Be alert: Sodium nitroprusside is a very potent agent

INDICATIONS

  • Accelerated hypertension
  • Sodium nitroprusside is a very potent agent
    • use only on the advice of a renal SpR/consultant
    • use only on wards (e.g. critical care unit/CCU) where continuous monitoring of BP (preferably via arterial line) is possible

PREPARATIONS

  • Sodium nitroprusside 50 mg ampoules/vials for reconstitution

DILUENTS

  • Glucose 5%

ADMINISTRATION

  • Administer sodium nitroprusside either in a 50 mL syringe via a syringe pump, or in 250 mL or 500 mL bags using a controlled infusion device for precise control of flow rate
    • choice of bag size or use of syringe pump depend on dosage, patient weight and fluid status and availability of equipment
  • Take care to avoid extravasation. Check infusion site regularly

How to start and adjust doses

  • Initially 0.3 microgram/kg/min by IV infusion
    • increase to 0.5 microgram/kg/min
    • then in increments of 0.5 microgram/kg/min according to response allowing 5–10 min between each increment
  • Maximum dose = 8 microgram/kg/min

Infusion via syringe pump

  • Reconstitute sodium nitroprusside with 2 mL of glucose 5%
  • Withdraw resulting solution and make up to 50 mL with glucose 5% (50 mg in 50 mL = 1 mg/mL)
    • mix thoroughly
  • Infusion solution has a faint orange-brownish tint. If it is highly coloured do not use
  • Sodium nitroprusside must be protected from light
    • immediately wrap syringe and tubing with foil provided
    • infusion solution is then stable for up to 24 hr from time of preparation
Pump rate of sodium nitroprusside (50 mg/50 mL) via syringe pump
Enter Patient Weight (kg) Enter Required Dosage (mcg/kg/min):

Infusion in a bag via a controlled-infusion device

Infusion rate of sodium nitroprusside via bag
Weight (kg) Enter Required Rate (mcg/kg/min):
  • Infusion solution has a faint orange-brownish tint. If it is highly coloured, do not use
  • Sodium nitroprusside must be protected from light
    • immediately wrap infusion bag and all parts of administration set with foil provided
    • infusion solution is then stable for up to 24 hr from time of preparation

MANAGEMENT

  • Aim to reduce diastolic BP to 110–115 mmHg over several hours
  • Patients already taking antihypertensive drugs and the elderly will be more sensitive to sodium nitroprusside
  • If BP not adequately reduced within 10 min at maximum dosage, discontinue infusion – see Accelerated (malignant) hypertension guideline for alternative

Monitoring

  • Monitor BP and symptoms carefully
  • Over-rapid reduction in BP may produce the following symptoms:
    • headache, dizziness, perspiration
    • nausea, retching, abdominal pain
    • palpitations, apprehension, retrosternal discomfort
  • If these occur, reduce infusion rate in decrements of 0.5 microgram/kg/min

Length of treatment

  • Sodium nitroprusside is metabolised to free cyanide, converted in the liver to thiocyanate
    • if response obtained, continue therapy only for a few hours to avoid risk of toxicity
  • If therapy required for >24 hr, consult manufacturer's literature on monitoring and management of potential toxicity
    • signs of toxicity include tachycardia, sweating, hyperventilation, arrhythmias, marked metabolic acidosis

Withdrawal

  • Start oral antihypertensive therapy while BP is being controlled by sodium nitroprusside
  • When finally withdrawing sodium nitroprusside, to prevent rebound increase in BP, reduce infusion rate gradually
    • reduce by 25–30% every 5 min, rechecking BP before each decrement

© 2022 The Bedside Clinical Guidelines Partnership.

Created by University Hospital North Midlands and Keele University School of Computing and Mathematics.

Research and development team: James Mitchell, Ed de Quincey, Charles Pantin, Naveed Mustfa