基层医疗机构早期慢性肾病综合管理项目的五年成果。

IF 2.5 Q1 MEDICINE, GENERAL & INTERNAL Annals of the Academy of Medicine, Singapore Pub Date : 2024-10-15 DOI:10.47102/annals-acadmedsg.2023399
Sky Wei Chee Koh, Ping Young Ang, Hung Chew Wong, Hui Qi Koh, Nurfaziela Binti Zainal, Cynthia Sze Mun Wong
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引用次数: 0

摘要

导言:降低和跟踪慢性肾脏病的整体方法(HALT-CKD)是新加坡于 2017 年推出的一项全国性计划,旨在防治慢性肾脏病。本研究旨在评估 HALT-CKD 计划的成果,并确定影响早期 CKD 患者疾病进展的因素:我们开展了一项回顾性队列研究,研究对象是 2017 年至 2018 年期间从新加坡 5 家综合医院招募的 21 至 80 岁 CKD 分期 G1-G3A 的成年患者。根据患者最后一次已知的血清肌酐水平,对其进展为晚期 CKD(G3B-G5)的主要结果时间进行了追踪,直至 2023 年 3 月。研究采用了描述性统计和 Cox 回归方法。在其他机构随访的患者、死亡的患者或未出现(或经历)结果而违约的患者均被剔除:我们对 3800 名患者(平均年龄:61.9 岁)进行了中位数为 4.7 年的研究。其中,尽管 HbA1c、血压和白蛋白尿水平有了统计学意义上的显著改善,但仍有 12.6% 的患者发展为晚期 CKD。年龄、女性性别、门诊、基线血肌酐、舒张压和 HbA1c 的增加明显缩短了 CKD 进展的时间。基线时的巨蛋白尿(危险比 [HR] 1.77,95% 置信区间 [CI] 1.19-2.61)和分析时的巨蛋白尿(HR 2.22,95% 置信区间 [CI] 1.55-3.19)明显加快了晚期 CKD 的进展。血管紧张素转换酶抑制剂(ACEi)/血管紧张素受体阻滞剂(ARB)剂量减少或停用的患者更早进展为晚期 CKD(HR 1.92,95% CI 1.50-2.45)。咨询和钠-葡萄糖共转运体-2抑制剂(SGLT2i)的使用并不能显著延缓CKD的进展:结论:保持最佳的 ACEi/ARB 剂量对延缓 CKD 进展至关重要。结论:保持最佳 ACEi/ARB 剂量是延缓 CKD 进展的关键,应避免过早停药或减少剂量。为应对日益加重的慢性肾脏病负担,需要进一步研究早期慢性肾脏病患者的咨询和 SGLT2i 的使用。
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Five-year outcomes of a holistic programme for managing early chronic kidney disease in primary care.

Introduction: Holistic Approach in Lowering and Tracking Chronic Kidney Disease (HALT-CKD) is a nationwide programme that was introduced in 2017 to combat CKD in Singapore. This study aims to evaluate outcomes of the HALT-CKD programme and identify factors influencing disease progression among early CKD patients.

Method: We conducted a retrospective cohort study involving adult patients aged 21 to 80 with CKD stages G1-G3A, recruited from 5 Singapore polyclinics between 2017 and 2018. The primary outcome-time to progression to advanced CKD (G3B-G5)-was tracked until March 2023, based on patients' last known serum creatinine levels. Descriptive statistics and Cox regression were used. Patients who followed up with other institutions, were deceased or defaulted without developing (or experiencing) the outcome were censored.

Results: We studied 3800 patients (mean age: 61.9 years) for a median of 4.7 years. Among them, 12.6% developed advanced CKD despite statistically significant improvements in HbA1c, blood pressure and albuminuria levels. Increasing age, female sex, clinic, baseline creatinine, diastolic blood pressure and HbA1c significantly shortened time to CKD progression. Macro-albuminuria at baseline (hazard ratio [HR] 1.77, 95% confidence interval [CI] 1.19- 2.61) and at analysis (HR 2.22, 95% CI 1.55-3.19) significantly accelerated advanced CKD progression. Patients who had their angiotensin-converting enzyme inhibitor (ACEi)/angiotensin receptor blocker (ARB) dose reduced or discontinued progressed to advanced CKD earlier (HR 1.92, 95% CI 1.50-2.45). Counselling and sodium-glucose cotransporter-2 inhibitor (SGLT2i) use did not significantly delay CKD progression.

Conclusion: Maintaining optimal ACEi/ARB dosage is essential to delay CKD progression. Premature cessation or reduction of this dosage should be discouraged. Further research on counselling and SGLT2i use in early CKD is needed to address the growing burden of CKD.

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