Hospitalization of patients with opioid use disorder (OUD) is increasing, yet little is known about opioid agonist therapy (OAT: methadone and buprenorphine) administration during admission.
Describe and examine patient- and hospital-level characteristics associated with OAT receipt during hospitalization in the Veterans Health Administration (VHA).
A total of 12,407 unique patients, ≥ 18 years old, with an OUD-related ICD-10 diagnosis within 12 months prior to or during index hospitalization in fiscal year 2017 from 109 VHA hospitals in the continental U.S.
OAT received during hospitalization.
Few admissions received OAT (n = 1914; 15%) and when provided it was most often for withdrawal management (n = 834; 7%). Among patients not on OAT prior to admission who survived hospitalization (n = 10,969), 2.0% (n = 203) were newly initiated on OAT with linkage to care after hospital discharge. Hospitals varied in the frequency of OAT delivery (range, 0 to 43% of qualified admissions). Patients with pre-admission OAT (adjusted odds ratio [AOR] = 15.30; 95% CI [13.2, 17.7]), acute OUD diagnosis (AOR = 2.3; 95% CI [1.99, 2.66]), and male gender (AOR 1.52; 95% CI [1.16, 2.01]) had increased odds of OAT receipt. Patients who received non-OAT opioids (AOR 0.53; 95% CI [0.46, 0.61]) or surgical procedures (AOR 0.75; 95% CI [0.57, 0.99]) had decreased odds of OAT receipt. Large-sized (AOR = 2.0; 95% CI [1.39, 3.00]) and medium-sized (AOR = 1.9; 95% CI [1.33, 2.70]) hospitals were more likely to provide OAT.
In a sample of VHA inpatient medical admissions, OAT delivery was infrequent, varied across the health system, and was associated with specific patient and hospital characteristics. Policy and educational interventions should promote hospital-based OAT delivery.
Surging opioid-related hospitalizations challenge the acute care delivery system in the United States (U.S.).1 Opioid-related hospitalizations are associated with increased readmissions2 and 12% of patients admitted with an OUD-related condition leave the hospital against medical advice.3 OUD-related admissions disproportionately burden public payers3,4 and cost more than non-opioid-related admissions.3,5 Opioid agonist therapy (OAT)—buprenorphine or methadone6—is provided infrequently and variably during hospitalization7 or upon discharge.8 Underutilization occurs although OAT delivery during hospitalization is feasible9,10 and OAT receipt is associated with decreased illicit opioid use upon discharge,9 reduced 30- and 90-day readmissions,11 and increased post-hospital substance use disorder (SUD) treatment engagement.11,12
Veterans are particularly vulnerable as they are twice as likely to die from accidental opioid overdose than non-veterans.13 OUD diagnoses within the Veterans Health Administration (VHA) have increased nearly twofold between 2004 (n = 30,093)14 and 2017 (n = 54,078).15 The VHA’s initiatives to increase OAT access16 include a system-wide requirement that all VHA facilities provide access to OAT16 and follow national OUD treatment guidelines.17 In fiscal year 2017, 41% (n = 22,179) of VHA patients with OUD received an OUD-related pharmacotherapy.15 At the facility-level, OUD-related pharmacotherapy delivery ranged from 2 to 76% across the VHA system.15 To date, little is known about inpatient practice for this patient population. This multi-hospital retrospective study examines variation in OAT delivery and receipt for hospitalized VHA patients with OUD.
Study Design and Cohort
A retrospective sample of unique acute medical and surgical inpatient admissions from fiscal year 2017 was extracted from the VHA Corporate Data Warehouse, a database containing national VHA patient electronic health record data. Eligible individuals were aged 18 or older with a primary or secondary OUD ICD-10 diagnosis from any source (inpatient, outpatient, and community care paid for by VHA) in the year preceding index hospitalization or during index hospitalization in fiscal year 2017. Facilities were restricted to “acute care hospitals” with at least 500 acute bed days of care delivered during the study period and at least 25 index admissions. Patients were excluded if they did not have a primary or secondary admission code, if they had an Elixhauser cancer flag,18 and if they had a hospital length of stay (LOS) greater than or equal to the 99th percentile (median 82 days, range 51 to 1652 days). The 99th percentile LOS cutoff was chosen to capture those admitted with OUD-related infections warranting 4 to 6 weeks of inpatient antibiotics and to exclude chronic hospitalization (see Fig. 1). The Veterans Affairs Portland Health Care System Institutional Review Board approved this study (no. 4045).
Variable selection and construction were informed by the existing literature, data availability, and prior qualitative research.19,20 Study variables included patient demographics (age, gender, race, ethnicity), patient diagnoses present on admission (co-occurring mental health and SUD diagnoses), admission characteristics (intensive care unit [ICU] or surgical services received), and admission-related diagnoses (OUD-related infection, OUD-related diagnoses). Hospital characteristics included admission volume, acute OUD diagnosis volume (the percentage of admissions with an acute OUD diagnosis during hospitalization), hospital geographic location, and hospital size.
Pharmacotherapy variables were coded for three time periods: (1) 30 days pre-admission; (2) during admission; and (3) 30 days post-admission. Non-OAT pharmacotherapy included benzodiazepines, non-OAT opioids (e.g., oxycodone), naltrexone, naloxone, inpatient use of first-line opioid withdrawal adjuvant (clonidine), and second-line withdrawal adjuvants (baclofen, gabapentin/pregabalin, tizanidine) (see Appendix Table 1 for additional details). Admission OAT was categorized by four OAT delivery scenarios (OAT continued, OAT initiated with linkage to care, OAT for withdrawal, and OAT sustained) (see Table 1). Categories and calculations involving post-admission care excluded patients who died during admission.
RStudio21,22,23,24,25,26,27 was used for data management and descriptive statistics. Multilevel logistic regression modeling used Stata28 with an alpha value of 0.05. The dependent variable (level 1) was any OAT received (yes/no) during hospitalization, and covariates were level 1 (patient) and level 2 (hospital) continuous, binary, or categorical variables (see Appendix Table 2 for model covariates). Covariate inclusion was based on literature review, study aims, and model fit. Comparative model fit for nested models used the log-likelihood ratio test, the Akaike information criterion, and the Bayesian information criterion. Regression coefficients, standard errors, adjusted odds ratios (AOR) with 95% confidence intervals, and the intraclass correlation coefficient (ICC) were reported. A sensitivity analysis examined whether a narrower OAT administration definition during hospitalization changed study findings.
The study cohort included 12,407 unique patients with index hospitalizations from 109 VHA acute care hospitals in the continental U.S. Most patients were male (n = 11,543; 93%), white (n = 8880; 72%) or Black (n = 2706; 22%), and non-Hispanic or Latino (n = 11,476; 93%) with a median age of 61 years (range 21 to 90). Over half of the patients (n = 8094; 65%) had at least one co-occurring mental health diagnosis and nearly half had at least one co-occurring SUD diagnosis (n = 6024; 49%).
The median length of hospital stay was 5 days (range 1 to 50 days). Nearly 20% of the patients (n = 2303) received ICU services and 6% (n = 779) received surgical services. OUD-related infection or primary or secondary OUD-related diagnoses occurred in 20% of admissions (n = 2491) and 1% of the patients died during admission (n = 119).
Pre- and Post-pharmacotherapy
Approximately one in ten patients received OAT in the 30 days prior to admission (n = 1325; 11.5%) and in the 30 days post-hospital discharge (n = 1420; 11.6%). Thirty percent of patients (n = 3766) had an opioid prescription filled in the 30 days before admission and 35% (n = 4250) filled an opioid prescription in the 30 days after discharge.
The majority of patients did not receive OAT during admission (n = 10,493; 85%). In the 15% of admissions with OAT (n = 1914), methadone was more common (n = 1049; 55%) than buprenorphine (n = 639; 33%). A small number of patients (n = 136; 7.1%) received more than one type of OAT and 4.7% (n = 90) had non-specific administration. For patients on OAT prior to admission (n = 1325), 65% (n = 867) had their OAT continued during admission and 35% (n = 458) had their OAT discontinued during admission—regardless of receipt post-admission.
Related to withdrawal management, 9% of patients received the VHA’s recommended first-line adjuvant for opioid withdrawal—clonidine—and 39% (n = 1089) received a second-line adjuvant (baclofen, gabapentin/pregabalin, or tizanidine).29 Over half of the patients (55%; n = 6765) received at least one non-OAT opioid (e.g., oxycodone) during admission.
Hospital OAT by Delivery Scenario
When hospital OAT was delivered for patients not on pre-admission OAT, it was most often provided as withdrawal management (n = 834; 44%) and infrequently initiated during hospitalization with linkage to care upon discharge (n = 203; 11%). For patients on pre-admission OAT, it was most often delivered as a sustained medication (n = 722; 38%)—OAT received before, during, and after admission—and less often continued during admission, but with subsequent discontinuation after discharge (n = 140; 8%) (see Table 2 for additional details on patient and admission-related characteristics and pharmacotherapy).
System-Wide OAT Delivery
Across the 109 VHA hospitals, the median OAT delivery frequency during admission was 11% (SD 0.10; range 0 to 43%). The data had a non-normal distribution skewed towards less OAT delivery (see Fig. 2). The frequency of OAT delivery scenario in each hospital varied. For example, two hospitals did not provide any OAT, and nearly half of the hospitals (48%; n = 52) did not have a single admission in which OAT was initiated with linkage to care (range 0 to 16 admissions). Measures of variation (ICC) are reported in Appendix Table 3.
Hospital- and Patient-Level Associations with OAT Receipt
In the fully specified model, 13 covariates were associated with hospital OAT receipt. Six covariates increased the odds of receiving OAT during hospitalization: pre-admission OAT receipt (AOR 15.3; 95% CI [13.2, 17.7]); an OUD diagnosis or OUD-related infection during admission (AOR 2.30; 95% CI [1.99, 2.66]); male gender (AOR 1.52; 95% CI [1.16, 2.01]); receipt of adjuvant medication for opioid withdrawal during admission (AOR 1.52; 95% CI [1.32, 1.75]); an opioid withdrawal diagnosis (AOR 1.47; 95% CI [1.12, 1.92]); and an increased length of hospital stay (AOR 1.04; 95% CI [1.03, 1.05]). Seven covariates were associated with decreased odds of OAT receipt: the receipt of pre-admission naltrexone (AOR 0.26; 95% CI [0.12, 0.56]); an unintentional overdose diagnosis (AOR 0.29; 95% CI [0.16, 0.52]); the receipt of admission naltrexone (AOR 0.31; 95% CI [0.14, 0.66]); pre-admission non-OAT opioid receipt (AOR 0.49; 95% CI [0.41, 0.58]); non-OAT opioid receipt during admission (AOR 0.53; 95% CI [0.46, 0.61]); surgical service receipt during admission (AOR 0.75; 95% CI [0.57, 0.99]); and having a co-occurring SUD diagnosis (AOR 0.77; 95% CI [0.67, 0.88]) (see Appendix Table 4).
Four hospital-level covariates were associated with hospital OAT receipt. Patients admitted to large-sized (AOR 2.04; 95% CI [1.39, 3.00]) and medium-sized (AOR 1.90; 95% CI [1.33, 2.70]) hospitals had increased odds of OAT receipt compared with small hospitals. Patients admitted to hospitals located in the northeast (AOR 1.80; 95% CI [1.30, 2.49]) and west (AOR 1.62; 95% CI [1.19, 2.22]) had increased odds of OAT receipt compared with those in the south (see Table 3 for the fully specified model output).
A pre-specified sensitivity analysis examined if a narrower OAT definition would change study findings, specifically, removing non-FDA-approved formulations of OAT for the treatment of OUD (e.g., injectable methadone) from the admission OAT variable. In this sensitivity analysis, surgical service received during admission was no longer statistically significant. No other differences were observed with statistical significance or the directionality of the relationships between covariates and the primary outcome (see Appendix Table 5).
This retrospective cohort analysis of 12,407 VHA hospitalized individuals with a past year or admission-related ICD-10 OUD diagnosis suggests that hospital OAT receipt was rare. This study is the first to examine hospital OAT delivery across multiple hospitals. A limited research base has examined hospital OAT delivery. A 10-year (2004 to 2014) retrospective chart review of patients with intravenous drug use–associated infective endocarditis—from a single Massachusetts hospital—observed that only 11% of OUD admissions had plans for OAT or naltrexone at discharge.7 Our national study confirms and expands upon these findings. Only 15% of patients in our study received any OAT during admission (n = 1914) and the vast majority (91%) of patients not on OAT prior to admission did not receive any OAT during hospitalization (n = 10,035).
Further, only 203 patients in our cohort were initiated on OAT and subsequently linked to care—a nationally recommend best-practice.6,30 Instead, patients naïve to OAT in the 30 days prior to admission were more likely to receive OAT for withdrawal management (n = 834; 7%), representing a missed opportunity to continue OUD treatment beyond hospitalization. Moreover, hospital admission interrupted ongoing outpatient OUD treatment. Over a third of patients had their outpatient OAT discontinued during admission. Contemporary guidance strongly recommends continuing outpatient OAT during admission, including for patients who are undergoing surgical procedures.6,31 It is possible that evolving practice recommendations were not reflected in our sample. Anesthesiologists may recommend buprenorphine discontinuation prior to surgery. However, only 6% of our cohort received surgery and only 12% of those patients were on OAT prior to admission; thus, it is unlikely that this is driving observed findings. Moreover, OAT discontinuation during admission may reflect challenges related to care transitions.20
Previous research in the VHA describes system-wide variation in OUD-related pharmacotherapy delivery, which ranged from 2 to 76% of qualified patients per facility.15 That analysis, however, did not examine variation specifically for hospital admissions. Our study aligns with and builds upon these prior findings. We observed OAT delivery frequency per hospital ranging from 0 to 43% of qualified admissions.
Prior VHA research suggests that specific patient characteristics are positively associated with OAT receipt including male gender, age 56 years or older, and those without a co-occurring mental health diagnosis.32 Gender disparities in SUD treatment and engagement have been described in other care delivery settings.33 Our study builds upon these findings, suggesting that women-identified patients may be less likely to receive OAT during hospitalization. Associations from this study also suggest that outpatient OAT preceding hospitalization influences subsequent hospital OAT delivery, highlighting the importance of OAT engagement prior to admission. Further, specific care received during admission decreased OAT receipt; for example, patients who received non-OAT opioids or surgical procedures were less likely to receive OAT during hospitalization. These two clinical scenarios should not influence hospital OAT administration. Finally, immutable hospital characteristics (e.g., size and location) influenced OAT delivery and may reflect unmeasurable internal hospital attributes (e.g., resources or culture).20 These findings could also reflect the contribution of elements outside the hospital, for example, local beliefs about addiction and availability of community-based treatment resources.20
This is an observational, unmatched, retrospective cohort study; thus, causal relationships cannot be established. There are limitations to the generalizability of study findings because of the cohort (Veterans, older, white, mostly men) and the health system setting (VHA); however, given that the VHA is an integrated health system that has prioritized OAT delivery, it is possible that VHA OAT delivery outperforms non-VHA hospitals. We elected to include patients with an OUD diagnosis in the prior year, not just patients with an admission diagnosis; thus, for 80% of patients, OUD was not the primary reason for hospitalization. The pragmatic study sample selection may be seen as a limitation, but we believe it reflects the realities of acute care delivery for patients hospitalized with complications related to OUD and other chronic illnesses. Patients in our cohort may have been misclassified with an OUD diagnosis and thus were not valid OAT candidates. The challenges of using diagnosis-based denominators for cross-facility comparisons are discussed elsewhere.34 Conversely, OUD is also underdiagnosed and eligible patients may have been inadvertently excluded. Further, our study only includes VHA pharmacotherapy data; thus, it is possible that patients received OAT after discharge at a non-VHA facility. Nonetheless, this is unlikely to significantly influence our results because there were only six cases with post-admission non-VHA OAT receipt in the original data extraction. Another study limitation was our inability to discern why OAT was not delivered (e.g., patients may have declined OAT). Finally, the study data are from 2017, a specific moment in time that does not capture potential changes in practice over time.
Implications for Practice, Research, and Policy
The findings from this study may motivate practice improvement, future research, and inform policy to increase hospital-based OAT delivery in the midst of the opioid-related overdose crisis.
National authorities recommend OAT continuation or initiation in the hospital6 and a National Academies of Science, Engineering, & Medicine consensus report concluded that: “Withholding or failing to have available all classes of FDA-approved medication for the treatment of opioid use disorder in any care or criminal justice setting is denying appropriate medical treatment”(p. 3).30 Further, hospitalization is a reachable moment for treatment initiation and engagement.35,36 Unfortunately, our study suggests that hospital OAT delivery frequency may be far from optimal. The current practice is not only a missed opportunity for treatment engagement, but may also cause harm by disrupting life-saving care.
A recent systematic review suggests that the provision of addiction-related services for hospitalized patients with OUD improves patient, provider, and health care outcomes.37 Interventions to improve OAT delivery may include an organizational intervention—the addiction consult service (ACS), which provides clinical, educational, and policy-based addiction services and programming in the hospital.38 ACSs, however, are unlikely to be available or feasible across all hospitals. Further, it is likely that many hospital providers have limited addiction training39 and are less confident in providing OAT and delivering other OUD-related services. To address this issue, the VHA and other national hospital decisionmakers could publish specific guidance promoting evidence-based addictions hospital care40 or create educational campaigns encouraging hospital-based OAT delivery. These initiatives would likely need to address provider knowledge gaps and addiction-related stigma,20,41 describe pathways to OAT after discharge, and identify policies impeding care inside and outside the hospital setting.20
Research should explore barriers to OAT initiation during hospitalization at the VHA and reasons for practice variation at patient, hospital, and system levels. Given the VHA’s prioritization of OUD treatment, it is possible that the VHA may be outperforming non-VHA hospitals. Future research may confirm this impression. Policymakers and researchers need to consider data access issues. One of the primary challenges to studying hospital OAT delivery is the widespread use of diagnosis-related groupings (DRG) in hospital billing. DRG billing allows hospitals to bill payers through a bundled payment algorithm to account for illness acuity.42 Study replication using Medicaid claims data, for example, is not feasible because most admission-related medications are not captured in the bundled claims data.
The VHA has already mandated national standards to enhance services for patients with OUD. Additional policy interventions outside the VHA may be warranted. Policies requiring all hospitals to offer OAT could be leveraged through hospital-related accrediting bodies (e.g., the Joint Commission). At present, there are no accreditation requirements related to hospital care for persons with OUD and SUDs. It is within the authority of the Joint Commission to require reporting and performance measurement for OAT and to mandate addiction-related technologies for hospital accreditation (e.g., presence of addiction physicians or ACS). Another approach is local legislation. In August 2018, the Massachusetts legislature passed House Bill 4866, Prevention and Access to Appropriate Care and Treatment of Addiction,43which requires Massachusetts’ emergency departments to offer OAT for patients with an opioid overdose and to link them to outpatient services.43 Similar policies could be created for inpatient service delivery. Finally, there is interest in reforming restrictive federal OAT policies, specifically, to abolish buprenorphine X-waiver requirements.44
In a retrospective, unmatched pragmatic VHA patient cohort, hospital OAT delivery varied widely, was infrequently delivered, and was most commonly administered as a continued outpatient medication or for withdrawal management. This study is the first multisite description of hospital OAT delivery and reveals characteristics that require further exploration to understand how to increase OAT access to patients hospitalized with OUD.
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Dr. Priest’s dissertation committee.
This study was funded by the National Institute on Drug Abuse (F30 DA044700, R33 DA035640, UG1 DA015815), the Greenlick Family Scholarship Fund, and the United States Department of Veterans Affairs Health Services Research & Development (IK2HX001516). The funding organizations were not involved in the design of the study, data collection, data analysis, the interpretation of data, or writing of the manuscript.
The Veterans Affairs Portland Health Care System Institutional Review Board approved this study (no. 4045).
Conflict of Interest
Dr. Lovejoy reports grants from VA Health Services Research & Development during the conduct of the study and grants from National Institutes of Health outside the submitted work. Dr. Priest reports grants from National Institutes of Health and the Greenlick Family Scholarship Fund during the conduct of the study. Drs. Englander, McCarty, and Shull have nothing to disclose.
The contents of the manuscript are those of the authors and do not represent the views of the US Department of Veterans Affairs or the US Government.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Dr. Priest’s dissertation defense (February 2019); AMERSA’s Annual Conference (November 2019); and OHSU Family Medicine Grand Rounds (November 2019).
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Cite this article
Priest, K.C., Lovejoy, T.I., Englander, H. et al. Opioid Agonist Therapy During Hospitalization Within the Veterans Health Administration: a Pragmatic Retrospective Cohort Analysis. J GEN INTERN MED 35, 2365–2374 (2020). https://doi.org/10.1007/s11606-020-05815-0
- opioid agonist therapy
- hospital medicine
- opioid use disorder