Terbutaline: Dosing, Indications, and Safety Profile
Acute Bronchospasm Management
For acute bronchospasm in adults, administer terbutaline 10 mg via nebulizer every 4-6 hours, or 0.25-0.5 mg subcutaneously, which provides effective bronchodilation within 5 minutes. 1, 2
Adult Dosing Regimens
Nebulized Administration:
- Standard dose: 10 mg nebulized, repeated every 4-6 hours if clinical improvement occurs 1
- For severe exacerbations with inadequate response, consider adding ipratropium bromide 500 µg to the nebulized terbutaline 1
- Drive the nebulizer with oxygen in acute severe asthma to simultaneously treat hypoxemia and bronchospasm 3
Subcutaneous Administration:
- Dose: 0.25 mg subcutaneously, repeated every 20 minutes for up to 3 doses 1
- Alternative dosing: 0.5 mg subcutaneously provides maximal bronchodilation with onset within 5 minutes 2
- This route is particularly effective when nebulized therapy is unavailable or poorly tolerated 1
Oral Maintenance:
- Start with 2.5 mg every 6-8 hours and adjust based on clinical response 2
- Oral terbutaline combined with aerosol administration represents a highly effective synergistic approach for maintenance therapy 2
Pediatric Dosing
For children with acute severe asthma, administer terbutaline 10 mg (or 0.3 mg/kg) nebulized, repeated every 1-4 hours if improvement occurs. 1
- If inadequate response after initial dose, repeat at 30 minutes after adding ipratropium bromide 250 µg (half the adult dose) 1
- Continue hourly nebulization for severe cases and consider hospital transfer 1
Tocolysis in Pregnancy
Terbutaline is classified as FDA Category C and TGA Category A for use in pregnancy, with evidence supporting its safety profile when used appropriately. 1
Acute Tocolysis Dosing
- Subcutaneous: 0.25 mg every 20 minutes for up to 3 doses for acute preterm labor 4
- After successful acute tocolysis, transition to oral maintenance: 20 mg/day divided into multiple doses 4
- Terbutaline provided more effective tocolysis with fewer adverse effects and better neonatal outcomes compared to salbutamol, with significantly higher gestational age at delivery and prolonged gestation 4
Continuous Subcutaneous Infusion
- Continuous subcutaneous terbutaline infusion after arrested preterm labor is associated with an extremely low incidence of serious adverse events (0.13% in a study of 9,359 patients) 5
- The most frequent serious adverse event was pulmonary edema (9 cases), with no maternal mortality 5
- Critical caveat: Patients with comorbidities and/or concomitant tocolysis with intravenous magnesium sulfate require close monitoring for serious adverse events 5
Important Pregnancy Considerations
- Systemic β2-agonists may have a tocolytic effect during delivery, potentially inhibiting uterine contractions 1
- Terbutaline is probably safe for breastfeeding 1
- SABAs (including terbutaline) are unlikely to cause structural anomalies, as observed risk in clinical studies is similar to the general population 1
Contraindications and Precautions
Absolute Contraindications
- Hypersensitivity to terbutaline or any component
- Patients at risk for cardiac arrhythmias (terbutaline may precipitate angina, particularly in elderly patients) 1
Critical Safety Warnings
Cardiovascular and Metabolic Effects:
- Systemic administration causes cardiovascular adverse effects including maternal and fetal tachycardia, maternal hyperglycemia, and neonatal hypoglycemia 1
- First treatment should be supervised in elderly patients due to risk of angina 1
- Monitor for tachycardia, myocardial irritability, and increased myocardial oxygen demand 1
Respiratory Considerations:
- In COPD patients with CO2 retention and acidosis, drive nebulizers with compressed air, NOT oxygen, to prevent worsening hypercapnia 6, 3
- Oxygen can be administered simultaneously via nasal cannula at 1-2 L/min if needed 6
Common Adverse Effects
Most Frequent Side Effects:
- Tachycardia (dose-dependent and more common than with salbutamol) 4
- Tremor (dose-dependent) 2
- Anxiety (significantly more common than salbutamol) 4
- Palpitations 2
- Maternal hyperglycemia (in pregnancy) 1
- Neonatal hypoglycemia (when used near term) 1
The incidence of side effects is clearly dose-dependent, supporting the recommendation to start with lower doses and titrate based on clinical response. 2
Clinical Decision Algorithm
For Acute Bronchospasm:
- Assess severity: respiratory rate >25/min, heart rate >110/min, peak flow <50% predicted indicates severe exacerbation 1
- Start with nebulized terbutaline 10 mg every 4-6 hours 1
- If inadequate response after first dose, add ipratropium 500 µg and continue combination every 4-6 hours 1
- For patients unable to use nebulizer, give 0.25 mg subcutaneously, repeat every 20 minutes up to 3 doses 1
- Transition to oral maintenance (2.5 mg every 6-8 hours) once stabilized 2
For Tocolysis:
- Acute preterm labor: 0.25 mg subcutaneously every 20 minutes for up to 3 doses 4
- After successful acute tocolysis, transition to oral 20 mg/day divided doses 4
- Critical: Avoid concomitant magnesium sulfate when possible; if necessary, monitor closely for pulmonary edema 5
- Monitor maternal pulse, blood glucose, and fetal heart rate 1
Important Clinical Pitfalls
- Excessive use should be avoided in pregnancy due to cumulative cardiovascular and metabolic effects 1
- Oral terbutaline after successful parenteral tocolysis does NOT reduce preterm birth rates when initiated at 24-34 weeks' gestation, though post-hoc analysis suggests benefit when started before 32 weeks 7
- Neonates exposed to terbutaline at term or during lactation should be observed for tachycardia, irritability, and hypoglycemia 1
- There is no evidence that subcutaneous terbutaline has advantages over inhaled β2-agonists for acute bronchospasm 1