19. INFECTION Infection remains a major source of morbidity and mortality in patients with MCS despite significant progress in the development of more durable VADs and advances in surgical techniques over the last decade [25, 176]. The most recent INTERMACS report showed that infection was still the fourth most common cause of death within 1 year after implant [25]. The International Society of Heart and Lung Transplantation recognized the importance of clearly defining infection in this unique population and commissioned an international working group of experts to develop definitions of infection in patients with MCS that were published in 2011 [363]. Hence, these international definitions are recommended for defining infection in Europe and are part of this European consensus document. 19.1 Evidence for preventing infection in preimplantation of mechanical circulatory support Nosocomial bloodstream infection (BSI) has been reported as a major source of morbidity and mortality in patients with MCS [472]. In general the risk of infection associated with catheters depends on type, location and duration in situ [473]. A recent study from the International Society of Heart and Lung Transplantation IMACS Registry, to which the EUROMACS Registry contributes, showed that early-onset BSI was associated with a significantly increased 24-month mortality rate and that 85% of these BSIs were not device related. There is an opportunity for infection prevention practices to decrease the BSI event rate in the intensive care unit and post-surgical settings, which may affect the 24-month survival rate [474]. Catheter-associated urinary tract infection is the most common nosocomial infection and is preventable by limiting the number of days of catheterization. As with indwelling catheters, a general proactive approach in patients with MCS of changing or reducing the duration of the catheters where possible to reduce the risk of infection is recommended as per other intensive care unit and post-surgical patients [475]. 19.2 Evidence for antimicrobial prophylaxis perioperatively In earlier studies, antimicrobial prophylaxis was broad spectrum and given for a prolonged duration. Two published multicentre surveys reported a wide variation in the different types of antimicrobial prophylaxis used in MCS implant surgery [476, 477]. More recently, MCS centres follow more general cardiac surgery prophylaxis guidelines and do not include broad spectrum gram-negative or fungal coverage. Cardiac surgery prophylaxis guidelines usually recommend a cephalosporin (cefazolin or cefuroxime) for 24–48 h, which can provide sufficient gram-positive and gram-negative coverage [26, 478–481]. Routine antifungal prophylaxis is not recommended [26]. 19.3 Evidence for managing infection in patients with mechanical circulatory support Whenever clinically feasible, infection should be excluded or appropriately treated before MCS implantation. In candidates for MCS before implantation, evaluation of suspected infection is no different from that in other patients and should be guided by clinical signs and symptoms. In patients with unexplained fever and/or leucocytosis, evaluation should include blood cultures, urinalysis, urine culture and chest radiogram, with additional imaging as needed until a diagnosis is established and the source has been treated and cleared. In all MCS candidates with suspected or proven infection, expert infection consultation is advisable. MCS candidates with BSI should be treated with targeted antimicrobial therapy [363]. For an active infection, there is insufficient evidence to define a minimum duration of antimicrobial therapy before proceeding to MCS implantation [26]. However, delaying MCS implantation is recommended where feasible until the following general goals are met: control of the source (e.g. incision and drainage of abscess, removal of infected catheter or tooth extraction for dental abscess); blood culture results have become negative after appropriate antibiotic treatment commenced; and illness and sepsis are resolved. Candidates for MCS with other infections (e.g. pneumonia, urinary tract infection) should be treated with appropriate antimicrobial therapy until resolution. Expert infection consultation should be sought in all cases of infection preimplantation and throughout the perioperative period. 19.4 Evidence for assessing a patient for postoperative infection after implantation of mechanical circulatory support The initial evaluation should include a careful history and review of symptoms. Physical examination of surgical wounds, driveline exit site and review of the LT-MCS device function are essential because early detection and treatment of a localized process may prevent progression to more serious VAD infections [26, 363]. In case of driveline exit site infection, the treatment includes increased frequency of dressing change, topical antiseptics and prolonged or lifelong antibiotics (suppressive treatment). In case of ascending driveline infection, surgical revision may be an option.