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MP-AzeFlu in Moderate-to-Severe Allergic Rhinitis: A Literature Review.
Klimek, Ludger; Berger, William E; Bousquet, Jean; Keith, Paul K; Smith, Peter; Sole, Dirceu; Scadding, Glenis; Kuhl, Hans Christian; Nguyen, Duc Tung; Kopietz, Ferdinand; Koltun, Arkady.
Afiliação
  • Klimek L; Center for Rhinology and Allergology, Wiesbaden, Germany.
  • Berger WE; Allergy and Asthma Associates of Southern California, Mission Viejo, California, USA.
  • Bousquet J; CHU Montpellier, Montpellier, France.
  • Keith PK; Charité - Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Smith P; Division of Allergy and Clinical Immunology, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Sole D; Queensland Allergy Services, Southport, Queensland, Australia.
  • Scadding G; Division of Allergy, Department of Pediatrics, Clinical Immunology and Rheumatology, Federal University of São Paulo/UNIFESP, São Paulo, Brazil.
  • Kuhl HC; Royal National Throat Nose and Ear Hospital, London, United Kingdom.
  • Nguyen DT; MEDA Pharma GmbH & Co. KG (A Mylan Company), Bad Homburg, Germany.
  • Kopietz F; MEDA Pharma GmbH & Co. KG (A Mylan Company), Bad Homburg, Germany.
  • Koltun A; MEDA Pharma GmbH & Co. KG (A Mylan Company), Bad Homburg, Germany.
Int Arch Allergy Immunol ; 182(11): 1026-1035, 2021.
Article em En | MEDLINE | ID: mdl-34082425
Allergic rhinitis (AR) is prevalent, and many patients present with moderate-to-severe symptomatic disease. The majority of patients are not satisfied with their AR treatment, despite the use of concurrent medications. These gaps underscore the need for treatment with more effective options for moderate-to-severe AR. The authors' objective was to review systematically the efficacy and safety of MP-AzeFlu for the treatment of AR. The primary outcomes studied were nasal, ocular, and total symptoms. Other outcomes included time to onset and of AR control, quality of life, and safety. Searches of PubMed and Cochrane databases were conducted on May 14, 2020, with no date restrictions, to identify publications reporting data on MP-AzeFlu. Clinical studies of any phase were included. Studies were excluded if they were not in English, were review articles, did not discuss the safety and efficacy of MP-AzeFlu for AR symptoms. Treatment of AR with MP-AzeFlu results in effective, sustained relief of nasal and ocular symptoms, and faster onset and time to control compared with intranasal azelastine or fluticasone propionate. Long-term use of MP-AzeFlu was safe, with benefits in children, adults, and adults aged ≥65 years. Other treatment options, including fluticasone propionate and azelastine alone or the combination of intranasal corticosteroids and oral antihistamine, do not provide the same level of efficacy as MP-AzeFlu in terms of rapid and sustained relief of the entire AR symptom complex. Furthermore, MP-AzeFlu significantly improves patient quality of life. MP-AzeFlu is a currently available combination that may satisfy all these patient needs and expectations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ftalazinas / Corticosteroides / Antialérgicos / Rinite Alérgica / Fluticasona / Antagonistas dos Receptores Histamínicos H1 Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Int Arch Allergy Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ftalazinas / Corticosteroides / Antialérgicos / Rinite Alérgica / Fluticasona / Antagonistas dos Receptores Histamínicos H1 Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Int Arch Allergy Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Alemanha