Activity estimation and biokinetic analysis of 99mTc-DMSA in renal infant patients using a gamma camera

P Teles1, J Costa2, D Costa3

  • 1Grupo de Protecção e Segurança Radiológica, Centro de Ciências e Tecnologias Nucleares (C2TN), CTN/IST, Pólo de Loures. Estrada Nacional 10 (km 139,7), 2695-066 Bobadela LRS, Portugal.

Insights

Paediatric biokinetic data for technetium-99m dimercaptosuccinic acid (99mTc-DMSA) was analyzed in infants. Results show lower kidney and liver absorbed doses compared to reference models, suggesting a need for updated paediatric dosimetry.

Area of Science:

  • Nuclear Medicine
  • Paediatric Dosimetry
  • Radiopharmaceutical Biokinetics

Background:

  • Accurate biokinetic data is crucial for nuclear medicine dosimetry, especially in children due to differing metabolism.
  • Existing paediatric biokinetic models may require adaptation compared to adult models.
  • In vivo infant data is essential for refining reference models and optimizing clinical protocols.

Purpose of the Study:

  • To analyze the biokinetic behavior of 99mTc-DMSA in infants.
  • To compare infant biokinetic data with the International Commission on Radiological Protection (ICRP) reference model.
  • To estimate absorbed doses in paediatric patients using study-specific biokinetic parameters.

Main Methods:

  • Studied 8 infants (4 months to 2 years) using gamma camera imaging.
  • Applied an adapted methodology from the MIRD 16 pamphlet for data analysis.
  • Estimated effective absorption, retention, and excretion half-lives and compared them to ICRP 128 parameters.

Main Results:

  • Obtained kidney residence time (2.56 h) differed by 30.8% from the ICRP 128 value (3.70 h).
  • Maximum kidney uptake (0.22/A0) was lower than the ICRP value (0.31/A0).
  • Estimated absorbed doses were 32.1% lower in the kidneys and 18.4% lower in the liver compared to ICRP 128.

Conclusions:

  • Infant biokinetics of 99mTc-DMSA differ from established adult/reference models.
  • Current reference models may overestimate absorbed doses in paediatric patients.
  • Updated paediatric biokinetic data can improve the accuracy of dosimetry and optimize clinical practice.

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