Antimicrobial resistance in chronic liver disease

被引:23
作者
Patel, Vishal C. [1 ,2 ,3 ,4 ]
Williams, Roger [1 ,2 ,4 ]
机构
[1] Inst Hepatol London, 111 Coldharbour Lane, London SE5 9NT, England
[2] Fdn Liver Res, 111 Coldharbour Lane, London SE5 9NT, England
[3] Kings Coll Hosp NHS Fdn Trust, Inst Liver Studies & Transplantat, Denmark Hill, London SE5 9RS, England
[4] Kings Coll London, Fac Life Sci & Med, James Black Ctr, Sch Immunol & Microbial Sci, 125 Coldharbour Lane, London SE5 9NU, England
关键词
Chronic liver disease; Cirrhosis; Multi-drug resistant organism; Antibiotic resistance; Antibiotic stewardship; Rapid diagnostic tests; Resistome; Immune modulation; Faecal microbial transplantation; SPONTANEOUS BACTERIAL PERITONITIS; DRUG-RESISTANCE; GUT MICROBIOME; PROBIOTIC VSLNUMBER-3; CIRRHOTIC-PATIENTS; BETA-BLOCKERS; THERAPY; INFECTIONS; TRANSLOCATION; STEWARDSHIP;
D O I
10.1007/s12072-019-10004-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
High levels of antimicrobial drug resistance deleteriously affecting the outcome of treatment with antibacterial agents are causing increasing concern worldwide. This is particularly worrying in patients with cirrhosis with a depressed immune system and heightened susceptibility to infection. Antibiotics have to be started early before results of microbiological culture are available. Current guidelines for the empirical choice of antibiotics in this situation are not very helpful, and embracing antimicrobial stewardship including rapid de-escalation of therapy are not sufficiently emphasised. Multi-drug resistant organism rates to quinolone drugs of up to 40% are recorded in patients with spontaneous bacterial peritonitis on prophylactic antibiotics, leading to a break-through recurrence of intra-peritoneal infection. Also considered in this review is the value of rifaximin-alpha, non-selective beta-blockers, and concerns around proton pump inhibitor drug use. Fecal microbial transplantation and other gut-targeting therapies in lessening gut bacterial translocation are a promising approach, and new molecular techniques for determining bacterial sensitivity will allow more specific targeted therapy.
引用
收藏
页码:24 / 34
页数:11
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