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2.
Acta Derm Venereol ; 103: adv00854, 2023 Jan 23.
Artículo en Inglés | MEDLINE | ID: mdl-36688701

RESUMEN

TREATgermany is an investigator-initiated prospective disease registry. It investigates physician- and patient-reported disease severity (Eczema Area and Severity Index (EASI), objective Scoring Atopic Dermatitis (oSCORAD), Investigator Global Assessment, Patient-Oriented Eczema Measure (POEM), Patient Global Assessment (PGA)), patient-reported symptoms (itch, sleep loss, depressive symptoms), therapy courses and dermatological quality of life (DLQI) in moderate-to-severe atopic dermatitis with SCORAD > 20. 1,134 atopic dermatitis patients (mean age 41.0 ± 14.7 years, 42.5% females) were enrolled by 40 German recruiting sites (dermatological clinics and practices) between June 2016 and April 2021. The current analysis focuses on itch scores obtained with a numerical rating scale (NRS)) documented for the previous 3 days prior to baseline visit. The results show that 97.2% (1,090 of 1,121) patients experienced itch. Itch severity correlated moderately with severity of atopic dermatitis oSCORAD (rho = 0.44 (0.39-0.48)) and EASI score (rho = 0.41 (0.36-0.46)). A strong correlation was found with self-reported disease severity as PGA (rho = 0.68 (0.65-0.71)), POEM sum score (rho = 0.66 (0.63-0.69)) and dermatological quality of life impairment DLQI (rho = 0.61 (0.57-0.65)). Itch as a subjective complaint is more closely correlated with patient-reported outcomes than with objective assessments by the physician.


Asunto(s)
Dermatitis Atópica , Eccema , Médicos , Femenino , Humanos , Adulto , Persona de Mediana Edad , Masculino , Dermatitis Atópica/diagnóstico , Calidad de Vida , Estudios Prospectivos , Índice de Severidad de la Enfermedad , Prurito , Medición de Resultados Informados por el Paciente , Sistema de Registros
4.
Am J Speech Lang Pathol ; 27(2): 536-552, 2018 05 03.
Artículo en Inglés | MEDLINE | ID: mdl-29466550

RESUMEN

Purpose: In a feasibility study for a randomized controlled trial of treatments for phonological disorders conducted over a period of 8 months, we examined 6 clinically relevant outcome measures. We took steps to reduce error variance and to maximize systematic variance. Method: Six children received traditional treatment (Van Riper, 1939), and 7 received expansion points (Smit, 2000), a treatment program with both phonological and traditional elements. Outcome measures, which were applied to both word list and conversational samples, included percentage of consonants correct (PCC; Shriberg & Kwiatkowski, 1982), PCC for late and/or difficult (L/D) consonants and number of L/D consonants acquired. Results: In repeated-measures analyses of variance, all measures showed significant differences from pretreatment to posttreatment, and the word list measures were associated with very high power values. In analyses of covariance for between-groups contrasts, the adjusted expansion points mean exceeded the adjusted traditional treatment mean for every measure; however, no differences reached significance. For the L/D PCC (conversation) measure, the contrast between groups was associated with a large effect size. Conclusion: We recommend that practitioners use outcome measures related to a word list. We recommend that researchers consider using L/D PCC on the basis of conversational samples to detect differences among treatment groups. Supplemental Materials: https://doi.org/10.23641/asha.5872677.


Asunto(s)
Determinación de Punto Final , Ensayos Clínicos Controlados Aleatorios como Asunto/métodos , Proyectos de Investigación , Acústica del Lenguaje , Trastorno Fonológico/terapia , Logopedia/métodos , Calidad de la Voz , Factores de Edad , Conducta Infantil , Lenguaje Infantil , Preescolar , Estudios de Factibilidad , Femenino , Humanos , Masculino , Inteligibilidad del Habla , Medición de la Producción del Habla , Trastorno Fonológico/diagnóstico , Trastorno Fonológico/psicología , Factores de Tiempo , Resultado del Tratamiento
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