Sanduzzi Zamparelli Stefano, Sanduzzi Zamparelli Alessandro, Bocchino Marialuisa
Division of Pneumology, A. Cardarelli Hospital, 80131 Naples, Italy.
Department of Clinical Medicine and Surgery, Section of Respiratory Diseases, University Federico II, Azienda Ospedaliera dei Colli-Monaldi Hospital, 80131 Naples, Italy.
Diagnostics (Basel). 2023 Jul 21;13(14):2437. doi: 10.3390/diagnostics13142437.
Interstitial lung diseases (ILDs) are a group of heterogeneous diseases characterized by inflammation and/or fibrosis of the lung interstitium, leading to a wide range of clinical manifestations and outcomes. Over the years, the literature has demonstrated the increased diagnostic accuracy and confidence associated with a multidisciplinary approach (MDA) in assessing diseases involving lung parenchyma. This approach was recently emphasized by the latest guidelines from the American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Association for the diagnosis of ILDs.
In this review, we will discuss the role, composition, and timing of multidisciplinary diagnosis (MDD) concerning idiopathic pulmonary fibrosis, connective tissue disease associated with ILDs, hypersensitive pneumonia, and idiopathic pneumonia with autoimmune features, based on the latest recommendations for their diagnosis.
The integration of clinical, radiological, histopathological, and, often, serological data is crucial in the early identification and management of ILDs, improving patient outcomes. Based on the recent endorsement of transbronchial cryo-biopsy in idiopathic pulmonary fibrosis guidelines, an MDA helps guide the choice of the sampling technique, obtaining the maximum diagnostic performance, and avoiding the execution of more invasive procedures such as a surgical lung biopsy. A multidisciplinary team should include pulmonologists, radiologists, pathologists, and, often, rheumatologists, being assembled regularly to achieve a consensus diagnosis and to review cases in light of new features.
The literature highlighted that an MDA is essential to improve the accuracy and reliability of ILD diagnosis, allowing for the early optimization of therapy and reducing the need for invasive procedures. The multidisciplinary diagnosis of ILDs is an ongoing and dynamic process, often referred to as a "working diagnosis", involving the progressive integration and re-evaluation of clinical, radiological, and histological features.
间质性肺疾病(ILDs)是一组异质性疾病,其特征为肺间质的炎症和/或纤维化,可导致广泛的临床表现和预后。多年来,文献表明多学科方法(MDA)在评估累及肺实质的疾病时,诊断准确性和可信度有所提高。美国胸科学会、欧洲呼吸学会、日本呼吸学会和拉丁美洲胸科学会关于ILDs诊断的最新指南最近强调了这种方法。
在本综述中,我们将根据特发性肺纤维化、与ILDs相关的结缔组织病、过敏性肺炎和具有自身免疫特征的特发性肺炎的最新诊断建议,讨论多学科诊断(MDD)的作用、组成和时机。
临床、放射学、组织病理学以及通常的血清学数据的整合对于ILDs的早期识别和管理至关重要,可改善患者预后。基于最近特发性肺纤维化指南中对经支气管冷冻活检的认可,MDA有助于指导采样技术的选择,获得最大诊断效能,并避免执行更具侵入性的程序,如外科肺活检。多学科团队应包括肺科医生、放射科医生、病理科医生,通常还包括风湿病学家,应定期组建以达成共识诊断,并根据新特征复查病例。
文献强调,MDA对于提高ILD诊断的准确性和可靠性至关重要,可实现治疗的早期优化并减少侵入性程序的需求。ILDs的多学科诊断是一个持续且动态的过程,通常称为“工作诊断”,涉及临床、放射学和组织学特征的逐步整合和重新评估。