A prospective, pragmatic non-inferiority study of emergency intubation success with the single-use i-view versus standard reusable video laryngoscope

被引:0
作者
Schauer, Steven G. [1 ,2 ,3 ,8 ]
Long, Brit J. [2 ,3 ,4 ]
April, Michael D. [3 ,5 ]
Resnick-Ault, Daniel [6 ]
Mendez, Jessica [1 ]
Arana, Allyson A. [4 ]
Bastman, Jill J. [6 ]
Davis, William T. [2 ,3 ,4 ]
Maddry, Joseph K. [1 ,2 ,3 ,4 ]
Ginde, Adit A. [6 ,7 ]
Bebarta, Vikhyat S. [4 ,6 ,7 ]
机构
[1] US Army, Inst Surg Res, Jbsa Ft Sam Houston, TX USA
[2] Brooke Army Med Ctr, JBSA, Jbsa Ft Sam Houston, TX USA
[3] Uniformed Serv Univ Hlth Sci, Bethesda, MD USA
[4] 59th Med Wing, Jbsa Lackland, TX USA
[5] 14th Field Hosp, Ft Stewart, GA USA
[6] Univ Colorado, Sch Med, Aurora, CO USA
[7] Univ Colorado, Ctr COMBAT Res, Aurora, CO USA
[8] 3698 Chambers Pass, Jbsa Ft Sam Houston, TX 78234 USA
关键词
airway; combat; disposable; emergency; i-view; laryngoscope; laryngoscopy; military; trauma; video; IRAQ;
D O I
10.1111/trf.17790
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionVideo laryngoscope (VL) technology improves first-pass success. The novel i-view VL device is inexpensive and disposable. We sought to determine the first-pass intubation success with the i-view VL device versus the standard reusable VL systems in routine use at each site.MethodsWe performed a prospective, pragmatic study at two major emergency departments (EDs) when VL was used. We rotated i-view versus reusable VL as the preferred device of the month based on an a priori schedule. An investigator-initiated interim analysis was performed. Our primary outcome was a first-pass success with a non-inferiority margin of 10% based on the per-protocol analysis.ResultsThere were 93 intubations using the reusable VL devices and 81 intubations using the i-view. Our study was stopped early due to futility in reaching our predetermined non-inferiority margin. Operator and patient characteristics were similar between the two groups. The first-pass success rate for the i-view group was 69.1% compared to 84.3% for the reusable VL group. A non-inferiority analysis indicated that the difference (-15.1%) and corresponding 90% confidence limits (-25.3% to -5.0%) did not fall within the predetermined 10% non-inferiority margin.ConclusionsThe i-view device failed to meet our predetermined non-inferiority margin when compared to the reusable VL systems with the study stopping early due to futility. Significant crossover occurred at the discretion of the intubating operator during the i-view month.
引用
收藏
页码:S201 / S209
页数:9
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