郭耀霞,红华,冯天鹰,尹海军,梁丹艳,吴国柱.速度向量成像评价乳腺癌患者蒽环类药物治疗后左心房收缩功能[J].中国医学影像技术,2021,37(1):54~58
速度向量成像评价乳腺癌患者蒽环类药物治疗后左心房收缩功能
Velocity vector imaging for evaluation on left atrial systolic function in breast cancer patients undergoing anthracycline therapy
投稿时间:2019-10-09  修订日期:2020-05-08
DOI:10.13929/j.issn.1003-3289.2021.01.012
中文关键词:  乳腺肿瘤  心房功能,左  蒽环素  超声检查
英文关键词:breast neoplasms  atrial function, left  anthracyclines  ultrasonography
基金项目:内蒙古自治区自然科学基金(2017MS0850)。
作者单位E-mail
郭耀霞 内蒙古自治区人民医院超声医学科, 内蒙古 呼和浩特 010010  
红华 内蒙古自治区人民医院超声医学科, 内蒙古 呼和浩特 010010 6622306hong@163.com 
冯天鹰 深圳市宝安区中心医院, 广东 深圳 518100  
尹海军 内蒙古自治区人民医院超声医学科, 内蒙古 呼和浩特 010010  
梁丹艳 内蒙古自治区人民医院超声医学科, 内蒙古 呼和浩特 010010  
吴国柱 内蒙古自治区人民医院超声医学科, 内蒙古 呼和浩特 010010  
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中文摘要:
      目的 应用速度向量成像(VVI)评价蒽环类药物对乳腺癌患者左心房收缩功能的影响。方法 选取30例接受蒽环类药物治疗的乳腺癌患者,采用VVI观察并比较治疗前、治疗第6、8周期及治疗结束6个月后左心房最小容积(LAVmin)、左心房P容积(LAVp)、左心房主动射血分数(LAAEF)和舒张晚期左心房峰值应变率(SRa)。结果 治疗第6周期LAVmin、LAVp、LAAEF与治疗前比较差异均无统计学意义(P均>0.05);第8周期LAVmin、LAVp及LAAEF与治疗前差异均有统计学意义(P均<0.05);第6周期及治疗结束6个月后LAVmin、LAVp及LAAEF与治疗第8周期差异均无统计学意义(P均>0.05)。治疗第6周期心肌6个节段SRa较治疗前升高(P<0.05),第8周期心肌6个节段SRa较治疗前及治疗第6周期时均减低(P均<0.05)。治疗结束6个月后间隔上段SRa较治疗第8周期升高(P<0.05),其他节段SRa差异均无统计学意义(P均>0.05)。结论 蒽环类药物影响左心房收缩功能,初期可在一定程度上代偿,最终出现失代偿,导致左心房收缩功能减低;利用VVI可准确加以评估。
英文摘要:
      Objective To evaluate the impact of anthracyclines on left atrial systolic function in breast cancer patients with velocity vector imaging (VVI). Methods Totally 30 breast cancer patients treated with anthracycline drugs were selected. Left atrial minimum volume (LAVmin), left atrial P volume (LAVp), left atrial active ejection fraction (LAAEF) and late diastolic peak left atrial strain rate (SRa) were observed and compared before and after 6 and 8 cycles of chemotherapy, also 6 months after the ending of chemotherapy. Results No significant difference of LAVmin, LAVp nor LAAEF was detected at the 6th cycles of chemotherapy and before chemotherapy (all P>0.05), while significant difference of LAVmin, LAVp and LAAEF were found at the 8th cycle and before chemotherapy (all P<0.05). No significant difference of LAVmin, LAVp and LAAEF at the 8th cycle of chemotherapy compared with those at the 6th cycle of chemotherapy and 6 months after the ending of chemotherapy (all P>0.05). Compared with that before chemotherapy, SRa of 6 segments of myocardium increased at the 6th cycle but decreased at the 8th cycle of chemotherapy (both P<0.05). Compared with that at the 6th cycle of chemotherapy, SRa of 6 segments of myocardium decreased at the 8th cycle of chemotherapy (P<0.05). Six months after the ending of chemotherapy, SRa in upper segment was higher than that at the 8th cycle of chemotherapy (P<0.05), and there was no significant difference of SRa in other segments (all P>0.05). Conclusion Anthracyclines had impact on left atrial systolic function, which could first be compensated to a certain extent, but eventually lead to decompensation and reduction of left atrium systolic function. VVI was able to sensitively and accurately evaluate the changes of left atrial systolic function during the above procedures.
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