重拾几十年前的智慧:纵向分析肾素-血管紧张素系统抑制剂及其对急性缺血性脑卒中的影响,以改善预后。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Sophie Samuel, Kyndol Craver, Charles Miller, Brittany Pelsue, Catherine Gonzalez, Teresa A Allison, Brian Gulbis, Huimahn Alex Choi, Seokhun Kim
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引用次数: 0

摘要

背景:虽然肾素-血管紧张素系统(RAS)抑制剂在控制血压方面有着悠久的历史,但由于半衰期长和肾衰竭问题,它们作为住院一线治疗的适用性可能受到限制:我们采用队列设计,评估了 RAS 抑制剂单独使用或与β-受体阻滞剂联合使用对死亡率的影响,同时探讨了相互作用,包括与终末期肾病和血清肌酐水平相关的相互作用。符合条件的受试者是年龄在 18 岁或 18 岁以上、有特定亚型并接受住院降压治疗的 AIS 患者。主要结果是死亡率。统计分析包括横断面分析和纵向分析,采用了广义线性模型、G计算和20天随访期的离散时间生存分析:在我们对 3058 名 AIS 患者进行的研究中,与未使用 RAS 抑制剂的患者(12.1%)相比,使用 RAS 抑制剂的患者的院内死亡率(2.2%)明显降低,相对风险 (RR) 为 0.18(95% CI 0.12-0.26)。使用 G 计算法进行的进一步分析表明,RAS 抑制剂可显著降低死亡率风险(0.0281 对 0.0913,风险差异 (RD) 为 6.31% 或 0.0631,95% CI 0.046-0.079)。亚组分析表明,肌酐水平低于和高于 1.3 毫克/分升的患者均有显著的统计学差异(RD -0.0510 vs. -0.0895),配对比较也有显著差异(-0.0385 或 3.85%,CI 0.023-0.054)。此外,纵向分析证实,每天摄入RAS抑制剂可使死亡风险持续降低0.93%:结论:RAS抑制剂可显著降低AIS患者的院内死亡率,这表明它在改善患者预后方面具有潜在的临床益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reviving Decades-Old Wisdom: Longitudinal Analysis of Renin-Angiotensin System Inhibitors and Its Effects on Acute Ischemic Stroke to Improve Outcomes.

Background: While renin-angiotensin system (RAS) inhibitors have a longstanding history in blood pressure control, their suitability as first-line in-patient treatment may be limited due to prolonged half-life and kidney failure concerns.

Methods: Using a cohort design, we assessed the impact of RAS inhibitors, either alone or in combination with beta-blockers, on mortality, while exploring interactions, including those related to end-stage renal disease and serum creatinine levels. Eligible subjects were Acute Ischemic Stroke (AIS) patients aged 18 or older with specific subtypes who received in-patient antihypertensive treatment. The primary outcome was mortality rates. Statistical analyses included cross-sectional and longitudinal approaches, employing generalized linear models, G-computation, and discrete-time survival analysis over a 20-day follow-up period.

Results: In our study of 3,058 AIS patients, those using RAS inhibitors had significantly lower in-hospital mortality (2.2%) compared to non-users (12.1%), resulting in a relative risk (RR) of 0.18 (95% CI: 0.12-0.26). Further analysis using G-computation revealed a marked reduction in mortality risk associated with RAS inhibitors (0.0281 vs. 0.0913, risk difference [RD] of 6.31% or 0.0631, 95% CI: 0.046-0.079). Subgroup analysis demonstrated notable benefits, with individuals having creatinine levels below and above 1.3 mg/dl exhibiting statistically significant RD (RD -0.0510 vs. -0.0895), and a significant difference in paired comparison (-0.0385 or 3.85%, CI 0.023-0.054). Additionally, longitudinal analysis confirmed a consistent daily reduction of 0.93% in mortality risk associated with the intake of RAS inhibitors.

Conclusions: RAS inhibitors are associated with a significant reduction in in-hospital mortality in AIS patients, suggesting potential clinical benefits in improving patient outcomes.

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