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Table 1 Clinical assessment of BAD-related stroke

From: Study protocol of Branch Atheromatous Disease-related stroke (BAD-study): a multicenter prospective cohort study

Items

Assessment

Demographics

Age, gender

Medications prior to stroke

Antiplatelet drugs, statins, anticoagulant drugs, and tirofiban

Medical history

Stroke, hypertension, diabetes mellitus, dyslipidemia, heart disease, chronic respiratory disease, autoimmune diseases, blood system disorders, and thyroid disorder

Personal history

Smoking, alcohol use, and daily activity

Family history

Cardiovascular and cerebrovascular diseases

Current stroke onset

Time information

Time of symptom onset, arrival at hospital, and enrollment

Stroke symptom

Types (ischemic stroke or transient ischemic attack [TIA]), and presentation (pure motor hemiparesis, pure sensory, sensorimotor syndrome, and others)

Blood pressure

(1) Arrival at hospital, enrollment, and each follow up;

(2) Monitor of blood pressure within 72 h after enrollment (≥ 3 times per day, interval time ≥ 2 h)

Heart rate

Arrival at hospital, enrollment, and each follow up

Intake and output volume

Monitor of intake and output volume within 72 h after enrollment

Stroke severity

National Institutes of Health Stroke Scale

Functional assessment

mRS

Activities of daily living

Barthel index

Reperfusion therapy

Data of intravenous thrombolysis, and change of NIHSS score

Medications after stroke

Antiplatelet drugs, lipid-lowering drugs including statins, anticoagulant drugs, antihypertensive drugs, antidiabetics, and other neuroprotective drugs

END

Therapies for END, and time of END occurrence

Use of tirofiban

Time, dosage, duration and side effects

  1. END Early neurological deterioration, TIA Transient ischemic attack, mRS Modified Ranking scale, NIHSS National institute of health stroke scale