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Treatment of vitamin D deficiency within a large integrated health care delivery system

机译:在大型综合医疗保健提供系统中治疗维生素D缺乏症

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Background: In the past decade, increasing attention has focused on identification and treatment of vitamin D deficiency although repletion outcomes of pharmacologic vitamin D therapy have not been examined at a population level. OBJECTIVE: To investigate population trends and outcomes of pharmacologic treatment of vitamin D deficiency. METHODS: We conducted a retrospective cohort study using data from an integrated health system with approximately 3.2 million members. Automated laboratory and pharmacy databases were used to identify patients aged 18 years or older with hypovitaminosis D (defined as a 25-hydroxy-vitamin D [25(OH)D] serum level < 20 nanograms [ng] per mL) who newly initiated pharmacologic ergocalciferol (50,000 international units [IU] per week) during 2007-2010 and did not have a prescription for ergocalciferol in the prior 12 months. Patients were required to be continuously enrolled for 12 months before and 6 months after ergocalciferol initiation. Age, gender, race/ethnicity, body mass index, and 25(OH)D levels were obtained from health plan electronic medical records and administrative, laboratory, and pharmacy databases. Outcome and predictors of repletion among the subset who received 12 weekly doses of 50,000 IU ergocalciferol (total dose 600,000 IU) were examined using multivariable logistic regression. RESULTS: There were 72,093 vitamin D-deficient patients who newly initiated pharmacologic ergocalciferol. During the study period, the use of ergocalciferol increased nearly 8-fold from 161 per 100,000 adult members in 2007 to 1,241 per 100,000 adult members in 2010. One-fifth (n = 14,727) had severe vitamin D deficiency (25[OH]D level < 10 ng per mL). Among 23,322 patients receiving 50,000 IU ergocalciferol for 12 weeks in whom subsequent 25(OH)D levels were measured between 90 and 365 days after the index ergocalciferol prescription date, 74.0% achieved 25(OH)D of at least 20 ng per mL, and 35.8% achieved 25(OH)D of at least 30 ng per mL. Increasing age (adjusted odds ratio [OR] 1.02, 95% CI 1.02-1.02) and higher baseline 25(OH)D level (OR 1.11, 95% CI 1.10-1.12) were associated with greater odds of successful repletion. Asian race (OR 0.80, 95% CI 0.73-0.88), Hispanic ethnicity (OR 0.71, 95% CI 0.65-0.77), and increasing overweight/obesity (OR 0.78, 95% CI 0.72-0.85 for body mass index [BMI], 25.0-29.9 kg/m2; OR 0.66, 95% CI 0.60-0.71 for BMI 30.0-39.9 kg/m2; OR 0.53, 95% CI 0.48-0.60 for BMI ≥ 40 kg/m2) were associated with lower odds of repletion compared with BMI 18.5-24.9 kg/m2. CONCLUSIONS: There is increasing recognition and treatment of vitamin D deficiency within the health care setting. Patients of younger age, Asian and Hispanic race/ethnicity, and those who are obese or with more severe vitamin D deficiency may be at greater risk for incomplete repletion using standard regimens and may require additional treatment to achieve optimal levels.
机译:背景:在过去的十年中,尽管尚未在人群中检查药物性维生素D治疗的补充结果,但越来越多的注意力集中在维生素D缺乏症的识别和治疗上。目的:探讨维生素D缺乏症的人群趋势和药物治疗结果。方法:我们进行了一项回顾性队列研究,使用了来自拥有约320万会员的综合医疗系统的数据。自动化的实验室和药房数据库用于识别年龄在18岁或以上的维生素D缺乏症(定义为25-羟基维生素D [25(OH)D]血清水平<20毫微克[ng] / mL)的患者,这些患者新开始药物治疗麦角钙化固醇(每周50,000国际单位[IU]),并且在之前的12个月内没有处方麦角钙化醇。要求患者在麦角钙化固醇开始前12个月和6个月后连续入组。年龄,性别,种族/民族,体重指数和25(OH)D水平是从健康计划电子病历以及行政,实验室和药房数据库获得的。使用多变量logistic回归分析了接受12周每周剂量50,000 IU麦角钙化醇(总剂量600,000 IU)的亚组中的结局和充盈预测。结果:有72,093名维生素D缺乏症患者新开始药理麦角钙化醇。在研究期间,麦角钙化固醇的使用量增加了近8倍,从2007年的100,000人中的161人增加到2010年的100,000人中的1,241人。五分之一(n = 14,727)患有严重的维生素D缺乏症(25 [OH] D浓度<10 ng / mL)。在23,322名接受50,000 IU麦角骨化醇的12周患者中,在指标麦角骨化醇处方日期后90至365天之间测量了25(OH)D的水平,其中74.0%的患者达到25(OH)D至少为20 ng / mL,并且35.8%的25(OH)D至少为30 ng / mL。年龄的增加(校正比值比[OR] 1.02,95%CI 1.02-1.02)和较高的基线25(OH)D水平(OR 1.11,95%CI 1.10-1.12)与成功补充的可能性更高。亚洲种族(OR 0.80,95%CI 0.73-0.88),西班牙裔种族(OR 0.71,95%CI 0.65-0.77),体重指数[BMI]的超重/肥胖增加(OR 0.78,95%CI 0.72-0.85) ,25.0-29.9 kg / m2;或BMI为30.0-39.9 kg / m2的0.66,95%CI为0.60-0.71; BMI≥40 kg / m2的为0.53,95%CI为0.48-0.60)与较低的补给几率相关而BMI为18.5-24.9 kg / m2。结论:在医疗机构中,对维生素D缺乏症的认识和治疗正在不断增加。年龄较小,亚洲和西班牙裔/种族的患者,以及肥胖或维生素D缺乏症更为严重的患者,采用标准方案可能存在更大的不完全补充风险,并且可能需要进行额外治疗才能达到最佳水平。

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