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Opioid Misuse and Dependence

NICE clinical guideline [CG52] Drug misuse in over 16s: opioid detoxification. Published: Jul 2007. Last reviewed: Dec 2024.

NICE BNF Treatment summaries Substance dependence

Department of Health & Social Care Guidance Oral methadone and buprenorphine: recommendations. Published: Dec 2024.

 

Opioid Misuse and Dependence

Pharmacology Overview

Opioids are a drug class, not one specific drug. Common examples include: [Ref]

  • Morphine
  • Codeine
  • Fentanyl
  • Oxycodone
  • Heroin (diamorphine)

MoA: [Ref]

  • Primarily a μ (mu) opioid receptor agonist
  • μ-receptor activation causes:
    • ↓ Presynaptic Ca²⁺ influx → ↓ neurotransmitter release
    • ↑ Postsynaptic K⁺ efflux → neuronal hyperpolarisation

Key opioid related medications:

  • Acute opioid toxicity / overdose → naloxone (opioid receptor antagonist)
  • Long-term management of opioid dependence
    • Methadone = full μ-opioid receptor agonist
    • Buprenorphine = partial μ-opioid receptor agonist and κ-opioid receptor antagonist

Opiates vs opioids

  • Opiates = naturally derived from opium, e.g. morphine and codeine
  • Opioids = broader term covering natural, semi-synthetic and synthetic opioid drugs, e.g. heroin, fentanyl, methadone

Clinical Features and Diagnosis

For clinical features, diagnosis and management of acute opioid toxicity / overdose, see the Opioid Toxicity and Overdose article.

Opioid Intoxication Features

This refers to the expected acute effects of opioid use: [Ref1][Ref2]

  • CNS features
    • Euphoria or a sense of relaxation
    • Analgesia
    • Sedation / drowsiness
  • Miosis
  • Pruritus
  • GI features
    • Nausea and vomiting
    • Constipation

Opioid Withdrawal Features

[Ref1][Ref2]

Objective signs
  • GI features
    • Nausea and vomiting
    • Diarrhoea
  • Secretory features
    • Excessive lacrimation
    • Rhinorrhoea
    • Sweating
  • Other:
    • Yawning
    • Piloerection (“chills” or goosebumps)
  • Physiological changes
    • Pupil dilatation (mydriasis)
    • Hyperthermia
    • Tachycardia
    • Hypertension

Opioid withdrawal and acute opioid toxicity often produce contrasting clinical signs:

  • GI
    • Withdrawal → diarrhoea
    • Toxicity → constipation
  • Pupil
    • Withdrawal → mydriasis (dilation)
    • Toxicity → miosis (constriction – “pin-point pupils”)
Subjective symptoms
  • Insomnia
  • Anxiety, restlessness
  • Low mood
  • Myalgia
  • Abdominal pain

Opioid withdrawal is highly distressing and physically unpleasant.  However, it is usually NOT life-threatening and rarely dangerous in itself.

Management

There are 2 broad consecutive phases:

  1. Detoxification (“getting clean”): short-term process of safely withdrawing opioids in a dependent patient while minimising withdrawal symptoms
  2. Relapse prevention (“staying clean”): following successful detoxification, treatment aims to maintain abstinence and reduce the risk of relapse

1. Detoxification

Detoxification Setting

1st line: community-based detoxification programme (up to 12 weeks) [NICE CG52]

Indications for residential and inpatient detoxification: [NICE CG52]

  • Failed previous community-based detoxification attempts
  • Patient suffers from significant comorbid physical or mental health problems that require structured medical and/or nursing care
  • Require complex polydrug detoxification (e.g. concurrent withdrawal from alcohol or benzodiazepines)
  • Patient experiencing severe social or housing instability

Patients who misuse both alcohol and opioids:

  • In community settings, alcohol detoxification should be completed before starting opioid detoxification
  • In inpatient settings, alcohol and opioid detoxification may be undertaken concurrently

Psychosocial Intervention

Contingency management is the only intervention with clear evidence of effectiveness [NICE CG52]

  • Also known as incentives for abstinence
  • Involves providing structured, voluntary incentives (like vouchers, modest financial rewards, clinical privileges) to reinforce positive behaviours such as drug-free urine screens or session attendance

Pharmacological Intervention

There are 2 main approaches to managing opioid withdrawal thus achieving detoxification:

  • Substitution therapy: use a longer-acting opioid agonist or partial agonist (e.g. methadone or buprenorphine) to replace the misused opioid and reduce the dose gradually
  • Symptomatic relief: use non-opioid adjunctive medications to relieve specific withdrawal symptoms

Substitution Therapy

1st line: [NICE CG52]

  • Methadone (opioid receptor full agonist), OR
  • Buprenorphine (opioid receptor partial agonist)

The choice between the 2 substitution agents depends on the following factors: [BNF][DHSC]

Factor Methadone Buprenorphine
Sedation level Methadone is more sedating

Some patients may prefer this greater sedative effect, particularly those with:

  • Increased anxiety during opioid withdrawal
  • A long history of opioid misuse
  • Concurrent misuse of sedative drugs or alcohol
Buprenorphine is less sedating than methadone

Therefore, preferred when maintaining alertness is important, e.g.:

  • Employment
  • Driving
  • Other skilled tasks
Overdose risk Methadone has a higher risk of overdose Buprenorphine has a lower risk of overdose due to its ceiling effect on respiratory depression

Therefore, may be preferred in patients with:

  • Low or uncertain level of opioid tolerance
  • Concurrent use of sedatives or alcohol
  • Significant comorbid cardiac or respiratory conditions
  • Concerns of unsupervised dosing (e.g. rural areas where supervised dispensing may not be available, those with mobility problems where regular pharmacy attendance is difficult)

To reduce the risk of precipitated withdrawal, the first dose of buprenorphine should be given when the patient is exhibiting signs of withdrawal, or 6-12 hours after the last use of the short-acting opioid. [BNF]

Buprenorphine can precipitate withdrawal if started while other opioid agonists are still active because its high μ-receptor affinity can displace full agonists while only partially activating the receptor.

Do NOT routinely use clonidine or dihydrocodeine in opioid detoxification. [NICE CG52]

Adjuvant / Symptomatic Treatment

Lofexidine (α2-adrenergic receptor agonist): reduces sympathetic outflow, helping relieve autonomic opioid withdrawal symptoms such as sweating, tachycardia and agitation [NICE CG52][BNF]

  • An alternative to standard opioid substitution (i.e. methadone and buprenorphine) in those with mild or uncertain dependence (often <18 y/o)
  • Can also be used as an adjuvant to standard opioid substitution (i.e. methadone and buprenorphine)

Symptom-directed management: [BNF]

  • Diarrhoea → loperamide 
  • Stomach cramps → mebeverine
  • Headache and myalgia → paracetamol and NSAIDs
  • Nausea and vomiting → metoclopramide or prochlorperazine
  • Insomnia → short-acting benzodiazepines or zopiclone

Topical rubefacients can be used to manage muscle pain associated with methadone hydrochloride withdrawal

2. Relapse Prevention

Psychosocial Intervention

Contingency management is the only intervention with clear evidence of effectiveness [NICE CG52]

  • Also known as incentives for abstinence
  • Involves providing structured, voluntary incentives (like vouchers, modest financial rewards, clinical privileges) to reinforce positive behaviours such as drug-free urine screens or session attendance

Pharmacological Intervention

Primary option: naltrexone [BNF]

  • MoA: opioid-receptor antagonist 
  • Naltrexone can only be initiated after successful detoxification and remaining opioid-free for at least 7-10 days [BNF]

Opioid Dependence in Pregnancy

Key points: [BNF]

  • Avoid acute opioid withdrawal during pregnancy as it can cause fetal compromise
  • Opioid substitution therapy is recommended during pregnancy because it carries a lower risk to the fetus than continued use of illicit drugs
    • 1st trimester: avoid withdrawal because it is associated with an increased risk of spontaneous miscarriage
    • 2nd trimester: if withdrawal is undertaken, methadone or buprenorphine should be reduced gradually
    • 3rd trimester: further withdrawal is not recommended because even mild maternal withdrawal is associated with fetal distress, stillbirth and neonatal mortality

If the patient is already stabilised on methadone or buprenorphine when pregnancy occurs, substitution therapy should generally be continued [BNF]

If the mother receives high doses of opioid substitution therapy, the neonate should be monitored for respiratory depression and signs of opioid withdrawal: [BNF]

  • Withdrawal features usually develop 24-72 hours after delivery and may be delayed for up to 2 weeks
  • Key features
    • High-pitched cry
    • Tachypnoea
    • Hungry but ineffective suckling
    • Excessive wakefulness
    • Hypertonicity and seizures (rare)

References

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