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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Intravenous thrombolysis and mechanical thrombectomy

Neurology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull

Synopsis

Select and prepare eligible patients for intravenous thrombolysis or mechanical thrombectomy while controlling avoidable delays, treatment-specific hazards and post-reperfusion complications.

  • Reperfusion decisions are made by an acute stroke service using disabling deficit, last-known-well, imaging, premorbid function, bleeding risk and patient wishes; age or NIHSS alone should not become an automatic exclusion.
  • NICE recommends tenecteplase or alteplase as intravenous thrombolysis options for selected acute ischaemic stroke within 4.5 hours when intracranial haemorrhage has been excluded and contraindications are addressed; use the locally commissioned stroke protocol.
  • Wake-up or later-presenting stroke may be thrombolysed when MRI or perfusion imaging demonstrates a favourable tissue pattern under current specialist protocols; clock time is not the only modern selection tool.
  • Mechanical thrombectomy is offered rapidly for eligible proximal intracranial large-vessel occlusion, commonly within 6 hours and in selected patients up to 24 hours using clinical and advanced-imaging criteria.
  • Do not withhold intravenous thrombolysis from an otherwise eligible patient merely because thrombectomy is planned; bridging treatment and transfer should proceed in parallel unless a specialist contraindication applies.
  • Before thrombolysis, blood pressure must be reduced to 185/110 mmHg or lower and glucose, anticoagulant exposure, recent bleeding or surgery and platelet or coagulation concerns must be evaluated without unnecessary testing delays.
  • After intravenous thrombolysis, maintain blood pressure below 180/105 mmHg for the first 24 hours under the stroke protocol, avoid antiplatelet and anticoagulant treatment for 24 hours, perform follow-up imaging before starting it, and investigate any neurological decline, headache, vomiting or hypertension immediately.
  • Thrombectomy care includes anaesthetic strategy, arterial access, reperfusion assessment and post-procedure blood-pressure planning at a specialist centre; successful recanalisation does not guarantee completed tissue recovery.

Key red flags

Suspected intracranial haemorrhage, active major bleeding or a known severe haemostatic abnormality requires immediate specialist review and usually precludes thrombolysis.

A direct oral anticoagulant taken recently, an elevated relevant drug level or uncertain exposure cannot be dismissed by a normal INR; use the local anticoagulant-specific pathway.

Blood pressure remaining above the treatment threshold despite careful protocol therapy prevents safe intravenous thrombolysis at that moment.

Basilar occlusion can deteriorate to coma or locked-in syndrome despite initially fluctuating symptoms and requires immediate thrombectomy-centre contact.

Airway swelling, haemodynamic instability, access-site expansion or any post-treatment neurological decline needs emergency senior and critical-care support.

Investigation priorities

01
Non-contrast CT brainFirst step

Exclude intracranial haemorrhage and assess the extent of established infarction before either reperfusion treatment.

Management branches

LYSEIntravenous thrombolysis decision

A patient has a disabling acute ischaemic stroke within a standard or imaging-selected treatment window.

  1. Confirm last-known-well, deficit and premorbid function, exclude haemorrhage on imaging and review anticoagulants, bleeding, procedures, blood pressure and glucose with the stroke physician.
  2. Correct a treatable pressure excess carefully to the protocol threshold and obtain only laboratory results that are clinically necessary before treatment.
  3. Discuss material benefit, symptomatic haemorrhage and uncertainty with the patient or appropriate representative without creating disproportionate delay.
  4. Administer the approved thrombolytic using the exact weight-based local protocol, document timestamps and begin protocolised post-treatment observations.

Key medicines

AlteplaseFor eligible acute ischaemic stroke, give 0.9 mg/kg intravenously to a maximum 90 mg, with 10% as an initial bolus and the remainder infused over 60 minutes.Use the complete stroke protocol for bleeding exclusions, anticoagulants, blood pressure and imaging; stop immediately for suspected intracranial bleeding or significant angioedema.
TenecteplaseFor eligible adult acute ischaemic stroke, give 0.25 mg/kg intravenously to a maximum 25 mg as a single bolus, using the dedicated stroke presentation and exact local weight-band protocol.Apply the full stroke thrombolysis exclusions and monitoring pathway; do not confuse the 25 mg stroke presentation or dose with higher-dose tenecteplase regimens used for myocardial infarction.
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Sources and review status6 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE NG128 stroke and TIA recommendationsNational thrombolysis and thrombectomy eligibility principles.
  • NICE TA264 alteplase for acute strokeTechnology appraisal for alteplase in acute ischaemic stroke.
  • NICE TA990 tenecteplase for acute strokeCurrent technology-appraisal recommendation for tenecteplase within 4.5 hours.
  • NICE IPG548 mechanical clot retrievalSafety and efficacy governance for mechanical thrombectomy.
  • National Clinical Guideline for Stroke acute careDetailed UK reperfusion and post-treatment care recommendations.
  • BNF alteplase monographUK medicine dosing, contraindications and adverse effects.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom