Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 13 de 13
Filter
Add more filters










Publication year range
8.
Pediatr Dermatol ; 40(4): 660-663, 2023.
Article in English | MEDLINE | ID: mdl-36451284

ABSTRACT

With the introduction of large-scale COVID-19 vaccination programs, a variety of cutaneous manifestations have been described. We present two girls (ages 12 and 5 years) who developed erythema nodosum (EN) 3 and 14 days after Pfizer-BioNTech COVID-19 vaccination, respectively. While EN after COVID-19 vaccination has been reported in adults, it is can also occur in children.


Subject(s)
COVID-19 Vaccines , COVID-19 , Erythema Nodosum , Adult , Child , Female , Humans , COVID-19/prevention & control , COVID-19 Vaccines/adverse effects , Erythema Nodosum/diagnosis , Erythema Nodosum/etiology , Vaccination/adverse effects
12.
Dermatol Ther ; 35(11): e15844, 2022 11.
Article in English | MEDLINE | ID: mdl-36124339

ABSTRACT

Apremilast is an oral small molecule approved for the treatment of psoriasis, psoriatic arthritis and oral ulcers associated with Behçet's disease. This research was conducted to describe the characteristics of patients who received treatment with apremilast for a skin disorder, either before, during, or after a biological treatment, with the aim of analyze the reasons that lead to start this drug in real clinical practice or suspend it for another. A total of 41 patients were enrolled: nine (22.0%) had received biological treatment prior to apremilast, seven (17.0%) both before and after apremilast and 25 (61.0%) after apremilast. One patient received concomitant treatment with adalimumab and apremilast. Most patients (85.4%) received apremilast as treatment for psoriasis. Reasons for starting apremilast were lack of efficacy with previous treatments (85.4%) and adverse effects or contraindication to previous treatments (14.6%), without statistically significant differences between patients who had received a previous biologic and those who had not. Drug survival was not influenced by previous biological treatment, but we found an increased risk of drug discontinuation in patients with chronic kidney disease (log-rank p = 0.028). The main reason of apremilast withdrawal was lack of adequate disease control (60.0%), most of whom required treatment with biologics. Therefore, despite the extensive development of new therapies for psoriasis and other dermatological conditions, apremilast is a widely used drug even in patients who are candidates for biologic treatment. Its initiation is more frequent due to poor disease control than because of other therapies contraindications.


Subject(s)
Arthritis, Psoriatic , Biological Products , Psoriasis , Humans , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Thalidomide/adverse effects , Arthritis, Psoriatic/drug therapy , Psoriasis/drug therapy , Psoriasis/chemically induced , Biological Products/adverse effects
SELECTION OF CITATIONS
SEARCH DETAIL
...