Using Virtual-Reality Simulation to Assess Performance in Endobronchial Ultrasound

被引:65
作者
Konge, Lars [1 ]
Annema, Jouke [4 ,5 ]
Clementsen, Paul [2 ]
Minddal, Valentina [2 ]
Vilmann, Peter [3 ]
Ringsted, Charlotte [6 ]
机构
[1] Univ Copenhagen & Capital Reg Denmark, Ctr Clin Educ, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, Gentofte Hosp, Dept Pulmonol, Hellerup, Denmark
[3] Univ Copenhagen, Herlev Hosp, Dept Surg Gastroenterol, DK-2730 Herlev, Denmark
[4] Leiden Univ, Med Ctr, Dept Pulmonol, Leiden, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Pulmonol, NL-1105 AZ Amsterdam, Netherlands
[6] Univ Toronto, Dept Anesthesia, Toronto, ON, Canada
关键词
Endobronchial ultrasound; Transbronchial needle aspiration; Virtual-reality simulator; BRONCHOSCOPY PERFORMANCE; NEEDLE-ASPIRATION; VALID ASSESSMENT; ASSESSMENT-TOOL; LUNG-CANCER; GUIDELINES;
D O I
10.1159/000350428
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: For optimal treatment of patients with non-small cell lung carcinoma, it is essential to have physicians with competence in endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA). EBUS training and certification requirements are under discussion and the establishment of basic competence should be based on an objective assessment of performance. Objectives: The aims of this study were to design an evidence-based and credible EBUS certification based on a virtual-reality (VR) EBUS simulator test. Methods: Twenty-two respiratory physicians were divided into 3 groups: experienced EBUS operators (group 1, n = 6), untrained novices (group 2, n = 8) and simulator-trained novices (group 3, n = 8). Each physician performed two standardized simulated EBUS-TBNA procedures. Simulator metrics with discriminatory ability were identified and reliability was explored. Finally, the contrasting-groups method was used to establish a pass/fail standard, and the consequences of this standard were explored. Results: Successfully sampled lymph nodes and procedure time were the only simulator metrics that showed statistically significant differences of p = 0.047 and p = 0.002, respectively. The resulting quality score (QS, i.e. sampled lymph nodes per minute) showed an acceptable reliability and a generalizability coefficient of 0.67. Reliability of 0.8 could be obtained by testing in 4 procedures. Median QS was 0.24 (range 0.21-0.26) and 0.098 (range 0.04-0.21) for groups 1 and 2, respectively (p = 0.001). The resulting pass/fail standard was 0.19. Group 3 had a median posttraining QS of 0.11 (range 0-0.17). None of them met the pass/fail standard. Conclusions: With careful design of standardized tests, a credible standard setting and appropriate transfer studies, VR simulators could be an important first line in credentialing before proceeding to supervised performance on patients. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:59 / 65
页数:7
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