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1.
Indian J Dermatol Venereol Leprol ; 84(4): 431-436, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-28485307

RESUMEN

BACKGROUND: Treatments for autoimmune blistering disease carry significant risks of medical complications and can affect the patient's quality of life. Recently, the Treatment of Autoimmune Bullous Disease Quality of Life questionnaire was developed in Australia. OBJECTIVE: The objective of this study was to evaluate the reliability and validity of the Chinese version of the Treatment of Autoimmune Bullous Disease Quality of Life questionnaire in Chinese patients with autoimmune blistering diseases. METHODS: The Chinese version of the Treatment of Autoimmune Bullous Disease Quality of Life questionnaire was produced by forward-backward translation and cross-cultural adaptation of the original English version. Autoimmune blistering disease patients recruited in the study self-administered the Chinese Treatment of Autoimmune Bullous Disease Quality of Life questionnaire, the Dermatology Life Quality Index and the 36-item Short-Form Health Survey. Reliability of the Chinese Treatment of Autoimmune Bullous Disease Quality of Life was evaluated using internal consistency and test-retest (days 0 and 7) methods. Validity was analyzed by face, content, construct, convergent and discriminant validity measures. RESULTS: A total of 86 autoimmune blistering disease patients were recruited for the study. Cronbach's alpha coefficient was 0.883 and the intraclass correlation coefficient was 0.871. Face and content validities were satisfactory. Convergent validity testing revealed correlation coefficients of 0.664 for the Treatment of Autoimmune Bullous Disease Quality of Life and Dermatology Life Quality Index and -0.577 for the Treatment of Autoimmune Bullous Disease Quality of Life and 36-item Short-Form Health Survey. With respect to discriminant validity, no significant differences were observed in the Treatment of Autoimmune Bullous Disease Quality of Life scores of men and women (t = 0.251, P = 0.802), inpatients and outpatients (t = 0.447, P = 0.656), patients on steroids and steroid-sparing medications (t = 0.672, P = 0.503) and patients with different autoimmune blistering disease subtypes (F = 0.030, P = 0.971). LIMITATIONS: Illiterate patients were excluded from the study. The patients were from a single hospital and most of their conditions were in a relatively stable status. CONCLUSION: The Chinese version of the Treatment of Autoimmune Bullous Disease Quality of Life questionnaire is a reliable and valid instrument to measure treatment burden and to serve as an end point in clinical trials in Chinese autoimmune blistering disease patients.


Asunto(s)
Enfermedades Autoinmunes/diagnóstico , Comparación Transcultural , Calidad de Vida , Enfermedades Cutáneas Vesiculoampollosas/diagnóstico , Encuestas y Cuestionarios/normas , Traducción , Adolescente , Adulto , Anciano , Enfermedades Autoinmunes/etnología , Enfermedades Autoinmunes/psicología , China/etnología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proyectos Piloto , Calidad de Vida/psicología , Reproducibilidad de los Resultados , Autoinforme/normas , Enfermedades Cutáneas Vesiculoampollosas/etnología , Enfermedades Cutáneas Vesiculoampollosas/psicología , Adulto Joven
2.
Artículo en Inglés | MEDLINE | ID: mdl-17050937

RESUMEN

A 23-year-old young woman presented with recurrent episodes of painful bruising along with linear erosions on the accessible areas of the body of nine years duration with a pseudo-ainhum of her left nipple for the past three months. Her case history included repeated visits to various physicians at different centers and an extensive investigative profile. A diagnosis of autoerythrocyte sensitization was made on the basis of the clinical history, dermatological examination complemented by a positive autoerythrocyte sensitization test, psychiatric evaluation and absence of any organic cause for her ailment. She was placed on psychiatric management and has remained symptom-free after six months follow-up. The case is reported for its rarity, as well as for the association of autoerythrocyte sensitization syndrome with frank dermatitis artefacta and pseudo-ainhum, which to the best of our knowledge has not yet been reported in the literature.


Asunto(s)
Enfermedades Autoinmunes/diagnóstico , Dermatitis/diagnóstico , Dermatitis/psicología , Eritrocitos/inmunología , Púrpura/diagnóstico , Púrpura/psicología , Adulto , Enfermedades Autoinmunes/complicaciones , Enfermedades Autoinmunes/psicología , Dermatitis/complicaciones , Femenino , Humanos , Pezones/patología , Trastornos Psicofisiológicos/complicaciones , Trastornos Psicofisiológicos/diagnóstico , Trastornos Psicofisiológicos/psicología , Púrpura/complicaciones , Síndrome
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