Effect of Preoperative Intravenous and Inhalational Dexmedetomidine on the Hemodynamic Response of Laryngoscopy: A Prospective Double-blinded Randomized Study.

IF 0.8 Q4 PHARMACOLOGY & PHARMACY
Journal of Research in Pharmacy Practice Pub Date : 2024-08-08 eCollection Date: 2023-10-01 DOI:10.4103/jrpp.jrpp_12_24
Shivanya Singh, Priyanka Gupta, Mridul Dhar, Arhan Pasha
{"title":"Effect of Preoperative Intravenous and Inhalational Dexmedetomidine on the Hemodynamic Response of Laryngoscopy: A Prospective Double-blinded Randomized Study.","authors":"Shivanya Singh, Priyanka Gupta, Mridul Dhar, Arhan Pasha","doi":"10.4103/jrpp.jrpp_12_24","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Laryngoscopy induces potent noxious stimuli causing reflex autonomic activation manifested by an increase in blood pressure and heart rate (HR). Various drugs with different routes have been tried to prevent this response. The literature comparing inhalational dexmedetomidine with intravenous (IV) dexmedetomidine to prevent laryngoscopy response is limited.</p><p><strong>Methods: </strong>A total of 150 American Society of Anesthesiologists Physical Status Class I/II, undergoing elective surgery requiring laryngoscopy and intubation, were included and randomized into two groups. Patients in Group D<sub>INH</sub> received nebulized dexmedetomidine (1 μg/kg) and in Group D<sub>IV</sub> received IV dexmedetomidine (0.5 μg/kg), 15 min before anesthesia induction. For blinding, nebulized or IV saline was used simultaneously. The primary outcome was to compare the mean arterial pressure (MAP) and HR at laryngoscopy, intubation, and 1, 5, and 10 min after intubation. The secondary outcome was to compare sedation, following the administration of dexmedetomidine, propofol consumption during induction, and any side effects.</p><p><strong>Findings: </strong>There was no significant difference in MAP (mmHg) postlaryngoscopy and intubation (immediate after intubation 78.5 ± 11.3 vs. 82.3 ± 16.0, <i>P</i> = 0.093). The mean HR was clinically similar in both groups postlaryngoscopy and intubation (immediate after intubation, 80.9 ± 12.5 vs. 76.3 ± 10.9). Patients in the D<sub>IV</sub> group were more sedated than the D<sub>INH</sub> (Ramsay Sedation Scale 3-4 vs. 1-2, <i>P</i> < 0.001). Bradycardia was seen in eight patients of the D<sub>IV</sub> group only.</p><p><strong>Conclusion: </strong>Preoperative nebulized dexmedetomidine is as effective as and safer than IV dexmedetomidine in preventing laryngoscopic response among adults.</p>","PeriodicalId":17158,"journal":{"name":"Journal of Research in Pharmacy Practice","volume":"12 4","pages":"123-129"},"PeriodicalIF":0.8000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11386063/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Research in Pharmacy Practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jrpp.jrpp_12_24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Laryngoscopy induces potent noxious stimuli causing reflex autonomic activation manifested by an increase in blood pressure and heart rate (HR). Various drugs with different routes have been tried to prevent this response. The literature comparing inhalational dexmedetomidine with intravenous (IV) dexmedetomidine to prevent laryngoscopy response is limited.

Methods: A total of 150 American Society of Anesthesiologists Physical Status Class I/II, undergoing elective surgery requiring laryngoscopy and intubation, were included and randomized into two groups. Patients in Group DINH received nebulized dexmedetomidine (1 μg/kg) and in Group DIV received IV dexmedetomidine (0.5 μg/kg), 15 min before anesthesia induction. For blinding, nebulized or IV saline was used simultaneously. The primary outcome was to compare the mean arterial pressure (MAP) and HR at laryngoscopy, intubation, and 1, 5, and 10 min after intubation. The secondary outcome was to compare sedation, following the administration of dexmedetomidine, propofol consumption during induction, and any side effects.

Findings: There was no significant difference in MAP (mmHg) postlaryngoscopy and intubation (immediate after intubation 78.5 ± 11.3 vs. 82.3 ± 16.0, P = 0.093). The mean HR was clinically similar in both groups postlaryngoscopy and intubation (immediate after intubation, 80.9 ± 12.5 vs. 76.3 ± 10.9). Patients in the DIV group were more sedated than the DINH (Ramsay Sedation Scale 3-4 vs. 1-2, P < 0.001). Bradycardia was seen in eight patients of the DIV group only.

Conclusion: Preoperative nebulized dexmedetomidine is as effective as and safer than IV dexmedetomidine in preventing laryngoscopic response among adults.

术前静脉注射和吸入右美托咪定对喉镜检查血流动力学反应的影响:一项前瞻性双盲随机研究。
目的喉镜检查会引起强烈的有害刺激,导致反射性自律神经激活,表现为血压和心率(HR)升高。人们尝试了各种不同途径的药物来防止这种反应。比较吸入右美托咪定和静脉注射右美托咪定预防喉镜检查反应的文献有限:方法:共纳入 150 名美国麻醉医师协会身体状况 I/II 级、接受需要喉镜检查和插管的择期手术的患者,并将其随机分为两组。DINH 组患者在麻醉诱导前 15 分钟接受雾化右美托咪定(1 μg/kg),DIV 组患者在麻醉诱导前 15 分钟接受静脉注射右美托咪定(0.5 μg/kg)。同时使用雾化或静脉注射生理盐水进行盲法。主要结果是比较喉镜检查、插管、插管后 1、5 和 10 分钟时的平均动脉压 (MAP) 和心率。次要结果是比较使用右美托咪定后的镇静效果、诱导过程中异丙酚的消耗量以及任何副作用:结果:喉镜检查和插管后的血压(毫米汞柱)无明显差异(插管后立即血压为 78.5 ± 11.3 vs. 82.3 ± 16.0,P = 0.093)。两组患者在喉镜检查和插管后的平均心率临床上相似(插管后立即心率为 80.9 ± 12.5 vs. 76.3 ± 10.9)。DIV 组患者的镇静程度高于 DINH 组(拉姆塞镇静量表 3-4 对 1-2,P <0.001)。只有 DIV 组的 8 名患者出现心动过缓:结论:在预防成人喉镜反应方面,术前雾化右美托咪定与静脉注射右美托咪定一样有效,而且更安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Research in Pharmacy Practice
Journal of Research in Pharmacy Practice PHARMACOLOGY & PHARMACY-
自引率
0.00%
发文量
8
审稿时长
21 weeks
期刊介绍: The main focus of the journal will be on evidence-based drug-related medical researches (with clinical pharmacists’ intervention or documentation), particularly in the Eastern Mediterranean region. However, a wide range of closely related issues will be also covered. These will include clinical studies in the field of pharmaceutical care, reporting adverse drug reactions and human medical toxicology, pharmaco-epidemiology and toxico-epidemiology (poisoning epidemiology), social aspects of pharmacy practice, pharmacy education and economic evaluations of treatment protocols (e.g. cost-effectiveness studies). Local reports of medication utilization studies at hospital or pharmacy levels will only be considered for peer-review process only if they have a new and useful message for the international pharmacy practice professionals and readers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信