Laterre Pierre-François
Department of Critical Care Medicine, St Luc University Hospital, Catholic University of Louvain, Brussels, Belgium.
Curr Opin Infect Dis. 2008 Aug;21(4):393-8. doi: 10.1097/QCO.0b013e328306ef2a.
Intra-abdominal infection management remains debated and evidence-based recommendations are often lacking despite numerous studies. These controversies are mainly explained by the limited number of powered and well designed randomized controlled trials. This review focuses on recent studies on antibiotic therapy for intra-abdominal infections and in particular for the management of severe acute pancreatitis.
For community-acquired intra-abdominal infection, early source control and antibiotic selection are well codified. In severe forms, every hour of delay between shock and antibiotherapy initiation reduces hospital survival. Antibiotics dose adjustment and continuous intravenous administration are suggested in critically ill patients and for difficult-to-treat pathogens. Shorter antibiotic treatment duration seems to offer similar clinical cure rates compared with prolonged therapy and could reduce emergence of resistance. For multidrug-resistant bacteria, the newly developed agents indications need to be better defined. In severe acute pancreatitis, antibiotic prophylaxis does not prevent necrosis infection nor does it reduce surgery requirement or mortality. Antibiotics should be given on demand. Infectious complications in pancreatitis are not reduced by probiotic prophylaxis and mortality is increased.
There is a growing evidence to support early, dose-adjusted, antimicrobial therapy in severe intra-abdominal infection, together with shorter treatment duration if source control is achieved. This could reduce emergence of resistance without affecting clinical cure rates. In severe acute necrotizing pancreatitis, antibiotic and probiotic prophylaxis to reduce infection or mortality should be avoided.
尽管有大量研究,但腹腔内感染的管理仍存在争议,且往往缺乏循证医学推荐。这些争议主要是由于有足够样本量且设计良好的随机对照试验数量有限。本综述重点关注腹腔内感染抗生素治疗的近期研究,尤其是重症急性胰腺炎的治疗。
对于社区获得性腹腔内感染,早期源头控制和抗生素选择已有明确规范。在重症病例中,休克与开始抗生素治疗之间每延迟一小时,都会降低患者的住院生存率。对于重症患者和难治疗病原体,建议调整抗生素剂量并持续静脉给药。与延长治疗相比,缩短抗生素治疗疗程似乎能提供相似的临床治愈率,且可减少耐药性的出现。对于多重耐药菌,新研发药物的适应证需要进一步明确。在重症急性胰腺炎中,抗生素预防不能预防坏死感染,也不能减少手术需求或降低死亡率。应按需使用抗生素。益生菌预防不能降低胰腺炎的感染并发症,反而会增加死亡率。
越来越多的证据支持在重症腹腔内感染中尽早进行剂量调整的抗菌治疗,若能实现源头控制,则治疗疗程可缩短。这可以减少耐药性的出现,而不影响临床治愈率。在重症急性坏死性胰腺炎中,应避免使用抗生素和益生菌预防以降低感染或死亡率。