What is the typical infusion rate of Isoprenaline (isoproterenol) in mL/minute via syringe pump?

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Isoprenaline Infusion Rate via Syringe Pump

For shock and hypoperfusion states, dilute 1 mg of isoprenaline in 500 mL of 5% dextrose and infuse at 0.5 to 5 mcg/minute (0.25 to 2.5 mL/minute of diluted solution), which can be increased up to 30 mcg/minute in advanced shock. 1

Standard Preparation and Infusion Rates

Adult Dosing for Shock

  • The FDA-approved preparation involves diluting 5 mL (1 mg) of isoprenaline in 500 mL of 5% Dextrose Injection, yielding a concentration of 2 mcg/mL 1
  • Initial infusion rate: 0.25 to 2.5 mL/minute of the diluted solution (equivalent to 0.5 to 5 mcg/minute) 1
  • In advanced stages of shock, rates exceeding 30 mcg/minute have been used, though this requires careful titration 1
  • Concentrations up to 10 times greater (20 mcg/mL) can be prepared when volume limitation is essential 1

Pediatric Dosing

  • The American Heart Association recommends an initial infusion rate of 0.1 mcg/kg/min in children, with the usual range being 0.1 to 1 mcg/kg/min 1
  • No well-controlled studies exist to establish definitive pediatric dosing, so these recommendations are based on expert consensus 1

Titration and Monitoring

Adjustment Parameters

  • Adjust the infusion rate based on heart rate, central venous pressure, systemic blood pressure, and urine flow 1
  • If heart rate exceeds 110 beats per minute, consider decreasing or temporarily discontinuing the infusion 1
  • Start at the lowest recommended dose and increase gradually based on patient response 1

Critical Monitoring Considerations

  • Syringe pump performance at low infusion rates can cause significant start-up delays (89 to 1622 seconds to reach steady-state flow) and flow irregularities during vertical displacement 2
  • Central venous pressure significantly impacts fluid delivery during pump start-up, with pressures of 10 and 20 mmHg causing retrograde flows and zero-drug delivery times of 3.22 and 4.51 minutes respectively 3
  • Clinical alertness is required during syringe changes, as connection of a new pump can result in significant antegrade or retrograde fluid volumes depending on central venous pressure 3

Alternative Indications and Dosing

Bronchospasm During Anesthesia

  • Dilute 1 mL (0.2 mg) to 10 mL with normal saline or 5% dextrose 1
  • Administer 10 to 20 mcg (0.5 to 1 mL of diluted solution) as bolus intravenous injection 1
  • The initial dose may be repeated when necessary 1

Repetitive Ventricular Arrhythmia in Brugada Syndrome

  • Administer 1-2 mcg as bolus injection, followed by continuous infusion at 0.15 mcg/min 4
  • This low-dose continuous infusion has been shown to suppress arrhythmic storm in Brugada syndrome patients for 1-3 days 4

Important Precautions

Contraindications and Warnings

  • Contraindicated in patients with tachycardia, ventricular arrhythmias, or angina pectoris 1
  • May induce cardiac arrhythmias and myocardial ischemia, especially in patients with coronary artery disease or cardiomyopathy 1
  • Contains sodium metabisulfite, which may cause allergic reactions including anaphylaxis in sulfite-sensitive patients 1

Drug Interactions

  • Should not be administered simultaneously with epinephrine, as both are direct cardiac stimulants and may induce serious arrhythmias 1
  • Effects may be potentiated by tricyclic antidepressants, MAO inhibitors, levothyroxine, and certain antihistamines (chlorpheniramine, tripelennamine, diphenhydramine) 1
  • Beta-adrenergic blocking drugs (e.g., propranolol) antagonize the cardiostimulating and bronchodilating effects 1

Administration Considerations

  • Inspect visually for particulate matter and discoloration; do not use if pinkish, darker than slightly yellow, or contains precipitate 1
  • Diluted solution should be used immediately and unused material discarded 1
  • Physiological responses reach >90% of steady state after 8 minutes of infusion, though plasma concentrations may not reach definite steady state even after 40 minutes 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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