糖尿病肾病高危初级保健患者的临床疗效:方法学挑战与 STOP-DKD 研究结果。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-10-01 Epub Date: 2024-07-18 DOI:10.1097/MLR.0000000000002043
Hayden B Bosworth, Uptal D Patel, Allison A Lewinski, Clemontina A Davenport, Jane Pendergast, Megan Oakes, Matthew J Crowley, Leah L Zullig, Sejal Patel, Jivan Moaddeb, Julie Miller, Shauna Malone, Huiman Barnhart, Clarissa J Diamantidis
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引用次数: 0

摘要

背景/目的:减缓糖尿病肾病(DKD)的进展至关重要。我们开展了一项随机对照试验,针对导致糖尿病肾病恶化的风险因素进行干预:与教育对照组相比,我们评估了以药剂师为主导的干预措施在 36 个月内对估计肾小球滤过率(eGFR)下降的影响,干预措施侧重于支持健康行为、药物管理和自我监测:我们将 138 人随机分配到干预组,将 143 人随机分配到对照组。基线时,eGFR 的平均值(标清)为 80.7 (21.7) mL/min/1.73m2 ,56% 的参与者患有慢性肾脏疾病和未控制的高血压病史,基线 SBP 为 134.3 mm Hg。对照组和干预组的胱抑素 C eGFR 从基线到 36 个月的平均(标度)降幅分别为 5.0 (19.6) 和 5.9 (18.6) mL/min/1.73m2 ,组间差异不显著(P=0.75):我们没有观察到不同研究组的临床结果有明显差异。结论:我们没有观察到不同研究组的临床结果有明显差异,但我们表明,患有 DKD 的人会参与药剂师指导的干预。DKD 风险因素未发生变化的潜在原因可归结为以下 5 大问题和挑战:(1)与招募 eGFR 低和血压控制不佳的患者有关;(2)干预措施的实施;(3)观察干预措施临床获益的时间有限;(4)潜在的共同干预或污染;以及(5)统计能力较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Outcomes Among High-Risk Primary Care Patients With Diabetic Kidney Disease: Methodological Challenges and Results From the STOP-DKD Study.

Background/objective: Slowing the progression of diabetic kidney disease (DKD) is critical. We conducted a randomized controlled trial to target risk factors for DKD progression.

Methods: We evaluated the effect of a pharmacist-led intervention focused on supporting healthy behaviors, medication management, and self-monitoring on decline in estimated glomerular filtration rate (eGFR) for 36 months compared with an educational control.

Results: We randomized 138 individuals to the intervention group and 143 to control. At baseline, mean (SD) eGFR was 80.7 (21.7) mL/min/1.73m 2 , 56% of participants had chronic kidney disease and a history of uncontrolled hypertension with a baseline SBP of 134.3 mm Hg. The mean (SD) decline in eGFR by cystatin C from baseline to 36 months was 5.0 (19.6) and 5.9 (18.6) mL/min/1.73m 2 for the control and intervention groups, respectively, with no significant between-group difference ( P =0.75).

Conclusions: We did not observe a significant difference in clinical outcomes by study arm. However, we showed that individuals with DKD will engage in a pharmacist-led intervention. The potential explanations for a lack of change in DKD risk factors can be attributed to 5 broad issues, challenges: (1) associated with enrolling patients with low eGFR and poor BP control; (2) implementing the intervention; (3) limited duration during which to observe any clinical benefit from the intervention; (4) potential co-intervention or contamination; and (5) low statistical power.

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CiteScore
7.20
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