379.4 ð ç« æ«éèš Summary
379.4.1 ð äžå¥è©±çžœçµ
CVST (cerebral venous sinus thrombosis) = thrombosis of cerebral venous sinuses (superior sagittal, transverse, sigmoid, cavernous) ± deep cerebral veins (straight sinus, internal cerebral, Galen); rare (3-4/million/yr) but underdiagnosed; female > male 3:1, often young; risk factors â pregnancy/postpartum (highest risk, postpartum 1st month especially) + OCP/HRT + infection (mastoiditis, sinusitis, otitis, meningitis, dental, periorbital) + malignancy + trauma + dehydration + nephrotic + systemic disease (lupus, IBD, Behçet, vasculitis) + COVID-19 + VITT (vaccine-induced immune thrombotic thrombocytopenia from adenoviral COVID vaccines 5-30 days post) + genetic thrombophilia (factor V Leiden, prothrombin G20210A, protein C/S/antithrombin deficiency, antiphospholipid syndrome); presentation variable â headache most common ~ 90% (progressive, may be thunderclap, worse with Valsalva) + papilledema (â ICP) + focal deficits (donât fit arterial territory!) + seizures (more common than arterial stroke) + altered LOC + cranial nerve palsies + encephalopathy; location-specific â superior sagittal sinus (bilateral parasagittal infarcts + leg weakness) + transverse-sigmoid (headache) + cavernous sinus (chemosis + proptosis + CN III/IV/V1/V2/VI palsies + painful ophthalmoplegia, often infectious S. aureus from face/orbit) + deep venous (bilateral thalamic + â LOC + devastating); diagnosis â MRV gold standard (direct visualization + empty delta sign filling defect) or CTV alternative (faster, comparable accuracy) + MRI venous infarcts donât follow arterial territory + hemorrhage common 30-40% + dural sinuses bright on T1/T2 (thrombus); workup â pregnancy test + D-dimer + thrombophilia workup (after acute phase ideally) + infection + malignancy imaging; treatment cornerstone is ANTICOAGULATION EVEN WITH HEMORRHAGE â IV heparin or LMWH acutely â warfarin INR 2-3 or DOAC (apixaban, rivaroxaban emerging) for 3-6 months provoked, 6-12 months idiopathic, indefinite for high-risk thrombophilia (APS, AT III) or recurrent; severe/deteriorating â endovascular thrombolysis or thrombectomy (TO-ACT 2020 mixed) + decompressive craniectomy life-saving for massive infarct; symptomatic anticonvulsants + analgesics + â ICP management; underlying treat infection + stop OCP + address malignancy; VITT-specific = IVIG + non-heparin anticoagulation (argatroban, bivalirudin, fondaparinux, DOACs) + AVOID heparin; prognosis generally favorable (75-80% functional recovery, mortality 5-10%, worse with deep venous/coma/deterioration/hemorrhage); TIA (transient ischemic attack) = TISSUE-BASED DEFINITION = transient neurological deficit + NO acute infarct on DWI MRI (previously time-based < 24 hr abandoned); average duration ~ 1 hr; high short-term stroke risk â 5% within 48 hr + 10% within 90 days â URGENT; ABCD2 score (Age ⥠60 1 + BP ⥠140/90 1 + Clinical unilateral weakness 2 or speech 1 + Duration ⥠60 min 2 or 10-59 min 1 + DM 1 = 0-7, high risk ⥠4); urgent workup within 24-48 hr â brain MRI with DWI (distinguishes TIA from stroke) + ECG + troponin + echocardiogram (consider TEE) + carotid imaging + Holter/ILR (occult AF) + glucose + lipids + hypercoagulable select + BP optimization; management â DAPT (ASA + clopidogrel à 21 days, CHANCE/POINT) for high-risk TIA (ABCD2 ⥠4) or minor stroke (NIHSS †3) then ASA monotherapy; alternative ASA + ticagrelor à 30 days (THALES) + CHANCE-2 (2021) ticagrelor + ASA better than clopidogrel + ASA in CYP2C19 LOF carriers; secondary prevention = stroke prevention (statin high-intensity + BP < 130/80 + DM + lifestyle + carotid + PFO closure + AF anticoagulation); TIA mimics â migraine with aura + seizure (Toddâs) + hypoglycemia + conversion + vestibular + syncopeã
379.4.2 ð æ²»ç粟èŠ
- CVST anticoagulation cornerstone (EVEN with hemorrhage)ïŒIV unfractionated heparin (target aPTT 1.5-2.5x normal) or LMWH (enoxaparin 1 mg/kg BID) acutely â transition to warfarin INR 2-3 or DOAC (apixaban, rivaroxaban) for 3-6 months provoked + 6-12 months idiopathic + indefinite for high-risk thrombophilia or recurrent
- CVST severe/deterioratingïŒendovascular thrombolysis (catheter-directed) or thrombectomy (TO-ACT 2020 mixed evidence â reserve for severe) + decompressive craniectomy for massive infarct + herniation
- CVST symptomaticïŒanticonvulsants for seizures + analgesics + â ICP management (head elevation, osmotherapy, CSF drainage)
- VITT (vaccine-induced immune thrombotic thrombocytopenia)ïŒIVIG 1 g/kg à 2 days + non-heparin anticoagulation (argatroban, bivalirudin, fondaparinux, DOACs apixaban/rivaroxaban) â AVOID heparin + monitor platelets + serotonin release assay for HIT
- cavernous sinus thrombosis (often infectious)ïŒIV antibiotics (vancomycin + ceftriaxone or other broad-spectrum, target Staph aureus) + anticoagulation + drainage of source (paranasal sinuses, mastoid, dental)
- TIA acuteïŒABC monitor + BP optimization (not too aggressive) + glucose + immediate aspirin 325 mg load + 81 mg/d
- TIA DAPT for high-risk (ABCD2 ⥠4 or minor stroke NIHSS †3)ïŒaspirin + clopidogrel 75 mg/d à 21 days (CHANCE/POINT) then aspirin monotherapy; alternative aspirin + ticagrelor à 30 days (THALES); CHANCE-2 ticagrelor + ASA preferred in CYP2C19 LOF carriers (Asian population particularly)
- TIA secondary preventionïŒsame as stroke â antiplatelet + high-intensity statin (atorvastatin 80 or rosuvastatin 20-40, LDL < 70) + BP < 130/80 + DM A1c < 7% + lifestyle + carotid intervention + PFO closure + AF anticoagulation
- pregnancy CVSTïŒLMWH throughout pregnancy (warfarin teratogenic) + plan for delivery + postpartum continue several months + future pregnancy LMWH prophylaxis
- IIH (idiopathic intracranial hypertension) DDx CVSTïŒalways rule out CVST first with MRV; if true IIH â acetazolamide + weight loss + LP
379.4.3 ð¯ ç§é«åž«çèåæé
- CVST risk factors (memorize): pregnancy/postpartum (highest) + OCP/HRT + infection (mastoiditis, sinusitis, dental) + malignancy + thrombophilia (genetic + APS) + COVID-19 + VITT (adenoviral COVID vaccines) + dehydration + IBD/lupus/Behçet
- CVST presentation atypical: headache most common (~ 90%, progressive or thunderclap) + seizures (MORE common than arterial stroke) + papilledema (â ICP) + focal deficits donât fit arterial territory; cavernous sinus thrombosis â chemosis + proptosis + painful ophthalmoplegia (CN III/IV/V1/V2/VI), often infectious S. aureus from face/orbit
- CVST diagnosis: MRV gold standard or CTV (empty delta sign on contrast); MRI shows venous infarcts (donât follow arterial territory) + hemorrhage common 30-40%
- CVST treatment cornerstone: ANTICOAGULATION EVEN WITH HEMORRHAGE â heparin/LMWH â warfarin (INR 2-3) or DOAC; duration 3-6 months provoked, 6-12 months idiopathic, indefinite for high-risk thrombophilia/recurrent
- VITT specific treatment: IVIG + non-heparin anticoagulation (argatroban, bivalirudin, fondaparinux, DOACs) â AVOID heparin (HIT-like mechanism with PF4 antibodies)
- TIA tissue-based definition: transient neurological deficit + NO acute infarct on DWI MRI (previously time-based < 24 hr abandoned); average ~ 1 hr
- TIA stroke risk: 5% within 48 hr + 10% within 90 days â urgent workup within 24-48 hr; many âTIAsâ actually small strokes on DWI (~ 30-50%)
- ABCD2 score for stroke risk after TIA: Age ⥠60 (1) + BP ⥠140/90 (1) + Clinical (unilateral weakness 2 or speech 1) + Duration (⥠60 min 2 or 10-59 min 1) + DM (1) = 0-7; high risk ⥠4
- DAPT for high-risk TIA/minor stroke: aspirin + clopidogrel à 21 days (CHANCE 2013 + POINT 2018) for ABCD2 ⥠4 or minor stroke (NIHSS †3) then ASA monotherapy; alternative ASA + ticagrelor à 30 days (THALES); CHANCE-2 (2021) ticagrelor + ASA preferred in CYP2C19 LOF carriers (relevant for Asian population â high prevalence)
- TIA urgent workup within 24-48 hr â brain MRI with DWI (distinguishes from stroke) + ECG + troponin + echocardiogram + carotid imaging + Holter/ILR for occult AF + hypercoagulable in select + initiate aspirin immediately; TIA mimics to consider â migraine with aura + seizure (Toddâs paralysis) + hypoglycemia + conversion + vestibular + syncope/presyncope