Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, 75 Francis St, Boston MA, 02115; Division of Rheumatology, Department of Internal Medicine III, Medical University Vienna, Vienna, Austria.
Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, 75 Francis St, Boston MA, 02115; Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA.
Semin Arthritis Rheum. 2015 Oct;45(2):167-73. doi: 10.1016/j.semarthrit.2015.06.010. Epub 2015 Jun 19.
To develop a multimorbidity index (MMI) based on health-related quality of life (HRQol).
The index was developed in an observational RA cohort. In all, 40 morbidities recommended as core were identified using ICD-9 codes. MMIs of two types were calculated: one by enumerating morbidities (MMI.count) and the other by weighting morbidities based on their association with HRQol as assessed by EQ-5D in multiple linear regression analysis (using β-coefficients; MMI.weight). MMIs were compared to the Charlson comorbidity index (CCI) and externally validated in an international RA cohort (COMORA Study).
In all, 544 out of 876 patients were multimorbid. MMI.count was in the range 1-16 (median = 2) and MMI.weight in the range 0-38 (median = 1). Both indices were more strongly associated with EQ-5D than CCI (Spearman: MMI.count = -0.20, MMI.weight = -0.26, and CCI = -0.10; p < 0.01). R(2) obtained by linear regression using EQ-5D as a dependent variable and various indices as independent variables, adjusted for age and gender, was the highest for MMI (R(2): MMI.count = 0.05, MMI.weight = 0.11, and CCI = 0.02). When accounting for clinical disease activity index (CDAI) R(2) increased: MMI.count = 0.18, MMI.weight = 0.22, and CCI = 0.17, still showing higher values of MMI compared with CCI. External validation in different RA cohorts (COMORA, n = 3864) showed good performance of both indices (linear regression including age, gender, and disease activity R(2) = 0.30 for both MMIs).
In our cohort, MMI based on EQ-5D performed better than did CCI. Findings were reproducible in another large RA cohort. Not much improvement was gained by weighting; therefore a simple counted index could be useful to control for the effect of multimorbidity on patient's overall well-being.
开发一种基于健康相关生活质量(HRQol)的多病症指数(MMI)。
该指数是在一项观察性类风湿关节炎队列研究中开发的。总共使用 ICD-9 代码确定了 40 种被推荐为核心的病症。计算了两种类型的 MMI:一种是通过枚举病症(MMI.count),另一种是通过基于与 HRQol 的关联对病症进行加权,该关联是通过多元线性回归分析(使用 β 系数)用 EQ-5D 评估的(使用β系数;MMI.weight)。将 MMI 与 Charlson 合并症指数(CCI)进行比较,并在国际类风湿关节炎队列(COMORA 研究)中进行外部验证。
总共 876 名患者中有 544 名患有多种病症。MMI.count 的范围为 1-16(中位数=2),MMI.weight 的范围为 0-38(中位数=1)。这两个指数与 EQ-5D 的相关性均强于 CCI(Spearman:MMI.count=-0.20,MMI.weight=-0.26,CCI=-0.10;p<0.01)。通过将 EQ-5D 作为因变量,将各种指数作为自变量进行线性回归,调整年龄和性别后,MMI 获得的 R2 值最高(R2:MMI.count=0.05,MMI.weight=0.11,CCI=0.02)。当考虑到临床疾病活动指数(CDAI)时,R2 增加:MMI.count=0.18,MMI.weight=0.22,CCI=0.17,与 CCI 相比,仍显示出更高的 MMI 值。在不同的类风湿关节炎队列(COMORA,n=3864)中的外部验证显示,这两个指数都表现良好(包括年龄、性别和疾病活动在内的线性回归 R2 均为 0.30)。
在我们的队列中,基于 EQ-5D 的 MMI 比 CCI 表现更好。在另一个大型类风湿关节炎队列中,该结果具有可重复性。加权没有带来太大改善;因此,简单的计数指数可能有助于控制多种病症对患者整体健康的影响。