community advisor
  • Contributing members
  • Guideline writing groups: Lead author, coauthors if applicable, and all committee leaders
Disclosure and management of conflicts of interest
  • Annual disclosure of financial relationships with commercial entities for the 12 months prior and upcoming is required of all individuals who work with the guidelines program, and includes disclosure for partners or spouses and primary professional affiliation.
  • The NYSDOH AI assesses all reported financial relationships to determine the potential for undue influence on guideline recommendations and, when indicated, denies participation in the program or formulates a plan to manage potential conflicts. Disclosures are listed for each committee member.
Evidence collection and review
  • Literature search and review strategy is defined by the guideline lead author based on the defined scope of a new guideline or update.
  • A comprehensive literature search and review is conducted for a new guideline or an extensive update using PubMed, other pertinent databases of peer-reviewed literature, and relevant conference abstracts to establish the evidence base for guideline recommendations.
  • A targeted search and review to identify recently published evidence is conducted for guidelines published within the previous 3 years.
  • Title, abstract, and article reviews are performed by the lead author. The JHU editorial team collates evidence and creates and maintains an evidence table for each guideline.
Recommendation development
  • The lead author drafts recommendations to address the defined scope of the guideline based on available published data.
  • Writing group members review the draft recommendations and evidence and deliberate to revise, refine, and reach consensus on all recommendations.
  • When published data are not available, support for a recommendation may be based on the committee’s expert opinion.
  • The writing group assigns a 2-part rating to each recommendation to indicate the strength of the recommendation and quality of the supporting evidence. The group reviews the evidence, deliberates, and may revise recommendations when required to reach consensus.
Review and approval process
  • Following writing group approval, draft guidelines are reviewed by all contributors, program liaisons, and a volunteer reviewer from the AI Community Advisory Committee.
  • Recommendations must be approved by two-thirds of the full committee. If necessary to achieve consensus, the full committee is invited to deliberate, review the evidence, and revise recommendations.
  • Final approval by the committee chair and the NYSDOH AI Medical Director is required for publication.
External reviews
  • External review of each guideline is invited at the developer’s discretion.
  • External reviewers recognized for their experience and expertise review guidelines for accuracy, balance, clarity, and practicality and provide feedback.
Update process
  • JHU editorial staff ensure that each guideline is reviewed and determined to be current upon the 3-year anniversary of publication; guidelines that provide clinical recommendations in rapidly changing areas of practice may be reviewed annually. Published literature is surveilled to identify new evidence that may prompt changes to existing recommendations or development of new recommendations.
  • If changes in the standard of care, newly published studies, new drug approval, new drug-related warning, or a public health emergency indicate the need for immediate change to published guidelines, committee leadership will make recommendations and immediate updates and will invite full committee review as indicated.
Recommendation Ratings Scheme
Strength Quality of Evidence
Rating Definition Rating Definition
A Strong 1 Based on published results of at least 1 randomized clinical trial with clinical outcomes or validated laboratory endpoints.
B Moderate * Based on either a self-evident conclusion; conclusive, published, in vitro data; or well-established practice that cannot be tested because ethics would preclude a clinical trial.
C Optional 2 Based on published results of at least 1 well-designed, nonrandomized clinical trial or observational cohort study with long-term clinical outcomes.
2† Extrapolated from published results of well-designed studies (including nonrandomized clinical trials) conducted in populations other than those specifically addressed by a recommendation. The source(s) of the extrapolated evidence and the rationale for the extrapolation are provided in the guideline text. One example would be results of studies conducted predominantly in a subpopulation (e.g., one gender) that the committee determines to be generalizable to the population under consideration in the guideline.
3 Based on committee expert opinion, with rationale provided in the guideline text.

Last updated on September 18, 2024