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Administration of Intravenous
FentaNYL During Labour
Misericordia
Community Hospital
POLICY and PROCEDURE
Labour and Delivery
Manual
Original Date
Revised Date
Next Review:
Approved by:
April 2013
Director, Women’s Health, Covenant Health, GNH/MCH
Facility Site Lead, Women’s Health, MCH
April 2015
Page 1 of 5
Purpose:
The purpose of this protocol is to ensure the safe administration of Intravenous FentaNYL
during labour.
Indications:
FentaNYL is a potent short acting opioid that is an effective intravenous analgesic when used
in active labour.
The MOREOB program (2012) recommends the use of narcotics during labour that have a
shorter half-life e.g. morphine or fentaNYL and discourages the use of Meperidine because of
the increased risk of negative neonatal effects related to its longer half-life. These include
respiratory depression, lack of responsiveness and impaired sucking reflex.
Stage of Labour
Latent Stage
Early Active Stage
Late Active Stage
Second Stage
Source: MORE
OB
Choices of Opioid in Labour
Nulliparous
IM Morphine
IM or IV Morphine
IV Morphine or FentaNYL
IV FentaNYL
Multiparous
IM Morphine
IV FentaNYL
IV FentaNYL
IV FentaNYL
(2012). Management of Labour
Methods of Action of Intravenous FentaNYL
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Has a rapid onset of action occurring 3-5 minutes after administration with a peak action
between 5 and 15 minutes.
Has a short duration of action (30-60 minutes after a single IV dose of up to 100
micrograms) probably due to its rapid distribution from plasma into the tissues rather
than metabolism and excretion.
Has a maternal half-life of less than one hour.
May be used within an hour of birth.
Is metabolized by the liver.
Is excreted mainly in the urine (metabolites and unchanged drug).
Results in less maternal sedation, nausea & vomiting than morphine.
Crosses the placenta in small amounts as is highly bound to protein.
Has a neonatal half-life of 1-6 hours.
Has not been associated with neonatal neurobehavioural depression.
Has been detected in breast milk but is considered compatible with breastfeeding.
Administration of Intravenous FentaNYL During Labour
Date Approved
April 2013
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Use with Caution
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Patients at high risk for emergent cesarean section (evidence of fetal compromise).
Preterm labour (higher risk of respiratory depression in the neonate.
Obesity (fentaNYL is very lipid soluble).
Patients who have received more than one dose of a longer acting narcotic. Lower
FentaNYL doses may be required.
Women with a history of difficult intubation.
Hypertensive disorders of pregnancy (increases sensitivity to hemodynamic effects of
fentaNYL.
Delivery anticipated within 30 minutes.
Renal impairment or hepatic disease (lower dosage may be required as fentaNYL
clearance may be reduced).
Pulmonary disease or myasthenia gravis.
Uncorrected hypotension or hypovolemia.
Contraindications
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Hypersensitivity to fentaNYL, and possible cross sensitivity to alfentanil, anileridine,
diphenoxylate, meperidine, remifentanil, and sufentanil.
Use of MAO inhibitors within 14 days.
Fetal acidosis/abnormal fetal heart tracing.
Maternal respiratory rate of less than 8 breaths per minute or with an oxygen saturation
of less than 94%.
Special Training and Equipment
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Special Training as per Edmonton Zone on line parenteral monograph for fentaNYL.
Ensure oxygen, Naloxone & Resuscitation equipment are readily available for the
mother and the neonate.
RN must have specialized clinical competency in direct IV medication administration.
Guidelines for Use
Assessment Prior to Administration
• Assess labour progress within 30 minutes prior to fentaNYL administration.
• Assess baseline maternal vital signs and pain score.
• Ensure fetal heart rate is normal as per SOGC (2007) and Edmonton Zone Women’s
Health Program (2011) Fetal Health Surveillance Guideline.
Education to Patient
• Education to patient should cover potential maternal and neonatal side effects of the IV
FentaNYL, its onset and peak times, effect on labour progress and potential effect on
breast feeding initiation. Document this education, patient verbal consent in chart.
Administration of Intravenous FentaNYL During Labour
Date Approved
April 2013
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Dilution Instructions
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Dilute 100 microgram (2mL of 50 micrograms/mL) of fentaNYL with 8 mL or normal
saline to obtain 10 mLs of solution with a concentration of 10 micrograms / mL.
Label syringe with patient name, medication, concentration, date, time & RN signature.
Administration
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Ensure an IV has been established and is infusing.
Initial Dose as ordered by the Physician.
- 50 – 100 mcg IV push over 1-2 minutes. Wait 5-10 minutes for effect.
- Repeat: 50 mcg IV Q 3-5 minutes until analgesia is effective to a maximum dose
of 300 mcq given in ½ hour.
- Notify physician when maximum dose is reached if patient remains in pain.
Monitoring
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Respiratory rate should be monitored prior to and 5 minutes following every dose.
Continuous O2 saturation monitoring is required.
Assess sedation scale and pain score 5 minutes after each dose is administered and
then Q30 minutes.
Subsequent doses should only be given if analgesia is inadequate.
Onset of action for IV fentaNYL is 3-5 minutes; duration of action is 30-60 minutes.
Patients should be closely monitored for signs of adverse reactions and possible
respiratory difficulty.
Naloxone should be readily available for Emergency administration.
Oxygen saturation and respiratory rate should be monitored for 30-45 minutes after the
last dose of fentaNYL. Respiratory depressant effect lasts longer than the analgesic
effect.
Maternal Potential Adverse Effects
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Respiratory depression, respiratory arrest, asystole, arrythmias, and hypotension have
recurred after the initial recovery following high or multiple doses of fentaNYL.
Frequent
• Respiratory depression (can occur 6-8 hours after administration).
• Bradycardia, orthostatic hypotension, sedation, nausea & vomiting.
Less Frequent
• Rigidity in respiration muscles in the chest and pharynx following rapid IV administration.
Rare
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Dizziness, euphoria, laryngospasm, allergic bronchospasm, and seizures.
Administration of Intravenous FentaNYL During Labour
Date Approved
April 2013
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Neonatal Potential Adverse Effects
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Respiratory depression.
Management of Adverse Reactions
In the event of an adverse reaction, the nurse should:
• Immediately stop the injection.
• Administer oxygen; assess oxygen saturation, initiate CPR and call a Code Blue if
required.
• Call for help immediately if the respiratory rate of less than 10 per minute or oxygen
saturation less than 92%. Charge Nurse to notify Anaesthetist/Physician stat.
• Prepare to administer Naloxone as ordered in the event of respiratory depression.
• Document the adverse reaction and steps take to reverse it.
Naloxone: As per on line drug monograph
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IV Naloxone is an opiate antagonist used to reverse opiate-induced respiratory
depression and overdose.
The dosage for opiate-induced respiratory depression is 0.4 to 2 mg IV initially; repeat at
2 to 3 minute intervals PRN. Maximum total dose of 10 mg.
The dose must be titrated to avoid interference with pain control.
If patient does not respond at this dose, the diagnosis of narcotic-induced or partial
narcotic-induced toxicity is questionable.
Monitor patients closely to detect re-emergence of opiate effects/toxicity.
Administer repeat doses of Naloxone as necessary for adequate reversal.
Neonatal Respiratory Depression:
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Call the Resuscitation Team stat.
Provide neonatal resuscitation as per the 2011 Neonatal Resuscitation Guidelines.
Assist the RST in administering Naloxone if required.
Ongoing Maternal / Fetal Assessment:
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Further maternal monitoring may be required depending on patient response, fentaNYL
dosage and need for repeated dose(s).
Assess other maternal vital signs as required or ordered.
Continue fetal health surveillance until patient is delivered.
Administration of Intravenous FentaNYL During Labour
Date Approved
April 2013
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References:
1.
Alberta Health Services. Parenteral Manual Edmonton Zone. FentaNYL Monograph,
November 10, 2011; version 6.
2.
Alberta Health Services. Parenteral Manual Edmonton Zone. Naloxone Monograph,
December 8, 2011; version 5.
3.
Alberta Perinatal Health Program. Module 06. Pain management in labour.
Retrieved August 23 from http://aphp.dapasoft.com
4.
British Columbia Perinatal Health Program. (2007). Obstetric Guideline 4. Pain Management
Options during Labour. Retrieved July 23, 2009 from
http://www.bcphp.ca//sites/bcrcp/files/Guidelines/Obstetrics/OB4PainManagement.pdf
5.
Canadian Pharmacists Association. (2012). Opioid monograph (2012). Retrieved 23 August
2012 from http://www.e-therapeutics.ca
6.
Edmonton Zone Women’s Health Zone Clinical Department Executive Committee. (2011)
Clinical Practice Guideline. Fetal Health Surveillance.
7.
Evans, R.J., Evans, M.K., Brown, Y.M.R., and Orschan, S.A., (2010). Canadian Maternity,
Newborn & Women’s Health Nursing. Philadelphia: Lippincott, Williams and Wilkins.
8.
Martindale: (The Complete Drug Reference). FentaNYL Citrate. Retrieved 23 August 2012
from Lexicomp online at: online.lexi.com/lco/action/doc/retrieve/docid/429/1251005
9.
MOREOB Program. (2012). Management of Labour. Retrieved 20 August 2012 from
http://www.moreob.ca
10.
Northern Alberta Neonatal Intensive Care Program. (2012, July). Delivery Resuscitation
Policy.p3.
11.
Reproductive Care Program of Nova Scotia. (2006). Guideline for the Administration of
FentaNYL for Pain Relief in Labour.
12.
Society of Obstetricians and Gynaecologists of Canada. (2007). Fetal Health Surveillance:
Antepartum and Intrapartum Consensus Guideline.
13.
Sturgeon Community Hospital (2010). Obstetrical Guideline: Intravenous Use of FentaNYL in
Labour. Number 3.3.13.