Ravera Maura, Mené Paolo, Degli Esposti Luca, Sangiorgi Diego, Di Rienzo Paolo
Ospedale Policlinico San Martino, Genova.
Sapienza Università di Roma, Azienda Ospedaliera Sant'Andrea, Roma.
G Ital Nefrol. 2023 Feb 27;40(1):2023-vol1.
This real-world study aimed to provide insights on the characteristics, drug utilization, and economic burden of chronic kidney disease non-dialysis-dependent (NDD-CKD) patients with anemia prescribed Erythropoiesis Stimulating Agents (ESA) in Italian clinical practice settings. A retrospective analysis was performed based on administrative and laboratory databases covering around 1.5 million subjects across Italy. Adult patients with a record for NDD-CKD stage 3a-5 and anemia during 2014-2016 were identified. Eligibility to ESA was defined as the presence of ≥ 2 records of Hb < 11 g/dL over 6 months, and patients eligible and currently treated with ESA were included. Overall, 101,143 NDD-CKD patients were screened for inclusion, of which 40,020 were anemic. A total of 25,360 anemic patients were eligible to ESA treatment and 3,238 (12.8%) were prescribed ESA and included. The mean age was 76.9 years and 51.1% was male. More frequently observed comorbidities were hypertension (over 90% in each stage), followed by diabetes (37.8-43.2%) and cardiovascular condition (20.5-28.9%). Adherence to ESA was observed in 47.9% of patients, with a downward trend while progressing across stages (from 65.8% stage 3a to 35% stage 5). A consistent proportion of patients did not have nephrology visits during the 2 years of follow-up. Costs were mainly due to all drugs (€4,391) followed by all-cause hospitalization (€3,591) and laboratory tests (€1,460). Findings from the study highlight an under-use of ESA in the management of anemia in NDD-CKD as well as a sub-optimal adherence to ESA and showed a great economic burden for anemic NDD-CKD patients.
这项真实世界研究旨在深入了解在意大利临床实践环境中,接受促红细胞生成素(ESA)治疗的非透析依赖性慢性肾脏病(NDD-CKD)合并贫血患者的特征、药物使用情况及经济负担。基于覆盖意大利约150万受试者的行政和实验室数据库进行了回顾性分析。确定了2014年至2016年期间患有NDD-CKD 3a-5期且合并贫血的成年患者。ESA治疗的入选标准为在6个月内有≥2次血红蛋白(Hb)<11 g/dL的记录,纳入符合条件且正在接受ESA治疗的患者。总体而言,筛查了101,143例NDD-CKD患者以纳入研究,其中40,020例贫血。共有25,360例贫血患者符合ESA治疗条件,3,238例(12.8%)接受了ESA治疗并被纳入研究。平均年龄为76.9岁,男性占51.1%。最常见的合并症是高血压(各阶段均超过90%),其次是糖尿病(37.8 - 43.2%)和心血管疾病(20.5 - 28.9%)。47.9%的患者对ESA治疗依从,且随着病情进展呈下降趋势(从3a期的65.8%降至5期的35%)。在2年随访期间,相当一部分患者未进行肾病科就诊。费用主要来自所有药物(4391欧元),其次是全因住院(3591欧元)和实验室检查(1460欧元)。该研究结果凸显了在NDD-CKD贫血管理中ESA使用不足以及对ESA的依从性欠佳,并显示贫血的NDD-CKD患者经济负担沉重。