Care Gaps Following Newly Detected Dipstick Proteinuria in Treated Hypertension: A Japanese Nationwide Database Study.

IF 4.6
Koya Nagase, Takahiro Imaizumi, Yuko Asano, Kenta Mitsubayashi, Nobuhiro Nishibori, Takaya Ozeki, Yoshihiro Nakamura, Masaki Okazaki, Shimon Kurasawa, Tsuyoshi Watanabe, Kazuhiro Furuhashi, Shoichi Maruyama
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引用次数: 0

Abstract

Aims: Clinical guidelines recommend follow-up quantitative testing after dipstick-positive proteinuria and, when proteinuria is confirmed, subsequent initiation of renin-angiotensin system inhibitors (RASi) in patients with hypertension. However, real-world adherence to these recommendations remains unclear. We investigated management patterns following newly detected dipstick proteinuria in patients with treated hypertension.

Methods: Using the JMDC claims database, we identified treated hypertensive patients with newly detected dipstick proteinuria (≥1+, with prior results <1+) between January 2005 and March 2025. The study outcomes were quantitative urine albumin/protein testing and RASi initiation. Cumulative incidence was estimated using the Kaplan-Meier method, and multivariable Cox models were used to identify factors associated with outcomes.

Results: The 365-day cumulative incidence of quantitative testing was 7.5% (95% CI: 7.2-7.7) in the overall population (n = 47,210), and that of RASi initiation was 13.2% (95% CI: 12.6-13.8) among baseline RASi non-users (n = 14,599). Both outcomes became more frequent with increasing dipstick grade but remained infrequent in the higher-grade groups: among patients with 2+ and 3+ proteinuria, quantitative testing was performed in 12.9% and 16.1%, respectively, and RASi initiation occurred in 17.5% and 21.7%, respectively. Temporal trend analysis indicated that RASi initiation rates showed no improvement (aHR per year: 1.01; 95% CI: 0.99-1.03).

Conclusion: Follow-up quantitative testing and RASi initiation after newly detected dipstick proteinuria were infrequent, even among patients with higher dipstick grades, and RASi initiation showed no clear improvement over time. These findings highlight opportunities to improve guideline-concordant urinary protein assessment and antihypertensive therapy.

在高血压治疗中新检测到试纸蛋白尿后的护理差距:日本全国数据库研究。
目的:临床指南推荐在尿试纸阳性蛋白尿后进行随访定量检测,当确认蛋白尿时,高血压患者随后开始使用肾素-血管紧张素系统抑制剂(RASi)。然而,现实世界对这些建议的遵守程度仍不清楚。我们研究了高血压患者新发现的试纸蛋白尿的处理模式。方法:使用JMDC声明数据库,我们确定了新检测到尿量≥1+的高血压患者,并有既往结果。结果:在总体人群(n = 47,210)中,365天的累积定量检测发生率为7.5% (95% CI: 7.2-7.7),在基线未使用RASi的人群(n = 14,599)中,RASi起始发生率为13.2% (95% CI: 12.6-13.8)。这两种结果都随着尿量表等级的增加而增加,但在较高等级组中仍然不常见:在2+和3+蛋白尿患者中,分别有12.9%和16.1%的患者进行了定量检测,分别有17.5%和21.7%的患者开始了RASi。时间趋势分析显示,RASi起始率无改善(aHR /年:1.01;95% CI: 0.99-1.03)。结论:随访定量检测和RASi启动在新检测到的试纸蛋白尿后很少发生,即使在较高试纸等级的患者中也是如此,并且随着时间的推移,RASi启动没有明显的改善。这些发现强调了改进尿蛋白评估和降压治疗的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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