Environmental Health Criteria 214
Environmental Health Criteria 214
Environmental Health Criteria 214
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HUMAN EXPOSURE ASSESSMENT<br />
of house dust mite allergens in air and dust (Oliver et al., 1995).<br />
Allergenic responses to dust mite allergens may be induced by<br />
short-duration high-concentration exposure events. Therefore, the<br />
clinical importance of integrated air samples may be more relevant in<br />
predicting prevalence of atopy to mites rather than predictive of<br />
acute health effects.<br />
At present no reliable information is available that will support<br />
adoption of a standardized method for air sampling of house dust mite<br />
allergens. According to an international workshop held in 1987<br />
(Platts-Mills & De Weck, 1989) airborne sampling has not been shown to<br />
be better than dust sampling to measure the level of mite infestation<br />
in homes or schools. This was confirmed by a second international<br />
workshop in 1990 (Platts-Mills et al., 1992). It was also stated that<br />
there are few or no data showing a relationship between airborne<br />
measurements and sensitization to house dust mites or symptoms. In<br />
contrast, a relationship is apparent between the concentrations of<br />
mite allergens in settled house dust and sensitization or symptoms.<br />
Therefore, air sampling was not recommended (Platts-Mills et al.,<br />
1992).<br />
9.2.2 Dust sampling for house dust mites<br />
Dust sampling for measurement of the level of mite infestation is<br />
accepted and recommended as the best-validated "index of exposure" to<br />
house dust mite allergens. The approach assumes that the quantity of<br />
allergens released into the air is a function of what is present in<br />
settled dust, or, conversely, that the measurement of allergen in<br />
settled dust is related to both the long-term dose a person receives<br />
and to the short-term airborne levels experienced during events that<br />
raise dust.<br />
Standardized sampling procedures to measure house dust mites and<br />
their allergens in house dust have been proposed (Platts-Mills & De<br />
Weck, 1989; Platts-Mills et al., 1992; EC, 1993; Dreborg et al.,<br />
1995). Sampling sites should be consistent throughout the study and<br />
preferably include the upper mattress surface and the floors of the<br />
living room and bedroom. Sampling can be conducted with vacuum<br />
cleaners equipped with a special attachment to collect dust on a paper<br />
filter. Vacuuming 1 m 2 of surface in 2 min is a commonly used<br />
sampling method. Depending on experiences with the amount of dust<br />
recovered in specific situations, investigators may have to modify the<br />
sampling procedures. Samples can also be obtained from upholstered<br />
furniture, soft toys and clothing. Alternative techniques for<br />
collecting dust samples include shaking blankets in a plastic bag and<br />
scraping flat surfaces higher than floor level with a piece of firm<br />
card. However, these techniques are less effective than collection by<br />
vacuum cleaner and not standardized. The dust samples may be sieved<br />
before analysis to obtain a sample of fine dust that can be weighed<br />
accurately. Unfortunately, dust samples may still vary in density<br />
after sieving. An alternate method for sampling airborne mite<br />
allergens is to collect settling dust on large Petri dishes over a<br />
period of 14 days (Tovey et al., 1992; Oliver et al., 1995). Brown<br />
(1994) developed a variation on the integrated settling method. A<br />
100-cm 2 piece of sticky tape is placed in contact with the surface<br />
for 24 h. Under low-power magnification (36×), the trapped mites are<br />
counted. Using an empirically derived collection efficiency of 30%,<br />
the number of live mites per area is estimated. However, this does not<br />
reflect the true extent of exposure to mite allergens (see section<br />
9.2.3.1).<br />
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