14.1 Poisoning And STOPP-START Flashcards

1
Q

What should be checked when thinking about medicine optimisation?

A

Checking repeat prescriptions
Full medication review - discussing each medicatio and condition with the patient
Ensure patient is taking the medications at the right time
Ensure they are taking medication in the intended way
Improving clinical outcomes - make sure it is the most beneficial and appropriate drug
Improve economy - best investment for each pound

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2
Q

Why is it useful to do medicine optimisation?

A

Because of polypharmacy - patients may be taking 4-6+ medicines a day
ADRs and DDIs are a common reason for admission to hospital in the elderly

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3
Q

What patients should be targeted for medication review?

A
  • Taking lots of medications - polypharmacy. The more drugs a patient is taking, the less good their adherence is likely to be
  • Complex medication regimens - taking drugs in a particular way at a particular time of day
  • Recently discharged (or admitted)
  • Frequent admissions to hospital - could be related to more management of their medications
  • Comorbidities
  • Medications prescribed from multiple sources
  • High risk medications – narrow therapeutic window, known and serious side effect profile
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4
Q

What are some of the pharmokinetic and dynamic changes in older people to think about when reviewing medication?

A
  • Body composition – increased fat, decreased body water and lean mass
  • Renal mass and function reduced
  • Hepatic function and blood flow decreased
  • GI absorption decrease, GI bleed risk increase
  • Baroreceptor sensitivity reduced - older patients tend to increase cardiac output instead of heart rate
  • Reduced first pass metabolism
  • Protein binding
  • Receptor expression level changes
  • Psychotropic drugs and extra pyramidal effects
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5
Q

Who might carry out a medication review?

A

GP
Hospital doctors
Specialist pharmacists

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6
Q

What things should we be thinking about when conducting a medication review?

A
Is the medication right for the patient
Time limited medication
Age - life expectancy and risk/benefit 
Measureable outcomes - able to tell whether or not the medication is effective
Cost 
Appropriate tests to support decisions
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7
Q

What is the function of the STOPP-START tool?

A

To aid in medication reviews

screening tool of older people’s prescriptions and screening tool to alert to right treatment

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8
Q

What group of people is STOPP-START used for?

A

Polypharmacy patients over 65

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9
Q

What is the aim of the STOPP-START tool?

A

Aim to highlight and prevent inappropriate prescribing → reduction in DDIs and or ADRs

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10
Q

What is the difference between drug toxicity and adverse drug reaction?

A

ADRs are typical of a drug being used at therapeutic doses
Drug toxicity more commonly associated with effects that occur at supra therapeutic doses - giving doses of an agent well above what we know causes a therapeutic benefit

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11
Q

What causes pharmalogical toxicity?

A

Most often predictable extension of desired effect
Secondary effect not related to primary aim of the treatment
An effect normally only seen in large overdose - too much drug, narrow therapeutic window

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12
Q

What drugs can cause pharmalogical toxicity in overdose?

A

B-blocker - myocardial depression
Opioids - respiratory depression
Theophylline - convulsions, arrhythmia
Carbamazepine/phenobarbital - respiratory depression

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13
Q

What is meant by biochemical toxicity?

A

A drug or active metabolite which causes cellular damage - macromolecules inc. structural proteins and enzymes.

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14
Q

How does biochemical toxicity occur?

A

Potentially harmful metabolites build up. If they are not inactivated they can cause cytotoxicity.
Balance of elimination of a drug or metabolites will dictate the potential harm that may be caused

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15
Q

How do we overcome biological toxicity?

A

Development of suitable pharmacological treatment.

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16
Q

Give an example of overcoming biological toxicity during overdosing

A

Acetyl cysteine - think donating in paracetamol overdose administered in three successive infusions at different concentrations over 21 hours.

17
Q

Give an example of overcoming biological toxicity at therapeutic levels

A

Cyclophosphamide used in severe RA produces highly toxic metabolites eliminated in urine. Can cause haemorrhagic cystitis due to damage to the bladder
Use Mensa alongside cyclophosphamide as has a thinly group for cytochrome toon and polar group. Also aggressive hydration

18
Q

What resources can we use to check biological and pharmalogical toxicity?

A

BNF

TOXBASE

19
Q

What are the 5 overdose management principles?

A
Prevention of absorption
Immediate actions
Supportive measures
Enhance elimination
Antidotes
20
Q

What are the immediate actions we can consider during an overdose?

A

Remove person from contact with the poison
Vital signs and injury
History
Evidence

21
Q

What are the supportive measures we can address in the event of an overdose?

A

Cardiac arrest = support any hypoxia, electrolyte and metabolic disturbance and cardiac toxicity
Arrhythmias = support hypoxia, electrolyte and metabolic disturbance and cardiac toxicity
Hypotension = support myocardial depression, peripheral vasodilation
Renal failure = hypotension, direct nephrotoxicity, rhabdomyolysis
Respiratory failure = direct neurotoxicity
Hepatic failure = direct hepatotoxicity
Seizures = hypoxia, direct neurotoxicity

22
Q

How do we prevent absorption in overdose?

A

Activated charcoal in large quantities. Not suitable for drowsy or comatose patients

23
Q

Why is gastric lovage not used in overdose?

A

Due to risk of aspiration

24
Q

How do we manage elimination in overdoses?

A

Continued activated charcoal
Sodium bicarbonate - alkaline diuresis
Haemodialysis

25
Q

Give some examples of competitive antagonist antidotes?

A

Naloxone

Atropine

26
Q

What are chelating agents?

A

Agents that form a complex with a drug to reduce the free drug. Used in overdose as an antidote. Some examples of overdose with cyanide lead and iron salt poisoning.

27
Q

Give some examples of drugs that work as an antidote via manipulating drug metabolism

A

Fomepizole

Acetylcysteine

28
Q

Give some examples of specific antidotes

A

Antibodies
Antivenoms
Digoxin-specific antibody