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Renal (99m)Tc-DMSA pharmacokinetics in pediatric patients

ABSTRACT: (99m)Tc-DMSA is one of the most commonly used pediatric nuclear medicine imaging agents. Nevertheless, there are no pharmacokinetic (PK) models for (99m)Tc-DMSA in children, and currently available pediatric dose estimates for (99m)Tc-DMSA use pediatric S values with PK data derived from a...

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Detalles Bibliográficos
Autores principales: Plyku, Donika, Ghaly, Michael, Li, Ye, Brown, Justin L., O’Reilly, Shannon, Khamwan, Kitiwat, Goodkind, Alison B., Sexton-Stallone, Briana, Cao, Xinhua, Zurakowski, David, Fahey, Frederic H., Treves, S. Ted, Bolch, Wesley E., Frey, Eric C., Sgouros, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292521/
https://www.ncbi.nlm.nih.gov/pubmed/34283316
http://dx.doi.org/10.1186/s40658-021-00401-7
Descripción
Sumario:ABSTRACT: (99m)Tc-DMSA is one of the most commonly used pediatric nuclear medicine imaging agents. Nevertheless, there are no pharmacokinetic (PK) models for (99m)Tc-DMSA in children, and currently available pediatric dose estimates for (99m)Tc-DMSA use pediatric S values with PK data derived from adults. Furthermore, the adult PK data were collected in the mid-70’s using quantification techniques and instrumentation available at the time. Using pediatric imaging data for DMSA, we have obtained kinetic parameters for DMSA that differ from those applicable to adults. METHODS: We obtained patient data from a retrospective re-evaluation of clinically collected pediatric SPECT images of (99m)Tc-DMSA in 54 pediatric patients from Boston’s Children Hospital (BCH), ranging in age from 1 to 16 years old. These were supplemented by prospective data from twenty-three pediatric patients (age range: 4 months to 6 years old). RESULTS: In pediatric patients, the plateau phase in fractional kidney uptake occurs at a fractional uptake value closer to 0.3 than the value of 0.5 reported by the International Commission on Radiological Protection (ICRP) for adult patients. This leads to a 27% lower time-integrated activity coefficient in pediatric patients than in adults. Over the age range examined, no age dependency in uptake fraction at the clinical imaging time was observed. Female pediatric patients had a 17% higher fractional kidney uptake at the clinical imaging time than males (P < 0.001). CONCLUSIONS: Pediatric (99m)Tc-DMSA kinetics differ from those reported for adults and should be considered in pediatric patient dosimetry. Alternatively, the differences obtained in this study could reflect improved quantification methods and the need to re-examine DMSA kinetics in adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40658-021-00401-7.