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本文引用的文献

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Clinical testing patterns and cost implications of variation in the evaluation of CKD among US physicians.美国医生对慢性肾脏病评估差异的临床检测模式及成本影响
Am J Kidney Dis. 2009 Aug;54(2):227-37. doi: 10.1053/j.ajkd.2008.12.044. Epub 2009 Apr 15.
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In the clinic. Chronic kidney disease.在临床上。慢性肾病。
Ann Intern Med. 2009 Feb 3;150(3):ITC2-1-15; quiz ITC2-16. doi: 10.7326/0003-4819-150-3-200902030-01002.
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Phosphorus binders and survival on hemodialysis.磷结合剂与血液透析患者的生存情况
J Am Soc Nephrol. 2009 Feb;20(2):388-96. doi: 10.1681/ASN.2008060609. Epub 2008 Dec 17.
4
Association of low-energy femoral fractures with prolonged bisphosphonate use: a case control study.低能量股骨骨折与长期使用双膦酸盐的关联:一项病例对照研究。
Osteoporos Int. 2009 Aug;20(8):1353-62. doi: 10.1007/s00198-008-0805-x. Epub 2008 Dec 9.
5
Awareness and knowledge of clinical practice guidelines for CKD among internal medicine residents: a national online survey.内科住院医师对慢性肾脏病临床实践指南的认知与了解:一项全国性在线调查
Am J Kidney Dis. 2008 Dec;52(6):1061-9. doi: 10.1053/j.ajkd.2008.06.022. Epub 2008 Oct 30.
6
Recent developments in the management of postmenopausal osteoporosis with bisphosphonates: enhanced efficacy by enhanced compliance.双膦酸盐治疗绝经后骨质疏松症的最新进展:通过提高依从性增强疗效。
J Intern Med. 2008 Oct;264(4):315-32. doi: 10.1111/j.1365-2796.2008.02010.x.
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Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis.成纤维细胞生长因子23与接受血液透析患者的死亡率
N Engl J Med. 2008 Aug 7;359(6):584-92. doi: 10.1056/NEJMoa0706130.
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Chronic kidney disease and bone fracture: a growing concern.慢性肾病与骨折:日益受到关注。
Kidney Int. 2008 Sep;74(6):721-31. doi: 10.1038/ki.2008.264. Epub 2008 Jun 18.
9
Chronic kidney disease, atherosclerosis, and cognitive and physical function in the geriatric group of the National Health and Nutrition Survey 1999-2002.1999 - 2002年美国国家健康与营养检查调查老年组中的慢性肾脏病、动脉粥样硬化以及认知和身体功能
Atherosclerosis. 2009 Jan;202(1):312-9. doi: 10.1016/j.atherosclerosis.2008.04.020. Epub 2008 Apr 24.
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Severely suppressed bone turnover and atypical skeletal fragility.严重抑制的骨转换和非典型骨骼脆性。
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慢性肾脏病矿物质和骨代谢异常的诊断和治疗。

Diagnosis and management of mineral metabolism in CKD.

机构信息

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

J Gen Intern Med. 2010 Jul;25(7):710-6. doi: 10.1007/s11606-010-1316-y. Epub 2010 Mar 30.

DOI:10.1007/s11606-010-1316-y
PMID:20352364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2881958/
Abstract

BACKGROUND

Chronic kidney disease (CKD) affects over 26 million Americans and is frequently complicated early in its course by disordered mineral metabolism and metabolic bone disease. Since CKD-related bone loss is often indistinguishable from osteoporosis by standard bone densitometry, many CKD patients may be inappropriately treated with bisphosphonates rather than CKD-specific therapies.

OBJECTIVE

To determine the prevalence of appropriate evaluation, diagnosis and management of metabolic bone disease among individuals with pre-dialysis CKD.

DESIGN AND PARTICIPANTS

Retrospective cohort study using electronic medical records of 69,215 ambulatory patients seen in the primary care clinics of an academic medical center.

MEASUREMENTS

Prevalence of CKD stages 3-4, frequency of diagnostic testing and treatment of metabolic bone disease.

MAIN RESULTS

Based on current diagnostic criteria and consistent with national data, CKD was present in 12% of the population. Bisphosphonates were used in 7.2% of patients, 20% of whom met criteria for CKD. Fewer than half of CKD patients underwent testing for parathyroid hormone (PTH) or 25-hydroxyvitamin D (25D) levels. Among those tested, vitamin D deficiency (25D <30 ng/ml) and secondary hyperparathyroidism (PTH >60 pg/ml) were present in 65% and 55%, respectively. Among patients with CKD, bisphosphonate use was nearly seven times as frequent as therapy with active vitamin D (12% vs. 1.7%, p < 0.0001), a primary treatment for CKD-associated metabolic bone disease.

CONCLUSIONS

Disordered mineral metabolism in CKD is common, under-diagnosed and under-treated. As a result, bisphosphonates may be prescribed inappropriately in patients with CKD.

摘要

背景

慢性肾脏病(CKD)影响着超过 2600 万的美国人,并且在其早期阶段经常伴有矿物质代谢紊乱和代谢性骨病。由于 CKD 相关的骨丢失通常与骨质疏松症无法通过标准骨密度测量区分,许多 CKD 患者可能会被不适当地用双膦酸盐治疗,而不是采用 CKD 特异性治疗。

目的

确定接受透析前 CKD 患者的代谢性骨病的评估、诊断和治疗是否合理。

设计和参与者

这是一项使用学术医疗中心初级保健诊所的电子病历进行的回顾性队列研究,共纳入了 69215 名门诊患者。

测量

CKD 3-4 期的患病率、代谢性骨病的诊断检测和治疗频率。

主要结果

根据目前的诊断标准,与全国数据一致,该人群中 CKD 的患病率为 12%。有 7.2%的患者使用了双膦酸盐,其中 20%的患者符合 CKD 的诊断标准。不到一半的 CKD 患者接受甲状旁腺激素(PTH)或 25-羟维生素 D(25D)水平检测。在接受检测的患者中,维生素 D 缺乏(25D<30ng/ml)和继发性甲状旁腺功能亢进症(PTH>60pg/ml)的发生率分别为 65%和 55%。在 CKD 患者中,双膦酸盐的使用频率几乎是活性维生素 D(12%对 1.7%,p<0.0001)的七倍,活性维生素 D 是治疗 CKD 相关代谢性骨病的主要药物。

结论

CKD 中的矿物质代谢紊乱很常见,但诊断不足且治疗不足。因此,双膦酸盐可能会被不适当地用于 CKD 患者。