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CHAPTER: Medication Administration Guidelines DUE FOR REVIEW: October 2018 ENDORSEMENT DATE: October 2015 AMENDMENT DATE/S:
St Vincent’s Hospital Melbourne Epidural Analgesia Infusions | Page 1 of 4
St. Vincent’s Hospital (Melbourne) Caritas Christi Hospice
St. George’s Health Service Prague House
EPIDURAL ANALGESIA INFUSIONS Dosing, Administration and Monitoring Guidelines
Protocol purpose and related documents
To provide guidance on the dosing, administration and monitoring of Epidural Analgesia Infusions, including Patient Controlled
Epidural Analgesia (PCEA).
Current protocols, policies and guidelines that may relate include:
Epidural Abscess protocol
Special Analgesia Nursing Observations policy
Epidural and Paravertebral Analgesia Protocols
Management Of Antithrombotic Agents In The Perioperative Period guideline
Clonidine medication management guideline
Prescribing requirements and restrictions
The order should be written by an Anaesthetist on the Analgesia Infusion Treatment Sheet (SV 754) specifying the background
infusion rate, bolus volume, and lockout period and the pump will be programmed accordingly.
Indication
Post-operative analgesia
Pain conditions where the pain can be managed by central blockade (e.g. fractured ribs, complex regional pain
syndrome, bony metastases)
Dosage and Administration
Medications used for epidural analgesia comprise a local anaesthetic e.g. ropivacaine/bupivacaine with or without an opioid
analgesic e.g. fentanyl. Clonidine or adrenaline can be added to any of the above to improve the quality of analgesia (see
Clonidine - for Pain Management medication management guideline).
These are administered NEAT (without dilution). The rate of infusion will be dictated by individual anaesthetic prescription as
found on the Analgesia Infusion Treatment sheet (SV 754). Examples of usual rates for these infusions would be 5-15mL/hr and
bolus doses 5-10mL with a lockout of 20-30minutes. Prescriptions are individualised according to the patient and surgical
incision.
Commercially available solutions used at SVHM:
Ropivacaine 0.2% (2 mg/mL), 200 mL Polybag
Ropivacaine 0.2% (2 mg/mL) + Fentanyl 2 microg/mL (400 microg /200 mL), 200 mL Polybag
Ropivacaine 0.2% (2 mg/mL) + Fentanyl 4 microg/mL (800 microg /200mL), 200mL Polybag
Bupivacaine 0.125%, 200 mL Polybag – limited stock - Only to be used if ropivacaine is unsuitable.
Not commercially available but made by Pharmacy:
Bupivacaine 0.2%, 0.25%, 200 mL ‘Plain’
The Pharmacy Department will prepare any anaesthetic solutions that are not commercially available. This includes
the addition of clonidine or adrenaline to epidural infusions ordered on the wards. Orders must be received during
Pharmacy working hours otherwise contact the on-call anaesthetist who will prepare the infusion solution.
CHAPTER: Medication Administration Guidelines DUE FOR REVIEW: October 2018 ENDORSEMENT DATE: October 2015 AMENDMENT DATE/S:
St Vincent’s Hospital Melbourne Epidural Analgesia Infusions | Page 2 of 4
Additives are NOT permitted to an epidural analgesia infusion bag unless authorised by the Department of Anaesthesia and
Acute Pain Medicine protocol. Additions will be made by the Pharmacy Department or the on-call anaesthetist (see above).
Common dose ranges for additions:
Clonidine – 300 to 450 microg /200 mL epidural infusion.
Adrenaline – 400 microg /200 mL epidural infusion.
Transitional analgesia following catheter removal:
IM/IV opioids can be given 1 to 2 hours after ceasing epidural infusions containing fentanyl
IV Patient Controlled Analgesia (PCA) analgesia can be commenced at the same time the epidural is ceased
Oral opioids e.g. oxycodone, can be given at the same time the epidural is ceased /removed or as soon as patient has
discomfort.
Adjuvant analgesia such as paracetamol, tramadol and NSAID’s (e.g. celecoxib) – there is no restriction on when these
can be administered. If there are no contraindications, these may be given in addition to the opioid patient controlled
analgesia and oral opioids.
The Acute Pain Service should be notified immediately if the transitional analgesia is inadequate.
Administration
Infusion Pump: All epidural infusions must be given via a REM Bodyguard pump (with a locked box if contains opioid).
On the pump, Select Epidural, and then select the correct epidural protocol from the pump menu as prescribed on the
Analgesia Infusion Treatment Sheet (SV754). These pumps are used for all epidural and peripheral nerve infusions and
will be primed and set up in PACU prior to the patient being transferred to the wards. If a patient is transferred to the
ward with the REM Bodyguard pump the Acute Pain Service (APS) team will see the patient 2-3 times daily and the APS
nurses will educate the ward nurses caring for the patient on how to use and alter the pump if required.
Tubing: The tubing for epidural infusions must not contain any accessible injection ports and should be colour-coded
(yellow stripe) or clearly labelled as ‘EPIDURAL INFUSION’.
PCEA (Patient Controlled Epidural Analgesia): the patient must clearly understand how to use the button for ‘wound
pain’ and to report numbness or tingling in the arms or hands. Orders will specify the background infusion rate, bolus
volume, and lockout period and the pump will be programmed accordingly.
Special Precautions and Contraindications
Anticoagulation: Epidural needle placement is contraindicated in therapeutically anticoagulated patients.
Patients receiving Heparin sodium or Low Molecular Weight Heparins (LMWH) require short-term medication
discontinuation prior to epidural needle insertion. Patients receiving oral anticoagulants require the anticoagulant to be
withheld for the appropriate number of days and bridging anticoagulation with LMWH/Heparin sodium to be started
prior to surgery/the epidural needle insertion - See the Epidural and Paravertebral Analgesia Protocol, and the
Management of Antithrombotic Agents in the Perioperative Period guideline.
o Manipulation of epidural catheter can ONLY be done by an Anaesthetic trainee or Anaesthetic Consultant
o Caution in patients with renal impairment – prolongs effect of LMWH
o Acute Pain Service must be notified before commencing IV unfractionated heparin in patients with an epidural
catheter
o For removal of epidural catheter - see Epidural and Paravertebral policy
Pregnancy and Breastfeeding - Medication dependent. Contact medicines information pharmacist for advice (4359).
Removal of epidural catheter
Removal of epidural catheter: Can ONLY be performed on written order of an anaesthetist. See the Epidural and Paravertebral
Analgesia Protocol and the Management of Antithrombotic Agents in the Perioperative Period guideline.
CHAPTER: Medication Administration Guidelines DUE FOR REVIEW: October 2018 ENDORSEMENT DATE: October 2015 AMENDMENT DATE/S:
St Vincent’s Hospital Melbourne Epidural Analgesia Infusions | Page 3 of 4
Monitoring
Refer to Special Analgesia Nursing Observation Policy ,
Special Analgesia Chart (SV 167) , and
Epidural and Paravertebral Analgesia Policy
PCEA – the patient must clearly understand how to use the button for ‘wound pain’ and to report numbness or tingling in
the arms or hands.
Adverse Effects and Overdose
Overdose: Signs and Symptoms of local anaesthetic or opioid toxicity see Reportable Observations section on the Special
Analgesia observation chart (SV 167) and Epidural and Paravertebral Analgesia Policy
Adverse Effects: See Special Analgesia Nursing Observations Policy and Special Analgesia Observation chart (SV167) under
Standard Orders and Reportable observations.
Drug Interactions (1, 2, 3, 4, 5)
Ropivacaine & Bupivacaine
When using ropivacaine as a single dose or for <24hours treatment, studies did not indicate any clinically relevant drug
interactions. If repeated administration or a long-term infusion is given, avoid potent CYP1A2 and CYP3A4 inhibitors such as
fluvoxamine and ketoconazole, as these may increase ropivacaine levels.
Other local anaesthetics and amide type Class III antiarrythmic drugs (eg/ amiodarone, mexiletine, lignocaine : consider ECG monitoring as cardiac effects may be additive
Clonidine - see the Clonidine medication management guideline for interactions
Adrenaline
Beta –blockers: (especially non-selective e.g. propanolol) may result in severe hypertension followed by reflex bradycardia
(even when used with a LA).
MAOIs: may inhibit the metabolism of adrenaline, increasing the risk of arrhythmias, hypertension and vasoconstriction.
Use combinations cautiously, monitoring ECG, BP and haemodynamic parameters.
TCAs: may also inhibit the metabolism of adrenaline (see above), however this is less likely to occur when used with LA.
Presentation and Storage
Commercially available solutions used at SVHM:
Ropivacaine 0.2% (2 mg/mL) (Ropivacaine Kabi®)Polybag 200mL
Ropivacaine 0.2% (2 mg/mL) + Fentanyl 2 microg/mL (400 microg/200 mL) (Naropin® with Fentanyl) Polybag
Ropivacaine 0.2% (2 mg/mL) + Fentanyl 4 microg/mL (800 microg/200mL) (Naropin® with Fentanyl) Polybag
o Store Ropivacaine Polybags below 25°C. Do not refrigerate. Do not freeze.
Bupivacaine 0.125%, 200 mL Polybag – limited stock - Only to be used if ropivacaine is unsuitable.
Not commercially available but made by Pharmacy if necessary:
Bupivacaine 0.2%, 0.25%, 200 mL ‘Plain’. Expires 48 hours after preparation.
Any local anaesthetic infusion preparation with addition of adrenaline or clonidine added expires 48 hours after preparation
REFERENCES 1. MIMS® Online. Ropivacaine hydrochloride (Ropivacaine Kabi®)0.2% solution for injection 200 mL Product Information.
MIMS Australia 2015, accessed 29/07/15 at https://www.mimsonline.com.au.acs.hcn.com.au/Search.
2. AusDI ®, Bupivacaine hydrochloride (Marcain®) Product Information, AusDI® 2.0r115, 009-2015 Health Communication
Network Limited 2009-2015 accessed 29/09/15 at http://ausdi.hcn.com.au/quickSearch.hcn
3. MIMS® Online. Clonidine hydrochloride (Catapres®) 150microg/mL ampoules, Product Information. MIMS Australia 2015,
accessed 29/07/15 on https://www.mimsonline.com.au.acs.hcn.com.au/Search
CHAPTER: Medication Administration Guidelines DUE FOR REVIEW: October 2018 ENDORSEMENT DATE: October 2015 AMENDMENT DATE/S:
St Vincent’s Hospital Melbourne Epidural Analgesia Infusions | Page 4 of 4
4. AMH 2015 [online]: Australian Medicines Handbook Pty Ltd, accessed online on 24/09/15 at
https://www.amhonline.amh.net.au/
5. Baxter K, Preston C. Stockley's Drug Interactions. London: Pharmaceutical Press accessed 23/09/15 at
http://www.medicinescomplete.com/
6. Acute Pain Management: Scientific Evidence (3rd Edition 2010). Australia and New Zealand College of Anaesthetists and
Faculty of Pain Medicine. Website: www.anzca.edu.au
7. Analgesic Expert Group. Therapeutic Guidelines: Analgesic Version 5. Melbourne: Therapeutic Guidelines Limited; 2007
8. Breivik, H. and G. Niemi (2001). “Does Adrenaline improve epidural bupivacaine and fentanyl analgesia after abdominal
surgery? (comment).” Anaesthesia and Intensive Care 29 (4):436-7.
9. Niemi, G. and H. Breivik (1998). “Adrenaline markedly improves thoracic epidural analgesia produced by a low-dose infusion
of bupivacaine, fentanyl and adrenaline after major surgery. A randomised, double-blind, cross-over study with and without
adrenaline.” Acta Anaesthesiologica Scandanavica 42(8):897-909.
10. Niemi, G. and H. Breivick (2003). “The minimally effective concentration of adrenaline in a low-concentration thoracic
epidural analgesia infusion of bupivacaine, fentanyl and adrenaline after major surgery. A randomised, double-blind dose
finding study.”
Acta Anaesthesiologica Scandinavica 47(4):439-50.
11. Scott, D.A. (2014). Acute Pain Service Manual. Department of Anaesthesia, St Vincent’s Hospital, Melbourne (anaesthetic
access only).
Authorship and Contributor Details
Primary Policy Author(s):
Andrew Stewart Consultant Anaesthetist, Anaesthetics Department
Wendy McDonald Acute Pain Nurse, Anaesthetics Department
Kim Choate Acute Pain Nurse, Anaesthetics Department
Noni Oborne Medicines Information Pharmacist, Pharmacy Department (July 2015)
Gedal Basman Medicines Information Pharmacist, Pharmacy Department (July 2010)
Others Consulted, including Committees:
Medication Guideline Review Group
Head of Department Responsible for policy:
Andrew Cording Chief Pharmacist, Pharmacy Department