SAMe-TT2R2 Score to Predict Time in Therapeutic Range of Vitamin K Antagonists in Asian and Non-Asian patients: A Systematic Review and Meta-analysis

IF 2.8 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Natnicha Poonchuay, Surasak Saokaew, Supatcha Incomenoy
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引用次数: 0

Abstract

Background

Sex, age, medical history, treatment, tobacco use, and race (SAMe-TT2R2) score helps detect patients at risk of suboptimal anticoagulation control. A score above two suggests poor control; however, non-Caucasian status being assigned two points might hinder the recognition of poor control in patients of other races.

Objective

To evaluate the SAMe-TT2R2 score’s ability to predict poor anticoagulation control [defined as time in therapeutic range (TTR) < 60–70%] in Asian and non-Asian populations on vitamin K antagonists (VKAs).

Methods

We searched PubMed, Cochrane Library, Scopus, SpringerLink, and Web of Science using the keyword “SAMe-TT2R2.” Articles published before April 2022 were screened. We gathered mean TTR and diagnostic accuracy data for different SAMe-TT2R2 thresholds and conducted meta-analyses using random-effects models.

Results

A total of 30 studies were included (N = 36,690). The overall mean TTR differences were − 4.88 and − 6.41 for the cutoffs of ≥ 3 and ≥ 4, respectively. For non-Asian patients, the mean TTR differences were − 3.86, − 5.12, and − 8.09 for the cutoffs ≥ 2, ≥ 3, and ≥ 4, respectively. For Asian patients, the mean TTR differences were − 3.99 and − 4.07 for the cut-offs ≥ 3 and ≥ 4, respectively. The highest positive likelihood ratio (LR+) for the Asian subgroup was 1.17 [95% confidence interval (CI): 1.06–1.28; I2 = 0%, p heterogeneity = 0.500] at cutoff ≥ 4 and for the non-Asian subgroup, at cut-off ≥ 3, the LR+ was 1.24 (95% CI 1.14–1.34; I2 = 0% p heterogeneity = 0.455). The lowest LR− was found at a lower cutoff for both races (at cutoff ≥ 3 and ≥ 2 for Asian and non-Asian subgroups, respectively). The pooled results of other accuracy parameters were modest at all cutoffs, except for the sensitivity at cutoff ≥ 3 in the Asian subgroup (83.05%).

Conclusion

Our study results suggest that a higher SAMe-TT2R2 score resulted in a greater reduction of TTR among Asian and all races. The accuracy parameters showed the highest sensitivity for poor TTR at the SAMe-TT2R2 cutoff of ≥ 3 for Asian patients. However, the ability to identify patients likely to have poor TTR was limited. Further research is needed to enhance the risk assessment for poor anticoagulation control with VKAs.

Registration

The protocol of this systematic review was registered in the International Prospective Register of Scientific Reviews: PROSPERO, registration number CRD42021291865.

Graphical Abstract

Abstract Image

预测亚裔和非亚裔患者服用维生素 K 拮抗剂治疗范围时间的 SAMe-TT2R2 评分:系统回顾与元分析》。
背景:性别、年龄、病史、治疗、烟草使用和种族(SAMe-TT2R2)评分有助于发现有抗凝控制不佳风险的患者。得分超过 2 分表明控制不佳;然而,非白种人被扣 2 分可能会妨碍识别其他种族患者控制不佳的情况:目的:评估 SAMe-TT2R2 评分预测服用维生素 K 拮抗剂(VKA)的亚裔和非亚裔人群抗凝控制不佳(定义为治疗范围内时间(TTR)< 60-70%)的能力:我们使用关键词 "SAMe-TT2R2 "检索了 PubMed、Cochrane Library、Scopus、SpringerLink 和 Web of Science。筛选了 2022 年 4 月之前发表的文章。我们收集了不同SAMe-TT2R2阈值的平均TTR和诊断准确率数据,并使用随机效应模型进行了荟萃分析:共纳入 30 项研究(N = 36,690)。阈值≥3和≥4的TTR总平均差异分别为-4.88和-6.41。对于非亚洲患者,截点≥2、≥3 和≥4 的平均 TTR 差异分别为 -3.86、-5.12 和 -8.09。对于亚洲患者,临界值≥3和≥4的平均TTR差异分别为-3.99和-4.07。亚裔亚组的最高正似然比(LR+)为截止值≥ 4 时的 1.17 [95% 置信区间(CI):1.06-1.28;I2 = 0%,异质性 = 0.500],而非亚裔亚组的截止值≥ 3 时的 LR+ 为 1.24 (95% CI 1.14-1.34;I2 = 0% ,异质性 = 0.455)。两个种族的最低 LR- 均出现在较低的临界值上(亚裔和非亚裔亚组的临界值分别为≥3 和≥2)。除了亚裔亚组在分界点≥3时的灵敏度(83.05%)外,其他准确度参数在所有分界点上的汇总结果都不高:我们的研究结果表明,SAMe-TT2R2 评分越高,亚裔和所有种族的 TTR 下降幅度越大。准确性参数显示,在 SAMe-TT2R2 临界值≥ 3 时,亚裔患者对 TTR 低的敏感性最高。然而,识别可能TTR不良患者的能力有限。需要进一步开展研究,以加强对 VKAs 抗凝控制不佳的风险评估:本系统综述的方案已在国际科学综述前瞻性注册中心(International Prospective Register of Scientific Reviews:PROSPERO,注册号为 CRD42021291865。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
3.30%
发文量
38
审稿时长
>12 weeks
期刊介绍: Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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