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使用冷冻球囊技术对心房颤动患者进行消融时脑动脉循环中的微栓塞——一项前瞻性观察研究的方案与方法

Microembolizations in the Arterial Cerebral Circulation in Patients with Atrial Fibrillation Ablation Using the Cryoballoon Technique-Protocol and Methodology of a Prospective Observational Study.

作者信息

Erkapic Damir, Aleksic Marko, Roussopoulos Konstantinos, Weipert Kay Felix, Sözener Korkut, Kostev Karel, Allendörfer Jens, Rosenbauer Josef, Guenduez Dursun, Tanislav Christian

机构信息

Department of Cardiology, Rhythmology and Angiology, Diakonie Klinikum Jung Stilling, 57074 Siegen, Germany.

Department of Cardiology and Angiology, University Clinic of Giessen, 35392 Giessen, Germany.

出版信息

Diagnostics (Basel). 2023 May 8;13(9):1660. doi: 10.3390/diagnostics13091660.

Abstract

There is considerable uncertainty regarding the impact of microembolic signals (MESs) on neuropsychological abilities in patients receiving pulmonary vein isolation and beyond using the cryoballoon technique. We conducted the largest prospective observational study on this topic, providing insights into the gradual unmasking of procedure-related MESs and their impacts on neuropsychological outcomes. MESs were continuously detected periprocedurally using transcranial Doppler ultrasonography. Neuropsychological status was evaluated comprehensively using the CERAD Plus test battery, which consists of 11 neuropsychological subtests. Patients with atrial fibrillation were included in the study with an equal distribution (50:50) of paroxysmal or persistent presentations. Of 167 consecutive eligible patients, 100 were included within the study enrollment period from February 2021 to August 2022. The study, including the documentation of all follow-up visits, ended in November 2022. This paper focuses on describing the study protocol and methodology and presenting the baseline data.

摘要

关于微栓塞信号(MESs)对接受肺静脉隔离及使用冷冻球囊技术的患者神经心理能力的影响,存在相当大的不确定性。我们针对这一主题开展了规模最大的前瞻性观察性研究,深入了解与手术相关的MESs的逐渐显现及其对神经心理结果的影响。在围手术期使用经颅多普勒超声持续检测MESs。使用由11个神经心理子测试组成的CERAD Plus测试组合全面评估神经心理状态。纳入心房颤动患者,阵发性或持续性表现的分布均衡(50:50)。在167例连续符合条件的患者中,100例在2021年2月至2022年8月的研究入组期内纳入研究。该研究包括所有随访记录,于2022年11月结束。本文重点描述研究方案和方法,并呈现基线数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d76/10178285/cd13354fe13c/diagnostics-13-01660-g001.jpg

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