Efficacy of iv infusion of magnesium sulphate and dromperidol on the management of neuropathic and somatosensory chronic pain - a two pain center study

IF 1 4区 医学 Q3 EMERGENCY MEDICINE
Signa Vitae Pub Date : 2021-09-15 DOI:10.22514/sv.2021.159
I. Chronakis, E. Chainaki, N. Polaki, I. Siafaka, A. Vadalouka
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引用次数: 0

Abstract

Introduction: Droperidol as a medicine has unique properties and it has been successfully used as analgesic, antipsychotic, antiemetic and as a sedative [1]. It is an antagonist for d2-dopamine, serotonin, histamine, and nicotinic and muscarinic cholinergic receptors. It is also a dose-dependent agonist/antagonist of GABA receptors and an agonist of a2 adrenergic receptors. Moreover, is a sodium channel blocker such as lidocaine and potentiate μ opioid receptors. Its multi-receptor action justifies its use as analgesic, antiemetic and antiphycotic medication [2]. Magnesium seems to function as an antagonist for NMDA receptors and it has been used for relief of acute and chronic pain [3, 4]. The aim of the current study is the evaluation of the efficacy of droperidol and magnesium co-administration on the patients with chronic pain. Method: All patients that attended the pain clinic for chronic pain and aged over 18 years old were included in the study. Patients with atrioventricular block any grade and patients with chronic renal failure were excluded from the study. All included patients received droperidol to the dose 2.5 mg maximum and 1 gr magnesium sulphate iv. DN4 questionnaire was used to assess the presence of neuropathic pain. VAS scale and NPS scale were used to assess the intensity of pain before and after the administration. Change in the pain scales calculated as a percentage. Results: 48 patients included in the study. 23 of them had neuropathic pain. There was a 40–50% reduction of the intensity of pain after iv administration of droperidol and magnesium. There weren’t any complications. Conclusions: The co-administration of magnesium and droperidol can relieve neuropathic and somatosensory pain. Long-term evaluation is needed.
静脉滴注硫酸镁和氟哌啶醇治疗神经性和体感慢性疼痛的疗效——一项双疼痛中心研究
引言:氟哌利多作为一种药物具有独特的性质,已成功地用作镇痛药、抗精神病药、止吐药和镇静剂[1]。它是d2多巴胺、血清素、组胺、烟碱和毒蕈碱胆碱能受体的拮抗剂。它也是GABA受体的剂量依赖性激动剂/拮抗剂和a2肾上腺素能受体的激动剂。此外,是一种钠通道阻滞剂,如利多卡因和增强μ阿片受体。其多受体作用证明了其作为镇痛、止吐和抗hycotic药物的用途[2]。镁似乎是NMDA受体的拮抗剂,已被用于缓解急性和慢性疼痛[3,4]。本研究的目的是评估氟哌利多和镁联合给药对慢性疼痛患者的疗效。方法:所有在疼痛门诊就诊的18岁以上慢性疼痛患者均纳入研究。任何级别的房室传导阻滞患者和慢性肾功能衰竭患者均被排除在研究之外。所有纳入的患者均接受了最大剂量为2.5 mg的氟哌利多和1gr的硫酸镁静脉注射。DN4问卷用于评估神经性疼痛的存在。VAS量表和NPS量表用于评估给药前后的疼痛强度。疼痛量表的变化以百分比计算。结果:48例患者纳入研究。其中23例有神经性疼痛。静脉注射氟哌利多和镁后,疼痛强度减轻了40-50%。没有任何并发症。结论:镁与氟哌利多合用可减轻神经性和体感疼痛。需要进行长期评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Signa Vitae
Signa Vitae 医学-急救医学
CiteScore
1.30
自引率
9.10%
发文量
0
审稿时长
3 months
期刊介绍: Signa Vitae is a completely open-access,peer-reviewed journal dedicate to deliver the leading edge research in anaesthesia, intensive care and emergency medicine to publics. The journal’s intention is to be practice-oriented, so we focus on the clinical practice and fundamental understanding of adult, pediatric and neonatal intensive care, as well as anesthesia and emergency medicine. Although Signa Vitae is primarily a clinical journal, we welcome submissions of basic science papers if the authors can demonstrate their clinical relevance. The Signa Vitae journal encourages scientists and academicians all around the world to share their original writings in the form of original research, review, mini-review, systematic review, short communication, case report, letter to the editor, commentary, rapid report, news and views, as well as meeting report. Full texts of all published articles, can be downloaded for free from our web site.
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