Screening, treatment initiation, and referral for substance use disorders
Steven L. Bernstein
Gail D’Onofrio
SimpleOriginal

Summary

SBIRT and STIR models offer effective, resource-sensitive ways to identify and treat substance use. Initiating treatment at first contact—especially in clinical care—can boost outcomes in nicotine and opioid use disorders.

2017

Screening, treatment initiation, and referral for substance use disorders

Keywords SBIRT; STIR; substance use disorders; pharmacotherapy; brief intervention; motivational interviewing; emergency department (ED); primary care; tobacco dependence; opioid dependence

Abstract

Substance use remains a leading cause of preventable death globally. A model of intervention known as screening, brief intervention, and referral to treatment (SBIRT) was developed decades ago to facilitate time- and resource-sensitive interventions in acute care and outpatient settings. SBIRT, which includes a psychosocial intervention incorporating the principles of motivational interviewing, has been shown to be effective in reducing alcohol consumption and consequences in unhealthy drinkers both in primary care and emergency department settings. Subsequently, SBIRT for unhealthy alcohol use has been endorsed by governmental agencies and professional societies in multiple countries. Although most trials support the efficacy of SBIRT for unhealthy alcohol use (McQueen et al. in Cochrane Database Syst Rev 8, 2011; Kaner et al. in Cochrane Database Syst Rev 2, 2007; O’Donnell et al. in Alcohol Alcohol 49(1):66–78, 2014), results are heterogenous; negative studies exist. A newer approach to screening and intervention for substance use can incorporate initiation of medication management at the index visit, for individuals willing to do so, and for providers and healthcare systems that are appropriately trained and resourced. Our group has conducted two successful trials of an approach we call screening, treatment initiation, and referral (STIR). In one trial, initiation of nicotine pharmacotherapy coupled with screening and brief counseling in adult smokers resulted in sustained biochemically confirmed abstinence. In a second trial, initiation of buprenorphine for opioid dependent individuals resulted in greater engagement in treatment at 30 days and greater self-reported abstinence. STIR may offer a new, clinically effective approach to the treatment of substance use in clinical care settings.

High risk health behaviors, including substance use, remain leading causes of preventable death globally. A model of intervention known as screening, brief intervention, and referral to treatment (SBIRT) was developed 20 years ago to facilitate time- and resource-sensitive interventions in acute care and outpatient settings. SBIRT, which includes a psychosocial intervention incorporating the principles of motivational interviewing, has been shown to be effective in reducing alcohol consumption and consequences in unhealthy drinkers both in primary care and emergency department settings (ED). Subsequently, SBIRT for unhealthy alcohol use has been endorsed by governmental agencies and professional societies in multiple countries, including the World Health Organization, American College of Emergency Physicians, the Committee on Trauma of the American College of Surgery, the Substance Abuse and Mental Health Services Administration and the United States Preventive Services Task Force, and the College of Family Physicians of Canada.

SBIRT appears to be an effective strategy for unhealthy alcohol use, although results from clinical trials are mixed, and treatment effects are modest. An additional challenge is that the term “SBIRT” has since been applied to other substances, such as tobacco and opioids. A third concern is that the effect of the site of care, reason for visit, interventionists’ training, or subject’s motivation to change behavior on SBIRT’s efficacy has not been adequately studied. A final concern is that the “brief intervention” component of SBIRT is restricted to behavioral treatments, and omits the many FDA-approved, efficacious pharmacotherapies for the treatment of alcohol, tobacco, and opioid use disorder.

Three recently published trials of brief intervention for individuals with substance use disorders found no benefit. Two were conducted in primary care settings [4, 5], and one in the ED [6]. Similarly, most studies of behavioral treatment for substance use or tobacco dependence in ED populations have been negative [7, 8].

To address some of the shortcomings of SBIRT, we have extended the model by adding the initiation of pharmacotherapy to the therapeutic options of the interventionist, at the index visit. Two recent studies using this model, performed by our group, were successful in decreasing tobacco and opioid use, respectively. This model, which we call screening, treatment initiation, and referral (STIR), represents a paradigm shift in the identification and treatment of individuals with substance use disorders.

We review two recent studies that support the use of STIR, and make recommendations. Both studies were clinical trials conducted in the ED [9, 10].

Bernstein et al. [9] randomized 778 adult smokers in an urban ED to a control or intervention group. Eligible subjects were adults presenting to the ED for any reason. The intervention consisting of an abbreviated version of a motivational interview, a referral faxed to the state smokers’ quitline, a phone call 2–3 days after enrollment, and the provision of six weeks of nicotine patches and gum. The first dose of patch or gum was ED-initiated. Patients in both groups received a brochure promoting the quitline and providing information about the health risks of smoking. At three months, the biochemically confirmed abstinence rate in the intervention group, 12.2% was significantly greater than the control group 4.9% (P < 0.001).

D’Onofrio et al. [10] randomized 329 adults with opioid dependence presenting to the ED (for any condition) to one of three groups: (1) a referral to community-based opioid addiction treatment services; (2) a traditional SBIRT intervention, consisting of a BNI with a facilitated, direct referral to addiction treatment services, or (3) a BNI, ED-initiated buprenorphine and referral to primary care to 10 weeks of continued medical management. The primary outcome for the study was engagement in addiction services treatment at 30 days after randomization.

The STIR strategy, ED-initiated buprenorphine, significantly increased patients’ engagement in addiction treatment at 30 days compared with the SBIRT and referral groups: 78, 45, and 37%, respectively (P < 0.001) and decreased self-reported illicit drug use. In addition, patients in the STIR group were less likely to be enrolled in inpatient addiction services at 30 days, compared to those in the SBIRT or referral groups. There were no differences in rates of negative urine tests.

In both trials, patients were screened for eligibility by trained research assistants. All were adults age 18 years or older, presenting to the ED for any medical or surgical condition; patients with primarily behavioral disorders (e.g. acute psychosis) were excluded. BNIs, conducted by the research assistants, typically lasted 10–15 min. BNIs adapted principles of motivational interviewing, and had four components: permission to discuss substance use, feedback on the health consequences of ongoing substance use, motivational enhancement, and negotiation and advice. In both studies, two-thirds of eligible subjects consented to enroll.

The standard SBIRT model focuses on alcohol. It consists of identifying individuals with risky levels of drinking, and engaging with them using techniques adapted from motivational interviewing or motivational enhancement. For individuals who meet criteria for alcohol use disorder, referral to follow-up in a treatment program is recommended. The referral may consist of giving the individual the contact information for treatment programs, or may involve phoning or electronic referral for a more definitive linkage to care. Printed materials may be provided. Interventions are generally delivered by clinicians, but may also be delivered by other healthcare personnel, or trained lay providers. Initiation of pharmacotherapy is not part of this traditional approach.

STIR adds pharmacotherapy to SBIRT, and may be efficacious for several reasons:

  • Salience of the acute care visit The ED visit has often been described as a “teachable moment,” in which an individual presenting with an acute illness or injury caused by a risky health behavior may be amenable to initiate a change in that behavior. Numerous theories of behavior change have been offered as conceptual models to explain the teachable moment phenomenon [11]. In our work we enroll patients who present to the ED with any condition, irrespective of whether it is caused or exacerbated by the substance use. In general, it is possible to discuss how their substance use may adversely affect treatment of the acute condition.

  • Additive or synergistic effects of pharmacotherapy In the treatment of tobacco dependence, a rich literature describes the enhanced efficacy of combination NRT compared to monotherapy, and medication and counseling together as more effective than either alone [12].

  • Lowering patients’ perceived barriers to medication use Substance users often have diminished access to primary care [13]. Beginning medication during the ED visit allows providers to educate patients on the benefits of medications such as opioid agonists or nicotine replacement therapies, answer questions, and demonstrate application of the nicotine patch.

  • Physicians and providers are comfortable prescribing medications Medical school and residencies traditionally offered limited training in the behavioral treatment of substance use [14], although this is evolving. STIR incorporates behavioral interventions, but allows physicians to use their traditional skills in medication management. For the physician unwilling or unable to provide a behavioral intervention, it is reasonable to begin pharmacotherapy. That said, additional training in the medication-assisted treatment of opioid and alcohol use disorders is likely to be needed.

Implementing a program of STIR requires attention to important operational details. These include:

Screening and assessment for eligibility for specific medications

Protocols for screening, medication eligibility, prescribing, management of withdrawal, and follow-up are needed. This includes partnering with community providers for ongoing care. That said, if STIR should occur in a primary care setting, that setting itself may become the site of follow-up care, in which case the “referral” is part of normal clinic workflow. Whether the clinical setting is primary care or ED, protocols should be sensitive to the need for efficiency and timeliness of care.

Of note, “assessment” may also entail determination of the patient’s willingness to change, although newer paradigms of screening for tobacco use would make treatment the default approach for individuals with identified substance use disorders [15]. The clinical efficacy of making treatment the default for other substances of abuse remains to be determined.

Delivery of the BNI

In our trials, the BNI was delivered by trained, nonclinical research personnel. BNIs were audiotaped and reviewed biweekly by research assistants and a psychologist. This model is not easily replicable, but physicians from diverse specialties can be trained to deliver BNIs [16].

Pharmacologic treatment

Our STIR trials focused on tobacco and opioids, two substances that are widely used and misused. Each has multiple effective, approved medications to treat dependence, with evidence to support reduction in subsequent healthcare utilization [17]. For tobacco, there are seven approved medications: nicotine patch, gum, lozenge, nasal spray, and inhaler, and varenicline and bupropion. For opioid dependence, both methadone and buprenorphine are approved, in addition to the use of naloxone for acute overdoses. In primary care settings, it may be appropriate to consider initiation of naltrexone for alcohol use disorders as well.

Additional scientific and clinical challenges remain. The efficacy of STIR should be confirmed with additional trials in other care settings. Whether the counseling component of STIR can be delivered effectively and reliably by the treating clinician needs to be assessed. In addition, STIR’s efficacy should be assessed for other substances that have effective, agency-approved pharmacotherapy. A good example is alcohol, for which medications such as naltrexone has shown efficacy in reducing use and craving.

Finally, in the United States, new models of care delivery, and enhanced insurance coverage for medication, spurred by the Affordable Care Act, may promote the implementation of STIR. Healthcare systems are increasingly incentivized to manage the health of populations. Integrating STIR into clinical workflows facilitates the treatment of substance use.

ED-based interventions for cigarette smoking and opioid dependence demonstrate that screening and treatment initiation, combining brief counseling, pharmacotherapy, and referral, promote abstinence and increased engagement in treatment. In the ED, STIR has the potential to narrow the gap between services needed and treatment. Its utility in other care settings deserves study. Given the prevalence of substance use, and its associated mortality, morbidity, and cost, we suggest that the moment is ripe for new models of treatment that will facilitate the identification and treatment of individuals with substance use disorders.

Abstract

Substance use remains a leading cause of preventable death globally. A model of intervention known as screening, brief intervention, and referral to treatment (SBIRT) was developed decades ago to facilitate time- and resource-sensitive interventions in acute care and outpatient settings. SBIRT, which includes a psychosocial intervention incorporating the principles of motivational interviewing, has been shown to be effective in reducing alcohol consumption and consequences in unhealthy drinkers both in primary care and emergency department settings. Subsequently, SBIRT for unhealthy alcohol use has been endorsed by governmental agencies and professional societies in multiple countries. Although most trials support the efficacy of SBIRT for unhealthy alcohol use (McQueen et al. in Cochrane Database Syst Rev 8, 2011; Kaner et al. in Cochrane Database Syst Rev 2, 2007; O’Donnell et al. in Alcohol Alcohol 49(1):66–78, 2014), results are heterogenous; negative studies exist. A newer approach to screening and intervention for substance use can incorporate initiation of medication management at the index visit, for individuals willing to do so, and for providers and healthcare systems that are appropriately trained and resourced. Our group has conducted two successful trials of an approach we call screening, treatment initiation, and referral (STIR). In one trial, initiation of nicotine pharmacotherapy coupled with screening and brief counseling in adult smokers resulted in sustained biochemically confirmed abstinence. In a second trial, initiation of buprenorphine for opioid dependent individuals resulted in greater engagement in treatment at 30 days and greater self-reported abstinence. STIR may offer a new, clinically effective approach to the treatment of substance use in clinical care settings.

A Critical Analysis of Screening, Treatment Initiation, and Referral (STIR) for Substance Use Disorders

The global burden of preventable mortality attributable to high-risk health behaviors, particularly substance use, necessitates the development of effective and efficient intervention strategies. The Screening, Brief Intervention, and Referral to Treatment (SBIRT) model, while widely adopted, exhibits limitations in efficacy and scope. Empirical evidence suggests modest treatment effects and inconsistent results across various clinical trials. Furthermore, the generalization of SBIRT beyond alcohol misuse to encompass tobacco and opioid dependence raises concerns regarding its adaptability and effectiveness across diverse substance use disorders. Methodological inconsistencies, including variations in intervention site, provider training, and patient motivation, further complicate the assessment of SBIRT's overall efficacy. The exclusion of FDA-approved pharmacotherapies from the "brief intervention" component represents a significant omission, limiting the model's potential impact.

Recent clinical trials have highlighted the limitations of relying solely on behavioral interventions for substance use disorders. Multiple studies, conducted in primary care and emergency department settings, have yielded null findings concerning the effectiveness of brief interventions alone. This underscores the need for a more comprehensive approach that integrates pharmacological treatments into the intervention paradigm.

In response to these shortcomings, the Screening, Treatment Initiation, and Referral (STIR) model was developed. This paradigm shift incorporates immediate pharmacotherapy initiation alongside brief counseling and referral. Preliminary research utilizing the STIR model has demonstrated promising results in reducing tobacco and opioid use. Two clinical trials conducted in emergency department settings provide supportive evidence for STIR's efficacy.

One study, involving adult smokers, showed significantly increased rates of biochemically confirmed abstinence among participants receiving immediate nicotine replacement therapy (NRT) and brief motivational interviewing compared to a control group. Another trial, focused on opioid dependence, revealed that immediate initiation of buprenorphine significantly enhanced engagement with addiction treatment services compared to both SBIRT and referral-only groups. These studies showcase the potential benefits of integrating pharmacotherapy into the initial intervention.

Methodological Considerations and Operational Aspects of STIR

Both studies employed rigorous methodologies, including randomization and standardized intervention protocols. Trained research assistants performed screenings and brief motivational interviews (BNIs). These interviews, lasting approximately 10–15 minutes, incorporated core elements of motivational interviewing. High participant enrollment rates (two-thirds of eligible subjects) suggest good feasibility. However, the reliance on trained research personnel raises questions regarding the model's generalizability to routine clinical practice.

The traditional SBIRT model, primarily focusing on alcohol misuse, entails identifying risky drinking patterns, employing motivational interviewing techniques, and referring patients with alcohol use disorders to treatment. The lack of pharmacotherapy integration distinguishes it from the STIR model.

Theoretical Underpinnings and Advantages of STIR

The enhanced efficacy of STIR may be attributed to several factors. The acute care setting presents a "teachable moment" where patients, often experiencing consequences of their substance use, may be more receptive to behavior change. The synergistic effects of combining pharmacotherapy with behavioral interventions represent a major advantage. Furthermore, STIR addresses barriers to medication access by initiating treatment immediately, facilitating patient education and providing support during the initial phase. The model leverages existing physician expertise in medication management, potentially overcoming limitations in behavioral intervention training.

Implementation Challenges and Future Directions

Successful STIR implementation requires well-defined protocols for screening, medication eligibility, prescribing, withdrawal management, and follow-up care. Collaboration with community providers is crucial for ensuring continuity of treatment. Further research is necessary to evaluate the efficacy of STIR across diverse settings and substance use disorders. Assessing the feasibility of clinicians delivering both behavioral and pharmacological interventions remains vital. Moreover, extending STIR to other substances with available pharmacotherapies, such as alcohol, warrants future investigation. Finally, evolving healthcare systems and insurance coverage may facilitate the broader adoption of STIR.

Conclusion

The STIR model offers a promising approach to addressing substance use disorders. By integrating immediate pharmacotherapy with brief counseling and referral, STIR potentially bridges the gap between identified need and treatment access. While further research is needed to confirm its efficacy and refine its implementation strategies, STIR demonstrates significant potential for improving outcomes in the management of substance use disorders.

Abstract

Substance use remains a leading cause of preventable death globally. A model of intervention known as screening, brief intervention, and referral to treatment (SBIRT) was developed decades ago to facilitate time- and resource-sensitive interventions in acute care and outpatient settings. SBIRT, which includes a psychosocial intervention incorporating the principles of motivational interviewing, has been shown to be effective in reducing alcohol consumption and consequences in unhealthy drinkers both in primary care and emergency department settings. Subsequently, SBIRT for unhealthy alcohol use has been endorsed by governmental agencies and professional societies in multiple countries. Although most trials support the efficacy of SBIRT for unhealthy alcohol use (McQueen et al. in Cochrane Database Syst Rev 8, 2011; Kaner et al. in Cochrane Database Syst Rev 2, 2007; O’Donnell et al. in Alcohol Alcohol 49(1):66–78, 2014), results are heterogenous; negative studies exist. A newer approach to screening and intervention for substance use can incorporate initiation of medication management at the index visit, for individuals willing to do so, and for providers and healthcare systems that are appropriately trained and resourced. Our group has conducted two successful trials of an approach we call screening, treatment initiation, and referral (STIR). In one trial, initiation of nicotine pharmacotherapy coupled with screening and brief counseling in adult smokers resulted in sustained biochemically confirmed abstinence. In a second trial, initiation of buprenorphine for opioid dependent individuals resulted in greater engagement in treatment at 30 days and greater self-reported abstinence. STIR may offer a new, clinically effective approach to the treatment of substance use in clinical care settings.

Summary

Substance use disorders represent a significant public health concern, contributing substantially to preventable mortality worldwide. The Screening, Brief Intervention, and Referral to Treatment (SBIRT) model, while widely adopted, has demonstrated mixed efficacy and limitations in its application beyond alcohol use. Recent trials highlighting the ineffectiveness of brief interventions alone underscore the need for enhanced approaches.

Limitations of SBIRT

While SBIRT has gained considerable support and adoption, its effectiveness is not consistently demonstrated across studies. The model's applicability to substances beyond alcohol is questionable, and crucial factors influencing its success, such as the intervention site, clinician training, and patient motivation, remain inadequately researched. Moreover, the exclusion of pharmacotherapy from the "brief intervention" component represents a notable limitation given the availability of effective FDA-approved medications for various substance use disorders.

A Novel Approach: Screening, Treatment Initiation, and Referral (STIR)

To address SBIRT’s shortcomings, a modified model—Screening, Treatment Initiation, and Referral (STIR)—incorporates immediate pharmacotherapy alongside brief behavioral interventions. This approach, evaluated in recent clinical trials, showed promising results in reducing tobacco and opioid use. The STIR model represents a paradigm shift by proactively initiating treatment during the initial patient encounter.

STIR Clinical Trial Results

Two studies support the efficacy of STIR. In a study of smokers, ED-initiated nicotine replacement therapy, coupled with brief counseling and referral, yielded significantly higher abstinence rates compared to a control group. Similarly, a trial involving individuals with opioid dependence demonstrated that ED-initiated buprenorphine, along with brief intervention and referral, significantly increased engagement with addiction treatment services and reduced self-reported illicit drug use compared to SBIRT and referral-only groups.

Operational Considerations for Implementing STIR

Successful STIR implementation necessitates careful consideration of operational details. This includes establishing clear protocols for screening and assessment of medication eligibility, appropriate prescribing practices, management of withdrawal symptoms, and ensuring seamless referral for ongoing care. The delivery of brief motivational interventions requires standardized training for clinicians, and the integration of pharmacotherapy needs to align with available FDA-approved medications for different substances.

Future Directions and Conclusion

Further research is needed to validate STIR’s efficacy across diverse settings and populations, and to explore its applicability to other substances with effective pharmacotherapies. The potential role of integrating STIR into various healthcare settings, coupled with evolving care delivery models and improved insurance coverage, highlights its potential to significantly impact substance use disorder treatment. The high prevalence of substance use disorders and their associated negative consequences warrant innovative and effective treatment approaches such as STIR.

Abstract

Substance use remains a leading cause of preventable death globally. A model of intervention known as screening, brief intervention, and referral to treatment (SBIRT) was developed decades ago to facilitate time- and resource-sensitive interventions in acute care and outpatient settings. SBIRT, which includes a psychosocial intervention incorporating the principles of motivational interviewing, has been shown to be effective in reducing alcohol consumption and consequences in unhealthy drinkers both in primary care and emergency department settings. Subsequently, SBIRT for unhealthy alcohol use has been endorsed by governmental agencies and professional societies in multiple countries. Although most trials support the efficacy of SBIRT for unhealthy alcohol use (McQueen et al. in Cochrane Database Syst Rev 8, 2011; Kaner et al. in Cochrane Database Syst Rev 2, 2007; O’Donnell et al. in Alcohol Alcohol 49(1):66–78, 2014), results are heterogenous; negative studies exist. A newer approach to screening and intervention for substance use can incorporate initiation of medication management at the index visit, for individuals willing to do so, and for providers and healthcare systems that are appropriately trained and resourced. Our group has conducted two successful trials of an approach we call screening, treatment initiation, and referral (STIR). In one trial, initiation of nicotine pharmacotherapy coupled with screening and brief counseling in adult smokers resulted in sustained biochemically confirmed abstinence. In a second trial, initiation of buprenorphine for opioid dependent individuals resulted in greater engagement in treatment at 30 days and greater self-reported abstinence. STIR may offer a new, clinically effective approach to the treatment of substance use in clinical care settings.

Summary

High-risk health behaviors, like substance abuse, are major preventable causes of death worldwide. The SBIRT (Screening, Brief Intervention, and Referral to Treatment) model, while effective in some cases for reducing alcohol use, has limitations. Recent studies show mixed results, and the model's application to other substances needs further research. Concerns exist regarding the impact of treatment location, interventionist training, and patient motivation on its success. Additionally, SBIRT mainly focuses on behavioral treatments and lacks the inclusion of FDA-approved medications.

Limitations of SBIRT

Some recent trials of brief interventions for substance use disorders have yielded disappointing results. Studies in both primary care and emergency departments (EDs) often show little to no benefit from behavioral interventions alone. This highlights a need for a more comprehensive approach.

A New Approach: STIR

To improve upon SBIRT, a new model called STIR (Screening, Treatment Initiation, and Referral) has been developed. STIR incorporates the immediate start of medication alongside brief counseling and referral. Initial studies show promise in reducing tobacco and opioid use.

STIR Trials and Results

Two ED-based clinical trials support the effectiveness of STIR. One trial on smokers showed significantly higher quit rates with the addition of nicotine patches and gum alongside brief counseling. Another study on opioid users demonstrated improved engagement in addiction treatment with the inclusion of buprenorphine.

Why STIR Works

Several factors contribute to STIR's success. The ED visit serves as a “teachable moment,” making patients more receptive to change. Combining medication and counseling provides a synergistic effect, greater than either alone. Starting treatment in the ED eliminates access barriers for patients. Lastly, STIR leverages physicians' comfort with prescribing medications while incorporating behavioral interventions.

Implementing STIR

Implementing STIR requires clear protocols for screening, medication eligibility, and ongoing care. The brief counseling component (BNI) can be delivered by trained healthcare personnel, not necessarily specialists. The use of various FDA-approved medications for different substances is key.

Future Directions for STIR

Further research is needed to validate STIR's effectiveness in different settings and with other substances. The reliability of clinicians delivering the brief counseling component also needs to be assessed. However, STIR shows great potential as a more effective model to address substance use disorders.

Abstract

Substance use remains a leading cause of preventable death globally. A model of intervention known as screening, brief intervention, and referral to treatment (SBIRT) was developed decades ago to facilitate time- and resource-sensitive interventions in acute care and outpatient settings. SBIRT, which includes a psychosocial intervention incorporating the principles of motivational interviewing, has been shown to be effective in reducing alcohol consumption and consequences in unhealthy drinkers both in primary care and emergency department settings. Subsequently, SBIRT for unhealthy alcohol use has been endorsed by governmental agencies and professional societies in multiple countries. Although most trials support the efficacy of SBIRT for unhealthy alcohol use (McQueen et al. in Cochrane Database Syst Rev 8, 2011; Kaner et al. in Cochrane Database Syst Rev 2, 2007; O’Donnell et al. in Alcohol Alcohol 49(1):66–78, 2014), results are heterogenous; negative studies exist. A newer approach to screening and intervention for substance use can incorporate initiation of medication management at the index visit, for individuals willing to do so, and for providers and healthcare systems that are appropriately trained and resourced. Our group has conducted two successful trials of an approach we call screening, treatment initiation, and referral (STIR). In one trial, initiation of nicotine pharmacotherapy coupled with screening and brief counseling in adult smokers resulted in sustained biochemically confirmed abstinence. In a second trial, initiation of buprenorphine for opioid dependent individuals resulted in greater engagement in treatment at 30 days and greater self-reported abstinence. STIR may offer a new, clinically effective approach to the treatment of substance use in clinical care settings.

Summary

Doctors are trying to help people stop using harmful substances like cigarettes and drugs. A new way to help, called STIR, is being tested. It's like an improved version of an older method called SBIRT.

What is STIR?

STIR is a plan to help people stop using harmful substances. It’s similar to SBIRT, but better. STIR helps people right away by giving them medicine and advice in the emergency room or doctor’s office. It also includes a plan for continuing help afterward.

How STIR Works

STIR works by giving people medicine to help them quit right then, along with helpful advice. Two studies showed this works well for people who smoke and people who use opioid drugs. In these studies, people who received medicine and advice in the emergency room did better than people who just got advice. STIR helps people get started and get more help if they need it.

More About STIR

STIR is still new, but early results look good. More studies are needed to see how well it works for other drugs and in different places. Doctors are excited because STIR may be a much better way to help many people.

Footnotes and Citation

Cite

Bernstein, S. L., & D’Onofrio, G. (2017). Screening, treatment initiation, and referral for substance use disorders. Addiction science & clinical practice, 12, 1-4.

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