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米氮平、加巴喷丁和昂丹司琼预防鞘内注射吗啡所致瘙痒的比较。

Comparison of mirtazapine, gabapentin and ondansetron to prevent intrathecal morphine-induced pruritus.

作者信息

Akhan Ayse, Subasi Ferhunde Dilek, Bosna Gulsen, Ekinci Osman, Pamuk Hakan, Batan Siddika, Ateser Rezzan Yagmur, Turan Gulden

机构信息

Department of Anesthesiology and Reanimation, Karabük Training and Research Hospital, Karabük, Turkey.

Department of Anesthesiology and Reanimation, Haydarpasa Numune Training and Research Hospital, Uskudar, Istanbul, Turkey.

出版信息

North Clin Istanb. 2016 Jun 10;3(1):53-59. doi: 10.14744/nci.2016.38233. eCollection 2016.

Abstract

OBJECTIVE

Antagonism of the central nervous system inhibitor neurotransmitter gamma-Aminobutyric acid (GABA) or serotonergic system activation is an important factor in the pathogenesis of intrathecal morphine-induced pruritus. This study tested the hypothesis that preoperative use of ondansetron, gabapentin or mirtazapine can prevent morphine-induced pruritus.

METHODS

We randomly allocated 80 patients of American Society of Anesthesiology (ASA) classification I and II physical status who were to undergo unilateral inguinal hernia or pilonidal sinus operations under spinal anesthesia into 4 equal groups. The first 3 groups received oral doses of 30 mg mirtazapine, 8 mg ondansetron, and 1200 mg gabapentin at 2 hours, 10 minutes, and 1 hour before surgery, respectively, and the fourth group was given a placebo. All patients received intrathecal injection of 15 mg of 0.5% hyperbaric bupivacaine and 0.2 mg morphine. Pruritus was evaluated at 0, 3, 6, 9, 12, and 24 hours after intrathecal morphine administration, and details of presence, onset time, duration, localization, and severity of pruritus were recorded.

RESULTS

Incidence of pruritus was significantly more frequent in the placebo group compared to ondansetron, gabapentin, and mirtazapine groups (70%, 55%, 35%, and 35%, respectively). In general, onset of pruritus was between 2 and 6 hours after intrathecal morphine injection; however, onset in the gabapentin group (mean±SD: 4.75±2.7 hours; p=0.019) was delayed compared to other groups. It was observed that pruritus persisted relatively longer in the ondansetron and placebo groups (mean±SD: 6±3.08; 5.82±2.96 hours, respectively; p=0.047). No statistical determination was made regarding location of pruritus. Severity of pruritus was greater in the placebo group (p=0.0001). Necessity for antipruritic treatment was not statistically significantly different between groups.

CONCLUSION

Incidence and severity of intrathecal morphine-induced pruritus decreased with use of each of all 3 drugs compared to placebo.

摘要

目的

中枢神经系统抑制性神经递质γ-氨基丁酸(GABA)的拮抗作用或血清素能系统激活是鞘内注射吗啡引起瘙痒的发病机制中的一个重要因素。本研究检验了术前使用昂丹司琼、加巴喷丁或米氮平可预防吗啡引起瘙痒的假设。

方法

我们将80例美国麻醉医师协会(ASA)分级为I级和II级身体状况、拟在脊髓麻醉下接受单侧腹股沟疝或藏毛窦手术的患者随机分为4组,每组人数相等。前三组分别在手术前2小时、10分钟和1小时口服30毫克米氮平、8毫克昂丹司琼和1200毫克加巴喷丁,第四组给予安慰剂。所有患者均接受鞘内注射15毫克0.5%的高压布比卡因和0.2毫克吗啡。在鞘内注射吗啡后0、3、6、9、12和24小时评估瘙痒情况,并记录瘙痒的存在、发作时间、持续时间、部位和严重程度等细节。

结果

与昂丹司琼、加巴喷丁和米氮平组相比,安慰剂组瘙痒发生率明显更高(分别为70%、55%、35%和35%)。一般来说,瘙痒发作在鞘内注射吗啡后2至6小时之间;然而,加巴喷丁组的发作时间(平均值±标准差:4.75±2.7小时;p = 0.019)比其他组延迟。观察到昂丹司琼组和安慰剂组瘙痒持续时间相对较长(平均值±标准差:分别为6±3.08;5.82±2.96小时;p = 0.047)。未对瘙痒部位进行统计学测定。安慰剂组瘙痒严重程度更高(p = 0.0001)。各组间抗瘙痒治疗的必要性无统计学显著差异。

结论

与安慰剂相比,使用这三种药物均可降低鞘内注射吗啡引起瘙痒的发生率和严重程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd9d/5175078/698d59a4ab2d/NCI-3-53-g001.jpg

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