Drugs and devices Mental health Poisoning
Poisoning or overdose
Last revised in March 2024
Poisoning denotes exposure to a substance that is dangerous to health or life. This may be a drug, household product, industrial chemical, plant or animal product
Poisoning or overdose: Summary
- In toxicology, poisoning is the state resulting from the administration of excessive amounts of any pharmaceutical agent. A poison may be a drug, household product, industrial chemical, or plant or animal derivative.
- Poisoning may be accidental or deliberate.
- Overdose is the use of a quantity of drug in excess of its intended or prescribed dose. It may be accidental or deliberate and involve the use of prescribed or illicit drugs.
- In the UK, paracetamol is the medication most commonly used in cases of deliberate overdose.
- Around 160,000 people are admitted to hospital in the UK each year with suspected poisoning.
- Prognosis depends on the type of poison, the quantity taken, and associated comorbidities.
- Initial assessment of people with suspected poisoning should include:
- Assessing the person's overall status — performing a rapid assessment of the airways, assessing the level of consciousness, measuring respiratory rate, and measuring the person's pulse, blood pressure and temperature.
- An examination should be performed and include general observations, a neurological examination, and checking for signs consistent with the substance(s) taken.
- If the person has deliberately self-poisoned, assessment should include the person's emotional and mental state, the risk of psychological harm and the risk of further self-harm or suicide, and any safeguarding concerns.
- Emergency transfer to hospital should be arranged for people if they have had a seizure, or if any of the following features are present:
- Unconscious, or reduced level of consciousness.
- Reduced respiratory rate or oxygen saturation is reduced.
- Hypotension.
- Tachycardia or bradycardia or an irregular pulse.
- Hypothermia or hyperthermia.
- Any other concerning clinical features are present, or the person's condition is deteriorating.
- If emergency transfer is not required a history should be taken and include details of the substance taken, relevant personal and medical details, and any symptoms the person is experiencing.
- The following cases should be urgently referred to hospital:
- All people who have deliberately self-poisoned.
- People who are symptomatic.
- People who have taken poisons with a delayed action.
- Where the type of poison is unknown.
- If a person refuses to go to hospital, the reasons should be determined, and information about the potential consequences of not receiving hospital treatment provided.
- If the person still refuses admission, and this is felt to be in their best interests, their capacity should be assessed and it should be considered whether a compulsory admission under the Mental Health Act is appropriate.
- If a person is judged to have diminished capacity and/or the presence of a significant mental health disorder, they should be referred for urgent hospital admission or urgent mental health assessment, depending on clinical judgement.
- In emergency situations, the person's capacity should be assessed. It will almost always be in the person's best interests to give urgent treatment without delay.
- Admission to hospital is not usually indicated for accidental poisoning with agents of low toxicity.
- Hospital assessment is not usually indicated if a person has accidentally taken an additional tablet of their own medication.
Have I got the right topic?
From birth onwards.
This CKS topic is largely based on expert opinion in narrative reviews Initial management of suspected poisoning in children and young people [Anderson, 2021], Principles of management of the poisoned patient [Morrison, 2020], Principles of assessment and diagnosis of the poisoned patient [Thanacoody, 2020a], Psychiatric assessment of self-poisoning [Martin, 2020], the National Institute for Health and Care Excellence (NICE) guideline Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], the British National Formulary (BNF) [BNF, 2022], the National Poisons Information Service (NPIS) Report 2020/21 [NPIS, 2021], and the toxicology database TOXBASE [TOXBASE, 2022].
This CKS topic covers advice on how to assess people who have been poisoned, when to refer to hospital, and the sources of information that can be used to guide management.
This CKS topic does not cover detailed information on how to treat individual cases of poisoning, since referral is advised in these circumstances.
There are separate CKS topics on Adverse drug reactions and Self-harm.
The target audience for this CKS topic is healthcare professionals working within the NHS in the UK, and providing first contact or primary healthcare.
How up-to-date is this topic?
Changes
March 2024 — minor update. Information about the Specialist Pharmacy Service (SPS) has been updated.
Previous changes
March 2022 — reviewed. A literature search was conducted in March 2022 to identify evidence-based guidelines, UK policy, systematic reviews, and key randomized controlled trials (RCTs) published since the last revision of the topic.
April to June 2017 — reviewed. Literature searches were conducted in April 2017 to identify evidence-based guidelines, UK policy, systematic reviews, and key randomized controlled trials published since the last revision of this topic. Changes include:
- A section on agents involved in poisoning and overdose has been added.
- Clinical situations where poisoning is a possibility and information about toxidromes (the syndrome of signs and symptoms caused by certain classes of substances, usually in overdose) have been added.
- The assessment of a person who has been poisoned has been revised in line with expert opinion in review articles and in the British National Formulary.
- The recommendations on when to admit someone who has been poisoned have been revised in line with guidelines from the National Institute for Health and Clinical Excellence on Self-harm: longer-term management (2011) and the Royal College of Psychiatrists on Managing self-harm in young people (2014) and expert advice in the British National Formulary.
- There have been minor changes on how to assess capacity in emergency situations.
May 2012 — revised. A literature search was conducted in April 2012 to identify evidence-based guidelines, UK policy, systematic reviews, and key RCTs published since the last revision of the topic. No changes to clinical recommendations have been made. The topic has has undergone minor structural changes to improve clarity and navigation, and information on assessing a person's capacity has been added.
July 2007 — minor update to text. The section on admission to hospital for people who refuse has been reworded, to highlight the difference between the use of common law and the Mental Health Act. Minor typographical correction made to the Clinical Summary. Issued in August 2007.
March to July 2007 — converted from CKS guidance to CKS topic structure. The evidence-base has been reviewed in detail, and recommendations are more clearly justified and transparently linked to the supporting evidence. This CKS topic also provides information on admission criteria for poisonings and what do to if someone refuses to go to hospital (against medical advice).
July 2006 — minor update. Revised information regarding the National Poisons Information Service (NPIS). Issued in July 2006.
October 2005 — minor technical update. Issued in November 2005.
August 2004 — updated to include National Institute for Health and Care Excellence recommendations for the short-term management of self-harm. Issued September 2004.
November 2003 — reviewed. Validated in March 2004 and issued in June 2004.
March 2001 — reviewed. Validated in March 2001 and issued in June 2001.
March 2000 — rewritten.
August 1997 — written, replacing previous guidance called Accidental poisoning by drugs; Other poisoning — non drug; Poisoning — animal or plant venom.
Update
New evidence
Evidence-based guidelines
No new evidence-based guidelines since 1 March 2022.
HTAs (Health Technology Assessments)
No new HTAs since 1 March 2022.
Economic appraisals
No new economic appraisals relevant to England since 1 March 2022.
Systematic reviews and meta-analyses
No new systematic reviews or meta-analysis which reach the CKS threshold for inclusion since 1 March 2022.
Primary evidence
No new primary evidence which reaches the CKS threshold for inclusion published since 1 March 2022.
New policies
No new national policies or guidelines since 1 March 2022.
New safety alerts
No new safety alerts since 1 March 2022.
Changes in product availability
No changes in product availability since 1 March 2022.
Goals and outcome measures
Goals
To support primary healthcare professionals to:
- Identify cases of potentially serious or intentional poisoning, and admit to hospital.
- Minimize the effects of mild poisoning.
Outcome measures
No outcome measures were found during the review of this topic.Audit criteria
No audit criteria were found during the review of this topic.QOF indicators
No QOF indicators were found during the review of this topic.QIPP - Options for local implementation
No QIPP indicators were found during the review of this topic.NICE quality standards
- People who have self-harmed are cared for with compassion and the same respect and dignity as any service user.
- People who have self-harmed have an initial assessment of physical health, mental state, safeguarding concerns, social circumstances and risks of repetition or suicide.
- People who have self-harmed receive a comprehensive psychosocial assessment.
Background information
What is it?
- In toxicology, poisoning is defined as the state resulting from the administration of excessive amounts of any pharmaceutical agent [WHO, 2014].
- A poison may be a drug, household product, industrial chemical, or plant or animal derivative [NPIS, 2021].
- The most common route of poisoning is by ingestion, but poisoning by inhalation, injection, skin/eye contamination, or bites may also occur.
- Poisoning may be accidental or deliberate:
- Accidental poisoning is where someone is exposed to a poison by an accidental action and develops symptoms [Sandilands, 2016].
- Poisoning is usually accidental in children aged under 6 years, and is most commonly due to exploration of their environment, where children place objects in their mouth and accidental ingestion occurs [Thanacoody, 2020b; BMJ, 2021a; NPIS, 2021].
- Accidental poisoning also occurs in adults as a result of exposure to drugs or chemicals, or less commonly occupational exposure, or as a result of natural toxins (for example, snake envenomation) [NPIS, 2021].
- Deliberate poisoning is part of the spectrum of deliberate self-harm. This encompasses both deliberate self-poisoning and deliberate self-injury. Deliberate self-poisoning is the deliberate ingestion of more than the prescribed amount of a medical substance, or of a substance not meant for human consumption, irrespective of the motive for the episode [NICE, 2004; Martin, 2020].
- Most poisoning in adults is related to self-harm [NPIS, 2021].
- In children aged over 11 years the frequency of poisoning increases into adolescence and is primarily the result of self-harm, rather than accidental poisoning [Thanacoody, 2020b; BMJ, 2021a].
- Older children and adolescents may also present with poisoning after experimenting with illicit drugs [BMJ, 2021a; NPIS, 2021].
- Accidental poisoning is where someone is exposed to a poison by an accidental action and develops symptoms [Sandilands, 2016].
- Overdose is a term used to describe the use of a quantity of drug in excess of its intended or prescribed dose and is a major cause of poisoning. It may be accidental or deliberate and involve the use of prescribed or illicit drugs [BMJ, 2020; NPIS, 2021].
- Accidental overdose may result from errors in drug administration, for example a person treating themselves for a cough-and-cold illness may inadvertently take different formulations that contain paracetamol [BMJ, 2020].
- Other contributory factors can include multiple medications, poor eyesight, and confusion.
- When referring to drugs of misuse, overdose may refer to adverse effects when the drug used, such as cocaine, or when quantities larger than physically tolerated are taken, such as with opioids [BMJ, 2019; BMJ, 2021b].
- Accidental overdose may result from errors in drug administration, for example a person treating themselves for a cough-and-cold illness may inadvertently take different formulations that contain paracetamol [BMJ, 2020].
Which agents are involved in poisoning and overdose?
- It is important to note that thousands of different drugs or chemicals may be involved in poisoning [NPIS, 2021].
- In the UK, the epidemiology of poisoning varies by geographical location, reflects prescribing practice, and access to potentially harmful products. Antidepressants, hypnotic, antipsychotics, and analgesics are the groups of medicines that are most commonly involved [Thanacoody, 2020b].
- In 2020/21, the most common enquiry on TOXBASE online related to paracetamol, which is the most common medication implicated in deliberate poisoning in adults. This was followed by ibuprofen, codeine, and sertraline. Other medicines commonly enquired about on TOXBASE, included: diazepam, quetiapine, pregabalin, mirtazapine, propranolol, and amitriptyline [NPIS, 2021].
- TOXBASE is a clinically-based toxicology database regularly updated and authenticated by the National Poisons Information Service, NPIS. See Information sources for further information.
- In its 2020/21 report, the National Poisons Information Service (NPIS) highlighted the following important causes of poisoning [NPIS, 2021]:
- Drugs of misuse — the number of TOXBASE accesses meeting the drugs of misuse criteria increased by 14.5%. Diazepam was the drug most commonly involved in online enquiries, followed by cocaine, cannabis, MDMA, and heroin.
- 2,4-dinitrophenol — this is a toxic industrial chemical. It blocks the normal mechanisms for storage of energy in the body, including fat, and although it is not a licensed medicine, it is sometimes ingested by users to produce weight reduction, ‘fat burning’ or ‘body sculpting’. In 2020/21 there were 7 exposures and one fatality.
- Pesticides — there were 667 exposures, most cases were not associated with toxicity, there were no episodes of exposure associated with severe toxicity, and there were no fatalities. Agents most commonly involved were permethrin, followed by glyphosate, brodifacoum, bromadiolone, and phenols/cresols.
- Carbon monoxide — there were 663 exposures during 2020, which were most commonly of low severity and associated with no symptoms or mild symptoms only. The most common cause were faulty domestic boilers. For further information, see the CKS topic on Carbon monoxide poisoning.
How common is it?
- It is difficult to calculate the exact frequency of poisoning. Sources of information about incidents of poisoning include mortality data on suicide and accidental poisoning, hospital admission rates, and enquiries to poisons information services [Thanacoody, 2020b].
- Around 160,000 people are admitted to hospital in the UK each year with suspected poisoning, and many more are managed in the community, including primary care and NHS advice services such as NHS 111, NHS 24 and NHS Direct [NPIS, 2021].
- Of the 54,757 hospital admissions in England for children under 5 due to poisoning between 2000 and 2011 [Mbeledogu, 2015]:
- 77% were due to poisoning with pharmaceuticals.
- 38% were non-opiate analgesics.
- Other causes of poisoning included organic solvents, corrosive substances, gases, soaps and detergents, pesticides, and alcohol.
- During the period 2020 to 2021 in the UK [NPIS, 2021]:
- There were 784,868 TOXBASE user sessions and over 2 million separate page views of TOXBASE entries.
- Contacts relating to children aged under 5 years account for over 25% of NPIS enquiries — less than 1% are clinically serious [Anderson, 2021].
- The NPIS received around 40,000 telephone calls about poison-related issues.
- This includes 852 exposures to drugs and chemicals during pregnancy, which were referred to the UK Teratology Information Service (UKTIS).
- There were 784,868 TOXBASE user sessions and over 2 million separate page views of TOXBASE entries.
- Self-poisoning is most commonly seen in younger adults, aged between 15 and 35. It is less common in the elderly, but has a greater impact on morbidity and mortality due to the availability of potentially harmful medicines and the impact of pre-existing comorbidities [Thanacoody, 2020b].
What is the prognosis?
- Prognosis depends on the type of poison, the quantity taken, and associated comorbidities.
- TOXBASE provides information on suggested toxic doses for drugs. In general, most people come to no harm after the ingestion of a small amount of a substance of low toxicity [NPIS, 2017].
- Poisoning in children:
- In preschool children medicines are frequently ingested in insufficient quantities to cause significant harm — less than 1% of cases are clinically serious. After an appropriate risk assessment no further investigations are needed where there has been ingestion of agents of low toxicity, or doses of potentially toxic substances that are too low to result in harm [Anderson, 2021].
- However, severe poisoning does occur. High-risk medications, where ingestion of one or two adult doses could be fatal for a 10-15 kg toddler, include methadone (which is particularly dangerous) and other opioids, tricyclic antidepressants, antipsychotics, calcium channel blockers, beta-blockers, flecainide, clonidine, and oral hypoglycaemics [Anderson, 2021].
- 28 children aged 4 years and under died from unintentional pharmaceutical poisoning between 2001 and 2013. Methadone was associated with over half of these deaths, tricyclic antidepressants with 3 deaths, heroin with 2 deaths, and iron in one death [Anderson, 2016].
- In 2020, there were 4,561 adult deaths due to drug poisoning registered in England and Wales, the highest number since records began in 1993 [ONS, 2021].
- Around 70% of these deaths were male.
- Drug poisoning deaths involve many substances, including controlled and non-controlled drugs, prescription drugs, and over-the-counter medicines.
- Half of all drug poisoning deaths involved an opiate, and 17% involved cocaine.
- Over half of all deaths involved more than one drug.
- In 2020, 2,996 of the adult deaths due to drug poisoning registered in England and Wales were due to drug misuse [ONS, 2021].
- These deaths include those arising from complications of drug misuse, such as deep vein thrombosis, or sepsis as a result of intravenous drug use.
- Overall death rates due to drug misuse were higher in men than women (76.3 deaths per million compared with 28.7 deaths per million).
- The 45-49-year-old age group had the highest fatality rate from drug misuse.
- 1337 deaths involved heroin and or morphine, 2263 involved any opioid, 476 any benzodiazepine, 777 cocaine, 344 pregabalin, and 118 involved gabapentin.
- Note: drug misuse death is labelled as such when the cause of death is drug abuse or drug dependence, or when the cause of death is drug poisoning and any of the substances controlled under the Misuse of Drugs Act 1971 are involved.
Diagnosis of poisoning or overdose
How is a person who has been poisoned or taken an overdose likely to present in primary care?
- Most people (including parents presenting with children) will present immediately after an accidental ingestion or inhalation of a known drug or chemical.
- Some people may present later, including parents presenting with children if they are not immediately aware of the poisoning when it occurs, and people who have intentionally poisoned themselves (or their friends or relatives).
- In most cases, a history of accidental ingestion, overdose or use of illegal drugs, is given by the person, a family member or a witness.
- In infants who are immobile, poisoning may be due to an accidental medication error by their carer.
- Children may have been found eating a poison, or with material around their mouth or on their clothes, or holding tablets or household chemicals by a parent or carer.
- Adolescents often present after disclosing to another person that they have taken a potentially harmful substance.
- If the episode of poisoning is unwitnessed, and the child or adolescent cannot, or does not, report what has happened to an adult, they may not present until their carer notices a change in their behaviour or they develop symptoms. Poisoned children and adolescents may present with altered behaviour or reduced consciousness, for which there is no obvious cause.
- Consider poisoning as a cause of altered level of consciousness in adults. Circumstantial evidence, such as tablets or empty medicine containers nearby or a suicide note (with no signs of physical violence), may provide a clue to the diagnosis.
- Other clinical situations where poisoning is a possibility include:
- Acute confusional states, for example from the use of illegal drugs.
- Hypoglycaemia, for example from sulfonylurea or meglitinide overdose.
- Abnormal liver function tests. Paracetamol overdose needs to be excluded if there are raised transaminases in combination with a prolonged prothrombin time.
- Unexplained seizures, which can be caused by drug toxicity from tricyclic antidepressants or cocaine.
- Abnormal bleeding, for example due to anticoagulants.
- Several people presenting with similar symptoms. Symptoms such as headache and confusion affecting members of the same household can be due to carbon monoxide poisoning. For further information, see the CKS topic on Carbon monoxide poisoning.
- Recurrent or chronic unexplained symptoms in children. Deliberate poisoning (as a form of Munchausen syndrome by proxy or fictitious disorder) is rare, but important to identify promptly. For more information, see the CKS topic on Child maltreatment - recognition and management.
Basis for recommendation
This information is based on expert opinion in narrative reviews Initial management of suspected poisoning in children and young people [Anderson, 2021], Principles of assessment and diagnosis of the poisoned patient [Thanacoody, 2020a], Assessment and diagnosis of the poisoned patient [Vale, 2016], Is the cause toxicological? [Thomas, 2016], and the British Medical Journal (BMJ) Best Practice guide Toxic ingestions in children [BMJ, 2021a].
What are the signs and symptoms of drugs commonly involved in poisoning or overdose?
- The diagnosis of poisoning cannot be made as a result of a single sign. The symptoms and signs which may be present following poisoning with certain drugs are listed in Table 1.
- In cases where it is unclear which poison(s) have been taken, the history and examination can sometimes be helpful in suggesting what class of substance might be involved. Table 2 includes a number of toxidromes, the syndrome of signs and symptoms caused by certain classes of substances, usually in overdose.
- Toxidromes are useful if the poisoning involves one drug, however, if multiple drugs have been ingested a constellation of symptoms may be present which makes diagnosis more complex.
Table 1. Symptoms and signs of drugs that are commonly involved in poisoning or overdose.
| Drug | Symptoms and signs |
|---|---|
| Paracetamol | Note: people who have ingested paracetamol are frequently asymptomatic. People who are suspected of taking a paracetamol overdose should be urgently admitted to hospital. Nausea and vomiting usually settle within 24 hours. If these continue, often with the development of right subcostal pain and tenderness, this suggests the development of hepatic necrosis. Liver damage is maximal after 3-4 days and may lead to liver failure, hypoglycaemia, encephalopathy, coma, and death. People may also present with coma, a reduced level of consciousness, or respiratory depression, if they have taken paracetamol with a drug that reduces the level of consciousness, such as opioids (for example a combined paracetamol/opioid preparation) or alcohol. |
| Aspirin | Hyperventilation, tinnitus, deafness, vasodilatation, and sweating. Coma if very severe poisoning. |
| Tricyclic and related antidepressants | Dry mouth, seizures, coma, cardiac conduction defects, and arrhythmias, hypothermia, hypotension, hyperreflexia, extensor plantar response, convulsions, and respiratory failure. There may be dilated pupils and urinary retention. |
| Selective serotonin re-uptake inhibitors (SSRIs) | Nausea, vomiting, agitation, tremor, nystagmus, drowsiness, sinus tachycardia. There may be convulsions. Rarely, severe poisonings may result in serotonin syndrome with marked neuropsychiatric effects, autonomic instability and neuromuscular hyperactivity. There may be hyperthermia, rhabdomyolysis, renal failure, and coagulation deficiencies. |
| Beta-blockers | Bradycardia, hypotension, syncope, conduction abnormalities and heart failure. Other features may include drowsiness, confusion, convulsions, hallucinations, and in severe cases coma. Effects vary depending on the beta-blocker. |
| Calcium-channel blockers | Nausea, vomiting, agitation, confusion, dizziness, and coma. Metabolic acidosis and hyperglycaemia may occur. Dihydropyridine calcium-channel blockers cause profound peripheral vasodilatation and severe hypotension. Verapamil and diltiazem can cause arrhythmias including complete heart block and asystole. |
| Iron salts | Nausea, vomiting, diarrhoea, abdominal pain, haematemesis, and rectal bleeding. Hypotension and hepatocellular necrosis can occur later. If severe poisoning: coma, shock and metabolic acidosis. |
| Lithium | Most cases of toxicity occur in people who are on long-term treatment with lithium, and whose excretion of lithium is reduced for example due to dehydration or infection. There is a delayed onset of symptoms in deliberate overdose (12 hours or more). Initially, apathy and restlessness followed by vomiting, diarrhoea, ataxia, tremor, weakness, dysarthria, and muscle twitching. If severe poisoning: electrolyte imbalance, dehydration, convulsions, renal failure, hypotension, and coma. |
| Theophylline | Onset of toxicity can be delayed if a modified-release preparation is involved. Severe vomiting, restlessness, agitation, dilated pupils, hyperglycaemia and tachycardia. More serious effects include haematemesis, convulsions and arrhythmias (supraventricular and ventricular). Hypokalaemia can develop quickly. |
| Benzodiazepines | Drowsiness, dysarthria, ataxia, and nystagmus. Respiratory depression and coma can also occur. |
| Antimalarials (quinine, chloroquine, hydroxychloroquine) | Rapid onset of life-threatening arrhythmias and intractable convulsions. Note: overdose with these is extremely dangerous and difficult to treat. The person should be referred to hospital urgently. |
| Phenothiazines and related drugs | Sinus tachycardia, arrhythmias, hypothermia, hypotension, reduced consciousness, and respiratory depression. Dystonic reactions may be seen with therapeutic doses. Seizures in severe cases. |
| Second-generation antipsychotic drugs | Drowsiness, hypotension, extrapyramidal symptoms, convulsions, ECG abnormalities such as QT prolongation. |
| Amphetamines | Initially excessive activity, wakefulness, hallucinations, paranoia, and hypertension. Later there may be convulsions, hyperthermia, exhaustion and coma. |
| Cocaine | Agitation, hypertension, tachycardia, dilated pupils, hallucinations, hyperthermia, hypertonia, and hyperreflexia and cardiac effects such as chest pain, arrhythmias, myocardial infarction. |
| Opioids | Drowsiness, coma, respiratory depression, pinpoint pupils. |
| Methylenedioxymethamfetamine (MDMA, ecstasy) | Delirium, coma, hyperthermia, rhabdomyolysis, acute renal failure, acute hepatitis, disseminated intravascular coagulation, adult respiratory distress syndrome, hyperreflexia, hypotension and intracerebral haemorrhage; hyponatraemia, convulsions, ventricular arrhythmias, delirium, coma. |
| Data from: [BNF, 2022] | |
Table 2. Toxidromes.
| Type of poisoning | Common agents | Toxic signs and symptoms |
|---|---|---|
| Anticholinergic | Antihistamines, tricyclic antidepressants, carbamazepine, phenothiazines. | Tachycardia, hyperthermia, mydriasis, warm and dry skin, urinary retention, loss of sweating, agitation/delirium, seizures. |
| Cholinergic | Carbamates and organophosphate insecticides, some mushrooms. | Salivation, lacrimation, miosis, urination, diarrhoea, bronchorrhoea, bronchospasm, bradycardia, hypotension, vomiting, muscle weakness. |
| Hallucinogenic | Amphetamines, cocaine, MDMA. | Hallucinations, panic, seizures, hypertension, tachycardia, tachypnoea. |
| Opioid | Morphine, heroin, codeine, methadone. | Hypoventilation, hypotension, miosis, sedation, bradycardia. |
| Sedative/hypnotic | Anticonvulsants, benzodiazepines, ethanol. | Ataxia, blurred vision, sedation, hallucinations, slurred speech, hypotonia, hyporeflexia, hypotension, nystagmus. |
| Serotonin | Serotonergic drugs (for example citalopram, tramadol, ecstasy) | Agitation, confusion, myoclonus, hyperreflexia, sweating, tremor, diarrhoea, incoordination/ataxia, fever. |
| Sympathomimetic | Amphetamines, cocaine, MDMA. | Tachycardia, hypertension, tachypnoea, mydriasis, agitation, seizures, hyperthermia, tremor, sweating. |
| Data from: [Anderson, 2013; Thanacoody, 2020a; BMJ, 2021a] | ||
Basis for recommendation
These recommendations are based on expert opinion in a narrative review Principles of assessment and diagnosis of the poisoned patient [Thanacoody, 2020a], the British Medical Journal (BMJ) Best Practice guides Paracetamol overdose in adults [BMJ, 2020], Toxic ingestions in children [BMJ, 2021a], the National Institute for Health and Care Excellence (NICE) guideline Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], the British National Formulary (BNF) [BNF, 2022], and the toxicology database TOXBASE [TOXBASE, 2022].
- It is recommended that paracetamol levels are checked for people who present with features consistent with opioid poisoning, and for unconscious people or people with reduced consciousness where drug overdose is a possibility [NICE, 2004; Thanacoody, 2020a].
- For more detailed information on toxidromes, see the TOXBASE information on Poisoning with an unknown substance [TOXBASE, 2022].
Management
Scenario: Management of poisoning or overdose
From birth onwards.
How should I assess a person who is suspected of being poisoned or taking an overdose?
- Most people should be seen (in person) after a poisoning episode or overdose.
- Advice may be offered over the telephone (without seeing the person) if the healthcare professional feels confident that the poisoning episode is not serious. For sources of information regarding the management of poisoning, see Information sources.
- If the person has collapsed and is unresponsive ensure the airway is open (in the absence of trauma) and check for normal breathing. If they are not breathing normally, start cardiopulmonary resuscitation (CPR) immediately, and call for an ambulance.
- Assess the person's overall status using the ABCDE approach.
- Perform a rapid assessment of the airway — remove any obstructions, assess evidence of any injury (for example from ingestion of a corrosive substance), and secure a patent airway.
- Assess the person's consciousness — the Glasgow coma scale is the method most commonly used.
- Measure respiratory rate — if a pulse oximeter is available, measure oxygen saturations.
- Note this may not be accurate if there is poor peripheral perfusion, or carboxyhaemoglobin or methaemoglobin.
- Measure the person's pulse, blood pressure and temperature.
- Arrange emergency transfer to hospital following the immediate assessment of the person if:
- The person is unconscious or has a reduced level of consciousness.
- There is a reduced respiratory rate or oxygen saturation is reduced.
- There is hypotension.
- There is tachycardia or bradycardia or an irregular pulse.
- There is hypothermia or hyperthermia.
- The person has had a seizure.
- There are any other concerning clinical features, or the person's condition is deteriorating.
- If emergency transfer is not required, take a history and ask the person (or friends, family members, or other health professionals if appropriate):
- What substance was taken — the amount, if any other medicines have been taken, and alcohol use.
- Note that the person's account of what and how much has been taken may not be accurate if they have impulsively ingested what is available, and they may estimate quantities in terms of mouthfuls, or handfuls. This can result in inconsistency between an unreliable history and laboratory blood and urine tests. It may be useful to prompt them to recall quantities in terms of strips or packets of drugs.
- When it was taken — try to establish the exact timing(s) of ingestion or contact (a single acute overdose, staggered or chronic). This is especially important in paracetamol poisoning.
- About the route of administration (mouth, inhalation, or injection).
- Why the substance was taken — if it was accidental, deliberate or a therapeutic error.
- If there is a risk of repetition.
- People who have self-harmed will need a further psychosocial assessment by another trained specialist (mental health worker, social worker) after the treatment of their physical problems.
- About other relevant details, such as age, weight, sex, medical history (including psychiatric history and history of self-harm), medication and factors that will affect the excretion or metabolism of the poison, such as renal or hepatic impairment.
- About any symptoms they may be experiencing, depending upon the substance(s) involved. See the section on Symptoms and signs of drugs that are commonly involved in poisoning or overdose.
- What substance was taken — the amount, if any other medicines have been taken, and alcohol use.
- Perform an examination, depending on the clinical situation. This may include:
- General observations — presence of track marks may indicate intravenous drug misuse, alcohol or solvents on the breath and stigmata of liver disease can suggest alcohol dependence, atypical bruising or fractures may raise safeguarding concerns, and skin blisters may be found in people who are, or have been, unconscious due to poisoning.
- A neurological examination (including pupils and eye movements).
- Abnormal movements — assess for acute dystonic movements (which can occur after exposure to antidopaminergics, such as antipsychotics), hypertonia, hyperreflexia, and extensor plantar response (which can occur after tricyclic antidepressant poisoning).
- Pupil size and reaction — widely dilated pupils that react poorly to light be due to agents with anticholinergic activity (for example tricyclic antidepressants), or sympathomimetic activity (for example, amfetamines). Pinpoint pupils (miosis) occur after exposure to opioids or agents with cholinergic activity (for example, pesticides).
- Eye movements — strabismus, internuclear ophthalmoplegia, dysconjugate roving eye movements and total external ophthalmoplegia may be seen in poisoning with tricyclic antidepressants, barbiturates, phenothiazines and anticonvulsants such as phenytoin and carbamazepine.
- Visual acuity and visual fields — blurring, loss of vision and tunnel vision may occur with some drugs (for example, quinine poisoning).
- Check for signs that are consistent with the poison or drug that has been taken, or if the poison is not known, compare the person's symptoms and examination findings to those commonly associated with known poisons, see toxidromes in the section on Symptoms and signs of drugs that are commonly involved in poisoning or overdose.
- If the person has deliberately self-poisoned:
- Conduct a preliminary psychosocial assessment — determine the person's mental capacity, their willingness to remain for further (psychosocial) assessment, their level of distress and the possible presence of mental illness.
- Where possible, the person should be seen alone for this assessment, to maintain confidentiality and allow the person to discuss any problems between themselves and friends or family.
- Assess the likely physical risk, the person's emotional and mental state, and the risk of further self-harm or suicide — identify the main clinical and demographic features and psychological characteristics associated with risk, in particular depression, hopelessness and continuing suicidal intent.
- Communicate the outcome of these assessments to other healthcare professionals who are involved in the person's care.
- For more information about an initial risk assessment in people who have self-poisoned, see the CKS topic on Self-harm.
- Assess any safeguarding concerns — this applies to people of all ages, including adults, older people, children and young people. It includes consideration of risks to the person who has self-harmed, any children or adults in the person's care and to other family members or significant others. For further information, see the CKS topic on Child maltreatment.
- Conduct a preliminary psychosocial assessment — determine the person's mental capacity, their willingness to remain for further (psychosocial) assessment, their level of distress and the possible presence of mental illness.
- Investigations are not routinely necessary or appropriate in primary care for those people who do not need emergency referral to hospital.
- Consult the poisons information database, TOXBASE, for information on the specific poison(s) involved, and manage accordingly. See the section on Information sources.
- Telephone the NPIS for advice if:
- Poisoning is severe or complex (for example multiple ingestions).
- The person has significant comorbidity.
- There are any uncertainties regarding the person's management after consulting TOXBASE online.
- The poison is unknown.
- Telephone the UK Teratology Information Service (UKTIS) for advice if the person is pregnant. See the section on Information sources.
Basis for recommendation
These recommendations are based on expert opinion in narrative reviews Initial management of suspected poisoning in children and young people [Anderson, 2021], Principles of management of the poisoned patient [Morrison, 2020], Principles of assessment and diagnosis of the poisoned patient [Thanacoody, 2020a], Psychiatric assessment of self-poisoning [Martin, 2020], Assessment and diagnosis of the poisoned patient [Vale, 2016], the British Medical Journal (BMJ) Best Practice guide Paracetamol overdose in adults [BMJ, 2020], the National Institute for Health and Care Excellence (NICE) guideline Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], the NICE quality standard Self-harm [NICE, 2013], a French consensus guideline Management of pharmaceutical and recreational drug poisoning [Mégarbane, 2020] the Royal College of Psychiatrists (RCP) report Managing self-harm in young people [Royal College of Psychiatrists, 2014], the British National Formulary (BNF) [BNF, 2022], the National Poisons Information Service (NPIS) Report 2020/21 [NPIS, 2021], and toxicology database TOXBASE [TOXBASE, 2022].
Investigations
- The recommendation that investigations are not routinely required in primary care is pragmatic, based on what CKS considers to be good medical practice.
- In most cases details of the substance people have been exposed to can be identified from the history allowing the risk of likely toxicity to be assessed.
- People who require further investigations should be admitted to hospital for assessment.
What sources of information should I use to guide the management of a person who has been poisoned or taken an overdose?
Sources of information and advice include:
- TOXBASE (www.toxbase.org).
- This is a clinically-based toxicology database and the first-line source of information for healthcare professionals. It is regularly updated by the National Poisons Information Service (NPIS), and provides information about the diagnosis, treatment and management of patients exposed to drugs, household products, and industrial and agricultural chemicals.
- It is available through the TOXBASE website or a mobile app and is free to all UK NHS healthcare units and healthcare professionals.
- A back-up site is available at www.toxbasebackup.org if the main site cannot be accessed.
- The Public Health England and NPIS information leaflet for healthcare professionals Low toxicity substances [NPIS, 2017].
- NPIS if there are complex cases or if there is any uncertainty about the degree of risk or management, for example:
- Severe or complex cases, including multiple ingestions.
- People with significant comorbidity.
- Cases where the poison is unknown.
- The NPIS advice line gives information and advice to NHS staff to assist them in deciding whether a person needs admission or can be managed at home. It also provides advice on the hospital management of people requiring admission.
- The NPIS is a network of units commissioned by Public Health England for the UK health departments.
- The service is available 24 hours a day via the central UK number 0344 892 0111. It consists of a network of poisons information specialists based, supported by a team of on-call consultant clinical toxicologists attached to major teaching hospitals.
- The service helps to reduce unnecessary hospital referrals and improves the care of those at risk of serious complications.
- In Northern Ireland, the Regional Medicines and Poison Information Service — this provides information during working hours. The NPIS takes out-of-hours enquiries.
- UK Teratology Information Service (UKTIS) in the event of poisoning in a pregnant woman — see www.uktis.org, or call 0344 892 0909.
- Information for healthcare professionals can be accessed online through TOXBASE, which contains the review documents produced by UKTIS on maternal exposures to drugs and chemicals, online through the UKTIS website, and by telephone.
- UKTIS is part of the NPIS and provides a national service on the safety of drugs and chemicals during pregnancy.
- Patient information leaflets are available through the Bumps (best use of medicines in pregnancy) website http://www.medicinesinpregnancy.org.
- Medicines information services can provide advice on many aspects of medicines therapy
- Primary care-based healthcare professionals in England can contact the Specialist Pharmacy Service for practical advice on when to restart drugs (if the person has taken additional doses accidentally or after acute toxicity has resolved), possible adverse effects, and can also direct healthcare professionals to further information (see Medicines Advice contact details – SPS - Specialist Pharmacy Service – The first stop for professional medicines advice).
- Details of services in Northern Ireland, Scotland and Wales, plus hospital-based services can be found at UKMI Contacts.
Basis for recommendation
The information is based on the National Poisons Information Service (NPIS) Report 2020/21 [NPIS, 2021], and the British National Formulary (BNF) [BNF, 2022].
When should I admit a person to hospital after an episode of poisoning or overdose?
- Consult TOXBASE for advice regarding the toxicity of a substance and whether the person requires admission. If there is any uncertainty after this, contact NPIS for advice, or discuss the case with a consultant from the nearest Accident and Emergency department. See the section on Information sources for further details.
- Arrange urgent hospital admission if advised.
- Refer all people who have deliberately self-poisoned urgently to accident and emergency — the nature and quantity of the ingested substances may not be clearly known to the person who has self-poisoned, making accurate risk assessment difficult.
- If available, send a sample of the suspected drug(s) or poison into hospital with them.
- Arrange for the person to be accompanied by an appropriate person if there is a risk of further self-harm, reluctance of the person to attend, or the person is very distressed.
- Arrange follow-up after hospital discharge according to a mutually agreed plan to ensure ongoing management of the person's psychosocial needs and treatment for identified issues or risk of further self-harm or suicide.
- Refer people who are symptomatic after taking or being exposed to a poison or drug urgently to hospital.
- Minor gastrointestinal upset alone is generally not considered an absolute indication for admission to hospital in people who have ingested a small amount of a substance considered to be of low toxicity — NPIS advises that a small glass of water (or milk or juice) may be given if there is mild gastrointestinal upset.
- Refer people who have taken poisons with delayed action urgently to hospital, even if the person appears well and is asymptomatic.
- Delayed-action medicines include aspirin, iron, paracetamol, tricyclic antidepressants, co-phenotrope, and all modified-release preparations.
- Note: salicylates may be present in some over-the-counter antacid preparations, and ingestion of topical liniments containing oil of wintergreen carries a high risk of salicylate poisoning — always consult TOXBASE for advice regarding the toxicity of a substance.
- Refer all people who have taken or been exposed to a drug that is unknown urgently to hospital.
- Consider admitting children, pregnant women, people with pre-existing comorbidities, or people taking concomitant medication, even if the drug is considered to have a good safety profile.
- In areas that are a significant distance away from an emergency department, and where there will likely be a delay in reaching hospital, consider initiating assessment and treatment in primary care following a discussion with the nearest Accident and Emergency consultant (for example, taking blood samples to test for paracetamol and other drugs).
- Consider child neglect if there are repeated presentations of accidental ingestion of poisons in a child. For more information, see the CKS topic on Child maltreatment - recognition and management.
Basis for recommendation
These recommendations are based on the National Institute for Health and Care Excellence (NICE) guideline Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], expert opinion in a narrative review Psychiatric assessment of self-poisoning [Martin, 2020], the British Medical Journal (BMJ) Best Practice guide Toxic ingestions in children [BMJ, 2021a], the Royal College of Psychiatrists (RCP) report Managing self-harm in young people [Royal College of Psychiatrists, 2014], the British National Formulary (BNF) [BNF, 2022], the National Poisons Information Service (NPIS) leaflet Low toxicity substances [NPIS, 2017], the toxicology database TOXBASE [TOXBASE, 2022], and what CKS considers good medical practice.
Admission
- The recommendation to consider admitting children, pregnant women, people with pre-existing comorbidities, or people taking concomitant medication, even if the drug is considered to have a good safety profile is pragmatic and based on what CKS considers good medical practice. These groups are more vulnerable to toxic effects of drugs, even those that have a good safety profile. Similarly, there is a risk of dangerous drug interactions in people who are taking concomitant medication.
How should I manage a person who does not need admission to hospital?
- Access information about the substance on TOXBASE, and use this as a guide to the person's management.
- For people who have ingested a substance considered to be of low toxicity — hospital assessment is not usually indicated for accidental poisoning. Advise the person:
- That they may experience mild gastrointestinal upset, and that if this occurs, they should drink a small glass of water, milk or juice.
- See the NPIS leaflet, Low toxicity substances.
- When to seek medical advice, for example if the gastrointestinal upset does not improve, becomes worse, or new symptoms develop.
- That they may experience mild gastrointestinal upset, and that if this occurs, they should drink a small glass of water, milk or juice.
- For people who have ingested a considerable quantity of a low toxicity substance, or if the person has symptoms other than mild gastrointestinal upset following ingestion of a low toxicity substance, follow advice from TOXBASE.
- Contact the NPIS if there are uncertainties after accessing TOXBASE, and refer the person to hospital if appropriate.
- For people who have accidentally taken an additional tablet of their own medication — hospital assessment is not usually indicated.
- Consider:
- The indications, maximum daily doses, toxic doses, adverse effects and interactions of the medicine.
- The person's past medical history (especially renal and liver impairment) and medication history.
- The person's age and social circumstances.
- Refer to the BNF or TOXBASE for information regarding individual medicines and the person's subsequent management. Seek advice where appropriate, for example a discussion with the medical consultant on call, or contact the UK Medicines Information (UKMI) service.
- Refer people who have exceeded the daily dose of two or more cardio-toxic agents for hospital assessment irrespective of the dose ingested.
- Restart the person on their medication when appropriate.
- Restarting medication may be complicated depending on the drug and dosing regimen. CKS cannot provide advice for individual drugs taken, due to the number of variables that must be considered.
- If there is any uncertainty about when to restart medication after an additional tablet has been taken, seek further advice. See the section on Information sources.
- Consider the cause of the error (for example, poor memory or confusion) and whether steps need to be taken to avoid future errors, such as supervision of medication or provision of a dosette box.
- Consider:
Basis for recommendation
These recommendations are based on the National Poisons Information Service Public (NPIS) leaflet Low toxicity substances [NPIS, 2017], the toxicology database TOXBASE [TOXBASE, 2022], and what CKS considers to be good medical practice.
- The recommendation that admission to hospital is not usually indicated if a person has accidentally taken an additional tablet of their own medication, and to refer to the BNF or TOXBASE, or seek advice from a medical consultant, the NPIS or the UK Medicines Information (UKMI) service, when deciding the person's subsequent management, is based on what CKS considers best medical practice.
- CKS cannot provide advice for individual drugs taken, due to the number of variables that must be considered. CKS advises in all cases to perform a full assessment, refer to the BNF and seek further advice where appropriate.
How should I manage a person who refuses admission to hospital after a poisoning?
- If a person refuses to go to hospital, determine the reason(s) and provide information about the potential consequences of not receiving hospital treatment and assessment.
- If the person still refuses admission, and this is felt to be in their best interests, assess their capacity, and consider whether a compulsory admission under The Mental Health Act, 1983 is appropriate.
- If possible, discuss this with the person's family, friends or carers taking into account the duty of confidentiality.
- If a person is judged to have diminished capacity and/or the presence of a significant mental health disorder, refer for urgent hospital admission or urgent mental health assessment, depending on clinical judgement.
- Document why capacity is in doubt and record details of the assessment process and findings.
- If there is uncertainty about whether a person has capacity to make informed decisions, seek advice from a psychiatrist or psychologist who has experience in assessing capacity. For more information, see How do I assess a person's capacity?
- If considering using the Mental Health Act, always seek help from the local community mental health team (CMHT) or crisis team, social services, and the on-call psychiatrist. Section 136 may be used by police to take people who appear to be suffering from a mental disorder and are in 'immediate need of care or control' from a public place to a place of safety and enable examination by a registered medical practitioner and interview by an Approved Mental Health Professional (AMHP). See The Mental Health Act (1983) for further information.
- In emergency situations, consider the person's capacity, but be aware that the steps reasonable when assessing capacity will be different to the steps in non-urgent cases. In such situations, it may be that capacity is only considered briefly. It will almost always be in the person's best interests to give urgent treatment without delay. See How do I assess a person's capacity? for further information.
- If the person is judged to have capacity, and does not have signs of a mental disorder, and is at a low risk of suicide, but is at risk from the effects of their overdose, by law they have the right to refuse hospital admission and/or to refuse lifesaving treatment. In these circumstances:
- Take all steps to persuade them to attend hospital or have treatment. If the person allows, involve family and carers.
- Seek advice from the NPIS, Emergency or Medical consultant, consultant psychiatrist or medical indemnity organisation.
- Follow the person up and reassess the clinical situation as soon as is clinically appropriate; provide information about the potential consequences of not receiving hospital treatment and assessment; and reassess capacity.
- Clearly document their wishes and that these are against medical advice.
How should I assess a person's capacity?
The Mental Capacity Act (2005)
- Mental capacity refers to the ability of a person to make a decision (or take a particular course of action) at a time when it is needed. It may change over time, for example, with changing levels of consciousness, emotional distress, or due to the effects of alcohol and/or drugs. Capacity may also vary according to the decision that needs to be made. The Mental Capacity Act (2005) states that all people aged 16 years and over are presumed to have capacity. It aims to balance a person's right to make decisions for themselves with their right to be protected from harm.
- The Mental Capacity Act (2005) has five key principles:
- Presumption of capacity — adults should always be presumed to have the capacity to make a decision unless the healthcare professional can prove otherwise.
- Maximizing decision-making capacity — the person must be given all practical support before it can be decided that they lack capacity. Support may involve extra time for assessment, repeating the assessment if capacity fluctuates, or using an interpreter or sign language.
- The freedom to make seemingly unwise decisions — if the person makes a seemingly unwise decision, this in itself is not proof of incapacity. Proof of incapacity depends on the process by which the decision is made, not the decision itself.
- Best interests — any decision or action taken on behalf of the person must be in their best interests. If the decision can be delayed until the person regains capacity, then it should be. A decision taken on another's behalf should take account of their wishes, including those expressed in an advance decision, and their beliefs and values. The decision-making process should involve, when appropriate, family, carers, and significant others.
- The least restrictive alternative — when a decision is made on the person's behalf, the healthcare professional must choose the alternative that interferes least with the person's rights and freedoms while still achieving the necessary goal.
- A person lacks capacity if, at the time the decision needs to be made, they are unable to make or communicate the decision because of an ‘impairment of, or a disturbance in the functioning of, the mind or brain’.
- Capacity may be impaired by a number of factors, including mental health disorders, learning disability, dementia, brain damage, or intoxication.
- When assessing a person's capacity, it may be useful to consider three questions:
- Does the person have an impairment of, or a disturbance in the functioning of, their mind or brain?
- Is the person unable to make a specific decision at the time it needs to be made for one or more of the reasons given in the Act?
- Is the person’s inability to make the specific decision at the time it needs to be made because of the impairment of, or disturbance in the functioning of, their mind or brain?
- Under the Act, a person is regarded as being unable to make a decision if they are unable to:
- Understand relevant information to the decision, or
- Retain that information, or
- Use or weigh that information as part of the decision-making process, or
- Communicate their decision (by talking, non-verbal communication, or any other means).
- The Mental Capacity Act also covers emergency situations. When someone who lacks capacity needs emergency medical treatment to save their life or prevent them coming to harm, the steps that are reasonable when assessing capacity and best interests will be different to the steps in non-urgent cases. In emergencies, it will almost always be in the person's best interest to give urgent treatment without delay. It is necessary to show that capacity has been considered, even if this has only been done so briefly.
- In emergency situations involving children or young people aged under 16, or when the intervention is for the protection of others, common law, or the 'doctrine of necessity', applies. The principles of common law state:
- The healthcare professional must reasonably believe that action is necessary to prevent harm to the person, or others.
- Actions must be proportionate to the likelihood of the person, or others, being harmed and the seriousness of this harm.
- In emergency situations involving children or young people aged under 16, or when the intervention is for the protection of others, common law, or the 'doctrine of necessity', applies. The principles of common law state:
- The Act does not generally apply to people aged under 16 years — care and treatment of children or young people aged under 16 is governed by common law.
- Most of the Act applies to young people aged 16-17 years.
- For young people aged 16–17 years who lack capacity, parents can consent on their behalf if the decision to be made is felt to be within parental control. Healthcare professionals are, however, able to give treatment regardless of whether parental consent has been given, as long as the principles of the Mental Capacity Act (2005) are followed, and the decision is judged to be in the young person's best interests.
- If a young person who self-harms and has capacity refuses to involve their family or carers in their treatment, or refuses consent to disclose issues relating to their safety to family or carers, confidential information can be shared if the benefits to the young person from sharing the information outweigh both the public and the individual’s interest in keeping the information confidential. Healthcare professionals must weigh the harm that is likely to arise from not sharing the information against the possible harm (both to the person, and to the overall trust between doctors and the person) arising from releasing that information [GMC, 2022].
- If information is shared without consent this should be explained to the individual and the reasons for the decision recorded.
The Mental Health Act (1983, amended 2007)
- The Mental Health Act (1983) allows compulsory admission of people who:
- Have a mental disorder of a nature and degree that warrant assessment or treatment in hospital, and
- Need to be admitted in the interests of their own health or safety, or for the protection of other people.
- Compulsory admission is arranged using the appropriate section of the Mental Health Act:
- Section 2 allows compulsory admission for up to 28 days for assessment.
- Section 3 allows compulsory admission for up to 6 months for treatment.
- Sections 2 and 3 require an application from an Approved Mental Health Professional (AMHP), or the person's nearest relative, and recommendations from two doctors; one of whom is section 12-approved (usually a psychiatrist) and one who has previous acquaintance with the person (usually the person's GP if at all practicable). Ideally, the person should be examined jointly by the two doctors with the AMHP also present. Where this is not possible, each doctor may carry out a separate examination. If the AMHP is not present, it is essential that at least one of the doctors discusses the person with the AMHP.
- Section 4 is used in exceptional cases to permit compulsory admission for up to 72 hours if there is urgent necessity, and undesirable delay would occur while trying to arrange admission under section 2.
- It requires an application from an AMHP (or, rarely, the person's nearest relative) and just one medical recommendation, preferably from a doctor with a previous acquaintance (usually the person's GP).
- Section 136 may be used by police to take people from a public place to a place of safety and enable examination by a registered medical practitioner and interview by an AMHP. The person's GP, where known, may be informed.
- Details of guidance and forms for the most common sections of the Mental Health Act can be accessed from the Department of Health and Social Care website http://www.gov.uk.
Basis for recommendation
These recommendations are based on the National Institute for Health and Care Excellence (NICE) guidelines Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], and Self-harm in over 8s: long-term management [NICE, 2011], the British Medical Association (BMA) Mental Capacity Act tool kit [BMA, 2016], the Office of the Public Guardian (OPG) Mental Capacity Act 2005. Code of practice [OPG, 2020], expert opinion in a narrative review When and how to treat patients who refuse treatment [Humphreys, 2014], and the General Medical Council (GMC) guidance Protecting children and young people. The responsibilities of all doctors [GMC, 2022], the Care Quality Commission (CQC) Brief guide: capacity and competence to consent in under 18s [CQC, 2019], and what CKS considers good medical practice.
Assessing capacity
- The recommendation to seek advice from a psychiatrist who has experience in assessing capacity if there is uncertainty about whether a person has capacity is based on what CKS considers to be good medical practice.
Seek advice if considering use of the Mental Health Act
- The recommendation to seek help from the local community mental health team (CMHT) or crisis team, social services, and the on-call psychiatrist if considering use of the Mental Health Act is based on expert opinion in narrative review [Humphreys, 2014] and what CKS considers to be good medical practice.
Assessing mental capacity in emergencies
- The recommendations on use of the Mental Capacity Act in emergency situations is based on expert opinion in a rapid response to the review article, When and how to treat patients who refuse treatment, [Humphreys, 2014; BMJ Rapid Responses, 2014] and the Mental Capacity Act Code of Practice [OPG, 2020].
Children aged under 16 years
- The recommendation that common law is applicable in emergency situations involving children aged under 16 years, or when the intervention is for the protection of others, is based on expert opinion in a review article [Humphreys, 2014; BMJ Rapid Responses, 2014].
Young people aged 16-17 years with capacity
- The CQC advises that [CQC, 2019]:
- Where a competent child refuses to allow information to be shared with their parent(s), there should be evidence that the risks of not sharing the information have been considered.
- Where it is thought to be in the child’s best interests to share information, there should be evidence of attempts to seek a compromise.
- Where it is the clinician’s opinion that it is necessary to share information in the best interests of the competent child, against their wishes, the Caldicott Guardian should be consulted.
- The recommendation regarding the management of a person who is judged to have capacity, and does not have signs of a mental disorder, and is at a low risk of suicide, but is at risk from the effects of their overdose is based on what CKS considers good medical practice.
- NICE advises that healthcare professionals should have access to legal advice in these circumstances [NICE, 2004].
How is poisoning managed in secondary care?
Medical management
- A further assessment will be carried out, which may include:
- Administration of antidotes, such as acetylcysteine, naloxone, and flumazenil, if appropriate.
- Blood and urine tests, such as toxicological investigations, full blood count, clotting, electrolytes, glucose, liver function tests, and arterial blood gases.
- ECG and imaging investigations.
- Plasma or serum monitoring. Drugs or poisons that require emergency measurement of their plasma or serum concentration in order to guide clinical management include:
- Carbamazepine.
- Carboxyhaemoglobin.
- Digoxin.
- Ethanol.
- Ethylene glycol.
- Iron.
- Lithium.
- Methanol.
- Methotrexate.
- Paracetamol.
- Salicylate.
- Theophylline.
- Valproate.
- Treatment will depend on the type of poison taken, and the severity of the episode.
- Most people will simply be observed, to make sure there are no worsening adverse effects, and that complications do not develop.
- The length of the observation will depend on the clinical circumstances.
- Prevention of absorption:
- Activated charcoal can bind to the poison and prevent absorption. The sooner it is given the more effective, but it may still be effective up to 1 hour after ingestion, or longer for modified release preparations or medicines with antimuscarinic properties. An important use is to prevent the absorption of medicines which are toxic in small amounts, such as antidepressants.
- In children this is only used if a potentially toxic amount of a drug that adsorbs to charcoal has been taken, the child has presented within 1 hour of ingestion, in the absence of contraindications, and after a risk-benefit analysis when this is being considered.
- Active elimination is suitable for a limited number of drugs:
- Repeated doses of activated charcoal enhance the elimination of some drugs even after they have been absorbed, such as carbamazepine, phenobarbital, quinine, theophylline, and dapsone.
- Alkalinisation of the urine for salicylate poisoning.
- Haemodialysis for ethylene glycol, lithium, methanol, phenobarbital, salicylates, and sodium valproate.
- Removal from the gastrointestinal tract:
- Gastric lavage is rarely required — it is indicated only if a life-threatening amount has been ingested within the previous hour, and the poison cannot be removed using other methods. It may be useful for drugs such as lithium and iron that are not absorbed by charcoal. Lavage should never be done if a petroleum distillate or a corrosive substance has been ingested.
- Whole bowel irrigation may be used if there has been poisoning with certain sustained-release or enteric-coated medicines, or in severe poisoning with iron or lithium salts. This should only be performed following discussion with the NPIS.
- Antidotes (if available) may be given for certain poisons, which either prevent the poison from working or reverse the effects of the poison.
- Acetylcysteine — paracetamol.
- Digoxin-specific antibody fragments — digoxin.
- Flumazenil injection — benzodiazepines. This reverses the central nervous system and respiratory depression. However, if the person has also taken a tricyclic antidepressant or has epilepsy, there must be caution, as flumazenil can cause seizures and arrhythmias.
- Glucagon injection — insulin, beta-blockers, calcium-channel blockers.
- Naloxone injection — morphine, heroin, opiates. In people with reduced consciousness due to suspected opioid poisoning, administration which leads to significant improvement in the person's condition within 1-2 minutes is highly suggestive of opioid poisoning.
- Desferrioxamine mesilate — iron salts.
- Fomepizole — ethylene glycol or methanol.
Psychiatric assessment and management of deliberate self-poisoning
- People who have deliberately self-poisoned should have a psychosocial assessment of their needs and risks by a specialist mental health professional while they are in hospital. The person's subsequent management is based on this assessment. This is likely to include:
- Events that preceded the episode of self-harm.
- Reasons for self-poisoning.
- Assessment of possible suicidal intent.
- Current personal difficulties and life issues.
- Problems with alcohol or substance misuse.
- Whether they have a psychiatric disorder.
- Personal risk factors (for example, low socioeconomic status, employment status).
- Psychiatric history and history of self-harm.
- Risk of further self-harm and suicide.
- The person's social supports and coping resources.
- Whether the person is willing to accept help, and the help that would most benefit the person.
- People who have a serious psychiatric disorder and/or are at a high risk of suicide are generally admitted for the treatment of the psychiatric disorder.
- Children and young people aged under 16 who have deliberately self-poisoned should be admitted overnight on a paediatric ward, and be assessed the next day by an appropriately experienced healthcare professional. Young people aged 16 and 17 do not always need to be admitted overnight.
Basis for recommendation
This information is based on expert opinion in narrative reviews Initial management of suspected poisoning in children and young people [Anderson, 2021], Principles of management of the poisoned patient [Morrison, 2020], Principles of assessment and diagnosis of the poisoned patient [Thanacoody, 2020a], Psychiatric assessment of self-poisoning [Martin, 2020], Psychiatric assessment and management of deliberate self-poisoning patients [Hawton, 2016], the National Institute for Health and Care Excellence (NICE) guideline Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], the Royal College of Psychiatrists (RCP) report Managing self-harm in young people [Royal College of Psychiatrists, 2014], and the British National Formulary (BNF) [BNF, 2022].
Supporting evidence
This CKS topic is largely based on expert opinion in narrative reviews Initial management of suspected poisoning in children and young people [Anderson, 2021], Principles of management of the poisoned patient [Morrison, 2020], Principles of assessment and diagnosis of the poisoned patient [Thanacoody, 2020a], Psychiatric assessment of self-poisoning [Martin, 2020], the National Institute for Health and Care Excellence (NICE) guideline Self-harm in over 8s: short-term management and prevention of recurrence [NICE, 2004], the British National Formulary (BNF) [BNF, 2022], the National Poisons Information Service (NPIS) Report 2020/21 [NPIS, 2021], and the toxicology database TOXBASE [TOXBASE, 2022]. The rationale for individual recommendations is discussed in the relevant basis for recommendation sections of this topic.
How this topic was developed
This section briefly describes the processes used in developing and updating this topic. Further details on the full process can be found in the About Us section and on the Clarity Informatics website.
Search strategy
Scope of search
A literature search was conducted for guidelines, systematic reviews and randomized controlled trials on primary care management of poisoning or overdose.
Search dates
April 2017 - March 2022
Key search terms
Various combinations of searches were carried out. The terms listed below are the core search terms that were used for Medline.
- exp Poisoning/, exp Overdose/, poison$.tw., overdose.tw.
- Overdos$.ti,ab. or OD.ti,ab. or over dos$.ti,ab.
- Paracetamol OR acetaminophen) AND (overdose OR toxicity OR risk prediction rules).ti,ab.
- Amfetamine AND (overdose OR toxicity OR risk prediction).ti,ab.
- Salicylate AND (overdose OR toxicity OR risk prediction).ti,ab.
- Cocaine AND (overdose OR toxicity OR risk prediction).ti,ab.
- Opioid AND (overdose OR toxicity OR risk prediction).ti,ab.
Sources of guidelines
- National Institute for Health and Care Excellence (NICE)
- Scottish Intercollegiate Guidelines Network (SIGN)
- Royal College of Physicians
- Royal College of General Practitioners
- Royal College of Nursing
- NICE Evidence
- World Health Organization
- Guidelines International Network
- TRIP database
- Agency for Healthcare Research and Quality
- Institute for Clinical Systems Improvement
- National Health and Medical Research Council (Australia)
- Royal Australian College of General Practitioners
- British Columbia Medical Association
- Canadian Medical Association
- Alberta Medical Association
- Michigan Quality Improvement Consortium
- Singapore Ministry of Health
- National Resource for Infection Control
- RefHELP NHS Lothian Referral Guidelines
- Medline (with guideline filter)
- Driver and Vehicle Licensing Agency
- NHS Health at Work (occupational health practice)
Sources of systematic reviews and meta-analyses
- The Cochrane Library:
- Systematic reviews
- Protocols
- Database of Abstracts of Reviews of Effects
- Medline (with systematic review filter)
- EMBASE (with systematic review filter)
Sources of health technology assessments and economic appraisals
- NIHR Health Technology Assessment programme
- The Cochrane Library:
- NHS Economic Evaluations
- Health Technology Assessments
- Canadian Agency for Drugs and Technologies in Health
- International Network of Agencies for Health Technology Assessment
Sources of randomized controlled trials
- The Cochrane Library:
- Central Register of Controlled Trials
- Medline (with randomized controlled trial filter)
- EMBASE (with randomized controlled trial filter)
Sources of evidence based reviews and evidence summaries
- Bandolier
- Drug and Therapeutics Bulletin
- TRIP database
- Central Services Agency COMPASS Therapeutic Notes
Sources of national policy
- Department of Health
- Health Management Information Consortium (HMIC)
Patient experiences
Sources of medicines information
The following sources are used by CKS pharmacists and are not necessarily searched by CKS information specialists for all topics. Some of these resources are not freely available and require subscriptions to access content.
Stakeholder engagement
Our policy
The external review process is an essential part of CKS topic development. Consultation with a wide range of stakeholders provides quality assurance of the topic in terms of:
- Clinical accuracy.
- Consistency with other providers of clinical knowledge for primary care.
- Accuracy of implementation of national guidance (in particular NICE guidelines).
- Usability.
Principles of the consultation process
- The process is inclusive and any individual may participate.
- To participate, an individual must declare whether they have any competing interests or not. If they do not declare whether or not they have competing interests, their comments will not be considered.
- Comments received after the deadline will be considered, but they may not be acted upon before the clinical topic is issued onto the website.
- Comments are accepted in any format that is convenient to the reviewer, although an electronic format is encouraged.
- External reviewers are not paid for commenting on the draft topics.
- Discussion with an individual or an organization about the CKS response to their comments is only undertaken in exceptional circumstances (at the discretion of the Clinical Editor or Editorial Steering Group).
- All reviewers are thanked and offered a letter acknowledging their contribution for the purposes of appraisal/revalidation.
- All reviewers are invited to be acknowledged on the website. All reviewers are given the opportunity to feedback about the external review process, enabling improvements to be made where appropriate.
Stakeholders
- Key stakeholders identified by the CKS team are invited to comment on draft CKS topics. Individuals and organizations can also register an interest to feedback on a specific topic, or topics in a particular clinical area, through the Getting involved section of the Clarity Informatics website.
- Stakeholders identified from the following groups are invited to review draft topics:
- Experts in the topic area.
- Professional organizations and societies (for example, Royal Colleges).
- Patient organizations, Clarity has established close links with groups such as Age UK and the Alzheimer’s Society specifically for their input into new topic development, review of current topic content and advice on relevant areas of expert knowledge.
- Guideline development groups where the topic is an implementation of a guideline.
- The British National Formulary team.
- The editorial team that develop MeReC Publications.
- Reviewers are provided with clear instructions about what to review, what comments are particularly helpful, how to submit comments, and declaring interests.
Patient engagement
Clarity Informatics has enlisted the support and involvement of patients and lay persons at all stages in the process of creating the content which include:
- Topic selection
- Scoping of topic
- Selection of clinical scenarios
- First draft internal review
- Second draft internal review
- External review
- Final draft and pre-publication
Our lay and patient involvement includes membership on the editorial steering group, contacting expert patient groups, organizations and individuals.
Evidence exclusion criteria
Our policy
Scoping a literature search, and reviewing the evidence for CKS is a methodical and systematic process that is carried out by the lead clinical author for each topic. Relevant evidence is gathered in order that the clinical author can make fully informed decisions and recommendations. It is important to note that some evidence may be excluded for a variety of reasons. These reasons may be applied across all CKS topics or may be specific to a given topic.
Studies identified during literature searches are reviewed to identify the most appropriate information to author a CKS topic, ensuring any recommendations are based on the best evidence. We use the principles of the GRADE and PICOT approaches to assess the quality of published research. We use the principles of AGREE II to assess the quality of published guidelines.
Standard exclusions for scoping literature:
- Animal studies
- Original research is not written in English
Possible exclusions for reviewed literature:
- Sample size too small or study underpowered
- Bias evident or promotional literature
- Population not relevant
- Intervention/treatment not relevant
- Outcomes not relevant
- Outcomes have no clear evidence of clinical effectiveness
- Setting not relevant
- Not relevant to UK
- Incorrect study type
- Review article
- Duplicate reference
Organizational, behavioural and financial barriers
Our policy
The CKS literature searches take into consideration the following concepts, which are discussed at the initial scoping of the topic.
- Feasibility
- Studies are selected depending on whether the intervention under investigation is available in the NHS and can be practically and safely undertaken in primary care.
- Organizational and Financial Impact Analysis
- Studies are selected and evaluated on whether the intervention under investigations may have an impact on local clinical service provision or national impact on cost for the NHS. The principles of clinical budget impact analysis are adhered to, evaluated and recorded by the author. The following factors are considered when making this assessment and analysis.
- Eligible population
- Current interventions
- Likely uptake of new intervention or recommendation
- Cost of the current or new intervention mix
- Impact on other costs
- Condition-related costs
- In-direct costs and service impacts
- Time dependencies
- Cost-effectiveness or cost-benefit analysis studies are identified where available.
We also evaluate and include evidence from NICE accredited sources which provide economic evaluations of recommendations, such as NICE guidelines. When a recommended action may not be possible because of resource constraints, this is explicitly indicated to healthcare professionals by the wording of the CKS recommendation.
Declarations of interest
Our policy
Clarity Informatics requests that all those involved in the writing and reviewing of topics, and those involved in the external review process to declare any competing interests. Signed copies are securely held by Clarity Informatics and are available on request with the permission of the individual. A copy of the declaration of interest form which participants are asked to complete annually is also available on request. A brief outline of the declarations of interest policy is described here and full details of the policy is available on the Clarity Informatics website. Declarations of interests of the authors are not routinely published, however competing interests of all those involved in the topic update or development are listed below. Competing interests include:
- Personal financial interests
- Personal family interest
- Personal non-financial interest
- Non-personal financial gain or benefit
Although particular attention is given to interests that could result in financial gains or losses for the individual, competing interests may also arise from academic competition or for political, personal, religious, and reputational reasons. An individual is not obliged to seek out knowledge of work done for, or on behalf of, the healthcare industry within the departments for which they are responsible if they would not normally expect to be informed.
Who should declare competing interests?
Any individual (or organization) involved in developing, reviewing, or commenting on clinical content, particularly the recommendations should declare competing interests. This includes the authoring team members, expert advisers, external reviewers of draft topics, individuals providing feedback on published topics, and Editorial Steering Group members. Declarations of interest are completed annually for authoring team and editorial steering group members, and are completed at the start of the topic update and development process for external stakeholders.
Competing interests declared for this topic:
None.
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