Working Group on Cardiovascular Magnetic Resonance, Experimental and Clinical Research Center - a joint cooperation between the Charité Medical Faculty and the Max-Delbrück Center for Molecular Medicine and HELIOS Hospital Berlin-Buch, Department of Cardiology and Nephrology, Lindenberger Weg 80, 13125, Berlin, Germany.
Clinic Agatharied, Department of Cardiology, Ludwig-Maximilians-University Munich, Norbert-Kerkel-Platz, 83734, Hausham, Germany.
J Cardiovasc Magn Reson. 2018 Feb 19;20(1):13. doi: 10.1186/s12968-018-0434-2.
Segmented phase-sensitive inversion recovery (PSIR) cardiovascular magnetic resonance (CMR) sequences are reference standard for non-invasive evaluation of myocardial fibrosis using late gadolinium enhancement (LGE). Several multi-slice LGE sequences have been introduced for faster acquisition in patients with arrhythmia and insufficient breathhold capability. The aim of this study was to assess the accuracy of several multi-slice LGE sequences to detect and quantify myocardial fibrosis in patients with ischemic and non-ischemic myocardial disease.
Patients with known or suspected LGE due to chronic infarction, inflammatory myocardial disease and hypertrophic cardiomyopathy (HCM) were prospectively recruited. LGE images were acquired 10-20 min after administration of 0.2 mmol/kg gadolinium-based contrast agent. Three different LGE sequences were acquired: a segmented, single-slice/single-breath-hold fast low angle shot PSIR sequence (FLASH-PSIR), a multi-slice balanced steady-state free precession inversion recovery sequence (bSSFP-IR) and a multi-slice bSSFP-PSIR sequence during breathhold and free breathing. Image quality was evaluated with a 4-point scoring system. Contrast-to-noise ratios (CNR) and acquisition time were evaluated. LGE was quantitatively assessed using a semi-automated threshold method. Differences in size of fibrosis were analyzed using Bland-Altman analysis.
Three hundred twelve patients were enrolled (n = 212 chronic infarction, n = 47 inflammatory myocardial disease, n = 53 HCM) Of which 201 patients (67,4%) had detectable LGE (n = 143 with chronic infarction, n = 27 with inflammatory heart disease and n = 31 with HCM). Image quality and CNR were best on multi-slice bSSFP-PSIR. Acquisition times were significantly shorter for all multi-slice sequences (bSSFP-IR: 23.4 ± 7.2 s; bSSFP-PSIR: 21.9 ± 6.4 s) as compared to FLASH-PSIR (361.5 ± 95.33 s). There was no significant difference of mean LGE size for all sequences in all study groups (FLASH-PSIR: 8.96 ± 10.64 g; bSSFP-IR: 8.69 ± 10.75 g; bSSFP-PSIR: 9.05 ± 10.84 g; bSSFP-PSIR free breathing: 8.85 ± 10.71 g, p > 0.05). LGE size was not affected by arrhythmia or absence of breathhold on multi-slice LGE sequences.
Fast multi-slice and standard segmented LGE sequences are equivalent techniques for the assessment of myocardial fibrosis, independent of an ischemic or non-ischemic etiology. Even in patients with arrhythmia and insufficient breathhold capability, multi-slice sequences yield excellent image quality at significantly reduced scan time and may be used as standard LGE approach.
ISRCTN48802295 (retrospectively registered).
分段相位敏感反转恢复(PSIR)心血管磁共振(CMR)序列是使用晚期钆增强(LGE)进行心肌纤维化无创评估的参考标准。已经引入了几种多切片 LGE 序列,以便在心律失常和屏气能力不足的患者中更快地采集。本研究的目的是评估几种多切片 LGE 序列检测和量化缺血性和非缺血性心肌疾病患者心肌纤维化的准确性。
前瞻性招募已知或疑似因慢性梗死、炎症性心肌病和肥厚型心肌病(HCM)而出现 LGE 的患者。在给予 0.2mmol/kg 基于钆的对比剂后 10-20 分钟采集 LGE 图像。采集了三种不同的 LGE 序列:分段、单切片/单屏气快速低角度激发 PSIR 序列(FLASH-PSIR)、多切片平衡稳态自由进动反转恢复序列(bSSFP-IR)和多切片 bSSFP-PSIR 序列在屏气和自由呼吸期间。使用 4 分制评分系统评估图像质量。评估了对比噪声比(CNR)和采集时间。使用半自动阈值方法定量评估 LGE。使用 Bland-Altman 分析分析纤维化大小的差异。
共纳入 312 名患者(n=212 例慢性梗死,n=47 例炎症性心肌病,n=53 例 HCM),其中 201 名患者(67.4%)可检测到 LGE(n=143 例慢性梗死,n=27 例炎症性心脏病,n=31 例 HCM)。多切片 bSSFP-PSIR 的图像质量和 CNR 最佳。与 FLASH-PSIR 相比,所有多切片序列的采集时间都明显缩短(bSSFP-IR:23.4±7.2s;bSSFP-PSIR:21.9±6.4s)。在所有研究组中,所有序列的平均 LGE 大小均无显著差异(FLASH-PSIR:8.96±10.64g;bSSFP-IR:8.69±10.75g;bSSFP-PSIR:9.05±10.84g;bSSFP-PSIR 自由呼吸:8.85±10.71g,p>0.05)。心律失常或多切片 LGE 序列屏气不足均不影响 LGE 大小。
快速多切片和标准分段 LGE 序列是评估心肌纤维化的等效技术,与缺血或非缺血病因无关。即使在心律失常和屏气能力不足的患者中,多切片序列也能以显著缩短的扫描时间提供出色的图像质量,可作为标准 LGE 方法使用。
ISRCTN48802295(回顾性注册)。