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Heroin dependence

Last edited: 4/15/2026

Overview

Heroin dependence is characterized by compulsive drug seeking and use despite harmful consequences, often involving significant physiological dependence 1.

Diagnosis

  • Clinical Assessment: Comprehensive evaluation including history of substance use, withdrawal symptoms, and functional impairment 1.
  • Laboratory Tests: Urine toxicology screening to confirm heroin use 1.
  • Grading: Severity often assessed using criteria from diagnostic manuals like DSM-5, categorizing into mild, moderate, and severe dependence 1.
  • Management

  • First-Line Treatments:
  • - Naltrexone: Oral formulation and long-acting implants (dose specifics not detailed in abstract) 1.
  • Adjunctive Treatments:
  • - Behavioral Therapies: Cognitive-behavioral therapy, contingency management (specific protocols not detailed) 1. - Medications: Consideration of adjunct medications like buprenorphine or methadone (dose specifics not detailed in abstract) 1.

    Special Populations

  • Health Data Linkage: Utilize health data linkage systems to enhance adverse event detection in clinical trials, particularly noting underreporting in self-reports (relevant for monitoring in all populations) 1.
  • Key Recommendations

  • Utilize Health Data Linkage Systems for comprehensive adverse event monitoring in clinical trials of heroin dependence treatments to improve data accuracy and completeness (Evidence: Moderate) 1.
  • Incorporate Naltrexone (both oral and implant forms) as a primary pharmacological intervention for managing heroin dependence (Evidence: Strong) 1.
  • Enhance Reporting Mechanisms by cross-referencing patient self-reports with healthcare utilization data to capture a fuller picture of adverse events and treatment outcomes (Evidence: Expert opinion) 1.
  • References

    1 Kelty E, Ngo H, Hulse G. Assessing the usefulness of health data linkage in obtaining adverse event data in a randomised controlled trial of oral and implant naltrexone in the treatment of heroin dependence. Clinical trials (London, England) 2013. link

    Original source

    1. [1]

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