Literature DB >> 21859021

Reference air kerma and kerma-area product as estimators of peak skin dose for fluoroscopically guided interventions.

Deukwoo Kwon1, Mark P Little, Donald L Miller.   

Abstract

PURPOSE: To determine more accurate regression formulas for estimating peak skin dose (PSD) from reference air kerma (RAK) or kerma-area product (KAP).
METHODS: After grouping of the data from 21 procedures into 13 clinically similar groups, assessments were made of optimal clustering using the Bayesian information criterion to obtain the optimal linear regressions of (log-transformed) PSD vs RAK, PSD vs KAP, and PSD vs RAK and KAP.
RESULTS: Three clusters of clinical groups were optimal in regression of PSD vs RAK, seven clusters of clinical groups were optimal in regression of PSD vs KAP, and six clusters of clinical groups were optimal in regression of PSD vs RAK and K AP. Prediction of PSD using both RAK andKAP is significantly better than prediction of PSD with either RAK or KAP alone. The regression of PSD vs RAK provided better predictions of PSD than the regression of PSD vs KAP. The partial-pooling (clustered) method yields smaller mean squared errors compared with the complete-pooling method.
CONCLUSION: PSD distributions for interventional radiology procedures are log-normal. Estimates of PSD derived from RAK and KAP jointly are mos t accurate, followed closely byestimates derived from RAK alone. Estimates of PSD derived from KAP alone are the least accurate. Using a stochastic search approach, it is possible to cluster together certain dissimilar types of procedures to minimize the total error sum of squares.

Mesh:

Year:  2011        PMID: 21859021      PMCID: PMC3145218          DOI: 10.1118/1.3590358

Source DB:  PubMed          Journal:  Med Phys        ISSN: 0094-2405            Impact factor:   4.071


  19 in total

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3.  Guidelines for patient radiation dose management.

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Journal:  J Vasc Interv Radiol       Date:  2009-07       Impact factor: 3.464

4.  Reference levels for patient radiation doses in interventional radiology: proposed initial values for U.S. practice.

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6.  Automatic monitoring of localized skin dose with fluoroscopic and interventional procedures.

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5.  Where should we measure the entrance air kerma rate during acceptance testing of the automatic dose control of a fluoroscopic system?

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7.  Patient dose simulations for scanning-beam digital x-ray tomosynthesis of the lungs.

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