RECOGNITION AND ASSESSMENT
- Withdrawal syndromes are specific to:
- type of drug involved
- route of administration
- frequency of use
- quantity used
- individual variation in sensitivity
- psychological state
- Mild symptoms occurring after withdrawal of a drug do not require routine medical intervention
- explaining to patient likely course of withdrawal reduces severity of withdrawal symptoms
- If treatment may be required suggest TAP
- Test (investigations) Assess (as described below) and Phone (drug agency that will continue input following discharge acute hospital)
Investigations
- Obtain witnessed urine sample or mouth swab for drug screen
- contact alcohol liaison team for screening tests
- Check patient’s prescribed medications with GP when surgery open
- if patient states they are taking opiate substitute, contact prescriber
- Pregnancy test, if indicated
Pregnancy
- Very detailed assessment and close management of withdrawal because of risks to fetus
- Refer to appropriate drug service and contact on-call obstetric team. See Management of a pregnant woman with a non-obstetric problem guideline
OPIATE WITHDRAWAL
Symptoms and signs
- Nausea, vomiting
- Diarrhoea
- Restlessness, anxiety
- Irritability, insomnia
- Muscle and bone pains
- Running eyes and nose
- Sneezing, yawning
- Sweating, flushing
- Dilated pupils, pilo-erection
- In a hospital setting assess opiate withdrawal severity
Immediate treatment
- Where withdrawal symptoms are of sufficient severity to warrant medical treatment, several options are available
Symptomatic treatment
- Nausea, vomiting and insomnia: promethazine hydrochloride 25 mg oral 12-hrly
- Somatic anxiety: propranolol 40 mg oral 8-hrly
- Diarrhoea: loperamide 4 mg single oral dose. Do not give loperamide if infective diarrhoea suspected
- Stomach cramps: hyoscine butylbromide 10–20 mg oral 6-hrly
- Pain: paracetamol 1 g oral 6-hrly or ibuprofen 400 mg oral 8-hrly if required
Opiate substitution
- Discuss initiation of opiate substitution with drug agency (based on geography) that will continue input following discharge from acute hospital
- Do not give substitutes unless a screening test confirms presence of opiates
- Drug of choice is methadone mixture (1 mg/1 mL)
- do not use injectable or tablet forms of methadone
- do not give alternative forms of opiate unless discussed with relevant drug agency
Initial dose
- Measure withdrawal symptoms at 6-hrly intervals for 24 hr
- if score >5, give methadone 1 mg per point (i.e. score of 5 = no dose, score of 7 = 7 mg)
- Following first four 6-hrly assessments, add up doses administered at these assessments
- sum will be the daily dose on which patient should continue
- If significant withdrawal symptoms persist and patient remaining in hospital, give the new daily dose and perform a further 24 hr cycle of 6-hrly assessments
- in order to decide dose to be given on day 3, add any extra methadone given on day 2 to the sum obtained from day 1
Maintenance dose
- Once stable dose has been achieved, give methadone as single daily dose
- with amount calculated from initial doses as described above
- Maximum dose in 24 hr should not exceed 50 mg without specialist advice
Subsequent management
- Aim to allow patient to stabilise on the dose of methadone reached by titration with any reductions arranged by continuing care teams once discharged
- On discharge, continuing prescription should be via local community services
Monitoring treatment
- Complete withdrawal table 6-hrly
Discharge and follow-up
- Contact agency that has agreed to continue prescribing
- allow as much warning as possible in order for necessary arrangements to be made
- relevant agency will confirm arrangements for prescription and appointment
- Do not write methadone prescription as a TTO
- Notify GP
SEDATIVE WITHDRAWAL
- Benzodiazepines and other sedative hypnotic drugs
- Alcohol. See Alcohol withdrawal guideline
Symptoms and signs
- Confusion
- Nystagmus
- Tremor
- Agitation, irritability
- Insomnia
- Pyrexia
- Hyperreflexia
- Weakness
- Convulsions
Immediate treatment
- In initial stages, treatment of sedative withdrawal is similar to that for alcohol. See Alcohol withdrawal guideline
- Once symptoms controlled, change to long-acting benzodiazepine (chlordiazepoxide, diazepam) in an equivalent dose (Table) to maintain clinical state
- Discuss a longer-term strategy with either Local drug management service or patient’s GP
GAMMA-HYDROXYBUTYRATE (GHB)
- GHB is a ‘party’ drug used for its euphoric effects. It may interact with other illicit or prescribed drugs (e.g. anti-convulsants or anti-psychotics)
Serious side effects
- Headaches
- Hallucinations
- Dizziness
- Confusion
- Nausea
- Vomiting
- Drowsiness
- Agitation
- Diarrhoea
- Sexual arousal
- Numbing of legs
- Vision problems
- Tightness of chest
- Mental changes
- Combativeness
- Memory loss
- Serious breathing and heart problems
- Seizures
- Coma
- Death
- Long-term use may lead to withdrawal symptoms
Management
- Patients may present to A&E in an intoxicated or comatose state
- most wake up within a few hours, but some require ventilation
- Due to short half-life, withdrawal symptoms require active management – use diazepam as indicated in Alcohol withdrawal guideline using CIWA-Ar assessment chart, Higher doses may be required
- Refer to local community drug and alcohol service
STIMULANT WITHDRAWAL
- There are no acute symptoms of stimulant withdrawal that need medical treatment as a matter of urgency. Insomnia and anxiety can be treated symptomatically
- Advice and support are valuable
- Depressive symptoms sometimes occur as a later withdrawal effect and can be treated with an antidepressant
- Refer to local community services
VOLATILE SUBSTANCES
- Commonly misused are butane, toluene, glues, petrol
- As there are no physical withdrawal syndromes, it is best to discontinue use abruptly
- Treatment of intoxication involves general supportive measures
- Refer to local community services
CANNABIS
- Treat anxiety and insomnia symptomatically
© 2022 The Bedside Clinical Guidelines Partnership.
Created by University Hospital North Midlands and Keele University School of Computing and Mathematics.
Research and development team: James Mitchell, Ed de Quincey, Charles Pantin, Naveed Mustfa