通过使用 "标志性椎体 "来消除在确定目标椎体水平时的可变性,从而使脊柱畸形手术中 "从未发生过 "错误部位手术。

IF 1.6 Q3 CLINICAL NEUROLOGY
Ritt R Givens, Matan S Malka, Kevin Lu, Amber Mizerik, Nicole Bainton, Thomas M Zervos, Benjamin D Roye, Lawrence G Lenke, Michael G Vitale
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引用次数: 0

摘要

目的:尽管引入了 "标准化计数 "方法,但脊柱水平计数错误和随后的错误水平手术(WLS)仍是患者安全的重要问题。我们小组之前的工作记录表明,尽管使用了包括脊柱畸形研究小组(SDSG)公约在内的这些系统,T12 的识别仍存在不一致性。为了帮助对术前手术水平进行一致且可重复的识别,本研究调查了一种新策略:使用 "标志性椎体"。假设与传统的 T12 定义方法相比,使用 "标志性椎体 "策略的个体在不同时间点之间的目标水平识别将达到较高的一致性:方法: 参与调查者分析了 99 张术前 X 光片,用 "最后一个双侧肋骨 "等简洁的描述识别并命名了 "标志性椎体"。然后,他们记下了建议的最低器械椎体 (LIV) 与标志椎体的相对距离(即比标志椎体低一个)。等待一段时间后,参与者使用他们对地标和 LIV 距离的书面描述来重新识别这些椎骨。Cohen's Kappa (k) 用于测量评分者之间的一致性。将地标策略与我们之前基于 SDSG 系统评估 T12 定义一致性的工作进行了比较:结果:在重新识别地标和目标椎体时,所有评分者都表现出完美或接近完美的一致性(k = 0.819-1.00;表 1A)。与定义 T12 的类似培训水平的评分者相比,所有培训水平的评分者在命名标志性椎体和目标椎体时的一致性更高(k = 0.34-0.91; 表 1B)。这种跨训练的高度一致性证明了该策略的通用性和普适性:结论:事实证明,使用地标策略能有效降低评分者内部的变异性,所有评分者之间的一致性完全接近完美,与定义T12相比,一致性一直较高:II级--前瞻性调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Making wrong site surgery a "never event" in spinal deformity surgery by use of a "landmark vertebra" to eliminate variability in identifying a target vertebral level.

Purpose: Despite the introduction of "standardized counting" methods, errors in counting spinal levels and subsequent wrong-level surgery (WLS) remain critically important patient safety concerns. Previous work by our group has documented inconsistency in the identification of T12 despite the use of these systems including the Spinal Deformity Study Group (SDSG) conventions. To assist with consistent and repeatable identification of proposed preoperative surgical levels, the current study investigates a new strategy: utilization of a "landmark vertebra". It was hypothesized that individuals using a "landmark vertebra" strategy will achieve high concordance with target level identification between distinct time points as compared to conventional methods defining T12.

Methods: Survey participants analyzed 99 pre-op radiographs, identifying and naming a "landmark vertebra" with concise descriptions like "last bilaterally ribbed vertebra." They then noted the proposed lowest instrumented vertebra's (LIV) distance relative to landmark (i.e., one below landmark). After a waiting period, participants used their written descriptions of the landmark and distance to LIV to reidentify these vertebrae. Cohen's Kappa (k) was used to measure intra-rater agreeability. The landmark strategy was compared to our previous work evaluating consistency in defining T12 based on the SDSG system.

Results: All raters showed perfect to near-perfect agreement when re-identifying the landmark and target vertebrae (k = 0.819-1.00; Table 1A). Raters at all training levels had higher agreeability in naming the landmark vertebra and target when compared to raters at similar training levels defining T12 (k = 0.34-0.91; Table 1B). This high agreement across training demonstrates the strategy's versatility and generalizability.

Conclusion: Utilization of a landmark strategy proved to be highly effective in reducing intra-rater variability, with perfect to near-perfect agreement among all raters and consistently higher agreeability when compared to defining T12.

Level of evidence: Level II-prospective survey.

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来源期刊
CiteScore
3.20
自引率
18.80%
发文量
167
期刊介绍: Spine Deformity the official journal of the?Scoliosis Research Society is a peer-refereed publication to disseminate knowledge on basic science and clinical research into the?etiology?biomechanics?treatment?methods and outcomes of all types of?spinal deformities. The international members of the Editorial Board provide a worldwide perspective for the journal's area of interest.The?journal?will enhance the mission of the Society which is to foster the optimal care of all patients with?spine?deformities worldwide. Articles published in?Spine Deformity?are Medline indexed in PubMed.? The journal publishes original articles in the form of clinical and basic research. Spine Deformity will only publish studies that have institutional review board (IRB) or similar ethics committee approval for human and animal studies and have strictly observed these guidelines. The minimum follow-up period for follow-up clinical studies is 24 months.
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