Double‐blinded randomized prospective trial of intranasal capsaicin treatment for nonallergic rhinitis
Autor: | Micah M. Gibson, Samuel Floren, Denna Zebda, Sorour Ahmadi, Amber U Luong, William C. Yao, Martin J. Citardi, Chauchau Pham, Zi Yang Jiang |
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Rok vydání: | 2020 |
Předmět: |
Visual analogue scale
Nasal congestion Placebo 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Nonallergic rhinitis Vasomotor Rhinitis Humans Immunology and Allergy Medicine Prospective Studies 030223 otorhinolaryngology Administration Intranasal Rhinitis business.industry medicine.disease Pathophysiology 030228 respiratory system Otorhinolaryngology chemistry Capsaicin Anesthesia Nasal administration Nasal Obstruction medicine.symptom business |
Zdroj: | International Forum of Allergy & Rhinology. 11:24-30 |
ISSN: | 2042-6984 2042-6976 |
DOI: | 10.1002/alr.22637 |
Popis: | Background Nonallergic rhinitis (NAR) is currently a diagnosis of exclusion with an unclear pathophysiologic mechanism and limited treatment options. In patients diagnosed with NAR based on symptoms, negative skin testing and positive optical rhinometry (ORM), the study's objective was to evaluate the therapeutic action of intranasal capsaicin in the management of rhinitic symptoms and the effect on ORM readings. Methods Patients with a history of NAR underwent screening by a diagnostic intranasal capsaicin challenge with ORM and skin-prick testing. Twenty-two NAR patients were enrolled and randomized to either treatment with 0.1mM capsaicin (n = 11) or placebo (n = 11). Treatment consisted of 5 consecutive intranasal applications separated by 1 hour with follow-up at 4 and 12 weeks. At each visit, subjects underwent intranasal capsaicin challenge with ORM reading and a visual analog scale scoring of rhinitis symptoms. Results Treatment with intranasal capsaicin resulted in a median change with improvement in total symptom score (TSS) of -5 from baseline vs an increase of 2 with placebo at 4 weeks, which remained significantly different between the groups at 12 weeks (p = 0.03). At 12 weeks posttreatment, 60% of the intervention group vs 80% of placebo-treated patients still met objective criteria for NAR by ORM. Conclusion Using ORM in the objective diagnosis of NAR, this trial showed that intranasal 0.1mM capsaicin not only improved rhinitic symptoms but also objectively reduced nasal reactivity and nasal congestion with a 40% responder rate at 12 weeks as noted by ORM. |
Databáze: | OpenAIRE |
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