Different doses of Dexmedetomidine in attenuating the pressor response to laryngoscopy in controlled hypertensive patient under general anesthesia

Rumana Afroz, Rabeya Begum, Mahin Muntakim, Taneem Mohammad, Subrata Mondal, Mohammad Jahid Iqbal, Md Ali Haider, M. Kabir
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Abstract

Background: Laryngoscopic manipulation and endotracheal intubation are always a matter of concernwhich capable of producing tachycardia, arrhythmias and hypertension which is generally well tolerated inhealthy patient. In Hypertensive patient cardiovascular response to laryngoscopy and intubation is exaggerated. Aims: To assess the effectiveness in attenuation of haemodynamic responses to laryngoscopy andendotracheal intubation with different doses of intravenous dexmedetomidine in controlled hypertensivepatients with no adverse effects. Methods: This prospective Randomized controlled trial was carried out with 60 patients belonging toAmerican Society of Anesthesiologists (ASA) Physical Status II posted for elective general anaesthesia.Patients were randomly divided into three groups with fixed card sampling, where, patients who receivedIV dexmedetomidine 0.5 μg/kg diluted to 50 ml with normal saline as infusion over 10 min was consideredas group A, patients who received IV dexmedetomidine 0.75 μg/kg diluted to 50 ml with normal salinewas considered as group B and patients who received IV dexmedetomidine 1 μg/kg diluted to 50 ml withnormal saline was considered as group C. The primary outcome measures were haemodynamic responseat 1, 3 and 5 min after intubation. The secondary outcome measures were to note down any adverseeffects associated with drugs. Result: The groups were well matched for their demographic data . Male to female ratio was 1:1 in allthree group. The mean height, weight and BMI were almost similar among three groups. In this studybaseline readings of SBP, DBP, MAP and HR were almost similar in all three groups and statistically notsignificant. Maximum intubation response was seen at 1 min post intubation in all the three groups. Themean SBP of group A varied from 144.8±8.4 mmHg to 118.5±4.4 mmHg that of group B varied from134.8±4.1 to 122.0±4.2 mmHg and then group C varied from 126.5±15.5 mmHg to 103.8±8.4 mmHgduring different evaluation period (p<0.05). The mean DBP of group A varied from 91.8±7.6 mmHg to72.4±5.8 mmHg that of group B varied from 81.3±5.2 to 70.3±2.5 mmHg and then group C varied from80.9±6.7 mmHg to 63.4±2.4 mmHg during different evaluation period (p<0.05). The mean MAP of groupA varied from 109.0±5.6 mmHg to 87.5±4.4 mmHg that of group B varied from 98.7±2.5 to 86.3±3.4mmHg and then group C varied from 95.5±9.2 mmHg to 76.5±3.4 mmHg during different evaluationperiod (p<0.05). The mean heart rate of group A varied from 94.5±12.7 bpm to 75.2±10.5 bpm that ofgroup B varied from 87.3±8.3 to 75.0±6.6 bpm and then group C varied from 81.1±7.2 bpm to 66.2±8.1bpm during different evaluation period (p<0.05). Conclusion: Dexmedetomidine in doses of 0.75 μg/kg was more effective compared to 0.05 μg/kg and1μg/kg in attenuating haemodynamic response to laryngoscopy and endotracheal intubation withoutproducing adverse effects in control hypertensive patients. JBSA 2020; 33(2): 69-77
不同剂量右美托咪定减轻全麻下控制高血压患者喉镜降压反应的研究
背景:喉镜操作和气管插管一直是一个值得关注的问题,可能产生心动过速、心律失常和高血压,而健康患者通常耐受良好。高血压患者对喉镜和插管的心血管反应被夸大。目的:评价不同剂量右美托咪定对无不良反应的控制性高血压患者喉镜和气管插管血流动力学反应的衰减效果。方法:本前瞻性随机对照试验纳入60例隶属于美国麻醉医师学会(ASA)物理状态II的择期全麻患者。采用固定卡片抽样法将患者随机分为三组,其中,给予0.5 μg/kg右美托咪定用生理盐水稀释至50 ml输液超过10 min的患者为A组;静脉注射右美托咪定0.75 μg/kg稀释至50 ml生理盐水组为B组,静脉注射右美托咪定1 μg/kg稀释至50 ml生理盐水组为c组。主要观察指标为插管后1、3、5 min血流动力学反应。次要结局指标是记录与药物相关的任何不良反应。结果:两组人口统计数据匹配良好。三组男女比例均为1:1。三组的平均身高、体重和身体质量指数几乎相似。在本研究中,三组患者的收缩压、舒张压、MAP和HR基线读数几乎相似,且无统计学意义。三组均在插管后1分钟出现最大插管反应。A组的平均收缩压在144.8±8.4 mmHg ~ 118.5±4.4 mmHg之间变化,B组在134.8±4.1 ~ 122.0±4.2 mmHg之间变化,C组在126.5±15.5 mmHg ~ 103.8±8.4 mmHg之间变化(p<0.05)。A组的平均舒张压变化范围为91.8±7.6 ~ 72.4±5.8 mmHg, B组的平均舒张压变化范围为81.3±5.2 ~ 70.3±2.5 mmHg, C组的平均舒张压变化范围为80.9±6.7 ~ 63.4±2.4 mmHg (p<0.05)。a组的平均MAP值在109.0±5.6 ~ 87.5±4.4 mmHg之间变化,B组在98.7±2.5 ~ 86.3±3.4mmHg之间变化,C组在95.5±9.2 ~ 76.5±3.4 mmHg之间变化(p<0.05)。各组患者的平均心率A组为94.5±12.7 ~ 75.2±10.5 bpm, B组为87.3±8.3 ~ 75.0±6.6 bpm, C组为81.1±7.2 ~ 66.2±8.1bpm (p<0.05)。结论:与0.05 μg/kg和1μg/kg剂量的右美托咪定相比,0.75 μg/kg剂量的右美托咪定能更有效地降低喉镜检查和气管插管患者的血流动力学反应,且无不良反应。JBSA 2020;33 (2): 69 - 77
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