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   <dc:title>Real-life effect of a microcrystalline tyrosine adjuvanted mite immunotherapy in patients with allergic rhinitis</dc:title>
   <dc:creator>Roger, Albert</dc:creator>
   <dc:creator>Malet, Alfons</dc:creator>
   <dc:creator>Moreno, Victoria</dc:creator>
   <dc:creator>Parra, Antonio</dc:creator>
   <dc:creator>Gutierrez, Diego</dc:creator>
   <dc:creator>Lleonart Bellfill, Ramon</dc:creator>
   <dc:creator>Moreno, Francisco</dc:creator>
   <dc:creator>Valero, Antonio</dc:creator>
   <dc:creator>Navarro, Begoña</dc:creator>
   <dc:creator>Hinojosa, Belén</dc:creator>
   <dc:creator>Justicia, José L.</dc:creator>
   <dc:subject>Àcars</dc:subject>
   <dc:subject>Rinitis</dc:subject>
   <dc:subject>Mites</dc:subject>
   <dc:subject>Rhinitis</dc:subject>
   <dcterms:abstract>Aim: Evaluate the effectiveness and safety of immunotherapy with Acarovac Plus((R)) in a 1-year prospective multicentered real-life study. Methods: A total of 118 adults with allergic rhinitis sensitized to Dermatophagoides received subcutaneous immunotherapy with Acarovac Plus. Treatment outcomes were evaluated at baseline, 6 months and 1 year after treatment initiation. Primary end point was the evolution of the combined symptom and medication score. Secondary end points included other effectiveness outcomes and measurement of product tolerability. Results: Acarovac Plus induced significant improvements in primary and secondary end points after 6 months compared with baseline. These differences persisted after 1 year of treatment (p &lt; 0.001; baseline vs 1 year): combined symptom and medication score (1.60 vs 0.79). No serious adverse events were recorded. Conclusion: Acarovac Plus for 1 year was effective and well tolerated in a real-life setting.</dcterms:abstract>
   <dcterms:issued>2021-02-09T09:36:19Z</dcterms:issued>
   <dcterms:issued>2021-02-09T09:36:19Z</dcterms:issued>
   <dcterms:issued>2020-01-01</dcterms:issued>
   <dcterms:issued>2021-02-08T10:12:28Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.2217/imt-2019-0205</dc:relation>
   <dc:relation>Immunotherapy, 2020, vol. 12, num. 1, p. 53-62</dc:relation>
   <dc:relation>https://doi.org/10.2217/imt-2019-0205</dc:relation>
   <dc:rights>cc by-nc-nd (c) Roger et al., 2020</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Future Medicine Ltd.</dc:publisher>
   <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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