首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Prevalence and correction of 25(OH) vitamin D deficiency in peritoneal dialysis patients.
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Prevalence and correction of 25(OH) vitamin D deficiency in peritoneal dialysis patients.

机译:腹膜透析患者中​​25(OH)维生素D缺乏症的发生率和校正。

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BACKGROUND: Peritoneal dialysis (PD) patients are at risk for 25(OH) vitamin D deficiency due to effluent loss in addition to traditional risk factors. OBJECTIVES: To measure 25(OH) vitamin D deficiency in prevalent PD patients, to evaluate a replacement dose, and to determine the effects of correction. METHODS: 25(OH) vitamin D levels were drawn on prevalent PD patients. Patients deficientin 25(OH) vitamin D were given ergocalciferol, 50000 IU orally once per week for 4 weeks. Patients scored muscle weakness, bone pain, and fatigue on a scale of 0 (none) to 5 (severe). Serum calcium, phosphate, parathyroid hormone (PTH), and 25(OH) vitamin D, and 1,25(OH)2 vitamin D levels were obtained before and after treatment. RESULTS: 25(OH) vitamin D levels were measured in 29 PD patients. Deficiency (<15 ng/mL) was found in 28/29 (97%); 25/29 (86%) had undetectable levels (<7 ng/mL). One course of ergocalciferol corrected the deficiency in all but 1 patient, who required a second course. Scores for muscle weakness and bone pain fell from pre- to posttreatment (p < 0.001). 1,25(OH)2 vitamin D levels rose post ergocalciferol (from 20 to 26 pg/mL, n = 20, p = 0.09). Serum calcium, phosphate, and PTH levels did not change with ergocalciferol. CONCLUSIONS: Most PD patients had marked 25(OH) vitamin D deficiency, which was readily and safely corrected with one course of 50000 IU ergocalciferol, having no effect on serum calcium, phosphorus, or PTH, but complaints of muscle weakness and bone pain decreased. A prospective, placebo-controlled double-blinded study is needed to determine whether replacement of 25(PH) vitamin D is beneficial in PD patients.
机译:背景:除了传统的危险因素外,由于流出物的丢失,腹膜透析(PD)患者还有25(OH)维生素D缺乏症的风险。目的:测量流行PD患者中25(OH)维生素D缺乏症,评估替代剂量,并确定矫正效果。方法:在PD患者中抽取25(OH)维生素D水平。维生素D 25(OH)缺乏症患者每周口服一次麦角钙化醇,50000 IU,共4周。患者的肌肉无力,骨痛和疲劳评分为0(无)至5(严重)。治疗前后分别获得血清钙,磷酸盐,甲状旁腺激素(PTH)和25(OH)维生素D和1,25(OH)2维生素D的水平。结果:29名PD患者中测得25(OH)维生素D水平。 28/29(97%)发现缺乏(<15 ng / mL); 25/29(86%)的水平达不到(<7 ng / mL)。一个疗程的麦角钙化固醇可纠正除一名患者外的所有患者的缺陷,需要第二疗程。肌肉无力和骨痛的评分从治疗前到治疗后下降(p <0.001)。麦角钙化固醇后1,25(OH)2维生素D含量升高(从20 pg / mL至26 pg / mL,n = 20,p = 0.09)。麦角钙化固醇不会改变血清钙,磷酸盐和PTH水平。结论:大多数PD患者具有明显的25(OH)维生素D缺乏症,可通过一个疗程的50000 IU麦角钙化醇轻松,安全地纠正维生素D缺乏症,对血清钙,磷或PTH无影响,但对肌肉无力和骨痛的抱怨减少。需要一项前瞻性,安慰剂对照的双盲研究来确定替代25(PH)维生素D对PD患者是否有益。

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