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首页> 外文期刊>Cardio-oncology. >Outcomes after transcatheter aortic valve replacement in cancer survivors with prior chest radiation therapy: a systematic review and meta-analysis
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Outcomes after transcatheter aortic valve replacement in cancer survivors with prior chest radiation therapy: a systematic review and meta-analysis

机译:经经胸腔血管瓣膜血管静脉抑制后的结果,具有先前的胸部放射治疗:系统审查和荟萃分析

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Background:Cancer survivors with prior chest radiation therapy (C-XRT) frequently present with aortic stenosis (AS) as the first manifestation of radiation-induced heart disease. They are considered high-risk for surgical valve replacement. Transcatheter aortic valve replacement (TAVR) is as an attractive option for this patient population but the outcomes are not well established in major clinical trials. The authors performed a systemic review and meta-analysis of clinical studies for the outcomes after TAVR in cancer survivors with prior C-XRT.Methods:Online databases were searched from inception to April 2020 for studies evaluating the outcomes of TAVR in patients with and without C-XRT. We analyzed the pooled estimates (with their 95% confidence intervals) of the odds ratio (OR) for the all-cause mortality at 30-day and 1-year follow-ups, 4-point safety outcomes (stroke, major bleed, access-related vascular complications and need for a pacemaker), a 2-point efficacy outcome (mean aortic valve gradient and left ventricular ejection fraction) and worsening of congestive heart failure (CHF). Four studies were included following 2054 patients with and without prior C-XRT exposure (164 patients and 1890 patients respectively).Results:The C-XRT group had similar 30-day mortality compared to the control group (OR 1.29, 95% CI 0.64 to 2.58, p?=?0.48). The 1-year mortality was higher in the C-XRT group (OR 1.97, CI 1.15 to 3.39, p?=?0.01). Apart from higher congestive heart failure (CHF) exacerbation in the C-XRT group (OR 2.03, CI 1.36 to 3.04, p?=?0.0006), TAVR resulted in similar safety and efficacy outcomes in both groups.Conclusion:TAVR in the C-XRT group has similar 30-day mortality, safety, and efficacy outcomes compared to the control group; however, they have higher 1-year mortality and CHF exacerbation. Including an oncologist to the cardiology team who considers cancer stage in the decision-making process and applying additional preoperative scores such as frailty indices may refine the risk assessment for these patients. The quality of analyzed data is modest, warranting randomized trials to assess the true benefits of TAVR in these patients.? The Author(s) 2020.
机译:背景:癌症幸存者与先前的胸部放射治疗(C-XRT)经常存在主动脉狭窄(AS)作为辐射诱导的心脏病的第一个表现。它们被认为是手术瓣膜置换的高风险。经膜管主动脉瓣置换(TAVR)是这种患者人口的有吸引力的选择,但在主要的临床试验中没有很好的成果。作者对癌症幸存者中TAVR后的结果进行了全身审查和荟萃分析,以先前的C-XRT.methods:从2002年4月开始搜查了在线数据库,以研究患有和没有的患者TAVR的结果。 C-XRT。我们分析了汇集估计(以95%的置信区间)在30天和1年后续后续次数,4分安全结果(中风,重大出血,访问 - 相关的血管并发症和需要起搏器),2点疗效结果(平均主动脉瓣梯度和左心室喷射部分)和充血性心力衰竭的恶化(CHF)。在2054例患者和未经证实的C-XRT暴露(分别为164名患者和1890名患者)后,包括四项研究。结果:与对照组(或1.29,95%CI 0.64)相比,C-XRT组具有相似的30天死亡率到2.58,p?=?0.48)。 C-XRT组的1年死亡率较高(或1.97,CI 1.15至3.39,P?= 0.01)。除了C-XRT组(或2.03,CI 1.36至3.04,P≥0.0006)中的较高充血性心力衰竭(CHF)加剧(CHF)加剧,TAVR在两组中导致两组的安全性和功效结果相似。结论:TAVR在C中与对照组相比,-XRT组具有类似的30天死亡率,安全性和疗效结果;然而,它们具有更高的1年死亡率和CHF恶化。包括肿瘤科学家对考虑决策过程中的癌症阶段的心脏病学团队,并应用额外的术前分数,如脆弱指数可能会对这些患者的风险评估进行细化。分析数据的质量是适度的,保证随机试验,以评估这些患者中TAVR的真正益处。作者2020年。

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