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[患有神经铁沉积脑白质营养不良(NBIA)患者的麻醉:伴有脑铁蓄积的神经退行性变]

[Anesthesia in patients with NBIA : Neurodegeneration with brain iron accumulation].

作者信息

Warnecke T, Schmitz J, Kerkhoff S, Hinkelbein J

机构信息

Klinik für Anästhesiologie, Intensiv- und Notfallmedizin, Evangelisches Klinikum Niederrhein, Fahrner Straße 133, 47169, Duisburg, Deutschland.

Klinik für Anästhesiologie und Operative Intensivmedizin, Universitätsklinikum Köln (AöR), Köln, Deutschland.

出版信息

Anaesthesist. 2018 Nov;67(11):871-877. doi: 10.1007/s00101-018-0488-4.

Abstract

BACKGROUND

Neurodegeneration with brain iron accumulation (NBIA) forms a group of rare hereditary diseases with rapid neurodegenerative progression due to an abnormal accumulation of iron in the basal ganglia. This causes extrapyramidal symptoms as well as dystonia and mental retardation. The most common form of NBIA is pantothenate kinase-associated neurodegeneration (PKAN, formerly Hallervorden-Spatz syndrome). There are multiple anesthesiological challenges with great implications for the clinical routine, particularly regarding the preparation for general anesthesia and the premedication visits. As with other orphan diseases, the available recommendations are mainly based on case reports.

OBJECTIVE AND METHODS

This article gives a short overview of complications associated with NBIA pertaining to general anesthesia. This includes anesthesia-relevant clinical symptoms and perioperative management. The published literature and case reports (available on PubMed) were reviewed to extract a set of recommendations.

RESULTS

So far only a few reports have included the anesthesia management of NBIA patients. Most of them refer to PKAN as the predominant type (50% of cases). Recommendations were found on www.orphananesthesia.eu and consensus guidelines on PKAN in general. In particular, dystonia-related restrictions in the maxillofacial area can complicate airway management and cause difficulties with respect to intubation. Furthermore, local or regional anesthesia as the sole anesthesia technique is not eligible/viable due to the reduced compliance of the patient. Special attention should be paid to a timely premedication visit and evaluation to ensure sufficient time to safely plan and prepare the anesthetic procedure.

CONCLUSION

The handling of NBIA patients requires good preparation, including an interdisciplinary team and customized time management. In principle, both general anesthesia as a balanced method and total intravenous anesthesia (TIVA) seem to be possible/viable options. The main focus is on airway management. Even after brief sedation in the context of diagnostic measures, the patient should be monitored for longer than usual.

摘要

背景

脑铁沉积神经变性病(NBIA)是一组罕见的遗传性疾病,由于基底神经节中铁异常蓄积,导致神经变性快速进展。这会引起锥体外系症状以及肌张力障碍和智力发育迟缓。NBIA最常见的形式是泛酸激酶相关神经变性病(PKAN,原称Hallervorden-Spatz综合征)。存在多种麻醉学挑战,对临床常规有重大影响,特别是在全身麻醉准备和术前访视方面。与其他罕见病一样,现有建议主要基于病例报告。

目的和方法

本文简要概述了与NBIA相关的全身麻醉并发症。这包括与麻醉相关的临床症状和围手术期管理。回顾已发表的文献和病例报告(可在PubMed上获取)以提取一组建议。

结果

到目前为止,仅有少数报告涉及NBIA患者的麻醉管理。其中大多数将PKAN作为主要类型(占病例的50%)。在www.orphananesthesia.eu上找到了相关建议以及关于PKAN的共识指南。特别是,颌面区域与肌张力障碍相关的限制会使气道管理复杂化,并在插管方面造成困难。此外,由于患者依从性降低,局部或区域麻醉作为唯一的麻醉技术不合适/不可行。应特别注意及时进行术前访视和评估,以确保有足够时间安全地规划和准备麻醉程序。

结论

处理NBIA患者需要做好准备,包括跨学科团队和定制的时间管理。原则上,全身麻醉作为一种平衡方法和全静脉麻醉(TIVA)似乎都是可行的选择。主要重点是气道管理。即使在诊断措施中进行短暂镇静后,也应比平时更长时间地监测患者。

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