Premedication of Oral Clonidine 2mcg/kg and 4mcg/kg for Analgesic and Pressure Response During First Twenty-four Hours After Upper Abdominal Surgery: A Comparative Study

Mohammmad Shaddam Hoshain Mondol, Md Abu Rasel Bhuiyan, Hasan Ali Talukder, Ishrat Jahan Shathi, A. Ali, Shukha Ranjan Das
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Abstract

Traditionally postoperative period analgesia was maintained by opoids and which frequently increasethe hospital stay time and cost by delayed bowel movement and others side effects. on the other handupper abdominal surgery is very much painful, usually Opiods are used as good analgesic, but havesome adverse effect and addiction effect; anaesthesiologists want to reduce its requirements. In upperabdominal surgery adequate analgesia, stable haemodynamic, early bowel movement, free from nauseaand vomiting is wanted, as a part of multimodal analgesic approach, premedication by clonidine is veryimportant for it analgesic, angiolytic and sedative properties. Alpha two (α–2) adrenoreceptor agonist,Clonidine exerts central sympatholytic effect for 8 to 10 hours as its half life is 9-12 h. So thatpremedication with oral clonidine causes reduction of anxiety, reduction of perioperative analgesicdrugs and also reduction of anaesthetic doses. In addition, clonidine increases cardiac baroreceptorreflex sensitivity to increase in systolic blood pressure, and thus stabilizes blood pressure. Clonidine israpidly and almost completely absorbed after oral administration with a time to maximum plasmaconcentration of between 1.5 and 2 hr and elimination half-life of 8 to 12 hr. But clonidine producesanalgesia in a dose dependent manner, achieving complete pain relief for up to 5 hours without sensoryor motor block at large doses (oral 7000 to 900 mcg) however large doss were associated withdisadvantage including hypotension, bradycardia and transient sedation. It also reported thatclonidine 150mcg intravenous (I/V) produce a similar analgesic effect to morphine 5mg in patient afterorthopedic surgery. Because of its dose, route, and surgical variation it is very much important tospecify the dose for upper abdominal surgery.The primary aim of this study to compare the effects of clonidine premedication at different doses (2 &4mcg/kg) on postoperative analgesia and hemodynamic status in upper abdominal surgery with largeincision area. (like- hepatobiliary surgery, gastrectomy, esophagectomy, hepatictomy, and whipplesoperations). JBSA 2022; 35 (2) : 17-21
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口服可乐定2mcg/kg和4mcg/kg前用药对上腹部手术后24小时镇痛和压力反应的比较研究
传统的术后镇痛是通过阿片类药物维持的,但由于排便延迟和其他副作用,经常增加住院时间和费用。另一方面上腹部手术非常痛苦,通常使用阿片类药物作为良好的镇痛药,但有一定的不良反应和成瘾效应;麻醉师想要减少它的需求。在上腹部手术中,需要充分的镇痛,稳定的血流动力学,早期的肠蠕动,无恶心和呕吐,作为多模式镇痛方法的一部分,可乐定的预用药对其镇痛,溶血管和镇静作用非常重要。α 2 (α-2)肾上腺受体激动剂,可发挥8 ~ 10小时的中枢交感神经溶解作用,其半衰期为9 ~ 12小时。因此,术前口服可减少焦虑,减少围手术期镇痛药物,减少麻醉剂量。此外,可乐定增加心脏压力感受器反射对收缩压升高的敏感性,从而稳定血压。口服可乐定吸收迅速且几乎完全,达到最大血浆浓度的时间为1.5至2小时,消除半衰期为8至12小时。但可乐定以剂量依赖的方式产生镇痛,在大剂量(口服7000至900微克)下可实现长达5小时的完全疼痛缓解而无传感器或运动阻滞,然而大剂量相关的缺点包括低血压、心动过缓和短暂性镇静。也有报道称,骨科术后患者静脉注射150毫克可乐定(I/V)的镇痛效果与吗啡5毫克相似。由于上腹部手术的剂量、途径和手术方式的不同,明确上腹部手术的剂量是非常重要的。本研究的主要目的是比较不同剂量可乐定(2和4微克/公斤)对大切口上腹部手术术后镇痛和血流动力学状态的影响。(如肝胆手术、胃切除术、食管切除术、肝切除术和鞭状手术)。JBSA 2022;35 (2): 17-21
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Premedication of Oral Clonidine 2mcg/kg and 4mcg/kg for Analgesic and Pressure Response During First Twenty-four Hours After Upper Abdominal Surgery: A Comparative Study Comparison between effects of Clonazepam and Dexmedetomidine as sedative in elective Caesarean section under Subarachnoid anaesthesia A Dose Response Study Of Oral clonidine as premedication in patients undergoing abdominal gynaecological surgery Blood Glucose Variability as a Predictor of Mortality for Septic Patients in Intensive Care Unit Postoperative pain relief in pediatric surgery patients: Effect of intravenous paracetamol in comparison with diclofenac suppository
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