ArticleBMC pulmonary medicine2026
From guidelines to reality: how do physicians really manage sarcoidosis?
Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Associations of Systemic Immune-Inflammation Index and Hematological Markers with Symptom Burden and Radiological Stage in Sarcoidosis.Diagnostics (Basel, Switzerland) · 2026Article
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundGuidelines exist for the diagnosis, treatment, and follow-up of sarcoidosis; however, considerable variation in clinical practice remains. This study aimed to evaluate the approaches of pulmonologists in Turkey to the management of patients with sarcoidosis through a survey.
methodsA web-based survey consisting of 26 questions regarding diagnostic and therapeutic approaches and follow-up strategies in patients with sarcoidosis was sent to the email groups of specialists. The study was designed as a multicenter project and targeted only pulmonology physicians. The responses provided by the participating physicians were analyzed statistically.
resultsNinety-seven pulmonologists participated in the survey. Stage I–II sarcoidosis was most frequently encountered, and endobronchial ultrasound was the preferred diagnostic modality across all stages. Routine evaluations commonly included laboratory tests, thoracic imaging, and pulmonary function testing. Systemic therapy was rarely initiated in stage I–II disease but was routinely used in stage III–IV disease, with glucocorticoids as first-line treatment and methotrexate as the most common second-line agent. Antifibrotic therapy was considered by approximately one-third of physicians for stage IV sarcoidosis. Follow-up intervals were generally 3–6 months for untreated patients and 3 months for treated patients.
conclusionsThere are individual and institutional variations in the diagnosis, treatment, and follow-up of sarcoidosis in Turkey, particularly in diagnostic methods and treatment duration. Considering the well-recognized environmental and racial differences in disease presentation, our findings highlight the need for a national diagnostic and treatment guideline for sarcoidosis.
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