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Spine adverse events severity system: content validation and interobserver reliability assessment.

机译:脊柱不良事件严重程度系统:内容验证和观察者间可靠性评估。

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STUDY DESIGN: A prospective validation study, preliminary single-center report. OBJECTIVE: The purpose of this study was to assess the content validity and interobserver reliability of a simple severity classification system for adverse events (AEs) associated with spinal surgery. SUMMARY OF BACKGROUND DATA: In the surgical literature what is defined as an AE, the severity of an AE, and the reporting of AEs are variable. Consequently, valid comparison of AEs within or among specialties or surgical centers for the same or different procedures is often impossible. METHODS: Since 2002, a Spine Adverse Events Severity system (SAVES) has been locally developed and prospectively used. AEs were graded as I (requires none/minimal treatment, minimal effect [<1-2 days] on length of stay [LOS]), II (requires treatment and/or increases LOS [3-7 days] with no long-term sequelae), III (requires treatment and/or increased LOS [>7 days] with long-term sequelae [>6 months]), and IV (death). Content validity of the grading system was assessed using the hospital chart abstraction (current defacto gold standard) compared with the SAVES from 200 randomly selected patients. Interobserver reliability was assessed in consecutive operative cases for 1 spine surgeon during a 1-year period (2006) using 3 raters (staff surgeon, fellow, and/or resident). RESULTS: The prospectively administered form reported a higher number of surgical AEs (n = 43 vs. n = 30) and a similar number of medical AEs (n = 31 vs. n = 27). Compared with the chart, the AE form displayed substantial agreement for number (70%; weighted Kappa [wK] = 0.60) and type (75%; wK = 0.67) of AE. The interobserver reliability was near perfect (kappa = 0.8) for the actual grade of AE and moderate (kappa = 0.5) for the criteria behind the grading (i.e., clinical effect of the AE or the effect of the AE on LOS or both). CONCLUSION: The result of this study demonstrates improved capture of surgical AEs using SAVES. Excellent interobserver reliability between surgeons at different level of training was demonstrated with minimal education or training regarding the use of SAVES.
机译:研究设计:前瞻性验证研究,初步的单中心报告。目的:本研究的目的是评估一种简单的严重度分类系统对脊柱手术相关不良事件(AE)的内容有效性和观察者间可靠性。背景数据概述:在外科手术文献中,定义为AE,AE的严重程度以及AE的报告是可变的。因此,对于相同或不同的程序,通常无法在专业或外科中心内或之间对有效不良事件进行有效的比较。方法:自2002年以来,脊柱不良事件严重性系统(SAVES)已在本地开发并预期使用。不良事件分级为I(不要求/最少治疗,对住院时间[LOS]的影响最小[<1-2天]),II(不要求长期治疗和/或增加LOS [3-7天])后遗症),III(需要长期治疗后遗症[> 6个月]和/或LOS [> 7天]增加和/或LOS增加>)和IV(死亡)。使用医院图表摘要(现行事实上的黄金标准)与200位随机选择的患者的SAVES进行比较,评估分级系统的内容有效性。在1年期间(2006年),由3名评估者(职员外科医生,研究员和/或住院医师)评估了1名脊柱外科医生在连续手术病例中的观察者间可靠性。结果:前瞻性给药形式报告了较高的外科手术不良事件数量(n = 43 vs. n = 30)和相似数量的医疗不良事件(n = 31 vs. n = 27)。与图表相比,AE表格显示AE的数量(70%;加权Kappa [wK] = 0.60)和类型(75%; wK = 0.67)基本一致。观察者之间的信度对于AE的实际等级几乎是完美的(kappa = 0.8),而对于评分背后的标准(即AE的临床效果或AE对LOS的影响或两者)的观察者间信度接近中等(kappa = 0.5)。结论:这项研究的结果表明使用SAVES可以更好地捕获外科手术AE。在接受SAVES培训或培训最少的情况下,证明了接受不同培训水平的外科医生之间出色的观察者间可靠性。

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