Lam John C, Stokes William
Division of Infectious Diseases, Department of Medicine, University of California Los Angeles, Los Angeles, CA.
Provincial Laboratory for Public Health, Alberta Precision Laboratories, Calgary.
J Clin Gastroenterol. 2023 Sep 1;57(8):774-781. doi: 10.1097/MCG.0000000000001871.
Pyogenic liver abscesses (PLAs) are a suppurative infection of the hepatic parenchyma responsible for significant morbidity and mortality. PLAs are categorized into a variety of mechanisms: (1) via the portal vein, (2) through the biliary tract, (3) via the hepatic artery, (4) from trauma, (5) contiguously via direct extension, and (6) cryptogenically. The pathogenesis of PLA, which informs treatment, can often be discerned based on host factors, clinical presentation, and causative microorganisms. The Streptococcus anginosus group, hypervirulent Klebsiella pneumoniae , and multidrug-resistant gram-negative pathogens have emerged as microbiologically challenging organisms to treat. The identification of hypervirulent K. pneumoniae should prompt for assessment for metastatic spread and consideration of prolonged antimicrobial treatment. Abdominal imaging is indispensable in characterizing PLAs and facilitating source control interventions. Source control remains the most critical aspect of PLA management, followed by antimicrobial therapy. Empiric antibiotics for PLAs are informed by the suspected etiology of PLA formation. Duration of antimicrobial therapy is individualized and dependent on multiple components, including the success of achieving source control, host factors, mechanism of PLA development, and the illness course of the individual-factoring in clinical, biochemical, and radiographic parameters.
化脓性肝脓肿(PLA)是肝实质的化脓性感染,可导致显著的发病率和死亡率。PLA可分为多种机制:(1)通过门静脉,(2)通过胆道,(3)通过肝动脉,(4)由创伤引起,(5)通过直接蔓延相邻组织,以及(6)病因不明。PLA的发病机制为治疗提供依据,通常可根据宿主因素、临床表现和致病微生物来判断。咽峡炎链球菌群、高毒力肺炎克雷伯菌和多重耐药革兰氏阴性病原体已成为在微生物学上难以治疗的病原体。高毒力肺炎克雷伯菌的鉴定应促使对转移性扩散进行评估,并考虑延长抗菌治疗时间。腹部影像学对于PLA的特征性诊断和促进源头控制干预不可或缺。源头控制仍然是PLA管理中最关键的方面,其次是抗菌治疗。PLA的经验性抗生素治疗依据PLA形成的可疑病因来确定。抗菌治疗的持续时间因人而异,取决于多个因素,包括实现源头控制的成功程度、宿主因素、PLA发展机制以及个体的病程,同时要考虑临床、生化和影像学参数。