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预防性左乙拉西坦在脑瘤手术后的持续时间:一项前瞻性随机试验。

Duration of Prophylactic Levetiracetam After Surgery for Brain Tumor: A Prospective Randomized Trial.

机构信息

Lillian S. Wells Department of Neurosurgery, University of Florida, Gainesville, Florida, USA.

Department of Neurology, University of Florida, Gainesville, Florida, USA.

出版信息

Neurosurgery. 2023 Jan 1;92(1):68-74. doi: 10.1227/neu.0000000000002164. Epub 2022 Sep 26.

Abstract

BACKGROUND

Levetiracetam is commonly used as a prophylactic antiseizure medication in patients undergoing surgical resection of brain tumors.

OBJECTIVE

To quantitate side effects experienced in patients treated with 1 week vs 6 weeks of prophylactic levetiracetam using validated measures for neurotoxicity and depression.

METHODS

Patients undergoing surgical resection of a supratentorial tumor with no seizure history were randomized within 48 hours of surgery to receive prophylactic levetiracetam for the duration of either 1 or 6 weeks. Patients were given oral levetiracetam extended release 1000 mg during the first part of this study. Owing to drug backorder, patients enrolled later in this study received levetiracetam 500 mg BID. The primary outcome was the change in the neurotoxicity score 6 weeks after drug initiation. The secondary outcome was seizure incidence.

RESULTS

A total of 81 patients were enrolled and randomized to 1 week (40 patients) or 6 weeks (41 patients) of prophylactic levetiracetam treatment. The neurotoxicity score slightly improved in the overall cohort between baseline and reassessment. There was no significant difference between groups in neurotoxicity or depression scores. Seizure incidence was low in the entire cohort of patients with 1 patient in each arm experiencing a seizure during the follow-up period.

CONCLUSION

The use of prophylactic levetiracetam did not result in significant neurotoxicity or depression when given for either 1 week or 6 weeks. The incidence of seizure after craniotomy for tumor resection is low regardless of duration of therapy.

摘要

背景

在接受脑瘤切除术的患者中,左乙拉西坦通常被用作预防性抗癫痫药物。

目的

使用神经毒性和抑郁的验证措施来量化接受 1 周和 6 周预防性左乙拉西坦治疗的患者的副作用。

方法

在手术后 48 小时内,无癫痫病史的患者随机分为两组,分别接受 1 或 6 周的预防性左乙拉西坦治疗。在本研究的第一部分,患者口服左乙拉西坦缓释片 1000mg。由于药物缺货,本研究后期入组的患者接受左乙拉西坦 500mg 每日两次治疗。主要结局是起始药物治疗 6 周后神经毒性评分的变化。次要结局是癫痫发作的发生率。

结果

共纳入 81 例患者,随机分为 1 周(40 例)或 6 周(41 例)预防性左乙拉西坦治疗组。在整个队列中,神经毒性评分在基线和重新评估之间略有改善。两组在神经毒性或抑郁评分方面无显著差异。在整个患者队列中,癫痫发作的发生率较低,每组各有 1 例患者在随访期间发生癫痫发作。

结论

在 1 周或 6 周的时间内给予预防性左乙拉西坦不会导致明显的神经毒性或抑郁。无论治疗持续时间如何,肿瘤切除术开颅术后癫痫发作的发生率都较低。

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