Literature DB >> 1373860

Biologic markers in hospital workers exposed to low levels of ethylene oxide.

P A Schulte1, M Boeniger, J T Walker, S E Schober, M A Pereira, D K Gulati, J P Wojciechowski, A Garza, R Froelich, G Strauss.   

Abstract

Operators of hospital sterilizers that use ethylene oxide were studied to determine if there was a relationship between exposure and a battery of biological markers. A total of 73 workers from nine hospitals in the United States (U.S.) and one hospital in Mexico City was evaluated for ethylene oxide exposure during four months prior to collection of peripheral blood. The frequency of hemoglobin adducts (p = 0.0006) and sister-chromatid exchanges (SCEs) (p = 0.002) increased with cumulative exposure to ethylene oxide in U.S. subjects when controlling by regression analysis for various confounding factors, including cigarette smoking. Hemoglobin adducts, but not SCEs, were also increased in Mexican subjects (p = 0.0012). Chromosomal micronuclei showed no consistent relationship with exposure. The U.S. study participants were classified by four-month cumulative exposure levels of 10 ppm-h (n = 8), greater than 0 to 32 ppm-h (n = 32) and greater than 32 ppm-h (n = 11) of ethylene oxide exposure. The group with an exposure of greater than 32 ppm-h had an increased frequency of hemoglobin adducts (p = 0.002) and SCEs (p = 0.0001) compared to the nonexposed group. The estimated mean of the 8-h time-weighted average (8-h TWA) exposure levels for the highest U.S. exposure group (greater than 32 ppm-h) was 0.16 +/- 0.007 ppm (mean +/- SD). A similar exposure-related differential was observed in the Mexican subjects for hemoglobin adducts (p = 0.04) but not for SCEs. The latter finding may have been due to longer shipping times for the specimens in the cytogenetic assays. The estimated mean of the 8-h TWA exposure levels for the highest Mexican exposure group (greater than 32 ppm-h) was 0.48 +/- 0.08 ppm. This study is the third to suggest that exposures less than the U.S. OSHA standard of 1 ppm 8-h TWA result in biochemical and biologic changes. It is not known whether these changes may be indicative of increased risk of disease; however, they do appear to reflect exposure to relatively low levels of ethylene oxide. The exact meaning of these changes is unknown.

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Year:  1992        PMID: 1373860     DOI: 10.1016/s0165-1218(10)80003-5

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  6 in total

1.  Evaluating OSHA's ethylene oxide standard: exposure determinants in Massachusetts hospitals.

Authors:  A D LaMontagne; K T Kelsey
Journal:  Am J Public Health       Date:  2001-03       Impact factor: 9.308

2.  Mortality study of ethylene oxide workers in chemical manufacturing: a 10 year update.

Authors:  M J Teta; L O Benson; J N Vitale
Journal:  Br J Ind Med       Date:  1993-08

3.  Evaluating OSHA's ethylene oxide standard: employer exposure-monitoring activities in Massachusetts hospitals from 1985 through 1993.

Authors:  A D LaMontagne; K T Kelsey
Journal:  Am J Public Health       Date:  1997-07       Impact factor: 9.308

4.  DNA-protein cross-links and sister chromatid exchange frequencies in lymphocytes and hydroxyethyl mercapturic acid in urine of ethylene oxide-exposed hospital workers.

Authors:  W Popp; C Vahrenholz; H Przygoda; A Brauksiepe; S Goch; G Müller; C Schell; K Norpoth
Journal:  Int Arch Occup Environ Health       Date:  1994       Impact factor: 3.015

Review 5.  Ethical considerations, confidentiality issues, rights of human subjects, and uses of monitoring data in research and regulation.

Authors:  P A Schulte; M H Sweeney
Journal:  Environ Health Perspect       Date:  1995-04       Impact factor: 9.031

Review 6.  Approaches to assessing genetic risks from exposure to chemicals.

Authors:  F H Sobels
Journal:  Environ Health Perspect       Date:  1993-10       Impact factor: 9.031

  6 in total

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