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首页> 外文期刊>JAMA neurology >Effect of Standard vs Intensive Blood Pressure Control on the Risk of Recurrent Stroke A Randomized Clinical Trial and Meta-analysis
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Effect of Standard vs Intensive Blood Pressure Control on the Risk of Recurrent Stroke A Randomized Clinical Trial and Meta-analysis

机译:标准VS强化血压控制对复发性脑卒中风险的影响,随机临床试验和荟萃分析

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IMPORTANCE The Systolic Blood Pressure Intervention Trial (SPRINT) demonstrated that a systolic blood pressure (BP) target less than 120 mm Hg was superior to less than 140 mm Hg for preventing vascular events. This trial excluded patients with prior stroke; therefore, the ideal BP target for secondary stroke prevention remains unknown. OBJECTIVE To assess whether intensive BP control would achieve fewer recurrent strokes vs standard BP control. DESIGN. SETTING, AND PARTICIPANTS Randomized clinical trial (RCT) of standard vs intensive BP control in an intent-to-treat population of patients who had a history of stroke. Patients were enrolled between October 20,2010, and December 7,2016. For an updated meta-analysis, PubMed and the Cochrane Central Library database were searched through September 30,2018, using the Medical Subject Headings and relevant search terms for cerebrovascular disease and for intensive BP lowering. This was a multicenter trial that included 140 hospitals in Japan; 1514 patients who had a history of stroke within the previous 3 years were approached, but 234 refused to give informed consent. INTERVENTIONS In total, 1280 patients were randomized 1:1 to BP control to less than 140/90 mm Hg (standard treatment) (n = 640) or to less than 120/80 mm Hg (intensive treatment) (n = 640). However, 17 patients never received intervention; therefore, 1263 patients assigned to standard treatment (n = 630) or intensive treatment (n = 633) were analyzed. main outcomes AND measures The primary outcome was stroke recurrence. RESULTS The trial was stopped early. Among 1263 analyzed patients (mean [SD] age, 67.2 [8.8] years; 69.4% male), 1257 of 1263 (99.5%) completed a mean (SD) of 3.9 (1.5) years of follow-up. The mean BP at baseline was 145.4/83.6 mm Hg. Throughout the overall follow-up period, the mean BP was 133.2/77.7 (95% Cl, 132.5-133.8/77.1-78.4) mm Hg in the standard group and 126.7/77.4 (95% Cl, 125.9-127.2/73.8-75.0) mm Hg in the intensive group. Ninety-one first recurrent strokes occurred. Nonsignificant rate reductions were seen for recurrent stroke in the intensive group compared with the standard group (hazard ratio [HR], 0.73; 95% Cl, 0.49-1.11; P = .15). When this finding was pooled in 3 previous relevant RCTs in a meta-analysis, the risk ratio favored intensive BP control (relative risk, 0.78; 95% Cl, 0.64-0.96; P = .02; absolute risk difference, -1.5%; 95% Cl, -2.6% to -0.4%; number needed to treat, 67; 95% Cl, 39-250). CONCLUSIONS AND RELEVANCE Intensive BP lowering tended to reduce stroke recurrence. The updated meta-analysis supports a target BP less than 130/80 mm Hg in secondary stroke prevention. TRIAL REGISTRATION ClinicalTrials.gov identifier: NCT01198496
机译:Indiantance收缩压干预试验(Sprint)表明,对于预防血管事件,细胞血压(BP)靶标少于120毫米Hg的优于小于140mm Hg。该试验排除了先前中风的患者;因此,用于次级行程预防的理想BP靶标仍然未知。目的评估密集型BP控制是否会达到较少的复发性笔划与标准BP控制。设计。设定和参与者随机化临床试验(RCT)标准的临床试验(RCT)在患有中风历史的患者的意图患者中。患者于2010年10月20日至12月7,2016之间注册。对于更新的元分析,通过医疗主题标题和脑血管病的相关搜索条件以及强化BP降低,搜索了PubMed和Cochrane中央库数据库。这是一项多中心试验,包括日本140家医院; 1514名患者在前3年内患有卒中史,但234岁拒绝提供知情同意。总共有1280名患者的干预率为1:1至BP对照至小于140/90 mm Hg(标准处理)(n = 640)或小于120/80mm hg(重症处理)(n = 640)。但是,17名患者从未收到过干预;因此,分析了1263名分配标准治疗(n = 630)或密集治疗(n = 633)的患者。主要结果和测量主要结果是中风复发。结果试验早期停止。在1263例分析的患者中(平均值[SD]年龄,67.2 [8.8岁),1263名(99.5%)的1257名(99.5%)完成了3.9(1.5)多年的平均值(SD)。基线的平均BP为145.4 / 83.6 mm Hg。在整个后续期间,平均BP为133.2 / 77.7(标准组95%CL,132.5-13.8 / 77.1-78.4)mm Hg,126.7 / 77.4(95%Cl,125.9-127.2 / 73.8-75.0 )在密集组中mm hg。发生九十一六次复发冲程。与标准组(危险比[HR],0.73; 95%CL,0.49-1.11; P = .15)相比,密集组中的复发性卒中的速率降低被视为不显着的速率降低。在荟萃分析中汇集了3个以前的相关RCT时,风险比率有利于强化BP控制(相对风险,0.78; 95%CL,0.64-0.96; P = .02;绝对风险差异,-1.5%; 95%Cl,-2.6%至-0.4%;治疗67; 95%Cl,39-250)所需的数量。结论和相关性强化BP降低倾向于减少卒中复发。更新的META分析支持次级笔划预防小于130/80 mm Hg的目标BP。试用注册CLINICLTIALS.GOV标识符:NCT01198496

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