BJR
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

British Journal of Radiology (2006) 79, 357-358
© 2006 British Institute of Radiology
doi: 10.1259/bjr/71189157

This Article
Right arrow Full Text (PDF)
Services
Right arrow Related articles in BJR
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Moores, B M
Right arrow Search for Related Content
PubMed
Right arrow Articles by Moores, B M

Correspondence

Authors' reply

I wish to thank B Wall for his comments on my letter and I would like to respond, first of all, to paragraphs 4 and 5 of his letter. Here, he appears to recommend an unproven optimization strategy for female patients, which is based upon the use of dose reference levels (DRLs) that are dependent upon the exposure of male patients. I believe that such an approach severely disadvantages female patients. It either ignores or neglects the well-known and significant differences in both entrance surface dose (ESD) and dose–area product (DAP) values for female patients, compared with those of males, as well as their own distinct optimization requirements.

A comparison of male and female ESD and DAP values measured during a national survey of doses to patients in the UK [1] and the corresponding DRLs presented in the National Protocol for Patient Dose Measurements [2] indicates that National and European adult patient DRLs are governed by the levels of exposure to male patients.

The reason for this lies, to a large extent, in the recommendation that the mean weight of an adult patient sample, in any ESD/DAP audit, should lie within 5 kg of 70 kg [2]. In the national patient dose survey [1], the average weight of female patients was roughly 60 kg whilst that of the male patients was 70 kg. Similar weight differences for female and male patients have also been noted in studies involving fluoroscopy [3] and radiography [4]. Also, the weights of female and male adult voxel phantoms, developed for computational radiation protection studies, have been designed around similar weight differences [57]. The decision to employ a single-weight dependent DRL value has never been scientifically justified as an effective basis for optimization of practices in respect of female patients.

As I indicated in my letter, results of the 1985 national survey [1] demonstrate that the mean ESD for female patients undergoing a PA chest X-ray examination was 30% lower than that of the male patients. Such differences in ESD were also noted, for example, for the AP abdomen (27%), lat thoracic spine (33%), lat lumbar spine (25%) examinations. Other studies have also shown similar differences in ESD [4], for PA chest (70%), knee (100%) and AP skull (70%), examinations.

The mean DAP value for female patients was significantly lower than that of male patients [1] for the PA chest (86%), thoracic spine (22%), barium meal (39%), IVU (43%), cholangiography and cholecystography (43%) examinations. Other studies have shown similar differences in DAP values for female patients [3]; barium meal (36%), barium swallow (45%) etc. In the case of the DAP values, such differences can arise from unknown variations in the ESD and field sizes employed.

Under present circumstances, local DRLs derived for patients in a women's hospital would not be relevant to females in a mixed-sex patient group of 70 kg average weight. Different audit standards, therefore, can exist for different female populations. Similarly, female DAP values for a PA X-ray examination of the chest may exceed their own population norm by up to 86% [1], due to unknown variations in either ESD or field size, before the need for an investigation is indicated. Such an indication may be dependent upon the patient mix, including weights, in the audit sample, as well as specifically radiation protection considerations. Why should easily demonstrable, optimized practices for female patients be hidden under patient sampling/weight considerations involving male patients?

Besides exposure differences for female patients, other factors merit consideration in respect of optimization strategies for female patients:

Given such extensive differences, why are female patients not considered to be a separate exposed group with its own DRL values, so that their own unique safety and imaging needs can demonstrably be given full and direct consideration in respect of radiation safety?

The main reason for the widespread installation of DAP meters on X-ray imaging equipment throughout the NHS [paragraph 2 of B Wall's comments] is due to the fact that funds were made available from central government (presumably on the advice of the NRPB), in the early 1990s, for the purchase and distribution of 200 DAP meters. Prior to this, extensive medical physics effort had been expended on developing the use of calibrated X-ray source data for patient dose assessments. This effort included the background science [12] and calibration methods [13]. Such an approach harmonises patient dose assessments in both radiotherapy and diagnostic radiology and is based upon over 50 years of scientific effort. Unfortunately this was ignored in the National Protocol [2].

The reduction in patient doses in diagnostic radiology over the past 20 years [paragraph 7 of B Wall's comments] is due to the introduction of rare earth intensifying screens in radiography and sodium iodide phosphors in fluoroscopic units. These initiatives have been supported by the introduction of low attenuation materials in table-tops and Bucky stands. The UK national dose audits have faithfully recorded their well-documented effects. Our manufacturer colleagues are to be commended upon their contribution to patient dose reduction.

Yours etc.,

B M Moores

1 Co-ordinator, Radiological Unification Strategies [RADIUS] Group, EC Radiation Protection Research Programme

Received for publication November 18, 2005. Revision received January 4, 2006. Accepted for publication January 11, 2006.

References

  1. Shrimpton PC, Wall BF, Jones DG, Fisher ES, Hillier MC, Kendall GM. A national survey of doses to patients undergoing a selection of routine x-ray examinations in English hospitals. NRPB-R200. Chilton, UK: National Radiological Protection Board 1986.
  2. National protocol for patient dose measurements in diagnostic radiology. Chilton, Didcot: National Radiological Protection Board 1992.
  3. Rowley KA, Hill SJ, Watkins R, Moores BM. An investigation into the levels of radiation exposure in diagnostic examinations involving fluoroscopy. Br J Radiol 1987;60:167–73.[Abstract]
  4. Gallini RE, Belletti S, Berna V, Giugni U. Adult and child doses in standardised x-ray examinations. Radiat Prot Dosim 1992;43:41–7.[Abstract]
  5. Zankl M, Fill U, Petoussi-Henss N, Regulla D. Organ dose conversion coefficients for external photon irradiation of male and female voxel models. Phys Med Biol 2002;47:2367–85.[CrossRef][Medline]
  6. Kramer R, Vieira JW, Khoury HJ, Lima FRA, Fuelle D. All about MAX: a male adult voxel phantom for Monte Carlo calculations in radiation protection dosimetry. Phys Med Biol 2003;48:1239–62.[CrossRef][Medline]
  7. Kramer R, Khoury HJ, Vieira JW, Loureiro ECM, Lima VJM, Lima FRA, et al. All about FAX: a female adult voxel phantom for Monte Carlo calculation in radiation protection dosimetry. Phys Med Biol 2004;49:5203–16.[CrossRef][Medline]
  8. Pascoal A, Patel R, Lawinski CP, Tabakov S. Optimization of tube voltage and dose for digital chest radiography – a study addressing patient size. In: Proceedings of UK Radiological Congress, 6–8 June, 2005. London, UK: British Institute of Radiology 2005. 2
  9. Wall BF, Rae S, Darby SC, Kendall GM. The NRPB survey: methods and results. Dosimetry in diagnostic radiology, CRS 40. Chapter 6, 44–55. The Hospital Physicists Association 1984.
  10. Goodenough DJ. Lessons learned in radiology. Proceedings of an international conference held in Malaga, Spain, 26–30 March 2001, 145–155. International Atomic Energy Agency 2001.
  11. Faulkner K, Moores BM. Radiation dose and somatic risk from computed tomography. Acta Radiologica 1987;28:483–8.[Medline]
  12. Harrison RM. Dose measurement in vivo and in vitro. CRS 40. Chapter 2, 8–17. The Hospital Physicist's Association. 1984.
  13. TGR 32 Measurement of the performance characteristics of diagnostic X-ray systems used in medicine. Part 1: X-ray tubes and generators. The Hospital Physicist's Association. 1984.

Related articles in BJR:

Response to "Radiation dose measurement and optimization"
B F Wall
BJR 2006 79: 356-357. [Full Text]  




This Article
Right arrow Full Text (PDF)
Services
Right arrow Related articles in BJR
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Moores, B M
Right arrow Search for Related Content
PubMed
Right arrow Articles by Moores, B M


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
BJR DMFR IMAGING  ALL BIR JOURNALS