右美托咪定与芬太尼对接受腹腔镜袖状胃切除术的病态肥胖患者拔管时间的影响

Q2 Medicine Anesthesiology and Pain Medicine Pub Date : 2024-05-15 DOI:10.5812/aapm-144776
Doha Mohammed Bakr, Rasha Behery Youssef, Maged Salah Mohamed, M. S. Khalil
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引用次数: 0

摘要

背景:袖带胃切除术(SG)是控制肥胖的有效方法。虽然阿片类药物因其血液动力学稳定性和减少术中应激的能力而被广泛使用,但也有副作用的报道。右美托咪定(DEX)是一种α2肾上腺素能受体激动剂,因其镇痛和节省麻醉剂的作用而备受关注,可提高术后恢复质量。研究目的本研究旨在比较芬太尼和右美托咪定(DEX)对腹腔镜袖状胃切除术(SG)后病态肥胖患者恢复的影响。研究方法这项随机双盲研究涉及 64 名患者,平均分为两组。右美托咪定组(D 组)在麻醉诱导前 15 分钟静脉注射负荷剂量右美托咪定(1 μg/kg),然后在诱导期间 60 秒内输注 10 毫升 0.9% 生理盐水。插管后,以 0.5 μg/kg/h 的剂量注射右美托咪定。芬太尼组(F 组)在诱导前 15 分钟内静脉注射与容量相匹配的 0.9% 生理盐水,在诱导期间 60 秒内静脉注射用 10 毫升 0.9% 生理盐水稀释的芬太尼(1 微克/千克)。插管后,以 1 μg/kg/hr 的速度持续输注芬太尼。结果右美托咪定组(D 组)拔管时间为 8.25 ± 2.7 分钟,明显短于芬太尼组(F 组)的 10.47 ± 2.17 分钟,P 值为 0.001。D 组的术中心率和平均动脉血压也明显低于 F 组。在到达麻醉后护理病房和术后 2 小时时,D 组的视觉模拟量表(VAS)疼痛评分明显低于 F 组(P 值 < 0.05)。此外,与 F 组(8 ± 2.38 毫克)相比,D 组在术后前 12 小时内的吗啡用量(5.75 ± 2.20 毫克)明显较低(P 值为 0.001)。结论对于接受腹腔镜袖状胃切除术的病态肥胖患者,右美托咪定(DEX)被证明是一种有效的麻醉选择。它不仅能缩短拔管时间,还能降低术后早期视觉模拟量表(VAS)疼痛评分和术后 12 小时内阿片类药物的用量。
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Dexmedetomidine Versus Fentanyl on Time to Extubation in Patients with Morbid Obesity Undergoing Laparoscopic Sleeve Gastrectomy
Background: Sleeve gastrectomy (SG) is an effective method for managing obesity. While opioids are used for their hemodynamic stability and their ability to reduce intraoperative stress, they also have reported side effects. Dexmedetomidine (DEX), an α2 adrenergic receptor agonist, is noted for its analgesic and anesthetic-sparing effects, leading to a higher quality of recovery. Objectives: The study aims to compare the effects of fentanyl and dexmedetomidine (DEX) on the recovery of morbidly obese patients following laparoscopic sleeve gastrectomy (SG). Methods: This randomized, double-blind study involved 64 patients, equally divided into two groups. The Dexmedetomidine group (Group D) received an intravenous (IV) loading dose of dexmedetomidine (1 μg/kg) over 15 minutes before anesthesia induction, followed by a 10 ml saline 0.9% infusion over 60 seconds during induction. Post-intubation, dexmedetomidine was administered at 0.5 μg/kg/h. The Fentanyl group (Group F) received a volume-matched saline 0.9% IV over 15 minutes pre-induction and fentanyl (1 μg/kg) diluted in 10 ml saline 0.9% IV over 60 seconds during induction. After intubation, a continuous fentanyl infusion was maintained at a rate of 1 μg/kg/hr. Results: Extubation time was significantly shorter in the Dexmedetomidine group (Group D) at 8.25 ± 2.7 minutes compared to the Fentanyl group (Group F) at 10.47 ± 2.17 minutes, with a P value of 0.001. Intraoperative heart rate and mean arterial blood pressure were also significantly lower in Group D than in Group F. Visual analogue scale (VAS) pain scores were significantly lower in Group D compared to Group F upon arrival at the post-anesthesia care unit and at 2 hours postoperatively (P-value < 0.05). Additionally, the morphine dose consumed in the first 12 hours after surgery was significantly lower in Group D (5.75 ± 2.20 mg) compared to Group F (8 ± 2.38 mg), with a P-value of 0.001. Conclusions: For morbidly obese patients undergoing laparoscopic sleeve gastrectomy, dexmedetomidine (DEX) proves to be an effective anesthetic choice. It not only reduces extubation time but also lowers early postoperative visual analogue scale (VAS) pain scores and opioid consumption within the first 12 hours following surgery.
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Anesthesiology and Pain Medicine
Anesthesiology and Pain Medicine Medicine-Anesthesiology and Pain Medicine
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