Thrombolytics for acute ischemic stroke: Difference between revisions
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== Background | ==Background== | ||
''[[EBQ:Studies_List_of_Thrombolytics_for_Acute_Stroke|see list of all thrombolytic trials in CVA for more details]]'' | ''[[EBQ:Studies_List_of_Thrombolytics_for_Acute_Stroke|see list of all thrombolytic trials in CVA for more details]]'' | ||
===NINDS Trial (treated within 3hrs)=== | ===NINDS Trial (treated within 3hrs)=== | ||
Benefits: | Benefits: | ||
*12% absolute risk reduction benefit (NNT = 8-9) at 3 months | *12% absolute risk reduction benefit (NNT = 8-9) at 3 months | ||
*Lower percentage of | *Lower percentage of patients who left hospital severely disabled | ||
*Comparable 3-month mortality rate (even with increased rate of ICH) | *Comparable 3-month mortality rate (even with increased rate of ICH) | ||
Risks: | Risks: | ||
| Line 15: | Line 15: | ||
==Studies Required== | ==Studies Required== | ||
*Physical exam: [[NIH Stroke Scale]] | *Physical exam: [[NIH Stroke Scale]] | ||
*Head CT | *[[Head CT]] | ||
*CBC ( | *CBC (hemoglobin, plt) | ||
*PT/PTT/INR | *PT/PTT/INR | ||
**Only need to wait for result if suspicion of abnormal value, | **Only need to wait for result if suspicion of abnormal value, patient has received heparin or warfarin, or use of anticoagulants is unknown | ||
*Glucose | *Glucose | ||
*ECG | *[[ECG]] | ||
*Urine pregnancy (pregnancy is relative contraindication) | *Urine pregnancy (pregnancy is relative contraindication) | ||
| Line 31: | Line 31: | ||
===Exclusion Criteria=== | ===Exclusion Criteria=== | ||
*Historical | *Historical | ||
**Stroke or head trauma in previous 3 months | **[[Stroke]] or [[head trauma]] in previous 3 months | ||
**Any history of intracranial hemorrhage | **Any history of [[intracranial hemorrhage]] | ||
**Major surgery in the previous 14 days | **Major surgery in the previous 14 days | ||
**GI or urinary tract bleeding in previous 21 days | **[[GI bleed|GI]] or [[hematuria|urinary tract]] bleeding in previous 21 days | ||
** | **[[Myocardial infarction]] in previous 3 months | ||
**Arterial puncture at noncompressible site in previous 7 days | **Arterial puncture at noncompressible site in previous 7 days | ||
*Clinical | *Clinical | ||
**Spontaneously clearing stroke symptoms | **Spontaneously clearing stroke symptoms | ||
**Only minor and isolated neurologic signs | **Only minor and isolated neurologic signs | ||
**Seizure at stroke onset | **[[Seizure]] at stroke onset | ||
*Persistent SBP >185 or DBP >110 despite treatment | *Persistent [[hypertension|SBP >185]] or DBP >110 despite treatment | ||
*Use of direct thrombin inhibitors or direct factor Xa inhibitors with elevated aPTT, INR, or factor Xa assay | *Use of direct thrombin inhibitors (e.g. [[dabigatran]], [[argatroban]]) or direct factor Xa inhibitors (e.g. [[rivaroxaban]], [[apixaban]]) with elevated aPTT, INR, or factor Xa assay | ||
*Active bleeding or acute trauma (fracture) on exam | *Active bleeding or acute [[trauma]] ([[fracture]]) on exam | ||
*Labs | *Labs | ||
**Platelets < 100K | **Platelets <100K | ||
**Serum glucose < 50 | **Serum glucose <50, >400 | ||
**INR > 1.7 or PT > 15 sec if on warfarin | **INR >1.7 or PT >15 sec if on warfarin | ||
**Elevated PTT if on heparin | **Elevated PTT if on heparin | ||
*Head CT | *[[Head CT]] | ||
**Evidence of hemorrhage | **Evidence of [[ICH|hemorrhage]] | ||
**Evidence of multilobar infarction | **Evidence of multilobar infarction with hypodensity involving >33% of cerebral hemisphere | ||
**Intracranial neoplasm, AVM, or aneurysm | **Intracranial neoplasm, [[AVM]], or aneurysm | ||
*Use of dabigatran within 48hrs is relative contraindication | *Use of dabigatran within 48hrs is relative contraindication | ||
===Relative Exclusion Criteria=== | ===Relative Exclusion Criteria=== | ||
*Minor or rapidly improving stroke symptoms | *Minor or rapidly improving stroke symptoms | ||
*Pregnancy | *[[Pregnancy]] | ||
*Seizure at onset | *[[Seizure]] at onset with postictal residual neuro impairments | ||
==tPA between 3-4.5hrs== | ==tPA between 3-4.5hrs== | ||
| Line 69: | Line 69: | ||
**Combination of both previous stroke and DM | **Combination of both previous stroke and DM | ||
**NIHSS score >25 | **NIHSS score >25 | ||
**Oral anticoagulant use regardless of INR | **Oral [[anticoagulant]] use regardless of INR | ||
==Administration== | ==Administration== | ||
{{TPA Stroke}} | |||
==tPA Complications== | ==tPA Complications== | ||
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*[[Angioedema]] | *[[Angioedema]] | ||
== See Also | ==See Also== | ||
*[[CVA (Main)]] | *[[CVA (Main)]] | ||
*[[Post-tPA Hemorrhage in CVA]] | *[[Post-tPA Hemorrhage in CVA]] | ||
*[[NIH Stroke Scale]] | *[[NIH Stroke Scale]] | ||
*[[EBQ: | *[[EBQ:Studies List of Thrombolytics for Acute Stroke|List of studies: Thrombolytics in CVA]] | ||
*[[Thrombolytics]] | |||
==References== | ==References== | ||
| Line 103: | Line 90: | ||
*AHA/ASA Guidelines | *AHA/ASA Guidelines | ||
[[Category: | [[Category:Neurology]] | ||
[[Category:Procedures]] | [[Category:Procedures]] | ||
Latest revision as of 22:44, 1 October 2019
Background
see list of all thrombolytic trials in CVA for more details
NINDS Trial (treated within 3hrs)
Benefits:
- 12% absolute risk reduction benefit (NNT = 8-9) at 3 months
- Lower percentage of patients who left hospital severely disabled
- Comparable 3-month mortality rate (even with increased rate of ICH)
Risks:
- 1% increase in mortality
- 5% increase in nonfatal intracranial hemorrhage
ECASS Trial (treated within 4.5hrs)
- Confirmed NINDS findings even when therapeutic window extended to 4.5hr
- As a result AHA/ASA now recommends tPA for patients presenting up to 4.5hr after symptom onset
Studies Required
- Physical exam: NIH Stroke Scale
- Head CT
- CBC (hemoglobin, plt)
- PT/PTT/INR
- Only need to wait for result if suspicion of abnormal value, patient has received heparin or warfarin, or use of anticoagulants is unknown
- Glucose
- ECG
- Urine pregnancy (pregnancy is relative contraindication)
tPA <3hr
Inclusion Criteria
- Diagnosis of ischemic stroke causing measurable neuro deficit
- Clear onset (last witnessed well) <3hr (see below for extension to <4.5hr)
- Age >18yr
Exclusion Criteria
- Historical
- Stroke or head trauma in previous 3 months
- Any history of intracranial hemorrhage
- Major surgery in the previous 14 days
- GI or urinary tract bleeding in previous 21 days
- Myocardial infarction in previous 3 months
- Arterial puncture at noncompressible site in previous 7 days
- Clinical
- Spontaneously clearing stroke symptoms
- Only minor and isolated neurologic signs
- Seizure at stroke onset
- Persistent SBP >185 or DBP >110 despite treatment
- Use of direct thrombin inhibitors (e.g. dabigatran, argatroban) or direct factor Xa inhibitors (e.g. rivaroxaban, apixaban) with elevated aPTT, INR, or factor Xa assay
- Active bleeding or acute trauma (fracture) on exam
- Labs
- Platelets <100K
- Serum glucose <50, >400
- INR >1.7 or PT >15 sec if on warfarin
- Elevated PTT if on heparin
- Head CT
- Evidence of hemorrhage
- Evidence of multilobar infarction with hypodensity involving >33% of cerebral hemisphere
- Intracranial neoplasm, AVM, or aneurysm
- Use of dabigatran within 48hrs is relative contraindication
Relative Exclusion Criteria
- Minor or rapidly improving stroke symptoms
- Pregnancy
- Seizure at onset with postictal residual neuro impairments
tPA between 3-4.5hrs
Inclusion Criteria
- Same as for <3hr
Exclusion Criteria
- All of the above plus:
- Age >80yr
- Combination of both previous stroke and DM
- NIHSS score >25
- Oral anticoagulant use regardless of INR
Administration
Alteplase
- NOTE - in stroke, do not give aspirin until 24 hours after giving tPA, as ASA with tPA does not improve outcomes and increases bleed risk[1]
- Do not give acutely heparin (or any anticoagulation) if giving tPA[2]
Dosing:
- 0.9mg/kg IV (max 90mg total)
- 10% of dose is administered as bolus; rest is given over 60min
- Neuro check Q15min x 2hr
- No anticoagulation/antiplatelets x 24hr
- Blood pressure (keep SBP <180, DBP <105)
If SBP is >180-230 or DBP is >120:
- Nicardipine 5 mg/hr by slow infusion (50 mL/hr) initially; may be increased by 2.5 mg/hr every 15 minutes; not to exceed 15 mg/hr OR
- Labetalol 10mg IV over 1–2 min; repeat dose q10–20min up to 300mg max OR
- Labetalol 10mg IV followed by infusion at 2–8 mg/min
If BP not controlled by above measures:
- Nitroprusside 0.5–10mcg/kg/min
- Continuous arterial monitoring advised
- Use with caution in patients with hepatic or renal insufficiency
tPA Complications
See Also
- CVA (Main)
- Post-tPA Hemorrhage in CVA
- NIH Stroke Scale
- List of studies: Thrombolytics in CVA
- Thrombolytics
References
- Hacke W, Kaste M, Bluhmi E, et al: Thrombolysis with alteplase 3 to 4.5 h after acute ischemic stroke. N Engl J Med 359(13): 1317, 2008
- ACEP/AAN Guidelines
- AHA/ASA Guidelines
- ↑ Zinkstok SM, Roos YB, ARTIS Investigators . Early administration of aspirin in patients treated with alteplase for acute ischaemic stroke: a randomised controlled trial. Lancet (2012) 380(9843):731–7.10.1016/S0140-6736(12)60949-0.
- ↑ Periprocedural Antithrombotic Treatment During Acute Mechanical Thrombectomy for Ischemic Stroke: A Systematic Review. Rob A. van de Graaf, Vicky Chalos, Gregory J. del Zoppo, Aad van der Lugt, Diederik W. J. Dippel, Bob Roozenbeek. Front Neurol. 2018; 9: 238.
