Biological Exposure Indices
Biological Exposure Indices
Biological Exposure Indices
1.1 Introduction
Biological monitoring – the measurement of a substance or its metabolites
in body fluids such as urine or blood – provides a complementary approach
to air monitoring for estimating exposure to workplace contaminants.
This applies where (as in most cases), the BEI has been derived from the
observed relationship between the measured air levels and measured
biological (e.g. blood or urine) levels as this knowledge enables
extrapolation from a WES to a BEI level. However, in some cases (such as
with lead), the relationship between the biological level and the potential
health effects has been approached more directly (e.g. by identifying
adverse effects as a function of blood lead levels).
1.3 Effectiveness
Biological monitoring has been widely used to monitor the uptake of
cumulative toxins (e.g. lead, mercury, organophosphate insecticides). It
also may be employed effectively where there is a significant potential for
increased uptake as a result of skin absorption, increased respiratory rate,
or exposure outside the workplace (even if there is no change in workplace
air levels).
The fact that a BEI has been listed for a particular substance does not
imply that biological monitoring is necessary. An appraisal of the exposure
should be made before considering monitoring requirements.
1.4 Biological Assays
Several conditions must be satisfied for a biological assay to be a reliable
indicator of exposure to a substance. The fate of the substance in the
human body must have been adequately researched, and a
time/concentration relationship must exist. It is not essential for the
concentration of the determinant to be zero in cases where there is no
occupational exposure, as long as the increase is measurably observable
above the background level.
Section 11 of the HSE Act requires the employer to give the results of
monitoring to affected employees. Where the monitoring results relate to
biological monitoring, the employer shall ensure that the results of each
worker’s monitoring is kept private and only made known to the worker,
the employer, and health professionals if necessary.
Assuming that there has been continual exposure over the working day,
the following potential sample periods (causing minimal disturbance of
working routines) have received most attention. The most appropriate
sample period for any given substance depends on how quickly it (or its
measured metabolite) is eliminated from the body:
End of Shift: The last two hours immediately following the end of the
working day. (Appropriate for substances “rapidly” eliminated, whose
measured levels could have fallen substantially if sampling was delayed
until just prior to the next shift).
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Workplace Exposure Standards and Biological Exposure Indices 7 edition
End of Work Week: After at least four days with exposure. (Appropriate
for substances eliminated more slowly and thus incompletely over 24
hours, causing some accumulation, with the highest levels observed on the
last day).
There are several reasons why the levels of the determinant may vary
between individuals, even under seemingly identical exposure situations.
Workers may differ in size, physical fitness and work practices, resulting in
differing uptakes, such as through variations in respiration rate/volume and
skin contact (and absorption). Further, there may be inter-individual
differences in metabolism and elimination rates of the absorbed substance
or contaminant.
This section should be read in conjunction with the Ministry of Business, Innovation and
Employment publication Guidelines for the Medical Surveillance of Lead Workers. The
overall objective of the surveillance outlined in the guidelines is to maintain the blood lead
levels of all workers below 1.5µmol/litre whole blood. Medical surveillance, including blood
lead monitoring, is extended to all those working with lead in a process that may result in
blood lead levels above 1.5µmol/litre whole blood.
An employee can return to work if their blood levels achieve 1.93 µmol/litre whole blood or
(2010)
below .