Epidural Analgesia in Labour CA4054 v5
Topics covered
Epidural Analgesia in Labour CA4054 v5
Topics covered
Document Control:
The care of women in labour requiring epidural analgesia
For Use In:
Delivery suite, Maternity Services
Search Keywords Labour, analgesia, epidural, regional anaesthesia, neuraxial
Document Author: Dr Joanna Walker, Consultant Anaesthetist
Document Owner: Women and Children Division
Maternity Clinical Guidelines Committee
Approved By:
Clinical Guidelines Assessment Panel
Ratified By: Clinical Safety and Effectiveness Sub-board
Date to be
reviewed by:
This document
Approval Date: 13th June 2023 remains current 13th June 2026
after this date
but will be
under review
Implementation Date: N/A
Version History:
Version Date Author Reason/Change
Dr Jonathon Francis,
V4.0 02/02/2018 Consultant
Anaesthetist
Updated: responsibilities for set-up,
indications/contraindications,
PIEB/PCEA prescription regimes,
Dr Joanna Walker.
recommended observations,
V5.0 26/05/2023 Consultant
trouble-shooting ineffective
Anaesthetist
epidurals and guidance on
neurological monitoring with labour
epidural have been added.
Distribution Control
Printed copies of this document should be considered out of date. The most up to
date version is available from the Trust Intranet.
Consultation
The following were consulted during the development of this document: Consultant
Obstetric Anaesthetist Group, Consultant Obstetrician Group, Practice Development
Midwife Group.
Inclusivity
Within this document we use the terms pregnant women, her/she. However, It is
important to acknowledge that it is not only people who identify as women for whom
it is necessary to access care. Maternity services and delivery of care must therefore
be appropriate, inclusive and sensitive to the needs of those individuals whose
gender does not identity does not align with the sex they were assigned at birth.
Contents Page
Quick reference ..........................................................................................................5
1.Introduction .............................................................................................................6
1.1.Rationale ...........................................................................................................6
1.2.Objective ...........................................................................................................6
1.3.Scope .................................................................................................................6
1.4.Glossary ............................................................................................................6
2.Responsibilities and Roles.....................................................................................7
2.1.Anaesthetists.....................................................................................................7
2.2.Midwives............................................................................................................7
2.3.Delivery Suite Co-Ordinator.............................................................................7
3.Processes to be followed .......................................................................................8
3.1.Indications ........................................................................................................8
3.1.1.Absolute Indication:......................................................................................8
3.1.2.Relative Indication:.......................................................................................8
3.2.Contraindications..............................................................................................8
3.2.1.Absolute Contraindications:..........................................................................8
3.2.2.Relative Contraindications (discuss with Consultant Anaesthetist):............8
3.3.Patient Consent.................................................................................................9
3.4.Insertion of an Epidural....................................................................................9
3.4.1.Midwife Actions:............................................................................................9
3.4.2.Anaesthetists Actions:................................................................................10
3.5.Setting up the epidural infusion pump.........................................................11
3.6.Establishing epidural analgesia for labour analgesia.................................11
3.7.Maintenance and monitoring of epidural for labour analgesia..................12
3.8.Changing the Epidural Bag............................................................................14
3.9.Patient Controlled Epidural Analgesia (PCEA) ...........................................15
3.10.Review of Patients with Epidurals During Labour....................................15
3.11.Trouble-Shooting Ineffective Epidurals......................................................15
3.12.Management of Complications of Epidural Analgesia..............................16
3.13.Emergency Drugs to be available on delivery suite at all times..............17
3.14.Mobilisation and positioning ......................................................................17
3.15.Caesarean sections and assisted deliveries in theatre............................17
3.16.Removal of epidural catheter.......................................................................17
3.17.Care of Epidural Related Equipment..........................................................18
3.17.1.Epidural trolleys........................................................................................18
3.17.2.Epidural pumps.........................................................................................18
3.18.Anaesthetic Follow-up .................................................................................18
Quick reference
1. Confirm indication/contraindication for epidural analgesia (see page 8)
2. Patient has read the Epidural information card
3. Check with Midwife in charge regarding safe staffing levels and provision of
one-to-one care
4. Informed verbal consent taken by Anaesthetist
Complete epidural anaesthetic chart (Appendix A)
5. Patent wide bore IV cannula (16-18G) in-situ
6. Midwife to establish adequate CTG monitoring and assess foetal wellbeing
(see Trust guideline for the use of Fetal Monitoring and Blood Sampling Trust
Doc ID 840)
7. Anaesthetist to insert epidural, prescribe, set up pump and connect to patient
Levobupivacaine 0.1% plus fentanyl 2micrograms/ml is the standard
infusion mix for labour analgesia
8. Ensure an anti-emetic and omeprazole are prescribed, with oxygen as
required
9. Ensure the following are available in the room:
Hartmann’s solution, emergency pre-filled syringe of ephedrine
10.Anaesthetist must be present for initial or ‘test-dose’ and first blood pressure
11.Midwife to record observations on epidural anaesthetic chart
Blood Pressure and Heart Rate: Every 5 minutes after initial dose for
20 minutes. Thereafter dependent on PIEB/PCEA regime (see page 11
Table 2: Epidural regime prescription and HR/BP monitoring)
Motor Score (straight leg raise): Every 1 hour
Sensory Score (upper and lower levels of sensation to cold): Every 1
hour
Pain Score: Every 1 hour
Any concerns with observations or epidural efficacy should be
escalated to the anaesthetist
12.A urinary catheter should be inserted following epidural placement (see Trust
guideline Bladder Care in Labour and Postnatally Trust Doc ID 12617)
13.Anaesthetist to review patient 30 minutes after insertion to ensure effective
analgesia achieved and if required further appropriate management
14.After insertion, anaesthetist to complete
http://nnvmpatweb01/obsaudit/2008/login.asp to facilitate patient follow-up
15.Refer to Appendix B for troubleshooting labour epidurals
16.Refer to page 16 for immediate management of labour epidural complications
17. Document epidural catheter removal on epidural chart, ensure appropriate
LMWH timings (if relevant) and continue neurological monitoring for resolution
of motor block (see page 16 and Appendix C)
1. Introduction
1.1. Rationale
Epidural analgesia is a well-established technique to reduce pain in labour.
This guideline aims to ensure effective and safe use of epidural analgesia on the
Delivery Suite; delivered via a closed system using BD Bodyguard epidural pumps.
Within this guideline the recommendations for monitoring women receiving epidural
analgesia for labour are based on those within the NICE Guideline (190) ‘Intrapartum
care for healthy women and babies: Pain relief’ and the OAA/AoA Safety Guideline:
‘Neurological monitoring after obstetric neuraxial blockade’.
1.2. Objective
The objective of this guideline is to:
Provide a clear explanation and guidance for the safe set-up, initiation,
maintenance and discontinuation of epidurals for labour analgesia in the
Delivery Suite.
Detail the management strategy for ineffective epidural analgesia,
complications, or side effects.
Clarify the responsibilities and roles of the multi-professional team in the
provision of epidural analgesia.
1.3. Scope
For use by Anaesthetists, Midwives and Obstetricians caring for women in labour
requiring epidural analgesia in the Delivery Suite only.
1.4. Glossary
The following terms and abbreviations have been used within this document:
Term Definition
AoA Association of Anaesthetists
BP Blood pressure
BMI Body mass index
OAA Obstetric Association of Anaesthetists
PCEA Patient Controlled Epidural Analgesia
PIEB Programmed Intermittent Epidural Bolus
SBP Systolic blood pressure
SLR Straight leg raise
2.2. Midwives
Inform the anaesthetist without delay, when an epidural has been requested
(or advised during consultation in antenatal care e.g. raised BMI)
Establish CTG monitoring (see Trust guideline for the use of Fetal Monitoring
and Blood Sampling Trust Doc ID 840)
Clinical care and monitoring of the patient receiving the epidural as described
within this guideline
Administer antacid (omeprazole 40mg) prophylaxis 12 hourly for duration of
epidural analgesia
Insert urinary catheter (see guideline Bladder Care in Labour and Postnatally
Trust Doc ID 12617)
Check patient pressure areas every 2 hours
Recognise and escalate concerns or complications
Complete appropriate documentation on the epidural anaesthetic chart
Epidural analgesia must only be considered where one to one midwifery care
can be provided by a midwife who has been assessed as competent
Facilitate escalation to another anaesthetist if delays from request to
attendance (>30 min) are anticipated
3. Processes to be followed
3.1. Indications
3.1.1. Absolute Indication:
Maternal request
3.2. Contraindications
3.2.1. Absolute Contraindications:
Patient Refusal
Administration of LMWH (prophylactic dose within the last 12 hours,
therapeutic dose within the last 24 hours)
Severe coagulopathy
Thrombocytopenia – Platelet < 80 109/L (with Platelet count <100 109/L check
coagulation and fibrinogen level)
Localised sepsis over insertion site
Hypovolaemia /cardiovascular instability
Raised intracranial pressure
Systemic infection
Mild coagulopathy
Pre-existing abnormalities of the vertebral column (e.g. previous spinal
surgery)
Pre-existing central or peripheral neurological conditions
Patients should be advised once an epidural is running, they will have reduced
mobility, greater levels of monitoring and a diet of still isotonic drinks or water only
(see guideline Maternity Clinical Guideline for Intrapartum Care Trust Doc ID:850)
Contact the anaesthetist on bleep 0011 or via Alertive without delay once the
patient has requested an epidural.
Collect the equipment and drugs required:
o Epidural trolley (containing sterile pack, sterile gown/gloves/hat,
chlorhexidine 0.5% in 70% alcohol, epidural mini-pack, ‘lock-it’ or device
to secure catheter, occlusive clear dressing, Mefix tape and emergency
pre-filled syringe of ephedrine).
Assess the epidural block 20-30 minutes after establishing pain relief (pain
scores, sensory level and SLR), at every shift change or at the request of the
midwife.
*Bolus is less than 10mls therefore there is no need to monitor BP unless concerns
The woman should be observed during and after each bolus and verbal contact
maintained.
Key Levels:
T4 – Nipple
T6 – Xiphoid
T8 – Midpoint between
the umbilicus and xiphoid
T10 – Umbilicus
L1 – Groin
S1 - Little toe
5. Pain Score
Ask the patient to rate her current pain every hour, on a scale of 0 (no pain)
to 10 (severe pain) and document on epidural chart
The woman needs to be instructed in how to use the Remote Dose Cord and when
to administer a bolus dose. The midwife should supervise the woman administer the
first two doses.
All boluses should be administered with the woman sitting on the bed.
The woman should only administer a bolus dose when she is sitting or lying
down on her side.
The bolus will be administered by using the Remote Dose Cord.
The woman should be asked to tell her midwife when she has administered a bolus
dose and asked to inform the midwife of any light-headedness, nausea, dizziness,
breathlessness or marked weakness of the legs. If the woman has any of these
symptoms, the midwife should remove the Remote Dosing Cord from the woman
and lay the woman in the left lateral position. The IV infusion rate should be
increased to give a fluid bolus of 250 mLs. The anaesthetist should be called to
attend. Maternal blood pressure and block height should be recorded and maternal
leg weakness assessed (see Section 3.11 Management of complications of epidural
analgesia).
If this proves ineffective then it can help to withdraw the catheter by 1cm, thus
altering the catheter position within the epidural space hopefully allowing the
anaesthetic to spread more effectively. Any adjustment of the catheter position must
only be done by an anaesthetist who should wear sterile gloves and a facemask.
The epidural catheter should be aspirated to check for blood/CSF before re-securing.
The epidural site must be kept as clean as possible and new clean dressings must
be applied afterwards.
Re-siting: If none of the above measures improve the effectiveness of the epidural
then it may be appropriate to remove the epidural and site another one. In this
scenario the woman needs to be made aware that although this is likely to improve
their pain relief there is a chance that the second epidural may fail as well. It may be
appropriate to discuss alternative options such as remifentanil PCA.
Problem Action
Hypotension If the woman feels unwell after a bolus or exhibits signs of
maternal hypotension (faintness, nausea, dizziness) or develops
sudden marked motor weakness of the legs (unable to straight
leg raise either leg) then no further boluses should be given.
Ephedrine
Phenylephrine
Naloxone
Atropine
Adrenaline
20% lipid emulsion (i.e. Intralipid 20% emulsion, Fresenius Kabi AB)
If the mother wishes and feels able to do so she should be encouraged to adopt
upright positions (see Trust guideline A Maternity Clinical Guideline for Intrapartum
Care Trust Docs ID 850)
If the patient has been to theatre, the epidural catheter is usually removed by the
anaesthetist; it may remain in situ if there are concerns with coagulopathy.
If any present: DO NOT remove the epidural catheter until discussed with the
anaesthetist.
If there are no concerns:
1. Using an aseptic technique, remove dressing and remove epidural catheter
with gentle traction. If resistance is encountered, do not persist and contact
the anaesthetist.
2. Apply appropriate small dressing to the area.
3. Record the time and that the catheter was ‘intact’ (presence of the blue tip) on
the epidural anaesthetic chart.
4. Complete a thromboembolic risk assessment. If LMWH is indicated, ensure it
is prescribed for > 4hrs after epidural catheter is removed.
5. Inform the patient of the expected time of return of bilateral straight leg raise
(approximately 4 hours after last epidural local anaesthetic dose).
6. The patient should not attempt to mobilise until it is recorded that full motor
power has returned.
7. Disposal of the remaining ‘bag mix’ solution should be made by two midwives
and documented on the epidural chart
When an epidural pump is in use, the number of the pump must be clearly
marked next to the patients name on the delivery suite board.
When the pump is no longer in use it should be cleaned and returned to the
equipment cupboard and plugged in to recharge.
4. Related Documents
5. References
National Institute for Health and Care Excellence. Clinical guideline [CG190]:
Intrapartum care for healthy women and babies, 2014 (revised 201) London:
NICE, 2017 https://www.nice.org.uk/guidance/cg190 (accessed 12/04/2023)
Yentis, S.M., Lucas, D.N., Brigante, L., Collis, R., Cowley, P., Denning, S.,
Fawcett, W.J. and Gibson, A. (2020), Safety guideline: neurological
monitoring associated with obstetric neuraxial block 2020. Anaesthesia, 75:
913-919. https://doi.org/10.1111/anae.14993
7. Appendices
7.1. Appendix A: Obstetric Neuraxial Analgesia Chart
A full assessment will only be required if: The impact is potentially discriminatory
under the general equality duty
Any groups of patients/staff/visitors or communities could be potentially
disadvantaged by the policy or function/service
The policy or function/service is assessed to be of high significance
IF IN DOUBT A FULL IMPACT ASSESSMENT FORM IS REQUIRED
The review of the existing policy re-affirms the rights of all groups and clarifies the
individual, managerial and organisational responsibilities in line with statutory and best
practice guidance.
When administering a manually administered epidural test dose, particularly when using 0.25% levobupivacaine, close monitoring for hypotension is necessary. If hypotension occurs, supportive measures should be employed, including increasing intravenous fluid administration under anaesthetist guidance .
To establish effective epidural analgesia, after administering a test dose of 10ml 0.1% levobupivacaine with fentanyl via pump, a clinician bolus of 5-15ml, if needed, can be administered to ensure analgesia. This is followed by setting the appropriate infusion regime like PCEA, PIEB, or a combination, with continuous monitoring and assessment to address any analgesia inadequacies .
Concerns after epidural removal, such as numbness, weakness, inability to perform a straight leg raise 4 hours post-analgesia, severe headache, or back pain, should prompt immediate notification of an anaesthetist. Further management follows the Trust guidelines on Postnatal Neurology Injuries and Inadvertent Dural Puncture .
Relative indications for early epidural analgesia in labour include labour augmentation, twin pregnancy, pre-eclampsia without severe thrombocytopenia or coagulopathy, high BMI, cardiovascular disease, respiratory disease, and other risk factors for general anaesthesia such as anticipated difficult airway .
Absolute contraindications for epidural analgesia include patient refusal, administration of low-molecular-weight heparin (LMWH) within the past 12 hours for prophylactic doses or 24 hours for therapeutic doses, severe coagulopathy, thrombocytopenia with platelet count less than 80 billion/L, localized sepsis over the insertion site, hypovolemia or cardiovascular instability, and raised intracranial pressure .
When the 'Near End' alarm is activated on the epidural infusion pump, the midwife should press 'Stop' to pause the pump, enter the Level 1 code to access the menu, select 'Change Bag', and attach a new pre-filled bag ensuring there is no air in the giving set. The 'Start' key is then pressed to confirm settings and restart the pump .
If analgesia remains unsatisfactory after two consecutive bolus doses or 30 minutes after any bolus, the midwife should contact an anaesthetist immediately for a review. The midwife should attempt positional adjustments or top-ups in the interim, but if these efforts do not improve analgesia, anaesthetic intervention is required .
If an epidural catheter disconnection is witnessed, wrap the end of the catheter in a sterile swab, call an anaesthetist immediately, and avoid further use until reviewed. If necessary, the catheter end can be cut and re-sterilized under the anaesthetist's instruction .
When changing the bag on an epidural infusion pump, the midwife should first acknowledge the 'Near End' alarm by stopping the pump, accessing the pump menu with the Level 1 code, selecting 'Change Bag', attaching a new bag without air in the giving set, and then starting the pump by confirming the settings with the 'Start' key .
In the first 30 minutes following an epidural block, blood pressure and heart rate should be recorded every 5 minutes, continuous CTG monitoring should be conducted, and the sensory block height to cold should be documented bilaterally after 20 minutes. The midwife must remain in the patient's room throughout this period .