Friedrich Rhea, Kernder Anna, Blank Norbert, Ernst Diana, Henes Jörg, Keyßer Gernot, Klemm Philipp, Krusche Martin, Meinecke Anna, Rech Jürgen, Schulz Nils, Schomburg Dirk, Vordenbäumen Stefan, Feist Eugen
Justus-Liebig-University Giessen, Giessen, Germany.
Helios Clinic Vogelsang-Gommern, Sophie-v.-Boetticher-Straße, 39245, Gommern, Germany.
Z Rheumatol. 2025 Feb;84(1):30-38. doi: 10.1007/s00393-024-01607-7. Epub 2024 Dec 12.
Adult-onset Still's disease (AOSD) is a rare autoinflammatory disease. Since it can lead to variable organ involvement, including life-threatening complications, and due to newly available therapeutic approaches, the German Society for Rheumatology and Clinical Immunology (Deutsche Gesellschaft für Rheumatologie und klinische Immunologie; DGRh) issued a newly developed S2e guideline in December 2022.
This study aims to investigate the influence of the new guideline on the diagnosis, management, and outcomes of AOSD.
Retrospective data from 168 patients diagnosed with AOSD between 2007 and 2023 (92 women and 76 men; average age 40.39 years) were captured at nine centers in Germany. Patient characteristics; results of laboratory, physical, and instrumental examinations; and therapeutic regimens were analyzed at three different timepoints.
After publication of the German AOSD guideline, the time to diagnosis was shorter (mean before: 18.56 months, mean after: 1.29 months) and fewer complications were recorded, especially with respect to macrophage activation syndrome. Although therapeutic approaches did not change over time, treatment side effects were lower in the recent observation periods. Of note, more patients have been diagnosed with cardiac (19% to 23.1%) and pulmonary (13.8% to 23.1%) manifestations of AOSD in recent years.
The new AOSD guideline has contributed to increased disease awareness, with earlier diagnosis and identification of extra-articular organ manifestations. Treatment side effects were less frequent, especially those related to glucocorticoids. However, there is still a need to further improve the management of AOSD.
成人斯蒂尔病(AOSD)是一种罕见的自身炎症性疾病。由于它可导致多种器官受累,包括危及生命的并发症,且鉴于新出现的治疗方法,德国风湿病与临床免疫学协会(Deutsche Gesellschaft für Rheumatologie und klinische Immunologie;DGRh)于2022年12月发布了新制定的S2e指南。
本研究旨在调查新指南对AOSD诊断、管理及预后的影响。
收集了2007年至2023年间在德国9个中心诊断为AOSD的168例患者(92例女性和76例男性;平均年龄40.39岁)的回顾性数据。在三个不同时间点分析了患者特征、实验室、体格和器械检查结果以及治疗方案。
德国AOSD指南发布后,诊断时间缩短(之前平均:18.56个月,之后平均:1.29个月),记录的并发症减少,尤其是巨噬细胞活化综合征方面。尽管治疗方法随时间未改变,但近期观察期内治疗副作用较低。值得注意的是,近年来更多患者被诊断出有AOSD的心脏(19%至23.1%)和肺部(13.8%至23.1%)表现。
新的AOSD指南提高了对该疾病的认识,实现了更早诊断和关节外器官表现的识别。治疗副作用更少见,尤其是与糖皮质激素相关的副作用。然而,AOSD的管理仍有进一步改善的必要。