首页> 外文期刊>Cureus. >Comparative Study of Intravenous Dexmedetomidine Sedation With Perineural Dexmedetomidine on Supraclavicular Approach Brachial Plexus Block in Upper Limb Orthopaedic Surgery
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Comparative Study of Intravenous Dexmedetomidine Sedation With Perineural Dexmedetomidine on Supraclavicular Approach Brachial Plexus Block in Upper Limb Orthopaedic Surgery

机译:静脉内甲肾上腺素镇静静脉内甲肾上腺素对上肢骨科手术中静脉内甲基宫内节育脉胸腺嘧啶的比较研究

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Background Dexmedetomidine is being used as an adjuvant analgesic, both as intravenous (IV) and intrathecal infusion.?The role of perineural (P) dexmedetomidine?has evoked attention recently. The aim of this study was to compare the effect?of IV dexmedetomidine and P dexmedetomidine as an adjunct to supraclavicular brachial plexus block in upper limb orthopaedic surgery. Methods Patients were randomly divided into two equal groups (n=20). Group I (IV dexmedetomidine) received dexmedetomidine 1 mcg/kg IV as loading dose over 10 minutes, followed by continuous?infusion of dexmedetomidine 0.4 mcg/kg/hr IV. Group P (P dexmedetomidine) received dexmedetomidine at 1 mcg/kg perineurally. After adequate motor response with the aid of peripheral nerve stimulator a supraclavicular block with 40 ml solution containing 5 mg/kg lignocaine (2%) with adrenaline (1:200,000) and 2 mg/kg of bupivacaine (0.5%) was injected to both the groups. Group P also received?dexmedetomidine perineurally with?block. Onset and duration of sensory and?motor block, Ramsay sedation score, hemodynamic parameters, and postoperative analgesia requirement were assessed along with side effects.?The data obtained were recorded as mean ± SD, ranges, numbers, and ratios. Results were analyzed using the chi-square test, the Mann-Whitney test for non-parametric data, and an unpaired ‘t’-test for parametric data. Statistical analysis was carried out using the SPSS (version 10, 2002; SPSS Inc., Chicago, IL, USA) for Windows statistical package. P value less than 0.05 was considered statistically significant. Results Mean onset of sensory block was earlier in group I?than in group P (p0.05) although mean onset of motor block was not significantly different (p0.05). Duration of sensory and motor blockade was longer in group I (p0.05). Patients in group I demonstrated lower pulse rate and lower systolic and diastolic blood pressures throughout the period with comparable SpOsub2/sub values. There was no difference in intraoperative Ramsay sedation scores in both groups, but postoperative Ramsay sedation scores at 9, 12, and 15 hours were better in group I (p0.05). The average time to rescue analgesia (visual analogue scale 4) was higher in group I (p0.05). Conclusion IV dexmedetomidine produced early onset of sensory block,?longer duration of sensory and motor block, and longer duration of analgesia as compared with P dexmedetomidine as an adjuvant to supraclavicular block with 5 mg/kg lignocaine (2%) and?2 mg/kg bupivacaine (0.5%) in upper limb orthopaedic surgeries.
机译:背景技术Dexmedetomidine被用作佐剂镇痛,无论是静脉内(IV)和鞘内输注。危及(P)德克梅哌啶胺的作用最近诱发了。本研究的目的是比较效果吗?IV德克梅哌咪唑和P德Xmedetomidine作为上肢整形外科术中的副肢体臂丛丛嵌段的辅助。方法将患者随机分为两组(n = 20)。 IV组(IV Dexmedetomidine)在10分钟内接受Dexmedetomidine 1mcg / kg IV作为装载剂量,然后连续α输注Dexmedetomidine 0.4mcg / kg / hr IV。组p(p dexmedetomidine)在11mcg / kg下接受Dexmedetomidine。在借助于外周神经刺激器的适当电动机响应之后,将含有肾上腺素(1:200,000)和2mg / kg Bupivacaine(0.5%)的肾上腺素(1:200,000)和2mg / kg的Bupivacaine(0.5%)的含有40ml溶液的溶液。群体。组P还收到了吗?甲醛海洋嘌呤(甲醛)感觉的发病和持续时间和持续时间和?马达块,拉丝镇静评分,血液动力学参数和术后镇痛要求以及副作用评估。获得的数据被记录为平均值±SD,范围,数量和比率。使用Chi-Square Test,非参数数据的Mann-Whitney测试和参数数据的未配对进行分析结果。使用SPSS(版本10,2002; SPSS Inc.,芝加哥,IL,USA)进行统计分析,用于Windows统计包。 P值小于0.05被认为是统计学意义的。结果意味着感觉块的发病率在I组中α比于P组(P <0.05)中(P <0.05),尽管电机块的平均发作没有显着差异(P> 0.05)。感觉和电机阻滞的持续时间在I组中更长(P <0.05)。患者患者在具有可比较的SPO 2 值的情况下,在整个期间均显示出较低的脉搏率和降低的收缩压和舒张血压。两组的术中Ramsay镇静分数没有差异,但在9,12和15小时的术后Ramsay镇静分数在I组中更好(P <0.05)。 I基团I(P> 0.05)恢复镇痛(视觉模拟尺度> 4)的平均时间较高。结论IV Dexmedetomidine产生的感觉块的早期发作,ω的持续时间较长,以及与P德Xmedetomidine相比,镇痛的持续时间较长,与副乳醛嵌段为5mg / kg lignocaine(2%)和β2mg / kg Bupivacaine(0.5%)在上肢骨科手术中。

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