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1.
An. otorrinolaringol. mex ; 45(1): 17-9, dic. 1999-feb. 2000. tab, CD-ROM
Article in Spanish | LILACS | ID: lil-292277

ABSTRACT

Objetivo: Evaluar la respuesta al tratamiento tópico con ciprofloxacina comparado con neomicina-polimixina -fluocinolona (NPF) en la otitis media crónica supurada (OMCs). Material y Métodos: Se realizó un ensayo clínico aleatorio de 36 pacientes (40 oídos), con OMCs, en dos grupos de 20 oídos, uno tratado con ciprofloxacina y el otro con NPF. Se aplicó tratamiento durante 10 días, registrando la respuesta como buena, regular o mala. Resultados: 36 pacientes, 21 mujeres (53 por ciento) y 19 hombres /47 por ciento), entre 15 y 71 años (media 38 de +- 18.5), en la bacteriología predominaron Staphylococcus aureus y Pseudomonas sp. La respuesta al 10§ día con ciprofloxacina fue buena en 17 (85 por ciento), regular en 1 (5 por ciento) y mala en 2 (10 por ciento). Con NPF fue buena en 16 (80 por ciento), regular en 3 (15 por ciento) y mala en 1 (5 por ciento). Las diferencias no fueron estadísticamente significantes. Conclusiones: La ciprofloxacina y la NPF son igualmente efectivos en el control de la otitis media crónica supurada.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Ciprofloxacin/therapeutic use , Fluocinonide/therapeutic use , Neomycin/therapeutic use , Otitis Media/drug therapy , Polymyxins/therapeutic use , Anti-Infective Agents, Local/therapeutic use , Anti-Inflammatory Agents/therapeutic use
3.
Korean Journal of Dermatology ; : 579-585, 1986.
Article in Korean | WPRIM | ID: wpr-186891

ABSTRACT

The aim of this stud y was to compare the epidermal thinning properties of four corticosteroid ointments applied under occlusion, using histology and histometry. The results were surnmerized as follows: 1.The stratum corneurn was dramatically thinned, appearing as a wispy layer of horny cells as apposed to the norrnal basket-weave configuration. this effect was prominent at sites treated with clobestasol propionate, fluocinonide, and fluocinolone acetonide. 2. With the histometry, visible epidermal thickness wa.s markedly reduced. This effect w is prominent in the following ascending order: fluocinolone acetonide, fluocienonide, clobestasol-17-propionate. Hydrocortisone was the least atrophogenic. 3. Clohestasol-17-propionate and fluocinonide caused significant flattening of dermo-epidermal junction, Fluocinolone acetonide and hydrocortisone caused less pronounced cbanges. 4. Marked capillary dilation af papilly dermis is caused by clobestasol-17-propionate, fluocinonide and fluocinolone acetonide.


Subject(s)
Humans , Adrenal Cortex Hormones , Atrophy , Capillaries , Dermis , Diethylpropion , Epidermis , Fluocinolone Acetonide , Fluocinonide , Hydrocortisone , Ointments
6.
Korean Journal of Dermatology ; : 115-120, 1980.
Article in Korean | WPRIM | ID: wpr-106061

ABSTRACT

lt is generally beIieved that several chemical mediators such as histamine, kinine, prustaglandin E and lysosomal enzyme are related to the pathogenesis of sunburn, but the exact mechenism of erythema is unknown. Recently, prostaglandins appear to be important mediators of ultraviolet erythema (UV-erythema) and several investigators has reported that the nonsteroidal antiinflammatory druga and corticosteroids supressed UV-erythema by inhibition of prostaglandin synthesis. This study was undertaken to evaluate the effect of topical nonsteroidaI antiinflammatary drugs and corticosteroids on UV-erythema induced by a artificial sunlamp. Nonsteroidal anti-inflammatory drugs (5% Bufexamac cream, 5% Ibuprofen cream, 5% Indomethacin cream) and corticosteroids(0.05% Fluocinonide cream, 0.5% Fluocortolone oint., 1%, Hydrocortisone cream) were applied immediately after 3~4 minimal erythema dose(MED) irradiation on back skin of 40 healthy volunteers and the delayed UV-erythema response was evaluated at 2, 4, 6, 8, 12, 24, 48 and 72 hours after irradiation, respectively. The resulta were as follows; 1) Minimal erythema dose(MED) was noted 4min. (62.5%), 3min. (25.0%), 5min. (22.5%). The averaged MED was 3. 63min. 2, MED has to be increased on site, applied nonsteroid and steroid agents topically, comparing with control site. 3) Blanching effect was detected in all cases of nonsteroid and steroid agents applicated topically, but in control site. 4) Average score in blanching effect was highest in 5% Indomethacin cream among nonsteroid agents(average score-2. 47) and 1% Hydrocortisone cream (average scoro -2. 63) among steroid agents.


Subject(s)
Humans , Adrenal Cortex Hormones , Bufexamac , Erythema , Fluocinonide , Fluocortolone , Healthy Volunteers , Histamine , Hydrocortisone , Ibuprofen , Indomethacin , Prostaglandins , Research Personnel , Skin , Sunburn , Ultraviolet Rays
7.
Korean Journal of Dermatology ; : 443-446, 1977.
Article in Korean | WPRIM | ID: wpr-101337

ABSTRACT

Puraotix-C(0.1% Clocortolone Picalats Cream) is a new di-halogenated topical corticosteroid, and used in trial for treating several kinds of dermatoses. We treated 30 patients with Purantix-C who had one of the following dermatoses; atopic dermatitis, neurodermatitis, pustulosis palmaris et plantsris, seborrheic dermatitis, pityriasis rosea, nummular eczema, psoriasis vulgaris, pruritus ani and pompolyx. Among these 30 patients, Purantix-C showed excellent or good result (66.7%) either unoccluded or occluded application, 2~3 times daily for 7~10 days. Comparing with Lidex(0.05% fluorocinonide cream) and purantix-C, both of them had similar effect on eczema and psoriatic groups but Lidex was more effective than Purantix-C for treating the patients with the pustulosis palmaris et plantaris. Purantix-C without containing perfume and coloring substapce was less irritative.


Subject(s)
Humans , Dermatitis, Atopic , Dermatitis, Seborrheic , Eczema , Fluocinonide , Neurodermatitis , Perfume , Pityriasis Rosea , Pruritus Ani , Psoriasis , Skin Diseases
8.
Korean Journal of Dermatology ; : 281-283, 1975.
Article in Korean | WPRIM | ID: wpr-156309

ABSTRACT

Lidex' cream (Fluocinonide 0.05% in FAPG base) is a new fluorina,ted topical corticosteroid, and its clinical effect was assessed by applying topically three to four times daily to the lesions of 50 patients with a variety of inflamrnatory skin condi- tions. The results revealed excellent effect in 16 patients, moderate effect in 23 patients, slight improvement in 9 patients, and no effect in 2 patients. No unfavorable side effects were noted except blanching. The findings suggest that fluocinonide is an excelIent addition to the topical corticosteroid agents that are available for clinical use at the present time.


Subject(s)
Humans , Fluocinonide , Skin
9.
Korean Journal of Dermatology ; : 109-112, 1975.
Article in Korean | WPRIM | ID: wpr-176143

ABSTRACT

Lidex(Fluacinonide) 0.05% in FAPG base is a new fluorinated topical corticosteroid. 30 patients with different steroid responsive dermatoaes were treated with 0. 05% Lidex. The diagnosis included atopic dermatitis, contact dermatitis, neurodermatitis, seborheic dermatitis, nummular eczema, psoriasis vulgaris, chronic eczema and pustulosis pahmaris et plantaris. In the majority of cases Lidex cream produced excellent to good result(70%) after unoccluded application 3 times daily for 10 days. Two patients complained burning or itching sensation after the initial application of Lidex. 0.05% Lidex was compared with 0. 25% Desoxymethasone cream and 0. 25% Fluocortolone cream and was found slightly more effective in Lidex.


Subject(s)
Humans , Burns , Dermatitis , Dermatitis, Atopic , Dermatitis, Contact , Desoximetasone , Diagnosis , Eczema , Fluocinonide , Fluocortolone , Neurodermatitis , Pruritus , Psoriasis , Sensation
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