Shastri Jay, Tran Anthony, Covit Andrew, Pepe John, Sherman Richard A
Division of Nephrology, Department of Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick, New Jersey 08903-0019, USA.
J Ren Nutr. 2008 Jul;18(4):370-4. doi: 10.1053/j.jrn.2008.04.011.
The Kidney Disease Outcomes Quality Initiative (K/DOQI) clinical practice guidelines for bone metabolism in chronic kidney disease recommend that calcium-based phosphate binders (CBPBs) be used in limited doses and be reduced or withheld when albumin-adjusted serum calcium exceeds target values, or when parathyroid hormone is below the target range. We sought to assess the pattern of CBPB use in a clinical practice setting.
This was a retrospective review.
We reviewed 283 patients at three hemodialysis units in New York and New Jersey in which 39 physicians practice.
Data collected included intact parathyroid hormone levels (from February and May, 2006), blood chemistries (from April and May, 2006), and the use of CBPBs, vitamin D, and cinacalcet. The use of CBPBs was classified as "consistent" or "inconsistent" with the guidelines 1 month after the blood tests of May 2006 (to allow time for dosing adjustments). Because cinacalcet was not available when the K/DOQI guidelines were published, a failure to reduce or stop CBPBs in the presence of elevated calcium levels was still considered to be "consistent" use if cinacalcet was initiated in the appropriate time frame (5 patients).
CBPBs were used in 172 of 283 patients (61%). In 10% (17 patients), doses exceeded the 1500-mg limit for calcium. Adjusted serum calcium levels exceeded 2.5 mmol/L (10.2 mg/dL) in 8 cases; CBPBs were not reduced or stopped in any of these. Similarly, CBPBs were reduced in only 2 of 27 patients on vitamin D, with an adjusted serum calcium level of 2.38 to 255 mmol/L (9.5 to 10.2 mg/dL). In all 10 patients with consecutive intact parathyroid hormone values of less than 150 ng/L (150 pg/mL), CBPBs were not discontinued or reduced.
Overall, 50 of 172 patients (29%) receiving CBPBs did so in a manner inconsistent with K/DOQI guidelines. The reasons for this inconsistency are speculative, and may include disagreement with the opinion-based recommendations, insufficient knowledge of the guidelines, or individual patient considerations (including cost, tolerance, and effectiveness).
《肾脏病预后质量倡议(K/DOQI)慢性肾脏病骨代谢临床实践指南》建议,应限制使用钙基磷结合剂(CBPB),当白蛋白校正的血清钙超过目标值,或甲状旁腺激素低于目标范围时,应减少剂量或停用。我们试图评估临床实践中CBPB的使用模式。
这是一项回顾性研究。
我们回顾了纽约和新泽西州三个血液透析单位的283例患者,这些单位有39名医生执业。
收集的数据包括完整的甲状旁腺激素水平(2006年2月和5月)、血液生化指标(2006年4月和5月),以及CBPB、维生素D和西那卡塞的使用情况。2006年5月血液检查1个月后(以便有时间进行剂量调整),CBPB的使用被分类为与指南“一致”或“不一致”。由于K/DOQI指南发布时西那卡塞尚未上市,如果在适当的时间范围内开始使用西那卡塞(5例患者),在血钙升高时未减少或停用CBPB仍被视为“一致”使用。
283例患者中有172例(61%)使用了CBPB。10%(17例)的患者剂量超过了钙的1500毫克限制。8例患者的校正血清钙水平超过2.5 mmol/L(10.2 mg/dL);这些患者中无一例减少或停用CBPB。同样,27例服用维生素D的患者中只有2例减少了CBPB,其校正血清钙水平为2.38至2.55 mmol/L(9.5至10.2 mg/dL)。在10例连续完整甲状旁腺激素值低于150 ng/L(150 pg/mL)的患者中,CBPB均未停用或减量。
总体而言,172例接受CBPB治疗的患者中有50例(29%)的使用方式与K/DOQI指南不一致。这种不一致的原因尚属推测,可能包括对基于观点的建议存在分歧、对指南的了解不足,或个别患者的考虑因素(包括成本、耐受性和有效性)。