An Assessment of Factors Which Influence the Effectiveness of the Modified In Vivo Technetium-99m-Erythrocyte Labeling Technique in Clinical Use

• Published in: The Journal of nuclear medicine (1978) Vol. 33; no. 12; pp. 2222 - 2225
• Main Authors: Kelly, Michael J, Cowie, Ailsa R, Antonino, Angelo, Barton, Howard, Kalff, Victor
• Format: Journal Article
• Language: English
• Published: United States Soc Nuclear Med 01-12-1992
• Subjects: Adult; Blood Volume; Erythrocytes; Humans; Isotope Labeling - instrumentation; Isotope Labeling - methods; Isotope Labeling - standards; Radionuclide Generators - standards; Technetium - standards; Time Factors
• ISSN: 0161-5505; 1535-5667

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 For each assessment duplicate or triplicate blood specimens were withdrawn from 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.