Persistence and healthcare utilization associated with the use of buprenorphine/naloxone film and tablet formulation therapy in adults with opioid dependence

Abstract

Background:

Buprenorphine/naloxone film was developed to improve retention in treatment and reduce public health risks over the tablet formulation for opioid dependence.

Objectives:

To compare patient persistence and resource utilization between formulations for the treatment of opioid dependence.

Methods:

A longitudinal, retrospective cohort analysis was conducted to compare persistence and healthcare costs in a private US insurance claims database. Previously untreated patients, who initiated treatment with buprenorphine/naloxone following the introduction of the film, were classified in two groups according to the initial prescription. Persistence was defined as the proportion of patients continuing treatment for at least 6 months. Resource utilization and related costs were calculated over the 6- and 12-month periods after treatment initiation.

Results:

Film and tablet groups included 2796 and 1510 patients enrolled over 9.76 and 13.76 months on average, respectively, from initiation of treatment. Patient characteristics were similar between groups. Mean prescribed doses were 14.62 and 14.26 mg/day in film and tablet groups. Among patients enrolled for at least 6 months from the initial treatment, persistence rates were 63.78% with film vs 58.13% with tablet. Time to treatment discontinuation was longer in the film group, with a hazard ratio of 0.818 (p = 0.0005, 95% CI = [0.730;0.916]) adjusted for baseline characteristics. Patients treated with film had significantly more outpatient visits (+4%, p = 0.0185) and lower probability to be hospitalized (−17%, p = 0.0158), resulting in lower total healthcare costs over the 12-month period after initiation (−27%, p < 0.0001).

Conclusions:

Patients treated with the film formulation of buprenorphine/naloxone appeared to stay longer on treatment, have a lower probability of hospital admission, and lower health care costs compared to patients treated with the tablet. This study, based on insurance claims data, has the advantage of reflecting real-world practice, but one cannot rule out the existence of bias due to differences in patient or prescriber profiles, despite adjustments made for observed characteristics at treatment initiation.

Keywords::

• Patient persistence
• Healthcare utilization
• Opioid dependence
• Buprenorphine/naloxone

Transparency

Declaration of funding

The study was sponsored by Reckitt-Benckiser.

Declaration of financial/other relationships

Reckitt-Benckiser has financial relations with ZRx Outcomes Research, which has financial relations with Creativ-Ceutical.

Acknowledgments

No assistance in the preparation of this article is to be declared.

Notes

*Reckitt Benckiser Pharmaceuticals, Inc., Package Insert, Richmond, VA.