Prospective adherence to specific immunotherapy in Europe (PASTE) survey protocol

dc.contributor.authorMakatsori, Melina
dc.contributor.authorSenna, Gianenrico
dc.contributor.authorPitsios, Constantinos
dc.contributor.authorLleonart Bellfill, Ramon
dc.contributor.authorKlimek, Ludger
dc.contributor.authorNunes, Carlos
dc.contributor.authorRukhadze, Maia
dc.contributor.authorRogala, Barbara
dc.contributor.authorGawlik, Radoslaw
dc.contributor.authorPanzner, Petr
dc.contributor.authorPfaar, Oliver
dc.contributor.authorCalderon, Moises
dc.date.accessioned2018-11-15T11:44:01Z
dc.date.available2018-11-15T11:44:01Z
dc.date.issued2015-04-27
dc.date.updated2018-07-24T12:31:39Z
dc.description.abstractBackground: Adherence to allergen immunotherapy is important for its effectiveness. There is currently limited data available on allergen immunotherapy adherence outside of clinical trials i.e. in real-life clinical practice. As part of a European Academy of Allergy and Clinical Immunology Immunotherapy Interest group initiative, we endeavoured to design a survey in order to prospectively evaluate adherence to subcutaneous and sublingual immunotherapy across different European countries. Method/Design: The inclusion criteria for this prospective, multi-country survey were set as: adults, starting clinically indicated allergen immunotherapy for respiratory allergic disorders or Hymenoptera venom allergy. An online survey was designed in order to enrol participants and assess adherence to immunotherapy. Eight countries (Czech Republic, Georgia, Germany, Greece, Italy, Poland, Portugal, Spain) were selected to reflect different parts of Europe and differences in allergens and routes of immunotherapy administration. Each country has an allocated National co-ordinator that has identified local Allergy departments willing to enrol participants in this survey. Each participant will be followed up for a total of three years. In order to assess adherence, a 4-monthly follow-up form detailing any missed doses and reasons will be completed online. In case of a participant discontinuing treatment, reasons for this will be recorded. Discussion: The use of online survey software has enabled us to make this survey a reality and reach clinicians in different countries. Forty-five centres have enrolled a total of over 1,350 participants. It is hoped that this prospective real life survey will enable us to gain a better understanding of reasons that affect adherence to subcutaneous and sublingual immunotherapy and assist in developing ways to improve this.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.pmid25918637
dc.identifier.urihttps://hdl.handle.net/2445/126129
dc.language.isoeng
dc.publisherBioMed Central Ltd
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1186/s13601-015-0060-0
dc.relation.ispartofClinical and Translational Allergy, 2015, vol. 5, num. 17
dc.relation.urihttps://doi.org/10.1186/s13601-015-0060-0
dc.rightscc by (c) Makatsori, Melina et al., 2015
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationImmunoteràpia
dc.subject.classificationMalalties de l'aparell respiratori
dc.subject.otherImmunotheraphy
dc.subject.otherRespiratory organs diseases
dc.titleProspective adherence to specific immunotherapy in Europe (PASTE) survey protocol
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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