肌少症是腹主动脉瘤修复后死亡率的重要预测因子。

JCSM clinical reports Pub Date : 2018-01-01
Joshua K Kays, Tiffany W Liang, Teresa A Zimmers, Daniel P Milgrom, Hamzah Abduljabar, Andrew Young, Bradford J Kim, Teresa M Bell, Andres Fajardo, Michael P Murphy, Leonidas G Koniaris
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引用次数: 0

摘要

目的:腹主动脉瘤(AAA)的修复可降低破裂和死亡的发生率。在癌症患者中,肌肉减少症与手术并发症和死亡率增加有关。肌少症对AAA修复后存活的影响尚未被描述。方法和结果:从印第安纳大学医学院接受AAA修复的患者中获得患者人口统计学、实验室、身体成分测量和生存数据,为期5年。进行单因素和多因素分析以确定与总生存率相关的因素。总体而言,58.2%表现为肌肉减少症。肌肉减少症患者年龄较大(71.8±8.3岁vs 66.8±8.1岁);p2;结论:这是第一个研究表明,超过一半的接受AAA修复的患者是肌肉减少,这种情况与死亡率增加有关。肌少症合并骨骼肌病的死亡率是单纯肌少症的两倍。CT扫描,而不是BMI,可以准确地识别肌肉减少症和肌骨化症。明确肌少症导致AAA修复后晚期死亡的机制,对于开发新的干预措施,提高这一高危人群的生存率至关重要。
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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Sarcopenia is a Significant Predictor of Mortality After Abdominal Aortic Aneurysm Repair.

Aims: Repair of abdominal aortic aneurysms (AAA) decreases the incidence of rupture and death. In cancer patients, sarcopenia has been associated with increased surgical complications and mortality. The impact of sarcopenia on survival after AAA repair has yet to be described.

Methods and results: Patient demographic, laboratory, body composition measurements and survival data were obtained from patients undergoing AAA repair at the Indiana University medical campus over a 5-year period. Univariate and multivariate analyses were performed to identify factors associated with overall survival. Overall, 58.2% presented with sarcopenia. Sarcopenic patients were older (71.8±8.3 versus 66.8±8.1 years; p<0.001), had lower body mass index (BMI) (26.3±5.2 versus 31.5±5.9 kg/m2; p<0.001), higher rates of myosteatosis (84.4% versus 52.%; p<0.001), greater AAA diameter (60.6±14.0 versus 57.8±11.7 mm; p=0.016), higher Charlson Comorbidity Index (CCI) (32.3% versus 25.1% ≥6; p=0.034), and increased rates of rupture (8.2% versus 3.8%; p=0.047). Sarcopenic and nonsarcopenic patients had no difference in 30-day morbidity (8.5% versus 8.5%; p=0.991) or mortality (3.7% versus 0.9%; p=0.07). Univariate analysis demonstrated age, sarcopenia, myosteatosis, CCI, and BMI to be associated with long-term survival. There was no correlation between BMI and sarcopenia. Both sarcopenia and myosteatosis resulted in decreased one-, three-, and five-year survivals compared to their counterparts. On multivariate analysis sarcopenia is independently associated with survival, conferring a 1.6-fold increase in death (p=0.04). The combination of sarcopenia plus myosteatosis doubled the risk of death compared to sarcopenia alone.

Conclusions: This is the first study to demonstrate that over half of all patients undergoing AAA repair are sarcopenic, a condition associated with increased mortality. Sarcopenia with myosteatosis is associated with double the mortality of sarcopenia alone. CT scan, but not BMI, accurately identifies sarcopenia and myosteatosis. Defining the mechanisms through which sarcopenia contributes to late death after AAA repair is critical to developing novel interventions that may improve survival in this high risk population.

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