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American Journal of Respiratory and Critical Care Medicine Vol 172. pp. 1230, (2005)
© 2005 American Thoracic Society


Correspondence

Screening for Chronic Beryllium Disease

To the Editor:

For practitioners treating and preventing chronic beryllium disease (CBD), the recent publication from the Environmental and Occupational Health Sciences Division at National Jewish Medical and Research Center (NJMRC) of their longitudinal experience with beryllium sensitization (BeS) progressing to CBD is a welcome validation of growing efforts to control this epidemic in beryllium workers (1). The total number of workers in the United States with potential for current exposure was recently estimated to be 134,000 (2), and an even larger number of former workers are at risk. The DOE nuclear weapons program has screened over 40,000 production and cleanup workers with the beryllium lymphocyte proliferation test (BeLPT), the largest cohort where the test has been deployed (3). Over 230 cases of CBD have been diagnosed in this cohort with over 750 additional workers sensitized.

CBD, which is preceded by BeS, is a slowly progressive disease. We would therefore expect BeS workers who are closely followed with the BeLPT and invasive diagnostic testing to have disease detection at its earliest stage. In his accompanying commentary, Dr. Cullen suggests that recently diagnosed cases of CBD do not have the "associated clinical manifestations of CBD" (4). However, after follow-up of 4.7 yr (1.6–10) over half showed an average 15.5% decline in DLCO and/or similar decline in O2max. Nevertheless, the article by Newman and coworkers (1) does leave open some questions about their clinical findings in CBD. What were the physiologic characteristics of the workers diagnosed with CBD at baseline who are not in their longitudinal study of BeS progression? How many of those CBD cases have required treatment? Are the nine individuals who progressed from BeS to CBD and had physiologic deficits the same workers?

Even in the absence of these data, Newman and coworkers have made a convincing argument for ongoing screening and surveillance of beryllium-exposed workers. Detecting a disease in its early stages before large reductions occur in function is beneficial as identified by Cullen and coworkers, in a previous paper (5). The experience with DOE workers shows that LPT testing provides the benefit of early detection. Longer follow-up in the DOE group, as with the NJMRC cohort, is likely to yield an increase in those with significant physiologic impairment. Considering the recent confirmation of the risk to workers in industries using low percentage beryllium alloys (6), even workers with relatively low exposures should be tested.

Tim K. Takaroa and Lew Pepperb

a University of Washington, Seattle, Washington
b Boston University, Boston, Massachusetts

FOOTNOTES

Conflict of Interest Statement: T.K.T. is a medical consultant to the Dept. of Labor Energy Employees Occupational Illness Compensation Program and advises on medical aspects of workers' beryllium claims. He was also paid as an expert on a panel evaluating the use of the beryllium lymphocyte proliferation test convened by Exponent and paid for by Brush Wellman, Inc. L.P. was the Chair of the Current Worker Beryllium Surveillance Program for Rocky Flats Workers. The program was managed by the Occupational and Environmental Health Program at National Jewish Medical Center. He received approximately $500–$1,000 per year for 3.5 years as the Panel Chair. He also received travel expenses, and food and lodging. He was a Visiting Professor and Lecturer at National Jewish Medical Center in 1999 and received $500.

REFERENCES

  1. Newman LS, Mroz MM, Balkissoon R, Maier LA. Beryllium sensitization progresses to chronic beryllium disease: a longitudinal study of disease risk. Am J Respir Crit Care Med 2005;171:54–60.[Abstract/Free Full Text]
  2. Henneberger PK, Goe SK, Miller WE, Doney B, Groce DW. Industries in the United States with airborne beryllium exposure and estimates of the number of current workers potentially exposed. J Occup Environ Hyg 2004;1:648–659.[Medline]
  3. Stange AW, Furman FJ, Hilmas DE. The beryllium lymphocyte proliferation test: relevant issues in beryllium health surveillance. Am J Ind Med 2004;46:453–462.[CrossRef][Medline]
  4. Cullen MR. Screening for chronic beryllium disease: one hurdle down, two to go. Am J Respir Crit Care Med 2005;171:3–4.[Free Full Text]
  5. Sood A, Beckett WS, Cullen MR. Variable response to long-term corticosteroid therapy in chronic beryllium disease. Chest 2004;126:2000–2007.[Abstract/Free Full Text]
  6. Schuler CR, Kent MS, Deubner DC, Berakis MT, McCawley M, Henneberger PK, Rossman MD, Kreiss K. Process-related risk of beryllium sensitization and disease in a copper-beryllium alloy facility. Am J Ind Med 2005;47:195–205.[CrossRef][Medline]




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Copyright © 2005 American Thoracic Society