scholarly journals Psychometric properties of the Spanish version of the once-daily Urticaria Activity Score (UAS) in patients with chronic spontaneous urticaria managed in clinical practice (the EVALUAS study)

2019 ◽  
Vol 17 (1) ◽  
Author(s):  
Ignacio Jauregui ◽  
Ana Gimenez-Arnau ◽  
Joan Bartra ◽  
Moises Labrador-Horrillo ◽  
Javier Ortiz de Frutos ◽  
...  
2019 ◽  
pp. 193-194
Author(s):  
Wiebke Sondermann

The recommended dose of omalizumab for the treatment of chronic spontaneous urticaria (CSU) is 300 mg every 4 weeks, but there is no recommendation for patients who do not benefit from this dose. Our aim is to present the experiences on the use of doses of omalizumab higher than those recommended for CSU patients and to propose a protocol for updosing. This was a retrospective analysis of patients treated with omalizumab for CSU from 2 urticaria centers in Istanbul and Barcelona. The weekly urticaria activity score and/or the Urticaria Control Test (UCT) were used to monitor response. In Barcelona, a stepwise updosing regimen was preferred (450 mg first, then increasing to 600 mg), while in Istanbul, direct updosing to 600 mg was chosen. In Istanbul, 81 (88%) patients were treated with 300 mg, while 11 (12%) received 600 mg of omalizumab. In Barcelona, 7 (8.8%), 45 (56.3%), 17 (21.3%), and 11 (13.8%) patients received 150, 300, 450, and 600 mg of omalizumab, respectively. Urticaria control was achieved in 82.6% of the patients with 300 mg and in 8.7% of the patients with 600 mg in Istanbul, while it was achieved with 150 mg in 10%, with 300 mg in 48.8%, with 450 mg in 16.3%, and with 600 mg in 6.3% of the patients in Barcelona. In total, 123 (71.5%) patients responded to 150-300 mg and 26 (15.1%) to 450-600 mg. When responders to 150-300 mg (n = 123) were compared with responders to 450-600 mg (n = 26), BMI was found to be higher, and pre-omalizumab UCT was found to be lower in patients receiving updosed omalizumab (p = 0.029). Baseline data of the patients, especially BMI and pre-oma UCT, might be useful to determine if the patient will require higher doses of omalizumab. We recommend a stepwise approach starting from 450 mg and then updosing to 600 mg in CSU patients who do not respond or partially respond to 300 mg of omalizumab after 3-6 months of treatment.


2018 ◽  
Vol 19 (2) ◽  
pp. 267-274 ◽  
Author(s):  
Kelly Hollis ◽  
Christina Proctor ◽  
Doreen McBride ◽  
Maria-Magdalena Balp ◽  
Lori McLeod ◽  
...  

2016 ◽  
Vol 13 (4-5) ◽  
pp. 82-87
Author(s):  
O G Elisyutina ◽  
E S Fedenko ◽  
E N Zemskaya ◽  
O V Shtyrbul

Background. To evaluate the efficacy and safety of Kestine® (ebastine) 20 mg sublingual tablets in spontaneous urticaria. Materials and methods. 25 adults suffered from spontaneous chronic urticaria, and 5 patients with acute urticaria aged from 18 to 56 years old (mean age 32,7±10,1) were included in the study. All patients received treatment with Kestine® (ebastine) 20 mg 1 sublingual tab. once daily during 28 days. Assessment of activity and severity of urticaria symptoms was carried out before the treatment, 2 and 4 weeks after the starting of the treatment. To assess the urticaria activity symptoms the urticaria activity score uAS and uAS 7 (for 7 days) were used. Results. The study showed high efficacy and safety of ebastine 20 mg sublingual tablets in the treatment of patients with chronic and acute urticaria. Control under the symptoms was achieved in 20 patients with chronic urticaria (mediana UAS7 before treatment 27 - Q1 - 21, Q3 - 34, after the treatment - 10 - Q1 - 4, Q3 - 12) and in 5 patients with acute urticaria on the 28th day of treatment. Thus Kestine® (ebastine) 20 mg can be recommended as the first line medication in the treatment of spontaneous urticaria.


2015 ◽  
Vol 18 (7) ◽  
pp. A426 ◽  
Author(s):  
M Balañá ◽  
A Valero ◽  
A Giménez Arnau ◽  
M Ferrer ◽  
I Jauregui ◽  
...  

2017 ◽  
Vol 38 (2) ◽  
pp. 136-142 ◽  
Author(s):  
Ebru Arik Yilmaz ◽  
Betul Karaatmaca ◽  
Pinar Gur Cetinkaya ◽  
Ozge Soyer ◽  
Bulent E. Sekerel ◽  
...  

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