Infections due to Acinetobacter baumannii have been frequently considered by clinicians and researchers not to be associated with considerable mortality [1]. Indeed, A. baumannii has been placed in the list of low-virulence pathogens [2]. These beliefs have generated relative widespread beliefs among members of the medical community that this microorganism is not a cause of considerable mortality in hospitalized patients, and have generated controversy on the issue of attributable mortality of A. baumannii infections [1, 3]. We recently performed a systematic review of the literature of cohort and case–control studies that focused on the issue [4]. The reviewed data suggest that infection with A. baumannii is associated with considerable mortality. In addition, we provided data regarding the impact of inappropriate empirical treatment of A. baumannii infections [5].

During the first 3 months of 2007, four new studies were added to the relevant literature. Specifically, investigators from the United States of America [6], Israel [7], Australia [8] and Korea [9] have provided their findings regarding the effect of A. baumannii infections in patients treated in the intensive care unit setting and also on medical and surgical wards. Another recent study from Israel compared A. baumannii bacteremia with Klebsiella pneumoniae bacteremia [10]. We summarize the findings of these five newer studies in Table 1.

Table 1 Comparison of patients with Acinetobacter baumannii (AB) infections with matched controls

The result of the main analysis of the latter study showed that A. baumannii remained significantly associated with mortality after adjustment for other important risk factors was performed [10]. Subgroup analyses in the same study again confirmed the association of A. baumannii with increased mortality in those patients not mechanically ventilated in the 30 days prior to bacteremia (multivariate analysis: odds ratio = 3.98, 95% confidence interval = 1.25–12.62) and in those patients not presenting with septic shock (odds ratio = 4.62, 95% confidence interval = 1.74–12.22).

In addition, in a recent letter to the editor, the summary findings of an older case–control study was reported that compared patients who were colonized or infected with multidrug-resistant A. baumannii with patients who were colonized or infected with multidrug-resistant Pseudomonas aeruginosa. Increased mortality was noted in the A. baumannii group (a statistically significantly result), even after adjusting for the stay in the intensive care unit [11].

Added to the findings of the previously available studies, we believe that these new data clearly show that infection of A. baumannii is associated with considerable mortality, even after adjustment for important potential confounders such as disease severity and the effect of the empirical antimicrobial treatment. While one could theoretically always argue that a specific risk factor may not have been included in the matching process of case–control and cohort studies (and thus differences in mortality may be attributed to this particular nonexamined risk factor), one has simultaneously to acknowledge the hazards of adjusting to all possible factors [12].

Someone may rightfully ask why not all relevant studies showed increased mortality of patients with A. baumannii infections compared with controls without such infections. There are various explanations for these apparently controversial findings. These explanations may include differences in patient populations, methodological characteristics of the studies, proportions of patients who received appropriate empirical treatment, as well as factors associated with the pathogen itself, including genetic factors that lead to differences in virulence.

If A. baumannii infection was not an independent contributor to increased mortality, then inappropriate treatment should not have any major effect on the outcome of patients. In an older study, mortality due to A. baumannii bacteremia treated with inappropriate antibiotics was 7.6% in excess (although not a statistically significant difference) compared with that of patients treated with appropriate antibiotics [13]. The finding of this study has to be interpreted considering that no excess mortality was found for any other bacteremia (possibly due to the small number of patients) except for bacteremia due to coagulase-negative Staphylococci [13]. In a study by our group, inappropriate treatment of A. baumannii bacteremia was associated with considerably increased (25.8%) mortality compared with that of patients treated with appropriate antibiotics – significance reached a trend (P = 0.1) since the total study population was small (40 patients) [5].

In the recently published study by Kwon and colleagues, a 44.5% increased mortality was noted in the group of patients with imipenem nonsusceptible A. baumannii bacteremia treated with inappropriate antibiotics compared with those patients with imipenem nonsusceptible A. baumannii bacteremia who received appropriate treatment (P = 0.007) [9]. Moreover, when 30-day mortality was examined in the total study population of cases and controls, a 43.7% excess mortality was noted when A. baumannii bacteremia was treated with inappropriate versus appropriate antibiotic therapy (P < 0.001) [9]. Also, in a study regarding risk factors for mortality related to nosocomial pneumonia due to various Gram-negative, Gram-positive and fungal pathogens, A. baumannii was the second most commonly cultured pathogen of 132 patients. In this study A. baumannii was significantly more predominant in nonsurvivors than in survivors (13.6% versus 5.1%, P = 0.04). Of the nonsurvivors, 85.9% received inappropriate therapy – inappropriate antibiotic therapy was independently associated with mortality (odds ratio = 14.5, 95% confidence interval = 5.08–41.44) in the study [14].

We believe that a fair interpretation of the available evidence, especially in light of the recently published findings, suggests that attributable mortality due to A. baumannii is no longer a controversial issue. The attention of the scientific community with interest in this pathogen should therefore be directed to the development and introduction of new antimicrobial agents effective against multidrug-resistant and pandrug-resistant A. baumannii, as well as to the implementation of infection control measures that may help control the evolving problem of A. baumannii infections that have taken epidemic dimensions in several parts of the word, especially in critically ill patients.