Chen Yi-Cheng, Hsu Chao-Wei, Chang Ming-Yang, Yeh Chau-Ting
Department of Gastroenterology-Hepatology, Liver Research Unit, Division of Hepatology, Taipei, Taiwan.
BMC Res Notes. 2013 Sep 2;6:349. doi: 10.1186/1756-0500-6-349.
Severe acute exacerbation in chronic hepatitis B could lead to mortality in some patients unless timely liver transplantation is performed. The baseline bilirubin level has been reported to be an important prognostic factor for mortality. Here we conducted a prospective observational study to examine the clinical performance of this predictor.
Twenty-one consecutive chronic hepatitis B patients experiencing severe acute exacerbation were treated with either telbivudine or entecavir. The clinical characteristics at baseline and week-2 were documented and correlated with mortality.
Of the 21 patients included, 9 had baseline bilirubin >10 mg/dL. Four of these 9 patients (44.4%) eventually died, whereas all other patients survived. During the initial 2-week period, the change of bilirubin was -1.2 mg/dl in the survivors, but was +8.05 mg/dl in the mortalities (P = 0.009). When this on-treatment factor was combined, 5 of the 21 patients had baseline bilirubin > 10 mg/dL plus an increase of bilirubin level at week-2. Of these 5 patients, 4 (80%) died. Thus, by combining the baseline and on-treatment bilirubin levels, a positive predictive value of 80% and a negative predictive value of 100% could be achieved. Other significant on-treatment mortality predictors (at week-2) included higher international normalized ratio of prothrombin time (2.75 vs. 1.3, P = 0.004), higher model for end-stage liver disease score (30 vs. 17, P = 0.006), lower alpha-fetoprotein level (36.3 vs. 459.6 ng/mL, P = 0.039), and more rapid deterioration of the estimated glomerular filtration rate (eGFR) (P = 0.008). Interestingly, during the course, deterioration of eGFR was statistically significant in entecavir-treated (P = 0.028), but not in telbivudine-treated patients. Additionally, the patients treated with telbivudine had significant increase in serum alpha-fetoprotein (27.9 to 191.9 ng/ml, P = 0.046) in the first 2 weeks, whereas the corresponding feature was not found in those treated with entecavir (P = 0.139).
In this prospective observational study, we discovered that the baseline and on-treatment bilirubin levels should be combined to achieve a better predictive value. Telbivudine might have a renoprotective effect in addition to its efficacy in viral suppression in patients with severe acute exacerbation.
慢性乙型肝炎的严重急性加重可能导致部分患者死亡,除非及时进行肝移植。据报道,基线胆红素水平是死亡率的重要预后因素。在此,我们进行了一项前瞻性观察性研究,以检验该预测指标的临床性能。
连续21例经历严重急性加重的慢性乙型肝炎患者接受替比夫定或恩替卡韦治疗。记录基线和第2周时的临床特征,并与死亡率进行关联分析。
纳入的21例患者中,9例基线胆红素>10mg/dL。这9例患者中有4例(44.4%)最终死亡,而其他所有患者均存活。在最初的2周内,存活者的胆红素变化为-1.2mg/dl,而死亡者为+8.05mg/dl(P=0.009)。当将该治疗期因素纳入时,21例患者中有5例基线胆红素>10mg/dL且第2周时胆红素水平升高。这5例患者中有4例(80%)死亡。因此,通过结合基线和治疗期胆红素水平,可实现80%的阳性预测值和100%的阴性预测值。其他显著的治疗期死亡率预测指标(第2周时)包括较高的国际标准化比值的凝血酶原时间(2.75对1.3,P=0.004)、较高的终末期肝病模型评分(30对17,P=0.006)、较低的甲胎蛋白水平(36.3对459.6ng/mL,P=0.039)以及估计肾小球滤过率(eGFR)更快的恶化(P=0.008)。有趣的是,在此过程中,恩替卡韦治疗组的eGFR恶化具有统计学意义(P=0.028),而替比夫定治疗组则无。此外,替比夫定治疗的患者在最初2周内血清甲胎蛋白显著升高(从27.9至191.9ng/ml,P=0.046),而恩替卡韦治疗组未发现相应特征(P=0.139)。
在这项前瞻性观察性研究中,我们发现应结合基线和治疗期胆红素水平以获得更好的预测价值。替比夫定在严重急性加重患者中除了具有病毒抑制作用外,可能还具有肾脏保护作用。