Department of Nephrology, Università degli Studi di Bari, Bari, Italy.
Intern Emerg Med. 2013 Aug;8(5):389-99. doi: 10.1007/s11739-011-0622-7. Epub 2011 May 18.
Prior longitudinal observational studies have examined the practice patterns and outcomes of anaemia management, including the use of erythropoiesis-stimulating agents (ESAs). Several dimensions of effectiveness remain unaddressed; especially considering the revised ESA label (target Hb levels between 10 and 12 g/dL), the recently published TREAT study, and the European approval of the first ESA biosimilar (HX575). Anecdotal evidence suggests that patient outcomes are influenced by physician-related variables and whether anaemia management is congruent with practice guidelines, but this has not been studied systematically. MONITOR-CKD5 is an international, prospective, observational, pharmacoepidemiological study evaluating the multi-level factors and outcomes of treatment with HX575 for renal anaemia in haemodialysis patients. Driven by a novel, integrated, multi-focal framework for post-approval observational studies, it examines determinants of response at both the patient and the physician level; integrates an advocated statistical methodology here to fore used mainly in the social and behavioural sciences; assesses factors potentially predictive of a poor treatment response; and evaluates the extent to which treatment is congruent with evidence-based guidelines, good practice evidence, and the revised ESA label. This pan-European study will recruit at least 1,000 patients from a minimum of 75 centres, and follow them for up to 24 months following initiation of anaemia management with biosimilar epoetin alfa. MONITOR-CKD5 will not only study the core issues addressed by prior observational studies but also aims to take knowledge discovery a step further by assessing outcomes across varying cohorts of patients, and examining the impact of evidence-based practice on clinical outcomes, differentiating, in the process, between physician-level and patient-level determinants.
先前的纵向观察性研究已经考察了贫血管理的实践模式和结果,包括使用红细胞生成刺激剂(ESA)。几个有效性维度尚未得到解决;特别是考虑到修订后的 ESA 标签(目标 Hb 水平在 10 到 12g/dL 之间)、最近发表的 TREAT 研究以及欧洲对首个 ESA 生物类似药(HX575)的批准。一些传闻证据表明,患者的结局受到医生相关变量的影响,以及贫血管理是否与实践指南一致,但这尚未得到系统研究。MONITOR-CKD5 是一项国际性、前瞻性、观察性、药物流行病学研究,评估了 HX575 治疗血液透析患者肾性贫血的多层次因素和结局。该研究受一种新颖的、综合的、多焦点的批准后观察性研究框架驱动,考察了患者和医生层面的反应决定因素;在这里整合了一种提倡的统计方法,这种方法主要以前用于社会和行为科学;评估了潜在预测治疗反应不良的因素;并评估了治疗与循证指南、良好实践证据和修订后的 ESA 标签的一致性程度。这项泛欧研究将从至少 75 个中心招募至少 1000 名患者,并在开始使用生物类似 epoetin alfa 进行贫血管理后对他们进行长达 24 个月的随访。MONITOR-CKD5 不仅将研究先前观察性研究中解决的核心问题,还旨在通过评估不同患者队列的结局并检查循证实践对临床结局的影响,进一步推进知识发现,在此过程中,区分医生层面和患者层面的决定因素。