An Updated Review on Treatment of Pulmonary Sarcoidosis and Multisystem Disease Monitoring
摘要
Sarcoidosis presents a complex challenge for clinicians in discerning the need for initiation of potentially toxic, but disease-modifying immunosuppressive therapies targeting granulomatous inflammation. In this review, we summarize the latest research on indications for treatment in high-risk pulmonary sarcoidosis and evidence supporting the most frequently utilized therapies. This article also addresses the initial evaluation of extrapulmonary manifestations of sarcoidosis to guide appropriate triage for multidisciplinary management of this highly morbid condition.
Recent findingsFor the management of high-risk pulmonary sarcoidosis, glucocorticoids remain the first-line therapeutic intervention for improving both symptoms and pulmonary function. While methotrexate is recommended as a steroid-sparing agent for persistent pulmonary sarcoidosis, there is an increasing role for the adjunctive use of TNF-alpha inhibition in refractory disease.
SummaryThe decision to initiate immunosuppressive therapy for sarcoidosis must be informed by the consideration of long-term risk for irreversible end-organ injury, the presence of significant impairment to an individual’s quality of life, and the risk for drug toxicity from treatment.