2011
DOI: 10.1016/j.jaci.2010.11.036
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Efficacy and safety of immunotherapy for allergies to Alternaria alternata in children

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Cited by 90 publications
(96 citation statements)
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References 42 publications
(28 reference statements)
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“…The primary diagnosis was asthma in 7 studies, 6,7,[11][12][13][14][15] rhinoconjunctivitis in 1 study, 16 and asthma with rhinitis/rhinoconjunctivitis in 5 studies. 8,9,[17][18][19] The majority of studies used a single allergen for SCIT. Dust mites were evaluated in 8 of the 13 studies.…”
Section: Resultsmentioning
confidence: 99%
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“…The primary diagnosis was asthma in 7 studies, 6,7,[11][12][13][14][15] rhinoconjunctivitis in 1 study, 16 and asthma with rhinitis/rhinoconjunctivitis in 5 studies. 8,9,[17][18][19] The majority of studies used a single allergen for SCIT. Dust mites were evaluated in 8 of the 13 studies.…”
Section: Resultsmentioning
confidence: 99%
“…Six RCTs with 550 subjects evaluated SCIT for control of asthma symptoms relative to placebo 11,15,18,19 or pharmacotherapy 13,17 (Table 1; Supplemental Appendix Table 4). Four studies evaluated a single allergen 11,13,18,19 and 2 used multiple allergens.…”
Section: Asthmamentioning
confidence: 99%
“…Children having allergic rhinitis/ asthma allergic to Alternaria utilized mold AIT or placebo for 3 years in a study by Kuna et al Symptom and medication scores were notably decreased in the AIT group following the 2nd and 3rd years, with a decline in the symptom scores by 63% after AIT. The AIT group had a significant decline in symptoms after a single dose nasal allergen challenge compared to their baseline and to the placebo group one year after completion of the 3 year AIT [15].…”
Section: Subcutaneous Allergen Immunotherapy (Sc-ait) For Alternaria mentioning
confidence: 90%
“…There is an absence of commercial extracts for many of the frequent fungi due to not growing on artificial media [26]. Published studies have also major limitations, including lack of placebo control, open design, utilization of unstandardized extracts, short follow-up time, or not have of a baseline observation periods [15].…”
Section: Limitations To Immunotherapymentioning
confidence: 99%
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