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引用次数: 0
摘要
背景:长期持续肾脏替代治疗(CKRT)的并发症尚未得到很好的描述。我们的目的是描述需要长期接受 CKRT 的儿童的矿物质代谢和骨骼情况:在这项单中心前瞻性观察研究中,我们招募了 37 名需要 CKRT ≥ 28 天并进行区域性枸橼酸盐抗凝治疗的患者。研究对象为接受 CKRT 的时间,研究结果为 25- 羟基维生素 D 和骨质疏松和/或骨折:结果:维生素 D 缺乏和不足的发生率分别为 17.2% 和 69.0%。29.7%的患者有骨质疏松和/或骨折的影像学检查结果。维生素 D 缺乏或不足与年龄或种族无关。接受 CKRT 治疗的时间和完整的 PTH 水平并不能预测维生素 D 水平。与其他主要诊断的儿童相比,患有慢性肝病的儿童更有可能出现骨质疏松和/或骨折,调整年龄和接受 CKRT 治疗的时间后,几率比(3.99(95%CI,1.58-2.91),p = 0.003):结论:维生素 D 缺乏和/或不足、骨质疏松和/或骨折在需要长期接受 CKRT 的儿童中很普遍。慢性肝病患 MBD 的风险可能更高。在接受 CKRT 治疗期间,可能需要更大剂量的维生素 D 才能维持正常水平。
Vitamin D and metabolic bone disease in prolonged continuous kidney replacement therapy: a prospective observational study.
Background: Complications of prolonged continuous kidney replacement therapy (CKRT) have not been well described. Our objective was to describe mineral metabolism and bone findings in children who required prolonged CKRT.
Methods: In this single center prospective observational study, we enrolled 37 patients who required CKRT for ≥ 28 days with regional citrate anticoagulation. Exposure was duration on CKRT and outcomes were 25-hydroxy vitamin D and osteopenia and/or fractures.
Results: The prevalence of vitamin D deficiency and insufficiency was 17.2% and 69.0%, respectively. 29.7% of patients had radiographic findings of osteopenia and/or fractures. There was no association between vitamin D deficiency or insufficiency with age or ethnicity. Time on CKRT and intact PTH levels were not predictive of vitamin D levels. Children with chronic liver disease were more likely to have osteopenia and/or fractures compared children with other primary diagnoses, odds ratio (3.99 (95%CI, 1.58-2.91), p = 0.003) after adjusting for age and time on CKRT.
Conclusion: Vitamin D deficiency and/or insufficiency, and osteopenia and/or fractures are prevalent among children who require CKRT for a prolonged period. The risk for MBD may be higher with chronic liver disease. Higher doses of vitamin D may be required to maintain normal levels while on CKRT.
期刊介绍:
BMC Nephrology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of kidney and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.