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http://hdl.handle.net/11452/30061
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ergün, Tülin | - |
dc.contributor.author | Seckin, Gençosmanoğlu Dilek | - |
dc.contributor.author | Alpsoy, Erkan | - |
dc.contributor.author | Sarıcam, Merve Hatun | - |
dc.contributor.author | Salman, Andaç | - |
dc.contributor.author | Onsun, Nahide | - |
dc.contributor.author | Sarıöz, Abdullah | - |
dc.date.accessioned | 2022-12-23T08:16:44Z | - |
dc.date.available | 2022-12-23T08:16:44Z | - |
dc.date.issued | 2016-10-28 | - |
dc.identifier.citation | Ergün, T. vd. (2017). ''Efficacy, safety and drug survival of conventional agents in pediatric psoriasis: A multicenter, cohort study''. Journal of Dermatology, 44(6), 630-634. | en_US |
dc.identifier.issn | 0385-2407 | - |
dc.identifier.uri | https://doi.org/10.1111/1346-8138.13713 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1111/1346-8138.13713 | - |
dc.identifier.uri | 1346-8138 | - |
dc.identifier.uri | http://hdl.handle.net/11452/30061 | - |
dc.description.abstract | The data on long-term efficacy, safety and drug survival rates of conventional systemic therapeutics in pediatric psoriasis is lacking. The primary aim of this study is to investigate acitretin, methotrexate, cyclosporin efficacy, safety and drug survival rates in pediatric patients as well as predictors of drug survival. This is a multicenter study including 289 pediatric cases being treated with acitretin, methotrexate and cyclosporin in four academic referral centers. Efficacy, adverse events, reasons for discontinuation, 1, 2- and 3-year drug survival rates, and determinants of drug survival were analyzed. A 75% reduction of Psoriasis Area and Severity Index score or better response rate was obtained in 47.5%, 34.1% and 40% of the patients who were treated with acitretin, methotrexate and cyclosporin, respectively. One-year drug survival rates for acitretin, methotrexate and cyclosporin were 36.3%, 21.1% and 15.1%, respectively. The most significant determinant of drug survival, which diminished over time, was treatment response whereas arthritis, body mass index and sex had no influence. Although all three medications are effective and relatively safe in children, drug survival rates are low due to safety concerns at this age group. Effective disease control through their rational use can be expected to improve survival rates. | en_US |
dc.description.sponsorship | Pfizer | en_US |
dc.description.sponsorship | Novartis | en_US |
dc.description.sponsorship | Merck & Company - Schering Plough Corporation | en_US |
dc.description.sponsorship | AbbVie | en_US |
dc.description.sponsorship | Merck & Company | en_US |
dc.description.sponsorship | Johnson & Johnson - Johnson & Johnson USA - Janssen Biotech Inc | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Dermatology | en_US |
dc.subject | Drug survival | en_US |
dc.subject | Efficacy | en_US |
dc.subject | Pediatric | en_US |
dc.subject | Psoriasis | en_US |
dc.subject | Systemic treatment | en_US |
dc.subject | Childhood psoriasis | en_US |
dc.subject | Etanercept | en_US |
dc.subject | Children | en_US |
dc.subject | Methotrexate | en_US |
dc.subject | Cyclosporine | en_US |
dc.subject | Adolescents | en_US |
dc.subject | Moderate | en_US |
dc.subject.mesh | Acitretin | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Cohort studies | en_US |
dc.subject.mesh | Cyclosporine | en_US |
dc.subject.mesh | Dermatologic agents | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Methotrexate | en_US |
dc.subject.mesh | Psoriasis | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.title | Efficacy, safety and drug survival of conventional agents in pediatric psoriasis: A multicenter, cohort study | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000402791900022 | tr_TR |
dc.identifier.scopus | 2-s2.0-85008244081 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı. | tr_TR |
dc.identifier.startpage | 630 | tr_TR |
dc.identifier.endpage | 634 | tr_TR |
dc.identifier.volume | 44 | tr_TR |
dc.identifier.issue | 6 | tr_TR |
dc.relation.journal | Journal of Dermatology | en_US |
dc.contributor.buuauthor | Bülbül, Başkan Emel | - |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 27943425 | tr_TR |
dc.subject.wos | Dermatology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q1 | en_US |
dc.contributor.scopusid | 6602518817 | tr_TR |
dc.subject.scopus | Pustulosis Palmoplantaris; Dermatologists; Diaper Rash | en_US |
dc.subject.emtree | Cyclosporin | en_US |
dc.subject.emtree | Etretin | en_US |
dc.subject.emtree | Methotrexate | en_US |
dc.subject.emtree | Cyclosporine | en_US |
dc.subject.emtree | Dermatological agent | en_US |
dc.subject.emtree | Etretin | en_US |
dc.subject.emtree | Methotrexate | en_US |
dc.subject.emtree | Adolescent | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Body mass | en_US |
dc.subject.emtree | Child | en_US |
dc.subject.emtree | Child care | en_US |
dc.subject.emtree | Cohort analysis | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Correlation analysis | en_US |
dc.subject.emtree | Cytopenia | en_US |
dc.subject.emtree | Disease duration | en_US |
dc.subject.emtree | Disease severity | en_US |
dc.subject.emtree | Drug dose increase | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Drug safety | en_US |
dc.subject.emtree | Drug tolerability | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Gastrointestinal disease | en_US |
dc.subject.emtree | Gastrointestinal symptom | en_US |
dc.subject.emtree | Global assessment of functioning | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Hyperlipidemia | en_US |
dc.subject.emtree | Kolmogorov Smirnov test | en_US |
dc.subject.emtree | log rank test | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Multicenter study | en_US |
dc.subject.emtree | Nausea | en_US |
dc.subject.emtree | Psoriasis | en_US |
dc.subject.emtree | Psoriasis area and severity index | en_US |
dc.subject.emtree | Psoriatic arthritis | en_US |
dc.subject.emtree | Randomized controlled trial | en_US |
dc.subject.emtree | School child | en_US |
dc.subject.emtree | Skin leishmaniasis | en_US |
dc.subject.emtree | Survival rate | en_US |
dc.subject.emtree | Treatment duration | en_US |
dc.subject.emtree | Treatment outcme | en_US |
dc.subject.emtree | Vomiting | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Psoriasis | en_US |
dc.subject.emtree | Patient monitoring | en_US |
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