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The Role of the Multidisciplinary Evaluation of Interstitial Lung Diseases: Systematic Literature Review of the Current Evidence and Future Perspectives

机译:间质肺病患者多学科评价的作用:系统文献综述当前证据和未来的观点

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The opportunity of a multidisciplinary evaluation for the diagnosis of interstitial pneumonias highlighted a major change in the diagnostic approach to diffuse lung disease. The new American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Latin American Thoracic Society guidelines for the diagnosis of idiopathic pulmonary fibrosis have reinforced this assumption and have underlined that the exclusion of connective tissue disease related lung involvement is mandatory, with obvious clinical and therapeutic impact. The multidisciplinary team discussion consists in a moment of interaction among the radiologist, pathologist and pulmonologist, also including the rheumatologist when considered necessary, to improve diagnostic agreement and optimize the definition of those cases in which pulmonary involvement may represent the first or prominent manifestation of an autoimmune systemic disease. Moreover, the proposal of classification criteria for interstitial lung disease with autoimmune features (IPAF) represents an effort to define lung involvement in clinically undefined autoimmune conditions. The complexity of autoimmune diseases, and in particular the lack of classification criteria defined for pathologies such as anti-synthetase syndrome, makes the involvement of the rheumatologist essential for the correct interpretation of the autoimmune element and for the application of classification criteria, that could replace clinical pictures initially interpreted as IPAF in defined autoimmune disease, minimizing the risk of misdiagnosis. The aim of this review was to evaluate the available evidence about the efficiency and efficacy of different multidisciplinary team approaches, in order to standardize the professional figures and the core set procedures that should be necessary for a correct approach in diagnosing patients with interstitial lung disease.
机译:多学科评价对间质肺炎的诊断的机会强调了弥漫性肺病诊断方法的重大变化。新的美国胸部社会,欧洲呼吸社会,日本呼吸社会和拉丁美洲胸胸部社会诊断的准则加强了这种假设,并强调了结缔组织疾病相关肺部受累的是强制性的,具有明显的临床和治疗的影响。多学科团队讨论在考虑必要时,放射科医生,病理学家和肺部学家之间的相互作用的时刻组成,以改善诊断协议,并优化肺部受累可能代表肺部受累的情况的定义自身免疫系统性疾病。此外,具有自身免疫特征(IPAF)的间质性肺病的分类标准的提议代表了在临床上未定义的自身免疫条件下定义肺部受累的努力。自身免疫疾病的复杂性,特别是对抗合成酶综合征如病理定义的缺乏分类标准,使风湿病学者的涉及能够对自身免疫元素的正确解释和应用程序的应用来说,这可能取代临床图片最初被解释为IPAF在定义的自身免疫疾病中,最大限度地减少了误诊的风险。本综述的目的是评估有关不同多学科团队方法的效率和功效的可用证据,以规范专业人格和核心集合程序,这些程序应该在诊断间质肺病患者中进行正确的方法。

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