Sharma Karan, Fultariya Lekhini, Reddy Mallimala Priya, Shah Kavita, Sharma Vishal
Internal Medicine, Poonam Multispeciality Hospital, Ahmedabad, IND.
Internal Medicine, Gujarat Cancer Society (GCS) Medical College, Hospital and Research Centre, Ahmedabad, IND.
Cureus. 2023 Aug 11;15(8):e43319. doi: 10.7759/cureus.43319. eCollection 2023 Aug.
Introduction While Light's criteria exhibit high sensitivity (98%) in detecting exudative pleural effusions, the capacity to rule out transudates is relatively limited. A previous study showed that approximately one-fifth of patients with congestive cardiac failure on diuretics also met the criteria for exudate. This study compares the diagnostic value of Light's criteria, the serum-effusion albumin gradient (SEAG) method, and pleural effusion glucose levels for accurately categorizing pleural effusion as transudate or exudate. Methodology We conducted this cross-sectional observational study in a tertiary care hospital in Ahmedabad, India. Two hundred patients with pleural effusion undergoing thoracentesis were included. Laboratory parameters measured in pleural fluid analysis included pleural fluid protein, pleural fluid lactate dehydrogenase (LDH), pleural fluid albumin, and pleural fluid glucose. Serum protein, serum LDH, and serum albumin were also collected. Mean values and standard deviations (SDs) were calculated for analysis. Results A significant difference was observed in the mean value of exudative and transudative effusions for each parameter (pleural fluid protein/serum fluid protein ratio, pleural fluid LDH/serum fluid LDH ratio, pleural fluid LDH, SEAG, and pleural fluid glucose) (P < 0.001). Light's criteria demonstrated the highest efficacy in diagnosing exudates (accuracy = 97.50%), while SEAG demonstrated the highest efficacy in diagnosing transudates (accuracy = 97.50%). Conclusion SEAG is an effective alternative diagnostic tool for identifying transudates misclassified by Light's criteria. Its use can contribute to prompt diagnosis and timely treatment of patients with pleural effusion, improving patient outcomes.
虽然莱特标准在检测渗出性胸腔积液方面具有较高的敏感性(98%),但其排除漏出液的能力相对有限。先前的一项研究表明,约五分之一使用利尿剂的充血性心力衰竭患者也符合渗出液的标准。本研究比较了莱特标准、血清-胸水白蛋白梯度(SEAG)法和胸水葡萄糖水平对准确将胸腔积液分类为漏出液或渗出液的诊断价值。
我们在印度艾哈迈达巴德的一家三级护理医院进行了这项横断面观察性研究。纳入了200例接受胸腔穿刺术的胸腔积液患者。胸水分析中测量的实验室参数包括胸水蛋白、胸水乳酸脱氢酶(LDH)、胸水白蛋白和胸水葡萄糖。还收集了血清蛋白、血清LDH和血清白蛋白。计算平均值和标准差(SD)进行分析。
每个参数(胸水蛋白/血清蛋白比值、胸水LDH/血清LDH比值、胸水LDH、SEAG和胸水葡萄糖)的渗出液和漏出液平均值存在显著差异(P < 0.001)。莱特标准在诊断渗出液方面显示出最高的效能(准确率 = 97.50%),而SEAG在诊断漏出液方面显示出最高的效能(准确率 = 97.50%)。
SEAG是一种有效的替代诊断工具,可用于识别被莱特标准误分类的漏出液。其应用有助于胸腔积液患者的及时诊断和治疗,改善患者预后。