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Autor(en):
Brockow, Knut; Grabenhorst, Petra; Abeck, Dietrich; Traupe, Bernd; Ring, Johannes; Hoppe, Udo; Wolf, Florian
Titel:
Effect of Gentian Violet, Corticosteroid and Tar Preparations in textitStaphylococcus-aureus-Colonized Atopic Eczema
Abstract:
Background: In atopic eczema (AE), skin colonization with Staphylococcus aureus plays a possible role in the pathophysiology of the disease. Methods: Thirty-eight patients with AE were screened for their cutaneous colonization with S. aureus. The antibacterial and clinical efficacy of topical therapy with the antiseptic dye gentian violet, a potent glucocorticosteroid or a tar solution (liquor carbonis detergens) was evaluated in vivo in 21 patients with a density of >104 CFU/cm2 and in vitro. Skin sites were treated twice daily for 4 days with the active drug or a corresponding control. Quantification of S. aureus was done daily during therapy as well as 3 days thereafter. The severity of the lesions was rated by a regional SCORAD. Results: In gentian-violet-treated skin, bacterial density decreased significantly in lesional (p < 0.001) and unaffected skin (p < 0.001). Bacterial densities did not decrease during therapy with glucocorticosteroid or liquor carbonis detergens but dropped afterwards. All therapeutics reduced the severity score, reduction being greatest for the glucocorticosteroid and lowest for liquor carbonis detergens. In vitro, a high antibactericidal efficacy was demonstrated only for gentian violet. Conclusions: Antibacterial therapy with gentian violet not only reduces S. aureus dramatically, but also reduces the severity of the eczema. Reduction of S. aureus after therapy with glucocorticosteroids and LCD seems to be secondary to improvement of the skin condition.
Stichworte:
Gentian violet; Staphylococcus aureus; Atopic eczema; Liquor carbonis detergens; Corticosteroids
Zeitschriftentitel:
Dermatology
Jahr:
1999
Band / Volume:
199
Heft / Issue:
3
Seitenangaben Beitrag:
231--236
Volltext / DOI:
doi:10.1159/000018253
Verlag / Institution:
S. Karger AG
Verlagsort:
Basel, Switzerland
Print-ISSN:
1421-9832
E-ISSN:
1421-9832
Hinweise:
Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.
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