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阿诺德-奇亚里畸形伴呼吸衰竭患者的静脉镇静

Intravenous Sedation in Arnold-Chiari Malformation With Respiratory Failure.

作者信息

Shionoya Yoshiki, Nakamura Eishi, Goi Takahiro, Nakamura Kiminari, Sunada Katsuhisa

机构信息

Department of Dental Anesthesia, Nippon Dental University Hospital, Tokyo, Japan.

Department of Dental Anesthesiology, Nippon Dental University School of Life Dentistry, Tokyo, Japan.

出版信息

Anesth Prog. 2019 Spring;66(1):37-41. doi: 10.2344/anpr-66-01-06.

DOI:10.2344/anpr-66-01-06
PMID:30883227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6424169/
Abstract

Type II Arnold-Chiari malformation (ACM) is an abnormality in which the cerebellum, pons, and medulla oblongata are displaced downward into the spinal cord. Type II ACM is often complicated by respiratory depression, sleep-disordered breathing, and deglutition disorder as a result of medullary dysfunction and impairment of the lower cranial nerves. Bending and stretching of the neck is restricted, and anesthetic management is problematic in patients with the disorder. We performed dental treatment twice under intravenous sedation in a patient with intellectual disability with type II ACM complicated by hypercapnic respiratory failure. Propofol was used for the first sedation procedure. Repeated bouts of respiratory depression occurred on that occasion, so the airway was managed manually by lifting the jaw. However, aspiration pneumonitis occurred postoperatively. A combination of dexmedetomidine and midazolam was used for sedation on the second occasion, and the intervention was completed uneventfully without any respiratory depression. Our experience with this patient highlights the need for selection of an agent for intravenous sedation that does not require neck extension and has minimal effect on respiration in patients with type II ACM, who are at high risk of respiratory depression and pulmonary aspiration.

摘要

II型阿诺德-奇亚里畸形(ACM)是一种小脑、脑桥和延髓向下移位至脊髓的异常情况。II型ACM常因延髓功能障碍和下颅神经受损而并发呼吸抑制、睡眠呼吸紊乱和吞咽障碍。颈部的弯曲和伸展受限,患有该疾病的患者麻醉管理存在问题。我们对一名患有II型ACM并伴有高碳酸血症呼吸衰竭的智障患者在静脉镇静下进行了两次牙科治疗。第一次镇静程序使用了丙泊酚。那次出现了反复的呼吸抑制发作,因此通过抬起下颌进行手动气道管理。然而,术后发生了吸入性肺炎。第二次镇静时使用了右美托咪定和咪达唑仑的组合,干预顺利完成,没有出现任何呼吸抑制。我们对这名患者的经验凸显了在II型ACM患者中选择一种不需要伸展颈部且对呼吸影响最小的静脉镇静药物的必要性,这类患者有呼吸抑制和肺误吸的高风险。

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引用本文的文献

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Anesthetic management in a patient with Arnold-Chiari malformation type 1,5: A case report.1例1型阿诺德-奇亚里畸形患者的麻醉管理:病例报告。
Clin Case Rep. 2022 Feb 4;10(2):e05194. doi: 10.1002/ccr3.5194. eCollection 2022 Feb.

本文引用的文献

1
A comparison of dexmedetomidine sedation with and without midazolam for dental implant surgery.右美托咪定镇静联合与不联合咪达唑仑用于牙种植手术的比较。
Anesth Prog. 2012 Summer;59(2):62-8. doi: 10.2344/11-11.1.
2
Sleep-disordered breathing in children with Chiari malformation type II and myelomeningocele.II型Chiari畸形和脊髓脊膜膨出患儿的睡眠呼吸障碍
Pediatr Int. 2012 Oct;54(5):623-6. doi: 10.1111/j.1442-200X.2012.03660.x. Epub 2012 Jul 19.
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Stridor at birth predicts poor outcome in neonates with myelomeningocele.出生时出现喘鸣预示着脊髓脊膜膨出新生儿预后不良。
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Postnatal ascent of the cerebellar tonsils in Chiari malformation Type II following surgical repair of myelomeningocele.脊髓脊膜膨出手术修复后 Chiari Ⅱ型畸形中小脑扁桃体的产后上升。
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Is synergy the rule? A review of anesthetic interactions producing hypnosis and immobility.协同作用是规律吗?关于产生催眠和不动效果的麻醉相互作用的综述。
Anesth Analg. 2008 Aug;107(2):494-506. doi: 10.1213/ane.0b013e31817b859e.
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A comparison of dexmedetomidine and midazolam for sedation in third molar surgery.右美托咪定与咪达唑仑用于第三磨牙手术镇静的比较。
Anaesthesia. 2007 Nov;62(11):1132-8. doi: 10.1111/j.1365-2044.2007.05230.x.
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Dexmedetomidine pharmacodynamics: part I: crossover comparison of the respiratory effects of dexmedetomidine and remifentanil in healthy volunteers.右美托咪定的药效学:第一部分:右美托咪定与瑞芬太尼对健康志愿者呼吸作用的交叉比较。
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