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Predicting mortality from change-over-time in the Charlson Comorbidity Index: A retrospective cohort study in a data-intensive UK health system

机译:根据Charlson合并症指数随时间的变化预测死亡率:英国数据密集型卫生系统的一项回顾性队列研究

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Multimorbidity is common among older people and presents a major challenge to health systems worldwide. Metrics of multimorbidity are, however, crude: focusing on measuring comorbid conditions at single time-points rather than reflecting the longitudinal and additive nature of chronic conditions. In this paper, we explore longitudinal comorbidity metrics and their value in predicting mortality. Using linked primary and secondary care data, we conducted a retrospective cohort study on adults in Salford, UK from 2005 to 2014 (n = 287,459). We measured multimorbidity with the Charlson Comorbidity Index (CCI) and quantified its changes in various time windows. We used survival models to assess the relationship between CCI changes and mortality, controlling for gender, age, baseline CCI, and time-dependent CCI. Goodness-of-fit was assessed with the Akaike Information Criterion and discrimination with the c-statistic. Overall, 15.9% patients experienced a change in CCI after 10 years, with a mortality rate of 19.8%. The model that included gender and time-dependent age, CCI, and CCI change across consecutive time windows had the best fit to the data but equivalent discrimination to the other time-dependent models. The absolute CCI score gave a constant hazard ratio (HR) of around 1.3 per unit increase, while CCI change afforded greater prognostic impact, particularly when it occurred in shorter time windows (maximum HR value for the 3-month time window, with 1.63 and 95% confidence interval 1.59–1.66). Change over time in comorbidity is an important but overlooked predictor of mortality, which should be considered in research and care quality management.
机译:多种疾病在老年人中很常见,对全世界的卫生系统提出了重大挑战。但是,多发病率的度量标准很粗糙:重点在于在单个时间点上测量合并症,而不是反映慢性病的纵向和累加性质。在本文中,我们探讨了纵向合并症指标及其在预测死亡率中的价值。利用相关的初级和二级保健数据,我们对2005年至2014年在英国索尔福德的成年人进行了一项回顾性队列研究(n = 287,459)。我们用查尔森合并症指数(CCI)衡量了多发病率,并量化了其在不同时间范围内的变化。我们使用生存模型评估CCI变化与死亡率之间的关系,控制性别,年龄,基线CCI和时间依赖性CCI。拟合优度使用Akaike信息准则进行评估,而歧视则使用c统计量进行评估。总体而言,10年后15.9%的患者CCI发生了变化,死亡率为19.8%。该模型包括性别和与时间相关的年龄,CCI和连续时间窗内的CCI变化,最适合数据,但与其他与时间相关的模型具有同等的歧视性。绝对CCI评分给出的恒定危险比(HR)每增加1个单位约1.3,而CCI变化则对预后产生更大的影响,尤其是在较短的时间范围内发生时(3个月时间范围内的最大HR值,为1.63和95%置信区间1.59–1.66)。合并症随时间的变化是重要但被忽视的死亡率预测指标,应在研究和护理质量管理中予以考虑。

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