Clinical experience with fortnightly buprenorphine/naloxone versus buprenorphine in Italy: preliminary observational data in an office-based setting

Clin Drug Investig. 2010:30 Suppl 1:33-9. doi: 10.2165/11536060-000000000-00000.

Abstract

Buprenorphine/naloxone is a new option for the management of opioid dependence. It has a reduced potential for abuse or misuse compared with methadone and buprenorphine alone, and has a long half-life allowing less frequent dosing. Buprenorphine/naloxone appears to be well suited for the management of opioid dependence in an office-based setting. The aim of this study was to evaluate the efficacy and safety of a buprenorphine/naloxone combination treatment in an office-based setting. Therefore, we evaluated the effect on misuse/diversion, quality of care, quality of life and service delivery. Seventy-eight patients were switched to buprenorphine/naloxone from either methadone or buprenorphine alone; the median duration of previous buprenorphine or methadone treatment was 10 years. Patients received buprenorphine/naloxone and were evaluated throughout a 1-year follow-up period. Treatment was self-administered by the patients every 2 weeks and the mean buprenorphine dosage at 1 year was 8 mg/day. Comparisons were made before and after the switch for patients who switched from buprenorphine alone to buprenorphine/naloxone. Switching to buprenorphine/naloxone was not associated with clinically relevant problems in 50% of patients studied. Buprenorphine/naloxone provided satisfactory coverage of withdrawal symptoms in 78.1% of patients, and 50% of patients were satisfied with buprenorphine/naloxone therapy. Seventy-eight per cent of patients reported improved psychosocial functioning. The majority of patients (approximately 85%) were negative for opioids during toxicological testing. A significantly higher proportion of treatment recipients were highly satisfied during buprenorphine/naloxone administration (p < 0.001 compared with buprenorphine given before the switch). Other outcomes were similar during buprenorphine and buprenorphine/naloxone administration. Fortnightly self-administration of buprenorphine/naloxone appeared to be cost saving for the clinic. Buprenorphine/naloxone is an effective and safe treatment option for the outpatient management of opioid dependence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Sublingual
  • Analgesics, Opioid / administration & dosage*
  • Analgesics, Opioid / adverse effects
  • Analgesics, Opioid / economics
  • Behavior, Addictive
  • Buprenorphine / administration & dosage*
  • Buprenorphine / adverse effects
  • Buprenorphine / economics
  • Cost-Benefit Analysis
  • Counseling
  • Delivery of Health Care
  • Drug Administration Schedule
  • Drug Combinations
  • Drug Costs
  • Female
  • Humans
  • Injections, Intravenous
  • Italy
  • Male
  • Naloxone / administration & dosage*
  • Naloxone / adverse effects
  • Naloxone / economics
  • Narcotic Antagonists / administration & dosage*
  • Narcotic Antagonists / adverse effects
  • Narcotic Antagonists / economics
  • Office Visits* / economics
  • Opioid-Related Disorders / drug therapy*
  • Opioid-Related Disorders / economics
  • Opioid-Related Disorders / psychology
  • Patient Satisfaction
  • Quality of Health Care
  • Substance Abuse Detection
  • Substance Abuse, Intravenous / diagnosis
  • Substance Abuse, Intravenous / prevention & control
  • Substance Withdrawal Syndrome / drug therapy*
  • Substance Withdrawal Syndrome / economics
  • Substance Withdrawal Syndrome / psychology
  • Time Factors
  • Treatment Outcome

Substances

  • Analgesics, Opioid
  • Drug Combinations
  • Narcotic Antagonists
  • Naloxone
  • Buprenorphine