Bartoletti Michele, Baldassarre Maurizio, Domenicali Marco, Lewis Russell E, Giannella Maddalena, Antognoli Agnese, Rinaldi Matteo, Zaccherini Giacomo, Verucchi Gabriella, Marconi Lorenzo, Tamè Mariarosa, Berardi Sonia, Napoli Lucia, Siniscalchi Antonio, Fabbri Angela, Biselli Maurizio, Tufoni Manuel, Pavarin Raimondo M, Trevisani Franco, Viale Pierluigi, Bernardi Mauro, Caraceni Paolo
Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
U.O. Infectious Disease, S. Orsola-Malpighi University Hospital, Bologna, Italy.
Open Forum Infect Dis. 2020 Nov 4;7(11):ofaa453. doi: 10.1093/ofid/ofaa453. eCollection 2020 Nov.
Bacterial and fungal infections (BFIs) are frequent in patients with cirrhosis and often trigger acute-on-chronic liver failure (ACLF). This prospective observational study aims to describe the interactions between BFI and ACLF in terms of mortality and related risk factors.
We performed a 2-center prospective observational study enrolling hospitalized patients with cirrhosis admitted for acute decompensation. Data were recorded at admission and during hospitalization. Survival was recorded up to 1 year.
Among the 516 patients enrolled, 108 (21%) were infected at admission, while an additional 61 patients (12%) developed an infection during hospital stay. In the absence of ACLF, the 1-year mortality rate of patients with BFI did not differ from that of patients without BFI (33% vs 31%; = .553). In contrast, those with ACLF triggered or complicated by BFI had a significantly higher mortality rate than those who remained free from BFI (75% vs 54%; = .011). Competing risk analysis showed that the negative impact of ACLF-related BFI on long-term prognosis was independent from Model for End-stage Liver Disease (MELD) incorporating serum sodium concentration score, comorbidity, and basal C-reactive protein level. Finally, multivariable logistic regression showed that higher MELD score ( < .001), QuickSOFA score ≥2 points ( = .007), and secondary bloodstream ( = .022) and multidrug-resistant pathogen isolation ( = .030) were independently associated with ACLF in patients with BFI.
This large prospective study indicated that the adverse impact of BFI on long-term survival in decompensated cirrhosis is not universal but is limited to those patients who also develop ACLF. Both disease severity and microbiological factors predispose infected decompensated patients to ACLF.
细菌和真菌感染(BFIs)在肝硬化患者中很常见,并且常常引发慢加急性肝衰竭(ACLF)。这项前瞻性观察性研究旨在描述BFIs与ACLF在死亡率及相关危险因素方面的相互作用。
我们进行了一项双中心前瞻性观察性研究,纳入因急性失代偿而住院的肝硬化患者。在入院时和住院期间记录数据。记录患者长达1年的生存情况。
在纳入的516例患者中,108例(21%)在入院时被感染,另有61例患者(12%)在住院期间发生感染。在没有ACLF的情况下,BFIs患者的1年死亡率与无BFIs患者的死亡率无差异(33%对31%;P = 0.553)。相比之下,由BFIs引发或并发ACLF的患者死亡率显著高于未发生BFIs的患者(75%对54%;P = 0.011)。竞争风险分析表明,与ACLF相关的BFIs对长期预后的负面影响独立于纳入血清钠浓度评分、合并症和基础C反应蛋白水平的终末期肝病模型(MELD)。最后,多变量逻辑回归显示,较高的MELD评分(P < 0.001)、快速序贯器官衰竭评估(QuickSOFA)评分≥2分(P = 0.007)、继发性血流感染(P = 0.022)和多重耐药病原体分离(P = 0.030)与BFIs患者发生ACLF独立相关。
这项大型前瞻性研究表明,BFIs对失代偿期肝硬化患者长期生存的不利影响并非普遍存在,而是仅限于那些同时发生ACLF的患者。疾病严重程度和微生物学因素均使感染的失代偿患者易发生ACLF。