使用二维斑点跟踪超声心动图评估犬单剂量康布他汀a4 -磷酸后的心脏毒性。

Gitte Mampaey, Arnaut Hellemans, Hilde de Rooster, Tom Schipper, Eline Abma, Bart J G Broeckx, Sylvie Daminet, Pascale Smets
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引用次数: 1

摘要

Combretastatin A4-phosphate (CA4P)是一种血管破坏剂,最近被描述用于治疗犬实体肿瘤。传统的超声心动图和脉冲波组织多普勒成像并没有显示狗的心脏毒性,然而,评估接受心脏毒性化疗的人类心肌损伤的金标准是二维斑点跟踪超声心动图。目前的研究评估了单剂量CA4P对狗的心脏毒性作用,使用峰值收缩应变测量和这些测量的可变性。回顾性分析了7只健康小猎犬和5只接受CA4P治疗的犬癌患者的超声心动图检查结果。测定CA4P给药前和给药后24 h的收缩区域纵向应变峰值(LSt)、收缩区域周向应变峰值(CSt)和收缩区域径向应变峰值(RSt)。将峰值收缩应变测量值与血清心肌肌钙蛋白I (cTnI)进行比较。为了量化观察者内部和观察者之间的测量变异性,选择了7个超声心动图检查,每个应变参数由3个观察者连续3天测量。CA4P治疗后,LSt和CSt的中位数分别下降了21.8% (p = 0.0005)和12.3% (p = 0.002),而RSt的中位数差异无统计学意义(p = 0.70)。LSt降低与血清cTnI值升高相关(Spearman ρ = -0.64, p = 0.02)。LSt、CSt和RSt的观察者内变异系数(CV)分别为9%、4%和13%,而相应的观察者间变异系数(CV)分别为11%、12%和20%。我们的研究结果表明,局部峰值收缩应变测量可能有助于血管破坏剂引起的心脏毒性的早期检测,并且LSt可能有希望用于犬癌症患者的随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Assessment of Cardiotoxicity after a Single Dose of Combretastatin A4-Phosphate in Dogs Using Two-Dimensional Speckle-Tracking Echocardiography.

Assessment of Cardiotoxicity after a Single Dose of Combretastatin A4-Phosphate in Dogs Using Two-Dimensional Speckle-Tracking Echocardiography.

Assessment of Cardiotoxicity after a Single Dose of Combretastatin A4-Phosphate in Dogs Using Two-Dimensional Speckle-Tracking Echocardiography.

Assessment of Cardiotoxicity after a Single Dose of Combretastatin A4-Phosphate in Dogs Using Two-Dimensional Speckle-Tracking Echocardiography.

Combretastatin A4-phosphate (CA4P) is a vascular disrupting agent that was recently described for the treatment of solid canine tumors. Conventional echocardiography and pulsed wave tissue Doppler imaging did not reveal cardiotoxicity in dogs, however, the gold standard for assessing myocardial damage in humans receiving cardiotoxic chemotherapeutics is two-dimensional speckle-tracking echocardiography. The current study evaluated the cardiotoxic effect of a single dose of CA4P in dogs using peak systolic strain measurements and the variability of these measurements. Echocardiographic examinations of seven healthy beagles and five canine cancer patients that received CA4P were retrospectively reviewed. Peak systolic regional longitudinal strain (LSt), peak systolic regional circumferential strain (CSt), and peak systolic regional radial strain (RSt) were measured before and 24 h after administration of CA4P. Peak systolic strain measurements were compared to serum cardiac troponin I (cTnI). To quantify intra- and inter-observer measurement variability, seven echocardiographic examinations were selected and each strain parameter was measured by three observers on three consecutive days. After CA4P administration, the median LSt and CSt values decreased by 21.8% (p = 0.0005) and 12.3% (p = 0.002), respectively, whereas the median RSt values were not significantly different (p = 0.70). The decrease in LSt was correlated with increased serum cTnI values (Spearman rho = -0.64, p = 0.02). The intra-observer coefficients of variation (CV) were 9%, 4%, and 13% for LSt, CSt, and RSt, respectively, while the corresponding interobserver CVs were 11%, 12%, and 20%. Our results suggest that regional peak systolic strain measurements may be useful for the early detection of cardiotoxicity that is caused by vascular disrupting agents and that LSt may be promising for the follow-up of canine cancer patients.

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