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1.
Acta Derm Venereol ; 102: adv00712, 2022 May 16.
Artículo en Inglés | MEDLINE | ID: mdl-35356990

RESUMEN

Real-world evidence, directly comparing the effectiveness of interleukin (IL)17-inhibitors, IL23-inhibitors, tumour necrosis factor alpha (TNF-α)-inhibitors and an IL12/23-inhibitor in psoriasis, is scarce. The aim of this study was to directly compare the first-year effectiveness of biologic therapies for psoriasis, corrected for confounders. This prospective, multicentre cohort study assessed BioCAPTURE data on etanercept, adalimumab, ustekinumab, secukinumab, ixekizumab, and guselkumab in 1,080 treatment episodes of 700 patients with psoriasis. The course of the mean absolute Psoriasis Area and Severity Index (PASI) and the proportion of patients who achieved PASI90/PASI75 were compared using linear mixed models and mixed logistic regression models respectively, corrected for baseline PASI, biologic naivety, and weight. Patients treated with adalimumab, ustekinumab, secukinumab, ixekizumab, or guselkumab all had a significantly lower mean PASI after 12 months compared with etanercept, and significantly higher overall odds of reaching PASI90 than those treated with etanercept. Patients treated with ixekizumab or guselkumab also had higher probabilities of reaching PASI90 than adalimumab, ustekinumab, and secukinumab. Relative to randomized controlled trials, the proportions of patients who reached PASI90/75 were lower in this real-world study.


Asunto(s)
Productos Biológicos , Psoriasis , Adalimumab/uso terapéutico , Productos Biológicos/efectos adversos , Estudios de Cohortes , Etanercept/uso terapéutico , Humanos , Factores Inmunológicos , Estudios Prospectivos , Psoriasis/diagnóstico , Psoriasis/tratamiento farmacológico , Índice de Severidad de la Enfermedad , Resultado del Tratamiento , Ustekinumab/uso terapéutico
2.
Dermatol Ther ; 32(6): e13143, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-31664756

RESUMEN

Patients often request treatment of their burdensome cutaneous warts. However, a safe and effective treatment for cutaneous warts is lacking. This study evaluates treatment outcome, side effects, and patient satisfaction after topical application of cantharidin 1% podophyllin 2% salicylic acid 30% (CPS1) solution in a large series of children and adults with cutaneous warts. Fifty-two children and 83 adults with warts, treated with CPS1 solution between October 2012 and October 2014, were included. Complete clearance of warts occurred in 86.5% of children and 62.7% of adults treated with CPS1 solution (p < .01). Resolution of warts was partial in 3.9 and 24.1% and absent in 9.6 and 13.2% of children and adults respectively. Side effects were present in 41.2% of children and 46.3% of adults (p = .7). Most common side effects were blistering, pain, and burning sensation. No serious adverse events occurred. On a 10-point scale, median patient satisfaction score was 9.0 (interquartile range 7.8-10.0) and 8.0 (interquartile range 5.1-9.7) for children and adults respectively (p < .01). CPS1 solution is a safe and promising treatment modality with a high clearance and high patient satisfaction rate for the management of cutaneous warts, particularly in children.


Asunto(s)
Cantaridina/administración & dosificación , Podofilino/administración & dosificación , Ácido Salicílico/administración & dosificación , Verrugas/tratamiento farmacológico , Administración Cutánea , Adulto , Factores de Edad , Cantaridina/efectos adversos , Niño , Estudios de Cohortes , Femenino , Humanos , Queratolíticos/administración & dosificación , Queratolíticos/efectos adversos , Masculino , Satisfacción del Paciente , Podofilino/efectos adversos , Estudios Retrospectivos , Ácido Salicílico/efectos adversos , Resultado del Tratamiento
3.
J Dermatolog Treat ; 35(1): 2304025, 2024 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-38263716

RESUMEN

Background: Little is known about the extent of impairments in work and activities of daily life (ADL) in patients with psoriasis, and the influence of contextual factors such as disease-related characteristics and treatment. Therefore, this study aimed to assess these impairments in patients with psoriasis who started using biologicals/small molecule inhibitors.Methods: Using data from the prospective BioCAPTURE registry, we collected patient, disease, and treatment parameters, as well as work/ADL impairments at baseline, 6 and 12 months. Changes in impairment parameters and correlations between impairment and patient/disease characteristics were assessed using generalized estimating equations.Results: We included 194 patients in our analysis. After biological initiation, disease activity decreased significantly (PASI 11.2 at baseline versus 3.9 at 12 months, p < 0.001). Work-for-pay in this cohort was lower than in the Dutch general population (53% versus 67%, p = 0.01). In patients who had work-for-pay, presenteeism improved over time (5% at baseline versus 0% at 12 months, p = 0.04). Up to half of the patients reported impairments in ADL, which did not change over time. Associations between impairments and contextual factors varied, but all impairments were associated with worse mental/physical general functioning.Conclusion: Patients with psoriasis using biologicals are less likely to have work-for-pay. Treatment improves the work productivity of employed patients, but we were unable to detect changes in ADL performance.


Asunto(s)
Actividades Cotidianas , Psoriasis , Humanos , Estudios Prospectivos , Cognición , Sistema de Registros
6.
J Dermatolog Treat ; 20(1): 67-9, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-18651300

RESUMEN

Efalizumab is therapeutically effective in moderate to severe plaque psoriasis. Rebound after discontinuing therapy affects approximately 14% of patients, while erythroderma occurs in less than 1% of the treated population. In this case report, we describe two non-responding patients with severe plaque psoriasis who developed erythroderma after treatment was ceased. Non-responders are more likely to suffer from rebound. This article emphasizes the importance of close monitoring of non-responders to efalizumab after discontinuance of treatment.


Asunto(s)
Anticuerpos Monoclonales/efectos adversos , Dermatitis Exfoliativa/etiología , Psoriasis/tratamiento farmacológico , Síndrome de Abstinencia a Sustancias/etiología , Adulto , Anticuerpos Monoclonales/uso terapéutico , Anticuerpos Monoclonales Humanizados , Dermatitis Exfoliativa/fisiopatología , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Monitoreo Fisiológico , Psoriasis/diagnóstico , Medición de Riesgo , Índice de Severidad de la Enfermedad , Síndrome de Abstinencia a Sustancias/fisiopatología , Factores de Tiempo , Insuficiencia del Tratamiento
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