Pharmocolgies Flashcards

1
Q

Adrenaline - Actions

A

Action

  • Stimulates the ALPHA and BETA receptors of the sympathetic nervous system to produce the “Fight” or “Flight” reaction
  • ALPHA stimulation causes peripheral vasoconstriction. It raises the perfusion pressure of vital organs during cardiac arrest and it decreases capillary permeability and increases blood pressure in anaphylaxis
  • BETA 1 stimulation causes increased myocardial excitability, tachycardia, and increased myocardial contractility
  • BETA 2 stimulation causes bronchodilation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Adrenaline - Uses

A

Use

C3 - Cardiac arrest
C7 - Bradycardia
C6 - Cardiogenic shock
M4 - Asthma
M16 - Anaphylaxis
M7 - Croup
O6 - Newborn resuscitation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Adrenaline - Adverse Effects

A

Adverse Effects

Tachycardia
Dysrhythmias, including ventricular fibrillation
Hypertension
Pupillary dilation
Anxiety
Nausea and vomiting
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Adrenaline - Preparation and Onset, Peak, Duration

A

Preparation

1mg in 1mL ampoule (1:1,000)
1mg in 10mL ampoule (1:10,000)

       Onset	Peak	Duration IM	30-90 sec	4-10 min	5-10 min IV	30 sec	       3-5 min	       5-10 min NEB	1-5 min	n/a	Up to 20 min
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Adrenaline - Infusion

A

Adrenaline infusion

Patients ≥ 16 years of age

Preparation: 1mg (10mL) 1:10,000 diluted in 90mL compound sodium lactate via burette with micro drip

Commence 5mcg/min (30 drops per min) and titrate whilst indicated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Adrenaline - Cardiac Arrest >16yrs

A

Cardiac arrest

Patients ≥ 16 years of age

1mg (10mL) 1:10,000 IV bolus
Repeat every 2nd cycle (approx. 4 min)
Maximum dose: no max
Note: During interhospital transports paramedics unable to obtain IV access may use existing IO access, if available.

2mg (2mL) 1:1,000 ETT bolus
Repeat every 2nd cycle (approx. 4 min)
Maximum dose: 10mg (10mL)

Following return of circulation post cardiac arrest
50mcg (0.5mL) 1:10,000 IV bolus every minute until systolic BP > 100mmHg or an adrenaline infusion is running.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Adrenaline - Cardiac Arrest <16yrs

A

Patients < 16 years of age

10mcg/kg (0.1mL/kg) 1:10,000 IV/IO bolus
Repeat every 2nd cycle (approx. 4 min)
Maximum dose: No max

100mcg/kg (0.1mL/kg) 1:1,000 ETT¹ bolus
Repeat every 2nd cycle (approx. 4 min)
Maximum bolus dose 2mg (2mL)
Maximum ETT dose: 5 total doses
¹ Patients < 1 year of age should have ETT dose diluted to 1mL in total with sodium chloride 0.9%
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Adrenaline - Severe/life threatening asthma

A

Severe / life threatening asthma

Patients ≥ 16 years of age

500mcg (0.5mL) 1:1,000 IM into lateral aspect of thigh
Repeat every 5 minutes whilst indicated
Maximum dose: no max

100mcg (1mL) 1:10,000 IV bolus if unresponsive to IM injection
Repeat every minute whilst indicated
Maximum dose: no max

Patients < 16 years of age

10mcg/kg (0.01mL/kg) 1:1,000 IM bolus into lateral aspect of thigh
Repeat every 5 minutes whilst indicated
Maximum dose: No max

10mcg/kg (0.1mL/kg) 1:10,000 IV bolus slowly if unresponsive to IM injection
Repeat every 5 minutes whilst indicated
Maximum bolus dose 100mcg (1mL)
Maximum dose: No max

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Adrenaline - Anaphylaxis Severe/ Life Threatening

A

Severe / life threatening anaphylaxis

Patients ≥ 16 years of age

500mcg (0.5mL) 1:1,000 IM² bolus into lateral aspect of thigh
Repeat every 5 minutes whilst indicated
Maximum dose: no max

Patients < 16 years of age

10mcg/kg (0.01mL/kg) 1:1,000 IM bolus into lateral aspect of thigh
Repeat every 5 minutes whilst indicated
Maximum dose: No max

*Adrenaline infusion is indicated for all patients ≥ 16 years of age unresponsive to a mininum of 4 IM injections (Authorised Paramedics Only)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Adrenaline - Croup

A

Severe croup

Patients < 16 years of age

500mcg/kg (0.5mL/kg) 1:1,000 NEB
Repeat 30 minutes if indicated
Maximum bolus dose: 5mg (5mL)
Maximum dose: No maximum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Aspirin - Type, action, onset, peak, duration, uses

A

Type: Non-steroidal anti-inflammatory drug

Action

Inhibits platelet aggregation thereby limiting thrombus enlargement in acute coronary syndrome
Reduces production of prostaglandins thereby relieving pain and fever

Route Onset Peak Duration
PO 2-10 min N/A 3-6 hrs
Use

C1 - Acute coronary syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Aspirin - Adverse Effects, Contraindications, Prep

A

Adverse effects

Allergic reactions, e.g. asthma, angioneurotic oedema, rhinitis, urticaria, laryngeal oedema and shock. Always check for history of previous reaction
Aggravation of any bleeding tendency
Gastric irritation (unlikely to be significant with one tablet)
Bleeding may take longer to stop

Contraindications
Allergy or hypersensitivity to aspirin
Active, suspected or known bleeding tendency
Patients < 16 years of age
Patients meeting T1 Major Trauma criteria
Preparation

300mg tablet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Aspirin - Dose

A

Acute coronary syndrome

Patients ≥ 16 years of age

300mg (1 tablet) chewed and swallowed, may be taken with a small amount of water if required
No repeat
Maximum dose: 1 dose

Aspirin administration is not contraindicated in patients with regular daily use of aspirin and/or warfarin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Benzyl Penicillin - Type, Action, Use, Adverse Effects

A

Benzyl Penicillin

Type: Antibiotic active against a range of bacteria

Action

Inhibits bacterial cell wall synthesis and causes cytolysis when the bacterium tries to divide

Use

M13 - Meningococcal septicaemia

Adverse effects

Hypersensitivity reactions may occur (including urticaria, angio-oedema, convulsions and anaphylaxis)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Benzyl Penicillin - Contraindications, Prep

A

Contraindication
Life threatening allergic reaction to penicillin

Preparation

600mg as a powder
IV/IO Administration: Dissolve 600mg in 10mL sodium chloride 0.9%
IM Administration: Dissolve 600mg in 2mL sodium chloride 0.9%
Note: Volume may vary after reconstitution

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Benzyl Penicillin - Dose

A

Meningococcal septicaemia

Age Route Dose Volume
<1 year IV/IO 300mg 5mL
1-<10 years IV/IO 600mg 10mL
≥10 years IV/IO 1200mg 20mL

Age. Route Dose Volume
<1 year. IM 300mg 1mL
1-<10 years IM 600mg 2mL
≥10 years IM 1200mg 4mL

All ages: No repeat dose, maximum dose: 1 dose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Clopidogrel - Type, Action, OPD, Uses

A

Clopidogrel

Type: Platelet receptor antagonist

Actions

Clopidogrel is a specific and potent inhibitor of platelet aggregation and limits propagation of thrombus by selectively inhibiting the binding of ADP to its platelet receptor
Clopidogrel is absorbed from the stomach and upper small bowel and begins to inhibit platelet function within 30 minutes

Route Onset Peak Duration
PO 2-10 min N/A 3-6 hrs

Uses

C13 - Cardiac reperfusion - Prehospital thrombolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Clopidogrel - Adverse Effects, Contraindications, Prep

A

Adverse effects

Allergic reactions (e.g. asthma, angioneurotic oedema, rhinitis, urticaria, laryngeal oedema and shock). Always check for history of previous reaction
Aggravation of any bleeding tendency
Gastric irritation (unlikely to be significant with current doses)
Bleeding may take longer to stop

Contraindications
Active or suspected or known bleeding tendency
Allergy or hypersensitivity to clopidogrel
Any exclusion via pre thrombolysis checklist
Patients < 18 years of age
Pregnancy or breastfeeding
Preparation

75mg tablet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Clopidogrel - Dose

A

Acute STEMI thrombolysis

Patients ≥ 18 - < 74 years of age

300mg (4 tablets) PO
No repeat
Maximum dose: 1 dose

Patients ≥ 74 years of age

75mg (1 tablet) PO
No repeat
Maximum dose: 1 dose

Warfarin and regular daily use of clopidogrel is not a contraindication to clopidogrel administration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Compound Sodium Lactate - Type, Action, Uses

A

Compound Sodium Lactate

Type: Crystalloid solution containing sodium chloride, calcium and potassium and lactate.

Action

Following intravenous infusion it is distributed throughout the extracellular fluid space, approximately 25% of the volume infused stays in the intravascular space for a variable period of time
Use

C6 - Cardiogenic shock
C9 - Hyperkalaemia
M8 - Dehydration
M21 - Hyperglycaemia
M25 - Medical hypoperfusion/hypovolaemia:
M13 - Meningococcal septicaemia
M16 - Anaphylaxis
M23 - Sepsis
E2 - Diving emergencies
T10 - Traumatic hypovolaemia
T23 - Trauma in pregnancy with any key sign of shock
T12 - Burns
T15 - Trapped patient
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Compound Sodium Lactate - Adverse Effects, Prep, Admin

A

Adverse effects

Pulmonary oedema
Hypothermia
When given in excess can contribute to coagulopathies (hypothermic & dilutional) and exacerbate acidosis
Preparation

500mL bag
Administration

Patients ≥ 16 years of age via pump set

Patients < 16 years of age via autostart burette and pump set

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Hartmanns - Dose - Burns, Traumatic Hypovolaemia

A

Burns

Indication:

> 20% TBSA - Patients ≥ 16 years of age
> 10% TBSA - Patients < 16 years of age
10mL/kg IV bolus 
Repeat 10mL/kg per hour whilst indicated 
Maximum dose: No max

Traumatic hypovolaemia

Patients ≥ 16 years of age

Indication:

Absence of a radial pulse for non head injured patients and Systolic BP < 100mmHg in head injured patients

250mL IV bolus
Repeat 250mL bolus until radial pulse is restored (no head injury) or BP > 100mmHg sys (with head injury)

Patients ≤ 16 years of age

Indication:

Any key sign of shock

10mL/kg IV/IO bolus
Repeat 10mL/kg bolus to maintain BP within age range:

≥ 13 years of age:
100mmHg

6 - < 13 years of age:
90mmHg

1 - < 6 years of age:
80mmHg

< 1 year of age:
70mmHg
Maximum dose: No max

Hypotension in traumatic brain injury is associated with poor outcomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Morphine basic info

A

Morphine

Type: Opioid analgesic

Action

Decreases pain perception and anxiety
Causes peripheral vasodilation
Route	Onset	Peak	Duration
IM	5-10 min	25-40 min	1-2 hrs
IV	2-5 min	10 min	1-2 hrs
Use

A6 - Pain management
Post intubation sedation
Adverse effects

↓ LOC
Respiratory depression
Hypotension
Nausea and vomiting
Contraindications
Altered LOC (V,P or U with the exception of patients requiring post intubation sedation)
Allergy or hypersensitivity to morphine
< 40 weeks corrected age
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Morphine prep and dose

A

Preparation

10mg in 1mL ampoule
10mg in 1mL ampoule diluted to 10mL with 9mL sodium chloride 0.9% (1mg:1mL)
Post intubation sedation: 10mg (1mL) morphine mixed with 10mg (2mL) midazolam and diluted with 7mL sodium chloride 0.9% to make morphine/midazolam solution (1mL = 1mg morphine and 1mg midazolam)
Note: During active labour morphine (IM dose only) may be administered if methoxyflurane is ineffective. Neonatal respiratory depression may occur therefore neonatal resuscitation equipment must be readily available.
Note: This pharmacology contains full doses. Consideration should be given to the administration of half the stated doses to patients with limited physiological reserves.

Pain management

Patients ≥ 16 - < 65 years of age

2.5 - 5mg (2.5 - 5mL) IV diluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 0.5mg/kg
This regime may be repeat 30 min after last administration if indicated

5 - 10mg (0.5 - 1mL) IM undiluted bolus
Repeat once after 15 min whilst indicated
Maximum dose: 2 doses
IM morphine should only be used where IV access or IN fentanyl is not available

Patients ≥ 65 years of age

1.25 - 2.5mg (1.25 - 2.5mL) IV diluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 0.25mg/kg
This regime may be repeated 30 min after last administration if indicated

2.5 - 5mg (0.25 - 0.5mL) IM undiluted bolus
Repeat once after 15 min whilst indicated
Maximum dose: 2 doses
IM morphine should only be used where IV access or IN fentanyl is not available

Patients ≥ 1 - < 16 years of age

100mcg/kg (0.1mL/kg) IV/IO diluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 0.5mg/kg
This regime may be repeated 30 min after last administration if indicated

100mcg/kg (0.01mL/kg) IM undiluted bolus
Repeat once after 15 min whilst indicated
Maximum dose: 2 doses

Patients Birth to < 1 year of age

100mcg/kg (0.1mL/kg) IM diluted bolus
Repeat once after 30 min whilst indicated
Maximum dose: 2 doses

Paramedics should adopt a conservative approach to the administration of analgesia in patients < 1 year of age. Where ever possible the patients actual weight should be ascertained to support medication calculation
Post intubation sedation

Patients ≥ 16 years of age

2.5mL IV morphine/midazolam solution bolus
Repeat every 3 min whilst indicated
Maximum dose: 15mL morphine/midazolam solution
This regime may be repeated 20 min after last administration if indicated

5mL IM morphine/midazolam solution if IV not available
Repeat every 15 min whilst indicated
Maximum dose: 15mL morphine/midazolam solution

Patients ≥ 6 months to < 16 years of age

0.1mL/kg IV/IO morphine/midazolam solution bolus
Repeat every 3 min whilst indicated
Maximum dose: 3 doses
This regime may be repeated 20 min after last administration if needed

0.1mL/kg IM morphine/midazolam solution bolus
Repeat every 15 min whilst indicated
Maximum dose: 3 doses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Clopidogrel

Type

A

Clopidogrel

Type: Platelet receptor antagonist

Actions

Clopidogrel is a specific and potent inhibitor of platelet aggregation and limits propagation of thrombus by selectively inhibiting the binding of ADP to its platelet receptor
Clopidogrel is absorbed from the stomach and upper small bowel and begins to inhibit platelet function within 30 minutes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Clopidogrel - uses, adverse effects

A

Uses

C13 - Cardiac reperfusion - Prehospital thrombolysis
Adverse effects

Allergic reactions (e.g. asthma, angioneurotic oedema, rhinitis, urticaria, laryngeal oedema and shock). Always check for history of previous reaction
Aggravation of any bleeding tendency
Gastric irritation (unlikely to be significant with current doses)
Bleeding may take longer to stop
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Clopidogrel - contraindications, prep

A

Contraindications
Active or suspected or known bleeding tendency
Allergy or hypersensitivity to clopidogrel
Any exclusion via pre thrombolysis checklist
Patients < 18 years of age
Pregnancy or breastfeeding
Preparation

75mg tablet

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

Clopidogrel - dose

A

Acute STEMI thrombolysis

Patients ≥ 18 - < 74 years of age

300mg (4 tablets) PO
No repeat
Maximum dose: 1 dose

Patients ≥ 74 years of age

75mg (1 tablet) PO
No repeat
Maximum dose: 1 dose

Warfarin and regular daily use of clopidogrel is not a contraindication to clopidogrel administration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Sodium compound lactate - type, action

A

Compound Sodium Lactate

Type: Crystalloid solution containing sodium chloride, calcium and potassium and lactate.

Action

Following intravenous infusion it is distributed throughout the extracellular fluid space, approximately 25% of the volume infused stays in the intravascular space for a variable period of time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

Sodium compound lactate - uses

A

Use

C6 - Cardiogenic shock
C9 - Hyperkalaemia
M8 - Dehydration
M21 - Hyperglycaemia
M25 - Medical hypoperfusion/hypovolaemia:
M13 - Meningococcal septicaemia
M16 - Anaphylaxis
M23 - Sepsis
E2 - Diving emergencies
T10 - Traumatic hypovolaemia
T23 - Trauma in pregnancy with any key sign of shock
T12 - Burns
T15 - Trapped patient
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Compound sodium lactate - adverse effects, prep

A

Adverse effects

Pulmonary oedema
Hypothermia
When given in excess can contribute to coagulopathies (hypothermic & dilutional) and exacerbate acidosis
Preparation

500mL bag
Administration

Patients ≥ 16 years of age via pump set

Patients < 16 years of age via autostart burette and pump set

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

Compound sodium lactate - dose

A

Burns

Indication:

> 20% TBSA - Patients ≥ 16 years of age
> 10% TBSA - Patients < 16 years of age
10mL/kg IV bolus 
Repeat 10mL/kg per hour whilst indicated 
Maximum dose: No max

Traumatic hypovolaemia

Patients ≥ 16 years of age

Indication:

Absence of a radial pulse for non head injured patients and Systolic BP < 100mmHg in head injured patients

250mL IV bolus
Repeat 250mL bolus until radial pulse is restored (no head injury) or BP > 100mmHg sys (with head injury)

Patients ≤ 16 years of age

Indication:

Any key sign of shock

10mL/kg IV/IO bolus
Repeat 10mL/kg bolus to maintain BP within age range:

≥ 13 years of age:
100mmHg

6 - < 13 years of age:
90mmHg

1 - < 6 years of age:
80mmHg

< 1 year of age:
70mmHg
Maximum dose: No max

Hypotension in traumatic brain injury is associated with poor outcomes
Trauma in pregnancy

Indication:

Trauma with any key sign of shock

Patients all ages:

250mL IV bolus
Repeat whilst indicated to maintain BP > 90mmHg
Maximum dose: No max

Medical hypoperfusion/hypotension

Patients all ages:

Indications:

≥ 2 key signs of shock
Meningococcal septicaemia
Suspected sepsis patient with hypotension
Moderate to severe anaphylaxis
20mL/kg IV bolus
Repeat whilst indicated
Maximum dose: No max

Cardiogenic shock

Patients ≥ 16 years of age

Indication:

Haemodynamic compromise and systolic BP < 90mmHg

10mL/kg IV bolus
Repeat once 10mL/kg per hour whilst indicated and Pt is unresponsive to adrenaline infusion
Maximum dose: 2 doses

Trapped patients / hyperkalaemia / hypergylcaemia

Patients all ages:

10mL/kg IV bolus
Repeat whilst indicated
Maximum dose: No max

Dehydration

All patients:

10mL/kg IV bolus
No repeat
Maximum dose: 1 dose

Newborn resusciation

Newborn patients:

Indication:

Pt unresponsive to CPR and adrenaline

10mL/kg IV/IO bolus
No repeat
Maximum dose: 1 dose

Use caution when flushing medications in patients < 16 years of age as excessive volume administration may inadvertently occur.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

Droperidol - type, action, onset

A

Droperidol

Type: Neuroleptic

Action

Droperidol produces marked tranquillisation and sedation
May ↓ BP due to direct vasodilatory effect and alpha block
Droperidol potentiates other CNS depressants, e.g. narcotic analgesics such as fentanyl and benzodiazepines such as midazolam
Route Onset Peak Duration
IM 3-10 min Up to 30 min 2-4 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

Droperidol - adverse effects, contraindications

A

Extrapyramidal reactions
Rarely, neuroleptic malignant syndrome (characterised by muscular rigidity, fever, hyperthermia, altered consciousness, and autonomic instability)
Contraindications
Patients with known or suspected hypersensitivity to droperidol
Patients with known or suspected or potential head injury
Patients < 14 years of age
Patients with Parkinson’s disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

Droperidol - use, prep

A

Use:

A7 - Management of acute severe behavioural disturbance - Aetiology non head injured patients

Preparation

10mg (2mL) ampoule (DORM™)

36
Q

Droperidol - dose

A

All Indications

Patients ≥ 14 - < 65 years of age

10mg IM bolus
Repeat once after 15 min if indicated
Maximum dose: 20mg

Patients ≥ 65 years of age and/or with limited physiological reserves

5mg IM bolus
Repeat once after 15 min if indicated
Maximum dose: 10mg

If indications for patient management persist 15 minutes post 2nd bolus of droperidol authorised paramedics may administer midazolam (P1, ALS, ICP) or ketamine (ALS,ICP) per current pharmacology regimens for patient management.

37
Q

Enoxoparin sodium - type, action, uses

A

Enoxaparin Sodium

Type: Low molecular weight antithrombotic

Actions

Induces a sustained release of tissue factor pathway inhibitor
Inhibits thrombin generation
Inhibits coagulation factors Xa and thrombin (anticoagulant)
Reduces reinfarction & ischaemia complications after lysis of STEMI
Uses

C13 - Cardiac reperfusion - Prehospital thrombolysis

38
Q

Enoxoparin sodium - adverse effects, contraindications, prep

A

Adverse effects

Aggravation of any bleeding tendency
Allergic reactions (e.g. asthma, angioneurotic oedema, rhinitis, urticaria, laryngeal oedema and shock)
Bleeding may take longer to stop
Contraindications
Allergy or hypersensitivity to enoxaparin sodium
Any exclusion per pre thrombolysis checklist
Preparation

60mg (0.6mL) pre filled syringe (Orange plunger)
100mg (1mL) pre filled syringe (Black plunger)

39
Q

Enoxoparin sodium - dose

A

ST elevation myocardial infarction

Patients ≥ 18 - < 75 years of age

1st dose: Discard 30mg (0.3mL) and attach sodium chloride primed microbore extension set prior to administering the remaining 30mg (0.3mL) IV as a bolus and flush with 30mL sodium chloride 0.9%. To be administered 15 minutes after the administration of tenecteplase

2nd dose: Weight adjusted 1mg/kg SC (to a maximum dose of 100mg) administered 15 minutes after the 1st dose of enoxaparin sodium

Patients ≥ 75 years of age

1st dose: NO IV DOSE

2nd dose: Weight adjusted 0.75mg/kg SC (to a maximum dose of 100mg) administered 15 minutes after the administration of tenecteplase

Weight adjusted table:
Always complete the pre-thrombolysis checklist prior to administration.

Patient's weight	< 75 SC - 1mg/kg	≥ 75 SC - 0.75mg/kg
kg	stone/lbs	mg	mL	mg	mL
40	6/4	40	0.40	30.0	0.30
45	7/1	45	0.45	33.7	0.35
50	7/12	50	0.50	37.5	0.35
55	8/9	55	0.55	41.2	0.40
60	9/6	60	0.60	45.0	0.45
65	10/3	65	0.65	48.7	0.50
70	11/0	70	0.70	52.5	0.50
75	11/11	75	0.75	56.2	0.55
80	12/8	80	0.80	60.0	0.60
85	13/5	85	0.85	63.0	0.65
90	14/2	90	0.90	67.5	0.65
95	14/13	95	0.95	71.2	0.70
100	15/10	100	1.00	75.0	0.75
105	16/7	100	1.00	78.7	0.80
110	17/4	100	1.00	82.5	0.80
115	18/1	100	1.00	86.2	0.85
120	18/12	100	1.00	90.0	0.90
125	19/9	100	1.00	93.7	0.95
130	20/6	100	1.00	97.5	1.00
135	21/3	100	1.00	100.0	1.0
40
Q

Fentanyl - type, action, use

A

Fentanyl

Type: Opioid analgesic

Action

Potent analgesic
Effective drug for intranasal use because it is rapidly absorbed across mucous membranes
Route	Onset	Peak	Duration
IN	2-3 min	N/A	30-60 min
Use

A6 - Pain management
First line moderate to severe pain management in patients < 16 years of age
Patients ≥ 16 years of age where morphine is ineffective or contraindicated
Note: During active labour fentanyl may be administered if methoxyflurane is ineffective. Neonatal respiratory depression may occur therefore neonatal resuscitation equipment must be readily available

41
Q

Fentanyl - adverse effects, contraindications, prep

A

Adverse effects

Respiratory depression
Hypotension
Nausea and vomiting
Contraindications
Altered LOC (V,P or U)
Epistaxis or occluded nasal passages
Patients < 1 year of age
Previous known allergy or adverse reaction
Preparation

600mcg in 2mL in a sealed vial
Route of administration

Intranasal (IN) via mucosal atomising device(MAD)

42
Q

Fexofenadine - type, action, prep, use

A

Fexofenadine

Type: Anti-histamine

Actions

Non-sedating anti-histamine
Route Onset Peak Duration
PO 15-30 min N/A 12-16 hrs
Use

M16 - Allergic reactions (localised, mild)

43
Q

Fexofenadine - adverse effects, contraindications, prep, dose

A

Adverse effects

Headache
Drowsiness
Nausea
Dry mouth
Contraindications
Allergy or hypersensitivity to fexofenadine
Patients < 12 years of age
Preparation

180mg tablet

Patients ≥ 12 years of age

180mg (1 tablet) PO
No Repeat
Maximum dose: 1 dose in 24 hours

44
Q

Glucagon - type, action, prep, use

A

Glucagon

Type: Pancreatic hormone

Action

Converts liver glycogen to glucose. Glucagon may not work if liver glycogen is depleted due to starvation or chronic liver disease
Route Onset Peak Duration
SC/ IM 4-7 min 8-10 min 11-30 min
Use

M21 - Hypoglycaemia

45
Q

Glucagon - adverse effects, contraindications, prep, dose

A

Adverse effects

Nausea and vomiting
Allergic reactions rarely occur
Preparation

1mg vial & syringe containing 1mL of sterile water

Dissolve the glucagon powder by adding the entire contents of the syringe to the vial containing the glucagon. The solution must be prepared immediately prior to use

Hypoglycaemia

Patients ≥ 16 years of age

1mg (1mL) of reconstituted solution SC/IM
No repeat
Maximum dose: 1 dose

Patients < 16 years of age

500mcg (0.5mL) of reconstituted solution SC/IM
No repeat
Maximum dose: 1 dose

46
Q

Glucose 10% - type, action, onset, use

A

Glucose 10%

Type: Hypertonic sugar solution for intravenous use

Actions

Principal energy source for body cells, especially the brain
Route Onset Peak
IV 30 sec 30 sec
Duration: Dependent on severity of hypoglycaemic episode
Use

M21 - Hypoglycaemia

47
Q

Glucose 10% - adverse effects, contraindications, prep, dose

A

Adverse effects

Tissue necrosis if extravasation from vein occurs
May aggravate brain damage in head injuries and strokes
May precipitate Wernicke’s encephalopathy in alcoholics with thiamine deficiency
Preparation

10% - 50g per 500mL bag
Hypoglycaemia

Patients ≥ 10 years of age

15g (150mL) IV bolus
Repeat whilst indicated
Maximum dose: No max

Patients < 10 years of age

0.5g/kg (5mL/kg) IV bolus
Repeat whilst indicated
Maximum bolus dose 15g (150mL)
Maximum dose: No max

Newborn

Indication: BGL < 3mmol/L
0.25g/kg (2.5mL/kg) IV/IO bolus
Repeat whilst indicated
Maximum dose: No max

IV line must be flushed with 10mL sodium chloride 0.9% at the completion of administration or prior to the administration of other medications

48
Q

Glucose gel - type, use, onset, action

A

Glucose Gel

Type: Hypertonic sugar solution for oral use

Action

Principal energy source for body cells, especially the brain
Route Onset Peak Duration
PO Within 15 min N/A N/A
Use

M21 - Hypoglycaemia

49
Q

Glucose gel - adverse effects, contraindications, onset, use

A

Adverse effects

May precipitate Wernicke's encephalopathy in alcoholics with thiamine deficiency
Contraindications
↓ LOC or altered gag reflex
Patients < 1 year of age
Preparation

37.5g tube containing glucose gel 40% (15g glucose)

Hypoglycaemia

Patients ≥ 1 years of age

15g (1 tube) PO
Repeat once after 15 minutes whilst indicated
Maximum dose: 2 doses

50
Q

GTN - type, action, onset, use

A

Glyceryl Trinitrate

Type: Vasodilator

Action

Dilates coronary arteries
Dilates systemic veins and arteries
Decreases preload, afterload and blood pressure
Route	Onset	Peak	Duration
SL	Within 2 min	N/A	Up to 30 min
Use

C1 - Acute coronary syndrome
C5 - Cardiogenic pulmonary oedema
M15 - Autonomic dysreflexia

51
Q

GTN - adverse effects, contraindications, prep

A

Adverse effects

Hypotension
Flushing
Headache
Contraindications
BP < 90mmHg systolic
Pulse rate < 50/min or > 150/min
Patients < 16 years of age
Use of drugs to treat erectile dysfunction e.g.
Sildenafil - Viagra® or Vardenafil - Levitra® - Within 24 hours
Tadalafil - Cialis® - within 96 hours
Preparation

600mcg tablet

Discard 3 months after opening the bottle as exposure reduces potency.
Bottles must have the date opened written on the label.
Unused ½ tablets of GTN must be discarded.

52
Q

GTN - dose

A

Patients ≥ 16 years of age

600mcg (1 tablet) SL
Repeat every 5 minutes whilst indicated (Monitor CP closely)
Maximum dose: 3 doses
This regime may be repeated 30 minutes after the last administration

Cardiogenic pulmonary oedema

Patients ≥ 16 years of age

600mcg (1 tablet) SL
Repeat every 5 minutes whilst indicated (Monitor CP closely)
Maximum dose: 3 doses
This regime may be repeated 30 minutes after the last administration

Autonomic dysreflexia

Patients ≥ 16 years of age

300mcg (½ tablet) SL
Repeat every 5 minutes whilst indicated (Monitor CP closely)
Maximum dose: 3 doses
Note: Patients with limited physiological reserves should receive an initial dose of 300mcg (½ tablet) with subsequent doses of either 300mcg or 600mcg depending on response to a max of 1.8mg (3 tablets)

53
Q

Hydrocortisone - type, action, onset, use

A

Hydrocortisone

Type: Corticosteroid

Action

Glucocorticoid drug that reduces inflammation and suppresses immune response
Route Onset Peak Duration
IV 1-2 hrs N/A 6-12 hrs
Use

M4 - Asthma
M24 - Adrenal crisis

54
Q

Hydrocortisone - adverse effects, contraindications, prep

A
Contraindications
Known or suspected allergy to corticosteroids, sodium succinate or sodium phosphate
Uncontrolled infection
Active peptic ulcer disease
Preparation

100mg vial
Reconstitute with 2mL normal saline 0.9% (50mg:1mL)

55
Q

Hydrocortisone - dose

A

Patients ≥ 16 years of age

100mg (2mL) IM/IV
No repeat
Maximum dose: 1 dose

Patients < 16 years of age

4mg/kg (0.08mL/kg) IM/IV
No repeat
Maximum bolus dose: 100mg
Maximum dose: 1 dose

NOTE: Patients < 6 years of age should not be administered hydrocortisone for moderate asthma. The indication for administration for patients < 6 years of age is Severe/Life Threatening Asthma and Symptomatic Adrenal Crisis ONLY.

56
Q

Ibuprofen - type, action, onset, use

A

Ibuprofen

Type: Non-steroidal anti-inflammatory

Actions

Provides anti-inflammatory and analgesic effects
Route Onset Peak Duration
PO 15-30 min N/A 3-4 hrs
Use

A6 - Pain management (Mild pain)

57
Q

Ibuprofen - adverse effects, contraindications, prep, dose

A

Adverse effects

G.I irritation
Hypersensitivity reactions may occur (e.g. anaphylaxis, asthma, angio-oedema, urticaria)
Contraindications
Active or suspected or known bleeding tendency
History of allergic reactions to NSAIDs
Patients with asthma who have a history of wheeze post NSAID administration or have not previously taken a NSAID
Active peptic ulcer disease or GI bleeding
Dehydration
Renal impairment
Pregnancy
Patients < 7 years of age
Preparation

200mg tablet
All uses

Patients ≥ 12 years of age

400mg (2 tablets) PO
Repeat after 4 hours whilst indicated
Maximum dose: 400mg (2 tablets) per dose, 1.2g (6 tablets) in 24 hours

Patients 7 - <12 years of age

200mg PO
Repeat after 4-6 hours whilst indicated
Maximum dose: 200mg per dose, 800mg in 24 hours

Reduced doses should be used in patients with advanced age, smaller than average size or general debility
Additional doses of ibuprofen are NOT to be left with patients as all medications left with patients MUST be labelled according to Ambulance Medication Management Policy

58
Q

Ipratropium bromide - type, action, use, onset

A

Ipratropium Bromide

Type: Anticholinergic bronchodilator

Action

Bronchodilation
Blocks vagal reflexes which mediate bronchoconstriction
Synergistic when used in combination with salbutamol
Route Onset Peak Duration
NEB 3-5 min N/A 2-4 hrs
Use

To relieve bronchospasm:
M4 - Asthma
M19 - Chronic obstructive pulmonary disease

59
Q

Ipratropium bromide - adverse effects, contraindications, prep, dose

A

Adverse effects

Mild anticholinergic effects, e.g. urine retention
Contraindications
Allergy or hypersensitivity to ipratropium bromide
Glaucoma
Preparation

500mcg in 1mL
250mcg in 1mL
All uses

Patients ≥ 6 years of age

500mcg (1mL) via nebuliser with 8L/min oxygen mixed with salbutamol
Repeat once whilst indicated
Maximum dose: 2 doses

Patients < 6 years of age

250mcg (1mL) via nebuliser with 8L/min oxygen mixed with salbutamol
Repeat once whilst indicated
Maximum dose: 2 doses

60
Q

Ketamine - type, action, use, onset

A

Ketamine

Type: Dissociative anaesthetic agent with analgesic effects

Action

Dissociates the central nervous system from painful stimuli. At low doses ketamine causes a trance like state characterised by analgesia and amnesia with retention of protective airway reflexes, spontaneous respirations and cardiovascular activity.
Route	Onset	Peak	Duration
IV	30 - 90 sec	< 5 min	10 - 15 min
IM	3 - 5 min	10 - 15 min	15 - 30 min
Use

A6 - Pain management
A7 - Management of acute severe behavioural disturbance

61
Q

Ketamine - adverse effects, contraindications, prep

A

Adverse effects

Distressing psychological reactions (e.g. agitation, hallucinations and/or dysphoria)
Nausea and vomiting
Muscle effects including increased tone, random purposeless movements
Contraindications
Suspected or known allergy to ketamine
Patients with known or suspected history of psychosis
Patients <14 years of age
Known 1st or 2nd trimester pregnancy
Preparation

200mg in 2mL vial
200mg (2mL) diluted to 20mL (10mg:1mL) with 18mL sodium chloride 0.9%

62
Q

Lignocaine - type, action, use, onset

A

Lignocaine

Type: Antiarrhythmic and local anaesthetic agent

Action

Blocks sodium channels reducing ventricular excitability and pain transmission
Route Onset Peak Duration
IV 1-4 min 5-10 min 20 min
Use

C3 - Cardiac arrest (VF or pulseless VT unresponsive to Amiodarone)
Local anaesthesia of the skin prior to cannulation (1% preparation only)

63
Q

Lignocaine - adverse, contraindications, prep dose

A

Adverse effects

Lignocaine may cause or exacerbate ventricular dysrhythmias
In high doses, may cause:
Neurological side effects (drowsiness, disorientation, agitation, muscle twitching, fits and coma)
Cardiac effects (hypotension, bradycardia, heart block/s and asystole)
Contraindications
Allergy or hypersensitivity to lignocaine
Preparation
For local anaesthesia prior to cannulation inject a small amount of lignocaine 1% subcutaneously until the skin is raised slightly
Lignocaine 2% - 100mg in 5mL polyampoule for IV bolus doses
Lignocaine 1% - 20mg in 2mL ampoule for local anaesthesia
As two concentrations are available: Read the label carefully and check with your partner.

64
Q

Methoxy - action, type, use, onset

A

Methoxyflurane

Type: Inhaled analgesic

Action

Central nervous system depressant
Route Onset Peak Duration
INH 2-3 min N/A Up to 30 min
Use

A6 - Pain management
Mild pain in children ≥ 1 years and < 12 years of age
Patients ≥ 1 years of age where a paramedic is not authorised to administer an opioid or an opioid is contraindicated, ineffective or refused
Multiple victim situations and/or initial pain management in environments which may present with safety concerns to facilitate prompt patient movement
Active labour

65
Q

Methoxy - adverse, contraindications, prep, dose

A

Adverse effects

↓ LOC
Renal damage in high doses
Contraindications
Malignant hyperthermia
Untreated renal failure
↓ LOC - V, P or U
Pre-eclampsia or eclampsia
Patients < 1 year of age
Acute behaviourally disturbed patients
Concurrent tetracycline use (e.g. doxycycline)
Preparation

3mL amber bottle sealed, with external inhaler
All uses

Patients ≥ 1 years of age

3mL inhaled via inhaler
Repeat once whilst indicated
Maximum dose: 6mL daily and 15mL weekly

Do not put any more than 3mL in inhaler at any time as this increases the risk of droplet inhalation
Do not use oxygen in conjunction with the inhaler
Methoxyflurane can only be administered twice in any one shift per paramedic and only 3mL of methoxyflurane in the back of the ambulance at any one time

66
Q

Maxolon - type, action, use, onset

A

Type: Anti-nauseant and anti-emetic

Action

Blocks central dopamine receptors
Route	Onset	Peak	Duration
IM	10-15 min	N/A	1-2 hrs
IV	3-5 min	N/A	1-2 hrs
Use

M6 - Nausea and Vomiting (Pts ≥ 16 years of age where odansetron is contraindicated or ineffective after 10 minutes)

67
Q

Maxolon - adverse, contra, prep, dose

A

Adverse effects

Restlessness, drowsiness and fatigue
Extrapyramidal / acute dystonic reactions including spasm of the facial muscles, trismus, rhythmic protrusion of the tongue, abnormal speech, spasm of the extra ocular muscles and unnatural positioning
Contraindications
Suspected bowel obstruction
Suspected or known haematemesis or melaena
Previous history of extrapyramidal / dystonic reaction
Allergy or hypersensitivity to metoclopramide
Patients < 16 years of age
Patients with Parkinson’s Disease
Preparation

10mg (2mL) ampoule
Severe nausea or vomiting

Patients ≥ 16 years of age

10mg (2mL) IM/IV Bolus
No repeat
Maximum dose: 1 dose

Metoclopramide is only to be administered if ondansetron is contraindicated or ineffective after 10 min

68
Q

Midaz - type, action, use, onset

A

Type: Benzodiazepine

Action

An anticonvulsant with anxiolytic and amnesic effects
Route	Onset	Peak	Duration
IM	5-10 min	15 min	30 min
IV	1-3 min	10 min	20 min
IN	1-3 min	12 min	20 min
Use

M9 - Seizures
T16 - Limb realignment and difficult extrication
A7 - Management of acute severe behavioural disturbance
Head injured patients unable to be administered ketamine (ALS & ICP Only)
Non head injured patients unable to be administered droperidol (P1, ALS & ICP)
Head injured patients < 14 years of age (ALS & ICP Only)
Non head injured patients < 14 years of age (P1, ALS & ICP)
Post intubation sedation
Post ketamine administration

69
Q

Midaz - adverse, contra, prep

A

Adverse effects

↓ LOC resulting in upper airway obstruction
Respiratory and cardiovascular depression which may be exacerbated in patients with limited physiological reserves and/or under the influence of alcohol or drugs
Preparation

5mg in 1mL ampoule
5mg in 1mL ampoule diluted to 5mL with 4mL sodium chloride 0.9% (1mg:1mL)
Post intubation sedation: 10mg (1mL) morphine mixed with 10mg (2mL) midazolam diluted with 7mL sodium chloride 0.9% to make morphine/midazolam solution (1mL = 1mg morphine and 1mg midazolam)

70
Q

Midaz - dose

A

Seizures

Patients ≥ 16 years of age

5mg IM undiluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 15mg

2.5mg IV diluted slow injection
Repeat every 3 min whilst indicated
Maximum dose: 15mg

Patients < 16 years of age

0.3mg/kg IN undiluted bolus via mucosal atomising device
No repeat
Maximum bolus dose: 5mg
Maximum dose: 0.3mg/kg

0.15mg/kg IM undiluted bolus if a vein is not available
Repeat every 5 min whilst indicated
Maximum bolus dose: 5mg
Maximum dose: 0.45mg/kg

0.15mg/kg IV diluted bolus
Repeat every 3 min whilst indicated
Maximum bolus dose: 2.5mg
Maximum dose: 0.45mg/kg

Management of acute severe behavioural disturbance

Patients ≥ 14 - < 65 years of age

5 - 10mg IM undiluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 15mg

2.5mg IV diluted slow injection
Repeat every 3 min whilst indicated
Maximum dose: 15mg

Patients ≥ 65 years of age

2.5 - 5mg IM undiluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 7.5mg

1.25mg IV diluted slow bolus
Repeat every 3 min whilst indicated
Maximum dose: 7.5mg

Patients < 14 years of age

0.15mg/kg IM undiluted bolus if a vein is not available
Repeat every 5 min whilst indicated
Maximum bolus dose: 5mg
Maximum dose: 0.45mg/kg (up to 15mg total maximum dose)

0.15mg/kg IV diluted bolus
Repeat every 3 min whilst indicated
Maximum bolus dose: 2.5mg
Maximum dose: 0.45mg/kg (up to 7.5mg total maximum dose)

71
Q

Morphine - type, action, use, onset

A

Morphine

Type: Opioid analgesic

Action

Decreases pain perception and anxiety
Causes peripheral vasodilation
Route	Onset	Peak	Duration
IM	5-10 min	25-40 min	1-2 hrs
IV	2-5 min	10 min	1-2 hrs
Use

A6 - Pain management
Post intubation sedation

72
Q

Morphine - adverse, contra, prep

A

Adverse effects

↓ LOC
Respiratory depression
Hypotension
Nausea and vomiting
Contraindications
Altered LOC (V,P or U with the exception of patients requiring post intubation sedation)
Allergy or hypersensitivity to morphine
< 40 weeks corrected age
Preparation

10mg in 1mL ampoule
10mg in 1mL ampoule diluted to 10mL with 9mL sodium chloride 0.9% (1mg:1mL)
Post intubation sedation: 10mg (1mL) morphine mixed with 10mg (2mL) midazolam and diluted with 7mL sodium chloride 0.9% to make morphine/midazolam solution (1mL = 1mg morphine and 1mg midazolam)
Note: During active labour morphine (IM dose only) may be administered if methoxyflurane is ineffective. Neonatal respiratory depression may occur therefore neonatal resuscitation equipment must be readily available.
Note: This pharmacology contains full doses. Consideration should be given to the administration of half the stated doses to patients with limited physiological reserves.

73
Q

Morphine - dose

A

Patients ≥ 16 - < 65 years of age

2.5 - 5mg (2.5 - 5mL) IV diluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 0.5mg/kg
This regime may be repeat 30 min after last administration if indicated

5 - 10mg (0.5 - 1mL) IM undiluted bolus
Repeat once after 15 min whilst indicated
Maximum dose: 2 doses
IM morphine should only be used where IV access or IN fentanyl is not available

Patients ≥ 65 years of age

1.25 - 2.5mg (1.25 - 2.5mL) IV diluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 0.25mg/kg
This regime may be repeated 30 min after last administration if indicated

2.5 - 5mg (0.25 - 0.5mL) IM undiluted bolus
Repeat once after 15 min whilst indicated
Maximum dose: 2 doses
IM morphine should only be used where IV access or IN fentanyl is not available

Patients ≥ 1 - < 16 years of age

100mcg/kg (0.1mL/kg) IV/IO diluted bolus
Repeat every 5 min whilst indicated
Maximum dose: 0.5mg/kg
This regime may be repeated 30 min after last administration if indicated

100mcg/kg (0.01mL/kg) IM undiluted bolus
Repeat once after 15 min whilst indicated
Maximum dose: 2 doses

Patients Birth to < 1 year of age

100mcg/kg (0.1mL/kg) IM diluted bolus
Repeat once after 30 min whilst indicated
Maximum dose: 2 doses

Paramedics should adopt a conservative approach to the administration of analgesia in patients < 1 year of age. Where ever possible the patients actual weight should be ascertained to support medication calculation

74
Q

Naloxone - type, action, use, onset

A

Type: Opioid antagonist

Action

Reverses symptoms caused by opioid analgesics:

Respiratory depression
Sedation
Hypotension
Route	Onset	Peak	Duration
IM	2-5 min	10-15 min	20 min approx.
IV	1-3 min	10-15 min	15 min approx.
Use

D1 - Drug overdose and poisoning

75
Q

Naloxone - adverse, contra, prep

A

Adverse effects

Opioid withdrawal (nausea, vomiting, sweating, tachycardia, hypertension & combative behaviour)
Pulmonary oedema in patients with pre existing cardiac disease
Dysrhythmias (VF, VT)
Nausea and vomiting
Contraindications
Neonates born to opioid addicted mothers due to risk of inducing opioid withdrawal
Preparation

400mcg in 1mL ampoule
400mcg in 1mL ampoule diluted to 4mL with 3mL sodium chloride 0.9% (100mcg in 1mL)

76
Q

Naloxone - dose

A

Life threatening opioid overdose

Patients ≥ 16 years of age

800mcg IV/IM undiluted bolus
Repeat 400mcg every 2 min whilst indicated
Maximum dose: 2mg

Patients < 16 years of age

10mcg/kg IV/IM diluted bolus
Repeat every 2 minutes whilst indicated
Maximum bolus dose 400mcg
Maximum dose: 2mg

Opioid overdose

Patients ≥ 16 years of age

100mcg IV diluted bolus
Repeat every 2 minutes whilst indicated
Maximum dose: 2mg

100mcg IM diluted bolus
Repeat every 5 minutes whilst indicated
Maximum dose: 2mg

Patients < 16 years of age

5mcg/kg IV/IM diluted bolus
Repeat every 5 minutes whilst indicated
Maximum bolus dose 100mcg
Maximum dose: 2mg

Etorphine or buprenorphine overdose

Patients ≥ 16 years of age

2mg IV/IM undiluted bolus
Repeat every 5 minutes whilst indicated
Maximum dose: No max (IV route preferred)

Patients < 16 years of age

10mcg/kg IV/IM diluted bolus
Repeat every 5 minutes whilst indicated
Maximum dose: No max (IV route preferred)

Additional information:

Opioid effects may exceed that of naloxone and renarcotisation is possible. Therefore repeat doses may be required

Naloxone is contraindicated in neonatal patients of opioid addicted mothers as serious withdrawal effects may occur. Hypoventilating newborns, due to maternal opiate use, will be hypercapnoeic and naloxone may provoke dysrhythmias, seizures and pulmonary oedema

Common opioid based medications

Generic name Brand name - examples
Buprenorphine Subutex®, Temgesic®, Norspan®
Codeine
Dextropropoxyphene / paracetamol Di-Gesic®, Capadex®, Paradex®
Diphenoxylate / atropine Lomotil®
Etorphine (veterinary drug) Immobilon®
Fentanyl
Heroin
Loperamide Imodium®
Methadone Bidone fort solution®, Physeptone tablets®
Morphine Kapanol®, MS Contin®, MS Mono®, Anamorph®
Oxycodone Endone®, OxyContin®, OxyNorm®
Pentazocine Fortral®
Pethidine
Various diarrhoea and cough medicines

77
Q

Ondansatron - type, action, use, onset

A

Ondansetron

Type: Anti-emetic and anti-nauseant

Actions

Blocks central and peripheral 5-HT3 receptors

Route Onset Peak Duration
IM 10-15 min N/A 1-2 hrs
IV 3-5 min N/A 1-2 hrs
Use

M6 - Nausea and vomiting
T13 - Suspected penetrating eye injury

78
Q

Ondansatron - adverse, contra, prep, dose

A

Adverse effects

Headache and/or flushing
Seizures and movement disorders
Visual disturbance
Hypersensitivity reactions (including anaphylaxis)
Contraindications
Concurrent apomorphine administration
Allergy or hypersensitivity to ondansetron
Patients < 2 years of age
Preparation

4mg in 2mL ampoule
Severe nausea and/or active vomiting & suspected penetrating eye injury

Patients ≥ 8 years of age

4mg (2mL) IM/IV bolus

No repeat Maximum dose: 1 dose

Patients ≥ 2 years of age to < 8 years of age

2mg (1mL) IM/IV bolus
No repeat
Maximum dose: 1 dose

Slow IV administration is preferred.
IM use only when IV not available

79
Q

Paracetamol - type, action, use, onset

A

Paracetamol

Type: Analgesic & antipyretic

Action

Temporary relief of pain and discomfort in arthritis, headache, muscular and neuralgic conditions; also reduces fever
Route Onset Peak Duration
PO 1-60 min N/A Up to 4 hrs
Use

A6 - Pain management (Mild pain)
Antipyretic in patients with a temperature ≥ 38.5°C

80
Q

Paracetamol - adverse, contra, prep, dose

A

Adverse effects

Nausea
Liver failure in overdose situations
Contraindications
Allergy or hypersensitivity to paracetamol
Multiple previous doses i.e. previous self-administration within 4/24 or 4g (8 tablets) within 24 hours
Patients < 7 years of age
Preparation

500mg tablet
500mg capseals™ (Pack of 4 for alternative referral options)
All uses

Patients ≥ 12 years of age

500 - 1000mg (1 - 2 tablets) PO
Repeat after 4 hours whilst indicated
Maximum dose: 1g (2 tablets) per dose, 4g (8 tablets) in 24 hours

Patients ≥ 7 - < 12 years of age

250 - 500mg (1/2 - 1 tablet) PO
Repeat after 4 hours whilst indicated
Maximum dose: 500mg (1 tablet) per dose, 2g (4 tablets) in 24 hours

Patients recommended with alternative treatment options may be administered 2 capseals™ of paracetamol from a new pack of 4. The remaining two in the original packaging may be left with the patient to enable a repeat dose after 4 hours. A maximum of 2 capseals™ only may be left with the patient.

81
Q

Salbutamol - type, action, use, onset

A

Salbutamol

Type: Sympathomimetic

Action

Stimulates beta 2 receptors in bronchial smooth muscle resulting in bronchodilation
Route Onset Peak Duration
NEB 2-5 min 5-10 min 1-2 hrs
Use

To relieve bronchospasm

M4 - Asthma
M19 - Chronic obstructive pulmonary disease

82
Q

Salbutamol - adverse, contra, prep, dose

A

Adverse effects

Dysrhythmias in large doses
Shakes and tremors
Preparation

5mg in 2.5mL nebule
2.5mg in 2.5mL nebule
Relieve bronchospasm

Patients ≥ 5 years of age

5mg (2.5mL) via nebuliser at 8L/min oxygen
Repeat whilst indicated
Maximum dose: No max

Patients < 5 years of age

2.5mg (2.5mL) via nebuliser at 8L/min oxygen
Repeat whilst indicated
Maximum dose: No max

If condition is severe/life threatening do not wait on scene for salbutamol to be effective.

Because two concentrations are available read the label carefully and check with your partner.

Special Operations Team (SOT) use only
Use

For use in circumstances where oxygen and nebulised salbutamol is not available
Note single use only - inhaler must be discarded after use

Preparation

Ventolin CFC-Free inhaler; pressurised MDI - 100mcg/actuation to be used in conjunction with a spacer

Dose

Each dose is to be administered as one puff into the spacer and four breaths via spacer

Patients ≥ 5 years of age

Mild to Moderate severity
4-12 puffs as required
Repeat whilst indications persist
Maximum dose: No max

Severe/life threatening severity
12 puffs as required
Repeat whilst indications persist
Maximum dose: No max

Patients < 5 years of age

Mild to Moderate severity
2-6 puffs as required
Repeat whilst indications persist
Maximum dose: No max

Severe/life threatening severity
6 puffs as required
Repeat whilst indications persist
Maximum dose: No max

83
Q

Tenectaplase - type, action, use

A

Tenecteplase

Type: Recombinant tissue plasminogen activating agent

Actions

Dissolves coronary artery thrombi facilitating myocardial reperfusion
Activates the fibrinolytic system to degrade the fibrin matrix of a thrombus
Use

C13 - Cardiac reperfusion - Prehospital thrombolysis

84
Q

Tentectaplase - adverse, contra, prep

A

Adverse effects

Intracranial haemorrhage
Reperfusion arrhythmias (usually self-limiting)
Aggravation of any bleeding tendency
Contraindications
Any exclusion per pre thrombolysis checklist
Patients <18 years of age
Preparation

50mg vial & syringe containing 10mL of sterile water
Dissolve the Tenecteplase powder completely by adding the entire contents of the syringe containing 10mL of sterile water to the vial. The solution must be prepared immediately before use. Avoid foaming the solution

85
Q

Tenectaplase - dose

A

ST elevation myocardial infarction

Patients ≥ 18 years of age

Weight adjusted dose (refer to table) IV bolus to a maximum 50mg (patients ≥ 18-74) and 25mg (patients ≥ 75) administered 15 minutes prior to the first dose of enoxaparin sodium (232)
No repeat
Maximum dose: 1 dose

Flush IV cannula with 10mL of sodium chloride 0.9% prior to administering Tenecteplase
Flush IV cannula with 30mL of sodium chloride 0.9% between administration of Tenecteplase and enoxaparin sodium
Do not administer through a line that may have contained glucose
Always complete the pre thrombolysis checklist prior to administration

Patient’s Stated Weight Tenecteplase (mg) / Vol of solution (mL)
KG Stone/Lbs ≥ 18 - < 75 ≥ 75
<60 < 9st 6lb 30mg / 6mL 15mg / 3mL
60-69 9st 6lb - 10st 13lb 35mg / 7mL 17.5mg / 3.5mL
70-79 11st - 12st 7lb 40mg / 8mL 20mg / 4mL
80-89 12st 8lb - 14st 2lb 45mg / 9mL 22.5mg / 4.5mL
>90 14st 3lb or more 50mg / 10mL 25mg / 5mL