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经皮经子宫胎儿脑内栓塞治疗有紧急新生儿失代偿风险的静脉汇管畸形:一项安全性和可行性临床试验的研究方案。

Percutaneous transuterine fetal cerebral embolisation to treat vein of Galen malformations at risk of urgent neonatal decompensation: study protocol for a clinical trial of safety and feasibility.

机构信息

Department of Neurosurgery, Boston Children's Hospital, Boston, Massachusetts, USA.

Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

BMJ Open. 2022 May 24;12(5):e058147. doi: 10.1136/bmjopen-2021-058147.

Abstract

INTRODUCTION

Although endovascular techniques have improved outcomes in vein of Galen malformations (VOGM), there is still a high rate of morbidity and mortality, particularly among cases with decompensation in the neonatal period. The dimension of the draining venous sinus on fetal imaging correlates with the risk of neonatal decompensation. In fetuses within this high-risk group who do not have end-organ injury, there is a theoretical therapeutic opportunity to reduce the arteriovenous shunt before the normal physiological changes of birth precipitate decompensation. This study investigates the safety and potential benefit of treating a VOGM in utero, which has not been previously studied.

METHODS AND ANALYSIS

This study aims to enroll 20 subjects: pregnant women with a fetus harbouring a high-risk VOGM (defined on MRI by a narrowest medial-lateral width greater than 8 mm in the draining venous sinus). Unfortunately, the subset of fetuses with in utero end-organ injury is ineligible, because the late stage of pathology is not amenable to recovery from a cerebrovascular intervention, likely not even in utero. This study aims to alter the physiology before such developments accrue.At or after 23 weeks of gestation, a transuterine transposterior fontanelle needle puncture to the torcular allows ultrasound-guided deployment of coils to embolise the draining venous malformation.This study has 97.5% power to detect major safety events at 30% or greater, and 80% power to detect a reduction in the rate of neonatal intervention from 80% to 30%. In the staged study design, an interval evaluation after 11 patients invokes study termination if safety events occur above the allowed threshold.

ETHICS AND DISSEMINATION

The institutional review boards at Mass General Brigham and Boston Children's Hospital (BCH) reviewed and approved this protocol. The BCH Department of Radiology and a patient family philanthropic donation fund this study. The trial results will be published in peer-reviewed journals and presented at scientific conferences.

TRIAL REGISTRATION NUMBER

NCT04434729.

摘要

简介

尽管血管内技术已改善了静脉巨腔畸形(VOGM)的预后,但仍存在较高的发病率和死亡率,尤其是在新生儿期失代偿的病例中。胎儿影像学上引流静脉窦的尺寸与新生儿失代偿的风险相关。在没有终末器官损伤的高危胎儿中,在出生的正常生理变化引发失代偿之前,有一个通过减少动静脉分流来治疗 VOGM 的理论治疗机会。本研究旨在探讨以前未研究过的宫内治疗 VOGM 的安全性和潜在益处。

方法和分析

本研究计划纳入 20 名受试者:怀有高危 VOGM 胎儿的孕妇(在 MRI 上定义为引流静脉窦的最窄内-外侧宽度大于 8mm)。不幸的是,由于病理的晚期阶段不能通过脑血管介入来恢复,即使在宫内也不行,因此不能将有宫内终末器官损伤的胎儿亚组纳入研究。本研究旨在在这些情况发生之前改变生理状态。在 23 周或之后,经子宫经后囟门针穿刺到脑上池,允许在超声引导下放置线圈以栓塞引流静脉畸形。本研究有 97.5%的效能在 30%或更高的水平上检测主要安全事件,80%的效能在降低新生儿干预率从 80%降至 30%。在分期研究设计中,如果安全事件发生在允许的阈值以上,在前 11 名患者的间隔评估后将终止研究。

伦理和传播

马萨诸塞州综合医院布列根和妇女医院(BCH)的机构审查委员会审查并批准了该方案。BCH 放射科和一个患者家庭慈善捐赠基金资助了这项研究。试验结果将发表在同行评议的期刊上,并在科学会议上报告。

试验注册号

NCT04434729。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a9a/9174825/4818d05273e1/bmjopen-2021-058147f01.jpg

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