Amiodarone Flashcards

1
Q

Drug Class of Amiodarone

A

Anti-arrhythmic

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2
Q

Presentation of Amiodarone

A

Ampoule, 150 mg/3 mL amiodarone

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3
Q

Schedule of Amiodarone

A

S4 (Restricted drugs).

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4
Q

Pharmacology of Amiodarone

A

Amiodarone prolongs the duration of the action potential and therefore the refractory period of atrial, nodal and ventricular tissues. It also reduces conduction across all cardiac tissue – including myocardial and conducting system cells. Amiodarone demonstrates electrophysiological properties across all Vaughan-Williams Class groups, which enables a broad spectrum of activity.

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5
Q

Metabolism of Amiodarone

A

The majority of amiodarone is excreted via the liver and GI tract 
 by biliary excretion; there may be some hepatic recirculation.

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6
Q

Indications of Amiodarone

A
  • Cardiac arrest (refractory VF OR pulseless VT)

* Sustained conscious VT (haemodynamically stable)

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7
Q

Contraindications of Amiodarone

A

• Cardiac arrest ( refractory VF or pulseless VT ): - Nil
• Sustained conscious VT (haemodynamically stable):
- KSAR or hypersensitivity to amiodarone
- severe conduction disorders (unless pacemaker 
 or AICD in situ)
- current amiodarone therapy
- concurrent anti-arrhythmic therapy that 

prolongs the QT interval
- pregnancy and/or lactation

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8
Q

Precautions of Amiodarone

A

• Cardiac arrest (refractory VF or pulseless VT):
- concurrent anti-arrhythmic therapy that prolongs the QT interval
- thyroid disease
• Sustained conscious VT (haemodynamically stable):
- hypotension
- thyroid disease

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9
Q

Side Effects of Amiodarone

A
  • Hypotension
  • Bradycardia
  • Nausea and/or vomiting
  • Peripheral paraesthesia
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10
Q

Routes of Administration Amiodarone

A

Intravenous injection (IV)
Intraosseous injection (IO)
Intravenous infusion (IV INF)

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11
Q

Onset time of Amiodarone IV

A

5 minutes

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12
Q

Duration time of Amiodarone IV

A

30 minutes

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13
Q

Half life of Amiodarone

A

14–110 days
 (with chronic dosing)

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14
Q

Special Notes of Amiodarone

A
  • If the patient is on oral amiodarone, the following cardiac arrest administration protocols continue to be authorised.
  • If lignocaine 2% has been administered to a patient with conscious VT that progresses into cardiac arrest, the following administration protocols continue to be authorised.
  • If the patient is in Torsade de Pointes due to suspected prolonged QT interval from excess amiodarone administration, magnesium sulphate administration is to be considered.
  • After completion of a risk/benefit analysis, the QAS authorises the administration of sodium chloride 0.9% (flush or running 
 IV line) following amiodarone administration in cardiac arrest, despite manufacturer’s recommendations.
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15
Q
Adult Dose of Amiodarone IV
Cardiac arrest (refractory VF or pulseless VT )
A

300 mg
Slow push over 2 minutes.

Repeated once at 150 mg after 5 minutes.
Total maximum dose – 450 mg.

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16
Q
Adult Dose of Amiodarone IO
Cardiac arrest (refractory VF or pulseless VT )
A

300 mg
Slow push over 2 minutes.

Repeated once at 150 mg after 5 minutes.
Total maximum dose – 450 mg.

17
Q

Adult Dose of Amiodarone IV INF

Sustained conscious VT (haemodynamically stable)

A

300 mg
infusion over 30 minutes.
Administer via SPRINGFUSOR® 30 mL.
Single dose only.
Syringe preparation: Mix 300 mg Amiodarone 
 6 mL) with 24 mL of glucose 5% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 300 mg /30 mL. 

Ensure syringes are appropriately labelled. Administer via SPRINGFUSOR® 30 mL at a rate 
 of 60 mL/hour (over 30 minutes).

18
Q
Paediatric Dose of Amiodarone IV
Cardiac arrest (refractory VF or pulseless VT )
A

5 mg/kg
Slow push over 2 minutes.
Single dose only.
Syringe preparation: Mix 150 mg (3 mL) 
 of amiodarone with 12 mL of glucose 5% 

(totalling 15 mL) in a 20 mL syringe to achieve 
 a final concentration of 10 mg/mL.

19
Q
Paediatric Dose of Amiodarone IO
Cardiac arrest (refractory VF or pulseless VT )
A

5 mg/kg
Slow push over 2 minutes.
Single dose only.
Syringe preparation: Mix 150 mg (3 mL) 
 of amiodarone with 12 mL of glucose 5% 

(totalling 15 mL) in a 20 mL syringe to achieve 
 a final concentration of 10 mg/mL.