TY - JOUR
T1 - Allergen immunotherapy for allergic rhinoconjunctivitis
T2 - a systematic review and meta-analysis
AU - Dhami, Sangeeta
AU - Nurmatov, Ulugbek
AU - Arasi, Stefania
AU - Khan, Tahir
AU - Asaria, Miqdad
AU - Zaman, Hadar
AU - Agarwal, Arnav
AU - Netuveli, Gopal
AU - Roberts, Graham
AU - Pfaar, Oliver
AU - Muraro, Antonella
AU - Ansotegui, Ignacio J
AU - Calderón, Moises A
AU - Cingi, Cemal
AU - Durham, Stephen R
AU - van Wijk, Ronald Gerth
AU - Halken, Susanne
AU - Hamelmann, Eckard
AU - Hellings, Peter
AU - Jacobsen, Lars
AU - Knol, Edward
AU - Linnemann, Desiree Larenas
AU - Lin, Sandra
AU - Maggina, Paraskevi
AU - Mösges, Ralph
AU - Elberink, Hanneke Oude
AU - Pajno, Giovanni
AU - Panwankar, Ruby
AU - Pastorello, Elide A
AU - Penagos, Martin
AU - Pitsios, Constantinos
AU - Rotiroti, Giuseppina
AU - Timmermans, Frans
AU - Tsilochristou, Olympia
AU - Varga, Eva-Maria
AU - Schmidt-Weber, Carsten
AU - Wilkinson, Jamie
AU - Williams, Andrew
AU - Worm, Margitta
AU - Zhang, Luo
AU - Sheikh, Aziz
N1 - This article is protected by copyright. All rights reserved.
PY - 2017/11
Y1 - 2017/11
N2 - Background: The European Academy of Allergy and Clinical Immunology (EAACI) is in the process of developing Guidelines on Allergen Immunotherapy (AIT) for Allergic Rhinoconjunctivitis. To inform the development of clinical recommendations, we undertook a systematic review to assess the effectiveness, cost-effectiveness, and safety of AIT in the management of allergic rhinoconjunctivitis. Methods: We searched nine international biomedical databases for published, in-progress, and unpublished evidence. Studies were independently screened by two reviewers against predefined eligibility criteria and critically appraised using established instruments. Our primary outcomes of interest were symptom, medication, and combined symptom and medication scores. Secondary outcomes of interest included cost-effectiveness and safety. Data were descriptively summarized and then quantitatively synthesized using random-effects meta-analyses. Results: We identified 5960 studies of which 160 studies satisfied our eligibility criteria. There was a substantial body of evidence demonstrating significant reductions in standardized mean differences (SMD) of symptom (SMD −0.53, 95% CI −0.63, −0.42), medication (SMD −0.37, 95% CI −0.49, −0.26), and combined symptom and medication (SMD −0.49, 95% CI −0.69, −0.30) scores while on treatment that were robust to prespecified sensitivity analyses. There was in comparison a more modest body of evidence on effectiveness post-discontinuation of AIT, suggesting a benefit in relation to symptom scores. Conclusions: AIT is effective in improving symptom, medication, and combined symptom and medication scores in patients with allergic rhinoconjunctivitis while on treatment, and there is some evidence suggesting that these benefits are maintained in relation to symptom scores after discontinuation of therapy.
AB - Background: The European Academy of Allergy and Clinical Immunology (EAACI) is in the process of developing Guidelines on Allergen Immunotherapy (AIT) for Allergic Rhinoconjunctivitis. To inform the development of clinical recommendations, we undertook a systematic review to assess the effectiveness, cost-effectiveness, and safety of AIT in the management of allergic rhinoconjunctivitis. Methods: We searched nine international biomedical databases for published, in-progress, and unpublished evidence. Studies were independently screened by two reviewers against predefined eligibility criteria and critically appraised using established instruments. Our primary outcomes of interest were symptom, medication, and combined symptom and medication scores. Secondary outcomes of interest included cost-effectiveness and safety. Data were descriptively summarized and then quantitatively synthesized using random-effects meta-analyses. Results: We identified 5960 studies of which 160 studies satisfied our eligibility criteria. There was a substantial body of evidence demonstrating significant reductions in standardized mean differences (SMD) of symptom (SMD −0.53, 95% CI −0.63, −0.42), medication (SMD −0.37, 95% CI −0.49, −0.26), and combined symptom and medication (SMD −0.49, 95% CI −0.69, −0.30) scores while on treatment that were robust to prespecified sensitivity analyses. There was in comparison a more modest body of evidence on effectiveness post-discontinuation of AIT, suggesting a benefit in relation to symptom scores. Conclusions: AIT is effective in improving symptom, medication, and combined symptom and medication scores in patients with allergic rhinoconjunctivitis while on treatment, and there is some evidence suggesting that these benefits are maintained in relation to symptom scores after discontinuation of therapy.
KW - Journal Article
KW - Review
KW - subcutaneous
KW - allergen
KW - allergen immunotherapy
KW - allergic rhinoconjunctivitis
KW - sublingual
KW - Humans
KW - Conjunctivitis, Allergic/therapy
KW - Desensitization, Immunologic/methods
KW - Allergens/immunology
KW - Databases, Factual
KW - Rhinitis, Allergic, Seasonal/therapy
U2 - 10.1111/all.13201
DO - 10.1111/all.13201
M3 - Journal article
C2 - 28493631
SN - 0105-4538
VL - 72
SP - 1597
EP - 1631
JO - Allergy
JF - Allergy
IS - 11
ER -