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前瞻性支付制度与种族/民族差异:美国终末期肾病患者贫血并发症的全国回顾性观察研究。

Prospective payment system and racial/ethnic disparities: a national retrospective observational study in anaemia complication among end-stage renal disease patients in the US.

机构信息

Centre for Public Health, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, UK.

出版信息

BMC Nephrol. 2020 Oct 6;21(1):423. doi: 10.1186/s12882-020-02081-4.

Abstract

BACKGROUND

A series of policy changes in 2011 altered reimbursement arrangements and guidance on use of erythropoiesis-stimulating agents for end-stage renal disease (ESRD) patients with anaemia in the US. While the policy changes were principally directed at care delivered in an outpatient setting, these had the potential to affect inpatient care also. This study used HCUP-NIS data (2008-2016) to examine trends in recorded anaemia among ESRD hospitalizations and analyse disparities in inpatient outcomes among ethnic groups following policy changes.

METHODS

The International Classification of Diseases codes were used to identify ESRD admissions, recorded anaemia due to chronic kidney disease (CKD), and to generate an age-adjusted Deyo-Charlson comorbidity index. Linear splines with a knot placed at the time point of policy changes and multivariable logistic regression were used to examine the likelihood of recorded anaemia, adjusted for a range of socio-demographic and clinical covariates. Difference-in-difference analyses investigated the impact of policies on recorded anaemia. Other outcomes included hospital cost, mortality and place of discharge.

RESULTS

The percentage of inpatient episodes with recorded anaemia arising from CKD increased from 26.2% in 2008 to 50.0% in 2016. Anaemia was more likely to be recorded as a complication of ESRD among minority ethnic groups and Native American admissions, in particular, (OR 1.20, 95%CI 1.15-1.25) relative to White American admissions; and these disparities widened following changes to reimbursement. Minorities were less likely to die in hospital and to be discharged to another healthcare facility, and (with the exception of Black American admissions) they were more expensive to treat.

CONCLUSIONS

Our findings provide evidence of an increase in recorded anaemia consistent with a shift of patients from outpatient to inpatient settings in the wake of changes to reimbursement enacted in 2011. In addition, the study highlights the existence of ethnic disparities that widened after the policy initiated reimbursement changes.

摘要

背景

2011 年的一系列政策变化改变了美国终末期肾病(ESRD)贫血患者的红细胞生成刺激剂使用的报销安排和使用指南。虽然这些政策变化主要针对门诊治疗,但它们也有可能影响住院治疗。本研究使用 HCUP-NIS 数据(2008-2016 年),研究政策变化后,记录的 ESRD 住院患者贫血趋势,并分析不同种族群体的住院结局差异。

方法

使用国际疾病分类代码识别 ESRD 入院、因慢性肾脏病(CKD)引起的记录性贫血,并生成年龄调整后的德约-查尔森共病指数。使用带有政策变化时间点结的线性样条和多变量逻辑回归来检查记录性贫血的可能性,同时调整了一系列社会人口统计学和临床协变量。差异中的差异分析研究了政策对记录性贫血的影响。其他结果包括医院成本、死亡率和出院地点。

结果

CKD 引起的住院患者中记录性贫血的比例从 2008 年的 26.2%增加到 2016 年的 50.0%。在少数民族和美洲原住民入院中,贫血更有可能被记录为 ESRD 的并发症,与白人美国人入院相比,这一比例更高(比值比 1.20,95%可信区间 1.15-1.25);而且,在报销方式改变后,这些差距扩大了。少数民族患者在医院死亡和出院到其他医疗机构的可能性较低,除了黑人患者外,他们的治疗费用更高。

结论

我们的研究结果提供了证据,表明随着 2011 年实施的报销政策的变化,记录的贫血患者数量增加,这与患者从门诊转移到住院治疗相一致。此外,该研究还强调了政策启动报销变化后扩大的种族差异的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01b/7541203/d6ab9c108ed4/12882_2020_2081_Fig1_HTML.jpg

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