首页> 外文期刊>Journal of Clinical and Diagnostic Research >Dexmedetomidine as an Additive toSpinal Anaesthesia in Orthopaedic Patients Undergoing Lower Limb Surgeries:A Randomized Clinical Trial Comparing Two Different Doses of Dexmedetomidine UC09-UC12
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Dexmedetomidine as an Additive toSpinal Anaesthesia in Orthopaedic Patients Undergoing Lower Limb Surgeries:A Randomized Clinical Trial Comparing Two Different Doses of Dexmedetomidine UC09-UC12

机译:右美托咪定可作为下肢手术骨科患者脊髓麻醉的添加剂:比较两种不同剂量右美托咪定UC09-UC12的随机临床试验

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Introduction: Use of dexmedetomidine as an additive to spinal anaesthesia is gaining popularity; but there seems to be no clear consensus on the ideal dose to be used. Because of dose related prolongation of duration of motor blockade along with increase in the incidence of side effects of dexmedetomidine namely hypotension and bradycardia, use of higher doses is not recommended.Aim: To evaluate the efficacy of two different doses of dexmedetomidine (3 μg and 5 μg) given in combination with 0.5% hyperbaric bupivacaine via intrathecal route with regard to the quality of anaesthesia namely the time to attain highest sensory and motor blockade, side effects of dexmedetomidine and time to first rescue analgesia.Materials and Methods: Sixty American Society of Anaesthesiologist (ASA) Grade I and II orthopaedic patients undergoing lower limb surgeries between the ages of 20-60 years and height >150 cm were randomly divided into two groups of 30 patients each: Group D3 to receive 3 μg of Inj. Dexmedetomidine (0.5 ml, reconstituted using normal saline) along with 12.5 mg (2.5 ml) of 0.5% hyperbaric bupivacaine and Group D5 to receive 5 μg of inj. Dexmedetomidine (0.5 ml, reconstituted using normal saline) along with 12.5 mg (2.5 ml) of 0.5% hyperbaric bupivacaine keeping the total volume of study drug constant in all 60 patients (3 ml). Data recordings were done for time to reach best sensory and motor block, intraoperative haemodynamic changes and time to first postoperative rescue analgesia. Statistical analysis was done using students t-test and Chi-square test with p-value of 0.05). The change in haemodynamics was similar (p>0.05). A statistically significant difference (p<0.001) was observed in time to first rescue analgesia after skin closure with Group D3 having 206.47 minutes while in Group D5 the time was 271.33 minutes.Conclusion: Used in a dose of 5 μg (in 0.5 ml volume) as an additive in spinal anaesthesia maximal beneficial effect of dexmedetomidine can be obtained without any side effects.
机译:简介:使用右美托咪定作为脊柱麻醉的添加剂正变得越来越流行。但对于理想的使用剂量似乎没有明确的共识。由于剂量相关的运动障碍持续时间的延长以及右美托咪定(即低血压和心动过缓)副作用的发生率增加,因此不建议使用更高剂量。目的:评估两种不同剂量右美托咪定(3μg和关于麻醉质量,即达到最高的感觉和运动阻滞时间,右美托咪定的副作用和首次抢救镇痛的时间,通过鞘内途径与5%的高压布比卡因组合使用5μg)。麻醉师(ASA)将年龄在20至60岁之间且身高大于150 cm的下肢手术的I级和II级骨科患者随机分为两组,每组30例:D3组接受3μg注射液。右美托咪定(0.5 ml,用生理盐水重建)与12.5 mg(2.5 ml)的0.5%高压布比卡因和D5组一起接受5μg注射液。右美托咪定(0.5毫升,用生理盐水重构)与12.5毫克(2.5毫升)的0.5%高压布比卡因一起使所有60例患者(3毫升)中的研究药物总量保持恒定。进行数据记录以达到最佳的感觉和运动阻滞时间,术中血流动力学变化以及首次术后抢救镇痛的时间。使用学生t检验和卡方检验(p值为0.05)进行统计分析。血流动力学变化相似(p> 0.05)。 D3组有206.47分钟的时间,而在D3组的时间为271.33分钟,在皮肤闭合后首次抢救镇痛的时间上有统计学上的显着差异(p <0.001)。结论:以5μg的剂量(0.5 ml量)使用)作为脊髓麻醉的添加剂,可以获得右美托咪定的最大有益作用,而没有任何副作用。

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