dc.contributor.author | Topaloğlu, Rezan | |
dc.contributor.author | Gülhan, Bora | |
dc.contributor.author | Çelegen, Kübra | |
dc.contributor.author | İnözü, Mihriban | |
dc.contributor.author | Hayran, Mutlu | |
dc.contributor.author | Düzova, Ali | |
dc.contributor.author | Ozaltin, Fatih | |
dc.date.accessioned | 2021-06-02T10:40:05Z | |
dc.date.available | 2021-06-02T10:40:05Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 2296-2360 | |
dc.identifier.uri | http://dx.doi.org/10.3389/fped.2019.00313 | |
dc.identifier.uri | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682627/ | |
dc.identifier.uri | http://hdl.handle.net/11655/23858 | |
dc.description.abstract | Background: Since the early 2000s rituximab (RTX) has been thought of as an alternative treatment for steroid-sensitive nephrotic syndrome (SSNS) and steroid-resistant nephrotic syndrome (SRNS)., Objective: This study aimed to determine the effects of RTX treatment on disease outcome and growth in pediatric SSNS and SRNS patients., Materials and Methods: The medical records of pediatric SSNS and SRNS patients that began RTX treatment at the mean age of 10.8 ± 5.1 years between 2009 and 2017 were retrospectively reviewed. Additionally, the effect of RTX on growth was evaluated based on patient height, weight, and BMI z scores., Results: The study included 41 children, of which 21 had SSNS and 20 had SRNS. Mean age at diagnosis of NS was 5.8 ± 4.7 years. Mean duration of post-RTX treatment follow-up was 2.3 ± 1.6 years. Among the SSNS patients, 6 and 11 patients were steroid free and calcineurin inhibitor free at the last follow-up visit, respectively. The 1-year cumulative steroid and calcineurin inhibitor doses both decreased after RTX treatment, as compared to before RTX (P = 0.001 and P = 0.015, respectively). The median height z-score at the time of RTX initiation was −1.2 and the median height z-score at the last follow-up visit was −0.6 (P = 0.044). The median BMI z-score decreased from 1.6 (IQR; 0.9–3.0) at the time RTX was initiated to 1.1 IQR; [(−0.7)−2.5] at the last follow-up visit (P = 0.007). At the last follow-up visit 4 SRNS patients had complete remission and 4 had partial remission. The 1-year cumulative steroid dosage in the SRNS patients decreased significantly after RTX, as compared to before RTX (P = 0.001). The median height z-score at the time of RTX initiation was −0.8 and the median height z-score at the last follow-up visit was −0.7 (P = 0.81). The median BMI z-score decreased from 0.3 at the time RTX was initiated to −0.1 at the last follow-up visit (P = 0.11)., Conclusion: RTX has a more positive effect on disease outcome and growth in SSNS patients than in those with SRNS. | |
dc.language.iso | en | |
dc.relation.isversionof | 10.3389/fped.2019.00313 | |
dc.rights | Attribution 4.0 United States | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.title | Rituximab For Children With Difficult-To-Treat Nephrotic Syndrome: Its Effects On Disease Progression And Growth | |
dc.title.alternative | Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:eu-repo/semantics/publishedVersion | |
dc.relation.journal | Frontiers In Pediatrics | |
dc.contributor.department | Çocuk Sağlığı ve Hastalıkları | |
dc.identifier.volume | 7 | |
dc.description.index | PubMed | |
dc.description.index | WoS | |
dc.description.index | Scopus | |