News
Ajmaline Intravenous for adults
Who can administer
Administration RESTRICTED - see Appendix 1
Important information
- This drug may only be used under supervision of a cardiologist in the Coronary Care unit
- Advanced cardio-pulmonary life-support systems must be immediately available (ref 1)
- Ensure isoprenaline injection has been ordered and is ready for use if required- see separate monograph.
- Unlicensed medicine - not routinely stocked in GUH - reorder when used
- This monograph refers specifically to the use of the drug in the diagnosis of Brugada syndrome
- There are numerous drug interactions (e.g. other antiarrhythmic drugs, enzyme inducers, drugs which cause QTc interval prolongation)
Available preparations
Gilurytmal injection 50mg per 10ml ampoule
Reconstitution
Already in solution
Draw up using a 5 micron filter needle
Infusion fluids
Not required-product ready for use
Methods of intravenous administration
Slow intravenous injection (for the diagnosis of Brugada syndrome)
- Administer each 10mg over one minute (ref 1) (see Dose below), followed by 5ml Glucose 5% (ref 3)
Dose in adults
Ajmaline challenge in the diagnosis of Brugada syndrome (ref 1,2)
- Administer 10mg every two minutes until termination indicated (see below) OR target dose of 1mg/kg (to a usual maximum total dose of 80mg)
- Check ECG and observations after each bolus
Drug administration should be terminated if (ref 1,2)
- Maximum dose reached, OR
- Diagnostic Brugada pattern in at least one ECG lead: J point or ST segment elevation of 2mm with coved ST elevation in more than one right precordial lead (positive result)
- Occurrence of ventricular ectopic beats or ventricular tachycardia
- Sinus arrest
- 2nd or 3rd degree AV nodal block
- Prolongation of QRS duration by more than 30%
Monitoring
- Monitor for tissue damage if extravasated (low pH) (ref 3)
- Continue ECG monitoring for at least 1 hour afterwards or until ECG normalises or any adverse effects resolve (ref 3)
- During testing monitor blood pressure and pulse at 5 minute intervals until recovery is evident (ref 3)
- Consider also monitoring SaO2 (ref 3)
- Serum sodium levels during administration should not exceed 145 to 150mmol/L(ref 3)
Further information
- Contains propylene glycol
Storage
- Store below 250C
References
SPC translated from German to English Dec 2010 (linked on Medusa IV website)
1: Ajmaline for the Diagnosis of Brugada Syndrome, Brighton and Sussex hospitals May 2020
2: Ajmaline test- Brugada syndrome. University Hospitals of Leicester 21/01/2022
3: Intravenous drug administration guide, Medusa , Review date 14/4/2016, - downloaded 09/05/2023
Therapeutic classification
Class 1a antiarrhythmic
IV Guide Type