Drug overdose Flashcards
What is the definition of drug overdose?
Taking more opiates than you should (Heroin and morphine are responsible for most drug-related deaths)
Describe the pathophysiology behind opioids
- Opioids are classified as agonists, partial agonists, or agonist-antagonists of the opioid receptors, which contributes to the specific clinical effects in overdose.
- Mu receptors mediate analgesia, sedation, respiratory depression, euphoria, gastrointestinal dysmotility, and physical dependence.
- Kappa receptors mediate analgesia, miosis, diuresis, and dysphoria.
- Less is known about delta receptors, which mediate analgesia, inhibition of dopamine release, and cough suppression.
- Sigma receptors are no longer considered opioid in character because they are not antagonised by naloxone.
Describe the epidemiology of drug overdose
ELDERLY are more at risk because they are more likely to be on opiates
What are the risk factors for opiate overdose?
- Mental health conditions
- Alcoholics
Morphine toxicity at a lower dose due to: - Hepatic impairment
- Renal impairment
- Hypotension
- Hypothyroidism
- Asthma (decreased respiratory reserve)
- There is increased risk of paracetamol toxicity in patients that are in glutathione deplete states. This includes eating disorders, HIV and malnutrition
What are some examples of opioids?
- Codeine
- Diamorphine
- Dihydrocodeine
- Fentanyl
- Loperamide
- Methadone
(most commonly due to): - Morphine
- Heroin
What are the symptoms of an opiate overdose?
- Constipation (if chronic)
- Drowsiness (if acute overdose)
- Nausea and vomiting
- Loss of appetite
- Sedation
- Craving the next dose
What signs of opiate overdose can be found on physical examination?
- Respiratory depression (bradypnoea)
- Altered mental status
- Hypotension and tachycardia
- Bilateral miosis (pinpoint pupils)
- Track/needle marks
- Rhinorrhoea
What investigations are used to diagnose/ monitor an opiate overdose?
- Toxicology screen (can take a few days, should start ABCDE approach)
- Paracetamol blood level (should be considered in patients who have self-poisoned)
- If in doubt, give a small test dose of naloxone : may show reversal of overdose signs
- ABG (respiratory depression)
- FBC
How would you manage an opiate overdose?
- Initial ventilation
- Initial naloxone (opioid antagonist- reverses overdose) administration: subcutaneously or intravenously every 2 to 3 minutes.
- Repeat doses of naloxone
- The duration of effect of most opioids is 4 hours or less, but some may last significantly longer. The effects of methadone, levomethadyl acetate (LAAM), and buprenorphine can last from 24 to 72 hours
What complications can arise from an opiate overdose?
- Hypoxia
- Aspiration
- ARDS
Describe the prognosis of an opiate overdose
Timely administration of naloxone, and appropriate ventilation prior to antidote, results in complete reversal of the effects of opioid overdose
What is meant by paracetamol overdose?
Paracetamol overdose is the excessive use of the medication paracetamol, also known as acetaminophen.
How can paracetamol overdose be classified?
- Acute overdose - excessive amounts in less than 1 hour, usually in context of self-harm)
- Staggered overdose - excessive amounts of paracetamol ingested over longer than 1 hour, usually in context of self harm)
- Therapeutic excess - excessive paracetamol taken with intent to treat pain or fever and without self-harm intent, ingested at dose greater than licensed daily dose (more than 75mg/kg/24 hours).
Describe the epidemiology of paracetamol overdose
Paracetamol is the most common agent for intentional self-harm in the UK. Paracetamol overdose accounts for 44% of all adult self-poisoning cases in the UK, with approximately 150,000 people admitted to hospital each year due to poisoning.
Describe the pathophysiology behind paracetamol overdose
- Involves the buildup of a toxic substance called NAPQI (N-acetyl-p-benzoquinone-imine).
- Normally, NAPQI is inactivated by glutathione, but during an overdose, glutathione stores are rapidly depleted, leaving NAPQI unmetabolised and resulting in liver and kidney damage. (most dmaage to liver- causes hepatotoxicity)