Extended-Release Naltrexone for Alcohol Dependence: Persistence and Healthcare Costs and Utilization
Published Online: June 17, 2011
William C. Bryson, MD, MPH; K. John McConnell, PhD; P. Todd Korthuis, MD, MPH; and Dennis McCarty, PhD
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.
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.
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