Department of Pulmonology and Internal Medicine, Mazumdar Shaw Medical Center, Narayana Health City, Bengaluru, India.
Department of Respiratory Medicine, Peterborough City Hospital, NHS, UK.
Indian J Tuberc. 2022 Jan;69(1):12-19. doi: 10.1016/j.ijtb.2021.03.002. Epub 2021 Mar 10.
Pleural effusions despite being so common, there is no much literature available regarding definite diagnosis for pleural effusions. Application of Light's criteria changed the approach to pleural effusion and till date remains a very useful step in the diagnosis of pleural effusions. Pleural fluid biochemistry and adenosine deaminase (ADA) enzyme levels play a significant role in the diagnosis of tubercular effusion. Studies have shown that levels of ADA are more often higher in tubercular effusion than in any other cause for it. But ADA levels can also be elevated in other types of parapneumonic effusions (PPEs), especially complicated PPEs. Hence it is difficult to distinguish a tubercular pleural effusion (TPE) from other PPEs based on pleural fluid ADA levels alone. LDH/ADA ratio as an indicator for ruling out tuberculosis was analyzed in few studies with high sensitivity and specificity. The pleural fluid cytology has a varying sensitivity, with a maximum of only 60% and it may increase with subsequent tapping. Closed pleural biopsy using a Cope or Abrams needle has a sensitivity up to 80% in cases of tuberculous effusion and 40%-73% in cases of Malignancies. Semi-rigid thoracoscopy not only allows for visualization of the pleura but also helps in procuring the biopsies under direct visualization from the abnormal looking areas. In cases of primary pleural malignancies like mesothelioma, pleurodesis can also be done in the same setting after taking the biopsy, hence reducing the number of procedures. Limitation of the semi-rigid thoracoscopy is smaller sample size and more superficial sampling of the pleura. Cryobiopsy and Electrocautery guided pleural biopsy using the IT knife are the modifications in the semi-rigid thoracoscopy to overcome the drawback of smaller sample size. While navigation band image guided pleuroscopy helps in better visualization of the vasculature of pleura during the biopsy. Management of pleural effusions has evolved over a period of time. Starting with a single criterion based on pleural fluid proteins to semi-rigid thoracoscopy. The inexhaustible research in this field suggests the desperate need for a gold standard procedure with cost effectiveness in the management of undiagnosed pleural effusions. Semi-rigid thoracoscopy has revolutionized the management of undiagnosed pleural effusions, but it has its own limitations. Various modifications have been proposed and tried to overcome the limitations to make it a cost-effective procedure.
尽管胸腔积液很常见,但关于胸腔积液的明确诊断,相关文献却并不多。Light 标准的应用改变了胸腔积液的处理方式,至今仍是胸腔积液诊断中非常有用的一步。胸腔液生化和腺苷脱氨酶 (ADA) 酶水平在结核性胸腔积液的诊断中起着重要作用。研究表明,ADA 水平在结核性胸腔积液中通常比其他任何原因引起的胸腔积液都高。但是,ADA 水平也可以在其他类型的类肺炎性胸腔积液 (PPE) 中升高,尤其是复杂的 PPE。因此,仅根据胸腔液 ADA 水平很难将结核性胸腔积液 (TPE) 与其他 PPE 区分开来。已有研究分析了 LDH/ADA 比值作为排除结核病的指标,其具有较高的灵敏度和特异性。胸腔液细胞学的灵敏度变化较大,最高只有 60%,且随着后续抽液可能会增加。使用 Cope 或 Abrams 针进行闭式胸膜活检在结核性胸腔积液中的灵敏度高达 80%,在恶性胸腔积液中的灵敏度为 40%-73%。半刚性胸腔镜不仅可以观察胸膜,还可以帮助在直视下从异常区域获取活检。在原发性胸膜恶性肿瘤(如间皮瘤)的情况下,在进行活检后也可以在同一部位进行胸膜固定术,从而减少手术次数。半刚性胸腔镜的局限性在于样本量较小,胸膜的采样较浅。冷冻活检和使用 IT 刀的电灼引导性胸膜活检是对半刚性胸腔镜的改进,以克服样本量较小的缺点。而导航带图像引导胸腔镜检查有助于在活检过程中更好地观察胸膜的血管。胸腔积液的管理在一段时间内已经发展起来。从基于胸腔液蛋白的单一标准开始,到半刚性胸腔镜。该领域的不懈研究表明,迫切需要一种具有成本效益的黄金标准程序,用于管理未明确诊断的胸腔积液。半刚性胸腔镜已经彻底改变了不明原因胸腔积液的管理,但它也有其自身的局限性。已经提出并尝试了各种改进方法来克服这些局限性,使其成为一种具有成本效益的方法。