Chronic Disease Research Group, Minneapolis Medical Research Foundation, Minneapolis, Minnesota, USA; Department of Medicine, Division of Nephrology, Hennepin County Medical Center, Minneapolis, Minnesota, USA; Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Chronic Disease Research Group, Minneapolis Medical Research Foundation, Minneapolis, Minnesota, USA.
Kidney Int. 2016 Oct;90(4):853-60. doi: 10.1016/j.kint.2016.04.026. Epub 2016 Jul 15.
The incidence and period prevalence of glomerulonephritis (GN) with resultant rates of death and end-stage renal disease (ESRD) in the United States are unknown. Therefore, we assessed the presumptive burden of GN in a 20% Medicare sample, 5,442,495 individuals, and an Optum Clinformatics Employer Group Health Plan sample of 13,712,946 individuals. GN was established using International Classification of Diseases, Ninth Revision, Clinical Modification claims-based algorithms. Outcomes were all-cause mortality and ESRD rates. Cox proportional hazards modeling was used to determine factors associated with outcomes in incident patients. For secondary (systemic immunologic disease) and primary GN, respectively, incidence rates per 100,000 patient-years were 134 (95% CI: 132-136) and 57 (56-58) in the Medicare cohort, and 10 (9-10) and 20 (19-21) in the health plan cohort. Period prevalence per 100,000 individuals was 917 (909-952) and 306 (302-311) in Medicare and 52 (51-54) and 70 (68-71) in the health plan. Death rates in incident Medicare patients were 3.9-fold higher for secondary and 2.7-fold higher for primary GN compared with no GN. ESRD rates were typically 1 to 2 orders of magnitude higher compared with no GN. In the Medicare cohort, women with incident secondary GN were less likely than men to progress to ESRD (hazard ratio: 0.70; 95% CI: 0.62-0.80) and death (0.82; 0.79-0.86). Black patients were more likely than white patients to progress to ESRD (secondary GN, 1.56; 1.31-1.85; primary GN, 1.57; 1.35-1.83), but not to death. Thus, in the United States, GN based on health claims data is associated with increased likelihood of progression to ESRD and death.
在美国,肾小球肾炎(GN)的发病率、期间患病率以及由此导致的死亡率和终末期肾病(ESRD)发病率均不明确。因此,我们评估了 Medicare 样本(20%,5442495 人)和 Optum Clinformatics 雇主团体健康计划样本(13712946 人)中 GN 的假定负担。GN 是通过国际疾病分类,第九修订版,临床修正基于索赔的算法确定的。结果为全因死亡率和 ESRD 发生率。使用 Cox 比例风险模型来确定与首发患者结局相关的因素。对于继发性(全身免疫性疾病)和原发性 GN,分别为每 10 万名患者年的发病率为 Medicare 队列中的 134(95%CI:132-136)和 57(56-58),健康计划队列中的 10(9-10)和 20(19-21)。每 10 万人的期间患病率为 Medicare 队列中的 917(909-952)和 306(302-311),健康计划队列中的 52(51-54)和 70(68-71)。与无 GN 相比,初次 Medicare 患者的继发性 GN 和原发性 GN 的死亡率分别高 3.9 倍和 2.7 倍。与无 GN 相比,ESRD 发生率通常高 1 到 2 个数量级。在 Medicare 队列中,与男性相比,患有首发继发性 GN 的女性进展为 ESRD(风险比:0.70;95%CI:0.62-0.80)和死亡(0.82;0.79-0.86)的可能性较低。黑人患者比白人患者更有可能进展为 ESRD(继发性 GN,1.56;1.31-1.85;原发性 GN,1.57;1.35-1.83),但不会死亡。因此,在美国,基于健康索赔数据的 GN 与进展为 ESRD 和死亡的可能性增加相关。