Dosimetric considerations of 99mTc-MDP uptake within the epiphyseal plates of the long bones of pediatric patients

被引:3
作者
Brown, Justin L. [1 ,2 ]
Sexton-Stallone, Briana [3 ]
Li, Ye [4 ,5 ]
Frey, Eric C. [4 ,5 ]
Treves, S. Ted [6 ,7 ]
Fahey, Frederic H. [6 ,7 ]
Plyku, Donika [5 ]
Cao, Xinhua [8 ]
Choi, Chansoo [9 ]
Kim, Chan Hyeong [9 ]
Sgouros, George [5 ]
Aris, John P. [10 ]
Bolch, Wesley E. [1 ]
机构
[1] Univ Florida, J Crayton Pruitt Family Dept Biomed Engn, Gainesville, FL 32611 USA
[2] Univ Florida, Coll Med, Med Phys Program, Gainesville, FL USA
[3] Harvard Med Sch, Boston Childrens Hosp, Boston, MA 02115 USA
[4] Johns Hopkins Univ, Dept Elect & Comp Engn, Baltimore, MD 21218 USA
[5] Johns Hopkins Univ, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD USA
[6] Harvard Med Sch, Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[7] Harvard Med Sch, Dept Radiol, Boston, MA 02115 USA
[8] Harvard Med Sch, Boston Childrens Hosp, Dept Radiol, Boston, MA 02115 USA
[9] Hanyang Univ, Dept Nucl Engn, Seoul, South Korea
[10] Univ Florida, Dept Anat & Cell Biol, Gainesville, FL USA
关键词
skeletal scintigraphy; Tc-99m MDP; dose reduction; optimization; computational phantoms; epiphyseal growth plates; organ dosimetry; administered activity guidelines; GROWTH;
D O I
10.1088/1361-6560/abb1db
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Skeletal scintigraphy is most performed in pediatric patients using the radiopharmaceutical Tc-99m labelled methylene diphosphonate (Tc-99m-MDP). Reference biokinetic models for Tc-99m-MDP indicate 50% of the administered activity is uniformly localized to the interior bone surfaces (trabecular and cortical regions), yet imaging data clearly show some preferential uptake to the epiphyseal growth plates of the long bones. To explore the dosimetric consequences of these regional activity concentrations, we have modified mesh-type computational phantoms of the International Commission on Radiological Protection (ICRP) reference pediatric series to explicitly include geometric models of the epiphyseal growth plates (2 mm in thickness) within the left/right, distal/proximal ends of the humeri, radii, ulnae, femora, tibia, and fibulae. Bone mineral activity from the ICRP Publication 128 biokinetic model for Tc-99m-MDP (ICRP 2015) was then partitioned to the growth plates at values of 0.5%, 4.4%, 8.3%, 12.2%, 16.1%, and 20%. Radiation transport simulations were performed to compute Tc-99m S-values and organ dose coefficients to the soft tissues and to bone site-specific regions of spongiosa. As the percentage of bone activity assigned to the growth plates was increased (from 0.5% to 20%), absorbed doses to the soft tissue organs, active bone marrow, bone endosteum (BE), as well as the detriment-weighted dose, were shown to decrease from their nominal values (no substantial growth plate activity), while epiphyseal plate self-doses increased. In the 15 year old male phantom, moving from 0.5% to 20% relative bone activity within the epiphyseal plates resulted in a 15% reduction in active marrow (AM) and BE dose, a 10% reduction in mean soft tissue and detriment-weighted dose, and a 6.3-fold increase in epiphyseal plate self-dose. In the newborn female phantom, we observed a 18% decrease in AM and BE dose, a 10% decrease in mean soft tissue dose, a 15% decrease in detriment-weighted dose, and 12.8-fold increase in epiphyseal plate self-dose. Increases (to 3 mm) and decreases (to 1 mm) in the assumed growth plate thickness of our models were shown to impact only the growth plate self-dose. Future work in differential quantification of Tc-99m-MDP activity-growth plates versus other bone surfaces-is required to provide clinically realistic data on activity partitioning as a function of patient age, and perhaps skeletal site. The phantom series presented here may be used to develop more optimized age-related guidance on Tc-99m-MDP administered activities to children.
引用
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页数:14
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