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Published on: October 5, 2018
Activity estimation and biokinetic analysis of 99mTc-DMSA in renal infant patients using a gamma camera
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.
Abstract:
Biokinetic data from the administration of radiopharmaceuticals is essential in nuclear medicine dosimetry. It has particular significance in children, as their metabolism is very different from adults. Biokinetic models for paediatric patients could therefore need to be adapted to better reflect their absorption, retention and excretion functions, when compared to adults. Obtaining quality in vivo infant or paediatric biokinetic data is then essential to improve the available reference models, which in turn can lead to the optimization of paediatric procedures and protocols in clinical practice. This study analyses the biokinetic behaviour of 99mTc-dimercaptosuccinic acid (DMSA), in 8 infants aged 4 months to 2 years old, through an imaging study using a gamma camera, and compares the obtained values with those obtained with the reference ICRP biokinetic model. The in vivo data was treated using an adapted methodology from the MIRD 16 pamphlet. Activity curves for the liver, the kidney and the whole body, were built, and new effective absorption, retention and excretion half-lives were estimated, and compared with the reference biokinetic parameters of ICRP 128. The obtained residence time in the kidneys of 2.56 h, has a deviation of 30.8% to the ICRP 128 value of 3.70 h. The obtained maximum uptake in the kidneys was of 0.22/A0, which compares to the value of 0.31/A0 for ICRP. The obtained biokinetic parameters were used to estimate the absorbed dose. The obtained dose values are smaller than the reference ICRP 128 ones by 32.1% in the kidneys, and 18.4% in the liver.
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