Qualitative evaluation of pharmacological strategy for connective tissue diseases with Guillain-Barré syndrome: a systematic review

对伴有格林-巴利综合征的结缔组织疾病的药物治疗策略进行定性评价:系统评价

阅读:2

Abstract

OBJECTIVE: To systematically evaluate the pharmacological management of Guillain-Barré syndrome occurring in the context of connective tissue diseases (CTD-GBS) and to investigate the relative efficacy of different treatment regimens on neurological outcomes. METHODS: Case reports and series regarding CTD-GBS were systematically retrieved from PubMed, Embase, and Web of Science databases. A Generalized Linear Mixed Model (GLMM) was utilized to assess independent associations between treatment regimens and neurological improvement, adjusting for key covariates including mechanical ventilation (as a baseline severity marker) and the year of publication. RESULTS: A total of 105 CTD-GBS patients were identified, with systemic lupus erythematosus (SLE) being the most prevalent subtype (n=73). Multivariable GLMM analysis suggested that, compared to intravenous immunoglobulin (IVIG) monotherapy, intensive combination regimens specifically glucocorticoids combined immunosuppressants (GC + IS) demonstrated a potential association with higher odds of clinical improvement (adjusted Odds Ratio [aOR] = 30.90; 95% CI: 6.58-145.00; p < 0.001). Mechanical ventilation was identified as an independent negative predictor of recovery (aOR = 0.43; p = 0.037), while the year of publication did not significantly influence outcomes (p = 0.344). Descriptive analysis within the SLE-GBS subgroup corroborated these trends, with the GC + IS regimen achieving a clinical improvement rate of 88.9%. CONCLUSION: Preliminary evidence suggests that intensive immunosuppressive combination therapy, notably GC + IS, may offer advantages over traditional IVIG monotherapy in improving short-term neurological outcomes for CTD-GBS patients. However, given the reliance on retrospective case-based evidence and the potential for confounding by indication, these findings should be interpreted as hypothesis-generating clinical clues rather than definitive guidelines. Future large-scale, prospective studies utilizing standardized functional assessment scales are urgently required to validate these preliminary observations.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。