Gerke Alicia K
Pulmonary and Critical Care Medicine, University of Iowa, 200 Hawkins Drive, Iowa City, IA 52242, USA.
J Clin Med. 2024 Jan 27;13(3):738. doi: 10.3390/jcm13030738.
The management of pulmonary sarcoidosis is a complex interplay of disease characteristics, the impact of medications, and patient preferences. Foremost, it is important to weigh the risk of anti-granulomatous treatment with the benefits of lung preservation and improvement in quality of life. Because of its high spontaneous resolution rate, pulmonary sarcoidosis should only be treated in cases of significant symptoms due to granulomatous inflammation, lung function decline, or substantial inflammation on imaging that can lead to irreversible fibrosis. The longstanding basis of treatment has historically been corticosteroid therapy for the control of granulomatous inflammation. However, several corticosteroid-sparing options have increasing evidence for use in refractory disease, inability to taper steroids to an acceptable dose, or in those with toxicity to corticosteroids. Treatment of sarcoidosis should be individualized for each patient due to the heterogeneity of the clinical course, comorbid conditions, response to therapy, and tolerance of medication side effects.
肺结节病的管理是疾病特征、药物影响和患者偏好之间复杂的相互作用。首先,权衡抗肉芽肿治疗的风险与肺保护及生活质量改善的益处非常重要。由于其高自发缓解率,肺结节病仅在因肉芽肿性炎症、肺功能下降或影像学上显著炎症可导致不可逆纤维化而出现明显症状的情况下才应进行治疗。长期以来,治疗的基础一直是使用皮质类固醇疗法来控制肉芽肿性炎症。然而,有越来越多的证据表明,几种皮质类固醇节省疗法可用于难治性疾病、无法将类固醇减至可接受剂量或对皮质类固醇有毒性的患者。由于临床病程、合并症、对治疗的反应以及对药物副作用的耐受性存在异质性,结节病的治疗应针对每位患者进行个体化。