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Placebo‐controlled study of the mite allergen‐reducing effect of tannic acid plus benzyl benzoate on carpets in homes of children with house dust mite sensitization and asthma
Author(s) -
Lau Susanne,
Wahn Julia,
Schulz Gabriele,
Sommerfeld Christine,
Wahn Ulrich
Publication year - 2002
Publication title -
pediatric allergy and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.269
H-Index - 89
eISSN - 1399-3038
pISSN - 0905-6157
DOI - 10.1034/j.1399-3038.2002.00073.x
Subject(s) - benzyl benzoate , medicine , allergen , mite , placebo , asthma , house dust mite , acaricide , sensitization , allergy , pyroglyphidae , dust mites , immunology , toxicology , chemistry , biology , botany , alternative medicine , organic chemistry , pathology
We studied the effect of a spray containing 1% benzyl benzoate, an acaricide, and 1% tannic acid (‘Lowal’; a protein‐denaturing substance), on concentrations of major allergens from house dust mite (HDM) species Dermatophagoides pteronyssinus and D. farinae ( Der p 1 and Der f 1, respectively) in carpets. In a double‐blind, placebo‐controlled study with crossover design, 30 homes of children with HDM sensitization and asthma were included. All houses showed ≥ 400 ng/g of Der p 1 + Der f 1 in carpet dust. The first treatment was performed on day 0 (group 1 active treatment, n = 15; group 2 placebo treatment, n = 15). After 2 and 8 weeks, dust samples were collected for quantification of mite allergens. After a 2‐week washout period, the second treatment was performed (group 1 placebo treatment; group 2 active treatment). Again, carpet dust was collected after 2 and 8 weeks. Twenty‐two of 30 families completed the trial: 14/15 in group 1 and eight of 15 in group 2. On day 0, there was no significant difference in mite allergen exposure between group 1 and group 2 (1,498 vs. 2,239 ng/g of Der p 1 + Der f 1, respectively). In group 1, the geometric mean for the difference of mite allergen concentration comparing day 0 and week 6 was 196 ng/g (95% CI: −7,161 and 8,401) for the first treatment (active) and 15 ng/g (95% CI: −1,079 and 1,292) for the second treatment (control). In group 2, the difference was 66 ng/g (95% CI: −398 and 1,515) for the first treatment (control) and 609 ng/g (95% CI: 186 and 9,264) for the second treatment (active). Comparing placebo and active treatment in total, there was a significant decrease following placebo treatment after 14 days (p = 0.026). After 8 weeks, active treatment was superior to placebo treatment (p = 0.049), but the allergen reduction achieved was < 20% (median 1,500 ng/g on day 0 vs. 1,250 ng/g after 8 weeks). We conclude that the slight mite allergen reduction on carpets achieved by the treatment with ‘Lowal’ is unlikely to achieve worthwhile clinical benefit either in the treatment of mite‐sensitive patients or in primary or secondary prophylaxis.