Discussion
Almost half of severely injured patients admitted to ICU who survived the first 48 hours, developed at least one infectious complication during hospital stay. Although there was no difference in ISS and physiological parameters, patients who later developed infectious complications had more often MODS, needed more blood products, and used more hospital resources (more ventilator days, longer stay in ICU and in hospital). There was however no difference in mortality between patients who later developed infectious complications and patients who did not. One per cent of the studied population died of an infectious complication.
Pneumonia was the most common infection followed by fracture-related infection. Median time to infection development was 12 days, although different infections developed during different time periods after admission.
Literature is equivocal on the relation between mortality and infectious complications. Some authors report higher mortality rates in patients who developed infectious complications,20 21 whereas others, including our own data, showed similar mortality rates.17 This discrepancy might be partly explained by the different infectious complications that have been reported; sepsis is for example more lethal than pneumonia or surgical site infections.21
Previous studies have shown comparable results regarding percentage and type of infectious complications; roughly half of severely injured patients developed infectious complications and the most common infectious complication was of respiratory origin.17 20 Different infections developed at different times during admission; Cole et al showed the same singularity in their study with early development of respiratory infections, and positive blood cultures, and later development of other infections.17 Results were however not entirely comparable, since different types of infections were registered in both studies. Several studies have shown that the neutrophil response is dependent on which bacterial species the cell is attempting to kill. It is likely that different types of infections are caused by different bacteria, and that some bacteria are better resistant to neutrophils than others, resulting in different times of development of infections.22 23 Possibly, exhaustion of the innate immune system with decreased response of neutrophils plays an important role in the selection of bacteria causing different infectious complications during different times after injury.
In our study age, the need for urgent laparotomy and MODS were independent predictors for development of infectious complications in patients with polytrauma. Other studies reported other independent predictors such as admission shock parameters,17 gender, blood transfusions, AIS chest, and GCS on scene.20 In our study, there was no difference in admission shock parameters between patients who later developed infections and patients who did not, although we did demonstrate that blood transfusion was associated with infectious complications. This association has been reported by others as well.17 20 24 25 The fact that admission shock parameters in our study were not associated with infections could be possibly explained by the fact that in our cohort parameters such as blood pressure and hemoglobin were within normal ranges on arrival in ED. This phenomenon in which severely injured patients in smaller service areas with short transport times do not have deranged physiologic parameters on arrival in the ED has been described earlier.6 7 These patients do not have the time to deteriorate because they are in the hospital before blood pressure, BD, and hemoglobin will change distinctly. One could argue that these patients were not severely injured at all. This is contradicted by the fact that patients had an ISS of 29, 31% had a pelvic fracture, 24% needed an urgent laparotomy, and they were all admitted to the ICU since that was one of the inclusion criteria. The studied cohort included the sickest patients with trauma admitted to our major trauma center. It is likely that the need for urgent laparotomy in our study reflects shock parameters in other studies. Furthermore, it is known that laparotomy as a second hit has an effect on the immune response and is associated with development of infections.20
As we have previously shown, MODS-related and ARDS-related death in trauma has decreased over the years and our previous studies have shown MODS- and ARDS-related death of less than 5%.5 6 Since both MODS/ARDS and infections are neutrophil-mediated complications, it is tempting to speculate that infectious complications are the residual (and less severe) effect of the diminishing more severe MODS and ARDS.
This theory seems to be in line with the timing of the complications. Nowadays, time to MODS development is early after injury (3 days after injury) as we have shown in previous studies,6 whereas median time to development of infectious complications was 12 (7–20) days in this study. This means that MODS precedes infectious complications. Since MODS-related mortality was very low in our cohort (2%), surviving patients may later develop infectious complications. This philosophy is confirmed by the fact that MODS was an independent predictor for infectious complications.
All patients admitted to ICU received SDD, selective oropharyngeal decontamination, and systemic prophylaxis with an intravenous third-generation cephalosporin. This policy was introduced to reduce the incidence of ICU-acquired respiratory tract infections.26 One could dispute that this could have influenced the micro-bacterial growth. However, first of all, all included patients received this regimen of antibiotic prophylaxis, so there was no difference in patients who later developed infectious complications and those who did not. Second, it has been previously shown that there was no overall ecological effect of prolonged antibiotic prophylaxis by counting resistant micro-organisms in ICU in countries where there is relatively low rates of resistant micro-organisms.27
One of the limitations of this study is that it was conducted at a single institution in which the clinical treatment and research were conducted by the same clinicians. Another limitation is that data on the type of bacteria that caused infections were not routinely collected. Furthermore, no pre-existing medical conditions were documented.
In conclusion, in this population of severely injured patients almost half of patients developed an infectious complication. With improvements of trauma and critical care death by complications such as MODS and ARDS has decreased. This success has likely resulted in a shift to less deleterious infectious complications. Future studies need to focus on the role of the immune system (eg, neutrophil function) on the development of infectious complications. Early recognition of development these complications might lead to possible prevention. This could also have a considerable beneficial impact on the use of hospital resources.