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Title
Effective dose assessment for participants in the National Lung Screening Trial undergoing posteroanterior chest radiographic examinations.
Pubmed ID
23789668 (View this publication on the PubMed website)
Publication
AJR Am J Roentgenol. 2013 Jul; Volume 201 (Issue 1): Pages 142-6
Authors
Kruger R, Flynn MJ, Judy PF, Cagnon CH, Seibert JA
Affiliations
  • Department of Radiology, Medical Physics Section, Marshfield Clinic, 1000 N Oak Ave, Marshfield, WI 54449-5777, USA. kruger.randell@marshfieldclinic.org
Abstract

OBJECTIVE: The National Lung Screening Trial (NLST) is a multicenter randomized controlled trial comparing low-dose helical CT with chest radiography in the screening of older current and former heavy smokers for early detection of lung cancer. Recruitment was launched in September 2002 and ended in April 2004, when 53,454 participants had been randomized at 33 screening sites. The objective of this study was to determine the effective radiation dose associated with individual chest radiographic screening examinations.

SUBJECTS AND METHODS: A total of 73,733 chest radiographic examinations were performed with 92 chest imaging systems. The entrance skin air kerma (ESAK) of participants' chest radiographic examinations was estimated and used in this analysis. The effective dose per ESAK for each examination was determined with a Monte Carlo-based program. The examination effective dose was calculated as the product of the examination ESAK and the Monte Carlo estimate of the ratio of effective dose per ESAK.

RESULTS: This study showed that the mean effective dose assessed from 66,157 postero-anterior chest examinations was 0.052 mSv. Additional findings were a median effective dose of 0.038 mSv, a 95th percentile value of 0.136 mSv, and a fifth percentile value of 0.013 mSv.

CONCLUSION: The effective dose for participant NLST chest radiographic examinations was determined and is of specific interest in relation to that associated with the previously published NLST low-dose CT examinations conducted during the trial.

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