Stepwise approach to screen high-risk individuals using the non-laboratory-based and laboratory-based CVD risk scoring.

Noushin Fahimfar, Sareh Eghtesad, Hossein Poustchi, Karim Kohansal, Sadaf G Sepanlou, Afshin Ostovar, Ali Esmaeili-Nadimi, Ehsan Bahramali, Farhad Pourfarzi, Samad Ghaffari, Azim Nejatizadeh, Farhad Moradpour, Ali Mousavizadeh, Farahnaz Joukar, Saeid Bitaraf, Vahid Mohammadkarimi, Farid Najafi, Seyed Vahid Hosseini, Ali Gohari, Arsalan Khaledifar, Motahareh Kheradmand, Kamal Khademvatani, Mohammad Hasan Lotfi, Alireza Ansari-Moghaddam, Reza Malekzadeh, Davood Khalili
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Abstract

Objective: We compared non-laboratory models' efficacy with standard laboratory-based model in identifying high-risk populations for cardiovascular disease (CVD) in resource-limited settings.

Methods: A national sample of 121 672 individuals aged 40-70 from the PERSIAN cohort was analyzed. Non-laboratory models, including the World Health Organization (WHO) and Iranian pooled-cohort CVD mortality models, were compared with the WHO laboratory-based model. Intra-class correlation coefficient (ICC) and concordance correlation coefficient (CCC) were utilized. Sensitivity and specificity of non-laboratory models were evaluated against the laboratory-based one at various risk thresholds. The number of reduced tests in the stepwise approach was calculated considering the Iranian census.

Results: Both non-laboratory and laboratory-based models showed similar trends in predicting CVD risks across age groups. Strong correlations and concordance were observed in both men (ICC: 94.4%, CCC:0.893) and women (ICC: 93.8%, CCC:0.883). Utilizing a 5% risk threshold for WHO non-laboratory and 2% for the Iranian pooled-cohort CVD mortality model as the initial step achieved high sensitivity (99.6%) and moderate specificity (52%) for identifying candidates for the second-step laboratory test. This approach effectively reduced the number of tests by 16 807 982.

Conclusion: Non-laboratory models, in a stepwise approach, offer a promising strategy to alleviate strain on financial resources and enhance healthcare system efficiency in resource-limited countries.

采用非实验室和实验室CVD风险评分逐步筛选高危人群。
目的:比较非实验室模型与标准实验室模型在资源有限环境下识别心血管疾病(CVD)高危人群的疗效。方法:对来自波斯队列的121,672名年龄在40-70岁之间的个体进行分析。非实验室模型,包括世界卫生组织(世卫组织)和伊朗合并队列心血管疾病死亡率模型,与世卫组织实验室模型进行了比较。采用类内相关系数(ICC)和一致性相关系数(CCC)。在不同的风险阈值下,对非实验室模型和实验室模型的敏感性和特异性进行了评估。考虑到伊朗的人口普查情况,计算了逐步方法的简化检验次数。结果:非实验室和基于实验室的模型在预测心血管疾病风险方面显示出相似的趋势。在男性(ICC: 94.4%, CCC:0.893)和女性(ICC: 93.8%, CCC:0.883)中均观察到强相关性和一致性。采用世卫组织非实验室5%的风险阈值和伊朗合并队列心血管疾病死亡率模型2%的风险阈值作为初始步骤,在确定第二步实验室检测候选人方面获得了高灵敏度(99.6%)和中等特异性(52%)。这种方法有效地减少了16 807 982次测试。结论:非实验室模型,在逐步的方法,提供了一个有希望的战略,以减轻财政资源紧张,提高医疗保健系统效率在资源有限的国家。
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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