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De novo Cardiac Valve Calcification after Hemodialysis in End-Stage Renal Disease Patients Predicts Future Cardiovascular Events: A Longitudinal Cohort Study

机译:De Novo心脏瓣膜钙化后血液透析后末期肾病患者预测未来心血管事件:纵向队列研究

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Background Cardiac valve calcification (CVC) in maintenance hemodialysis patients is associated with adverse cardiovascular outcomes. However, whether de novo CVC in incident hemodialysis patients predicts future cardiovascular events is unknown. Methods This study included 174 patients newly receiving hemodialysis without CVC as reflected by echocardiography between January 2005 and December 2014. De novo CVC was determined with echocardiography once every 6 months until December 2016. Results The median follow-up was 66 months (range, 19–141). De novo CVC developed in 80 out of 174 (45.98%) subjects 58 developed aortic valve calcification (AVC) alone, 42 developed mitral valve calcification (MVC) alone, and 20 developed both AVC and MVC. The median time from baseline to de novo CVC was 46 months (range, 3–120) for AVC and 50 months (range, 13–127) for MVC. Patients who developed CVC had a higher major adverse cardiovascular events (MACE) rate than those who did not (AVC 30/58 [51.72%] vs. 23/116 [19.83%]; MVC 25/42 [59.52%] vs. 28/132 [21.21%]). Multivariate time-dependent Cox regression showed an association between MACE with both de novo AVC and MVC (AVC hazard ratio [HR] 3.2, 95% confidence interval [CI] 1.55–6.63; MVC HR 5.95, 95% CI 2.90–12.20). Conclusions De novo CVC is an independent risk factor for MACE in hemodialysis patients, and regular CVC screening among hemodialysis patients without preexisting CVC may be helpful to identify patients at increased risk of adverse cardiovascular outcomes.
机译:背景技术维持血液透析患者的心脏瓣膜钙化(CVC)与不良心血管结果有关。然而,在入射血液透析患者中​​是否德诺科CVC预测未来的心血管事件是未知的。方法本研究包括174例新接受血液透析患者,无需CVC,由2005年1月至2014年12月反映。De Novo CVC在2016年12月之前每6个月均每6个月内测定一次。结果66个月(范围,19 -141)。 De Novo CVC在174个(45.98%)的70个受试者58中,仅开发了主动脉瓣钙化(AVC),42个仅开发二尖瓣钙化(MVC),20个开发的AVC和MVC。从基线到De Novo CVC的中位时间为AVC和50个月(范围,13-127)为46个月(范围,3-120)。开发CVC的患者具有比没有(AVC 30/58 [51.72%]与23/116 [19.83%]; MVC 25/42 [59.52%]的患者的主要不良心血管事件(SMACE)率更高/ 132 [21.21%])。多变量时间依赖性Cox回归显示阶段与De Novo AVC和MVC(AVC危险比[HR] 3.2,95%置信区间[CI] 1.55-6.63; MVC HR 5.95,95%CI 2.90-12.20)之间的关联。结论De Novo CVC是血液透析患者术术的独立危险因素,血液透析患者的常规CVC筛查,无预先存在的CVC可能有助于识别患者增加不良心血管结果的患者。

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