Drug Therapy Protocols: Magnesium sulphate · PDF file• Magnesium sulphate for the...

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Drug Therapy Protocols: Magnesium sulphate Disclaimer and copyright ©2018 Queensland Government All rights reserved. Without limiting the reservation of copyright, no person shall reproduce, store in a retrieval system or transmit in any form, or by any means, part or the whole of the Queensland Ambulance Service (‘QAS’) Clinical practice manual (‘CPM’) without the prior written permission of the Commissioner. The QAS accepts no responsibility for any modification, redistribution or use of the CPM or any part thereof. The CPM is expressly intended for use by QAS paramedics when performing duties and delivering ambulance services for, and on behalf of, the QAS. Under no circumstances will the QAS, its employees or agents, be liable for any loss, injury, claim, liability or damages of any kind resulting from the unauthorised use of, or reliance upon the CPM or its contents. While effort has been made to contact all copyright owners this has not always been possible. The QAS would welcome notification from any copyright holder who has been omitted or incorrectly acknowledged. All feedback and suggestions are welcome, please forward to: [email protected] This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/. Date May, 2018 Purpose To ensure a consistent procedural approach to Magnesium sulphate administration. Scope Applies to all QAS clinical staff. Author Clinical Quality & Patient Safety Unit, QAS Review date May, 2021 Information security This document has been security classified using the Queensland Government Information Security Classification Framework (QGISCF) as UNCLASSIFIED and will be managed according to the requirements of the QGISF. URL https://ambulance.qld.gov.au/clinical.html

Transcript of Drug Therapy Protocols: Magnesium sulphate · PDF file• Magnesium sulphate for the...

Page 1: Drug Therapy Protocols: Magnesium sulphate · PDF file• Magnesium sulphate for the purpose of treating marine envenomation is only to be administered and carried by appropriately

Drug Therapy Protocols: Magnesium sulphate

Disclaimer and copyright©2018 Queensland Government

All rights reserved. Without limiting the reservation of copyright, no person shall reproduce, store in a retrieval system or transmit in any form, or by any means, part or the whole of the Queensland Ambulance Service (‘QAS’) Clinical practice manual (‘CPM’) without the prior written permission of the Commissioner.

The QAS accepts no responsibility for any modification, redistribution or use of the CPM or any part thereof. The CPM is expressly intended for use by QAS paramedics when performing duties and delivering ambulance services for, and on behalf of, the QAS.

Under no circumstances will the QAS, its employees or agents, be liable for any loss, injury, claim, liability or damages of any kind resulting from the unauthorised use of, or reliance upon the CPM or its contents.

While effort has been made to contact all copyright owners this has not always been possible. The QAS would welcome notification from any copyright holder who has been omitted or incorrectly acknowledged.

All feedback and suggestions are welcome, please forward to: [email protected]

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Date May, 2018

Purpose To ensure a consistent procedural approach to Magnesium sulphate administration.

Scope Applies to all QAS clinical staff.

Author Clinical Quality & Patient Safety Unit, QAS

Review date May, 2021

Information security

This document has been security classified using the Queensland Government Information Security Classification Framework (QGISCF) as UNCLASSIFIED and will be managed according to the requirements of the QGISF.

URL https://ambulance.qld.gov.au/clinical.html

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Drug classElectrolyte

Pharmacology Magnesium is an important cofactor in multiple processes. It causes vasodilation and bronchodilation through inhibition

of smooth muscle contraction. Magnesium ions also possess

anticonvulsant and anti-dysrrhythmic properties.[1–3]

MetabolismMagnesium is filtered in the kidneys and excreted predominantly

in urine with small amounts in faeces and saliva.[1]

Presentation

Onset (IV) Duration (IV) Half-life

Immediate 30 minutes

• Ampoule, 10 mmol (2.5 g)/5 mL, magnesium sulphate

Variable

Magnesium sulphate

Precautions

• Renal impairment

Contraindications

• Allergy and/or Adverse Drug Reaction

• Atrioventricular (AV) block

• Renal failure

Indications

• Box jellyfish (Chironex fleckeri) envenomation

(unresponsive to antivenom therapy)[4]

• Eclampsia

• Irukandji syndrome (with intractable pain

unrelieved by narcotic analgesia AND/OR

systolic BP > 160 mmHg)[4]

• Torsades de Pointes

• Severe life-threatening asthma (only in patients

who have required IV salbutamol AND/OR IM/IV

adrenaline (epinephrine))

Side effects

• Pain at the cannulation site

• Magnesium toxicity

- hypotension/respiratory depression

- loss of deep tendon reflexes

May, 2018

Figure 4.30

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Special notes

• Magnesium sulphate for the purpose of treating marine

envenomation is only to be administered and carried by

appropriately trained QAS paramedics within the following

response catchments:

- Coastal QAS stations in the Wide Bay LASN and north; and

- Tin Can Bay (Cooloola Coast) and Rainbow Beach QAS

stations in the Sunshine Coast LASN.

• Irukandji syndrome is described as a tropical sting (usually

minimal discomfort) followed in 15–40 minutes by significant

systemic symptoms of pain, agitation, restlessness, and

clinically associated with signs of catecholamine excess.[1]

• All cannulae and IV lines must be flushed thoroughly with sodium chloride 0.9% following each medication

administration.

Schedule

• Unscheduled.

Routes of administration

Intravenous injection (IV)

Intraosseous injection (IO)

Intravenous infusion (IV INF)

Adult dosages

Magnesium sulphate

CCP

CCP IV

IO

Irukandji syndrome (with intractable pain unrelieved by narcotic analgesia AND/OR systolic BP > 160 mmHg)

CCP

ACP2

ECC

P

ACP2

E

CCP

ACP2

E

QAS Clinical Consultation and Advice Line consultation and approval required in all situations.

10 mmol over 20 minutesRepeated once at 20 minutes.Total maximum dose 20 mmol.Administer via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 15 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®syringe to achieve a final concentration of 10 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

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Adult dosages (cont.)

IV

IO

Box jellyfish (Chironex fleckeri ) envenomation (unresponsive to antivenom therapy)

CCP

CCP

ACP2

E

Eclampsia Eclampsia Eclampsia

IV

IO

CCP

CCP 20 mmol over 20 minutes

Administer via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 20 mmol (10 mL) of magnesium sulphate with 10 mL of sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 20 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

20 mmol over 20 minutesAdminister via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 20 mmol (10 mL) of magnesium sulphate with 10 mL of sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 20 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

10 mmol over 20 minutesRepeated once at 20 minutes.Total maximum dose 20 mmol.Administer via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 15 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®syringe to achieve a final concentration of 10 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

10 mmol over 20 minutesRepeated once at 20 minutes.Total maximum dose 20 mmol.Administer via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 15 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®syringe to achieve a final concentration of 10 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

Adult dosages (cont.)

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Adult dosages (cont.)

Torsades de PointesTorsades de PointesTorsades de Pointes

IV

IO

IV

IO

Adult dosages (cont.)

Severe life-threatening asthma (only in patients who have required IV salbutamol and/or IM/IV adrenaline (epinephrine))CC

PCC

P

CCP

CCP

Magnesium sulphate

10 mmol over 10 minutesRepeated once at 10 minutes.Total maximum dose 20 mmol.Administer via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 5 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®syringe to achieve a final concentration of 10 mmol/10 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 10 mins).

10 mmol over 20 minutesAdminister via SPRINGFUSOR® 30 mLSingle dose only.

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 15 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®syringe to achieve a final concentration of 10 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

10 mmol over 20 minutesAdminister via SPRINGFUSOR® 30 mLSingle dose only.

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 15 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®syringe to achieve a final concentration of 10 mmol/20 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 20 mins).

10 mmol over 10 minutesRepeated once at 10 minutes.Total maximum dose 20 mmol.Administer via SPRINGFUSOR® 30 mL

Syringe preparation: Mix 10 mmol (5 mL) of magnesium sulphate with 5 mL sodium chloride 0.9% in a 30 mL SPRINGFUSOR®

syringe to achieve a final concentration of 10 mmol/10 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 10 mins).

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Paediatric dosages

IV

IO

• Irukandji syndrome (with intractable pain unrelieved by narcotic analgesia AND/OR systolic BP > 160 mmHg)

• Box jellyfish (Chironex fleckeri ) envenomation (unresponsive to antivenom therapy)

0.1 mmol/kg over 15 minutes(rounded up to the nearest 0.5 mmol)Administer via SPRINGFUSOR® 30 mL

Single dose not to exceed 5 mmol.Repeated once at 10 minutes.

Total maximum dose 10 mmol.

Syringe preparation: Mix 0.1 mmol/kg of magnesium sulphate with sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 0.1 mmol/kg in 15 mL. Ensure syringe is appropriately la-belled. Administer via SPRINGFUSOR® at a rate of60 mL/hour (over 15 mins)

Torsades de Pointes (cont.) Torsades de Pointes (cont.) Torsades de Pointes (cont.)

IV

IO

Paediatric dosages (cont.)

0.1 mmol/kg over 10 minutes(rounded up to the nearest 0.5 mmol)Administer via SPRINGFUSOR® 30 mL

Single dose not to exceed 5 mmol. Repeated once at 10 minutes. Total maximum dose 10 mmol.

Syringe preparation: Mix 0.1 mmol/kg of magnesium sulphate with sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 0.1 mmol/kg/10 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 10 mins).

CCP

CCP

CCP

Magnesium sulphate

ACP2

E

0.1 mmol/kg over 10 minutes(rounded up to the nearest 0.5 mmol)Administer via SPRINGFUSOR® 30 mL

Single dose not to exceed 5 mmol.Repeated once at 10 minutes.

Total maximum dose 10 mmol.

Syringe preparation: Mix 0.1 mmol/kg of magnesium sulphate with sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 0.1 mmol/kg/10 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of60 mL/hour (over 10 mins).

QAS Clinical Consultation and Advice Line consultation and approval required in all situations.

CCP

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IV

IO

Paediatric dosages (cont.)

0.1 mmol/kg over 10 minutes(rounded up to the nearest 0.5 mmol)Administer via SPRINGFUSOR® 30 mL

Single dose not to exceed 5 mmol.

Syringe preparation: Mix 0.1 mmol/kg of magnesium sulphate with sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 0.1 mmol/kg/10 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 10 mins).

Severe life-threatening asthma (only in patients who have required IV salbutamol and/or IM/IV adrenaline (epinephrine))

0.1 mmol/kg over 10 minutes(rounded up to the nearest 0.5 mmol)Administer via SPRINGFUSOR® 30 mL

Single dose not to exceed 5 mmol.

Syringe preparation: Mix 0.1 mmol/kg of magnesium sulphate with sodium chloride 0.9% in a 30 mL SPRINGFUSOR® syringe to achieve a final concentration of 0.1 mmol/kg/10 mL. Ensure syringe is appropriately labelled. Administer via SPRINGFUSOR® at a rate of 60 mL/hour (over 10 mins).

CCP

CCP

Magnesium sulphate

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