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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 />

http://www.inchem.org/documents/ehc/ehc/ehc<strong>214</strong>.htm<br />

Page 153 of 284<br />

6/1/2007

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