首页> 外文OA文献 >Prospective Evaluation of Sedation-Related Adverse Events in Pediatric Patients Ventilated for Acute Respiratory Failure
【2h】

Prospective Evaluation of Sedation-Related Adverse Events in Pediatric Patients Ventilated for Acute Respiratory Failure

机译:对因急性呼吸衰竭而通气的小儿患者的镇静相关不良事件进行前瞻性评估

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。

摘要

Objectives: Sedation-related adverse events in critically ill pediatric patients lack reproducible operational definitions and reference standards. Understanding these adverse events is essential to improving the quality of patient care and for developing prevention strategies in critically ill children. The purpose of this study was to test operational definitions and estimate the rate and site-to-site heterogeneity of sedation-related adverse events. Design: Prospective cohort study. Setting: Twenty-two pediatric intensive care units in the United States enrolling baseline patients into a prerandomization phase of a multicenter trial on sedation management. Patients: Pediatric patients intubated and mechanically ventilated for acute respiratory failure. Data Extraction: Analysis of adverse event data using consistent operational definitions from a Web-based data management system. Measurements and Main Results: There were 594 sedation-related adverse events reported in 308 subjects, for a rate of 1.9 adverse events per subject and 16.6 adverse events per 100 pediatric intensive care unit days. Fifty-four percent of subjects had at least one adverse event. Seven (1%) adverse events were classified as severe, 347 (58%) as moderate, and 240 (40%) as mild. Agitation (30% of subjects, 41% of events) and pain (27% of subjects, 29% of events) were the most frequently reported events. Eight percent of subjects (n = 24) experienced 54 episodes of clinically significant iatrogenic withdrawal. Unplanned endotracheal tube extubation occurred at a rate of 0.82 per 100 ventilator days, and 32 subjects experienced postextubation stridor. Adverse events with moderate intraclass correlation coefficients included: Inadequate sedation management (intraclass correlation coefficient = 0.130), clinically significant iatrogenic withdrawal (intraclass correlation coefficient = 0.088), inadequate pain management (intraclass correlation coefficient = 0.080), and postextubation stridor (intraclass correlation coefficient = 0.078). Conclusions: Operational definitions for sedation-related adverse events were consistently applied across multiple pediatric intensive care units. Adverse event rates were different from what has been previously reported in single-center studies. Many adverse events have moderate intraclass correlation coefficients, signaling site-to-site heterogeneity.
机译:目的:危重儿科患者中与镇静有关的不良事件缺乏可重复的操作定义和参考标准。了解这些不良事件对于提高患者护理质量和制定重症儿童的预防策略至关重要。这项研究的目的是测试操作定义并估计与镇静有关的不良事件的发生率和部位间异质性。设计:前瞻性队列研究。地点:美国的22个儿科重症监护室将基线患者纳入多中心镇静管理试验的随机化前阶段。患者:因急性呼吸衰竭而插管并进行机械通气的小儿患者。数据提取:使用基于Web的数据管理系统中一致的操作定义来分析不良事件数据。测量和主要结果:在308名受试者中报告了594次与镇静有关的不良事件,每名受试者小儿重症监护病房每100天有1.9次不良事件和16.6次不良事件。 54%的受试者患有至少一种不良事件。七种(1%)不良事件被分类为严重,347(58%)为中度,240(40%)为轻度。躁动(受试者的30%,事件的41%)和疼痛(受试者的27%,事件的29%)是最频繁报告的事件。 8%的受试者(n = 24)经历了54次临床上明显的医源性戒断发作。计划外气管插管的发生率为每100呼吸机天0.82的发生率,并且32名受试者经历了拔管后喘鸣。具有中等组内相关系数的不良事件包括:镇静管理不当(组内相关系数= 0.130),临床上显着的医源性戒断(组内相关系数= 0.088),疼痛处理不充分(组内相关系数= 0.080)和拔管后喘鸣(组内相关系数) = 0.078)。结论:镇静相关不良事件的手术定义在多个儿科重症监护病房中得到一致应用。不良事件发生率与单中心研究以前报道的发生率不同。许多不良事件具有中等的组内相关系数,表明位点间异质性。

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