Pitocin (Oxytocin) Guidelines for Labor Induction and Postpartum Hemorrhage Management
Labor Induction and Augmentation
Oxytocin should be administered exclusively via intravenous infusion with continuous monitoring, starting at 1-2 mU/min and increasing by no more than 1-2 mU/min at intervals of at least 15-40 minutes, with immediate discontinuation if uterine hyperstimulation or fetal distress occurs. 1
Preparation and Initial Dosing
- Prepare the infusion by combining 10 units (1 mL) of oxytocin with 1,000 mL of physiologic electrolyte solution to create a concentration of 10 mU/mL 1
- Use an infusion pump or similar device for accurate flow rate control—this is mandatory, not optional 1
- Begin infusion at 1-2 mU/min as the initial dose 1
- Increase the dose gradually by increments of no more than 1-2 mU/min until achieving a contraction pattern similar to normal labor 1
Critical Monitoring Requirements
- Continuously monitor fetal heart rate, resting uterine tone, and the frequency, duration, and force of contractions 1
- When using intrauterine pressure catheter (IUPC), monitor both contraction amplitude and baseline resting tone—external tocodynamometry cannot reliably assess these parameters 2
- Maintain continuous ECG monitoring and pulse oximetry as clinically indicated, particularly in high-risk patients 3
Immediate Action Thresholds
- If baseline intrauterine pressure reaches 40 mmHg, immediately discontinue oxytocin 4
- Reposition patient to left lateral decubitus position 4
- Administer supplemental oxygen at 6-10 L/min 4
- Initiate IV fluid bolus if not already running 4
- Perform vaginal examination to assess for rapid descent, cord prolapse, or signs of rupture 4
- Consider tocolysis with terbutaline if fetal heart rate abnormalities develop 4
Special Considerations for VBAC Patients
- Oxytocin induction in VBAC candidates carries a 1.1% (95% CI 0.9-1.5%) risk of uterine rupture 5
- This risk is significantly lower than prostaglandin E2 (2%) or misoprostol (13%) 5
- Misoprostol is absolutely contraindicated in third trimester for patients with prior cesarean delivery 5
- Oxytocin use decreases the likelihood of successful VBAC but remains acceptable when medically indicated 5
HIV-Positive Patients
- Use oxytocin as needed to expedite delivery in HIV-positive women choosing vaginal delivery 5
- Avoid invasive monitoring procedures such as scalp electrodes 5
Postpartum Hemorrhage Management
For postpartum hemorrhage control, administer 10-40 units of oxytocin in 1,000 mL of non-hydrating diluent via slow IV infusion at a rate necessary to control uterine atony, or give 10 units intramuscularly after placental delivery. 1
Intravenous Administration
- Add 10-40 units to 1,000 mL of non-hydrating diluent 1
- Run at a rate necessary to control uterine atony 1
- In high-risk cardiac patients, maintain infusion rate below 2 U/min (approximately 33 mU/min) to avoid systemic hypotension 3
Intramuscular Administration
- Give 10 units (1 mL) after delivery of the placenta 1
- This route is acceptable for routine prophylaxis 1
Critical Safety Considerations
- Never administer oxytocin as a rapid IV bolus—this causes severe hypotension, tachycardia, and uterine hyperstimulation 3
- In patients with structural heart disease, obstructive valve lesions, or hypertrophic cardiomyopathy, use only slow infusion to avoid hypotension and tachycardia 3
- Continue hemodynamic monitoring for at least 24 hours after delivery due to significant fluid shifts 3
Alternative Agents
- Methylergonovine is contraindicated due to >10% risk of vasoconstriction and hypertension 5, 3
- Prostaglandin F analogues are useful alternatives unless increased pulmonary artery pressure is undesirable 5
- Ergotamine should be avoided in patients with respiratory disease due to bronchospasm risk 3
Incomplete or Inevitable Abortion
- Infuse 10 units of oxytocin in 500 mL of physiologic saline or 5% dextrose in saline 1
- Run at 20-40 drops/minute 1
- Curettage is generally considered primary therapy in first trimester 1
Common Pitfalls to Avoid
- Do not rely on external tocodynamometry alone during oxytocin administration—it cannot accurately measure baseline intrauterine pressure or contraction intensity 2
- Do not continue oxytocin if uterine hyperactivity or fetal distress occurs—the infusion can be abruptly stopped and oxytocic effects will rapidly wane 1
- Do not use oxytocin for elective induction—it is indicated for medical induction only 1
- In patients with severe bronchiectasis, oxytocin may cause acute hypoxemia resistant to supplemental oxygen 3