TY - JOUR
T1 - Allergen immunotherapy for allergic rhinoconjunctivitis
T2 - A systematic review and meta-analysis
AU - Dhami, S.
AU - Nurmatov, U.
AU - Arasi, S.
AU - Khan, T.
AU - Asaria, M.
AU - Zaman, H.
AU - Agarwal, A.
AU - Netuveli, G.
AU - Roberts, G.
AU - Pfaar, O.
AU - Muraro, A.
AU - Ansotegui, I. J.
AU - Calderon, M.
AU - Cingi, C.
AU - Durham, S.
AU - van Wijk, R. Gerth
AU - Halken, S.
AU - Hamelmann, E.
AU - Hellings, P.
AU - Jacobsen, L.
AU - Knol, E.
AU - Larenas-Linnemann, D.
AU - Lin, S.
AU - Maggina, P.
AU - Mösges, R.
AU - Oude Elberink, H.
AU - Pajno, G.
AU - Panwankar, R.
AU - Pastorello, E.
AU - Penagos, M.
AU - Pitsios, C.
AU - Rotiroti, G.
AU - Timmermans, F.
AU - Tsilochristou, O.
AU - Varga, E. M.
AU - Schmidt-Weber, C.
AU - Wilkinson, J.
AU - Williams, A.
AU - Worm, M.
AU - Zhang, L.
AU - Sheikh, A.
N1 - Publisher Copyright:
© 2017 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.
PY - 2017
Y1 - 2017
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 Methods: We searched nine international biomedical databases for published, in-progress, and unpublished evidence.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 - allergen
KW - allergen immunotherapy
KW - allergic rhinoconjunctivitis
KW - subcutaneous
KW - sublingual
UR - http://www.scopus.com/inward/record.url?scp=85023623258&partnerID=8YFLogxK
U2 - 10.1111/all.13201
DO - 10.1111/all.13201
M3 - Review article
C2 - 28493631
AN - SCOPUS:85023623258
SN - 0105-4538
VL - 72
SP - 1597
EP - 1631
JO - Allergy: European Journal of Allergy and Clinical Immunology
JF - Allergy: European Journal of Allergy and Clinical Immunology
IS - 11
ER -