D2.235 - Urticaria Voices: Patient-reported disease burden and treatment experiences in Chronic Spontaneous Urticaria in China - A real-world evidence study (UV in China)
Background
Chronic spontaneous urticaria (CSU) is characterized by recurring itchy wheals (hives) and/or angioedema lasting >6 weeks without identifiable triggers, affecting 1.29% of China’s population. As studies on CSU in China are largely epidemiological with few patient-reported perspectives, studying real-world patient outcomes is important. This study investigated Chinese CSU patients' perspectives on disease burden, treatment patterns and unmet needs, assessing gaps between current management outcomes and treatment expectations.
Method
Cross-sectional study using 40-minute online surveys. Patients recruited through online panels. Eligibility: adults ≥18 years with physician-confirmed CSU diagnosis, currently receiving treatment. Descriptive analysis stratified by disease control and treatment type.
Results
The study included 400 CSU patients (55% male, mean age 35.9 years). Symptoms onset occurred 1-5 years prior in 71% patients, with a mean disease duration of 5.31 years (SD 4.89). Based on Urticaria Control Test (UCT) scores (<12), 35% patients had inadequately controlled disease, while Patient Global Impression of Severity (PGIS) self-assessment showed better perceived control (mild/no symptoms 92%). Diagnoses were predominantly made by dermatologists (94%), 86% had consulted 1+ additional dermatologists since diagnosis; 57% reported no fixed visit schedule while 42% had less than 2 visits annually. Quality of life was affected: sleep disturbance reported by 79% inadequately controlled patients, with worsening during exacerbations. Most patients (82%) were currently receiving second-generation antihistamines, and 1/3 had taken Traditional Chinese Medicine with/without medical advice in the past. Patients rated complete symptom control as most important treatment goal, mean importance ~8.5/10 (=10 extremely important), but only 16% considered it achievable with current treatments – 9% among inadequately controlled.
Conclusion
This study identified inadequate disease control in 35% of Chinese CSU patients despite active treatment, accompanied by quality-of-life impairment. The discordance between patient treatment priorities and perceived achievability, together with irregular follow-up patterns across all control levels, suggest current therapeutic and care delivery limitations. These findings suggest opportunities for more effective treatments and structured management approaches to optimise CSU care in China.
