Kelly M J, Cowie A R, Antonino A, Barton H, Kalff V
Department of Nuclear Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
J Nucl Med. 1992 Dec;33(12):2222-5.
This study assessed factors which may contribute to suboptimal image quality when the modified in vivo erythrocyte labeling technique is used with standard clinical 99mTc activities. For each assessment duplicate or triplicate blood specimens were withdrawn from > or = 10 patients, into syringes containing 700-900 MBq 99mTc as pertechnetate. After incubation the percent of 99mTc which was not bound to erythrocytes at blood re-injection time (%Unbound 99mTc), was measured and compared when one of four factors was varied. The most significant results, in descending order of measured effect were: [table: see text] Our data suggest that the requirements for optimal erythrocyte labeling with standard clinical 99mTc activities are: (A) Erythrocyte tinning time between 10 and 30 min; (B) blood volume > or = 3 ml; (C) blood incubation time > or = 20 min; and (D) Generator ingrowth time < or = 24 hr.
本研究评估了在使用标准临床99mTc活度的改良体内红细胞标记技术时,可能导致图像质量欠佳的因素。对于每次评估,从≥10名患者身上采集两份或三份血样,注入含有700 - 900 MBq高锝酸盐形式的99mTc的注射器中。孵育后,在重新注入血液时测量未与红细胞结合的99mTc的百分比(未结合99mTc百分比),并在改变四个因素之一时进行比较。按测量效应从大到小排序,最显著的结果如下:[表格:见原文]我们的数据表明,使用标准临床99mTc活度进行最佳红细胞标记的要求为:(A)红细胞锡化时间在10至30分钟之间;(B)血容量≥3 ml;(C)血液孵育时间≥20分钟;以及(D)发生器生长时间≤24小时。