Suppr超能文献

重症监护病房患者拔管后喘鸣。危险因素评估及套囊漏气试验的重要性。

Post-extubation stridor in intensive care unit patients. Risk factors evaluation and importance of the cuff-leak test.

作者信息

Jaber Samir, Chanques Gérald, Matecki Stefan, Ramonatxo Michèle, Vergne Christine, Souche Bruno, Perrigault Pierre-François, Eledjam Jean-Jacques

机构信息

Department of Anesthesiology, Intensive Care and Transplantation Unit (DAR B), Chu de Montpellier Hopital Saint Eloi, 80, avenue Augustin Fliche, 34295 Montpellier Cedex 5, France.

出版信息

Intensive Care Med. 2003 Jan;29(1):69-74. doi: 10.1007/s00134-002-1563-4. Epub 2002 Nov 22.

Abstract

OBJECTIVE

To evaluate the incidence and identify factors associated with the occurrence of post-extubation stridor and to evaluate the performance of the cuff-leak test in detecting this complication.

DESIGN

Prospective, clinical investigation.

SETTING

Intensive care unit of a university hospital.

PATIENTS

Hundred twelve extubations were analyzed in 112 patients during a 14-month period.

INTERVENTION

A cuff-leak test before each extubation.

MEASUREMENTS AND RESULTS

The incidence of stridor was 12%. When we chose the thresholds of 130 ml and 12% to quantify the cuff-leak volume, the sensitivity and the specificity of the test were, respectively, 85% and 95%. The patients who developed stridor had a cuff leak significantly lower than the others, expressed in absolute values (372+/-170 vs 59+/-92 ml, p<0.001) or in relative values (56+/-20 vs 9+/-13%, p<0.001). Stridor was associated with an elevated Simplified Acute Physiology Score (SAPS II), a medical reason for admission, a traumatic or difficult intubation, a history of self-extubation, an over-inflated balloon cuff at admission to ICU and a prolonged period of intubation. These results provide a framework with which to identify patients at risk of developing a stridor after extubation.

CONCLUSION

A low cuff-leak volume (<130 ml or 12%) around the endotracheal tube prior to extubation is useful in identifying patients at risk for post-extubation stridor.

摘要

目的

评估拔管后喘鸣的发生率,确定与拔管后喘鸣发生相关的因素,并评估套囊漏气试验在检测该并发症方面的性能。

设计

前瞻性临床研究。

地点

一所大学医院的重症监护病房。

患者

在14个月期间,对112例患者的112次拔管进行了分析。

干预措施

每次拔管前进行套囊漏气试验。

测量与结果

喘鸣发生率为12%。当我们选择130 ml和12%的阈值来量化套囊漏气量时,该试验的敏感性和特异性分别为85%和95%。发生喘鸣的患者套囊漏气量明显低于其他患者,以绝对值表示(372±170 vs 59±92 ml,p<0.001)或以相对值表示(56±20 vs 9±13%,p<0.001)。喘鸣与简化急性生理学评分(SAPS II)升高、入院的医学原因、创伤性或困难插管、自行拔管史、入住重症监护病房时球囊套囊过度充气以及插管时间延长有关。这些结果提供了一个框架,用以识别拔管后有发生喘鸣风险的患者。

结论

拔管前气管导管周围套囊漏气量低(<130 ml或12%)有助于识别有拔管后喘鸣风险的患者。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验