- 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
- 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
- 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
- 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们。
- 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
- 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
右美托咪定在急性呼吸衰竭危重患儿中的应用
右美托咪定在急性呼吸衰竭危重患儿中的应用
Dexmedetomidine Use in Critically Ill Children With Acute Respiratory Failure
摘要翻译: 田 磊
原文摘要:
OBJECTIVE:
Care of critically ill children includes sedation but current therapies are suboptimal. To
describe dexmedetomidine use inchildren supported on mechanical ventilation for acute respiratory
failure.
DESIGN:
Secondary analysis of data from the Randomized Evaluation of Sedation Titration for Respiratory
Failure clinical trial.
SETTING:
Thirty-one PICUs.
PATIENTS:
Data from 2,449 children; 2 weeks to 17 years old.
INTERVENTIONS:
Sedation practices were unrestrained in the usual care arm. Patients were categorized as
receivingdexmedetomidine as a primary sedative, secondary sedative, periextubation agent, or never
prescribed. Dexmedetomidine exposure and sedation and clinical profiles are described.
MEASUREMENTS AND MAIN RESULTS:
Of 1,224 usual care patients, 596 (49%) received dexmedetomidine. Dexmedetomidine as a primary
sedative patients (n = 138; 11%) were less critically ill (Pediatric Risk of Mortality III-12 score median,
6 [interquartile range, 3-11]) and when compared with all other cohorts, experienced more episodic
agitation. In the intervention group, time in sedation target improved from 28% to 50% within 1 day of
initiating dexmedetomidine as a primary sedative. Dexmedetomidine as a secondary sedative usual care
patients (n = 280; 23%) included more children with severe pediatric acute respiratory distress
syndrome or organfailure. Dexmedetomidine as a secondary sedative patients experienced more
inadequate pain (22% vs 11%) and sedation (31% vs 16%) events. Dexmedetomidine as a
periextubation agent patients (n = 178; 15%) were those known to not tolerate an awake, intubated
state and experienced a shorter ventilator weaning process (2.
原创力文档


文档评论(0)