DO NOT USE - ALL INFORMATION LIKELY INCORRECT IF NOT ACTIVELY DANGEROUS
Please use current guidelines available on the UHNM intranet for patient treatment
Please use current guidelines available on the UHNM intranet for patient treatment
- There is no upper age limit for this treatment
- Cardiogenic shock and ventricular arrhythmias are not contraindications to thrombolysis
INDICATIONS
- Default treatment for STEMI in the UK is primary PCI (pPCI)
- Role of thrombolysis is limited to cases where there is a delay in the system, that means that pPCI is unlikely to be achieved within 120 min, then a thrombolytic strategy should be deployed
- Aim should be to deliver thrombolysis within 10 min of taking decision that the patient will not achieve pPCI within the 120 min window
- Once thrombolysis delivered, arrange transfer to a pPCI centre
- Typical STEMI criteria apply
- presentation within 12 hr of onset of symptoms
- typical cardiac chest pain persisting for >30 min
- >1 mm ST segment elevation in 2 or more precordial leads or 2 or more bipolar leads or >1 mm ST segment depression in leads V1–V3 (suggesting acute posterior infarction) or LBBB with any of the following in leads V1–V3:
- >1 mm ST segment depression
- >1 mm ST segment elevation where QRS complex positive
- >5 mm ST segment elevation where QRS complex negative
CONTRAINDICATIONS
- Absolute:
- active bleeding
- Relative:
- major trauma/major surgery within previous 4 weeks
- stroke/TIA within previous 3 months
- confirmed subarachnoid haemorrhage at any time
- traumatic cardiac massage or intracardiac injection
- known bleeding disorder
- active dyspepsia or history of GI haemorrhage
- sustained systolic BP ≥180 mmHg
- proliferative retinopathy
- recent head injury
- pericarditis
- INR >2.0
STANDARD AGENT IS TENECTEPLASE (METALYSE®)
- Administer tenecteplase based on body weight, with a maximum dose of 10,000 units (tenecteplase 50 mg) according to table below. However, any bolus, fibrin specific thrombolytic is acceptable (such as alteplase – check BNF for treatment regimen). For patients aged >75 yr use half dose of bolus thrombolytic
Choose a body weight:
Tenectoplase: 6000 units; 30mg with corresponding volume of reconstituted solution 6 mL
Tenectoplase: 7000 units; 35mg with corresponding volume of reconstituted solution 7 mL
Tenectoplase: 8000 units; 40mg with corresponding volume of reconstituted solution 8 mL
Tenectoplase: 9000 units; 45mg with corresponding volume of reconstituted solution 9 mL
Tenectoplase: 10000 units; 50mg with corresponding volume of reconstituted solution 10 mL
- Administer by giving unfractionated heparin 5000 units by IV bolus, followed by tenecteplase administered as a single IV bolus over approximately 10 seconds, then give unfractionated heparin 1000 units/hr via infusion pump for 48 hr, adjusting dose to maintain APTT ratio 1.5-2.0
COMPLICATIONS
- Hypotension - if occurs de novo, review for cardiogenic shock, mitral regurgitation or tamponade. If thrombolysis being administered, stop IV infusion and recommence at a slower rate after BP has recovered
- Bradycardia - usually responds to atropine 300 microgram IV
- Ventricular tachycardia or idioventricular rhythm - usually self-limiting and requires no therapy. If sustained - see Cardiac arrhythmias guideline
- Avoid arterial puncture, central venous cannulation and IM injections in patients undergoing thrombolytic therapy, unless essential to patient care
Last reviewed: 2024-02-12