-
Adrenaline - Presentation
- 1 mg in 1 mL glass ampoule (1:1,000)
- 1 mg in 10 mL glass ampoule (1:10,000)
-
Adrenaline - Pharmacology & Metabolism
- A naturally occurring alpha and beta-adrenergic stimulant
- Actions:
- - Increases HR by increasing SA node firing rate (Beta 1)
- - Increases conduction velocity through the A-V node (Beta 1)
- - Increases myocardial contractility (Beta 1)
- - Increases the irritability of the ventricles (Beta 1)
- - Causes bronchodilatation (Beta 2)
- - Causes peripheral vasoconstriction (Alpha)
- Metabolism by monoamine oxidase and other enzymes in the blood, liver and around nerve
- endings; excreted by the kidneys
-
Adrenaline - Primary emergency indications
- 1. Cardiac arrest - VF/VT, Asystole or PEA
- 2. Inadequate perfusion (cardiogenic or non-cardiogenic/non-hypovolaemic)
- 3. Bradycardia with poor perfusion
- 4. Anaphylaxis
- 5. Severe asthma - imminent life threat not responding to nebulised therapy, or
- unconscious with no BP
- 6. Croup
-
Adrenaline - Contraindication
1. Hypovolaemic shock without adequate fluid replacement
-
Adrenaline - Precautions
- Consider reduced doses for:
- 1. Elderly / frail Pts
- 2. Pts with cardiovascular disease
- 3. Pts on monoamine oxidase inhibitors
4. Higher doses may be required for Pts on beta blockers
-
Adrenaline - Side effects
- 1. Sinus tachycardia
- 2. Supraventricular arrhythmias
- 3. Ventricular arrhythmias
- 4. Hypertension
- 5. Pupillary dilatation
- 6. May increase size of MI
- 7. Feeling of anxiety/palpitations in the conscious Pt
-
Adrenaline - Special notes
- IV Adrenaline should be reserved for life threatening situations.
- IV effects:
- Onset: 30 sec
- Peak: 3 – 5 min
- Duration: 5 – 10 min
- IM effects:
- Onset: 30 – 90 sec
- Peak: 4 – 10 min
- Duration: 5 – 10 min
-
Aspirin - Presentation
- 300 mg chewable tablets
- 300 mg soluble or water dispersible tablets
-
Aspirin - Pharmacology
An analgesic, antipyretic, anti-inflammatory and antiplatelet aggregation agent
- Actions:
- - To minimise platelet aggregation and thrombus formation in order to retard the
- progression of coronary artery thrombosis in ACS
- - Inhibits synthesis of prostaglandins - anti-inflammatory actions
-
Aspirin - Metabolism
Converted to salicylate in the gut mucosa and liver; excreted mainly by the kidneys
-
Aspirin - Primary emergency indication
1. ACS
-
Aspirin - Contraindications
- 1. Hypersensitivity to aspirin / salicylates
- 2. Actively bleeding peptic ulcers
- 3. Bleeding disorders
- 4. Suspected dissecting aortic aneurysm
- 5. Chest pain associated with psychostimulant OD if SBP >160 mmHg
-
Aspirin - Precautions
- 1. Peptic ulcer
- 2. Asthma
- 3. Pts on anticoagulants
-
Aspirin - Side effects
- 1. Heartburn, nausea, gastrointestinal bleeding
- 2. Increased bleeding time
- 3. Hypersensitivity reactions
-
Aspirin - Special notes
Aspirin is C/I for use in acute febrile illness in children and adolescents
- The anti-platelet effects of Aspirin persist for the natural life of platelets.
- Onset: n/a
- Peak: n/a
- Duration: 8 - 10 days
-
Ceftriaxone - Presentation
1 g sterile powder in a glass vial
-
Ceftriaxone - Pharmacology & Metabolism
- P - Cephalosporin antibiotic
- M - Excreted unchanged in urine (33% - 67%) and in bile
-
Ceftriaxone - Primary emergency indication
- 1. Suspected meningococcal septicaemia
- 2. Severe sepsis (consult only)
-
Ceftriaxone - Contraindication
1. Allergy to Cephalosporin antibiotics
-
Ceftriaxone - Precautions
1. Allergy to Penicillin antibiotics
-
Ceftriaxone - Side effects
-
Ceftriaxone - Special notes
- Usual dose: adult 1 g, child 50 mg/kg (max. 1 g)
- Ceftriaxone IV must be made up to 10 mL using sterile water and
- dose administered over 2 min
- Ceftriaxone IM must be made up to 4 mL using 1% Lignocaine and
- dose administered in lateral upper thigh
- IM/IV effects:
- Onset: n/a
- Peak: n/a
- Duration: n/a
-
Fentanyl - Presentation
- 100 mcg in 2 mL glass ampoule
- 200 mcg in 1mL glass vial (IN use only)
- 600 mcg in 2 mL glass vial (IN use only)
-
Fentanyl - Pharmacology
- A synthetic opioid analgesic
- Actions:
- CNS effects:
- - Depression – leading to analgesia
- - Respiratory depression – leading to apnoea
- - Dependence (addiction)
- Cardiovascular effects:
- - Decreases conduction velocity through the A-V node
-
Fentanyl - Metabolism
By the liver; excreted by the kidneys
-
Fentanyl - Primary emergency
indications
- 1. Sedation to facilitate intubation
- 2. Sedation to maintain intubation
- 3. Drug facilitated intubation
- 4. Analgesia – IV/IN
-
Fentanyl - Contraindication
1. Known hypersensitivity
-
Fentanyl - Precautions
RICEPRK
- 1. Respiratory depression, e.g. COPD
- 2. Impaired renal / hepatic function
- 3. Current asthma
- 4. Elderly/frail patients
- 5. Pts on monoamine oxidase inhibitors
- 6. Rhinitis, rhinorrhea or facial trauma (IN route)
- 7. Known addiction to opioids
-
Fentanyl - Side effects
RARB
- Respiratory depression
- Apnoea
- Rigidity of the diaphragm and intercostal muscles
- Bradycardia
-
Fentanyl -
- Fentanyl is a Schedule 8 drug under the Poisons Act and its use must be carefully
- controlled with accountability and responsibility
Respiratory depression can be reversed with Naloxone
100 mcg Fentanyl is equivalent in analgesic activity to 10 mg Morphine
- IV effects:
- Onset: Immediate
- Peak: < 5 min
- Duration: 30 - 60 min
-
Glyceryl Trinitrate (GTN) - Presentation
- 0.6 mg tablets
- Transdermal GTN Patch (50 mg 0.4 mg/hr release)
-
Glyceryl Trinitrate (GTN) - Pharmacology
Principally, a vascular smooth muscle relaxant
- Actions:
- - Venous dilatation promotes venous pooling and reduces venous return to the heart
- (reduces preload)
- - Arterial dilatation reduces systemic vascular resistance and arterial pressure
- (reduces afterload)
- The effects of the above are:
- - Reduced myocardial O2
- demand
- - Reduced systolic, diastolic and mean arterial blood pressure, whilst usually
- maintaining coronary perfusion pressure
- - Mild collateral coronary arterial dilatation may improve blood supply to ischaemic
- areas of myocardium
- - Mild tachycardia secondary to slight fall in blood pressure
- - Preterm labour: Uterine quiescence in pregnancy
-
Glyceryl Trinitrate (GTN) - Primary emergency indication
- 1. Chest pain with ACS
- 2. Acute LVF
- 3. Hypertension associated with ACS
- 4. Autonomic dysreflexia
- 5. Preterm labour (consult)
-
Glyceryl Trinitrate (GTN) - Contraindication
- 1. Known hypersensitivity
- 2. Sildenafil Citrate (Viagra) or Vardenafil (Levitra) administration in the previous24 hr or Tadalafil (Cialis) administration in the previous 4 days (PDE5 inhibitors)
- 3. Systolic blood pressure < 110 mmHg tablet
- 4. Systolic blood pressure < 90 mmHg patch
- 5. Heart rate > 150 bpm
- 6. Bradycardia HR < 50 bpm (excluding autonomic dysreflexia)
- 7. VT
- 8. Inferior STEMI with systolic BP < 160 mmHg
- 9. Right ventricular MI
-
Glyceryl Trinitrate (GTN) - Precautions
- 1. No previous administration
- 2. Elderly Pts
- 3. Recent MI
- 4. Concurrent use with other tocolytics
- [Tocolytics (also called anti-contraction medications or labor repressants) are medications used to suppress premature labor]
-
Glyceryl Trinitrate (GTN) - Side effects
- Tachycardia
- Hypotension
- Headache
- Skin flushing (uncommon)
- Bradycardia (occasionally)
-
Glyceryl Trinitrate (GTN) - Special notes (some selected only)
- - Since both men and women can be prescribed Sildenafil Citrate (Viagra) or
- Vardenafil (Levitra) or Tadalafil (Cialis) all Pts should be asked if and when they last
- had the drug to determine if GTN is C/I
- - Tadalafil (Cialis) may also be prescribed to men for Rx of benign prostatic
- hypertrophy. This is a new indication for the drug and may lead to an increased
- number of Pts under this Rx regimen.
- Interhospital transfer:
- The IV dose is to be prescribed and signed by the referring hospital medical officer.
- Infusions usually run in the range of 5 mcg/min to 200 mcg/min and increased 3 - 5
- mcg/min.
- S/L effects:
- Onset: 30 sec – 2 min
- Peak: 5 - 10 min
- Duration: 15 - 30 min
- Intravenous effects
- Onset: 30 sec – 1 min
- Peak: 3 - 5 min
- Duration: 15 - 30 min
- Transdermal effect
- Onset: Up to 30 min
- Peak: 2 hr
-
Ipratropium Bromide - Presentation
250 mcg in 1 mL nebule or polyamp
-
Ipratropium Bromide - Pharmacology
Anticholinergic bronchodilator
- Actions:
- - Allows bronchodilatation by inhibiting cholinergic bronchomotor tone (i.e. blocks vagal reflexes which mediate bronchoconstriction
-
Ipratropium Bromide - Metabolism
Excreted by the kidneys
-
Ipratropium Bromide - Primary emergency indication
1. Severe respiratory distress associated with bronchospasm
-
Ipratropium Bromide - Contraindication
1. Known hypersensitivity to Atropine or its derivatives
-
Ipratropium Bromide - Precautions
- 1. Glaucoma
- 2. Avoid contact with eyes
-
Ipratropium Bromide - Side effects
HANDS TP
- Headache
- Acute angle closure glaucoma secondary to direct eye contact (rare)
- Nausea
- Dry mouth
- Skin rash
- Tachycardia (rare)
- Palpitations (rare)
-
Ipratropium Bromide - Special notes
- Ipratropium Bromide must be nebulised in conjunction with Salbutamol and is to be
- administered as a single dose only.
- Onset: 3 - 5 min
- Peak 1.5 - 2 hr
- Duration: 6 hr
-
Methoxyflurane - Presentation & Pharmacology
3 mL glass bottle
- Pharma:
- Inhalational analgesic agent at low concentrations
-
Methoxyflurane - Metabolism
- Excreted mainly by the lungs
- By the liver
-
Primary emergency indication
1. Pain relief
-
Methoxyflurane - Contraindication
- 1. Pre-existing renal disease / renal impairment
- 2. Concurrent use of tetracycline antibiotics
- 3. Exceeding total dose of 6 mL in a 24 hr period
-
Methoxyflurane - Precautions
- 1. The Penthrox™ inhaler must be hand-held by the Pt so that if unconsciousness
- occurs it will fall from the Pt’s face. Occasionally the operator may need to assist
- but must continuously assess the level of consciousness
- 2. Pre-eclampsia[Pre-eclampsia is a serious condition of pregnancy characterised by high blood pressure, protein in the urine and swelling of the hands, feet and face.]
- 3. Concurrent use with Oxytocin may cause hypotension
-
Methoxyflurane - Side effects
- Drowsiness
- Decrease in blood pressure and bradycardia (rare)
- Exceeding the maximum total dose of 6 mL in a 24 hr period may lead to
- renal toxicity
-
Methoxyflurane - Special notes
- The maximum initial priming dose for Methoxyflurane is 3 mL. This will provide
- approximately 25 min of analgesia and may be followed by one further 3mL dose
- once the initial dose is exhausted if required. Analgesia commences after 8 - 10
- breaths and lasts for approximately 3 - 5 min once discontinued.
Do not administer in a confied space. Ensure adequate ventilation in ambulance
-
Metoclopramide - Presentation
10 mg in 2 mL polyamp
-
Metoclopramide - Pharmacology
Antiemetic
- Actions:
- - Accelerates gastric emptying and peristalsis
- - Dopamine receptor antagonist
-
Metoclopramide - Metabolism
By the liver; excreted by the kidneys
-
Metoclopramide - Primary emergency indication
- 1. Nausea / vomiting associated with
- - Chest pain / discomfort of a cardiac nature
- - Opioid administration for pain
- - Cytotoxic or radiotherapy
- - Previously diagnosed migraine
- - Severe gastroenteritis
- 2. Prophylaxis:
- - Awake spinal immobilised Pts
- - Eye trauma
-
Metoclopramide - Contraindication
- 1. Children
- 2. Suspected bowel obstruction or perforation
- 3. Gastrointestinal haemorrhage
-
Metoclopramide - Side effects
DLDME
- Drowsiness
- Lethargy
- Dry mouth
- Muscle tremor
- Extrapyramidal reactions (usually the dystonic type)
-
Metoclopramide - Special notes
- Not effective for established motion sickness.
- Not effective for nausea prophylaxis in the setting of opioid administration.
- IV effects:
- Onset: 1 – 3 min
- Peak: n/a
- Duration: 10 – 30 min
- IM effects:
- Onset: 10 – 15 min
- Peak: n/a
- Duration: 1 – 2 hr
-
Midazolam - Presentation
- 5 mg in 1 mL glass ampoule
- 15 mg in 3 mL glass ampoule
-
Midazolam - Pharmacology
Short acting CNS depressant
- Actions:
- - Anxiolytic
- - Sedative
- - Anti-convulsant
-
Midazolam - Metabolism
In the liver; excreted by the kidneys
-
Midazolam - Primary emergency indication
- 1. Status epilepticus
- 2. Sedation to enable intubation (RSI / IFS)
- 3. Post intubation sedation
- 4. Sedation to enable synchronised cardioversion
- 5. Sedation in the agitated Pt (including Pts under the Mental Health Act 2014)
- 6. Sedation in psychostimulant OD
-
Midazolam - Contraindications
1. Known hypersensitivity to benzodiazepines
-
Midazolam - Precautions
- 1. Reduced doses may be required for the elderly/frail, Pts with chronic renal failure,
- CCF or shock
- 2. The CNS depressant effects of benzodiazepines are enhanced in the presence of
- narcotics and other tranquillisers including alcohol
- 3. Can cause severe respiratory depression in Pts with COPD
- 4. Pts with myasthenia gravis
-
Midazolam - Side effects
- Depressed level of consciousness
- Respiratory depression
- Loss of airway control
- Hypotension
-
Midazolam - Special notes
- IM effects:
- Onset: 3 – 5 min
- Peak: 15 min
- Duration: 30 min
- IV effects:
- Onset: 1 – 3 min
- Peak: 10 min
- Duration: 20 min
-
Morphine - Presentation
10 mg in 1 mL glass ampoule
-
Morphine - Pharmacology
- CNS effects:
- - Depression (leading to analgesia)
- - Respiratory depression
- - Depression of cough reflex
- - Stimulation (changes of mood, euphoria or dysphoria, vomiting, pin-point pupils)
- - Dependence (addiction)
- Cardiovascular effects:
- - Vasodilatation
- - Decreases conduction velocity through the A-V Node
-
Morphine - Metabolism
By the liver; excreted by the kidneys
-
Morphine - Primary emergency indication
- 1. Pain relief
- 2. Acute LVF with shortness of breath and full field crackles
- 3. Sedation to maintain intubation
- 4. Sedation to enable intubation
- 5. RSI
-
Morphine - Contraindications
- 1. Known hypersensitivity
- 2. Late second stage of labour
-
Morphine - Precautions
EHRCRKAP
- 1. Elderly/frail patients
- 2. Hypotension
- 3. Respiratory depression
- 4. Current asthma
- 5. Respiratory tract burns
- 6. Known addiction to opioids
- 7. Acute alcoholism
- 8. Pts on monoamine oxidase inhibitors
-
Morphine - Side effects
- CNS effects:
- - Drowsiness
- - Respiratory depression
- - Euphoria
- - Nausea, vomiting
- - Addiction
- - Pin-point pupils
- Cardiovascular effects:
- - Hypotension
- - Bradycardia
-
Morphine - Special notes
- Morphine is a Schedule 8 drug under the Poisons Act and its use must be
- carefully controlled with accountability and responsibility.
- Side effects of Morphine can be reversed with Naloxone.
- Occasional wheals are seen in the line of the vein being used for IV injection. This is
- not an allergy, only a histamine release.
- IV effects:
- Onset: 2 – 5 min
- Peak: 10 min
- Duration: 1 – 2 hr
- IM effects:
- Onset: 10 – 30 min
- Peak: 30 – 60 min
- Duration: 1 – 2 hr
-
Naloxone - Presentation
- 0.4 mg in 1 mL glass ampoule
- 2 mg in 5 mL (prepared syringe)
-
Naloxone - Pharmacology
An opioid antagonist
- Action:
- - Prevents or reverses the effects of opioids
-
Naloxone - Metabolism
By the liver
-
Naloxone - Primary emergency indication
- 1. Altered conscious state and respiratory depression secondary to administration of
- opioids or related drugs.
-
Naloxone - Contraindications
1. Nil of significance in the above indication
-
Naloxone - Precautions
- 1. If Pt is known to be physically dependent on opioids, be prepared for a combative
- Pt after administration.
- 2. Neonates.
-
Naloxone - Side effects
- Symptoms of opioid withdrawal:
- - Sweating, goose flesh, tremor
- - Nausea and vomiting
- - Agitation
- - Dilatation of pupils, excessive lacrimation
- - Convulsions
-
Naloxone - Special notes
- Naloxone reverses the effects of opioids with none of the actions produced by other
- opioid antagonists when no opioid is present in the body. (For example, it does not
- depress respiration or cause pupillary constriction). In the absence of opioids, Naloxone has no perceivable effects.
- Following an opioid associated cardiac arrest Naloxone should not be administered.
- Maintain assisted ventilation.
Following head injury Naloxone should not be administered. Maintain assisted ventilation if required.
- IV effects:
- Onset: 1 – 3 min
- Peak: n/a
- Duration: 30 – 45 min
- IM effects:
- Onset: 1 – 3 min
- Peak: n/a
- Duration: 30 – 45 min
-
Prochlorperazine (Stemetil) - Presentation
12.5 mg in 1 mL glass ampoule
-
Prochlorperazine (Stemetil) - Primary emergency indication
- 1. Rx or prophylaxis of nausea / vomiting for
- - Motion sickness
- - Planned aeromedical evacuation
- - Known allergy or C/I to Metoclopramide administration
- - Headache irrespective of nausea / vomiting
- - Vertigo
-
Prochlorperazine (Stemetil) - Contraindications
- 1. Circulatory collapse
- 2. CNS depression
- 3. Previous hypersensitivity
- 4. Children
-
Prochlorperazine (Stemetil) - Precautions
- 1. Circulatory collapse
- 2. CNS depression
- 3. Previous hypersensitivity
- 4. Children
-
Prochlorperazine (Stemetil) - Side effects
SHEBS D
- Drowsiness
- Blurred vision
- Hypotension
- Sinus tachycardia
- Skin rash
- Extrapyramidal reactions (usually the dystonic type)
-
Prochlorperazine (Stemetil) - Special notes
- IM effect
- Onset: 20 min
- Peak: 40 min
- Duration: 6 hr
-
Prochlorperazine (Stemetil) - Pharmacology
- An anti-emetic
- Action:
- - Acts on several central neuro-transmitter systems
-
Salbutamol - Presentation
- 5 mg in 2.5 mL polyamp
- 500 mcg in 1 mL glass ampoule
- 5 mg in 5 mL glass ampoule
- pMDI (100 mcg per actuation)
-
Salbutamol - Pharmacology
- A synthetic beta adrenergic stimulant with primarily beta 2 effects
- Action:
- - Causes bronchodilatation
-
Salbutamol - Metabolism
By the liver; excreted by the kidneys
-
Salbutamol - Primary emergency indication
- 1. Respiratory distress with suspected bronchospasm:
- - asthma
- - severe allergic reactions
- - COPD
- - smoke inhalation
- - oleoresin capsicum spray exposure
-
Salbutamol - Contraindications
1. IV Salbutamol is no longer indicated for adult Pts
-
Salbutamol - Precautions
- 1. Large doses of IV Salbutamol have been reported to cause intracellular metabolic
- acidosis
-
Salbutamol - Side effects
- Sinus tachycardia
- Muscle tremor (common)
-
Salbutamol - Special notes
- IV Salbutamol has no advantage over nebulised Salbutamol provided that adequate
- ventilation is occurring.
- Salbutamol nebules / polyamps have a shelf life of one month after the wrapping
- is opened. The date of opening of the packaging should be recorded and the drug
- should be stored in an environment of < 30°C
- Although infrequently used, Salbutamol by IV infusion may be required during
- interhospital transfers of some women in premature labour
- The dose is to be prescribed and signed by the referring hospital medical officer
- Nebulised effects:
- Onset: 5 – 15 min
- Peak: n/a
- Duration: 15 – 50 min
- IV effects:
- Onset: 1 – 2 min
- Peak: n/a
- Duration: 30 – 60 min
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