Antibiotic prophylaxis for surgical site infection in people undergoing liver transplantation

Background Surgical site infection is more frequent in liver transplantation than in other types of solid organ transplantation with different antibiotics. Studies have shown that the rate of surgical site infection varies from 8.8% to 37.5% after liver transplantation. Therefore, antimicrobial prophylaxis is likely an essential tool for reducing these infections. However, the literature lacks evidence indicating the best prophylactic antibiotic regimen that can be used for liver transplantation. Objectives To assess the benefits and harms of antibiotic prophylactic regimens for surgical site infection in people undergoing liver transplantation. Search methods We searched the Cochrane Hepato‐Biliary Group Controlled Trials Register, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, Science Citation Index Expanded and Latin American Caribbean Health Sciences Literature (LILACS). The most recent search was performed on 11 September 2015. Selection criteria All eligible randomised clinical trials comparing any antibiotic regimen versus placebo, versus no intervention or versus another antibiotic regimen for surgical site infection in liver transplant recipients, regardless of age, sex and reason for transplantation. Quasi‐randomised studies and other observational studies were considered for data on harm if retrieved with search results for randomised clinical trials. Data collection and analysis Two review authors selected relevant trials, assessed risk of bias of studies and extracted data. Main results The electronic search identified 786 publications after removal of duplicates. From this search, only one seemingly randomised clinical trial, published in form, fulfilled the inclusion criteria of this review. This trial was conducted at Shiraz Transplant Centre, Shiraz, Iran, where investigators randomly assigned a total of 180 consecutive liver transplant recipients. We judged the overall risk of bias of the trial published in form as high. Researchers reported no numerical data but mentioned that 163 participants met the inclusion criteria after randomisation, and hence were included in the analyses. Most probably, the 17 excluded participants were high‐risk liver transplant recipients. Trial authors concluded that they could find no differences between the two antibiotic regimens ‐ ceftriaxone plus metronidazole versus ampicillin‐sulbactam plus ceftizoxime ‐ when given to liver transplant recipients. Review authors could not