1. A retrospective analysis omalizumab treatment patterns in patients with chronic spontaneous urticaria: a real-world study in Belgium
- Author
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K. Allewaert, Hilde Lapeere, L Vandebuerie, A. Stockman, Vito Sabato, H. Rabijns, Julien Lambert, M. Moutschen, R. Schrijvers, Martine Grosber, Marie Baeck, L de Montjoye, Skin function and permeability, Dermatology, Vrije Universiteit Brussel, UCL - SSS/IREC/PNEU - Pôle de Pneumologie, ORL et Dermatologie, and UCL - (SLuc) Service de dermatologie
- Subjects
Adult ,Male ,Pediatrics ,medicine.medical_specialty ,Histamine Antagonists ,Omalizumab ,Dermatology ,INTERVALS ,VALIDATION ,Drug Administration Schedule ,Medication Adherence ,ANGIOEDEMA ,Belgium ,Anti-Allergic Agents ,Medicine and Health Sciences ,MANAGEMENT ,medicine ,Humans ,Chronic Urticaria ,Allergy and Eczema ,Medical prescription ,Adverse effect ,Retrospective Studies ,Angioedema ,business.industry ,CHRONIC IDIOPATHIC/SPONTANEOUS URTICARIA ,Guideline ,Middle Aged ,medicine.disease ,LIFE ,Clinical trial ,Treatment Outcome ,Infectious Diseases ,GUIDELINE ,EXPERIENCE ,Female ,Original Article ,Observational study ,QUALITY INDEX DLQI ,Human medicine ,medicine.symptom ,business ,CHRONIC IDIOPATHIC URTICARIA ,Anaphylaxis ,medicine.drug - Abstract
BACKGROUND: Chronic spontaneous urticaria (CSU) is characterized by the repeated occurrence of persistent hives and/or angioedema for ≥6 weeks, without specific external stimuli. H1 -antihistamines have long been the standard of care of CSU, but many patients remain uncontrolled even at 4× the approved dose. Add-on therapy with omalizumab has proven effective in clinical trials, but little is known about omalizumab treatment in Belgium. OBJECTIVE: To collect real-world clinical data on omalizumab treatment in adults with CSU in Belgium. METHODS: This was an observational, retrospective chart review of adults with CSU, who initiated omalizumab treatment between August 2014 and December 2016 (maximum 28 months follow-up). RESULTS: In total, 235 patients were included (median time from symptom onset to diagnosis, 5.4 months; median time from diagnosis to commencing omalizumab, 6.7 months). Treatments used before/after commencing omalizumab did not always adhere to guidelines; many patients (26.4%/11.1%) received first-generation H1 -antihistamines, while 20.4% used omalizumab monotherapy after initiating treatment. The mean interval between omalizumab administrations was 4.8 (SD 1.7) weeks; 67.8% of patients had ≥1 interval prolongation and/or shortening. Mean baseline 7-day Urticaria Activity Score (UAS7) was 32.0 (SD 6.05); this improved to 12.6 (SD 11.2) after 1 month of omalizumab. About 67.2% of patients reached UAS7 ≤ 6 (well controlled) during the study. A total of 87 patients stopped omalizumab and never restarted before the end of the observation period; the most prevalent reason was remission of symptoms (49.4% of patients), followed by lack of effect (12.6%), lost to follow-up (6.9%) and adverse events (3.4%). Headache was the most common adverse event (n = 8/82). No anaphylaxis was reported. CONCLUSIONS: This study revealed that patients initiated on omalizumab in Belgium had severe CSU at baseline, and showed substantial improvements after 1 month of treatment. Greater adherence to the prescription of guideline-recommended medications is needed for the treatment of CSU. ispartof: Journal Of The European Academy Of Dermatology And Venereology vol:34 issue:1 pages:127-134 ispartof: location:England status: published
- Published
- 2020