Division of Neurology, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
JAMA Neurol. 2018 Jul 1;75(7):850-859. doi: 10.1001/jamaneurol.2018.0454.
Response to intensive blood pressure (BP) lowering in acute intracerebral hemorrhage (ICH) might vary with the degree of underlying cerebral small vessel disease.
To characterize cerebral microbleeds (CMBs) in acute ICH and to assess the potential for interaction between underlying small vessel disease (as indicated by CMB number and location) and assignment to acute intensive BP targeting for functional outcomes and hematoma expansion.
DESIGN, SETTING, AND PARTICIPANTS: Preplanned subgroup analyses in the Antihypertensive Treatment of Acute Cerebral Hemorrhage 2 (ATACH-2) trial were performed. The ATACH-2 was an open-label international randomized clinical trial that investigated optimal acute BP lowering in 1000 patients with acute ICH. Analyses followed the intent-to-treat paradigm. Participants were enrolled between May 2011 and September 2015 and followed up for 3 months. Eligible participants were aged at least 18 years with ICH volumes less than 60 mL on computed tomography (CT) and a Glasgow Coma Scale score of at least 5 on initial assessment, in whom study drug could be initiated within 4.5 hours of symptom onset. Eight hundred thirty-three participants were excluded, leaving 167 who had an interpretable axial T2*-weighted gradient-recalled echo sequence on magnetic resonance imaging to assess CMBs for inclusion in these subgroup analyses.
The primary outcome of interest was death or disability (modified Ranking Scale score, 4-6) at 3 months. The secondary outcome of interest was hematoma volume expansion of at least 33% on a CT scan obtained 24 hours after randomization compared with the entry scan.
A total of 167 patients were included; their mean (SD) age was 61.9 (13.2) years, and 98 (58.7%) were male. Cerebral microbleeds were present in 120 patients. Forty-six of 157 (29.3%) patients had poor outcome (modified Ranking Scale score, ≥4), and hematoma expansion was observed in 29 of 144 (20.1%) patients. Risk of poor outcome was similar for those assigned to intensive vs standard acute BP lowering among patients with CMBs (relative risk, 1.19; 95% CI, 0.61-2.33; P = .61) and those without CMBs (relative risk, 1.42; 95% CI, 0.43-4.70; P = .57), and no significant interaction was observed (interaction coefficient, 0.18; 95% CI, -1.20 to 1.55; P = .80). Risk of hematoma expansion was also similar, and no significant interaction between treatment and CMBs was observed (interaction coefficient, 0.62; 95% CI, -1.08 to 2.31; P = .48).
Cerebral microbleeds are highly prevalent among patients with ICH but do not seem to influence response to acute intensive BP treatment.
ClinicalTrials.gov Identifier: NCT01176565.
急性脑出血(ICH)患者强化降压治疗的反应可能因潜在的脑小血管疾病程度而异。
对急性 ICH 患者的脑微出血(CMB)进行特征描述,并评估潜在的小血管疾病(以 CMB 数量和位置表示)与急性强化血压目标治疗之间的潜在相互作用,以评估功能结局和血肿扩大。
设计、地点和参与者:对 Antihypertensive Treatment of Acute Cerebral Hemorrhage 2(ATACH-2)试验进行了预先计划的亚组分析。ATACH-2 是一项开放标签的国际随机临床试验,研究了 1000 例急性 ICH 患者的最佳急性血压降低。分析遵循意向治疗原则。参与者于 2011 年 5 月至 2015 年 9 月期间入组,并随访 3 个月。符合条件的参与者年龄至少 18 岁,CT 显示 ICH 体积小于 60mL,初始评估时格拉斯哥昏迷量表评分为至少 5 分,可在症状发作后 4.5 小时内开始研究药物治疗。833 名参与者被排除在外,留下 167 名有可解释的轴向 T2*-weighted gradient-recalled echo 序列的磁共振成像,用于评估 CMB,以纳入这些亚组分析。
主要关注的结局是 3 个月时的死亡或残疾(改良 Rankin 量表评分,4-6)。次要关注的结局是与入组扫描相比,随机分组后 24 小时获得的 CT 扫描显示血肿体积扩大至少 33%。
共纳入 167 名患者;他们的平均(标准差)年龄为 61.9(13.2)岁,98 名(58.7%)为男性。120 名患者存在 CMB。157 名患者中有 46 名(29.3%)预后不良(改良 Rankin 量表评分,≥4),29 名患者(20.1%)观察到血肿扩大。在有 CMB 的患者和没有 CMB 的患者中,强化急性降压治疗与标准急性降压治疗的不良预后风险相似(相对风险,1.19;95%CI,0.61-2.33;P=0.61),也没有观察到显著的交互作用(交互系数,0.18;95%CI,-1.20 至 1.55;P=0.80)。血肿扩大的风险也相似,治疗与 CMB 之间也没有观察到显著的交互作用(交互系数,0.62;95%CI,-1.08 至 2.31;P=0.48)。
ICH 患者中 CMB 非常普遍,但似乎不会影响对急性强化降压治疗的反应。
ClinicalTrials.gov 标识符:NCT01176565。