Exclusion criteria for thrombolytic therapy with rtPA for acute stroke order set Goal: Door-to-needle time: 60 minutes | ||
Absolute exclusion criteria: All answers must be “NO” | ||
Onset of symptoms or the “last seen normal” is >4.5 h |
Yes |
No |
CT evidence of cerebral hemorrhage |
Yes |
No |
Clinical presentation consistent with subarachnoid hemorrhage even if CT scan normal |
Yes |
No |
Blood pressure >185/110 mm Hg and not treatable |
Yes |
No |
Blood glucose level <2.7 mmol/L (48.6 mg/dL) |
Yes |
No |
Significant head trauma, brain surgery, or spinal surgery within 3 months |
Yes |
No |
History of intracranial hemorrhage (in previous 6 months) |
Yes |
No |
Recent minor stroke (1 month) or moderate to severe stroke (3 months) |
Yes |
No |
Active internal, gastrointestinal, or urinary bleeding within 21 days |
Yes |
No |
Arterial puncture at a noncompressible site in previous 7 days |
Yes |
No |
Platelet count <100×109/L |
Yes |
No |
IV heparin received within 48 h, resulting in abnormally elevated aPTT >40 s |
Yes |
No |
Low-molecular-weight heparin at full anticoagulant levels |
Yes |
No |
Warfarin use with INR >1.7 |
Yes |
No |
Direct oral anticoagulants (rivaroxaban, dabigatran, apixaban) taken within previous 48 ha |
Yes |
No |
Relative contraindications: Consider eligibility on an individual basis based on benefits and risks | ||
Rapidly improving neurologic signs or NIHSS <4 |
Yes |
No |
History of arteriovenous malformation or aneurysm |
Yes |
No |
Profound stroke with obtundation, fixed eye deviation, and complete hemiplegia, or NIHSS >24 |
Yes |
No |
Acute cerebral infarct with ASPECTS ≤5 |
Yes |
No |
Recent large myocardial infarction or pericarditis within 3 months |
Yes |
No |
Blood glucose level >22.2 mmol/L (399.6 mg/dL) |
Yes |
No |
Recent major surgery or trauma (cardiac, thoracic, abdominal, orthopedic) within 14 days |
Yes |
No |
History of bleeding diathesis or liver failure |
Yes |
No |
Seizure at onset of stroke with residual postictal neurologic deficits |
Yes |
No |
Pregnancy |
Yes |
No |
Age <18 years |
Yes |
No |
Summary eligibility assessment: All answers must be checked | ||
1. The patient meets inclusion criteria: acute ischemic stroke symptom and symptom onset <4.5 h. |
Yes |
No |
2. The patient does not have any of the absolute exclusion criteria. |
Yes |
No |
3. The patient may have one or more of the relative contraindications, but potential benefits of alteplase exceed potential risks. |
Yes |
No |
Alteplase (rtPA) to be given (YES or NO): |
Yes |
No |
a Some experts consider the reversal of dabigatran with idarucizumab and the use of rtPA in selected patients.Evidence 36Strong recommendation (benefits clearly outweigh downsides; right action for all or almost all patients). High Quality of Evidence (high confidence that we know true effects of the intervention). Wardlaw JM, Murray V, Berge E, et al. Recombinant tissue plasminogen activator for acute ischaemic stroke: an updated systematic review and meta-analysis. Lancet. 2012 Jun 23;379(9834):2364-72. Doi: 10.1016/S0140-6736(12)60738-7. Epub 2012 May 23. Review. PMID: 22632907; PMCID: PMC3386494. Wardlaw JM, Murray V, Berge E, del Zoppo GJ. Thrombolysis for Acute Ischemic Stroke, Update August 2014. Stroke. 2014;45(11):e222-e225. doi: 10.1161/STROKEAHA.114.007024. Berge E, Whiteley W, Audebert H, et al. European Stroke Organisation (ESO) guidelines on intravenous thrombolysis for acute ischaemic stroke. Eur Stroke J. 2021 Mar;6(1):I-LXII. doi: 10.1177/2396987321989865. Epub 2021 Feb 19. PMID: 33817340; PMCID: PMC7995316. | ||
aPTT, activated partial thromboplastin time; ASPECTS, Alberta Stroke Program Early CT Score; CT, computed tomography; INR, international normalized ratio; NIHSS, National Institutes of Health Stroke Scale; PO, oral; rtPA, recombinant tissue plasminogen activator. |