A week seems to be weak: tailoring duration of antibiotic treatment in Gram-negative ventilator-associated pneumonia

The optimal length of antimicrobial therapy has not been extensively studied for a great majority of infections and, in critically ill patients affected by ventilator-associated pneumonia, is a persisting and unsolved issue confronting clinicians. The integration of biomarkers, clinical judgment, and microbiologic eradication might help to define a shorter duration for some ventilator-associated pneumonia episodes due to non-fermenting Gram-negative bacilli, but until these strategies are implemented in clinical practice for individualizing antibiotic treatment, a short-course duration does not seem to tailor a long benefit.


Introduction
In the previous issue of Critical Care, Kollef and colleagues [1] compared 7 days of doripenem with 10 days of imipenem in patients with ventilator-associated pneu monia (VAP) caused by Gram-negative bacilli (GNB). Th e 7-day course arm was found to have non-signifi cant higher rates of clinical failure and mortality compared with the 10-day course arm. On the basis of the reported data, an independent data monitoring committee, which was blinded to treatment arm assignment, wisely decided to stop the present trial.
Th e impact of potential resistant microorganisms (PRMs), including non-fermenting GNB (NF-GNB), that cause nosocomial infection is a major health problem [2] and contributes to unfavorable clinical outcome and increased resource utilization [3]. Th e greater hospital mortality associated has been attributed to the increased occur rence of inadequate initial antibiotic treatment and viru lence factors [4]. Although several guidelines recommend treating patients according to defi ned patient risk factors, the consideration of intensive care unit (ICU) ecology must provide a more rational basis for selecting initial therapy for VAP patients before culture results are available [5,6].
Th e optimal length of antimicrobial therapy has not been extensively studied for a great majority of infections and, in critically ill patients aff ected by VAP, is a persisting and unsolved issue confronting clinicians. Does a shorter duration achieve a longer benefi t? Th e answer is not easy. In clinical practice, several strategies have been used for shorter antibiotic therapy in VAP. Micek and colleagues [7] performed a randomized prospective study in patients with VAP and found that reevaluation strategies decreased antibiotic duration (6.0 ± 4.9 days versus 8.0 ± 5.6 days). Chastre and colleagues [8] performed a randomized study that found that an 8-day duration of treatment was associated with an outcome similar to that of a 15-day treatment in terms of mortality, ventilator-free days, and stay in the ICU; interestingly, there were no diff erences in super-infection and relapse of pneu monia, but for primary infections caused by NF-GNB, a higher percentage of patients developed documented pulmonary infection recurrence in the 8-day than the 15-day group (41% versus 26%). Nevertheless, a retro spective study could not fi nd a higher recurrence rate in patients with NF-GNB-caused VAP who received not more than 8 days of antibiotic therapy compared with at least 9 days. Also, in the study by Kollef and colleagues [1], the clinical pulmonary infection score (CPIS) was similar for the fi rst 8 days of treatment and remained stable in the 1-week course but in the 10-day arm continued to decrease. In a study by Singh and colleagues [9] more than a decade ago, antibiotics were maintained for 10 to 21 days for patients with a high CPIS, but for

Abstract
The optimal length of antimicrobial therapy has not been extensively studied for a great majority of infections and, in critically ill patients aff ected by ventilator-associated pneumonia, is a persisting and unsolved issue confronting clinicians. The integration of biomarkers, clinical judgment, and microbiologic eradication might help to defi ne a shorter duration for some ventilator-associated pneumonia episodes due to non-fermenting Gram-negative bacilli, but until these strategies are implemented in clinical practice for individualizing antibiotic treatment, a short-course duration does not seem to tailor a long benefi t.

© 2010 BioMed Central Ltd
A week seems to be weak: tailoring duration of antibiotic treatment in Gram-negative ventilator-associated pneumonia Full list of author information is available at the end of the article those with a low CPIS (<6), the antibiotic either was free choice or was based on a reevaluation strategy after 72 hours: the antibiotic was stopped if the score decreased or remained constant and was continued if the CPIS increased. No diff er ences in mortality and ICU stay were found; how ever, less time on antibiotic therapy and lower cost were achieved in the reevaluation group.
Current guidelines for VAP recommend a fi xed duration of antibiotic therapy (7 to 8 days) for patients with uncomplicated VAP with good clinical response but not for patients with VAP episodes caused by NF-GNB [10]. One of the several unique characteristics and patho genic properties of NF-GNB is the structure of the outer membrane. In recent years, there have been some notable studies that might help clinicians to better customize treatment duration and that include the use of a single biomarker or a combination of them. Although biomarkers have been extensively investigated for the manage ment of infections from diff erent sources in critically ill patients, the number of patients with VAP included is low for solid recommendations [11]. On the other hand, microbiologic eradication might be a useful end-point [12]. Montravers and colleagues [13], in a study of quantitative cultures of bronchoscopic protected specimen brush (PSB) obtained after the administration of eff ective antibiotic therapy, showed complete eradication of the causative organisms after only 3 days of treatment in two thirds of patients. More recently, Mueller and colleagues [14] found that the use of repeat bronchoalveolar lavage decreased the duration of antibiotic therapy for NF-GNB VAP from 14 to 10 days, but this approach requires an invasive technique.

Conclusions
In summary, it is clear that a period of 7 days of antibiotic treatment in NF-GNB is not enough, and more explor atory trials for VAP due to NF-GNB are clearly not recommended. Until a strategy based on the integration of clinical judgment, dynamic changes in biomarkers, and microbiologic eradication can be implemented for tailoring antibiotic treatment in daily clinical practice, a week of antibiotic treatment seems to be weak.