• No se han encontrado resultados

Capítulo 2. Marco de referencia

3. Normatividad incidente

3.5. Norma urbana Bogotá

Fentanyl citrate86

Fentanyl Citrate (fentanyl) is a short-acting opioid which binds with receptors at many sites within the CNS, alters pain reception, increases pain threshold.Fentanyl has no active metabolites and produces less maternal sedation, nausea, and vomiting than morphine. Indications and Clinical Use:

It is administered intravenously as an analgesic for pain relief in labour. Fentanyl is useful in early active labour with cervix at least 3-4 cm dilated and effacing, when a multiparous woman having a rapid, intense labour is requesting analgesia, and for women who wish pain relief and have a contraindication to epidural analgesia or where epidural is not available. Contraindications:

Fentanyl should not be used when the woman has PIH, is hypotensive or hypovolemic, has liver or kidney disease, is obese (BMI greater than 35), in preterm labour, at high risk of emergency cesarean delivery (e.g. breech) or has respiratory compromise (e.g. severe asthma, cystic fibrosis) or allergy or prior intolerable side effects to Fentanyl (hallucinations) or known hypersensitivity to Fentanyl .

Fentanyl should not be used in the presence of non-reassuring fetal heart tones or in the second stage of labour. Fentanyl should be used with caution in multiple pregnancy, where a woman has a history of difficult intubation or who has already received more than one dose of a longer acting narcotic in labour.

Fentanyl should not be administered within one half hour of anticipated delivery. Warnings and Precautions:

Naloxone should be readily available for administration to the mother or neonate. Physician consultation immediately after administration is required if Naloxone needs to be given. May cause CNS depression, which may impair physical or mental abilities.

Use with caution in patients with a history of drug abuse or acute alcoholism. Use with caution in patients with hepatic dysfunction, renal impairment, pre-existing respiratory compromise (hypoxia and/or hypercapnia).

One to one care must be provided. Monitor maternal vital signs, including respirations, and sedation scores for 30 minutes after IV Fentanyl administration, then hourly for 4 hours. Monitor maternal oxygen saturation for 5 minute periods if bolus does of 2 mcg/kg or total doses >200 mcg/hr are used or if morphine or meperidine has been administered IM in the 3 hours preceding IV fentanyl administration. A physician should be consulted if O2

saturations fall below 94%. Pregnancy:

Category C Lactation: Category L2

86 Items have been requested, but are not yet approved for inclusion in Schedule A

Refer Standards, Limits & Conditions for Prescribing, Ordering & Administering Drugs Midwives Regulation, Schedules A and B

Bylaws for the College of Midwives of BC Current Revision: March 17, 2014

Standard Fifteen page 81 of 85

Adverse Reactions:

Fentanyl can depress maternal and newborn respiration. Extra caution should be observed if fentanyl use continues for more than 5 hours or a total dose of 300 mcg has been

administered. The larger the maternal dose, the more likely the neonate is to be depressed. O2 saturation monitoring of the newborn is advised for at least 2 hrs after birth whenever >250 mcg have been given. As with any narcotic, watch for aspiration, drowsiness, hypotension, obtunded reflexes in addition to respiratory depression.

Dosage and Administration:

Dilute 100 micrograms (2mls – 2cc ampoule) into 8mls normal saline to obtain 10 mls solution (concentration 10mcg/ml) and give IV during a contraction. The recommended weight-based dose is 0.5 mcg/kg over 30 seconds waiting 5 minutes for effect and repeating every 5 minutes until satisfactory pain relief or a total maximum dose of 2mcg/kg/hr (or 200mcg/hr, or 4 doses in 1 hr) has been given. Alternatively, with continuous maternal O2 saturation monitoring, doses up to 1mcg/kg (max 100mcg) can be given initially with repeat dosing every 15 -20 minutes to a total of 200mcg/hr (or 2 doses). Once a total dose of 3 mcg/kg has been administered epidural or other alternate pain relief measures should be considered.

Onset of Action:

3 -5- minutes, takes peak effect in 5 – 15 minutes Duration of Action:

<1 hour, a maternal T ½ of <1 hour and a neonatal T ½ of 1 – 6 hours.

Morphine sulphate87

Morphine sulphate (morphine) is an opioid. Binds to opiate receptors in the CNS, causing inhibition of pain pathways, altering perception and pain response; producing generalized CNS depression.

Indications and Clinical Use:

Can be administered intramuscularly as an analgesic for pain relief in labour.

Morphine is often administered with Gravol® to counteract the side effects of nausea and vomiting. (The two drugs are compatible in a syringe for only 15 minutes.)

Morphine has a similar analgesic action as Demerol® (Meperidine), but with less nausea and fewer significant side effects for the neonate. As Morphine is more sedating and has a longer half life than Fentanyl, it should be reserved for early labour analgesia when

intramuscular administration will provide longer relief, or for women who do not want IV access in labour.

Contraindications:

Hypersensitivity to morphine sulfate or any component of the formulation; acute alcoholism, seizure disorders.

Morphine should not be used in the presence of non-reassuring fetal heart tone, in late first stage, active labour, or the second stage of labour.

87 Items have been requested, but are not yet approved for inclusion in Schedule A

Refer Standards, Limits & Conditions for Prescribing, Ordering & Administering Drugs Midwives Regulation, Schedules A and B

Bylaws for the College of Midwives of BC Current Revision: March 17, 2014

Standard Fifteen page 82 of 85

Warnings and Precautions:

Naloxone should be readily available for administration to the mother or neonate. Physician consultation immediately after administration is required if Naloxone needs to be given. Use with caution in patients with a history of drug abuse or acute alcoholism with severe hepatic impairment, in patients with renal impairment, with pre-existing respiratory compromise (hypoxia and/or hypercapnia), with seizure disorders or with thyroid dysfunction. Assess maternal and fetal well-being prior to and after morphine administration. Determine cervical dilation prior to administration; generally a nullipara should be <7 cm and a multipara <4 cm. As with other opioids, morphine can depress maternal and newborn respiration. The larger the maternal dose, the more likely the neonate is to be depressed. As with any narcotic, watch for aspiration, drowsiness, hypotension, obtunded reflexes, in addition to respiratory depression and urinary retention.

Pregnancy: Category C Lactation: Category L3

Adverse Reactions:

Circulatory depression, flushing, shock bradycardia, hypotension, drowsiness, dizziness, confusion, headache, pruritus, chest pain, hypertension, tachycardia, vasodilation, amnesia, anxiety, hallucination, nervousness, restlessness, seizure, slurred speech, rash.

Dosage and Administration: 10 – 15 mg IM every 4 hours or

3 – 5 mg dose IV bolus every 10 minutes prn for 1 -2 hours of relief

IV administration may be particularly appropriate for the nulliparous woman seeking pain relief in early active first stage. Morphine should not be administered subcutaneously as consistency of uptake and effectiveness cannot be determined. Morphine is often

administered with Gravol® to counteract the side effects of nausea and vomiting. (The two drugs are compatible in a syringe for only 15 minutes.)

Onset of Action:

15 – 20 minutes, peak effect is in 40-50 minutes Duration of Action:

3 – 4 hours

Morphine has a maternal T ½ life of 1 hour and a neonatal T ½ life of 6 hours. It has no active metabolites. Morphine may be used up to 4 hours prior to anticipated delivery. Most infants delivered 3 hours after a dose have been found to have no detectable cord levels. The CMBC is awaiting changes to federal drug regulations in order for midwives to prescribe fentanyl citrate and morphine sulphate independently.

Dimenhydrinate

(Gravol®) isnot a controlled substance but has been included here for reference purposes.

Gravol® is categorized in a class of drugs called antihistamines. Competes with histamine

for H1-receptor sites on effector cells in the respiratory tract, gastrointestinal tract and blood

vessels; blocks chemoreceptor trigger zones

.

Appendix 1a

Refer Standards, Limits & Conditions for Prescribing, Ordering & Administering Drugs Midwives Regulation, Schedules A and B

Bylaws for the College of Midwives of BC Current Revision: March 17, 2014

Standard Fifteen page 83 of 85

Indications and Clinical Use:

Can be administered intramuscularly as an analgesic for pain relief in labour. Gravol® is often given with morphine to counteract the side effects of nausea and vomiting. (The two drugs are compatible in a syringe for only 15 minutes.) While it is considered safe, Gravol® may produce some sedation.

Contraindications:

Hypersensitivity or previous reactions to dimenhydrinate or any component of the formulation.

Warnings and Precautions:

Use with caution in patients with asthma, peptic ulcer or cardiac arrhythmias and thyroid dysfunction. Pregnancy: Category B Lactation; Category L2 Adverse Reactions:

Palpitations, hypotension, confusion, nervousness, restlessness, headache, insomnia, tingling, heaviness and weakness of hands, vertigo, dizziness, blurred vision, nasal

stuffiness, dryness of nose and throat; nausea, vomiting, diarrhea, constipation, dry mouth; tightness of chest, wheezing.

Dosage and Administration:

Usual Concentration: each ml contains 50mg

50 – 100 mg PO every 4-6 hours, maximum dose 400 mg/day

25 - 50 mg IM,IV, every 4 hours, maximum dose 100mg every 4 hours 25 mg IV should be administered slowly over 2 min

Onset of Action: 20 to 30 minutes Duration of Action: 3 to 6 hours

Refer Standards, Limits & Conditions for Prescribing, Ordering & Administering Drugs Midwives Regulation, Schedules A and B

Bylaws for the College of Midwives of BC Current Revision: March 17, 2014

Standard Fifteen page 84 of 85

Drug Index

Documento similar