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