Comparison of Weight-Adjusted Dose versus Fixed Dose Ondansetron in Preventing Shivering Following Spinal Anaesthesia for Caesarean Deliveries

Rajib Hazarika, Ananya Choudhury
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Abstract

BACKGROUND Spinal anaesthesia is the preferred method of anaesthesia in parturients undergoing both elective and emergency lower-segment caesarean section. A common complication of spinal anaesthesia is shivering. Shivering increases perioperative heart rate and oxygen consumption by 5 times and also increases the metabolic demand by 100 times, thereby increasing chances of myocardial ischemia, hypoxia, hypoxemia and later lactic acidosis. In this study, we wanted to compare the incidence of shivering following spinal anaesthesia when a weight-adjusted dose versus a fixed dose of ondansetron is used during caesarean delivery. METHODS This was a hospital-based randomized double-blinded (patient and observer blinded) single hospital-based study conducted among 190 pregnant patients who underwent elective caesarean delivery under spinal anaesthesia in the Department of Anaesthesiology and Critical Care, Gauhati Medical College and Hospital, Guwahati from 1st August 2021 to 31st July 2022 after obtaining clearance from Institutional Ethics Committee and written informed consent from the study participants. The patients were divided into two groups: group 1 (patients who received a weight-adjusted dose of ondansetron at 0.1mg/kg) and group 2 (patients who received fixed-dose ondansetron). RESULTS Shivering occurred in 11 patients (11.6 %) in group 1 and 21 patients (22.1 %) in group 2, but there was no statistical difference between the two groups (p-value 0.053) (using the chi-square test). 10 patients (10.5 %) developed grade I shivering and 1 patient (1.1 %) developed grade II shivering in group 1. In group 2, 10 patients (10.5 %) developed grade I shivering and 11 patients (11.6 %) developed grade II shivering (P-value - 0.0163) which was statistically significant (using chi-square test). Nausea occurred in 2 patients (2.1 %) in group 2 while no incidence of nausea was seen in group 1. Incidence of headache was seen in both groups; 1 patient (1.1 %). There was no statistical difference between the adverse effects of the groups. CONCLUSIONS The severity of shivering was lower in the weight-adjusted dose at 0.1 mg/kg ondansetron group in patients undergoing spinal anaesthesia for caesarean delivery. The incidence of shivering was comparable in both the weight-adjusted dose and fixed-dose ondansetron groups. The incidence of nausea, vomiting, headache and pruritus did not differ significantly among the groups.
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体重调整剂量与固定剂量昂丹司琼预防剖宫产脊髓麻醉后颤抖的比较
背景脊柱麻醉是选择性和紧急下段剖腹产产妇的首选麻醉方法。脊椎麻醉的常见并发症是颤抖。颤抖使围手术期心率和耗氧量增加5倍,代谢需求增加100倍,从而增加心肌缺血、缺氧、低氧血症和后期乳酸酸中毒的机会。在这项研究中,我们想比较在剖腹产期间使用重量调整剂量和固定剂量的昂丹司琼时,脊柱麻醉后颤抖的发生率。方法这是一项基于医院的随机双盲(患者和观察者盲)单医院研究,对高哈蒂医学院和医院麻醉与危重症科190名在脊髓麻醉下接受选择性剖腹产的孕妇进行了研究,在获得机构伦理委员会的批准和研究参与者的书面知情同意后,古瓦哈提于2021年8月1日至2022年7月31日。患者分为两组:第1组(接受体重调整剂量为0.1mg/kg的昂丹司琼的患者)和第2组(接受固定剂量昂丹司酮的患者)。结果第一组11例(11.6%)和第二组21例(22.1%)出现颤抖,但两组之间无统计学差异(p值0.053)(卡方检验)。在第1组中,10名患者(10.5%)出现I级颤抖,1名患者(1.1%)出现II级颤抖。在第2组中,10名患者(10.5%)出现I级颤抖,11名患者(11.6%)出现II级颤抖(P值-0.0163),具有统计学意义(使用卡方检验)。第2组有2名患者(2.1%)出现恶心,而第1组没有出现恶心。两组患者均有头痛发生率;1例(1.1%)。两组的不良反应之间没有统计学差异。结论:在接受剖宫产脊柱麻醉的患者中,体重调整剂量为0.1mg/kg的昂丹司琼组的颤抖严重程度较低。体重调整剂量组和固定剂量昂丹司琼组的颤抖发生率相当。恶心、呕吐、头痛和瘙痒的发生率在各组之间没有显著差异。
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