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灌注压力与脑梗死(PPCI)试验——体外循环期间平均动脉压对预防心脏手术后脑并发症的重要性:一项随机对照试验的研究方案

Perfusion Pressure Cerebral Infarct (PPCI) trial - the importance of mean arterial pressure during cardiopulmonary bypass to prevent cerebral complications after cardiac surgery: study protocol for a randomised controlled trial.

作者信息

Vedel Anne G, Holmgaard Frederik, Rasmussen Lars Simon, Paulson Olaf B, Thomsen Carsten, Danielsen Else Rubæk, Langkilde Annika, Goetze Jens P, Lange Theis, Ravn Hanne Berg, Nilsson Jens C

机构信息

Department of Cardiothoracic Anaesthesiology, Heart Centre, Rigshospitalet, University of Copenhagen, Blegdamsvej 9, DK-2100, Copenhagen, Denmark.

Department of Anaesthesia, Centre of Head and Orthopaedics, Rigshospitalet, University of Copenhagen, Blegdamsvej 9, DK-2100, Copenhagen, Denmark.

出版信息

Trials. 2016 May 17;17(1):247. doi: 10.1186/s13063-016-1373-6.

Abstract

BACKGROUND

Debilitating brain injury occurs in 1.6-5 % of patients undergoing cardiac surgery with cardiopulmonary bypass. Diffusion-weighted magnetic resonance imaging studies have reported stroke-like lesions in up to 51 % of patients after cardiac surgery. The majority of the lesions seem to be caused by emboli, but inadequate blood flow caused by other mechanisms may increase ischaemia in the penumbra or cause watershed infarcts. During cardiopulmonary bypass, blood pressure can be below the lower limit of cerebral autoregulation. Although much debated, the constant blood flow provided by the cardiopulmonary bypass system is still considered by many as appropriate to avoid cerebral ischaemia despite the low blood pressure.

METHODS/DESIGN: The Perfusion Pressure Cerebral Infarct trial is a single-centre superiority trial with a blinded outcome assessment. The trial is randomising 210 patients with coronary vessel and/or valve disease and who are undergoing cardiac surgery with the use of cardiopulmonary bypass. Patients are stratified by age and surgical procedure and are randomised 1:1 to either an increased mean arterial pressure (70-80 mmHg) or 'usual practice' (40-50 mmHg) during cardiopulmonary bypass. The cardiopulmonary bypass pump flow is fixed and set at 2.4 L/minute/m(2) body surface area plus 10-20 % in both groups. The primary outcome measure is the volume of the new ischaemic cerebral lesions (in mL), expressed as the difference between a baseline, diffusion-weighted, magnetic resonance imaging scan and an equal scan conducted 3-6 days postoperatively. Secondary endpoints are the total number of new ischaemic cerebral lesions, postoperative cognitive dysfunction at discharge and 3 months postoperatively, diffuse cerebral injury evaluated by magnetic resonance spectroscopy and selected biochemical markers of cerebral injury. The sample size will enable us to detect a 50 % reduction in the primary outcome measure in the intervention compared to the control group at a significance level of 0.05 and with a power of 0.80.

DISCUSSION

This is the first clinical randomised study to evaluate whether the mean arterial pressure level during cardiopulmonary bypass influences the development of brain injuries that are detected by diffusion-weighted magnetic resonance imaging.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT02185885 . Registered on 7 July 2014.

摘要

背景

在接受体外循环心脏手术的患者中,1.6% - 5%会发生致残性脑损伤。弥散加权磁共振成像研究报告称,心脏手术后高达51%的患者出现类似中风的病变。大多数病变似乎是由栓子引起的,但其他机制导致的血流不足可能会增加半暗带的缺血情况或导致分水岭梗死。在体外循环期间,血压可能低于脑自动调节的下限。尽管存在诸多争议,但许多人仍认为体外循环系统提供的恒定血流适合避免脑缺血,尽管血压较低。

方法/设计:灌注压力脑梗死试验是一项单中心优效性试验,采用盲法评估结果。该试验将210例患有冠状动脉和/或瓣膜疾病且正在接受体外循环心脏手术的患者进行随机分组。患者按年龄和手术方式分层,在体外循环期间按1:1随机分为平均动脉压升高组(70 - 80 mmHg)或“常规做法”组(40 - 50 mmHg)。两组的体外循环泵流量固定,设定为2.4 L/分钟/平方米体表面积加10% - 20%。主要结局指标是新的缺血性脑病变体积(以毫升为单位),表示为基线弥散加权磁共振成像扫描与术后3 - 6天进行的同等扫描之间的差异。次要终点包括新的缺血性脑病变总数、出院时和术后3个月的术后认知功能障碍、通过磁共振波谱评估的弥漫性脑损伤以及选定的脑损伤生化标志物。样本量将使我们能够在显著性水平为0.05、检验效能为0.80的情况下,检测到干预组与对照组相比主要结局指标降低50%。

讨论

这是第一项评估体外循环期间平均动脉压水平是否会影响通过弥散加权磁共振成像检测到的脑损伤发生情况的临床随机研究。

试验注册

ClinicalTrials.gov,NCT02185885。于2014年7月7日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b5/4869311/2cfb2268edd1/13063_2016_1373_Fig1_HTML.jpg

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