应激高血糖比和血红蛋白与RDW比预测溶栓治疗卒中的预后:一项回顾性队列研究。

IF 2 Q1 EMERGENCY MEDICINE
Archives of Academic Emergency Medicine Pub Date : 2025-08-07 eCollection Date: 2025-01-01 DOI:10.22037/aaemj.v13i1.2730
Sarawut Krongsut, Nat Na-Ek
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引用次数: 0

摘要

高应激性高血糖比(SHR)和低血红蛋白与红细胞分布宽度比(HB/RDW)都是已知的急性缺血性卒中(AIS)死亡率的预测因子。本研究旨在评估高SHR(≥1.18)和低HB/RDW(≤0.76)在脑卒中溶栓治疗患者中的预测作用。方法:我们回顾性收集345例接受溶栓治疗的AIS患者的资料。HB/RDW值通过重组前组织纤溶酶原激活物全血计数获得;而空腹血糖(FPG)和糖化血红蛋白(HbA1c)水平在8-14小时的夜间禁食后的早晨测量。根据SHR和HB/RDW水平将患者分为四组。我们使用具有稳健方差的多变量泊松回归来估计风险比(rr)和95%置信区间(ci)。模型评估了住院死亡率(IHM)、早期神经系统恶化(END)以及出院和3个月时功能结局的相关性,调整了年龄、性别、既往卒中、既往残疾、心肌梗死、心房颤动、心力衰竭、慢性肾脏疾病和恶性肿瘤。进一步进行倾向得分加权分析作为敏感性分析。结果:345例患者中,仅有37例属于高SHR (SHR+)和低HB/RDW (HB/RDW+)组。住院期间死亡65例(18.8%)。与SHR- HB/RDW-组相比,SHR+ HB/RDW+组发生IHM(校正RR: 9.97, 95% CI: 4.95-20.08)、END(校正RR: 2.95, 95% CI: 1.51-5.77)、3个月死亡率(校正RR: 6.23, 95% CI: 3.49-11.12)和3个月功能不良结局(校正RR: 2.86, 95% CI: 2.01-4.06)的风险显著较高。在敏感性分析中,这些关联仍然很强。SHR≥1.18和HB/RDW≤0.76联合预测IHM, AuROC为0.78 (95% CI: 0.73-0.83)。虽然联合生物标志物提高了敏感性和净效益,但其AUROC在统计学上并不优于单个标志物。结论:入院时的高SHR和低HB/RDW水平联合显著预测溶栓治疗AIS的不良预后,比单独使用任何一种生物标志物都更好。在更大的、不同的队列中进一步验证是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stress Hyperglycemia Ratio and Hemoglobin to RDW Ratio in Predicting the Outcomes of Thrombolysis-Treated Stroke: A Retrospective Cohort Study.

Stress Hyperglycemia Ratio and Hemoglobin to RDW Ratio in Predicting the Outcomes of Thrombolysis-Treated Stroke: A Retrospective Cohort Study.

Stress Hyperglycemia Ratio and Hemoglobin to RDW Ratio in Predicting the Outcomes of Thrombolysis-Treated Stroke: A Retrospective Cohort Study.

Stress Hyperglycemia Ratio and Hemoglobin to RDW Ratio in Predicting the Outcomes of Thrombolysis-Treated Stroke: A Retrospective Cohort Study.

Introduction: High stress hyperglycemia ratio (SHR) and low hemoglobin-to-red blood cell distribution width ratio (HB/RDW) are each known predictors of mortality in acute ischemic stroke (AIS). This study aimed to assess the predictive performance of high SHR (≥1.18) and low HB/RDW (≤0.76) together in stroke patients treated with thrombolysis.

Methods: We retrospectively collected data from 345 AIS patients treated with thrombolysis. HB/RDW values were obtained from pre-recombinant tissue plasminogen activator complete blood counts; while fasting plasma glucose (FPG) and glycated hemoglobin (HbA1c) levels were measured in the morning after an 8-14-hour overnight fast. Patients were categorized into four groups based on SHR and HB/RDW levels. We used multivariable Poisson regression with robust variance to estimate risk ratios (RRs) and 95% confidence intervals (CIs). Models assessed associations with in-hospital mortality (IHM), early neurological deterioration (END), and functional outcomes at discharge and 3 months, adjusting for age, sex, prior stroke, pre-existing disability, myocardial infarction, atrial fibrillation, heart failure, chronic kidney disease, and malignancy. Propensity score weighting analysis was further conducted as a sensitivity analysis.

Results: Among 345 patients, only 37 were in the high SHR (SHR+) and low HB/RDW (HB/RDW+) group. A total of 65 patients (18.8%) died during hospitalization. The SHR+ HB/RDW+ group had significantly higher risks of IHM (adjusted RR: 9.97, 95% CI: 4.95-20.08), END (adjusted RR: 2.95, 95% CI: 1.51-5.77), 3-month mortality (adjusted RR: 6.23, 95% CI: 3.49-11.12), and poor 3-month functional outcomes (adjusted RR: 2.86, 95% CI: 2.01-4.06) compared to the SHR- HB/RDW- group. These associations remained robust across sensitivity analyses. The combination of SHR ≥1.18 and HB/RDW ≤0.76 predicted IHM with an AuROC of 0.78 (95% CI: 0.73-0.83). Although the combined biomarker improved sensitivity and net benefit, its AUROC was not statistically superior to that of individual markers.

Conclusions: Combined high SHR and low HB/RDW levels at admission significantly predict poor outcomes in thrombolysis-treated AIS, performing better than either biomarker alone. Further validation in larger, diverse cohorts is warranted.

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来源期刊
Archives of Academic Emergency Medicine
Archives of Academic Emergency Medicine Medicine-Emergency Medicine
CiteScore
8.90
自引率
7.40%
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0
审稿时长
6 weeks
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