Department of Epidemiology, School of Public Health, Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, MOE Key Laboratory of Geriatric Diseases and Immunology Suzhou Medical College of Soochow University Suzhou China.
Department of Epidemiology Tulane University School of Public Health and Tropical Medicine New Orleans LA.
J Am Heart Assoc. 2023 Oct 17;12(20):e030692. doi: 10.1161/JAHA.123.030692. Epub 2023 Oct 7.
Background We aimed to evaluate the relationships between the magnitude of systolic blood pressure (SBP) reduction and achieved SBP in the acute phase of ischemic stroke onset and subsequent clinical outcomes. Methods and Results This study was a secondary analysis of CATIS (China Antihypertensive Trial in Acute Ischemic Stroke), a multicenter randomized controlled trial of 4071 patients with acute ischemic stroke. SBP reduction was defined as the proportional SBP changes from baseline to 24 hours after randomization, and achieved SBP was the mean of SBP measurements at day 7. The study outcomes included functional outcome of death or major disability (modified Rankin Scale score ≥3), death, and cardiovascular events at 3 months after recruitment. Compared with the reference group of increase or no change in SBP within the first 24 hours, the odds ratios (95% CIs) of functional outcome of death or major disability were 0.62 (0.47-0.83) and 0.61 (0.42-0.87) for the reduction of 11% to 20% and >20%, respectively. Compared with participants in highest achieved SBP group (≥160 mm Hg) at day 7, odds ratios or hazard ratios of lower achieved SBP (<130 mm Hg) were 0.54 (95% CI, 0.37-0.80) for functional outcome, and 0.36 (95% CI, 0.17-0.80) for death or cardiovascular events. Conclusions A moderate magnitude of SBP reduction and a lower early achieved SBP were associated with a decreased risk of poor functional outcome, death, and cardiovascular events after acute ischemic stroke. Further studies are warranted to confirm these findings. REGISTRATION: URL: ClinicalTrials.gov; Unique identifier: NCT01840072.
背景 本研究旨在评估缺血性脑卒中发病急性期收缩压(SBP)降幅和达到的 SBP 水平与随后临床结局之间的关系。
方法和结果 本研究是 CATIS(中国急性缺血性脑卒中降压试验)的二次分析,该研究是一项纳入 4071 例急性缺血性脑卒中患者的多中心随机对照试验。SBP 降幅定义为随机分组后 24 小时内 SBP 的相对变化,达到的 SBP 为第 7 天 SBP 测量值的平均值。研究结局包括招募后 3 个月时的功能结局(死亡或重度残疾,改良 Rankin 量表评分≥3 分)、死亡和心血管事件。与第 1 天内 SBP 增加或不变的参考组相比,SBP 降幅为 11%20%和>20%的患者发生死亡或重度残疾的比值比(95%CI)分别为 0.62(0.470.83)和 0.61(0.420.87)。与第 7 天达到最高 SBP 组(≥160mmHg)的患者相比,达到的 SBP 较低组(<130mmHg)的比值比或风险比为 0.54(95%CI,0.370.80),功能结局为 0.36(95%CI,0.17~0.80)。
结论 中等幅度的 SBP 降幅和较低的早期达到的 SBP 与急性缺血性脑卒中后不良功能结局、死亡和心血管事件风险降低相关。需要进一步的研究来证实这些发现。
网址:ClinicalTrials.gov;注册号:NCT01840072。