超高压瓣膜对持续性症状性分流过度引流的作用。

Iván Federico Narváez Moscoso, Bienvenido Ros López, Sara Iglesia Moroño, Julia Casado Ruiz, Raquel Simón Wolter, Miguel Ángel Arráez Sánchez
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引用次数: 0

摘要

简介分流过度引流是脑室腹腔分流术的长期并发症之一。治疗难治性病例可能需要进一步提高瓣膜开放压力和反虹吸装置。本文旨在描述这一组合在部分患者中的效果:方法:回顾性队列研究,包括 2003-2022 年间的 18 名儿科患者。这些患者之前使用的分流管被替换为 SOPHYSA Polaris® SPVA-300 瓣膜和升级的固定或可调式反重力装置的组合。研究人员收集了以下变量:脑积水病因、首次分流术的年龄和瓣膜类型、分流术翻修次数、其他外科手术、纳入时的年龄、临床和放射学结果以及随访时间。对定量变量采用均值、中位数和范围进行描述性分析,对定性数据采用百分比和频率进行分析:首次分流的中位年龄为两个月(0-67)。纳入前分流手术的平均次数为三次。有七名患者尝试过移除分流器,但未获成功;有两名患者接受了 ETV,并取得了暂时的成功。两名患者曾进行过颅骨扩张手术。患者入院时的平均年龄为 9.1 岁(2.7-15.2 岁)。更换和升级分流系统后,94.4%(17/18)的患者临床症状得到改善,83.3%(15/18)的患者放射学症状得到改善。中位随访时间为 21 个月:结论:在考虑采取更具侵入性的治疗措施之前,通过结合使用超高压阀门和升级后的在线反虹吸装置来优化分流系统,是治疗难治性症状性分流过度引流的有效且安全的策略。
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Utility of very high-pressure valves in persistent symptomatic shunt overdrainage.

Introduction: Shunt overdrainage is one of the long-term complications associated with ventriculoperitoneal shunts. Treatment of refractory cases may require further upgrading of both the valve opening pressure and antisiphon device. The aim of this paper is to describe the results of this combination in a selected group of patients.

Methods: Retrospective cohort study that included 18 pediatric patients between 2003-2022. Previous shunts were exchanged for the combination of a SOPHYSA Polaris® SPVA-300 valve and upgraded fixed or adjustable antigravitatory devices. The following variables were collected: etiology of the hydrocephalus, age at first shunt and type of valve, number of shunt revisions, other surgical procedures, age at inclusion, clinical and radiological outcomes, and follow-up time. A descriptive analysis was done with means, medians and ranges for quantitative variables; percentages and frequencies for the analysis of qualitative data.

Results: The median age at first shunt was two months (0-67). The mean number of shunt revisions before inclusion was three. Shunt removal was attempted in seven patients without success; temporary success was observed in two patients who underwent ETV. Two patients had previous cranial expansions. The mean age at inclusion was 9.1 years (2.7-15.2). After the shunt system was exchanged and upgraded, clinical improvement was observed in 94.4% (17/18) of patients, and radiological improvement was observed in 83.3% (15/18) of patients. The median follow-up was 21 months.

Conclusions: Before considering more invasive therapeutic measures, shunt system optimization by the combination of very high-pressure valves and upgraded in-line antisiphon devices is a valid and safe strategy for refractory symptomatic shunt overdrainage.

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