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用于评估手术麻醉患者痛觉的 Analgesia Nociception Index (ANI) 和 Nociception Level Index (NOL) 的有效性描述:系统评价。

Description of the validity of the Analgesia Nociception Index (ANI) and Nociception Level Index (NOL) for nociception assessment in anesthetized patients undergoing surgery: a systematized review.

机构信息

Ingram School of Nursing, McGill University, Montréal, Canada.

Centre for Nursing Research and Lady Davis Institute, Jewish General Hospital - CIUSSS West-Central Montréal, Montréal, Canada.

出版信息

J Clin Monit Comput. 2022 Jun;36(3):623-635. doi: 10.1007/s10877-021-00772-3. Epub 2021 Nov 16.

Abstract

Maintaining optimum analgesia in anesthetized patients is challenging due to the inability to self-report pain or exhibit pain-related behaviours. The Analgesia Nociception Index (ANI) (based on heart rate variability [HRV]) and the Nociception Level Index (NOL) (based on HRV, photoplethysmography, skin conductance, and temperature) both include HRV and provide continuous index monitoring for nociception assessment. The research question was: "What are the validation strategies of the NOL and ANI for nociception assessment in anesthetized patients?". The objectives were to describe and analyze the validation strategies and results. A systematized review was conducted using a comprehensive search with keywords under three concepts (nociception/pain, ANI/NOL, and validity) in four databases. A quality assessment using an adapted GRADE approach for measurement tools, and a risk of bias assessment using QUADAS-2 tool were performed by two reviewers. Out of 525 results, 15 validation studies were included. Strategies included hypothesis testing, discriminative, and criterion validation. Significant changes in ANI/NOL values were found in response to nociceptive stimuli at different opioid concentrations (hypothesis testing). Higher ANI/NOL values were observed during nociceptive stimuli (discriminative). AUCs ranging from 0.83 to 0.99 were obtained to detect nociceptive stimuli (criterion). Both technologies performed superiorly in detecting nociceptive stimuli compared to individual monitoring of HR and blood pressure. Although the aforementioned validation strategies are deemed appropriate, in the absence of a gold standard, criterion validation findings should be interpreted with caution. Moreover, reliability could be examined using test-retest with consistent ANI/NOL values during a stable time-interval.

摘要

由于麻醉患者无法自我报告疼痛或表现出与疼痛相关的行为,因此维持最佳镇痛效果具有挑战性。镇痛/伤害感受指数(ANI)(基于心率变异性[HRV])和伤害感受水平指数(NOL)(基于 HRV、光容积描记法、皮肤电导和温度)均包含 HRV,并提供用于伤害感受评估的连续指数监测。研究问题是:“用于评估麻醉患者伤害感受的 NOL 和 ANI 的验证策略是什么?”。目的是描述和分析验证策略和结果。使用综合搜索,在四个数据库中使用三个概念(伤害感受/疼痛、ANI/NOL 和有效性)的关键字进行了系统评价。使用针对测量工具的改编版 GRADE 方法进行了质量评估,并使用 QUADAS-2 工具进行了偏倚风险评估。在 525 项研究结果中,有 15 项验证研究被纳入。策略包括假设检验、判别和标准验证。在不同阿片类药物浓度下,ANI/NOL 值对伤害性刺激的变化有显著差异(假设检验)。在伤害性刺激期间观察到较高的 ANI/NOL 值(判别)。获得了 0.83 至 0.99 的 AUC 以检测伤害性刺激(标准)。与单独监测 HR 和血压相比,这两种技术在检测伤害性刺激方面表现更好。尽管上述验证策略被认为是合适的,但在没有金标准的情况下,应谨慎解释标准验证结果。此外,可以使用具有一致 ANI/NOL 值的测试-再测试来检查可靠性,在稳定的时间间隔内。

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