Perspective - (2025) Volume 12, Issue 1
Received: 28-Jan-2025, Manuscript No. JPD-25-168981;
Editor assigned: 31-Jan-2025, Pre QC No. P-168981;
Reviewed: 11-Feb-2025, QC No. Q-168981;
Revised: 18-Feb-2025, Manuscript No. R-168981;
Published:
25-Feb-2025
, DOI: 10.37421/2684-4281.2025.12.500
Citation: Braxton, Greyson. “Long-Term Outcomes in Patients with Chronic Urticaria: A Retrospective Review.” J Dermatol Dis 12 (2025): 500.
Copyright: © 2025 Braxton H. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
The study cohort consisted of over 600 patients, with a female predominance and a mean age at diagnosis of 38 years. The majority were diagnosed with chronic spontaneous urticaria, while approximately one-third had identifiable triggers consistent with inducible forms such as cold urticaria, pressure urticaria, or cholinergic urticaria. Disease duration varied considerably, with a median time to remission of 36 months. Around 50% of patients achieved remission within five years, while a smaller subset continued to have active disease beyond a decade. Interestingly, patients with CSU tended to achieve remission earlier than those with CIndU, suggesting different underlying pathophysiological mechanisms and natural histories. A significant proportion of patients had associated atopic conditions, including allergic rhinitis, asthma and atopic dermatitis, while a smaller number showed evidence of autoimmune thyroiditis, positive antinuclear antibodies, or other autoimmune markers. The presence of autoimmune comorbidities was associated with longer disease duration and more refractory symptoms. Elevated serum total IgE and positive autologous serum skin test (ASST) results were also more common in those with persistent disease. These findings support the hypothesis that an autoimmune component plays a role in a subset of patients with chronic urticaria, contributing to disease chronicity and resistance to standard antihistamine therapy [2].
First-line treatment for chronic urticaria remains non-sedating second-generation H1-antihistamines. In practice, many patients required higher-than-standard doses to achieve symptom control. For those unresponsive to antihistamines, treatment escalation included leukotriene receptor antagonists, short courses of systemic corticosteroids for acute flares and immunomodulatory agents such as cyclosporine. The introduction of omalizumab, a monoclonal anti-IgE antibody, marked a breakthrough in the management of antihistamine-refractory CSU. In this review, omalizumab was effective in over 70% of patients who received it, with many reporting significant improvement within the first three months of therapy. Those who responded early to omalizumab were more likely to achieve long-term remission even after discontinuation, while non-responders often had coexisting inducible urticaria or autoimmune features.
Patient adherence to therapy and regular follow-up were crucial in achieving disease control. Individuals who were engaged in their treatment plans, educated about the disease and managed in a multidisciplinary setting had better outcomes and higher remission rates. Psychological support played a significant role, as a high burden of anxiety and depression was noted among patients with persistent urticaria. Chronic itch, sleep disruption and the visibility of lesions often led to social embarrassment and emotional distress, necessitating the inclusion of mental health professionals in comprehensive care models.
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