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clonidine
clonidine
clonidine
PHARMACY GUIDELINE
Background
Clonidine is an alpha2 receptor agonist which is licensed for the treatment of hypertension.
Due to its seda9ve and an9hypertensive effects, clonidine may also be used as an unlicensed
treatment, with the consent of a Consultant Intensivist for:
• Alcohol withdrawal reac9ons
• Opiate withdrawal reac9ons
• Agita9on with tachycardia and hypertension, especially during weaning from the ven9lator.
• Autonomic storm aBer trauma9c brain injury.
• As an addi9onal seda9ve when adequate seda9on cannot be maintained using standard drugs.
The half-life of clonidine is 10 – 20 hours, rising to up to 41 hours in end stage renal failure.
Cau4ons
Clonidine should be used with extreme cau9on in pa9ents with hypotension, bradycardia, low cardiac
output or impaired leB ventricular func9on.
Enhanced hypotensive effects will be seen when other hypotensive drugs are given concurrently.
Concurrent use with haloperidol may produce QT prolonga9on.
Use with cau9on in Raynaud’s syndrome or other occlusive peripheral vascular disease.
Use with cau9on in pa9ents with a history of depression as it can worsen the condi9on.
Unsafe in porphyria.
Example calcula4on
Infusion rate: The infusion rate can be calculated from the following equa9on:
Date: DTC Jan 2017 Revision Date: Jan 2019 Authors: JW/OC
DEPARTMENT OF CRITICAL CARE Clonidine Version 1
PHARMACY GUIDELINE
Using a 750microgram in 50mL (15micrograms/mL) clonidine solu4on the following specifies the infusion
rate (mL per hour) required for different pa4ent weights:
** Infusion rates (mL/hr) have been rounded down for ease of administra9on
Intravenous Bolus
Method of administra4on
Appropriate in acute agita9on in a hypertensive, tachycardia pa9ent. Dilute dose to 10mL with sodium
chloride 0.9% to facilitate slow administra9on and give by slow IV injec9on over 10-15 minutes to avoid a
possible transient hypertensive effect.
Ideally administer centrally due to low pH. Alterna9vely if giving peripherally, it is less likely to cause damage
on extravasa9on when diluted in sodium chloride.
50micrograms tds may be 9trated to a maximum of 250micrograms tds.
Dose must not be withdrawn suddenly. Wean off gradually to minimise rebound hypertension and agita9on.
References
1. Intensive Care Society. Medication Concentrations in Critical Care Areas 2010
2. Injectable Medicines Guide Clonidine Monograph. Accessed on 18/06/2016 via http://medusa.wales.nhs.uk
3. Paw H and Shulman R (2010) Handbook of Drugs in Intensive Care (4th ed.) University Press, Cambridge.
4. White R and Bradnam V (2011) Handbook of Drug Administration via Enteral Feeding Tubes (2nd ed.) Padstow,
5. Pharmaceutical Press.BNF online accessed on 18/06/2016.
6. Summary of Product Characteristics Cetapres Ampoules 150mcg. Boehringer Ingelheim Ltd last revised 10/06/2014.
The use of this guideline is subject to professional judgement and accountability. This guideline has been
prepared carefully and in good faith for use within the Department of Critical Care at Brighton and Sussex
University Hospitals.The decision to implement this guideline is at the discretion of the on-call critical care
consultant in conjunction with appropriate critical care medical/ nursing staff.
Date: DTC Jan 2017 Revision Date: Jan 2019 Authors: JW/OC