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持续静脉输注利多卡因用于治疗阿片类药物无法控制的疼痛。

Continuous Intravenous Lidocaine Infusion for the Management of Pain Uncontrolled by Opioid Medications.

作者信息

Reeves David J, Foster Alexandra E

出版信息

J Pain Palliat Care Pharmacother. 2017 Sep-Dec;31(3-4):198-203. doi: 10.1080/15360288.2017.1313356. Epub 2017 May 10.

DOI:10.1080/15360288.2017.1313356
PMID:28489478
Abstract

Limited data exist describing the outcomes of patients receiving continuous lidocaine infusions. The objective of this study was to evaluate the effect of use of continuous lidocaine infusions for pain management at a community teaching hospital. A retrospective chart review was performed that included adult patients receiving continuous systemic lidocaine infusions for the treatment of pain. Twenty-one patients were included in the analysis. Dosing ranged from 0.25 to 2.8 mg/kg/h, with a median infusion time of 64 hours. Eight patients (38%) experienced a response (≥20% reduction in pain score during the infusion compared with prior to the infusion). Among responding patients, there was a decrease in pain scores at rest after starting lidocaine (compared with prior to lidocaine) (6.5 vs. 3.7, P = .001) that was maintained 24 hours after lidocaine discontinuation. There were no differences in pain scores before, during, or after lidocaine in the entire study sample. A difference in oral morphine equivalent intake was present comparing usage during the infusion vs. day +1 (P = .006) and day +2 (P < .001). Similarly, a difference was present comparing morphine equivalent usage on day -2 with day +2 (P = .008) and day -1 with day +1 (P = .006). Continuous infusions of systemic lidocaine appear to be beneficial in some patients experiencing uncontrolled pain and may improve pain scores while decreasing opioid requirements. Overall beneficial effects of systemic lidocaine may last longer than the infusion itself.

摘要

关于接受持续利多卡因输注的患者预后的描述性数据有限。本研究的目的是评估在一家社区教学医院使用持续利多卡因输注进行疼痛管理的效果。进行了一项回顾性病历审查,纳入了接受持续全身性利多卡因输注以治疗疼痛的成年患者。21名患者纳入分析。给药剂量范围为0.25至2.8mg/kg/h,中位输注时间为64小时。8名患者(38%)有反应(与输注前相比,输注期间疼痛评分降低≥20%)。在有反应的患者中,开始使用利多卡因后静息时的疼痛评分降低(与使用利多卡因前相比)(6.5对3.7,P = 0.001),且在停用利多卡因24小时后仍保持。在整个研究样本中,利多卡因使用前、使用期间和使用后的疼痛评分无差异。比较输注期间与第1天(P = 0.006)和第2天(P < 0.001)的口服吗啡等效剂量摄入量存在差异。同样,比较第-2天与第2天(P = 0.008)以及第-1天与第1天(P = 0.006)的吗啡等效剂量使用情况也存在差异。持续全身性输注利多卡因似乎对一些疼痛未得到控制的患者有益,可能会改善疼痛评分,同时减少阿片类药物的需求。全身性利多卡因的总体有益效果可能比输注本身持续时间更长。

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