Suppr超能文献

小儿复发性多软骨炎的临床表现和治疗的系统文献综述。

Systematic Literature Review of the Presentation and Management of Pediatric Relapsing Polychondritis.

机构信息

University of Nevada, Reno School of Medicine, USA.

Department of Otolaryngology - Head and Neck Surgery, University of California, Davis, USA.

出版信息

Ann Otol Rhinol Laryngol. 2024 Nov;133(11):933-939. doi: 10.1177/00034894241275474. Epub 2024 Aug 20.

Abstract

INTRODUCTION

Pediatric Relapsing Polychondritis (RP) is a rare autoimmune disorder that causes inflammation and damage to cartilage in children. Common symptoms include pain, swelling and deformities in the ears, nose, trachea, joints, and eyes. The lack of research on the pediatric population necessitates further evaluation of the literature on pediatric RP to summarize existing patterns in presentation, management, and treatment.

METHODS

A systematic review was conducted on PubMed and Embase from 1947 to April 2023 on RP in patients under 21 years old abiding by the 2020 PRISMA checklist. Only patient presentations meeting McAdam criteria for RP and including information on management were included.

RESULTS

From the 304 initial studies, 54 studies were included for final analysis with a total of 68 patients, who were predominantly female (65%). With a median diagnostic delay of 1 year, the mean age of onset was 12 years old. The most common symptoms on presentation included bilateral auricular chondritis (69%), nasal cartilage inflammation (62%), and respiratory tract chondritis (63%). The most commonly reported information in the literature for the initial workup usually included CT/MRI (72%), bronchoscopy (57%), biopsy (51%), and labs (88%), which most commonly displayed elevated ESR (59%). The most common medications were corticosteroids (91%) and methotrexate (35%) and the most common procedural treatment was tracheostomy (38%). The most efficacious treatment options were monoclonal antibodies (87%, n = 15) and corticosteroids (66%, n = 62) used in 22% and 91% of patients, respectively. The most commonly used monoclonal antibody therapy was infliximab (13%, n = 9).

CONCLUSION

The most common presentation for pediatric RP includes chondritis of the ear, nose, and respiratory tract. The most effective treatment options include corticosteroids and monoclonal antibody therapy, such as infliximab. Our findings highlight increasing remission achieved with anti-rheumatic drugs and monoclonal antibody treatment, especially alongside corticosteroids.

摘要

简介

儿科复发性多软骨炎(RP)是一种罕见的自身免疫性疾病,可导致儿童软骨发炎和损伤。常见症状包括耳朵、鼻子、气管、关节和眼睛疼痛、肿胀和畸形。由于对儿科人群的研究不足,需要进一步评估儿科 RP 的文献,以总结现有表现、管理和治疗模式。

方法

对 1947 年至 2023 年 4 月期间在 21 岁以下患者中进行的关于 RP 的 PubMed 和 Embase 进行了系统评价,遵循 2020 年 PRISMA 清单。仅纳入符合 McAdam 标准的 RP 患者表现并包含管理信息的研究。

结果

从 304 项初始研究中,有 54 项研究最终纳入分析,共有 68 名患者,其中大多数为女性(65%)。中位诊断延迟 1 年,平均发病年龄为 12 岁。就诊时最常见的症状包括双侧耳廓软骨炎(69%)、鼻软骨炎(62%)和呼吸道软骨炎(63%)。文献中最常报告的初始检查通常包括 CT/MRI(72%)、支气管镜检查(57%)、活检(51%)和实验室检查(88%),其中最常显示 ESR 升高(59%)。最常用的药物是皮质类固醇(91%)和甲氨蝶呤(35%),最常用的程序治疗是气管切开术(38%)。最有效的治疗选择是单克隆抗体(87%,n=15)和皮质类固醇(66%,n=62),分别在 22%和 91%的患者中使用。最常用的单克隆抗体治疗是英夫利昔单抗(13%,n=9)。

结论

儿科 RP 的最常见表现包括耳、鼻和呼吸道的软骨炎。最有效的治疗选择包括皮质类固醇和单克隆抗体治疗,如英夫利昔单抗。我们的发现强调了抗风湿药物和单克隆抗体治疗,特别是与皮质类固醇联合治疗,可实现更高的缓解率。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验