Nuclear Medicine Department, "Evaggelismos" General Hospital, Athens, Greece.
Ann Nucl Med. 2012 Apr;26(3):234-40. doi: 10.1007/s12149-011-0564-1. Epub 2012 Jan 12.
To evaluate the degree of interobserver agreement in the visual interpretation of (123)I-FP-CIT studies and to investigate for potential associations between visual and semi-quantitative parameters.
Eighty-nine (123)I-FP-CIT studies were blindly reviewed by 3 independent observers: a consultant, a resident doctor and a radiographer. They classified every study as either "normal" or "abnormal" and assigned visual (123)I-FP-CIT uptake scores (2: normal, 1: reduced and 0: no uptake) in basal ganglia nuclei (right and left putamina and caudate nuclei) on every scan. Striatal (123)I-FP-CIT binding ratios were calculated using crescent-ROI software. The interobserver agreement for the interpretation of studies and for visual score assignment was evaluated by means of κ statistics. We investigated for associations of binding ratios with visual scores and clinical parameters; patients' clinical diagnoses served as the reference standard.
There was excellent interobserver agreement (κ 0.89-0.93) in classifying studies as "normal" or "abnormal" and fine agreement in assignment of visual scores (κ 0.71-0.80 for putamina and 0.50-0.79 for caudate nuclei). Nuclei with scores of 1 and 0 showed significantly reduced binding ratios (about 30 and 50%, respectively) compared with the nuclei scored as 2. ROC analysis indicated the optimal cutoff point of striatal binding ratio at 3.8 (sensitivity 98.5%, specificity 95%) for the detection of parkinsonian syndromes. Striatal binding ratios were negatively associated with age in normal subjects and disease duration in Parkinson's disease patients.
Visual interpretation of (123)I-FP-CIT studies showed very good interobserver agreement. We found significant associations among visual, semi-quantitative and clinical parameters.
评估(123)I-FP-CIT 研究中视觉解读的观察者间一致性,并研究视觉和半定量参数之间的潜在关联。
3 名独立观察者(顾问、住院医师和放射技师)对 89 项(123)I-FP-CIT 研究进行了盲法审查。他们将每一项研究分为“正常”或“异常”,并在每一次扫描中对基底节核(右侧和左侧壳核和尾状核)的视觉(123)I-FP-CIT 摄取评分(2:正常,1:减少,0:无摄取)进行赋值。使用新月形 ROI 软件计算纹状体(123)I-FP-CIT 结合比。通过 κ 统计评估观察者间对研究的解释和视觉评分赋值的一致性。我们研究了结合比与视觉评分和临床参数之间的关联;患者的临床诊断作为参考标准。
将研究分为“正常”或“异常”的观察者间一致性极好(κ 值为 0.89-0.93),而视觉评分赋值的一致性也很好(壳核的κ 值为 0.71-0.80,尾状核的κ 值为 0.50-0.79)。评分 1 和 0 的核与评分 2 的核相比,结合比显著降低(分别约为 30%和 50%)。ROC 分析表明,纹状体结合比的最佳截断值为 3.8(帕金森综合征的检测敏感性为 98.5%,特异性为 95%)。在正常受试者中,纹状体结合比与年龄呈负相关,在帕金森病患者中与疾病持续时间呈负相关。
(123)I-FP-CIT 研究的视觉解读具有非常好的观察者间一致性。我们发现视觉、半定量和临床参数之间存在显著关联。