A Utilitarian Perspective on Risk Quantification for Clinical Significance in Binary Outcomes

IF 1.7 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Inquiry-The Journal of Health Care Organization Provision and Financing Pub Date : 2024-04-24 DOI:10.1177/00469580241248134
Junhui Park
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Abstract

Null hypothesis significance testing (NHST) in medical research is increasingly being supplemented by estimation statistics, focusing on effect sizes (ESs) and confidence intervals (CIs). This study evaluates the expression of ESs and CIs for binary outcomes. A utilitarian framework is proposed, emphasizing the number of beneficiaries and the impact level. To evaluate clinical significance, minimal clinically important risk difference (MCIRD) is proposed based on event magnitude (EM). Within this framework, risk difference (RD) is introduced as the primary measure. To assess the performance of RD, we compared its statistical power against other measures (risk ratio, RR; odds ratio, OR; Cohen’s h) in individual study scenarios, and visual information conveyance in meta-analysis scenarios. RDs maintain statistical power in comparison to other measures in individual studies. They provide clarity on the true impact of clinical interventions without compromising statistical integrity. Meta-analytic results indicate that using RDs directly enhances transparency, uncovers heterogeneity, and addresses misaligned assumptions. This approach, by quantifying clinical effectiveness under a utilitarian perspective, facilitates the applicability of research to patient care and encourages shared decision-making. The study advocates for reporting baseline risks (BRs) with RDs and recommends a standardized presentation of these statistics. In a utilitarian perspective, adopting RD as the preferred ES can foster a transparent, patient-focused research ethos. This aids in accurately presenting the magnitude and variability of treatment effects, offering a new direction in methodology.
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二元结果临床意义风险量化的功利主义视角
医学研究中的零假设显著性检验(NHST)越来越多地辅以估计统计,重点是效应大小(ES)和置信区间(CI)。本研究评估了二元结果的效应大小和置信区间的表达。研究提出了一个功利主义框架,强调受益人数和影响程度。为评估临床意义,提出了基于事件量级(EM)的最小临床重要风险差异(MCIRD)。在此框架内,引入了风险差异 (RD) 作为主要衡量标准。为了评估 RD 的性能,我们比较了 RD 与其他测量指标(风险比,RR;比值比,OR;Cohen's h)在单项研究中的统计能力,以及在荟萃分析中的视觉信息传达能力。与单项研究中的其他测量方法相比,风险系数保持了统计能力。在不影响统计完整性的前提下,它们能使临床干预措施的真实影响更加清晰。元分析结果表明,使用 RDs 可以直接提高透明度、发现异质性并解决假设不一致的问题。这种方法从功利的角度量化临床效果,有利于将研究成果应用于患者护理,并鼓励共同决策。该研究提倡报告基线风险(BRs)与RDs,并建议对这些统计数据进行标准化表述。从功利主义的角度来看,采用 RD 作为首选 ES 可以培养一种透明的、以患者为中心的研究精神。这有助于准确表述治疗效果的大小和可变性,为研究方法提供了一个新的方向。
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来源期刊
CiteScore
2.50
自引率
0.00%
发文量
192
审稿时长
>12 weeks
期刊介绍: INQUIRY is a peer-reviewed open access journal whose msision is to to improve health by sharing research spanning health care, including public health, health services, and health policy.
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