Effect of Intrathecal Bupivacaine Temperature Variation on Prophylaxis of Shivering in Urologic Patients Undergoing Spinal Anesthesia.

IF 1.5 Q2 ANESTHESIOLOGY
Anesthesiology Research and Practice Pub Date : 2026-10-08 eCollection Date: 2026-01-01 DOI:10.1155/anrp/1005074
Emad M Abdelhafez, Hala Gomaa, Sherif M Abdelaziz, Esraa Sayed Ewais Muhammad, Heba Bakr
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Abstract

Background: Postspinal shivering is a frequent complication of spinal anesthesia (SA) and is particularly relevant in urological procedures, where perioperative heat loss can be exacerbated by irrigation fluids. Modifying the temperature of the intrathecal local anesthetic may affect thermoregulatory responses and the properties of the blockade.

Methods: This prospective, randomized, double-blind, controlled trial was conducted in 96 patients (ASA I-II, aged 18-60 years) undergoing elective urological procedures under SA. Participants received intrathecal hyperbaric bupivacaine 0.5% (15 mg) combined with fentanyl 25 μg at one of three temperatures: 4°C (cold; n = 32), 24°C (room; n = 32), or 37°C (warm; n = 32). Shivering was graded using the validated Crossley and Mahajan scale. The primary endpoint was the incidence of clinically significant shivering (Grade ≥ 3) throughout the observation period, evaluated at 10-min intervals.

Results: Cold bupivacaine demonstrated a significantly higher incidence of clinically significant shivering (Grade ≥ 3) (81.3%) compared with the room-temperature (34.4%) and warm (25%) groups (p < 0.001). The post hoc analysis showed that the difference between the room-temperature and warm groups was not significant. Pharmacological intervention requirements were substantially elevated in the cold group (43.8%, 15.6%, 15.6%; p = 0.01). Warm bupivacaine accelerated sensory and motor block onset (p = 0.001) while reducing residual motor blockade.

Conclusion: Warmed intrathecal bupivacaine significantly reduces PSS incidence and severity while optimizing block characteristics without compromising safety in urological patients. Trial Registration: ClinicalTrials.gov identifier: NCT07081516.

布比卡因鞘内温度变化对预防泌尿科脊髓麻醉患者寒战的影响。
背景:脊髓后寒战是脊髓麻醉(SA)的常见并发症,尤其与泌尿外科手术相关,其中围手术期热损失可因冲洗液而加剧。改变鞘内局麻药的温度可能会影响热调节反应和阻滞的性质。方法:该前瞻性、随机、双盲、对照试验纳入96例(ASA I-II,年龄18-60岁)在SA下择期行泌尿外科手术的患者。参与者在4°C(冷,n = 32)、24°C(室温,n = 32)或37°C(暖,n = 32)三种温度之一的鞘内注射布比卡因0.5% (15 mg)和芬太尼25 μg。颤抖是用经过验证的Crossley和Mahajan量表进行分级的。主要终点是整个观察期间临床显著性寒战(≥3级)的发生率,每隔10分钟评估一次。结果:冷布比卡因组临床显著性寒战(≥3级)发生率(81.3%)明显高于常温组(34.4%)和温组(25%)(p p = 0.01)。温布比卡因加速了感觉和运动阻滞的发生(p = 0.001),同时减少了残留的运动阻滞。结论:加热鞘内布比卡因可显著降低PSS的发生率和严重程度,同时优化阻滞特性,同时不影响泌尿科患者的安全性。试验注册:ClinicalTrials.gov标识符:NCT07081516。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
29
审稿时长
18 weeks
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