影响腹主动脉瘤生长速度的因素。墨西哥队列分析

Vascular and endovascular surgery Pub Date : 2024-11-01 Epub Date: 2024-07-21 DOI:10.1177/15385744241265758
Luis O Bobadilla-Rosado, Javier E Anaya-Ayala, Eros Santos-Chavez, Julio Navarro, Ignacio Martinez-Quesada, Hugo Laparra-Escareno, Nina Mendez-Dominguez, Carlos A Hinojosa
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摘要

目的:腹主动脉瘤(AAA)的生长过程尚不完全清楚。本研究旨在分析墨西哥队列中与 AAA 直径变化相关的风险因素:在这项观察性研究中,我们分析了 2014 年至 2021 年期间在计算机断层扫描(CT)研究中报告有 AAA 并进行了后续 CT 检查的所有患者。我们根据 2 型糖尿病诊断和用药史(糖尿病与非糖尿病、二甲双胍摄入与非二甲双胍摄入、他汀与非他汀摄入)将其分组。我们使用配对 t 检验比较了随访前后 AAA 的直径。我们还进行了多变量分析,以确定与增长速度相关的独立变量。统计分析在 Stata 17 中进行:在研究期间,72 名(39.77%)患者进行了 CT 随访。平均年龄为 75 岁(±9.05),男性 52 人(72.22%)。根据二甲双胍摄入量比较不同时间段的肾下最大直径,发现只有未摄入二甲双胍组存在显著差异(42.05 ± 12.54 vs45.34 ± 12.06 [P = 0.02]),相反,摄入二甲双胍组的随访测量结果无显著差异(36.13 ± 7.04 vs 37.00 ± 4.51; P = 0.57)。在多变量分析中,诊断时的 AAA 最大直径与显著增长的增长率相关(系数 = 0.06,P < 0.05):结论:AAA直径似乎会随着时间的推移发生非线性变化,并受到不同流行病学和临床因素的影响。在我们研究的人群中,二甲双胍的摄入似乎促进了 AAA 直径增长的稳定性。
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Factors that Influence Growth Rates of Abdominal Aortic Aneurysms. Analysis of a Mexican Cohort.

Objective: Abdominal Aortic Aneurysms (AAA) growth remains a process not fully understood. The objective of this study was to analyze risk factors associated with changes in AAA diameter in a Mexican cohort.

Methods: An observational study in which we analyzed the entirely of patients in which an AAA was reported in a Computed Tomography (CT) study from 2014 to 2021 who had a follow-up CT. We divided them by groups depending on the diagnosis of type 2 diabetic mellitus and pharmacological history (diabetic vs non-diabetic, metformin vs non-metformin intake and statin vs non-statin intake). We compared pre and post follow-up AAA diameters using paired t-tests. A multivariate analysis was performed in order to identify independent variables associated with an increased growth rate. Statistical analysis was performed on Stata 17.

Results: During the studied period 72 (39.77%) patients had a follow-up CT. Mean age was 75 years (±9.05) and 52 (72.22%) were men. When comparing infra-renal largest diameter through time based on metformin intake, a significant difference was found only in the metformin non-intake group (42.05 ± 12.54 vs45.34 ± 12.06 [P = 0.02]), in contrast the metformin intake group measures were non-significantly different (36.13 ± 7.04 vs 37.00 ± 4.51; P = 0.57) through follow-up. In the multivariate analysis AAA largest diameter at diagnosis correlated with significantly increased growth rate (coeff = 0.06, P < 0.05).

Conclusions: AAA diameters appear to change through time in a non-linear pattern influenced by different epidemiological and clinical factors. Metformin intake appears to promote a stability in AAA diameter growth in our studied population.

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