ergotrate
ergonovine
(er-goe-noe-veen) ergonovine,ergometrine
(trade name),Ergotrate
(trade name)Classification
Therapeutic: none assignedPharmacologic: oxytocics
Indications
Action
Therapeutic effects
Pharmacokinetics
Time/action profile (uterine contractions)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
PO | 5–15 min | unknown | ≥3 hr |
Contraindications/Precautions
Adverse Reactions/Side Effects
Central nervous system
- dizziness
- headache
Ear, Eye, Nose, Throat
- tinnitus
Respiratory
- dyspnea
Cardiovascular
- arrhythmias
- chest pain
- hypertension
- palpitations
Gastrointestinal
- nausea (most frequent)
- vomiting (most frequent)
Dermatologic
- sweating
Miscellaneous
- allergic reactions
Interactions
Drug-Drug interaction
Excessive vasoconstriction may result when used with other vasopressors, such as dopamine or nicotine.May ↑ the risk of adverse reactions with bromocriptine.Route/Dosage
Oxytocic
Availability (generic available)
Nursing implications
Nursing assessment
- Monitor BP, pulse, and respirations every 15–30 min until transfer to the postpartum unit, then every 1–2 hr. Report hypertension, chest pain, arrhythmias, headache, or change in neurologic status.
- Monitor amount and type of vaginal discharge. Report symptoms of hemorrhage (increased bleeding, hypotension, pallor, tachycardia) immediately.
- Palpate uterine fundus; note position and consistency. Notify health care professional if fundus fails to contract in response to ergonovine. Assess patient if cramping is severe; dose may be decreased.
- Assess for signs of ergotism (cold, numb fingers and toes; nausea; vomiting; diarrhea; headache; muscle pain; weakness).
- If patient fails to respond to ergonovine, check serum calcium level. Correction of hypocalcemia may restore responsiveness.
- Lab Test Considerations: May cause ↓ serum prolactin level, which inhibits synthesis of breast milk. Toxicity, initially manifested as ergotism, may cause seizures and gangrene. Seizures are treated with anticonvulsants. Vasodilators and heparin may be ordered to improve circulation to extremities.
Potential Nursing Diagnoses
Ineffective tissue perfusion (Indications)Risk for injury (Side Effects)
Implementation
- Do not administer solution that is discolored or contains a precipitate.
- Oral: Administration is usually limited to 48 hr postpartum, by which time the danger of hemorrhage from uterine atony has passed.
- Tablets may be administered SL.
- Intramuscular: The preferred route is IM. Firm uterine contractions are produced within a few minutes. Dose may need to be repeated every 2–4 hr for full therapeutic effect.
Intravenous Administration
- pH: 2.7–3.5.
- The IV route is reserved for severe uterine bleeding. Diluent: Dilute with 5 mL of 0.9% NaCl.
- Rate: Administer slow IV push over at least 1 min through Y-site injection of an IV of D5W or 0.9% NaCl.
Patient/Family Teaching
- Review symptoms of toxicity with patient. Instruct the patient to report occurrence of these immediately.
- Inform patient that uterine cramping demonstrates effectiveness of therapy.
- Explain need for pad count to determine degree of bleeding. Instruct patient to report immediately an increase in degree of bleeding or passage of clots.
- Instruct patient to report breastfeeding difficulties.
- Caution patient not to smoke while receiving ergonovine; nicotine is also a vasoconstrictor.
Evaluation/Desired Outcomes
- Uterine contraction and cramping in the prevention or cessation of uterine hemorrhage after delivery or abortion.