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儿童肥厚型心肌病性心原性猝死的危险因素:系统评价和荟萃分析。

Risk factors for sudden cardiac death in childhood hypertrophic cardiomyopathy: A systematic review and meta-analysis.

机构信息

1 Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital, London, UK.

2 University College London Institute of Cardiovascular Science, London, UK.

出版信息

Eur J Prev Cardiol. 2017 Jul;24(11):1220-1230. doi: 10.1177/2047487317702519. Epub 2017 May 9.

Abstract

Aims To perform a systematic literature review and meta-analysis of clinical risk factors for sudden cardiac death (SCD) in childhood hypertrophic cardiomyopathy. Methods Medline and PubMed databases were searched for original articles published in English from 1963 through to December 2015 that included patients under 18 years of age with a primary or secondary end-point of either SCD or SCD-equivalent events (aborted cardiac arrest or appropriate implantable cardioverter-defibrillator discharge) or cardiovascular death (CVD). Results Twenty-five studies (3394 patients) met the inclusion criteria. We identified four conventional major risk factors that were evaluated in at least four studies and that we found to be statistically associated with an increased risk of death in at least two studies: previous adverse cardiac event (pooled hazard ratio [HR] 5.4, 95% confidence interval [CI] 3.67-7.95, p < 0.001); non-sustained ventricular tachycardia (pooled HR 2.13, 95% CI 1.21-3.74, p = 0.009); unexplained syncope (pooled HR 1.89, 95% CI 0.69-5.16, p = 0.22); and extreme left ventricular hypertrophy (pooled HR 1.80, 95% CI 0.75-4.32, p = 0.19). Left atrial diameter did not meet the major risk factor criteria; however, this is likely to be an additional significant risk factor. 'Minor' risk factors included a family history of SCD, gender, age, symptoms, electrocardiogram changes, abnormal blood pressure response to exercise and left ventricular outflow tract obstruction. Conclusions A lack of well-designed, large, population-based studies in childhood hypertrophic cardiomyopathy means that the evidence base for individual risk factors is not robust. We have identified four clinical parameters that are likely to be associated with increased risk of SCD, SCD-equivalent events or CVD. Multi-centre prospective studies are needed in order to further determine the relevance of these factors in predicting SCD in childhood hypertrophic cardiomyopathy and to identify novel risk markers. Condensed abstract A systematic review and meta-analysis of clinical risk factors predicting sudden cardiac death in childhood hypertrophic cardiomyopathy was performed, identifying four 'major' factors: previous adverse cardiac event; non-sustained ventricular tachycardia; syncope; and extreme left ventricular hypertrophy. Well-designed multi-centre studies are required in the future in order to confirm these findings.

摘要

目的

对儿童肥厚型心肌病中心律失常性猝死(SCD)的临床危险因素进行系统文献回顾和荟萃分析。

方法

检索 1963 年至 2015 年 12 月期间发表的英文原始文章,纳入主要终点为 SCD 或 SCD 等效事件(心搏骤停或合适的植入式心脏复律除颤器放电)或心血管死亡(CVD)的年龄在 18 岁以下的儿童患者的研究。

结果

25 项研究(3394 例患者)符合纳入标准。我们确定了四个常规主要危险因素,这些危险因素至少在四项研究中进行了评估,并且我们发现它们与至少两项研究中死亡风险增加具有统计学关联:既往不良心脏事件(合并危险比 [HR]5.4,95%置信区间 [CI]3.67-7.95,p<0.001);非持续室性心动过速(合并 HR 2.13,95%CI 1.21-3.74,p=0.009);不明原因晕厥(合并 HR 1.89,95%CI 0.69-5.16,p=0.22);和极度左心室肥厚(合并 HR 1.80,95%CI 0.75-4.32,p=0.19)。左心房直径不符合主要危险因素标准;然而,这可能是一个额外的重要危险因素。“次要”危险因素包括 SCD 的家族史、性别、年龄、症状、心电图改变、运动时血压反应异常和左心室流出道梗阻。

结论

由于缺乏设计良好、大型、基于人群的儿童肥厚型心肌病研究,因此个体危险因素的证据基础并不稳健。我们已经确定了四个可能与 SCD、SCD 等效事件或 CVD 风险增加相关的临床参数。需要进行多中心前瞻性研究,以进一步确定这些因素在预测儿童肥厚型心肌病 SCD 中的相关性,并确定新的风险标志物。

简明摘要

对预测儿童肥厚型心肌病中心律失常性猝死的临床危险因素进行了系统评价和荟萃分析,确定了四个“主要”因素:既往不良心脏事件;非持续室性心动过速;晕厥;和极度左心室肥厚。未来需要进行设计良好的多中心研究来证实这些发现。

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