Extended-Release Naltrexone for Alcohol Dependence: Persistence and Healthcare Costs and Utilization

Supplements and Featured PublicationsEconomic Considerations for the Treatment of Opioid and Alcohol Dependence
Volume 17
Issue 8 Suppl


Evaluate persistence with treatment, healthcare costs, and utilization in stably enrolled Aetna Behavioral Health members receiving extended-release naltrexone (XR-NTX) for alcohol use dependence compared with oral medications and psychosocial therapy only.

Study Design: Historical cohort study.

Methods: Aetna beneficiaries with stable enrollment (at least 6 months before and after index treatment) who initiated pharmacotherapy with XR-NTX (n = 211), disulfiram (n = 1043), oral naltrexone (n = 1408), acamprosate (n = 2479), or psychosocial therapy only (n = 6374) for alcohol use disorders between January 1, 2007, and December 31, 2008, were extracted and deidentified from Aetna’s nationwide claims and utilization database. Survival analysis compared persistence with XR-NTX versus oral pharmacotherapies. Difference-in-differences analysis compared healthcare costs and utilization among patients receiving XR-NTX versus oral pharmacotherapies and psychosocial therapy only. Multivariate analyses controlled for demographics.

Results: Patients taking acamprosate and disulfiram were more likely to discontinue treatment than patients taking naltrexone, and patients given oral naltrexone were more likely to discontinue treatment than those given XR-NTX. Outpatient behavioral health treatment visits increased in all study groups. Nonpharmacy healthcare costs and utilization of inpatient and emergency services decreased in the XR-NTX group relative to other study groups.


Patients receiving XR-NTX persisted with treatment longer than patients receiving oral alcohol use—disorder medications or psychosocial therapy only, and had decreased inpatient and emergency healthcare costs and utilization compared with those receiving other medications.

(Am J Manag Care. 2011;17:S213-S221)

The US Food and Drug Administration approved 3 medications for treatment of alcohol dependence disorder in the past 15 years: oral naltrexone (NTX) in 1994; acamprosate in 2004; and extended-release naltrexone (XR-NTX) in 2006. A fourth medication, disulfiram, was approved in 1949. Adoption of alcohol pharmacotherapies, however, has remained limited. One analysis estimates that fewer than 9% of Americans with alcohol dependence fill prescriptions.1

Reasons for limited adoption of alcohol use-disorder (AUD) medications are numerous, including lack of organizational support, incompatibility with treatment model and philosophy, limited provider exposure to information, provider concerns regarding efficacy and side effects, and reimbursement difficulties.2-4 The 2 most commonly cited barriers to adoption of oral NTX in a 2001 survey of addiction physicians were poor adherence and medication cost.4

Poor adherence is a recognized problem among alcohol dependence pharmacotherapies. Side effects, difficulty “feeling” the effect of medication, and lack of understanding of the need for consistent dosing contribute to discontinuation.5 Acamprosate requires dosing 3 times daily and disulfiram produces unpleasant deterrent effects when alcohol is consumed. Oral NTX has a narrow therapeutic window.6 Approximately 15% to 20% of patients continue to fill prescriptions for oral NTX regularly over 6 months.7-9 Kranzler and colleagues found that persistence (a surrogate for adherence) was associated with lower utilization of expensive inpatient healthcare services.9 Subsequent work reported that patients taking oral NTX decreased healthcare spending relative to control patients with and without AUD diagnoses, even when the cost of treatment was included.10

XR-NTX was developed with improved pharmacokinetic properties and a monthly dosing regimen to address the adherence limitations of oral AUD pharmacotherapies.11 Despite these pharmacokinetic advantages, XR-NTX prescribing remains limited due in part to its high cost, the complexity of delivery (must be administered by a qualified healthcare professional), and lack of information about the medication.1,12 Available data suggest that XR-NTX is associated with fewer heavy drinking days and longer time to first drink than placebo over 12-week13 and 24-week14-16 periods. Studies conducted in primary care clinics17 and privately funded substance abuse treatment clinics12 found that 70% to 75% of patients who initiated treatment with XR-NTX returned for a second injection, and adherence was associated with decreased alcohol consumption.17 Patients who received XR-NTX, moreover, incurred lower healthcare costs and decreased utilization in the 6 months following treatment initiation compared with those who took oral pharmacotherapies.18

This study takes a different analytic approach and uses a different patient population from those employed by Mark and colleagues18 to compare treatment adherence and healthcare costs of XR-NTX with oral medications and psychosocial therapy. We hypothesized that (1) treatment adherence would be greater for XR-NTX, given its unique pharmacokinetics, and (2) XR-NTX would be associated with decreased healthcare costs (excluding the cost of the medication itself) and utilization of inpatient and emergency treatment.


Study Design

For this historical cohort study, the population of interest included all continuously enrolled Aetna Behavioral Health (Aetna) members who began pharmacologic or psychosocial treatment for AUDs between January 1, 2007, and December 31, 2008. Patient-level data on allowed behavioral, physical, and prescription drug claims are stored in an integrated national database. Aetna uses the database to coordinate management of physical healthcare with services for alcohol, drug, and mental health problems among members who receive physical, behavioral health, and pharmacy benefits from Aetna. Concurrent review of claims and utilization data identified patients with AUD diagnoses.

Patients were eligible if they met all inclusion criteria: (1) claims review flagged the patient as treated for an AUD, and (2) a prescription for AUD pharmacotherapy (XR-NTX, oral NTX, acamprosate, or disulfiram) was filled or psychosocial therapy was initiated. Treatment initiation (the index date) for the psychosocial therapy only group was the date of the first claim with a full psychiatric evaluation (Current Procedural Terminology code 90801) and an AUD diagnosis.

There were 4 exclusion criteria: (1) lack of continuous enrollment for 6 months before and after the index date; (2) single claims over $25,000; (3) prescriptions for AUD pharmacotherapies in the 3 months prior to the index date; or (4) prescriptions for multiple AUD pharmacotherapies during the 6 months following the index date. The exclusion criteria were designed to eliminate loss to follow-up (number 1), remove outliers (number 2), and prevent exposure misclassification (numbers 3 and 4). Patients receiving psychosocial therapy were only excluded if they had taken AUD pharmacotherapy at any time in the past. All pharmacotherapy patients who met selection criteria were included, as well as a random sample of psychosocial therapy only patients.

There were 73,292 Aetna beneficiaries with AUD diagnoses between January 1, 2007, and December 31, 2008, and 12,994 (18%) with at least 1 claim for an alcohol dependence medication: 241 given XR-NTX; 3779 given oral NTX; 6059 given acamprosate; and 2915 given disulfiram. A total of 13,968 patients comprised the random sample of those receiving psychosocial therapy only. After exclusion criteria, the final analytic data set contained 211 patients given XR-NTX, 1408 given oral NTX, 2479 given acamprosate, 1043 given disulfiram, and 6374 given psychosocial therapy only. The Oregon Health & Sciences Institutional Review Board determined that the study was a secondary analysis of deidentified data and qualified for exemption.


Primary outcome variables were (1) persistence with medication; (2) healthcare spending; and (3) healthcare utilization. Spending and utilization data were aggregated over 6 months before and after the index date.

Persistence measured the number of consecutive days the patients had alcohol dependence pharmacotherapy in their possession. Patients were considered to be in possession of AUD pharmacotherapy from the date they filled a prescription until the date the prescription should have been exhausted. Nonpersistence (discontinuation) was defined as the first time after the index date that patients went more than 10 consecutive days without medication in their possession. The 10-day cutoff was determined empirically. Patients who refilled their prescriptions within 10 days tended to continue to fill them regularly, whereas patients who waited 10 days or longer to refill tended to discontinue.

Healthcare spending measured total nonpharmacy healthcare costs recorded in the Aetna claims database during the 6-month pre- and post-index periods, including out-of-pocket and health plan expenses. Healthcare utilization encompassed inpatient admissions, days spent in inpatient treatment, outpatient behavioral health visits, and emergency department (ED) visits. Outpatient behavioral health visits included psychosocial therapy (psychiatrist and therapist visits) and outpatient visits to hospitals/inpatient facilities (intensive outpatient treatment, partial hospitalization).

Primary predictors were (1) time relative to initiation of AUD treatment and (2) medication (study) group. There were 5 distinct study groups: XR-NTX, oral NTX, acamprosate, disulfiram, and psychosocial therapy only. The dichotomous time variable tested the 6-month pre-index period versus the 6-month post-index period.

Covariates included age, sex, beneficiary status, plan type, region, pretreatment period mental health and substance abuse diagnoses, and pretreatment period physical health diagnoses. Age was a 4-level categorical variable (<35 years, 35-44 years, 45-54 years, and >55 years). Region was a 6-level categorical variable (West, Southwest, North Central, Southeast, Mid Atlantic, and Northeast).

Comorbidities included physical health, mental health, or substance use disorders diagnosed in the 6-month pretreatment period. Diagnoses were grouped into mental health and substance abuse (MH/SA) categories by International Classification of Diseases, 9th Revision code following Ettner et al.19 The MH/SA groups represented schizophrenia and other non-mood psychosis, bipolar disorder, major depression, anxiety disorders, and drug use disorders. The Charlson Comorbidity Index (CCI) represented physical health comorbidities.20 Due to low prevalence of physical health comorbidities, the CCI score was collapsed into a 3-level categorical variable (0, 1-2, 3 or more).

Statistical Analysis

Survival analysis compared persistence with XR-NTX versus oral pharmacotherapies. Discontinuation of medication was the “failure event,” and it was defined as allowing 10 days to elapse after a prescription was exhausted without refill. Prescriptions filled after the first episode of discontinuation were not included in the analysis. Patients who remained persistent at 180 days were censored at that time. The primary predictor was study group (XR-NTX, oral NTX, acamprosate, disulfiram). Covariates included all demographic variables and pretreatment comorbidity indicators. Kaplan-Meier survival curves plotted persistence over the 180-day follow-up period. A Cox proportional hazards model compared the risk of discontinuation for XR-NTX versus oral pharmacotherapies.

Difference-in-differences analysis estimated the impact of XR-NTX versus oral NTX, acamprosate, disulfiram, and psychosocial therapy only on healthcare costs and utilization. We compared the change in healthcare costs and utilization that each group experienced in the 6-month period before versus after treatment initiation for XR-NTX and the other therapy groups. Primary predictors were (1) a time dummy variable that had the value of 1 in the posttreatment period and 0 in the pretreatment period and (2) 4 study group dummy variables with XR-NTX as the reference group. Interactions between the time and study group dummy variables were the primary estimands of interest and tested the difference (between XR-NTX and comparison groups) in the differences (between pretreatment and posttreatment).

A 2-part model estimated the difference-in-differences for average spending per patient per half year.21 Logistic regression determined the probability of any spending and utilization, and generalized linear modeling determined average spending conditional on use. Negative binomial regression modeled utilization outcomes. We used the method of recycled predictions, based on the estimated regression model, to calculate the average effects of the predictor variables on spending/utilization. Bootstrapping (500 replications) generated 95% confidence intervals. Demographic variables were included as covariates in all regression models. Pretreatment comorbidities were not included in the cost and utilization analyses due to poor overlap between study groups. All analyses were conducted using Stata/IC version 11.0 (StataCorp, College Station, Texas).


Table 1 summarizes the characteristics of the 5 study groups. Overall, the population was 62% men, and mean age was 41 years. Most had a preferred provider organization (PPO) health plan (72%) and no physical (85%) or mental health (79%) comorbidities. Study groups significantly differed with respect to sex, age, geographic region of residence, plan type (HMO vs PPO), beneficiary status (subscriber vs dependent), and pretreatment physical health, mental health, and substance abuse diagnoses. Psychosocial therapy only patients were younger, more likely to be male, and less likely to have physical health, mental health, or drug use-disorder comorbidities than patients receiving medication-assisted treatment. XR-NTX and acamprosate groups had the highest prevalence of pretreatment physical health comorbidities (25%), while the XR-NTX and oral NTX groups had the highest prevalence of mental health (41%) and drug abuse (14%) comorbidities.


Survival analysis assessed duration of alcohol pharmacotherapy. Figure 1 provides Kaplan-Meier survival curves for each study group. Most (89%) patients began treatment with 30-day index prescriptions. Each study group had a steep drop in persistence at 40 days (10 days after expiration of the 30-day index prescriptions). Approximately 40% of patients receiving XR-NTX filled a second prescription, as opposed to 30% given oral NTX, 25% given acamprosate, and 20% given disulfiram. The XR-NTX group had the highest level of persistence (15%) after the full 6 months of follow-up.

Table 2 presents the results of Cox proportional hazards regression models that compared the risk of discontinuation for XR-NTX versus oral pharmacotherapies. The analysis controlled for demographics and all pretreatment comorbidities. Patients taking oral medications were more likely to discontinue treatment than those given XR-NTX (P <.05). Throughout the 6-month follow-up, patients taking oral NTX, disulfiram, and acamprosate were 27%, 47%, and 49% more likely to discontinue treatment than those receiving XR-NTX, respectively. Patients taking disulfiram and acamprosate were 16% and 17% more likely to discontinue treatment than those given oral NTX (P <.05).

Expenditures and Utilization

Figures 2A and 2B display the difference-in-differences estimates comparing the posttreatment and pretreatment differences in average costs and utilization between XR-NTX and other therapies. Mean expenditure and utilization per patient per 6 months in the pretreatment and posttreatment periods, pre/post differences, and comparisons of the pre/post differences between the XR-NTX and other therapies (the difference-in-differences) are located in the eAppendix. All analyses controlled for demographics.

Mean pretreatment spending and utilization of outpatient psychosocial therapy (psychiatrist and therapist visits), outpatient visits to behavioral health hospitals/inpatient facilities, inpatient services, and emergency services were higher in the XR-NTX group (mean = $7882) than all comparison groups: oral NTX = $7388; acamprosate = $6312; disulfiram = $5369; and psychosocial only = $4137 (see electronic appendix for detail). Patients receiving psychosocial therapy only had very low utilization of outpatient behavioral health services in the pretreatment period, and the lowest average pretreatment spending.

All study groups increased outpatient psychosocial therapy visits in the posttreatment period. On average, there was 1 additional psychosocial therapy visit in the posttreatment period for every 1 to 2 medication-assisted patient(s) or 33 psychosocial therapy only patients. The increases in utilization of outpatient psychosocial therapy did not significantly differ between the XR-NTX and oral pharmacotherapy groups, but the increase in the XR-NTX group was significantly greater (P <.05) than in psychosocial therapy only.

Outpatient visits to behavioral health hospitals/inpatient facilities (intensive outpatient treatment, partial hospitalization) increased in the posttreatment period compared with the pretreatment period for all study groups. There were 1 to 2 additional visits in the posttreatment period for each patient receiving medication-assisted treatment, and nearly 5 additional visits per psychosocial therapy only patient. Increases did not significantly differ between XR-NTX and oral medication groups, but the increase in the XR-NTX group was significantly less (P <.05) than in psychosocial therapy only.

Utilization of inpatient hospital and ED services decreased following treatment initiation compared with pretreatment levels in all study groups, more so for patients given XR-NTX than those given other therapies. Compared with pretreatment utilization levels, 1 admission (average length of stay, 5 days) was prevented in the posttreatment period for every 2 XR-NTX patients, 5 oral medication patients, and 13 psychosocial therapy only patients. One ED visit was prevented for every 4 XR-NTX patients, 6 oral NTX, acamprosate, or psychosocial therapy only patients, and 9 disulfiram patients. Patients given XR-NTX spent fewer days receiving inpatient treatment than those given disulfiram or psychosocial therapy only (P <.05).

Nonpharmacy healthcare spending decreased significantly in the posttreatment period compared with the pretreatment period for the XR-NTX and oral medication groups, but increased for the psychosocial therapy only group. Spending in the XR-NTX group decreased nearly $2700 per patient per half year compared with those in the psychosocial therapy only group (P <.01).


Aetna Behavioral Health provided claims data from their national database to examine persistence with AUD medications and healthcare costs incurred. Study patients were drawn from a “real world” population, meaning that patients received AUD pharmacotherapy based on their regular providers’ clinical judgment. Compared with patients receiving psychosocial therapy alone, AUD pharmacotherapies were prescribed to those who were older and sicker. Patients given XR-NTX had more comorbid diagnoses, higher pretreatment spending, and greater utilization of outpatient behavioral health services, inpatient services, and emergency services than any other group.

Controlling for demographics and pretreatment physical health, mental health, and drug abuse comorbidities, patients taking XR-NTX persisted with treatment longer than patients receiving oral pharmacotherapies. Patients receiving oral NTX or XR-NTX persisted with treatment significantly longer than those given acamprosate and disulfiram, suggesting a naltrexone drug effect. Patients given XR-NTX persisted with treatment significantly longer than those given oral NTX, indicating a naltrexone delivery mode effect as well. However, persistence needs to be interpreted carefully, since no direct information on alcohol-related health outcomes was available.

Although direct health outcomes were not available in this study, cost and utilization outcomes were. XR-NTX patients decreased nonpharmacy healthcare spending and utilization of inpatient and emergency services relative to oral pharmacotherapies and psychosocial therapy only. One potential explanation for the decrease in spending and utilization is that patients were avoiding necessary healthcare. Arguing against avoidance is the observation that utilization of outpatient behavioral health services increased in all groups. Further evidence to suggest that patients were not simply avoiding healthcare in the posttreatment period lies in the statistic that over 90% of each medication group had nonzero healthcare spending in both pretreatment and posttreatment periods (data not shown). The relatively healthy psychosocial therapy only group had lower proportions of patients with nonzero healthcare spending in the pretreatment (87%) and posttreatment (74%) periods.

This study demonstrated persistence, utilization, and spending patterns similar to those reported in other analyses.5,7-10,14,17,18,22 Lower levels of persistence in the current study may reflect a more stringent definition of persistence, differences in the health of the study populations, or unique features of the Aetna Behavioral Health system. Spending outcomes differed from a recent study10 of oral NTX spending and utilization because we did not include pharmacy costs in the analyses, but overall patterns were similar. Notably, our cost and utilization results replicated findings that suggest that XR-NTX is associated with decreased healthcare costs and utilization compared with oral medications when treating alcohol dependence.18,22 The consistency of results across different patient populations and different analytic approaches lends robustness to these findings. We have also demonstrated an advantage of XR-NTX over oral medications in terms of persistence with treatment. Prior work has found that persistence with XR-NTX is associated with improved drinking outcomes,17 and nonpersistence with oral NTX has been linked with increased healthcare utilization.9 The persistence benefit with XR-NTX provides a plausible explanation for the observed cost and utilization advantages, but the relationship between persistence, health outcomes, and costs/utilization demands further study.

Study Strengths

There were several strengths in this study’s design and analytic approach. The data come from Aetna’s nationwide claims and utilization database, which provides a geographically diverse sample of patients and accurate cost and utilization information. All patients included in the study were continuously enrolled with Aetna Behavioral Health for at least 6 months before and after treatment initiation, so there was no loss to follow-up. Survival analysis provided temporal data on medication persistence throughout the follow-up period. The difference-in-differences analytic approach minimized the effects of unmeasured confounding factors by controlling for time-independent baseline differences between groups. Available confounders were explicitly accounted for in multivariate regression models.

Study Limitations

In addition to its strengths, this study was subject to several limitations. First, treatment was not randomly allocated and the study was limited in its capacity to control for underlying differences between study groups. Considerable differences in demographics, pretreatment comorbid diagnoses, and pretreatment utilization patterns between study groups suggest that unmeasured factors could have influenced treatment allocation and confounded outcome measurements. Important variables that were not available included AUD severity and psychometrics, such as motivation to change drinking behavior. High pretreatment utilization suggests that XR-NTX was prescribed to patients with more severe AUDs. Severity is likely to be a negative confounder that biases the results toward the null, but the overall confounding effects of unmeasured factors and nonrandom treatment allocation is unknown. At the same time, the number of patients receiving each medication reflected current utilization patterns and the number in each group was relatively large. The large number of patients increased confidence in the stability of the results.

The application of selection criteria to study groups with considerable underlying differences could have introduced selection bias. A lower proportion of patients who received XR-NTX (13%) were excluded, compared with those who received an oral medication or psychosocial therapy only (54% to 64%). Excluded patients are likely to represent individuals who lost their jobs and lacked continuous enrollment, individuals who were prescribed 2 or more AUD medications, and individuals with single claims over $25,000. These exclusions should preferentially omit individuals with relatively poor outcomes, thereby biasing our results toward the null.

The difference-in-differences method is a repeated measures design that renders the analysis susceptible to regression to the mean. We cannot exclude the possibility that regression to the mean is responsible for the observed spending and utilization patterns over time. The analysis is also susceptible to types I and II statistical errors. However, the consistency of the results across several outcomes increased confidence that the observed differences were not statistical artifacts. It is unlikely that such consistency would be observed if the results were attributable to chance.


Continuously enrolled patients with AUDs who were prescribed XR-NTX persisted with treatment longer and experienced larger decreases in nonpharmacy healthcare spending and utilization than those who received oral medications or psychosocial therapy only. Although this study was not able to account for the cost of medication, XR-NTX demonstrated favorable persistence and utilization patterns among a cohort of patients in clinical practice. Future research on this topic is necessary to clarify the associations between persistence, healthcare spending and utilization, and direct health outcomes. Cost-effectiveness analyses of XR-NTX and oral medications would provide critical information for practicing clinicians and insurance providers.

The analysis was completed as William Bryson’s MPH thesis with the support of his Oregon Health and Sciences University thesis advisory committee (Dennis McCarty, Chair, John McConnell, Todd Korthuis). Aetna Behavioral Healthcare provided the data.

Author affiliations: Duke University School of Medicine, Durham, North Carolina (WCB); Department of Public Health and Preventive Medicine, Oregon Health and Sciences University, Portland, OR (WCB, PTK, DM); Department of Emergency Medicine, Oregon Health and Sciences University, Portland, OR (KJM); Department of Internal Medicine, Oregon Health and Sciences University, Portland, OR (PTK).

Funding source: This study was completed without external funding. Aetna Behavioral Healthcare provided the data. Dr Korthuis’ time was supported by the National Institutes of Health, National Institute on Drug Abuse (K23DA019809).

Author disclosures: Dr McCarty reports consultation for Purdue Pharma and has a grant application pending with the National Institutes of Health. Dr Bryson, Dr Korthuis, and Dr McConnell report no relationship or financial interest with any entity that would pose a conflict of interest with the subject matter of this article.

Authorship information: Concept and design (WCB, PTK, DM); acquisition of data (WCB, DM); analysis and interpretation of data (WCB, KJM, PTK); drafting of the manuscript (WCB, KJM, DM); critical revision of the manuscript for important intellectual content (WCB, PTK); statistical analysis (WCB, KJM); and supervision (PTK, DM).

Address correspondence to: Dennis McCarty, PhD, Department of Public Health and Preventive Medicine, Oregon Health and Sciences University, 3181 SW Sam Jackson Park Rd, Portland, OR 97239. E-mail: mccartyd@ohsu.edu.

1. Mark TL, Kassed CA, Vandivort-Warren R, Levit KR, Kranzler HR. Alcohol and opioid dependence medications: prescription trends, overall and by physician specialty. Drug Alcohol Depend. 2009;99:345-349.

2. Thomas CP, Wallack SS, Lee S, McCarty D, Swift R. Research to practice: adoption of naltrexone in alcoholism treatment. J Subst Abuse Treat. 2003;24:1-11.

3. Fuller BE, Rieckmann T, McCarty D, Smith KW, Levine H. Adoption of naltrexone to treat alcohol dependence. J Subst Abuse Treat. 2005;28:273-280.

4. Mark TL, Kranzler HR, Song X. Understanding US addiction physicians’ low rate of naltrexone prescription. Drug Alcohol Depend. 2003;71:219-228.

5. Weiss RD. Adherence to pharmacotherapy in patients with alcohol and opioid dependence. Addiction. 2004;99:1382-1392.

6. Volpicelli JR, Rhines KC, Rhines JS, Volpicelli LA, Alterman AI, O’Brien CP. Naltrexone and alcohol dependence: role of patient compliance. Arch Gen Psychiatry. 1997;54:737-742.

7. Harris KM, DeVries A, Dimidjian K. Trends in naltrexone use among members of a large private health plan. Psychiatr Serv. 2004;55:221.

8. Hermos JA, Young MM, Gagnon DR, Fiore LD. Patterns of dispensed disulfiram and naltrexone for alcoholism treatment in a veteran patient population. Alcohol Clin Exp Res. 2004;28:1229-1235.

9. Kranzler HR, Stephenson JJ, Montejano L, Wang S, Gastfriend DR. Persistence with oral naltrexone for alcohol treatment: implications for healthcare utilization. Addiction. 2008;103:1801-1808.

10. Kranzler HR, Montejano LB, Stephenson JJ, Wang S, Gastfriend DR. Effects of naltrexone treatment for alcohol-related disorders on healthcare costs in an insured population. Alcohol Clin Exp Res. 2010;34:1090-1097.

11. Johnson BA. Naltrexone long-acting formulation in the treatment of alcohol dependence. Ther Clin Risk Manag. 2007;3:741-749.

12. Abraham AJ, Roman PM. Early adoption of injectable naltrexone for alcohol use disorders: findings in the private treatment sector. J Stud Alcohol Drugs. 2010;71:460-466.

13. Kranzler HR, Wesson DR, Billot L. Naltrexone depot for treatment of alcohol dependence: a multicenter, randomized, placebo-controlled clinical trial. Alcohol Clin Exp Res. 2004;28:1051-1059.

14. Pettinati HM, Gastfriend DR, Dong Q, Kranzler HR, O’Malley SS. Effect of extended-release naltrexone (XR-NTX) on quality of life in alcohol-dependent patients. Alcohol Clin Exp Res. 2009;33:350-356.

15. Garbutt JC, Kranzler HR, O’Malley SS, et al. Efficacy and tolerability of long-acting injectable naltrexone for alcohol dependence: a randomized controlled trial. JAMA. 2005;293:1617-1625.

16. O’Malley SS, Garbutt JC, Gastfriend DR, Dong Q, Kranzler HR. Efficacy of extended-release naltrexone in alcohol-dependent patients who are abstinent before treatment. J Clin Psychopharmacol. 2007;27:507-512.

17. Lee JD, Grossman E, DiRocco D, et al. Extended-release naltrexone for treatment of alcohol dependence in primary care. J Subst Abuse Treat. 2010;39:14-21.

18. Mark TL, Montejano LB, Kranzler HR, Chalk M, Gastfriend DR. Comparison of healthcare utilization among patients treated with alcoholism medications. Am J Manag Care. 2010;16:879-888.

19. Ettner SL, Frank RG, McGuire TG, Hermann RC. Risk adjustment alternatives in paying for behavioral health care under Medicaid. Health Serv Res. 2001;36:793-811.

20. D’Hoore W, Sicotte C, Tilquin C. Risk adjustment in outcome assessment: the Charlson comorbidity index. Methods Inf Med. 1993;32:382-387.

21. Manning WG, Mullahy J. Estimating log models: to transform or not to transform? J Health Econ. 2001;20:461-494.

22. Baser O, Chalk M, Rawson R, Gastfriend DR. Alcohol dependence treatments: comprehensive healthcare cost, utilization outcomes, and pharmacotherapy persistence. Am J Manag Care. 2011;17(8):S222-S234.

© 2023 MJH Life Sciences
All rights reserved.