Arnaud Laurent, Fabry-Vendrand Caroline, Todea Remus, Vidal Blandine, Cottin Juliette, Bureau Isabelle, Bouée Stéphane, Thabut Gabriel
Service de Rhumatologie, Hôpitaux Universitaires de Strasbourg, Centre National de Référence des Maladies Systémiques Auto-immunes Rares Est Sud-Ouest, INSERM UMRS-1109, Université de Strasbourg, Strasbourg, France
AstraZeneca, Tour Carpe Diem, Courbevoie, France.
Lupus Sci Med. 2025 Feb 18;12(1):e001428. doi: 10.1136/lupus-2024-001428.
Oral glucocorticoids (OCS) remain one of the most important treatments for SLE but are associated with damage. Evidence regarding the real-world use of OCS in nationwide SLE populations is currently lacking. The aim of this study was to analyse OCS use and SLE treatments in French patients with SLE at the national level.
The nationwide French health insurance claims database, which contains pseudonymised data for ≈66 million people, was used. Prevalent patients with SLE (International Classification of Diseases, 10th Revision code M32, recorded as a chronic condition or associated with hospital stay) were identified over the year 2019. SLE treatments were captured through actual drug deliveries by pharmacies and mean daily OCS doses (prednisone equivalent) were calculated for the year 2019.
The 2019 French prevalent SLE population comprised 31 852 patients (86.3% of women, with a mean age of 49.7 (±15.9) years) with a mean disease duration of 7.1 (±6.2) years. Among these, 48.3% were treated with OCS. The mean daily OCS dose was ≤5 mg/day in 35.9%, more than 5 mg but <7.5 mg/day in 6.4% and ≥7.5 mg/day in 6.0%. The use of other SLE treatments was significantly increased in patients with higher doses of OCS (p<0.0001). Potential complications of OCS, including cardiovascular diseases, infections and osteoporosis, were significantly increased in patients with SLE receiving more than 5 mg of OCS per day (p<0.0001, for all). Strikingly, 13.6% of patients receiving mean daily OCS doses >5 mg/day were not treated with antimalarial, immunosuppressant or biologic drugs for SLE.
In total, 48.2% of French patients with SLE were treated with OCS in 2019, including 12.4% at a mean dose >5 mg/day, with an increased risk of OCS complications and a limited use of antimalarials, immunosuppressants or biologics. These results highlight the urgent need for the implementation of more robust OCS-sparing strategies in SLE.
口服糖皮质激素(OCS)仍然是系统性红斑狼疮(SLE)最重要的治疗方法之一,但会带来损害。目前缺乏关于全国SLE人群中OCS实际使用情况的证据。本研究的目的是在国家层面分析法国SLE患者中OCS的使用情况和SLE治疗情况。
使用了包含约6600万人匿名数据的法国全国健康保险理赔数据库。通过识别2019年患有SLE的现患患者(国际疾病分类第10版代码M32,记录为慢性病或与住院相关)。通过药房实际药品发放情况获取SLE治疗信息,并计算2019年的平均每日OCS剂量(泼尼松等效剂量)。
2019年法国SLE现患人群包括31852名患者(86.3%为女性,平均年龄49.7(±15.9)岁),平均病程7.1(±6.2)年。其中,48.3%接受OCS治疗。平均每日OCS剂量≤5mg/天的患者占35.9%,超过5mg但<7.5mg/天的患者占6.4%,≥7.5mg/天的患者占6.0%。OCS剂量较高的患者使用其他SLE治疗方法的比例显著增加(p<0.0001)。接受SLE治疗且每日OCS剂量超过5mg的患者发生OCS潜在并发症(包括心血管疾病、感染和骨质疏松症)的比例显著增加(所有p<0.0001)。令人惊讶的是,平均每日OCS剂量>5mg/天的患者中有13.6%未接受抗疟药、免疫抑制剂或生物制剂治疗SLE。
2019年,总计48.2%的法国SLE患者接受了OCS治疗,其中12.4%的患者平均剂量>5mg/天,OCS并发症风险增加,抗疟药、免疫抑制剂或生物制剂的使用有限。这些结果凸显了在SLE中实施更有力的OCS节约策略的迫切需求。