Khandwalla Hashim E, Fasakin Yemi, El-Serag Hashem B
Sections of Gastroenterology and Health Services Research, Michael E. DeBakey Veterans Affairs Medical Center and Baylor College of Medicine, 2002 Holcombe Boulevard, Houston, TX 77030, USA.
Am J Gastroenterol. 2009 Jun;104(6):1401-5. doi: 10.1038/ajg.2009.117. Epub 2009 Apr 21.
Serum-ascites albumin gradient (SAAG) has been used extensively in the diagnostic workup of patients with ascites. A SAAG level of <1.1 g/dl is usually thought of as a result of nonportal hypertension etiologies, including malignancies, tuberculous peritonitis, and nephrotic syndrome. However, the predictive value of a low SAAG in patients with existing cirrhosis in whom the pretest probability of portal hypertension is high is not clear.
We identified all patients with a SAAG of <1.1 g/dl during a 5-year period at a single large veterans affairs medical center. Cirrhosis was defined by clinical, histological, and radiological features. Nonportal hypertension causes of low SAAG were identified, including bacterial peritonitis, peritoneal carcinomatosis, nephrogenous ascites, tuberculous peritonitis, chylous ascites, and pancreatic ascites.
We identified 92 patients (76 with cirrhosis and 16 with no cirrhosis) with ascites and a SAAG of <1.1 g/dl. Of the 76 patients with cirrhosis, only 29 (38%) had an identifiable cause, most commonly primary bacterial peritonitis (11, 38%), followed by peritoneal carcinomatosis or malignant ascites (8, 28%) and nephrotic syndrome (5, 17%). There were 47 patients with cirrhosis and a low SAAG for whom no etiology was identified. Thirty-three patients underwent a repeat paracentesis, 24 (73%) of whom changed to a high SAAG. On the other hand, the 16 patients with no cirrhosis had significantly lower SAAG (0.66 vs. 0.81), and most (12, 75%) had an identifiable cause of ascites.
Evaluation of a SAAG <1.1 g/dl in patients with known cirrhosis has low yield and is less likely to be helpful than that in patients without cirrhosis. A repeat paracentesis as part of the workup is recommended. Further studies of low SAAG cutoffs are needed.
血清腹水白蛋白梯度(SAAG)已广泛应用于腹水患者的诊断检查。SAAG水平<1.1g/dl通常被认为是非门静脉高压病因所致,包括恶性肿瘤、结核性腹膜炎和肾病综合征。然而,对于门静脉高压验前概率较高的肝硬化患者,低SAAG的预测价值尚不清楚。
我们在一家大型退伍军人事务医疗中心确定了5年内所有SAAG<1.1g/dl的患者。肝硬化由临床、组织学和放射学特征定义。确定了低SAAG的非门静脉高压病因,包括细菌性腹膜炎、腹膜癌病、肾源性腹水、结核性腹膜炎、乳糜性腹水和胰源性腹水。
我们确定了92例腹水且SAAG<1.1g/dl的患者(76例肝硬化患者和16例无肝硬化患者)。在76例肝硬化患者中,只有29例(38%)有可识别的病因,最常见的是原发性细菌性腹膜炎(11例,38%),其次是腹膜癌病或恶性腹水(8例,28%)和肾病综合征(5例,17%)。有47例肝硬化且SAAG低的患者未查明病因。33例患者接受了重复腹腔穿刺术,其中24例(73%)的SAAG变为高值。另一方面,16例无肝硬化的患者SAAG明显较低(0.66对0.81),且大多数(12例,75%)有可识别的腹水病因。
对已知肝硬化患者SAAG<1.1g/dl进行评估的阳性率较低,且与无肝硬化患者相比,帮助可能较小。建议作为检查一部分进行重复腹腔穿刺术。需要对低SAAG临界值进行进一步研究。