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高分辨率自由呼吸晚期钆增强心血管磁共振诊断 COVID-19 感染后的心肌损伤。

High-resolution Free-breathing late gadolinium enhancement Cardiovascular magnetic resonance to diagnose myocardial injuries following COVID-19 infection.

机构信息

Department of Cardiovascular Imaging, Groupe Hospitalier Sud, CHU Bordeaux, Pessac, France; IHU LIRYC, Electrophysiology and Heart Modeling Institute, Université de Bordeaux - INSERM U1045, Avenue du Haut Lévêque, Pessac, France; Department of Diagnostic and Interventional Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Department of Cardiovascular Imaging, Groupe Hospitalier Sud, CHU Bordeaux, Pessac, France.

出版信息

Eur J Radiol. 2021 Nov;144:109960. doi: 10.1016/j.ejrad.2021.109960. Epub 2021 Sep 20.

DOI:10.1016/j.ejrad.2021.109960
PMID:34600236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8450147/
Abstract

PURPOSE

High-resolution free-breathing late gadolinium enhancement (HR-LGE) was shown valuable for the diagnosis of acute coronary syndromes with non-obstructed coronary arteries. The method may be useful to detect COVID-related myocardial injuries but is hampered by prolonged acquisition times. We aimed to introduce an accelerated HR-LGE technique for the diagnosis of COVID-related myocardial injuries.

METHOD

An undersampled navigator-gated HR-LGE (acquired resolution of 1.25 mm) sequence combined with advanced patch-based low-rank reconstruction was developed and validated in a phantom and in 23 patients with structural heart disease (test cohort; 15 men; 55 ± 16 years). Twenty patients with laboratory-confirmed COVID-19 infection associated with troponin rise (COVID cohort; 15 men; 46 ± 24 years) prospectively underwent cardiovascular magnetic resonance (CMR) with the proposed sequence in our center. Image sharpness, quality, signal intensity differences and diagnostic value of free-breathing HR-LGE were compared against conventional breath-held low-resolution LGE (LR-LGE, voxel size 1.8x1.4x6mm).

RESULTS

Structures sharpness in the phantom showed no differences with the fully sampled image up to an undersampling factor of x3.8 (P > 0.5). In patients (N = 43), this acceleration allowed for acquisition times of 7min21s ± 1min12s at 1.25 mm resolution. Compared with LR-LGE, HR-LGE showed higher image quality (P = 0.03) and comparable signal intensity differences (P > 0.5). In patients with structural heart disease, all LGE-positive segments on LR-LGE were also detected on HR-LGE (80/391) with 21 additional enhanced segments visible only on HR-LGE (101/391, P < 0.001). In 4 patients with COVID-19 history, HR-LGE was definitely positive while LR-LGE was either definitely negative (1 microinfarction and 1 myocarditis) or inconclusive (2 myocarditis).

CONCLUSIONS

Undersampled free-breathing isotropic HR-LGE can detect additional areas of late enhancement as compared to conventional breath-held LR-LGE. In patients with history of COVID-19 infection associated with troponin rise, the method allows for detailed characterization of myocardial injuries in acceptable scan times and without the need for repeated breath holds.

摘要

目的

高分辨率自由呼吸晚期钆增强(HR-LGE)已被证明对诊断非阻塞性冠状动脉急性冠脉综合征有价值。该方法可能有助于检测与 COVID 相关的心肌损伤,但由于采集时间延长而受到阻碍。我们旨在引入一种加速 HR-LGE 技术来诊断与 COVID 相关的心肌损伤。

方法

开发并验证了一种欠采样导航门控 HR-LGE(采集分辨率为 1.25mm)序列,结合先进的基于补丁的低秩重建,在体模和 23 例结构性心脏病患者(试验队列;15 名男性;55±16 岁)中进行了验证。20 例实验室确诊的 COVID-19 感染伴肌钙蛋白升高的患者(COVID 队列;15 名男性;46±24 岁)前瞻性地在我院中心接受了拟议序列的心血管磁共振(CMR)检查。与传统的屏气低分辨率 LGE(LR-LGE,体素大小为 1.8x1.4x6mm)相比,比较了自由呼吸 HR-LGE 的图像清晰度、质量、信号强度差异和诊断价值。

结果

在体模中,结构清晰度在采样因子高达 x3.8 时与完全采样图像无差异(P>0.5)。在患者(N=43)中,这种加速允许在 1.25mm 分辨率下采集 7 分 21 秒±1 分 12 秒的时间。与 LR-LGE 相比,HR-LGE 显示出更高的图像质量(P=0.03)和相当的信号强度差异(P>0.5)。在结构性心脏病患者中,LR-LGE 上的所有 LGE 阳性节段也在 HR-LGE 上检测到(80/391),而 HR-LGE 上仅检测到 21 个增强节段(101/391,P<0.001)。在 4 例有 COVID-19 病史的患者中,HR-LGE 呈阳性,而 LR-LGE 要么呈阴性(1 例微梗死和 1 例心肌炎),要么不确定(2 例心肌炎)。

结论

与传统的屏气低分辨率 LGE 相比,欠采样的自由呼吸各向同性 HR-LGE 可检测到晚期增强的附加区域。在伴有肌钙蛋白升高的 COVID-19 感染病史的患者中,该方法可在可接受的扫描时间内对心肌损伤进行详细特征描述,且无需重复屏气。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/6c101be19d9c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/626123f5c5f5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/375ee47f043d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/e014f4c9d6eb/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/d44b61664c3b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/cf21820ec41a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/6c101be19d9c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/626123f5c5f5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/375ee47f043d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/e014f4c9d6eb/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/d44b61664c3b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/cf21820ec41a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df99/8661040/6c101be19d9c/gr6.jpg

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