首页> 美国卫生研究院文献>other >The safety and efficacy of dexmedetomidine-remifentanil in children undergoing flexible bronchoscopy
【2h】

The safety and efficacy of dexmedetomidine-remifentanil in children undergoing flexible bronchoscopy

机译:右美托咪定-瑞芬太尼在进行柔性支气管镜检查的儿童中的安全性和有效性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Flexible bronchoscopy is more and more used for diagnosis and management of various pulmonary diseases in pediatrics. As poor coordination of children, the procedure is usually performed under general anesthesia with spontaneous or controlled ventilation to increase children and bronchoscopists’ safety and comfort. Previous studies have reported that dexmedetomidine (DEX) could be safely and effectively used for flexible bronchoscopy in both adulate and children. However, there is no trial to evaluate the dose-finding of safety and efficacy of dexmedetomidine-remifentanil (DEX-RF) in children undergoing flexible bronchoscopy.The objective of this study is to evaluate the dose-finding of safety and efficacy of DEX-RF in children undergoing flexible bronchoscopy.One hundred thirty-five children undergoing flexible bronchoscopy with DEX-RF were divided into 3 groups: Group DR1 (n = 47, DEX infusion at 0.5 μg·kg–1 for 10 minutes, then adjusted to 0.5–0.7 μg kg–1 h–1; RF infusion at 0.5 μg kg–1 for 2 minutes, then adjusted to 0.05–0.2 μg kg–1 min–1), Group DR2 (n = 43, DEX infusion at 1 μg kg–1 for 10 minutes, then adjusted to 0.5–0.7 μg kg–1 h–1; RF infusion at 1 μg kg–1 for 2 minutes, then adjusted to 0.05–0.2 μg kg–1 min–1), Group DR3 (n = 45, DEX infusion at 1.5 μg kg–1 for 10 minutes, then adjusted to 0.5–0.7 μg kg–1 h–1; RF infusion at 1 μg kg–1 for 2 minutes, then adjusted to 0.05–0.2 μg kg–1 min–1). Ramsay sedation scale of the 3 groups was maintained 3. Anesthesia onset time, total number of intraoperative children movements, hemodynamics (heart rate, arterial pressure, pulse oxygen saturation (SpO2), respiratory rate), total cumulative dose of dexmedetomidine and remifentanil, the amount of midazolam and lidocaine, time to first dose of rescue midazolam and lidocaine, postoperative recovery time, adverse events, bronchoscopist satisfaction score were recorded.Anesthesia onset time was significantly shorter in DR3 group (14.23 ± 5.45 vs 14.45 ± 5.12 vs 11.13 ± 4.51 minutes, respectively, of DR1, DR2, DR3, P = 0.003). Additionally, the perioperative hemodynamic profile was more stable in group DR3 than that in the other 2 groups. Total number of children movements during flexible bronchoscopy was higher in DR1 group than the other 2 groups (46.81% 22/47 vs 34.88% 15/43 vs 17.78% 8/45, respectively, of DR1, DR2, DR3, P = 0.012). Total doses of rescue midazolam and lidocaine were significantly higher in DR1 and DR2 groups than that of DR3 group (P = 0.000). The time to first dose of rescue midazolam and lidocaine was significantly longer in DR3 group than DR1 and DR2 groups (P = 0.000). Total cumulative dose of dexmedetomidine was more in DR2 and DR3 groups (P = 0.000), while the amount of remifentanil was more in DR1 and DR2 groups (P = 0.000). The time to recovery for discharge from the PACU was significantly shorter in DR1 group compared with the other 2 groups (P = 0.000). Results from bronchoscopist satisfaction score showed significantly higher in DR2 and DR3 groups than that of DR1 group (P = 0.025). There were significant differences among the 3 groups in terms of the overall incidence of hypertension, tachycardia, hypoxemia, and cough (P < 0.05).Though it required longer recovery time, high dose of DEX-RF, which provided better stable hemodynamic profiles and bronchoscopist satisfaction score, less amount of rescue scheme, and children movements, could be safely and efficacy used in children undergoing flexible bronchoscopy.
机译:柔性支气管镜越来越多地用于儿科各种肺部疾病的诊断和管理。由于儿童的协调性较差,因此通常在全身麻醉下自发或控制通气进行手术,以增加儿童和支气管镜医师的安全性和舒适度。先前的研究报道,右美托咪定(DEX)可以安全有效地用于成年和儿童的柔性支气管镜检查。但是,尚无试验评估柔性支气管镜检查儿童右美托咪定-瑞芬太尼(DEX-RF)的安全性和有效性的剂量确定性。进行柔性支气管镜检查的儿童的射频。135例接受DEX-RF柔性支气管镜的儿童分为3组:DR1组(n = 47,DEX输注剂量为0.5μg·kg –1 ) 10分钟,然后将其调整为0.5–0.7μgkg –1 h –1 ;以0.5μgkg –1 射频输注2分钟,然后调整为0.05–0.2μgkg –1 min –1 ),DR2组(n = 43,以1μgkg -1 10分钟,然后调整为0.5–0.7μgkg –1 h –1 ; RF输注量为1sμgkg –1 2分钟,然后调整为0.05–0.2μgkg –1 min –1 ),DR3组(n = 45,以1.5inμgkg –1 <输注DEX / sup> 10分钟,然后将其调整为0。 5–0.7μgkg –1 h –1 ;以1μgkg -1 射频输注2分钟,然后调整为0.05–0.2μg kg -1 min -1 。维持3组的Ramsay镇静规模。3麻醉开始时间,术中儿童运动总数,血液动力学(心率,动脉压,脉搏氧饱和度(SpO2),呼吸频率),右美托咪定和瑞芬太尼的总累积剂量,记录咪达唑仑和利多卡因的量,首次使用咪达唑仑和利多卡因的时间,术后恢复时间,不良事件,支气管镜医师满意度评分。DR3组的麻醉起效时间明显缩短(14.23±5.45 vs 14.45±5.12 vs 11.13±4.51分钟,分别为DR1,DR2,DR3,P = 0.003)。此外,DR3组的围手术期血流动力学特征比其他两组更稳定。 DR1组的柔性支气管镜检查儿童活动总数高于其他两组(DR1,DR2,DR3,P = 0.012分别为46.81%22/47比34.88%15/43对17.78%8/45) 。 DR1和DR2组的抢救性咪达唑仑和利多卡因的总剂量显着高于DR3组(P = 0.000)。在DR3组中,首次给予救援用咪达唑仑和利多卡因的时间明显长于DR1和DR2组(P = 0.000)。右美托咪定的总累积剂量在DR2和DR3组中较高(P = 0.000),而瑞芬太尼的量在DR1和DR2组中较高(P = 0.000)。 DR1组的PACU出院恢复时间明显短于其他2组(P = 0.000)。 DR2和DR3组的支气管镜医师满意评分结果显着高于DR1组(P = 0.025)。在高血压,心动过速,低氧血症和咳嗽的总发生率方面,三组之间存在显着差异(P <0.05),尽管需要更长的恢复时间,高剂量的DEX-RF才能提供更好的稳定血流动力学特征和支气管镜医师的满意度评分,较少的营救方案和儿童活动可以安全且有效地用于接受柔性支气管镜检查的儿童。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号