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Effect of respiratory motion on internal radiation dosimetry
Author(s) -
Xie Tianwu,
Zaidi Habib
Publication year - 2014
Publication title -
medical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 180
eISSN - 2473-4209
pISSN - 0094-2405
DOI - 10.1118/1.4898118
Subject(s) - dosimetry , absorbed dose , nuclear medicine , imaging phantom , internal dosimetry , respiratory system , monte carlo method , irradiation , radiation , photon , medicine , physics , nuclear physics , optics , mathematics , statistics
Purpose: Estimation of the radiation dose to internal organs is essential for the assessment of radiation risks and benefits to patients undergoing diagnostic and therapeutic nuclear medicine procedures including PET. Respiratory motion induces notable internal organ displacement, which influences the absorbed dose for external exposure to radiation. However, to their knowledge, the effect of respiratory motion on internal radiation dosimetry has never been reported before. Methods: Thirteen computational models representing the adult male at different respiratory phases corresponding to the normal respiratory cycle were generated from the 4D dynamic XCAT phantom. Monte Carlo calculations were performed using the mcnp transport code to estimate the specific absorbed fractions (SAFs) of monoenergetic photons/electrons, the S ‐values of common positron‐emitting radionuclides (C‐11, N‐13, O‐15, F‐18, Cu‐64, Ga‐68, Rb‐82, Y‐86, and I‐124), and the absorbed dose of 18 F‐fluorodeoxyglucose ( 18 F‐FDG) in 28 target regions for both the static (average of dynamic frames) and dynamic phantoms. Results: The self‐absorbed dose for most organs/tissues is only slightly influenced by respiratory motion. However, for the lung, the self‐absorbed SAF is about 11.5% higher at the peak exhale phase than the peak inhale phase for photon energies above 50 keV. The cross‐absorbed dose is obviously affected by respiratory motion for many combinations of source‐target pairs. The cross‐absorbed S ‐values for the heart contents irradiating the lung are about 7.5% higher in the peak exhale phase than the peak inhale phase for different positron‐emitting radionuclides. For 18 F‐FDG, organ absorbed doses are less influenced by respiratory motion. Conclusions: Respiration‐induced volume variations of the lungs and the repositioning of internal organs affect the self‐absorbed dose of the lungs and cross‐absorbed dose between organs in internal radiation dosimetry. The dynamic anatomical model provides more accurate internal radiation dosimetry estimates for the lungs and abdominal organs based on realistic modeling of respiratory motion. This work also contributes to a better understanding of model‐induced uncertainties in internal radiation dosimetry.