<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(1)</volume><submitter>Mirrahimi B</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To evaluate the effects of dietary eicosapentaenoic acid (EPA) in children with atopic dermatitis.&lt;h4>Methods&lt;/h4>Forty-eight children with atopic dermatitis were randomly allocated to receive either 250 mg twice daily EPA (n = 24) or placebo (n = 24) for 4 weeks. The absolute improvement in the SCORing Atopic Dermatitis (SCORAD) index and the necessity to use topical corticosteroids was evaluated.&lt;h4>Results&lt;/h4>Based on an intention-to-treat analysis, after 2 weeks the scores decreased to 30.50 ± 8.91 and 38.34 ± 10.52 in the EPA and placebo groups, respectively (p = 0.015). Per-protocol analysis showed a decrease in scores to 18.01 ± 10.63 in the EPA group and to 30.11 ± 9.58 in the placebo group (p = 0.001). After 2 weeks, corticosteroid was needed in 11 (50.0%) patie</pubmed_abstract><journal>The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG</journal><pagination>29-35</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9901318</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Evaluating the Effect of Eicosapentaenoic Acid in Children With Atopic Dermatitis: A Randomized Triple-Blind Clinical Trial.</pubmed_title><pmcid>PMC9901318</pmcid><pubmed_authors>Mohebbi R</pubmed_authors><pubmed_authors>Mirrahimi B</pubmed_authors><pubmed_authors>Moazemi M</pubmed_authors><pubmed_authors>Jamshidi E</pubmed_authors><pubmed_authors>Esmaily H</pubmed_authors><pubmed_authors>Mir M</pubmed_authors><pubmed_authors>Eslami N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluating the Effect of Eicosapentaenoic Acid in Children With Atopic Dermatitis: A Randomized Triple-Blind Clinical Trial.</name><description>&lt;h4>Objective&lt;/h4>To evaluate the effects of dietary eicosapentaenoic acid (EPA) in children with atopic dermatitis.&lt;h4>Methods&lt;/h4>Forty-eight children with atopic dermatitis were randomly allocated to receive either 250 mg twice daily EPA (n = 24) or placebo (n = 24) for 4 weeks. The absolute improvement in the SCORing Atopic Dermatitis (SCORAD) index and the necessity to use topical corticosteroids was evaluated.&lt;h4>Results&lt;/h4>Based on an intention-to-treat analysis, after 2 weeks the scores decreased to 30.50 ± 8.91 and 38.34 ± 10.52 in the EPA and placebo groups, respectively (p = 0.015). Per-protocol analysis showed a decrease in scores to 18.01 ± 10.63 in the EPA group and to 30.11 ± 9.58 in the placebo group (p = 0.001). After 2 weeks, corticosteroid was needed in 11 (50.0%) patie</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-25T19:18:23.877Z</modification><creation>2024-10-18T03:12:44.443Z</creation></dates><accession>S-EPMC9901318</accession><cross_references><pubmed>36777980</pubmed><doi>10.5863/1551-6776-28.1.29</doi></cross_references></HashMap>