Habib Shahid, Yarlagadda Sandeep, Carreon Teresia A, Schader Lindsey M, Hsu Chiu-Hsieh
Liver Institute PLLC, 5295 E. Knight Dr, Tucson, AZ 85712, USA.
Tucson Medical Center, 5301 E Grant Rd, Tucson, AZ 85712, USA.
Gastroenterology Res. 2020 Oct;13(5):199-207. doi: 10.14740/gr1255. Epub 2020 Oct 31.
Infection in acute-on-chronic liver failure (ACLF) patients is known to cause higher mortality. The current approach is to culture all patient samples. There are no published data evaluating fungal infections in acutely decompensated patients. In this study, we aim to identify clinical factors predictive of infections within ACLF patients and assess workup compliance within 24 h of hospital admission.
We retrospectively analyzed the charts of 457 ACLF patients seen at the University of Arizona between January 1, 2014 and December 31, 2014. We used logistic regression to identify potential risk indicators for bacterial, fungal, and any infections. In order to proceed to a systemic infection workup, the following parameters were assessed: complete blood count, urinalysis, urine culture, bacterial blood culture, chest X-ray, and ascitic fluid analysis in patients with ascites. Additionally, serological markers were also assessed in patient samples. Systemic inflammatory response syndrome (SIRS) was defined as the presence of two or more of the following criteria: temperature > 38 °C or < 36 °C, heart rate > 90 beats/min, respiratory rate > 20 breaths/min, white blood cell count > 12,000 or < 4,000 cells/mm or > 10% bands.
An established infection was observed in 60.61% of ACLF patients. SIRS criteria predicted infections with concordance statistic (C-statistic) of 0.71 (odds ratio (OR) 6.85, 95% confidence interval (CI): 4.33, 10.85) for any infection, 0.63 (OR 2.88, 95% CI: 1.96, 4.23) for bacterial infection, and 0.53 (OR 1.32, 95% CI: 0.59, 2.96) for fungal infection. After including other significant variables (over 10 additional variables), predictive ability improved, C-statistic 0.83 (95% CI: 0.77, 0.90) for any infection and 0.71 (95% CI: 0.65, 0.77) for bacterial infections. The combination of model for end-stage liver disease (MELD) and hemoglobin (Hb) predicted fungal infections with C-statistic 0.74 (95% CI: 0.63, 0.84). Workup within 24 h of admission was obtained in 12% of patients.
Fungal infections in ACLF patients results in an increased mortality rate. Elevated MELD and low Hb in combination predict fungal infections. Compliance is very poor to obtain diagnostic workup efficiently, better tools are needed to predict infection upon admission.
已知急性慢性肝衰竭(ACLF)患者发生感染会导致更高的死亡率。目前的方法是对所有患者样本进行培养。尚无已发表的数据评估急性失代偿患者中的真菌感染情况。在本研究中,我们旨在确定ACLF患者感染的临床预测因素,并评估入院24小时内的检查依从性。
我们回顾性分析了2014年1月1日至2014年12月31日在亚利桑那大学就诊的457例ACLF患者的病历。我们使用逻辑回归来确定细菌、真菌及任何感染的潜在风险指标。为了进行系统性感染检查,评估了以下参数:全血细胞计数、尿液分析、尿培养、细菌血培养、胸部X光以及有腹水患者的腹水分析。此外,还对患者样本中的血清学标志物进行了评估。全身炎症反应综合征(SIRS)定义为存在以下两项或更多标准:体温>38°C或<36°C、心率>90次/分钟、呼吸频率>20次/分钟、白细胞计数>12,000或<4,000个细胞/mm或>10%杆状核细胞。
60.61%的ACLF患者观察到确诊感染。SIRS标准预测感染的一致性统计量(C统计量)对于任何感染为0.71(比值比(OR)6.85,95%置信区间(CI):4.33,10.85),对于细菌感染为0.63(OR 2.88,95%CI:1.96,4.23),对于真菌感染为0.53(OR 1.32,95%CI:0.59,2.96)。纳入其他显著变量(超过10个额外变量)后,预测能力有所提高,对于任何感染C统计量为0.83(95%CI:0.77,0.90),对于细菌感染为0.71(95%CI:0.65,0.77)。终末期肝病模型(MELD)和血红蛋白(Hb)的组合预测真菌感染的C统计量为0.74(95%CI:0.63,0.84)。12%的患者在入院24小时内进行了检查。
ACLF患者中的真菌感染导致死亡率增加。MELD升高和Hb降低共同预测真菌感染。有效进行诊断检查的依从性非常差,需要更好的工具来预测入院时的感染情况。