Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC), VA Cooperative Studies Program, VA Boston Healthcare System, Boston, MA, USA.
Nephrol Dial Transplant. 2010 Jul;25(7):2237-44. doi: 10.1093/ndt/gfp758. Epub 2010 Jan 18.
Erythropoiesis-stimulating agents (ESAs) are frequently used to treat anaemia of chronic kidney disease (CKD) in the dialysis setting; however, few data are available regarding factors influencing initiation of ESAs and other therapies in non-dialysis patients.
A retrospective cohort study of Veterans Health Administration data from 2003 to 2005 for 89 585 patients identified as having CKD and anaemia based on two outpatient estimated glomerular filtration rates <60 ml/min/1.73 m(2) and at least one outpatient haemoglobin (Hb) <11 g/dL. Hb levels, patient demographics, clinical and provider characteristics and procedures predicted ESA treatment initiation over 1 year of follow-up. Multivariable logistic and pooled logistic survival models identified predictors of ESA initiation.
Overall, 6381 subjects (7.1%) initiated ESAs within 1 year of the index Hb; initiation was more common (8.6%) for patients with Hb <10 g/dL. Iron therapy use varied by initial Hb levels (27.6% to 52.4%) as did transfusions (12.5% to 42.8%); each was more common at lower Hb levels. Hbs rose to above 11 g/dL for 25-50% of patients in the absence of any treatment or by transfusion/iron therapy. Factors predicting time to ESA initiation included: nephrologist [odds ratio (OR = 2.3)] or haematologist care (OR = 2.2) and iron therapy (OR = 1.6). Transfusions increased for patients with increasing follow-up time.
Iron therapy is more common than ESA treatment in patients with CKD and Hbs <11 g/dL in the VA. Correction of anaemia in the absence of any ESA treatment was common at higher Hbs levels, but much less so when Hb levels fell below 10 g/dL.
促红细胞生成素刺激剂(ESAs)常用于治疗透析患者的慢性肾脏病(CKD)相关贫血;然而,关于非透析患者中影响 ESA 及其他治疗方法起始的因素的数据较少。
本研究为 2003 年至 2005 年退伍军人健康管理局数据的回顾性队列研究,共纳入 89585 例患者,根据两次门诊估算肾小球滤过率(eGFR)<60 ml/min/1.73 m 2 和至少一次门诊血红蛋白(Hb)<11 g/dL,确定其患有 CKD 和贫血。在 1 年的随访期间,Hb 水平、患者人口统计学、临床和提供者特征及程序预测 ESA 治疗的起始。多变量逻辑和汇总逻辑生存模型确定 ESA 起始的预测因素。
总体而言,6381 例患者(7.1%)在索引 Hb 后 1 年内开始使用 ESA;Hb<10 g/dL 的患者中起始 ESA 的比例更高(8.6%)。铁剂治疗的使用因初始 Hb 水平而异(27.6%至 52.4%),输血也因初始 Hb 水平而异(12.5%至 42.8%);Hb 水平越低,两者越常见。在没有任何治疗或输血/铁剂治疗的情况下,25%至 50%的患者的 Hbs 升高至 11 g/dL 以上。预测 ESA 起始时间的因素包括:肾病医生(优势比[OR] = 2.3)或血液科医生(OR = 2.2)治疗和铁剂治疗(OR = 1.6)。随着随访时间的增加,输血患者数量增加。
在退伍军人健康管理局,与 Hb<11 g/dL 的 CKD 患者相比,铁剂治疗比 ESA 治疗更为常见。在 Hb 水平较高时,即使不进行任何 ESA 治疗,贫血也能得到纠正,但在 Hb 水平低于 10 g/dL 时,这种情况就不那么常见了。