Abstract
During the coronavirus disease 2019 (COVID-19) pandemic, we also experienced a worsening opioid overdose epidemic. Untreated opioid use disorder (OUD) in persons with human immunodeficiency virus (HIV) is associated with worse HIV-related outcomes. Buprenorphine is a safe, evidence-based medication for OUD and is effective in reducing opioid craving and overdose and improving outcomes along the HIV care continuum. Despite the longstanding evidence supporting the benefits of buprenorphine, there remains an implementation gap in the uptake of buprenorphine prescribing in HIV care settings. To improve integration of OUD care and HIV primary care, we recommend (1) all HIV clinicians obtain a buprenorphine waiver, (2) teaching on OUD should be integrated into infectious diseases and HIV continuing medical education, and (3) previously validated models of integrated care should be leveraged to urgently expand access to buprenorphine for persons with HIV and OUD.
Keywords: buprenorphine, HIV, opioid use disorder, substance use disorder
HIV clinicians care for many persons with opioid use disorder, and buprenorphine is safe and effective in reducing overdose deaths and improving HIV-related outcomes. HIV clinicians should obtain a buprenorphine waiver to reduce barriers to prescribing in primary care settings.
Although the infectious diseases (ID) community has focused on the coronavirus disease 2019 (COVID-19) pandemic for over 2 years, we have also found ourselves in the midst of an epidemic of opioid overdoses [1]. As human immunodeficiency virus (HIV) clinicians, we care for many patients with opioid use disorder (OUD), and persons with HIV (PWH) and untreated OUD experience worse HIV-related outcomes, including reduced access and adherence to antiretrovirals (ARVs), decreased retention in care, and increased morbidity and mortality [2, 3]. Buprenorphine is an evidence-based, first-line medication for OUD (MOUD); it is effective in reducing opioid craving, illicit opioid use, and overdose deaths [4], and for PWH, it improves engagement and retention in HIV care, ARV adherence, and HIV viral suppression [5, 6]. Thus, there is an urgent need to expand access to MOUD to our patients.
For decades we have known the evidence suggesting the benefits of MOUD [4, 7, 8], yet there remains an implementation gap in the uptake of buprenorphine prescribing in HIV care settings. Buprenorphine can be prescribed by any physicians and advanced practice providers who obtain a special waiver from the Drug Enforcement Agency, commonly known as an “X-waiver.” Despite the availability of this life-saving, evidence-based treatment for OUD, fewer than 15% of individuals with OUD in the United States receive MOUD [9], and only 3% of primary care physicians in the United States have buprenorphine waivers [10].
A critical way to reduce barriers to MOUD for PWH is by increasing the number of HIV providers in the United States with buprenorphine waivers. In this study, we call for every HIV provider to obtain a buprenorphine waiver, and we discuss additional strategies to integrate buprenorphine prescribing into HIV primary care.
INTEGRATE BUPRENORPHINE PRESCRIBING INTO HUMAN IMMUNODEFICIENCY VIRUS CARE SETTINGS: A CALL TO ACTION
Primary care settings are effective in treating OUD and are an opportunity to extend the reach of MOUD [11]. Human immunodeficiency virus clinicians are not only HIV specialists; we are also primary care practitioners (PCPs), and, as such, we are well positioned to treat OUD. Studies demonstrate improved outcomes with integrated HIV and OUD treatment compared with referrals for treatment, which perpetuate fragmented, siloed care for a population already facing barriers to accessing healthcare [12]. In one systematic review, prioritizing offering buprenorphine/naloxone in HIV clinics was associated with improved HIV outcomes, whereas offering referral for medications did not [13].
Like the HIV care continuum, we need to optimize the cascade of care for PWH and OUD by streamlining access to MOUD. With years of research to support MOUD as the gold standard for treating OUD, it is our time as HIV providers to meet the goals of implementing buprenorphine prescribing in HIV primary care settings. Our call is for HIV providers to adopt feasible, evidence-based strategies to integrate buprenorphine prescribing into HIV care, starting with obtaining a buprenorphine waiver. In a recently published call for action, authors described opportunities to integrate OUD care into hospital settings [14]; we have adapted these suggestions to OUD care in HIV care settings (Table 1).
Table 1.
Action Opportunities | |
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INDIVIDUAL HIV CLINICIANS |
|
HIV Clinics and Programs |
|
HIV National Guidelines and Policies |
|
Abbreviations: ADAP, AIDS Drug Assistance Programs; HIV, human immunodeficiency virus; ID, infectious diseases; OUD, opioid use disorder.
Encourage All Human Immunodeficiency Virus Providers to Obtain a Buprenorphine Waiver
Qualified practitioners can apply for a buprenorphine waiver by visiting the Substance Abuse and Mental Health Services Administration (SAMHSA) website and completing an application online (Table 2). Historically, clinicians were required to complete an educational training; however, in April 2021, the US Department of Health and Human Services enabled clinicians to prescribe buprenorphine for OUD for up to 30 patients without this requirement. Human immunodeficiency virus care settings should normalize obtaining an X-waiver as standard of care; this can be accomplished through an opt-out system, requiring waivers as part of onboarding or recredentialing processes, or by having dedicated staff to submit applications on clinicians’ behalf.
Table 2.
|
Abbreviations: APRN, advanced practice registered nurse; DEA, Drug Enforcement Administration; MD, Doctor of Medicine; PA, physician assistant; SAMHSA, Substance Abuse and Mental Health Services.
For APRNs who are required by State law to be supervised to prescribe Schedule III, IV, or V medications, a supervising physician’s name and DEA number must be provided.
For most HIV providers applying for the first time, the 30-patient level waiver is the appropriate waiver selection. Practitioners who are board certified in addiction medicine or addiction psychiatry may apply for a waiver at the 100-patient level.
Increase Education on Opioid Use Disorder to Human Immunodeficiency Virus Providers
We recommend integrating OUD treatment into ID/HIV training and continuing medical education (CME). One barrier to prescribing buprenorphine is lack of knowledge and confidence [24]. Studies have shown that dedicated training sessions improve clinician confidence in prescribing MOUD [25], and increasing training to identify and treat OUD is aligned with suggested actions from a National Academies of Sciences, Engineering, and Medicine workshop [26]. Education should be focused on identifying OUD through screening as part of routine clinical care, prescribing MOUD, and discussing harm reduction strategies with patients. For trainees, education should be integrated into training curricula through didactics, conferences, or elective rotations. For practicing HIV clinicians, education can be integrated into CME by collaborating with local behavioral health and addiction specialists.
Leverage Previously Validated Models of Care to Integrate Human Immunodeficiency Virus and Opioid Use Disorder Services
One barrier to integration of buprenorphine into HIV primary care is the lack of behavioral health resources within the clinic building. Although studies have shown benefit to MOUD with and without adjunctive counseling [27], comprehensive substance use care can be offered through validated models of care. This is particularly important for rural communities, where there is a growing population of people who inject drugs but a scarcity of buprenorphine prescribers.
The ECHO model of care extends access to specialty care to underserved populations or rural areas using video-conferencing technology to mentor local PCPs to treat complex diseases. This model of care successfully delivered care to treat hepatitis C infections in underserved communities [28]. Similarly, this model of telementoring could extend our ability to deliver OUD treatment in HIV care settings, even in the absence of onsite behavioral health specialists.
Another barrier to the uptake of buprenorphine prescribing may be that physicians perceive the workload for managing OUD as too high for a single provider. Collaborative care models, such as The Massachusetts Model, include nurse program directors, nurse care managers, program coordinators, and physicians who share clinical responsibilities, rather than relying on physicians alone. By delivering MOUD as a collaborative team, the Massachusetts Model demonstrated effective use of physician time, comparable outcomes to physician-centered approaches, and increased access to OUD treatment [29]. Other models of care to integrate HIV and OUD services (including the integration of HIV testing and treatment into addiction medicine settings) have been described in detail previously [13, 19, 20, 30–32].
CONCLUSIONS
Like HIV, OUD should be diagnosed and treated at time of presentation. We have learned through caring for PWH that there is “no wrong door” to entry to care. Rapid initiation of ARVs leads to improved linkage of care along the HIV care continuum and decreases time to viral suppression [33]. Similarly, when PWH present for primary care with OUD, HIV providers should be capable and willing to treat them with MOUD. As HIV providers, we are often the only PCPs our patients see, and to provide optimal HIV primary care, we must be empowered to treat comorbid conditions and adapt to tackle important health crises of our time, whether that be the COVID-19 pandemic or opioid crisis. By offering counseling alone or relying on referrals for MOUD, we are missing critical opportunities to intervene on OUD and improve both HIV and OUD outcomes. One of the first steps you can take toward improving care for your patients with HIV and OUD is to obtain a buprenorphine waiver today to treat OUD.
Acknowledgments
Potential conflicts of interest. All authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest.
Contributor Information
A Wendy Fujita, Division of Infectious Diseases, Emory University Department of Medicine, Atlanta, Georgia, USA.
J Deanna Wilson, Division of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Amy J Kennedy, Division of General Internal Medicine, University of Washington School of Medicine, VA Puget Sound Healthcare System, Seattle, Washington, USA.
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