Association of 24-hour Blood Pressure Variability With Early Outcomes in Patients With Acute Non Cardiogenic Ischemic Stroke
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Stroke
- Sponsor
- Dongguan People's Hospital
- Enrollment
- 260
- Locations
- 1
- Primary Endpoint
- early neurological deterioration
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
Previous studies on the association between blood pressure variation (BPV) in acute ischemic stroke and functional outcomes yield conflicting result. The obscured definition and measurement of BPV engenders considerable confounding factors, making it difficult to interpret. We aim to investigate the predictive role of 24-hour BPV on early outcomes in acute non-cardiogenic ischemic stroke.
Detailed Description
This is a perspective registered cohort study. Patients with acute non-cardiogenic ischemic stroke are included into the study. During the first 24 hours after admission, the 24 hours blood pressure monitoring is to be taken and used to calculate various parameters of hour-to-hour blood pressure variability, including standard deviation(SD), coefficient of variation (CV), variation independent of mean(VIM) and average real variability (ARV) of systolic blood pressure (SBP) and diastolic blood pressure (DBP). The demographic and clinical data are also recorded. This is an observational sturdy, thus the caring physician make clinical decisions according to individual patient's condition. The endpoints are defined as early neurological deterioration, functional outcome(modified Rankin scale\<3 as good outcome) at discharge and 3 months.
Investigators
Zhu Shi
deputy director of neurology department
Dongguan People's Hospital
Eligibility Criteria
Inclusion Criteria
- •acute ischemic stroke
Exclusion Criteria
- •cardiogenic cerebral embolisms due to atrial fibrillation, pronounced heart valve diseases or valve replacement operation;
- •isolated sensory symptoms, isolated visual changes, isolated dizziness, or vertigo, without explicit MRI-DWI evidence for acute cerebral infarcts;
- •coexisting severe systematic diseases on admission such as acute coronary syndrome, malignant tumor, plasma dialysis therapy for renal failure, cirrhosis, rheumatic disease which would influence patients' independent functions .
Outcomes
Primary Outcomes
early neurological deterioration
Time Frame: 7 days after admission
NIHSS increase by 4 points or continuous consciousness deterioration
Secondary Outcomes
- good functional outcome at 14 days(up to 14 days in-hospital)
- good functional outcome at 3 months(3 months)