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强化降压与脑出血中的斑点征:一项随机临床试验的二次分析

Intensive Blood Pressure Reduction and Spot Sign in Intracerebral Hemorrhage: A Secondary Analysis of a Randomized Clinical Trial.

作者信息

Morotti Andrea, Brouwers H Bart, Romero Javier M, Jessel Michael J, Vashkevich Anastasia, Schwab Kristin, Afzal Mohammad Rauf, Cassarly Christy, Greenberg Steven M, Martin Renee Hebert, Qureshi Adnan I, Rosand Jonathan, Goldstein Joshua N

机构信息

Division of Neurocritical Care and Emergency Neurology, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston.

J. P. Kistler Stroke Research Center, Massachusetts General Hospital, Harvard Medical School, Boston.

出版信息

JAMA Neurol. 2017 Aug 1;74(8):950-960. doi: 10.1001/jamaneurol.2017.1014.

Abstract

IMPORTANCE

The computed tomographic angiography (CTA) spot sign is associated with intracerebral hemorrhage (ICH) expansion and may mark those patients most likely to benefit from intensive blood pressure (BP) reduction.

OBJECTIVE

To investigate whether the spot sign is associated with ICH expansion across a wide range of centers and whether intensive BP reduction decreases hematoma expansion and improves outcome in patients with ICH and a spot sign.

DESIGN, SETTING, AND PARTICIPANTS: SCORE-IT (Spot Sign Score in Restricting ICH Growth) is a preplanned prospective observational study nested in the Antihypertensive Treatment of Acute Cerebral Hemorrhage II (ATACH-II) randomized clinical trial. Participants included consecutive patients with primary ICH who underwent a CTA within 8 hours from onset at 59 sites from May 15, 2011, through December 19, 2015. Data were analyzed for the present study from July 1 to August 31, 2016.

MAIN OUTCOMES AND MEASURES

Patients in ATACH-II were randomized to intensive (systolic BP target, <140 mm Hg) vs standard (systolic BP target, <180 mm Hg) BP reduction within 4.5 hours from onset. Expansion of ICH was defined as hematoma growth of greater than 33%, and an unfavorable outcome was defined as a 90-day modified Rankin Scale score of 4 or greater (range, 0-6). The association among BP reduction, ICH expansion, and outcome was investigated with multivariable logistic regression.

RESULTS

A total of 133 patients (83 men [62.4%] and 50 women [37.6%]; mean [SD] age, 61.9 [13.1] years) were included. Of these, 53 (39.8%) had a spot sign, and 24 of 123 without missing data (19.5%) experienced ICH expansion. The spot sign was associated with expansion with sensitivity of 0.54 (95% CI, 0.34-0.74) and specificity of 0.63 (95% CI, 0.53-0.72). After adjustment for potential confounders, intensive BP treatment was not associated with a significant reduction of ICH expansion (relative risk, 0.83; 95% CI, 0.27-2.51; P = .74) or improved outcome (relative risk of 90-day modified Rankin Scale score ≥4, 1.24; 95% CI, 0.53-2.91; P = .62) in spot sign-positive patients.

CONCLUSIONS AND RELEVANCE

The predictive performance of the spot sign for ICH expansion was lower than in prior reports from single-center studies. No evidence suggested that patients with ICH and a spot sign specifically benefit from intensive BP reduction.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT01176565.

摘要

重要性

计算机断层血管造影(CTA)斑点征与脑出血(ICH)扩大相关,可能标识出最有可能从强化降压治疗中获益的患者。

目的

研究斑点征在广泛的多个中心中是否与ICH扩大相关,以及强化降压是否能减少血肿扩大并改善有斑点征的ICH患者的预后。

设计、地点和参与者:SCORE-IT(限制ICH生长的斑点征评分)是一项预先计划的前瞻性观察性研究,嵌套于急性脑出血降压治疗II(ATACH-II)随机临床试验中。参与者包括2011年5月15日至2015年12月19日期间在59个地点发病8小时内接受CTA检查的连续性原发性ICH患者。本研究于2016年7月1日至8月31日对数据进行分析。

主要结局和测量指标

ATACH-II试验中的患者在发病4.5小时内被随机分为强化降压组(收缩压目标值<140 mmHg)和标准降压组(收缩压目标值<180 mmHg)。ICH扩大定义为血肿增长超过33%,不良预后定义为90天改良Rankin量表评分为4分或更高(范围为0 - 6)。采用多变量逻辑回归研究降压、ICH扩大和预后之间的关联。

结果

共纳入133例患者(83例男性[62.4%]和50例女性[37.6%];平均[标准差]年龄为61.9[13.1]岁)。其中,53例(39.8%)有斑点征,123例无缺失数据的患者中有24例(19.5%)发生ICH扩大。斑点征与ICH扩大相关,敏感性为0.54(95%CI,0.34 - 0.74),特异性为0.63(95%CI,0.53 - 0.72)。在对潜在混杂因素进行校正后,强化血压治疗与斑点征阳性患者的ICH扩大显著减少(相对风险,0.83;95%CI,0.27 - 2.51;P = 0.74)或预后改善(90天改良Rankin量表评分≥4的相对风险,1.24;95%CI,0.53 - 2.91;P = 0.62)无关。

结论与相关性

斑点征对ICH扩大的预测性能低于单中心研究的既往报告。没有证据表明有斑点征的ICH患者能从强化降压中特别获益。

试验注册

clinicaltrials.gov标识符:NCT01176565。

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