Nicolas Amélie, Leroy Sylvie, Mouthon Luc, Uzunhan Yurdagul, Cottin Vincent, Mekinian Arsene, Queyrel Viviane, Hachulla Eric, Gachet Benoit, Launay David, Martis Nihal
Department of Internal Medicine and Clinical Immunology, Centre de Référence des Maladies Auto-immunes Systémiques Rares du Nord et Nord-Ouest de France (CeRAINO), University Hospital of Lille, Rue Michel Polonovski, Hôpital Huriez, CHU Lille, F-59000 Lille, France.
Univ. Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, Lille, France.
Ther Adv Musculoskelet Dis. 2023 May 9;15:1759720X231159712. doi: 10.1177/1759720X231159712. eCollection 2023.
Interstitial lung disease (ILD) is the leading cause of mortality in systemic sclerosis (SSc).
We performed an overview of the diagnostic approaches, follow-up and treatment strategies used in France for the management of SSc-associated ILD (SSc-ILD).
A structured nationwide online survey was submitted to participants the French Medical Societies for Internal Medicine and Pneumology, and research groups on SSc-ILD from May 2018 to June 2020. The 79 multiple-choice and 9 open-ended questions covered the screening of ILD at baseline, monitoring of patients with established SSc-ILD and its management. Fourteen optional vignettes exploring different clinical phenotypes of SSc-ILD were submitted to evaluate therapeutic decisions.
All of the 93 participants screened SSc patients for ILD at baseline with 83 (89%) participants relying on a systematic chest computed tomography (CT) scan. Pulmonary function tests (PFT) were prescribed by 87 (94%) participants at baseline and during follow-up. Treatment was started based on abnormal PFT (95%), chest CT scan characteristics (89%), worsening dyspnoea (72%) and drop in SpO during 6-min walk tests (66%). First-line therapy was cyclophosphamide (CYC) (89%), mycophenolate mofetil (MMF) (83%) and prednisone (73%). Rituximab as second-line immunosuppressive therapy (41%) was preferred to antifibrotic agents (18%), and a median daily prednisone dose of 10 mg (interquartile range, 10-15) was prescribed by 73% participants. Extensive SSc-ILD with worsening PFT (95%), regardless of diffusing capacity for carbon monoxide values and skin extension, were more likely to be treated, and CYC was favoured over MMF ( < 0.01). Extensive SSc-ILD with disease duration of less than 5 years was also a criterium for treatment initiation.
This overview of practices in diagnosis, follow-up and treatment of SSc-ILD in France describes real-life management of patients. It highlights heterogeneity in this management and gaps in current strategies that should be addressed to improve and harmonize clinical practices in SSc-ILD.
间质性肺病(ILD)是系统性硬化症(SSc)的主要死亡原因。
我们对法国用于管理系统性硬化症相关间质性肺病(SSc-ILD)的诊断方法、随访及治疗策略进行了综述。
全国性结构化在线调查
2018年5月至2020年6月,向法国内科和肺病医学协会的参与者以及SSc-ILD研究小组开展了全国性结构化在线调查。79个多项选择题和9个开放式问题涵盖了基线时ILD的筛查、确诊SSc-ILD患者的监测及其管理。提交了14个探索SSc-ILD不同临床表型的可选病例 vignettes,以评估治疗决策。
所有93名参与者在基线时均对SSc患者进行了ILD筛查,其中83名(89%)参与者依靠系统性胸部计算机断层扫描(CT)。87名(94%)参与者在基线和随访期间开具了肺功能测试(PFT)。治疗基于PFT异常(95%)、胸部CT扫描特征(89%)、呼吸困难加重(72%)以及6分钟步行试验期间SpO下降(66%)而开始。一线治疗为环磷酰胺(CYC)(89%)、霉酚酸酯(MMF)(83%)和泼尼松(73%)。作为二线免疫抑制治疗,利妥昔单抗(41%)比抗纤维化药物(18%)更受青睐,73%的参与者开具的泼尼松中位日剂量为10毫克(四分位间距,10-15)。无论一氧化碳弥散量值和皮肤受累范围如何,PFT恶化的广泛SSc-ILD(95%)更有可能接受治疗,且CYC比MMF更受青睐(P<0.01)。疾病持续时间少于5年的广泛SSc-ILD也是开始治疗的标准。
此次对法国SSc-ILD诊断、随访及治疗实践的综述描述了患者的实际管理情况。它突出了这种管理的异质性以及当前策略中的差距,应加以解决以改善和统一SSc-ILD的临床实践。