Department of Medical Sciences, Clinical Epidemiology, Uppsala University, Uppsala, Sweden
The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
BMJ Open. 2024 Apr 19;14(4):e074064. doi: 10.1136/bmjopen-2023-074064.
Identify the windows of opportunity for the diagnosis of chronic kidney disease (CKD) and the prevention of its adverse outcomes and quantify the potential population gains of such prevention.
Observational, population-wide study of residents in the Stockholm and Skåne regions of Sweden between 1 January 2015 and 31 December 2020.
All patients who did not yet have a diagnosis of CKD in healthcare but had CKD according to laboratory measurements of CKD biomarkers available in electronic health records.
We assessed the proportions of the patient population that received a subsequent diagnosis of CKD in healthcare, that used guideline-directed pharmacological therapy (statins, renin-angiotensin aldosterone system inhibitors (RAASi) and/or sodium-glucose cotransporter-2 inhibitors (SGLT2i)) and that experienced adverse outcomes (all-cause mortality, cardiovascular mortality or major adverse cardiovascular events (MACE)). The potential to prevent adverse outcomes in CKD was assessed using simulations of guideline-directed pharmacological therapy in untreated subsets of the study population.
We identified 99 382 patients with undiagnosed CKD during the study period. Only 33% of those received a subsequent diagnosis of CKD in healthcare after 5 years. The proportion that used statins or RAASi was of similar size to the proportion that didn't, regardless of how advanced their CKD was. The use of SGLT2i was negligible. In simulations of optimal treatment, 22% of the 21 870 deaths, 27% of the 14 310 cardiovascular deaths and 39% of the 22 224 MACE could have been avoided if every patient who did not use an indicated medication for their laboratory-confirmed CKD was treated with guideline-directed pharmacological therapy for CKD.
While we noted underdiagnosis and undertreatment of CKD in this large contemporary population, we also identified a substantial realisable potential to improve CKD outcomes and reduce its burden by treating patients early with guideline-directed pharmacological therapy.
确定慢性肾脏病(CKD)诊断的机会窗口和预防其不良结局,并量化这种预防的潜在人群获益。
对 2015 年 1 月 1 日至 2020 年 12 月 31 日期间瑞典斯德哥尔摩和斯科讷地区的居民进行了一项观察性、全人群研究。
所有尚未在医疗保健中诊断为 CKD 但根据电子健康记录中可用的 CKD 生物标志物实验室测量结果患有 CKD 的患者。
我们评估了随后在医疗保健中诊断为 CKD 的患者人群比例、使用指南指导的药物治疗(他汀类药物、肾素-血管紧张素-醛固酮系统抑制剂(RAASi)和/或钠-葡萄糖共转运蛋白-2 抑制剂(SGLT2i))以及经历不良结局(全因死亡率、心血管死亡率或主要不良心血管事件(MACE))的患者比例。通过对研究人群中未经治疗亚组进行指南指导的药物治疗模拟,评估了预防 CKD 不良结局的潜力。
我们在研究期间确定了 99382 例未诊断的 CKD 患者。只有 33%的患者在 5 年内随后在医疗保健中诊断为 CKD。使用他汀类药物或 RAASi 的比例与未使用的比例相似,无论他们的 CKD 有多严重。SGLT2i 的使用微不足道。在最佳治疗模拟中,如果对每个未使用实验室确诊 CKD 指示药物的患者进行 CKD 指南指导的药物治疗,可以避免 21870 例死亡中的 22%、14310 例心血管死亡中的 27%和 22224 例 MACE 中的 39%。
尽管我们在这个大型当代人群中注意到 CKD 的诊断不足和治疗不足,但我们也确定了通过早期使用指南指导的药物治疗治疗患者来改善 CKD 结局和减轻其负担的可观的可实现潜力。