Knight Tyler G, Ryan Kellie, Schaefer Caroline P, D'Sylva Lynell, Durden Emily D
Covance Market Access Services, Inc., Gaithersburg, MD 20878, USA.
J Manag Care Pharm. 2010 Oct;16(8):605-15. doi: 10.18553/jmcp.2010.16.8.605.
Anemia in patients with chronic kidney disease (CKD) is associated with increased morbidity and mortality, decreased quality of life, and substantial health care costs. Iron therapy is recommended, usually in combination with an erythropoiesis-stimulating agent (ESA), in many CKD patients with anemia and low iron levels to raise hemoglobin levels to a range of 10 to 12 grams per deciliter; iron deficiency is defined by a ferritin score less than 100 micrograms (mcg) per liter and transferrin saturation (TSAT) less than 20%.
To examine the use of intravenous (IV) iron and its associated economic and clinical outcomes in Medicare beneficiaries with stage 3 or stage 4 CKD and anemia.
This was a retrospective cohort analysis using 2006 and 2007 Medicare 5% Standard Analytic Files (SAF). Use of therapy with IV iron and/or ESAs was identified among patients diagnosed with CKD and anemia. The study index quarter was the first quarter in 2006 during which the patient had primary or secondary diagnoses of both CKD and anemia. Based on the receipt of IV iron or ESA treatment in the index quarter, patients were classified into 1 of 4 treatment groups: IV iron and ESA; IV iron without ESA; ESA without IV iron; neither IV iron nor ESA. Therapy with oral iron was not measurable with this database. Clinical and economic outcomes, including the progression to advanced CKD stages, development of anemia, mortality, hospitalization, and net Medicare reimbursement (i.e., not including patient or supplemental plan contribution) for all-cause health care services, were examined for 1 year following the index quarter. Between-group differences were tested using Pearson chi-square for categorical variables and the Kruskal-Wallis nonparametric test for reimbursement. Multivariate logistic regression models were estimated to assess the associations of mortality, inpatient hospitalization, skilled nursing facility (SNF) admission, and hospice care with treatment regimen, controlling for patient demographic and clinical characteristics.
Of the 4,310 study patients with both CKD and anemia, 2,913 (67.6%) received neither IV iron nor ESA; 984 (22.8%) received ESA without IV iron; 277 (6.4%) received IV iron and ESA; and 136 (3.2%) received IV iron without ESA in the index quarter. Logistic regression analyses showed that patients receiving neither IV iron nor ESA (reference group) were at increased risk of death compared with patients receiving both IV iron and ESA (OR = 0.62, 95% CI = 0.42-0.90). Additionally, patients receiving neither IV iron nor ESA were more likely to be hospitalized compared with patients receiving both IV iron and ESA (OR = 0.66, 95% CI = 0.50-0.87), IV iron without ESA (OR = 0.55, 95% CI = 0.38-0.79), and ESA without IV iron (OR = 0.73, 95% CI = 0.62-0.87). Further, patients not receiving IV iron or ESA were more likely to be admitted to an SNF than patients receiving both IV iron and ESA (OR = 0.44, 95% CI = 0.32-0.61), IV iron without ESA (OR = 0.57, 95% CI = 0.36-0.88), and ESA without IV iron (OR = 0.56, 95% CI = 0.47-0.67). Patients receiving neither IV iron nor ESA in the index quarter had the highest mean [SD] total Medicare reimbursement per patient in the subsequent year ($42,353 [$52,887]) compared with patients receiving IV iron without ESA ($28,654 [$32,068]), IV iron and ESA ($34,152 [$30,506]), or ESA without IV iron ($38,172 [$35,591], P = 0.001).
Use rates of IV iron and ESA in a sample of Medicare enrollees with CKD and anemia in 2006 suggest that anemia management therapies may be underutilized; however, oral iron therapy use was not measurable with the study database, and therapies initiated after the index quarter were not measured. Patients not treated with IV iron or ESA had significantly higher rates of hospitalization and SNF admission than patients treated with either IV iron or ESA. Further, mortality was significantly higher in patients receiving neither IV iron nor ESA than in patients who received IV iron and ESA. Additionally, total all-cause health care costs were higher among patients receiving neither IV iron nor ESA treatment compared with patients treated with IV iron and/or ESA.
慢性肾脏病(CKD)患者的贫血与发病率和死亡率增加、生活质量下降以及大量医疗保健费用相关。对于许多贫血且铁水平低的CKD患者,建议进行铁剂治疗,通常与促红细胞生成素(ESA)联合使用,以将血红蛋白水平提高到每分升10至12克的范围;铁缺乏的定义为铁蛋白水平低于每升100微克(mcg)且转铁蛋白饱和度(TSAT)低于20%。
研究静脉注射(IV)铁剂在患有3期或4期CKD及贫血的医疗保险受益人中的使用情况及其相关的经济和临床结果。
这是一项回顾性队列分析,使用2006年和2007年医疗保险5%标准分析文件(SAF)。在诊断为CKD和贫血的患者中确定IV铁剂和/或ESA治疗的使用情况。研究索引季度是2006年的第一季度,在此期间患者有CKD和贫血的原发性或继发性诊断。根据索引季度接受IV铁剂或ESA治疗的情况,患者被分为4个治疗组之一:IV铁剂和ESA;仅IV铁剂;仅ESA;既不使用IV铁剂也不使用ESA。该数据库无法测量口服铁剂治疗情况。在索引季度后的1年里,检查临床和经济结果,包括进展到晚期CKD阶段、贫血的发生、死亡率、住院情况以及所有原因医疗保健服务的医疗保险净报销(即不包括患者或补充计划缴费)。使用Pearson卡方检验对分类变量进行组间差异检验,使用Kruskal-Wallis非参数检验对报销情况进行检验。估计多变量逻辑回归模型以评估死亡率、住院治疗、熟练护理机构(SNF)入院和临终关怀护理与治疗方案之间的关联,并控制患者的人口统计学和临床特征。
在4310例患有CKD和贫血的研究患者中,2913例(67.6%)在索引季度既未接受IV铁剂也未接受ESA;984例(22.8%)仅接受ESA而未接受IV铁剂;277例(6.4%)接受IV铁剂和ESA;136例(3.2%)仅接受IV铁剂而未接受ESA。逻辑回归分析表明,与接受IV铁剂和ESA的患者相比,既未接受IV铁剂也未接受ESA的患者(参照组)死亡风险增加(OR = 0.62,95%CI = 0.42 - 0.90)。此外,与接受IV铁剂和ESA的患者相比,既未接受IV铁剂也未接受ESA的患者住院可能性更大(OR = 0.66,95%CI = 0.50 - 0.87),与仅接受IV铁剂而未接受ESA的患者相比(OR =