Elimination of artifacts caused by residual radiopharmaceutical activity in injection site in myocardial perfusion imaging on Discovery NM 530c semiconductor gamma camera.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Aleksandra Owczarek, Zbigniew Adamczewski, Anna Plachcinska, Pawel Cichocki
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引用次数: 0

Abstract

Background: Cardiac gamma cameras dedicated for myocardial perfusion imaging (MPI) perform studies faster and acquire higher quality images than traditional cameras. However, they are susceptible to some artifacts. We observed a previously unreported artifact, caused by residual radiopharmaceutical activity in injection site in cubital fossa caught in camera field of view. This study aims to assess the impact of these artifacts on image quality and the possibility of their elimination. Study included 50 male patients referred for MPI using Discovery NM 530c gamma camera, in whom radiopharmaceutical activity in injection site was observed in stress or rest study. In such cases, image acquisition was immediately repeated, with the patient and the camera kept in the same position, after covering the injection site with a special lead shield. Obtained images were assessed by two experienced nuclear medicine physicians using a 0-4 point scale in each segment (where 0-normal perfusion, and 4-complete lack of perfusion). Summed stress, rest and difference scores (SSS, SRS and SDS, respectively) were calculated for the entire myocardium and 3 main vascular territories.

Results: SSS, SRS and SDS were most frequently assessed as abnormal in RCA territory. Radiopharmaceutical activity in injection site was observed more frequently in stress studies (84% of cases). Covering injection site with a shield changed the assessment of SSS, SRS or SDS from normal to abnormal and vice versa in almost 20% of studies. The most frequently affected vascular territories were LAD and RCA. Elimination of the artifact changed final diagnosis in almost 1/5 of patients, most often by eliminating previously visible significant stress-induced perfusion defects (patients in whom such change occurred did not report any cardiovascular events in one-year follow-up).

Conclusions: Artifacts caused by radiopharmaceutical activity in injection site reduce image quality and can potentially generate or hide perfusion defects. They can be observed mainly in patients examined in prone position, after radiopharmaceutical injection in cubital fossa. These artifacts can be eliminated by a lead shield, which can change the final assessment of MPI study in 20% of the patients.

背景:与传统相机相比,专门用于心肌灌注成像(MPI)的心脏伽马相机能更快地进行研究,获得更高质量的图像。但是,它们容易受到一些伪影的影响。我们观察到了一种以前未报道过的伪影,它是由肘窝注射部位残留的放射性药物活性在相机视野中造成的。本研究旨在评估这些伪影对图像质量的影响以及消除这些伪影的可能性。研究对象包括50名使用Discovery NM 530c伽马相机进行骨髓造影的男性患者。在这种情况下,用特制的铅屏蔽罩覆盖注射部位后,立即重复采集图像,病人和相机保持在同一位置。获取的图像由两名经验丰富的核医学医生用 0-4 分制对每个区段进行评估(0-正常灌注,4-完全无灌注)。计算整个心肌和 3 个主要血管区域的应激、静息和差异总分(分别为 SSS、SRS 和 SDS):结果:在 RCA 区域,SSS、SRS 和 SDS 最常被评估为异常。应激研究中更常观察到注射部位的放射性药物活性(84% 的病例)。在近 20% 的研究中,用防护罩覆盖注射部位会使 SSS、SRS 或 SDS 的评估从正常变为异常,反之亦然。最常受影响的血管区域是 LAD 和 RCA。消除伪影改变了近1/5患者的最终诊断,最常见的是消除了之前可见的明显应激诱导灌注缺陷(发生这种改变的患者在一年的随访中未报告任何心血管事件):结论:注射部位放射性药物活性造成的伪影降低了图像质量,有可能产生或掩盖灌注缺陷。这些伪影主要出现在肘窝注射放射性药物后俯卧位接受检查的患者身上。这些伪影可以通过铅屏蔽消除,但这可能会改变 20% 患者 MPI 研究的最终评估结果。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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