<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Du Y</submitter><funding>Xi'an medical key project for science and technology</funding><funding>Tangdu hospital discipline promotion project</funding><funding>Shaanxi Innovative Team for Science and Technology</funding><funding>Tangdu hospital foundation for social recruitment talent</funding><funding>National Natural Science Foundation of China</funding><funding>Tangdu hospital clinical research project</funding><funding>the National Natural Science Foundation of China</funding><funding>Tangdu hospital innovation development foundation</funding><funding>Shaanxi Province Health Research and Innovation Team for Cognitive Dysfunction Disease</funding><pagination>180-191</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11752089</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To determine the efficacy and safety of combined low-dose rituximab with conventional therapy for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) treatment.&lt;h4>Methods&lt;/h4>Total 73 patients with CIDP were enrolled for the retrospective cohort study, and divided into conventional first-line therapy cohort (n = 40) and combined low-dose rituximab (100 mg per infusion) cohort (n = 33). The outcome measures include scores of I-RODS, mRS, INCAT, ONLS, TSS, and COMPASS 31 scale at baseline and regular four visits (4, 16, 28, and 52 weeks), as well as proportion of favorable response and outcome, corticosteroids dosage, and deterioration occurrence during follow-up.&lt;h4>Results&lt;/h4>Compared to conventional therapy cohort, combined rituximab cohort presented bette</pubmed_abstract><journal>Annals of clinical and translational neurology</journal><pubmed_title>Efficacy and safety of combined low-dose rituximab regimen for chronic inflammatory demyelinating polyradiculoneuropathy.</pubmed_title><pmcid>PMC11752089</pmcid><funding_grant_id>2024JCRH022</funding_grant_id><funding_grant_id>2023TD-06</funding_grant_id><funding_grant_id>2021SHRC011</funding_grant_id><funding_grant_id>2024RS-CXTD-87</funding_grant_id><funding_grant_id>2024JH-YXZD-0047</funding_grant_id><funding_grant_id>2021LCYJ040</funding_grant_id><funding_grant_id>2018QYTS010</funding_grant_id><funding_grant_id>82171406</funding_grant_id><funding_grant_id>82271457</funding_grant_id><funding_grant_id>2019QYTS002</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Hou T</pubmed_authors><pubmed_authors>Du Y</pubmed_authors><pubmed_authors>Hao Y</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Jiang P</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Dang Y</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Yan Q</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Chen F</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>Yao D</pubmed_authors><pubmed_authors>Zhu W</pubmed_authors><pubmed_authors>Zhu T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and safety of combined low-dose rituximab regimen for chronic inflammatory demyelinating polyradiculoneuropathy.</name><description>&lt;h4>Objective&lt;/h4>To determine the efficacy and safety of combined low-dose rituximab with conventional therapy for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) treatment.&lt;h4>Methods&lt;/h4>Total 73 patients with CIDP were enrolled for the retrospective cohort study, and divided into conventional first-line therapy cohort (n = 40) and combined low-dose rituximab (100 mg per infusion) cohort (n = 33). The outcome measures include scores of I-RODS, mRS, INCAT, ONLS, TSS, and COMPASS 31 scale at baseline and regular four visits (4, 16, 28, and 52 weeks), as well as proportion of favorable response and outcome, corticosteroids dosage, and deterioration occurrence during follow-up.&lt;h4>Results&lt;/h4>Compared to conventional therapy cohort, combined rituximab cohort presented bette</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-05T11:35:26.766Z</modification><creation>2025-04-05T11:35:26.766Z</creation></dates><accession>S-EPMC11752089</accession><cross_references><pubmed>39660535</pubmed><doi>10.1002/acn3.52270</doi></cross_references></HashMap>