Methadone-related deaths in Norway

Jean-Paul Bernard1, Ingrid Havnes, Lars Slørdal

  • 1Norwegian Institute of Public Health, Division of Forensic Medicine and Drug Abuse Research, Oslo, Norway. jpbern28@hotmail.com

Abstract

Insights

Methadone-related deaths in Norway averaged one weekly from 2000-2006. Most deaths involved intoxication, often with other drugs, and few victims were in opioid maintenance treatment (OMT).

Area of Science:

  • Forensic Toxicology
  • Public Health
  • Pharmacology

Background:

  • Methadone, used in opioid maintenance treatment (OMT), carries risks of adverse effects and fatal toxicity.
  • Increased availability of methadone may correlate with a rise in methadone-related fatalities.
  • This study examined methadone-related deaths in Norway between 2000 and 2006.

Purpose of the Study:

  • To investigate the trends and characteristics of methadone-related deaths in Norway.
  • To assess the role of OMT in methadone-related fatalities.
  • To inform strategies for controlling methadone diversion and reducing mortality.

Main Methods:

  • Forensic toxicological investigations identified methadone-positive samples from 2000-2006.
  • Demographic and toxicological data were collected for deceased individuals.
  • Cases were cross-referenced with the Norwegian Cause of Death Registry and OMT registers.

Main Results:

  • A total of 312 individuals died from methadone use between 2000-2006, predominantly males aged 36.
  • Methadone-related intoxication caused 85% of deaths, frequently involving co-ingestion of other substances like benzodiazepines and opioids.
  • Only 22% of deceased individuals were enrolled in OMT at the time of death; OMT patients had higher mortality from non-intoxication causes (e.g., disease).

Conclusions:

  • An average of one methadone-related death occurred weekly during the study period.
  • A significant majority of methadone-related deaths involved individuals not registered in OMT programs.
  • Findings highlight the critical need for controlling medication diversion from OMT programs to prevent fatalities.

Related Concept Videos

Opioid Analgesics: Synthetic and Semisynthetic Opioids01:15

Opioid Analgesics: Synthetic and Semisynthetic Opioids

Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
Opioid Analgesics: Morphine and Other Natural Cogeners01:20

Opioid Analgesics: Morphine and Other Natural Cogeners

Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
Drug Toxicity: Dose-Dependent Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...
Phase II Reactions: Methylation Reactions01:17

Phase II Reactions: Methylation Reactions

Methylation is a phase II biotransformation process involving the attachment of a methyl group to a substrate. Enzymes known as methyltransferases orchestrate this reaction.
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...
Analgesia and Pain Management01:25

Analgesia and Pain Management

Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
Drugs Affecting Neurotransmitter Synthesis01:29

Drugs Affecting Neurotransmitter Synthesis

Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase, which converts...