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代理 SARC-F 的临床验证:评估依赖老年人肌少症的实用工具。

Clinical validation of SARC-F by proxy as a practical tool to evaluate sarcopenia in dependent older adults.

机构信息

Department of Internal Medicine, Division of Geriatrics, Istanbul Medical School, Istanbul University, Capa, Istanbul 34093, Türkiye.

Department of Public Health, Istanbul Medical School, Istanbul University, Capa, Istanbul 34093, Türkiye.

出版信息

J Geriatr Oncol. 2023 Nov;14(8):101630. doi: 10.1016/j.jgo.2023.101630. Epub 2023 Sep 22.

DOI:10.1016/j.jgo.2023.101630
PMID:37741772
Abstract

INTRODUCTION

Sarcopenia is a prevalent disorder in older adults with significant adverse outcomes and regular screening is recommended for those at risk. The SARC-F questionnaire is the most commonly recommended screening tool for sarcopenia. However, as a self-reported tool, it cannot be applied to dependent individuals with communication problems. We hypothesized that implementation of the proxy-reported SARC-F (SARC-F by proxy) would be non-inferior in screening sarcopenia when compared with the standard SARC-F. Thus, we aimed to investigate the clinical validity of the SARC-F by proxy in identifying sarcopenia in older adults and to compare its performance with the standard SARC-F. Additionally, we aimed to determine the ideal cut-off of SARC-F by proxy in screening sarcopenia.

MATERIALS AND METHODS

This is a validation study including older adults aged ≥60 years without communication problems and their close proxies. The participants were recruited from a geriatric outpatient clinic of a tertiary health center and a nursing home. Standard SARC-F was transformed to SARC-F by proxy and administered to the proxies of older adults, and standard SARC-F was administered to the patients simultaneously in different rooms. We defined sarcopenia as probable and confirmed by the EWGSOP2 consensus report. We performed receiver operating characteristics (ROC) and sensitivity/specificity analyses of SARC-F by proxy for diagnosing sarcopenia and compared its performance with standard SARC-F by the DeLong test.

RESULTS

We included 172 older adults (median age: 72; 44.8% female) and 107 proxies in close contact (median age: 55, 63.2% female). The prevalence of probable and confirmed sarcopenia was 18.9% and 12.9%, respectively. For both definitions, area under the curve (AUC) values of SARC-F by proxy and standard SARC-F were moderate and similar [probable sarcopenia: 0.619 and 0.624 (p = 0.9); confirmed sarcopenia 0.613 and 0.645 (p = 0.7), respectively]. The best balance between sensitivity and specificity was achieved with a SARC-F by proxy score of ≥2 for both sarcopenia definitions (sensitivity levels were 74.7% and 77.8%, and specificity levels were 50.0% and 49.6%, for probable and confirmed sarcopenia, respectively).

DISCUSSION

SARC-F by proxy showed a similar, non-inferior performance compared to the standard SARC-F in the evaluation of sarcopenia. Our results suggest that it can be used instead of standard SARC-F to screen sarcopenia in older patients with communication problems. Further validation studies in different populations are warranted to support our findings.

摘要

简介

肌少症是老年人中普遍存在的疾病,会产生严重的不良后果,建议对高危人群进行常规筛查。SARC-F 问卷是最常被推荐用于肌少症筛查的工具。然而,作为一种自我报告的工具,它不能用于有沟通问题的依赖个体。我们假设代理报告的 SARC-F(SARC-F by proxy)在筛查肌少症方面与标准 SARC-F 相比具有非劣效性。因此,我们旨在研究代理报告的 SARC-F(SARC-F by proxy)在识别老年人肌少症方面的临床有效性,并比较其与标准 SARC-F 的性能。此外,我们旨在确定 SARC-F by proxy 筛查肌少症的理想截断值。

材料与方法

这是一项验证性研究,纳入了年龄≥60 岁、无沟通问题且有密切亲属的老年人及其亲属。参与者来自一家三级保健中心的老年门诊和一家疗养院。对老年人的亲属进行标准 SARC-F 转化为 SARC-F by proxy,并同时在不同房间对患者进行标准 SARC-F 测试。我们根据 EWGSOP2 共识报告将肌少症定义为可能和确诊。我们对 SARC-F by proxy 进行了诊断肌少症的受试者工作特征(ROC)和敏感性/特异性分析,并通过 DeLong 检验比较了其与标准 SARC-F 的性能。

结果

我们纳入了 172 名老年人(中位年龄:72 岁,44.8%为女性)和 107 名密切接触的亲属(中位年龄:55 岁,63.2%为女性)。可能和确诊的肌少症患病率分别为 18.9%和 12.9%。对于这两种定义,SARC-F by proxy 和标准 SARC-F 的曲线下面积(AUC)值均为中等且相似[可能的肌少症:0.619 和 0.624(p=0.9);确诊的肌少症:0.613 和 0.645(p=0.7)]。对于这两种肌少症定义,SARC-F by proxy 评分≥2 时均能达到最佳的敏感性和特异性平衡(敏感性水平分别为 74.7%和 77.8%,特异性水平分别为 50.0%和 49.6%)。

讨论

SARC-F by proxy 在评估肌少症方面与标准 SARC-F 具有相似的、非劣效的性能。我们的研究结果表明,在有沟通问题的老年患者中,它可以替代标准 SARC-F 进行肌少症筛查。需要在不同人群中进行进一步的验证研究来支持我们的发现。

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