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3.
Rev. MVZ Córdoba ; 22(2): 5829-5836, May-Aug. 2017. tab
Article in English | LILACS | ID: biblio-896927

ABSTRACT

ABSTRACT Objective. To determine Trypanosoma cruzi (T. cruzi), Leishmania mexicana (L.mexicana) and Leishmania braziliensis (L.braziliensis) circulating antibodies in dogs from Chontalpa region in Tabasco, Mexico using ELISA diagnostic techniques Fe-SOD and Western blot. Materials and methods. For this study, 119 serums were obtained from domiciled dogs. Serums were tested for antibodies against T. cruzi, L. mexicana and L. braziliensis, using ELISA and Western Blot sod as diagnostic test. The antigenic fraction used in both tests was the Fe-SOD excreted by the species of Leishmania and Trypanosoma. Results. The obtained frequency in this study was 3.36% for T. cruzi, 9.24% for L. mexicana and 10.08% for L. braziliensis. Conclusions. The present study has demonstrated the presence of antibodies to these parasites in Chontalpa region from Tabasco, Mexico.


RESUMEN Objetivo. Determinar la frecuencia de anticuerpos circulantes de Trypanosoma cruzi (T. cruzi), Leishmania mexicana (L. mexicana) y Leishmania braziliensis (L. braziliensis) en una población de perros usando ELISA Fe-SOD y Western blot en la región Chontalpa del estado de Tabasco, México. Materiales y métodos. Para este estudio se obtuvieron 119 sueros de perros domiciliados, con el consentimiento previo de los propietarios. Los sueros fueron analizados para detectar anticuerpos contra T. cruzi, L. mexicana, y L. braziliensis, usando como prueba diagnóstica ELISA-sod y Western Blot. La fracción antigénica utilizada en las dos pruebas fue la Fe-SOD excretada por las especies de Trypanosoma y Leishmania. Resultados. La frecuencia obtenida en este estudio fue de 3.36% para T. cruzi, 9.24% para L. mexicana y 10.08% L. braziliensis. Conclusiones. El presente estudio demostró la presencia de anticuerpos para estos parásitos en la región Chontalpa del estado de Tabasco, México.

6.
Actas dermo-sifiliogr. (Ed. impr.) ; 101(1): 47-53, ene.-feb. 2010. tab, ilus
Article in Spanish | IBECS | ID: ibc-77076

ABSTRACT

Introducción: La experiencia clínica demuestra que la suspensión del tratamiento con etanercept en pacientes con psoriasis en la semana 24, como indica la ficha técnica del fármaco, produce en algunos casos rebrote de la enfermedad. Existen diversos ensayos que avalan el uso de etanercept a largo plazo con un buen perfil de seguridad y eficacia. Material y métodos: Estudio observacional, retrospectivo, en el que se recogió a 43 pacientes con psoriasis en placas de moderada a grave, con y sin artropatía, tratados con etanercept de forma continua durante más de 24 semanas. Resultados: El etanercept se administró durante un tiempo promedio de 57 semanas, y disminuyó el PASI (Psoriasis Area Severity Index) de forma global de un valor basal de 22,5 a 4,3.ResultadosAdemás, con el tratamiento continuo, la mayor parte de los pacientes mantuvieron puntuaciones PASI inferiores al 50% o incluso al 75%. Por otra parte, algunos pacientes que no alcanzaron mejorías significativas en su puntuación PASI en las primeras 24 semanas pueden conseguirlo prolongando el tratamiento. Todo ello con una baja incidencia de efectos adversos (13 pacientes [30,2%]) y de características leves. Conclusiones: Exponemos nuestra experiencia clínica con el tratamiento con etanercept a largo plazo en pacientes con psoriasis de moderada a grave, con y sin artropatía asociada, y demostramos un perfil favorable de eficacia y seguridad (AU)


Introducción: La experiencia clínica demuestra que la suspensión del tratamiento con etanercept en pacientes con psoriasis en la semana 24, como indica la ficha técnica del fármaco, produce en algunos casos rebrote de la enfermedad. Existen diversos ensayos que avalan el uso de etanercept a largo plazo con un buen perfil de seguridad y eficacia. Material y métodos: Estudio observacional, retrospectivo, en el que se recogió a 43 pacientes con psoriasis en placas de moderada a grave, con y sin artropatía, tratados con etanercept de forma continua durante más de 24 semanas. Resultados: El etanercept se administró durante un tiempo promedio de 57 semanas, y disminuyó el PASI (Psoriasis Area Severity Index) de forma global de un valor basal de 22,5 a 4,3.ResultadosAdemás, con el tratamiento continuo, la mayor parte de los pacientes mantuvieron puntuaciones PASI inferiores al 50% o incluso al 75%. Por otra parte, algunos pacientes que no alcanzaron mejorías significativas en su puntuación PASI en las primeras 24 semanas pueden conseguirlo prolongando el tratamiento. Todo ello con una baja incidencia de efectos adversos (13 pacientes [30,2%]) y de características leves. Conclusiones: Exponemos nuestra experiencia clínica con el tratamiento con etanercept a largo plazo en pacientes con psoriasis de moderada a grave, con y sin artropatía asociada, y demostramos un perfil favorable de eficacia y seguridad (AU)


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Psoriasis/therapy , Receptors, Tumor Necrosis Factor/therapeutic use , /therapeutic use , Efficacy , Treatment Outcome , Signs and Symptoms , Retrospective Studies , Safety , Methotrexate/therapeutic use , Tinea/complications , Tinea Pedis/therapy , Onychomycosis/complications , Onychomycosis/epidemiology
7.
Actas Dermosifiliogr ; 101(1): 47-53, 2010.
Article in Spanish | MEDLINE | ID: mdl-20109392

ABSTRACT

BACKGROUND: Clinical experience has shown that, in patients with psoriasis, suspending treatment with etanercept at week 24, as indicated in the prescribing information, may lead to a rebound effect. Several clinical trials support long-term use of etanercept, which was shown to have a good safety and efficacy profile. MATERIAL AND METHODS: This was a retrospective, observational study of 43 patients with moderate to severe plaque psoriasis, with and without joint involvement, who received continuous treatment with etanercept for more than 24 weeks. RESULTS: Etanercept was administered for a mean of 57 weeks. Overall, the Psoriasis Area and Severity Index (PASI) score decreased from a baseline value of 22.5 to 4.3 after treatment. In addition, with continuous treatment, most patients maintained decreases in PASI scores of 50% and even of 75%. Some patients without significant improvement in their PASI score in the first 24 weeks did manage to achieve significant results after prolonged treatment. These outcomes were achieved with a low incidence of adverse effects (reported in 13 patients [30.2%]), which were generally mild. CONCLUSION: We present our clinical experience with long-term etanercept treatment in patients with moderate to severe psoriasis, with and without associated joint involvement. The efficacy and safety profiles were found to be favorable.


Subject(s)
Anti-Inflammatory Agents/therapeutic use , Immunoglobulin G/therapeutic use , Psoriasis/drug therapy , Receptors, Tumor Necrosis Factor/therapeutic use , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Adult , Aged , Anti-Inflammatory Agents/adverse effects , Arthritis, Psoriatic/drug therapy , Biological Products/therapeutic use , Combined Modality Therapy , Cyclosporine/therapeutic use , Drug Evaluation , Etanercept , Female , Humans , Immunoglobulin G/adverse effects , Male , Methotrexate/therapeutic use , Middle Aged , Psoriasis/radiotherapy , Retrospective Studies , Severity of Illness Index , Tretinoin/therapeutic use , Ultraviolet Therapy , Young Adult
10.
Actas Dermosifiliogr ; 100(1): 53-60, 2009.
Article in Spanish | MEDLINE | ID: mdl-19268112

ABSTRACT

INTRODUCTION: Contact dermatitis to cosmetics is a common problem in the general population, although its prevalence appears to be underestimated. We reviewed cases of allergic contact dermatitis to cosmetics diagnosed in our dermatology department over a 7-year period with a view to identifying the allergens responsible, the frequency of occurrence of these allergens, and the cosmetic products implicated. METHODS: Using the database of the skin allergy department, we undertook a search of all cases of allergic contact dermatitis to cosmetics diagnosed in our department from January 2000 through October 2007. RESULTS: In this period, patch tests were carried out on 2,485 patients, of whom 740 were diagnosed with allergic contact dermatitis and the cause was cosmetics in 202 of these patients (170 women and 32 men), who accounted for 27.3 % of all cases. A total of 315 positive results were found for 46 different allergens. Allergens most often responsible for contact dermatitis in a cosmetics user were methylisothiazolinone (19 %), paraphenylenediamine (15.2 %), and fragrance mixtures (7.8 %). Acrylates were the most common allergens in cases of occupational disease. Half of the positive results were obtained with the standard battery of the Spanish Group for Research Into Dermatitis and Skin Allergies (GEIDAC). The cosmetic products most often implicated among cosmetics users were hair dyes (18.5 %), gels/soaps (15.7 %), and moisturizers (12.7 %). CONCLUSION: Most patients affected were women. Preservatives, paraphenylenediamine, and fragrances were the most frequently detected cosmetic allergens, in line with previous reports in the literature. Finally, in order to detect new cosmetic allergens, cooperation between physicians and cosmetics producers is needed.


Subject(s)
Allergens/adverse effects , Cosmetics/adverse effects , Dermatitis, Allergic Contact/etiology , Acrylic Resins/adverse effects , Beauty Culture , Dermatitis, Allergic Contact/epidemiology , Dermatitis, Occupational/epidemiology , Dermatitis, Occupational/etiology , Emollients/adverse effects , Female , Hair Preparations/adverse effects , Humans , Male , Perfume/adverse effects , Phenylenediamines/adverse effects , Retrospective Studies , Soaps/adverse effects , Spain/epidemiology , Thiazoles/adverse effects
12.
Actas dermo-sifiliogr. (Ed. impr.) ; 100(1): 53-60, ene. 2009. tab, ilus
Article in Spanish | IBECS | ID: ibc-128210

ABSTRACT

Introducción: La dermatitis de contacto por cosméticos es un problema frecuente entre la población general, sin embargo, parece ser que su prevalencia está infraestimada. Revisamos en este trabajo los casos de dermatitis de contacto alérgica por cosméticos diagnosticados en el Departamento de Dermatología en un periodo de 7 años con el objetivo de detectar los alergenos responsables, la frecuencia de los mismos, así como los productos cosméticos implicados. Métodos: Utilizando la base de datos de la sección de Alergia Cutánea se realiza una búsqueda de todos los casos de dermatitis de contacto alérgica por cosméticos diagnosticados en nuestro departamento entre enero de 2000 y octubre de 2007. Resultados: Durante este periodo se realizaron pruebas epicutáneas a 2.485 pacientes. De todos ellos, 740 fueron diagnosticados de una dermatitis de contacto alérgica, 202 pacientes (170 mujeres/32 varones), es decir, el 27,3 % lo fueron por cosméticos. Se detectaron un total de 315 parches positivos y 46 alergenos diferentes. Los alergenos que con más frecuencia produjeron una dermatitis de contacto en el usuario fueron las metilisotiazolinonas (19 %), la parafenilendiamina (15,2 %) y la mezcla de perfumes (7,8 %). Los acrilatos fueron los alergenos más frecuentes en aquellos casos que tenían un origen laboral. Con la batería estándar del Grupo Español en Investigación en Dermatitis y Alergia Cutánea (GEIDAC) se detectaron la mitad de las pruebas positivas. Los productos cosméticos implicados con mayor frecuencia en el usuario fueron los tintes capilares (18,5 %), los geles/jabones (15,7 %) y las cremas hidratantes (12,7 %). Conclusión: La mayoría de los pacientes afectados fueron mujeres. Los conservantes, la parafenilendiamina y los perfumes fueron los alergenos cosméticos más frecuentes, tal y como había sido publicado previamente en la literatura. Finalmente, con el objetivo de detectar nuevos alergenos cosméticos debe existir colaboración entre los facultativos y las casas comerciales (AU)


Introduction: Contact dermatitis to cosmetics is a common problem in the general population, although its prevalence appears to be underestimated. We reviewed cases of allergic contact dermatitis to cosmetics diagnosed in our dermatology department over a 7-year period with a view to identifying the allergens responsible, the frequency of occurrence of these allergens, and the cosmetic products implicated. Methods: Using the database of the skin allergy department, we undertook a search of all cases of allergic contact dermatitis to cosmetics diagnosed in our department from January 2000 through October 2007. Results: In this period, patch tests were carried out on 2485 patients, of whom 740 were diagnosed with allergic contact dermatitis and the cause was cosmetics in 202 of these patients (170 women and 32 men), who accounted for 27.3% of all cases. A total of 315 positive results were found for 46 different allergens. Allergens most often responsible for contact dermatitis in a cosmetics user were methylisothiazolinone (19%), paraphenylenediamine (15.2%), and fragrance mixtures (7.8%). Acrylates were the most common allergens in cases of occupational disease. Half of the positive results were obtained with the standard battery of the Spanish Group for Research Into Dermatitis and Skin Allergies (GEIDAC). The cosmetic products most often implicated among cosmetics users were hair dyes (18.5%), gels/soaps (15.7%), and moisturizing creams (12.7%). Conclusion: Most patients affected were women. Preservatives, paraphenylenediamine, and fragrances were the most frequently detected cosmetic allergens, in line with previous reports in the literature. Finally, in order to detect new cosmetic allergens, cooperation between physicians and cosmetics producers is needed (AU)


Subject(s)
Humans , Male , Female , Acrylic Resins/adverse effects , Allergens/adverse effects , Allergens , Cosmetics/adverse effects , Dermatitis, Allergic Contact/epidemiology , Dermatitis, Allergic Contact/etiology , Emollients/adverse effects , Thiazoles/adverse effects , Beauty Culture , Dermatitis, Occupational/epidemiology , Dermatitis, Occupational/etiology , Hair Preparations/adverse effects , Spain/epidemiology , Perfume/adverse effects , Soaps/adverse effects , Phenylenediamines/adverse effects , Retrospective Studies
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