Department of Nephrology, Ajou University School of Medicine, 164, Worldcup-ro, Yeongtong-gu, Suwon, Gyeonggi-do 16499, Republic of Korea.
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, 123, Cheomdangwagi-ro, Buk-gu, Gwangju 61005, Republic of Korea.
Biomed Res Int. 2021 Nov 22;2021:5504873. doi: 10.1155/2021/5504873. eCollection 2021.
Chronic kidney disease-mineral bone disorder (CKD-MBD) is the most common complication in CKD patients. Although there is a consensus on treatment guidelines for CKD-MBD, it remains uncertain whether these treatment recommendations reflect actual practice. Therefore, the aim of this study was to investigate the CKD-MBD medication trend in real-world practice. This was a retrospective and observational study using a 12-year period database transformed into a common data model from three tertiary university hospitals. Study populations were subjects initially diagnosed as CKD. The date of diagnosis was designated as the index date. New patients were categorized year to year from 2008 to 2019 with a fixed observation period of 365 days to check the prescription of CKD-MBD medications including calcium-containing phosphate binder, noncalcium-containing phosphate binder, aluminium hydroxide, vitamin D receptor activator (VDRA), and cinacalcet. The numbers of CKD patients in the three hospitals were 7555, 2424, and 5351, respectively. The proportion for patients with CKD-MBD medication prescription decreased yearly regardless of hospital and CKD stage ( for trend < 0.05). The use of aluminium hydroxide disappeared steadily while the use of VDRA increased annually in all settings. Despite these changes in prescription patterns, the mean value for CKD-MBD-related serologic markers was almost within target range. The proportion of the population within the target value was not significantly changed. Irrespective of hospital and CKD stage, similar trends of prescription for CKD-MBD medications were observed in real-world practice. Further research with a distributed network study may be helpful to understand medication trends in CKD-MBD treatment.
慢性肾脏病-矿物质和骨异常(CKD-MBD)是 CKD 患者最常见的并发症。尽管 CKD-MBD 的治疗指南已经达成共识,但这些治疗建议是否反映实际情况仍不确定。因此,本研究旨在调查真实世界实践中 CKD-MBD 药物治疗趋势。这是一项回顾性和观察性研究,使用了来自三所三级大学医院的 12 年数据库转化为通用数据模型。研究人群为最初被诊断为 CKD 的患者。诊断日期被指定为索引日期。新患者按 2008 年至 2019 年逐年分类,固定观察期为 365 天,以检查 CKD-MBD 药物的处方,包括含钙磷酸盐结合剂、非含钙磷酸盐结合剂、氢氧化铝、维生素 D 受体激动剂(VDRA)和西那卡塞。三所医院的 CKD 患者人数分别为 7555、2424 和 5351。无论医院和 CKD 分期如何,CKD-MBD 药物处方的比例均逐年下降(趋势<0.05)。尽管处方模式发生了这些变化,但 CKD-MBD 相关血清标志物的平均值几乎仍在目标范围内。目标值范围内的人口比例没有明显变化。无论医院和 CKD 分期如何,真实世界实践中 CKD-MBD 药物处方均呈现出相似的趋势。具有分布式网络研究的进一步研究可能有助于了解 CKD-MBD 治疗中的药物趋势。