Pouwels Xavier G L V, van Mil Dominique, Kieneker Lyanne M, Boersma Cornelis, van Etten Ronald W, Evers-Roeten Birgitte, Heerspink Hiddo J L, Hemmelder Marc H, Langelaan Marloes L P, Thelen Marc H M, Gansevoort Ron T, Koffijberg Hendrik
Health Technology and Services Research Department, Technical Medical Centre, Faculty of Behavioral, Management, and Social Sciences, University of Twente, Enschede, the Netherlands.
Department of Internal Medicine, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.
EClinicalMedicine. 2024 Jan 17;68:102414. doi: 10.1016/j.eclinm.2023.102414. eCollection 2024 Feb.
Chronic kidney disease (CKD) is often detected late, leading to substantial health loss and high treatment costs. Screening the general population for albuminuria identifies individuals at high risk of kidney events and cardiovascular disease (CVD) who may benefit from early start of preventive interventions. Previous studies on the cost-effectiveness of albuminuria population screening were inconclusive, but were based on survey or cohort data rather than an implementation study, modelled screening as performed by general practitioners rather than home-based screening, and often included only benefits with respect to kidney events. We evaluated the cost-effectiveness of home-based general population screening for increased albuminuria based on real-world data obtained from a prospective implementation study taking into account prevention of CKD as well as CVD events.
We developed an individual-level simulation model to compare home-based screening using a urine collection device with usual care (no home-based screening) in individuals of the general population aged 45-80, based on the THOMAS study (Towards HOMe-based Albuminuria Screening). Cost-effectiveness was assessed from the Dutch healthcare perspective with a lifetime horizon. The costs of the screening process and benefits of preventing CKD progression (dialysis and kidney transplantation) and CVD events (non-fatal myocardial infarction, non-fatal stroke, fatal CVD event) were reflected. Albuminuria detection led to treatment of identified risk factors. The model subsequently simulated CKD progression, the occurrence of CVD events, and death. The risks of experiencing CVD events were calculated using the SCORE2 CKD risk prediction model and individual-level data from the THOMAS study. Relative treatment effectiveness, quality of life scores, resource use, and cost inputs were obtained from literature. Model outcomes were the number of CKD and CVD-related events, total costs, quality-adjusted life years (QALYs), and the incremental cost-effectiveness ratio (ICER) per QALY gained by screening versus usual care. All results were obtained through probabilistic analysis.
The absolute difference between screening versus usual care in lifetime probability of dialysis, kidney transplantation, non-fatal myocardial infarction, non-fatal stroke, and fatal CVD events were 0.2%, 0.05%, 0.6%, 0.6%, and 0.2%, respectively. This led to relative decreases compared to usual care in lifetime incidence of these events of 10.7%, 11.1%, 5.1%, 4.1%, and 1.6%, respectively. The incremental costs and QALYs of screening were €1607 and 0.17 QALY, respectively, which led to a corresponding ICER of €9225/QALY. The probability of screening being cost-effective for the Dutch willingness-to-pay threshold for preventive population screening of €20,000/QALY was 95.0%. Implementing the screening in the subgroup of 45-64 years old reduced the ICER (€7946/QALY), whereas implementing screening in the subgroup of 65-80 years old increased the ICER (€10,310/QALY). A scenario analysis assuming treatment optimization in all individuals with newly diagnosed risk factors or known risk factors not within target range reduced the ICER to €7083/QALY, resulting from the incremental costs and QALY gain of €2145 and 0.30, respectively.
Home-based screening for increased albuminuria to prevent CVD and CKD events is likely cost-effective. More health benefits can be obtained by screening younger individuals and better optimization of care in individuals identified with newly diagnosed or known risk factors outside target range.
Dutch Kidney Foundation, Top Sector Life Sciences & Health of the Dutch Ministry of Economic Affairs.
慢性肾脏病(CKD)往往发现较晚,导致大量健康损失和高昂的治疗费用。对普通人群进行蛋白尿筛查可识别出肾脏事件和心血管疾病(CVD)高风险个体,这些个体可能从早期开始的预防性干预中获益。以往关于蛋白尿人群筛查成本效益的研究尚无定论,且基于调查或队列数据而非实施研究,将筛查模拟为全科医生进行而非居家筛查,并且通常仅纳入了肾脏事件方面的益处。我们基于一项前瞻性实施研究获得的真实世界数据,评估了居家进行普通人群蛋白尿筛查的成本效益,同时考虑了CKD以及CVD事件的预防。
我们开发了一个个体水平的模拟模型,以比较在45 - 80岁普通人群中使用尿液收集装置进行居家筛查与常规护理(不进行居家筛查)的效果,该模型基于THOMAS研究(迈向居家蛋白尿筛查)。从荷兰医疗保健的角度,以终身视角评估成本效益。反映了筛查过程的成本以及预防CKD进展(透析和肾移植)和CVD事件(非致命性心肌梗死、非致命性中风、致命性CVD事件)的益处。蛋白尿检测导致对已识别的风险因素进行治疗。该模型随后模拟了CKD进展、CVD事件的发生和死亡。使用SCORE2 CKD风险预测模型和THOMAS研究的个体水平数据计算发生CVD事件的风险。相对治疗效果、生活质量评分、资源使用和成本投入均来自文献。模型结果包括CKD和CVD相关事件的数量、总成本、质量调整生命年(QALY)以及筛查与常规护理相比每获得一个QALY的增量成本效益比(ICER)。所有结果均通过概率分析获得。
筛查与常规护理相比,透析、肾移植、非致命性心肌梗死、非致命性中风和致命性CVD事件终身概率的绝对差异分别为0.2%、0.05%、0.6%、0.6%和0.2%。这导致这些事件的终身发病率与常规护理相比分别相对降低了10.7%、11.1%、5.1%、4.1%和1.6%。筛查的增量成本和QALY分别为1607欧元和0.17 QALY,相应的ICER为9225欧元/QALY。对于荷兰预防性人群筛查每QALY支付意愿阈值20000欧元,筛查具有成本效益的概率为95.0%。在45 - 64岁亚组中实施筛查降低了ICER(7946欧元/QALY),而在65 - 80岁亚组中实施筛查则增加了ICER(10310欧元/QALY)。一项情景分析假设对所有新诊断出风险因素或已知风险因素不在目标范围内的个体进行治疗优化,将ICER降至7083欧元/QALY,这是由于增量成本和QALY增益分别为2145欧元和0.30。
居家进行蛋白尿筛查以预防CVD和CKD事件可能具有成本效益。筛查较年轻个体以及更好地优化对新诊断出或已知风险因素不在目标范围内个体的护理可获得更多健康益处。
荷兰肾脏基金会、荷兰经济事务部生命科学与健康顶级部门。