RESUMEN
We aimed to prepare guidelines for the management of diabetic ulcer/gangrene with emphasis on the diagnosis and treatment of skin symptoms. They serve as a tool to improve the quality of the diagnosis and treatment in each patient and, further, to improve the level of the care for diabetic ulcer in Japan by systematically presenting evidence-based recommendations for clinical judgments by incorporating various viewpoints.
Asunto(s)
Pie Diabético/terapia , Gangrena/terapia , Aldehído Reductasa/antagonistas & inhibidores , Antibacterianos/administración & dosificación , Eliminación de Componentes Sanguíneos , Desbridamiento , Pie Diabético/complicaciones , Pie Diabético/diagnóstico , Nefropatías Diabéticas/diagnóstico , Gangrena/diagnóstico , Gangrena/etiología , Humanos , Oxigenoterapia Hiperbárica , Isquemia/diagnóstico , Isquemia/etiología , Terapia de Presión Negativa para Heridas , Aparatos Ortopédicos , Osteomielitis/diagnóstico por imagen , Osteomielitis/tratamiento farmacológico , Osteomielitis/etiología , Diálisis Renal/efectos adversos , Cicatrización de HeridasRESUMEN
Burns are a common type of skin injury encountered at all levels of medical facilities from private clinics to core hospitals. Minor burns heal by topical treatment alone, but moderate to severe burns require systemic management, and skin grafting is often necessary also for topical treatment. Inappropriate initial treatment or delay of initial treatment may exert adverse effects on the subsequent treatment and course. Therefore, accurate evaluation of the severity and initiation of appropriate treatment are necessary. The Guidelines for the Management of Burn Injuries were issued in March 2009 from the Japanese Society for Burn Injuries as guidelines concerning burns, but they were focused on the treatment for extensive and severe burns in the acute period. Therefore, we prepared guidelines intended to support the appropriate diagnosis and initial treatment for patients with burns that are commonly encountered including minor as well as moderate and severe cases. Because of this intention of the present guidelines, there is no recommendation of individual surgical procedures.
Asunto(s)
Quemaduras/diagnóstico , Quemaduras/terapia , Fluidoterapia/métodos , Índice de Severidad de la Enfermedad , Cicatrización de Heridas , Administración Cutánea , Corticoesteroides/administración & dosificación , Corticoesteroides/uso terapéutico , Antibacterianos/uso terapéutico , Antiinfecciosos Locales/uso terapéutico , Vendajes , Broncoscopía , Quemaduras/clasificación , Quemaduras por Inhalación/diagnóstico , Quemaduras por Inhalación/terapia , Humanos , Hidroterapia , Pulmón/diagnóstico por imagen , Pomadas/administración & dosificación , Pomadas/uso terapéutico , Pronóstico , Radiografía , Sulfadiazina de Plata/uso terapéutico , Tétanos/prevención & control , Toxoide Tetánico/uso terapéutico , Infección de Heridas/prevención & controlAsunto(s)
Antígenos CD8/análisis , Linfoma Cutáneo de Células T/patología , Linfoma de Células T Periférico/patología , Neoplasias Cutáneas/patología , Femenino , Humanos , Inmunohistoquímica , Linfoma Cutáneo de Células T/tratamiento farmacológico , Linfoma Cutáneo de Células T/metabolismo , Linfoma de Células T Periférico/tratamiento farmacológico , Linfoma de Células T Periférico/metabolismo , Persona de Mediana Edad , Terapia PUVA , Neoplasias Cutáneas/tratamiento farmacológico , Neoplasias Cutáneas/metabolismo , Resultado del TratamientoRESUMEN
BACKGROUND: Atopic dermatitis (AD) is an allergic skin disease that follows a clinical course of 'flare-up' and remission. Histamine and tryptase are inducers of pruritus and non-sedating second-generation antihistamines, including fexofenadine, are widely used for treatment of allergic skin disorders. OBJECTIVE: We assessed the efficacy of a second-generation antihistamine in AD patients and examined its pharmacological effects on chemical mediators. METHODS: The scoring atopic dermatitis (SCORAD) instrument and visual analogue scale (VAS) for pruritus were used to assess disease severity in 349 AD patients. Twenty patients with moderate AD symptoms, who had not received any treatment for 2 weeks, were randomly assigned into two groups. Ten patients underwent fexofenadine and emollient treatment (Group 1) and 10 received fexofenadine and steroid treatment (Group 2) for 1 week. SCORAD and VAS for pruritus, and blood histamine and tryptase levels were evaluated before and after treatment. RESULTS: SCORAD and VAS improved in both Group 1 (p=0.01 and p=0.006, respectively) and Group 2 (p<0.001 and p=0.001, respectively). The improvement in Group 1 showed a significant correlation with the diminution rate of blood tryptase levels (SCORAD: r=0.83 and p=0.013, respectively; VAS: r=0.81, p=0.015, respectively). End-point plasma tryptase levels were significantly lower than baseline levels in Group 2 (p=0.046). Histamine levels did not show any significant changes in either group. CONCLUSION: These results suggest that second-generation antihistamine therapy reduces AD pruritus, resulting in the effective clinical treatment for AD. In addition, monitoring tryptase levels during antihistamine therapy in moderate AD treatment may prove to be useful in establishing treatment effects.