MP-AzeFlu Improves the Quality-of-Life of Patients with Allergic Rhinitis

被引:4
|
作者
van Weissenbruch, Ranny [1 ]
Klimek, Ludger [2 ]
Galffy, Gabriella [3 ]
Emmeluth, Melanie [4 ]
Koltun, Arkady [5 ]
Kopietz, Ferdinand [4 ]
Duc Tung Nguyen [6 ]
Kuhl, Hans Christian [4 ]
Pohl, Wolfgang [7 ]
Scadding, Glenis K. [8 ]
Price, David [9 ,10 ]
Mullol, Joaquim [11 ]
机构
[1] Wilhelmina Ziekenhuis, Dept ENT Head & Neck Surg, Assen, Netherlands
[2] Zentrum Rhinol & Allergol, Dept Otorhinolaryngol & Head & Neck Plast Surg, Wiesbaden, Germany
[3] Pulmonol Hosp, Torokbalint, Hungary
[4] MEDA Pharma GmbH & Co KG, Global Med Affairs, Bad Homburg, Germany
[5] Mylan Inc, Canonsburg, PA USA
[6] MEDA Pharma GmbH & Co KG, GBK Clin Affairs, Bad Homburg, Germany
[7] Inst Clin & Expt Pneumol, Dept Resp & Pulm Dis, Karl Landsteiner Gesell, Vienna, Austria
[8] Roy Natl Throat Nose & Ear Hosp, London, England
[9] Univ Aberdeen, Ctr Acad Primary Care, Div Appl Hlth Sci, Aberdeen, Scotland
[10] Observat & Pragmat Res Inst, Singapore, Singapore
[11] Univ Barcelona, ENT Dept, Rhinol Unit & Smell Clin, CIBERES,Hosp Clin Barcelona,IDIBAPS, Barcelona, Catalonia, Spain
来源
关键词
azelastine hydrochloride; daily activities; fluticasone propionate; sleep; VISUAL ANALOG SCALE; INTRANASAL THERAPY; FLUTICASONE; AZELASTINE; SEVERITY; MP29-02; ASTHMA; IMPACT; RISK;
D O I
10.2147/JAA.S277734
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: Patients with poorly controlled allergic rhinitis (AR) experience nasal symptoms, sleep disturbances, activity impairment, and decreased quality-of-life (QoL). MP-AzeFlu is safe and effective for moderate-to-severe seasonal and perennial AR, but its impact on QoL requires investigation in the real-world, especially among phenotypes of immunoglobulin (Ig)E-mediated AR. This subanalysis of an observational study evaluated response to MP-AzeFlu via assessment of sleep quality and trouble with daily activities. Patients and Methods: This multicenter, prospective, non-interventional, real-life study included a convenience sample of patients with a history of moderate-to-severe AR presenting with acute AR symptoms (visual analog scale [VAS] >= 50 mm). Over approximately 14 days of treatment with MP-AzeFlu (137 mu g azelastine HCL and 50 mu g fluticasone propionate administered via single 0.137-mL spray in each nostril twice daily), changes in sleep quality and trouble with daily work, school, social, and outdoor activities were evaluated using a VAS for the entire study population and for four subgroups based on IgE response phenotype. VAS scores ranged from "not at all troubled" (0 mm) to "extremely troubled" (100 mm). Results: Following MP-AzeFlu treatment, mean VAS scores for sleep quality impairment and work or school impairment decreased from 55.2 mm at baseline to 22.1 mm and 57.6 mm at baseline to 23.0 mm, respectively, after similar to 14 days. Similar results were observed for mean VAS scores for impairment of social activity (55.1 mm to 22.4 mm) and impairment of outdoor activity (64.4 mm to 25.0 mm). For all VAS scores, results were similar across populations, regardless of phenotype of IgE-mediated disease, comorbidity, age, and sex. Conclusion: MP-AzeFlu relieves symptoms and improves patient-reported QoL, illustrated by better sleep quality and less impairment of work, school, social, and outdoor activities after 14 days. The QoL benefits of MP-AzeFlu were consistent regardless of the phenotype of IgE-mediated disease.
引用
收藏
页码:633 / 645
页数:13
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