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一名4个月大儿童硬膜外导管置入术后出现霍纳综合征。

Horner Syndrome After Epidural Catheter Placement in a 4-Month-Old Child.

作者信息

Avila Andrea, Liu John, Kohen Maryo C

出版信息

J Pediatr Ophthalmol Strabismus. 2018 Jan 31;55:e1-e3. doi: 10.3928/01913913-20170907-02.

DOI:10.3928/01913913-20170907-02
PMID:29384560
Abstract

Although there are reports of iatrogenic Horner syndrome in the adult population, pediatric cases are rare. The current report presents a case of acquired Horner syndrome that occurred after an epidural catheter was placed for pain control. Horner syndrome completely resolved after removing the catheter and no imaging or further work-up was necessary. [J Pediatr Ophthalmol Strabismus. 2018;55:e1-e3.].

摘要

尽管在成人中存在医源性霍纳综合征的报道,但儿科病例罕见。本报告介绍了一例在放置硬膜外导管用于疼痛控制后发生的获得性霍纳综合征病例。拔除导管后霍纳综合征完全缓解,无需影像学检查或进一步评估。[《小儿眼科与斜视杂志》。2018年;55:e1 - e3。]

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J Pediatr Ophthalmol Strabismus. 2018 Jan 31;55:e1-e3. doi: 10.3928/01913913-20170907-02.
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Two cases of Horner syndrome after administration of an epidural test dose that did not recur with subsequent epidural activation.两例硬膜外试验剂量给药后出现霍纳综合征,后续硬膜外激活时未再复发。
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