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首页> 外文期刊>Journal of cardiovascular magnetic resonance : >Myocardial fibrosis in Eisenmenger syndrome: a descriptive cohort study exploring associations of late gadolinium enhancement with clinical status and survival
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Myocardial fibrosis in Eisenmenger syndrome: a descriptive cohort study exploring associations of late gadolinium enhancement with clinical status and survival

机译:艾森曼格综合征的心肌纤维化:一项描述性队列研究,探讨晚期g增强与临床状态和生存的关系

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BackgroundA relationship between myocardial fibrosis and ventricular dysfunction has been demonstrated using late gadolinium enhancement (LGE) in the pressure-loaded right ventricle from congenital heart defects. In patients with Eisenmenger syndrome (ES), the presence of LGE has not been investigated. The aims of this study were to detect any myocardial fibrosis in ES and describe major clinical variables associated with the finding.MethodsFrom 45 subjects screened, 30 subjects (age 43?±?13?years, 20 female) underwent prospective cardiovascular magnetic resonance with LGE to quantify biventricular volume and function as well as maximal and submaximal exercise during a single visit. Standard cine acquisitions were obtained for ventricular volume and function. Further imaging was performed after administration of 0.1?mmol/kg gadolinium contrast. Regions of LGE were evaluated qualitatively and quantitatively by manual contouring of identified areas, with total area expressed as a percentage of mass. Patients were followed prospectively (mean follow up 7.4?±?0.4?years) and any deaths recorded. Patients with LGE findings were compared to those without.ResultsLGE was present in 22/30 (73%) patients, specifically in RV myocardium (70%), RV trabeculae (60%), LV myocardium (33%) or LV papillary muscles (30%), though in small amounts (mean 1.4% of total ventricular mass, range 0.16 – 6.0%). Those with any LGE were not different in age, history of arrhythmia, desaturation, nor hemoglobin, nor ventricular size, mass, or function. Exercise capacity was low, but also not different between those with and without LGE. Similarly no significant associations were found with amount of fibrosis. There were five deaths among patients with LGE, versus two in patients without, but no difference in survival (log rank =0.03, P?=?0.85).ConclusionsMyocardial fibrosis by LGE is common in ES, though not extensive. The presence and quantity of LGE did not correlate with ventricular size, function, degree of cyanosis, exercise capacity, or survival in this pilot study. More data are clearly required before recommendations for routine use of LGE in these patients can be made.
机译:背景已证明先天性心脏缺陷在压力负荷的右心室中使用晚期late增强(LGE)可以证明心肌纤维化与心室功能障碍之间的关系。在艾森曼格综合征(ES)的患者中,尚未调查LGE的存在。本研究的目的是检测ES中是否存在心肌纤维化,并描述与该发现相关的主要临床变量。方法从接受筛选的45名受试者中,对30名受试者(年龄43?±?13?岁,20名女性)进行了LGE前瞻性心血管磁共振检查。量化单次就诊时的双心室容量和功能以及最大和次最大运动。对于心室容积和功能获得标准的电影采集。给予0.1?mmol / kg contrast造影剂后进行进一步成像。 LGE区域通过手动绘制轮廓确定区域进行定性和定量评估,总面积表示为质量百分比。对患者进行了前瞻性随访(平均随访7.4±0.4)年,并记录了死亡人数。结果发现LGE存在于22/30(73%)患者中,特别是RV心肌(70%),RV小梁(60%),LV心肌(33%)或LV乳头肌( 30%),尽管数量很少(平均占总心室质量的1.4%,范围为0.16-6.0%)。患有任何LGE的患者的年龄,心律不齐,去饱和史,血红蛋白,心室大小,质量或功能均无差异。运动能力低,但有和没有LGE的人的运动能力也没有差异。同样,没有发现纤维化程度的显着相关性。 LGE患者中有5例死亡,而无LGE患者中有2例死亡,但生存率无差异(log rank = 0.03,P≤0.85)。结论LGE心肌纤维化在ES中很常见,尽管并不广泛。在这项初步研究中,LGE的存在和数量与心室大小,功能,紫osis程度,运动能力或生存率无关。在可以推荐这些患者常规使用LGE之前,显然需要更多数据。

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