What is the treatment for opioid addiction?

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Last updated: December 6, 2025View editorial policy

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Treatment of Opioid Use Disorder

Medication-assisted treatment (MAT) combining FDA-approved medications with behavioral therapy is the standard of care for opioid use disorder, with three primary options: buprenorphine, methadone, and naltrexone—each proven to reduce relapse, prevent overdoses, and decrease mortality. 1

First-Line Medication Options

Buprenorphine (Preferred for Most Settings)

  • Buprenorphine is a partial mu-opioid receptor agonist with high receptor affinity that reduces cravings and withdrawal while having a ceiling effect on respiratory depression, making it safer than full agonists like methadone. 2
  • FDA-approved for patients 16 years and older, with extensive evidence supporting efficacy in adults and growing evidence in adolescents. 1
  • Can be prescribed in primary care settings by physicians who complete 8 hours of training and obtain a DEA waiver (though recent regulations have simplified this process). 1
  • Critical initiation requirement: Buprenorphine must ONLY be started when patients are in active opioid withdrawal to avoid precipitated withdrawal—confirm using both history and physical examination with the Clinical Opiate Withdrawal Scale (COWS). 2
  • Therapeutic dose range is 8-16 mg daily, with 16 mg being optimal for most patients. 2

Methadone (Gold Standard for Severe Cases)

  • Methadone is a full opioid agonist with a long half-life that has been established as highly effective for treating opioid addiction. 1
  • Can be initiated at any stage of withdrawal, unlike buprenorphine, making it advantageous for patients in acute distress. 3
  • Federal regulations restrict methadone to certified Opioid Treatment Programs (OTPs), and most programs prohibit admission of patients younger than 18 years. 1, 4
  • Requires daily supervised administration initially, which limits accessibility but ensures compliance. 4

Naltrexone (For Highly Motivated Patients)

  • Naltrexone is an opioid antagonist with high affinity for opioid receptors that blocks euphoric effects of opioids and reduces cravings. 1, 5
  • Has very limited potential for misuse or diversion compared to opioid agonists. 1
  • Extended-release injectable formulation (Vivitrol, 380 mg monthly) reduces adherence burden and is FDA-approved for opioid use disorder. 5, 6
  • Patients must be completely opioid-free for a minimum of 7-10 days (for short-acting opioids) or up to 2 weeks (for buprenorphine/methadone) before initiating naltrexone to avoid precipitating severe withdrawal. 6
  • Most effective in highly motivated populations such as healthcare professionals, criminal justice populations, and those who cannot or do not wish to take continuous opioid agonist therapy. 5, 6
  • May be particularly beneficial for adolescents and young adults with co-occurring alcohol use disorder or those in unstable housing situations. 1

Essential Treatment Components

Behavioral Therapy Integration

  • Medication alone is insufficient—buprenorphine and methadone must be combined with counseling and behavioral therapies to provide comprehensive "whole-patient" care. 2
  • Behavioral interventions include cognitive-behavioral therapy, contingency management, relapse prevention, and motivational enhancement therapy. 1
  • The addition of psychosocial care significantly reduces treatment dropouts and rates of opioid use during treatment and at follow-up. 5

Monitoring Requirements

  • Conduct regular urine drug testing to assess for continued illicit opioid use. 2
  • Assess patients using DSM-5 criteria for opioid use disorder during follow-up visits. 2
  • Offer hepatitis C and HIV screening as part of comprehensive care, given the association with intravenous drug use. 1, 2
  • For naltrexone: perform liver function tests at baseline and every 3-6 months due to potential hepatotoxicity at supratherapeutic doses. 5, 6

Special Populations

Adolescents and Young Adults

  • The American Academy of Pediatrics recommends that pediatricians consider offering medication-assisted treatment to adolescent and young adult patients with severe opioid use disorders or refer to other providers for this service. 1
  • Adolescents are at particularly high risk for addiction due to enhanced neuroplasticity of their developing brains, which allows them to condition to drugs more rapidly. 1
  • Buprenorphine is FDA-approved for patients 16 years and older, with no age-specific safety concerns identified to date. 1
  • Federal regulations prohibit most methadone programs from admitting patients younger than 18 years. 1

Pregnant Patients

  • Buprenorphine alone (Subutex) is preferred over buprenorphine/naloxone combination (Suboxone) during pregnancy. 2

Acute Pain Management in Patients on MAT

  • For patients on buprenorphine maintenance requiring acute pain management, continue the usual buprenorphine dose and use short-acting opioid analgesics as needed for breakthrough pain. 2
  • Buprenorphine's high binding affinity may block effects of other opioids at lower doses, potentially requiring higher analgesic doses. 2
  • Patients on naltrexone cannot receive opioid pain relief—oral naltrexone should be held for 2-3 days prior to elective procedures if opioids are expected; extended-release naltrexone should be held for 24-30 days after the last injection. 5

Common Pitfalls and How to Avoid Them

Precipitated Withdrawal with Buprenorphine

  • Never initiate buprenorphine until objective withdrawal symptoms are present (COWS score typically ≥8-12)—starting too early precipitates severe withdrawal. 2
  • Patients must be opioid-free including tramadol before starting. 6

Precipitated Withdrawal with Naltrexone

  • Perform naloxone challenge test if there is any question of occult opioid dependence before initiating naltrexone. 6
  • Do not perform the challenge in patients showing clinical signs of withdrawal or whose urine contains opioids. 6
  • If switching from buprenorphine or methadone, patients may be vulnerable to precipitated withdrawal for as long as 2 weeks. 6

Overdose Risk After Treatment Discontinuation

  • Patients who discontinue naltrexone have increased risk of opioid overdose and death due to decreased opioid tolerance—provide opioid overdose education and naloxone. 5
  • This applies to all MAT discontinuation, as tolerance decreases during treatment. 5

Underutilization and Access Barriers

  • Despite proven efficacy, medications for opioid use disorder are severely underutilized—less than 50% of addiction treatment programs offer MAT, and only 34% of opioid-dependent patients in treatment receive medication. 1
  • Confusion, stigma, and limited resources restrict access, particularly for adolescents and young adults. 1
  • Policies and attitudes that prevent patients from accessing life-saving medication may be harmful to patient health. 1

Treatment Outcomes and Prognosis

  • Opioid use disorder is a chronic relapsing neurologic disorder with low rates of spontaneous recovery, but outcomes can be significantly improved with medication-assisted treatment. 1
  • MAT reduces relapse rates, prevents overdoses, prevents HIV transmission, and improves quality of life. 1
  • Recovery is an expectable result of comprehensive, continuing care and monitoring—addiction should be managed as a chronic condition requiring continuous treatment. 1
  • Successful outcomes with MAT are as likely as for other chronic diseases such as diabetes, hypertension, and asthma. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Buprenorphine Treatment for Opioid Use Disorder

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Naltrexone Treatment for Opioid and Alcohol Dependence

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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