{"title":"COMPARATIVE EVALUATION OF DEXMEDETOMIDINE AND PROPOFOL INFUSION FOR HYPOTENSIVE ANESTHESIA DURING ACDF SURGERY: A PROSPECTIVE RANDOMIZED TRIAL","authors":"Akanksha Ratanpal, Abhinav Bishnoi, Sumeet Kumar","doi":"10.36106/gjra7900723","DOIUrl":null,"url":null,"abstract":"Background: Intense bleeding during general anesthesia is the major limitation during ACDF surgery. It\naffects operative eld visibility and increases complications. Hypotensive anesthesia is preferred to\nimprove surgical outcomes. This study aimed to compare the efcacy of Propofol and Dexmedetomidine infusion for\nhypotensive anesthesia in patients undergoing ACDF surgery. To compare the efcacy and safety of Objective:\nDexmedetomidine and Propofol for hypotensive anesthesia in ACDF surgeries. This prospective Materials and methods:\nrandomized trial was conducted in 60 adult patients who were scheduled for ACDF under general anesthesia. Patients were\nrandomly divided into two groups: group P (n = 30) received Propofol infusion of 100-150mcg/kg/min and group D (n = 30)\nreceived dexmedetomidine with a loading dose of 1 mcg/kg diluted in 10 mL 0.9% saline to be infused over 10 min after\ninduction, followed by maintenance infusion of 0.4-0.8 mcg/kg/h. The infusions were titrated to maintain mean arterial pressure\n(MAP) between 60 and 70 mm Hg. Hemodynamic control, Intraoperative blood loss, Quality of the surgical eld and patient recovery were recorded. In our study, the mean arterial pressure and heart rate were signi Results: cantly lower in group D\nthroughout the surgery than in group P. Blood loss was signicantly higher in group P (615.18 ± 18.15 ml) than in group D (480.50\n± 14.50 ml). The Surgical eld visibility was comparable between the groups. The awakening time was signicantly shorter in\ngroup D than group P. In our study, we observed that both Dexmedetomidine and Propofol Conclusion: are efcacious and safe\nfor controlled hypotension during ACDF; however, Dexmedetomidine provides better hemodynamic control and is associated\nwith lesser degree of sedation without any signicant adverse effects.","PeriodicalId":12664,"journal":{"name":"Global journal for research analysis","volume":"48 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global journal for research analysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36106/gjra7900723","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Intense bleeding during general anesthesia is the major limitation during ACDF surgery. It
affects operative eld visibility and increases complications. Hypotensive anesthesia is preferred to
improve surgical outcomes. This study aimed to compare the efcacy of Propofol and Dexmedetomidine infusion for
hypotensive anesthesia in patients undergoing ACDF surgery. To compare the efcacy and safety of Objective:
Dexmedetomidine and Propofol for hypotensive anesthesia in ACDF surgeries. This prospective Materials and methods:
randomized trial was conducted in 60 adult patients who were scheduled for ACDF under general anesthesia. Patients were
randomly divided into two groups: group P (n = 30) received Propofol infusion of 100-150mcg/kg/min and group D (n = 30)
received dexmedetomidine with a loading dose of 1 mcg/kg diluted in 10 mL 0.9% saline to be infused over 10 min after
induction, followed by maintenance infusion of 0.4-0.8 mcg/kg/h. The infusions were titrated to maintain mean arterial pressure
(MAP) between 60 and 70 mm Hg. Hemodynamic control, Intraoperative blood loss, Quality of the surgical eld and patient recovery were recorded. In our study, the mean arterial pressure and heart rate were signi Results: cantly lower in group D
throughout the surgery than in group P. Blood loss was signicantly higher in group P (615.18 ± 18.15 ml) than in group D (480.50
± 14.50 ml). The Surgical eld visibility was comparable between the groups. The awakening time was signicantly shorter in
group D than group P. In our study, we observed that both Dexmedetomidine and Propofol Conclusion: are efcacious and safe
for controlled hypotension during ACDF; however, Dexmedetomidine provides better hemodynamic control and is associated
with lesser degree of sedation without any signicant adverse effects.
背景:全身麻醉期间的大量出血是 ACDF 手术的主要限制因素。它影响手术,增加并发症。低血压麻醉是改善手术效果的首选。本研究旨在比较丙泊酚和右美托咪定输注用于ACDF手术患者低血压麻醉的效果。目的:比较右美托咪定和丙泊酚在ACDF手术中用于低血压麻醉的有效性和安全性。这项前瞻性材料与方法:随机试验在 60 名计划接受 ACDF 全身麻醉的成年患者中进行。患者被随机分为两组:P 组(n = 30)接受 100-150 毫克/千克/分钟的丙泊酚输注,D 组(n = 30)接受右美托咪定输注,负荷剂量为 1 毫克/千克,用 10 毫升 0.9% 生理盐水稀释,在诱导后 10 分钟内输注,随后维持输注 0.4-0.8 毫克/千克/小时。输注量经过滴定,以将平均动脉压(MAP)维持在 60 至 70 毫米汞柱之间。对血流动力学控制、术中失血量、手术质量 eld 和患者恢复情况进行了记录。在我们的研究中,D组的平均动脉压和心率显著低于D组:cantly lower in group D throughout the surgery than group P. Blood loss was signicantly higher in group P (615.18 ± 18.15 ml) than group D (480.50 ± 14.50 ml).两组的手术 eld 可见度相当。在我们的研究中,我们观察到右美托咪定和丙泊酚对于控制 ACDF 期间的低血压都是有效cacious 和安全的;然而,右美托咪定能提供更好的血流动力学控制,并且镇静程度较低,没有任何明显cant 的不良反应。