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培哚普利对轻度早期缺血性脑卒中正常血压患者脑灌注和肾灌注的影响:一项随机对照试验

Effect of perindopril on cerebral and renal perfusion on normotensives in mild early ischaemic stroke: a randomized controlled trial.

作者信息

Nazir Fozia S, Overell James R, Bolster Alison, Hilditch Tom E, Lees Kennedy R

机构信息

Division of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

出版信息

Cerebrovasc Dis. 2005;19(2):77-83. doi: 10.1159/000082783. Epub 2004 Dec 17.

Abstract

BACKGROUND AND PURPOSE

Blood pressure reduction is central to secondary prevention after stroke, but the optimal time to start therapy is unknown. Cerebral autoregulation is impaired early after ischaemic insult, and any changes in systemic blood pressure may be reflected in cerebral perfusion. However, early initiation in hospital may better assure continued long-term treatment. We have investigated the effect of the angiotensin-converting enzyme inhibitor perindopril on blood pressure, global and focal cerebral blood flow (CBF) and glomerular filtration rate (GFR) in a normotensive acute stroke population.

METHODS

Twenty-five patients within 4-8 days of mild ischaemic stroke/transient ischaemic attack and with diastolic blood pressure 70-90 mm Hg were randomized to receive perindopril 2 or 4 mg daily versus placebo according to estimated GFR. Mean arterial blood pressure (MABP), internal carotid artery (ICA) flow and middle cerebral artery velocity (MCAv) were measured prior to dosing, over the following 24 h and at 2 weeks. Brain hexamethyl propylene amino oxide single photon emission computed tomography (SPECT) was performed before dosing and at estimated time of peak drug effect (6-8 h after first dose). GFR measurement using a (51)Cr-ethylene diamine tetraacetic acid technique was undertaken prior to medication and repeated at 2 weeks.

RESULTS

MABP was reduced throughout the first 24 h with a mean MABP reduction of 9.3 mm Hg (95% CI 7.4-11.3 mm Hg), maximal placebo corrected fall of 12.5 mm Hg at 10 h post-dose, p = 0.005. No significant change occurred in ICA flow, MCAv or CBF measured by SPECT: change from baseline in symptomatic hemisphere CBF was -0.02 (SD 3.11) ml/100 g/min (treated group) compared with 0 (SD 3.01) (placebo group). Similarly, no significant change was observed in cortical CBF. Mean within-group change in GFR was 2.7 +/- 10.1 in the treated group and -4.3 +/- 6.7 in the placebo group (p = NS).

DISCUSSION

Antihypertensive therapy with perindopril may be introduced in the first week after mild ischaemic stroke in normotensive patients without affecting global or regional CBF or affecting GFR.

摘要

背景与目的

降低血压是卒中后二级预防的核心,但开始治疗的最佳时机尚不清楚。缺血性损伤后早期脑自动调节功能受损,全身血压的任何变化都可能反映在脑灌注上。然而,在医院早期开始治疗可能更好地确保长期持续治疗。我们研究了血管紧张素转换酶抑制剂培哚普利对血压正常的急性卒中患者的血压、全脑和局部脑血流量(CBF)以及肾小球滤过率(GFR)的影响。

方法

25例轻度缺血性卒中/短暂性脑缺血发作后4 - 8天且舒张压为70 - 90 mmHg的患者,根据估计的GFR随机分为每日接受2 mg或4 mg培哚普利组与安慰剂组。在给药前、随后的24小时内及2周时测量平均动脉血压(MABP)、颈内动脉(ICA)血流和大脑中动脉速度(MCAv)。在给药前及估计的药物效应峰值时间(首剂后6 - 8小时)进行脑六甲基丙烯胺氧化物单光子发射计算机断层扫描(SPECT)。用药前采用(51)Cr - 乙二胺四乙酸技术测量GFR,并在2周时重复测量。

结果

在最初的24小时内MABP持续降低,平均MABP降低9.3 mmHg(95%可信区间7.4 - 11.3 mmHg),给药后10小时安慰剂校正后的最大降幅为12.5 mmHg,p = 0.005。ICA血流、MCAv或SPECT测量的CBF无显著变化:治疗组有症状半球CBF相对于基线的变化为 - 0.02(标准差3.11)ml/100 g/min,而安慰剂组为0(标准差3.01)。同样,皮质CBF也无显著变化。治疗组GFR的组内平均变化为2.7±10.1,安慰剂组为 - 4.3±6.7(p = 无显著性差异)。

讨论

对于血压正常的患者,在轻度缺血性卒中后的第一周即可开始使用培哚普利进行降压治疗,且不影响全脑或局部CBF,也不影响GFR。

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