Bellolio M Fernanda, Gilmore Rachel M, Stead Latha G
Department of Emergency Medicine, Mayo Clinic, Genrose Building-G410, 200 First Street SW, Rochester, Minnesota, USA, 55905.
Cochrane Database Syst Rev. 2011 Sep 7(9):CD005346. doi: 10.1002/14651858.CD005346.pub3.
Patients with hyperglycaemia concomitant with an acute stroke have greater stroke severity and greater functional impairment when compared to those with normoglycaemia at stroke presentation.
To determine whether maintaining serum glucose within a specific normal range (4 to 7.5 mmol/L) in the first 24 hours of acute ischaemic stroke influences outcome.
We searched the Cochrane Stroke Group Trials Register (June 2010), CENTRAL (The Cochrane Library 2010, Issue 2), MEDLINE (1950 to June 2010), EMBASE (1980 to June 2010), CINAHL (1982 to June 2010), Science Citation Index (1900 to June 2010), and Web of Science (ISI Web of Knowledge) (1993 to June 2010). In an effort to identify further published, unpublished and ongoing trials we searched ongoing trials registers and SCOPUS.
Eligible studies were randomised controlled trials comparing intensively monitored insulin therapy versus usual care in adult patients with acute ischaemic stroke.
Two review authors independently extracted the study characteristics, study quality, and data to estimate the odds ratio (OR) and 95% confidence interval (CI), mean difference (MD) and standardised mean difference (SMD) of outcome measures.
We included seven trials involving 1296 participants (639 participants in the intervention group and 657 in the control group). We found that there was no difference between treatment and control groups in the outcome of death or disability and dependence (OR 1.00, 95% CI 0.78 to 1.28) or final neurological deficit (SMD -0.12, 95% CI -0.23 to 0.00). The rate of symptomatic hypoglycaemia was higher in the intervention group (OR 25.9, 95% CI 9.2 to 72.7). In the subgroup analyses of diabetes mellitus (DM) versus non-DM, we found no difference for the outcomes of death and dependency or neurological deficit.
AUTHORS' CONCLUSIONS: With the current evidence, we found that the administration of intravenous insulin with the objective of maintaining serum glucose within a specific range in the first hours of acute ischaemic stroke does not provide benefit in terms of functional outcome, death, or improvement in final neurological deficit and significantly increased the number of hypoglycaemic episodes. Specifically, those who were maintained within a more tight range of glycaemia with intravenous insulin experienced a greater risk of symptomatic and asymptomatic hypoglycaemia than those individuals in the control group.
与急性卒中发作时血糖正常的患者相比,伴有高血糖的急性卒中患者卒中严重程度更高,功能障碍更严重。
确定在急性缺血性卒中的最初24小时内将血清葡萄糖维持在特定正常范围(4至7.5毫摩尔/升)是否会影响预后。
我们检索了Cochrane卒中组试验注册库(2010年6月)、CENTRAL(Cochrane图书馆2010年第2期)、MEDLINE(1950年至2010年6月)、EMBASE(1980年至2010年6月)、CINAHL(1982年至2010年6月)、科学引文索引(1900年至2010年6月)以及科学网(ISI知识网络)(1993年至2010年6月)。为了识别更多已发表、未发表及正在进行的试验,我们检索了正在进行的试验注册库和SCOPUS。
符合条件的研究为随机对照试验,比较了对成年急性缺血性卒中患者进行强化监测的胰岛素治疗与常规治疗。
两位综述作者独立提取研究特征、研究质量和数据,以估计结局指标的比值比(OR)和95%置信区间(CI)、均值差(MD)和标准化均值差(SMD)。
我们纳入了7项试验,涉及1296名参与者(干预组639名参与者,对照组657名参与者)。我们发现,治疗组和对照组在死亡、残疾和依赖结局(OR 1.00,95%CI 0.78至1.28)或最终神经功能缺损方面无差异(SMD -0.12,95%CI -0.23至0.00)。干预组有症状性低血糖发生率更高(OR 25.9,95%CI 9.2至72.7)。在糖尿病(DM)与非糖尿病亚组分析中,我们发现死亡、依赖或神经功能缺损结局方面无差异。
根据目前的证据,我们发现,在急性缺血性卒中最初数小时内给予静脉胰岛素以将血清葡萄糖维持在特定范围内,在功能结局、死亡或最终神经功能缺损改善方面并无益处,且显著增加了低血糖发作次数。具体而言,与对照组个体相比,通过静脉胰岛素将血糖维持在更严格范围内的患者发生有症状和无症状低血糖的风险更高。