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Early-Onset Ventilator-Associated Pneumonia in Adults Randomized Clinical Trial: Comparison of 8 versus 15 Days of Antibiotic Treatment

  • Gilles Capellier ,

    Affiliations Réanimation médicale adulte, Pôle Urgences-SAMU-Réanimation CHU, Besancon, Doubs, France, EA 3920, Univ-Fcomte, Besancon, Doubs, France

  • Hélène Mockly,

    Affiliation Pôle pharmaceutique, CHU, Besancon, Doubs, France

  • Claire Charpentier,

    Affiliation Service de réanimation chirurgicale adulte, Hôpital Central, Nancy, Lorraine, France

  • Djillali Annane,

    Affiliation Service médico-chirurgical adulte, CHU Raymond Poincaré - Assistance Publique Hôpitaux de Paris, Garches, Ile de France, France

  • Gilles Blasco,

    Affiliation Service de réanimation chirurgicale adulte, CHU, Besancon, Doubs, France

  • Thibault Desmettre,

    Affiliations Réanimation médicale adulte, Pôle Urgences-SAMU-Réanimation CHU, Besancon, Doubs, France, EA 3920, Univ-Fcomte, Besancon, Doubs, France

  • Antoine Roch,

    Affiliations Service de Réanimation médicale - URMITE, Assistance Publique Hôpitaux de Marseille, Marseille, Bouches du Rhône, France, CNRS-UMR 6236, Université de la Méditerranée Aix-Marseille II, Marseille, Bouches du Rhône, France

  • Christophe Faisy,

    Affiliation Service de réanimation médicale adulte, HEGP-Assistance Publique Hôpitaux de Paris, Paris, Ile de France, France

  • Joel Cousson,

    Affiliation Service de réanimation polyvalente adulte, Hôpital Robert Debré, Reims, Champagne, France

  • Samuel Limat,

    Affiliations Pôle pharmaceutique, CHU, Besancon, Doubs, France, EA 4267, Univ-Fcomte, Besancon, Doubs, France

  • Mariette Mercier,

    Affiliations Laboratoire de Biostatistique, CHU, Besancon, Doubs, France, EA3181, Univ-Fcomte, Besancon, Doubs, France

  • Laurent Papazian

    Affiliations Service de Réanimation médicale - URMITE, Assistance Publique Hôpitaux de Marseille, Marseille, Bouches du Rhône, France, CNRS-UMR 6236, Université de la Méditerranée Aix-Marseille II, Marseille, Bouches du Rhône, France

Early-Onset Ventilator-Associated Pneumonia in Adults Randomized Clinical Trial: Comparison of 8 versus 15 Days of Antibiotic Treatment

  • Gilles Capellier, 
  • Hélène Mockly, 
  • Claire Charpentier, 
  • Djillali Annane, 
  • Gilles Blasco, 
  • Thibault Desmettre, 
  • Antoine Roch, 
  • Christophe Faisy, 
  • Joel Cousson, 
  • Samuel Limat



The optimal treatment duration for ventilator-associated pneumonia is based on one study dealing with late-onset of the condition. Shortening the length of antibiotic treatment remains a major prevention factor for the emergence of multiresistant bacteria.


To demonstrate that 2 different antibiotic treatment durations (8 versus 15 days) are equivalent in terms of clinical cure for early-onset ventilator-associated pneumonia.


Randomized, prospective, open, multicenter trial carried out from 1998 to 2002.


The primary endpoint was the clinical cure rate at day 21. The mortality rate was evaluated on days 21 and 90.


225 patients were included in 13 centers. 191 (84.9%) patients were cured: 92 out of 109 (84.4%) in the 15 day cohort and 99 out of 116 (85.3%) in the 8 day cohort (difference = 0.9%, odds ratio = 0.929). 95% two-sided confidence intervals for difference and odds ratio were [−8.4% to 10.3%] and [0.448 to 1.928] respectively. Taking into account the limits of equivalence (10% for difference and 2.25 for odds ratio), the objective of demonstrative equivalence between the 2 treatment durations was fulfilled. Although the rate of secondary infection was greater in the 8 day than the 15 day cohort, the number of days of antibiotic treatment remained lower in the 8 day cohort. There was no difference in mortality rate between the 2 groups on days 21 and 90.


Our results suggest that an 8-day course of antibiotic therapy is safe for early-onset ventilator-associated pneumonia in intubated patients.

Trial Registration NCT01559753


Pneumonia is the second-most-common nosocomial infection and accounts for around 15% of infections acquired in hospitals. The incidence rate varies from 1% in medical departments to 20% in intensive care units (ICU!) [1]. Intubation and mechanical ventilation (MV) are known risk factors for the acquisition of nosocomial pneumonia [2]. Ventilator-associated pneumonia (VAP) is a common, serious condition and therefore poses a real public health problem, particularly in ICU where the mortality rate for ventilated patients lies above 50% [3], [4]. VAP is defined as having either an early- or a late-onset according to whether it begins before or after the first 5 to 7 days of hospitalization [4]. During early-onset ventilator-associated pneumonia (EOVAP), the normal bacterial flora consists of Haemophilus influenzae, Streptococcus pneumoniae, methicillin-sensitive Staphylococcus aureus, Moraxella catarrhalis and non multiresistant Escherichia coli [5], [6]. The bacteria isolated may vary due to antibiotic treatment, recent hospitalization and ICU ecology [7], [8], [9], [10]. Several recent studies have evaluated the impact of antibiotic treatment duration on clinical cure and recurrence rates. In a randomized prospective study, Chastre et al. found no clear advantage in prolonging antibiotic treatment to 15 days compared with 8 days when treating late-onset VAP [11]. Other authors [12], [13], [14] have evaluated the use of clinical scores (CPIS) and biological markers (Procalcitonin - PCT) for reducing treatment duration [15]. Resolution of infectious parameters after appropriate antibiotic treatment occurs within 6 days and justifies shorter treatment durations [16]. Although many textbooks do not specify the optimal duration [17], the latest learned society guidelines recommend limiting treatment to 8 days, particularly when appropriate initial antibiotic treatment is administered, and in the absence of isolated nonfermenting gram negative bacilli [18], [19], [20]. Current recommendations are mainly based on one single randomized prospective study related to late-onset VAP [11]. Our randomized, controlled trial comparing 2 antibiotic regimens (8 days versus 15 days) for the treatment of patients with EOVAP who had been ventilated for less than 8 days, was carried out to provide further evidence on the best length of treatment in this ICU population.

Some of the results of these studies have been previously presented [21], [22].


The protocol for this trial and supporting consort checklist are available as supporting information; see checklist S1 and protocol S1.

Inclusion criteria

Patients included in the study were over the age of 18 and had developed EOVAP under invasive mechanical ventilation. The pneumonia was defined as having an early-onset if the patient had been ventilated for more than 24 hours and less than 8 days [23], [24], [25]. A EOVAP diagnosis was considered in the presence of at least 2 or 3 of the following clinical criteria: temperature ≥38.3°C, leukocyte count >10000/mm3, excessive purulent or mucopurulent bronchial secretion; and the radiological criterion described by Weinberg [26] (Table 1): increase of 2 points in radiological score compared to chest x-ray on admission, or no improvement of a maximum score (11 or 12) on admission. The diagnosis of pneumonia was confirmed by bronchoalveolar lavage (BAL) culture of ≥104 colony-forming units/ml for at least one bacterial species.

Randomization for treatment duration (8 versus 15 days) was carried out if the bacteria identified in significant concentrations in the BAL samples were susceptible to the authorized antibiotics while for streptococci, a low level resistance to aminoglycosides was not taken into account (Figure 1). Randomization is allocated in each centre by a dedicated randomization table. The assigned treatment arm is communicated by fax at the latest at D5 by the main investigator center.

Figure 1. Design of the study governing inclusion of a new patient according to BAL bacteriological results and follow up criteria.

The exclusion criteria are detailed in table 2. The study protocol had received local ethics committee and CCPPRB (Comite Consultatif de Protection des Personnes dans la Recherche Biomedicale de Franche Comte, number 97/189) approval. Each patient or a member of their family had signed an informed consent form, and written informed consent was obtained from all participants involved in the study.

Treatment initiation

Patients received immediate treatment, according to the standardized severity criteria (Table 3) and direct bacteriological results from BAL samples if available. If immediate antibiotic treatment was initiated, only patients who had been receiving appropriate treatment from the outset were included.

Table 3. Indications for antibiotic treatment before bacteriology results.

All patients included in the study were treated with beta-lactams for 8 or 15 days combined with an aminoglycoside for the first 5 days (Table 4). In the event of a secondary pulmonary infection or the development of extrapulmonary infections, all antibiotics could be used according to the bacteriological data. Once the patient had been included in the protocol, BAL samples were taken for intubated patients prior to making any changes to antibiotic treatment (Table 5).

Table 5. Definition of secondary infections requiring the initiation of antibiotic treatment for more than 48 hours.

Patients were followed up daily during hospitalization in ICU. The onset of intercurrent adverse events associated with the treatment was recorded throughout the follow up (Table 6). All intercurrent infectious events were documented according to the clinical orientation based on appropriate sampling.

Evaluation criteria

Primary criteria for evaluating recovery.

The primary endpoint of the present study was the clinical cure rate at day 21. Complete clinical recovery was determined by the absence of the following criteria: death, septic shock (except when associated with a documented non-respiratory infection), intercurrent adverse event attributable to the protocol (or for which attributability to the protocol could not be ruled out) requiring modified antibiotic treatment (Table 6), and patients who relapsed. A relapse was defined by a new infectious pulmonary event caused by the same pathogen identified in the initial BAL fluid (regardless of its susceptibility profile), associated with clinical and radiological signs of nosocomial pneumonia (occurring ≥4 days of treatment) or a worsening of 2 points of the baseline SOFA score.

Secondary criteria.

The study focused on establishing the determinants of clinical response on day 21: incidence of secondary nosocomial infections; number of patients on antibiotic treatment; total number of days of antibiotic treatment; duration of MV; number of patients still under ventilation; number of patients still in ICU; length of stay in ICU on day 21; and mortality rate at 3 months. The following set of complementary results enabled a better characterization of the study cohorts: isolated pathogens; frequency of positive hemocultures; and proportion of patients receiving first-line or secondary treatment (Table 3).

Statistical analysis

The trial was designed to show equivalence in the clinical response rates between the 2 treatment groups. A sample size of 220 patients was determined to be adequate to demonstrate equivalence with a power of 80% and a basal response rate of 90%. The limits of the 95% confidence interval (CI) for the difference between the response rates in the 2 treatments groups were calculated, and the equivalence accepted if it did not exceed 10%.

Comparisons of baseline patient characteristics and secondary criteria between the 2 cohorts were performed using the t-test for continuous variables and the chi-square test or Fisher's exact test for categorical variables.

The efficacy analysis was conducted using an intent-to-treat approach. Difference (d) and odds-ratio (OR) of response rates and their 95% CIs were used to test the equivalence between the 2 cohorts [28], [29].

All P values were two-sided. Data are presented as mean values with the standard deviation in brackets for normal distribution variables, and as median and quartile values for others (SAS institute inc. USA version 9.1).


Patient characteristics

225 patients (109 in the 15 d cohort and 116 in the 8 d cohort) were included and evaluated in 13 different centers over a period of 4 years from 1998 to 2002, and 6 of the centers recruited 96% of patients (figure 2). The patients' baseline characteristics were comparable in the 2 groups (Table 7). The cause of coma was traumatic in 38.9% and 40.5% of patients in the 15 d and 8 d cohorts respectively.

Figure 2. Data regarding number of patients included, treated according to protocol and followed up at 21 and 90 days.

Table 7. Admission characteristics of the study patients according to the duration of antibiotic treatment.


There were no significant differences between the proportions of gram-negative bacilli (p = 0.32) and gram-positive cocci (p = 0.65) from one group to the other. 32.9% of the pathogens isolated in BAL samples were MSSA in the 15 d cohort, and 28.2% in the 8 d cohort. The samples were multimicrobial for 54.1% of patients in the 15 d cohort and 37.9% of patients in the 8 d cohort (p = 0.03), but the antibiotics used were active on all pathogens. The bacteria isolated in the BAL samples are shown in Table 8. For 2 (15 d cohort) and 3 (8 d cohort) patients, several strains of MSSA were isolated in the BAL fluid. One MSSA pathogen was identified in the BAL samples of 58 patients in the 15 d cohort and 45 patients in the 8 d cohort (p = 0.35).

18 patients (8 in the 15 d cohort, 10 in the 8 d cohort) presented at least one positive hemoculture during the 24 hours of BAL sampling. For 7 of these patients, the isolated pathogen in the hemoculture was the same as in the BAL fluid. We found 5 MSSA, 1 pneumococcus and 1 Escherichia coli. For the remaining 11 patients, the pathogen was not isolated in the BAL fluid or in an another focus of infection. We found 6 Staphylococcus epidermidis or negative coagulase, 1 enterococcus, 3 streptococci and 1 MSSA. The mortality rate for patients with positive hemoculture did not differ from the overall study population (p = 0.82; Fischer's exact test).

Treatment duration and compliance

Immediate treatment was initiated following BAL in 77 (71%) and 81 (70%) patients in the 15 d and 8 d cohorts respectively. The mean durations for first-line treatment were 13.1 (3.6) days and 7.8 (1.6) days for the 15 d and 8 d cohorts respectively (p<0.01).

Principal criteria

According to our judgment criteria, a total of 191 out of the 225 patients (84.9%) included in the study were cured; 92 out of 109 (84.4%) in the 15 d cohort and 99 out of 116 (85.3%) in the 8 d cohort (d = 0.9%, OR = 0.929). 95% two-sided CIs for difference and OR were [−8.4% to 10.3%] and [0.448 to 1.928] respectively. Taking into account the limits of equivalence (10% for difference and 2.25 for OR), the protocol objective of demonstrating equivalence between the 2 treatment regimens was fulfilled.

Secondary objectives

The mortality rate evaluated on day 21 was comparable in the 2 cohorts. 19 patients died, 9 (8.3%) in the 15 d cohort and 10 (8.6%) in the 8 d cohort (p = 0.92). The median delay between antibiotic treatment initiation and death was also comparable in the 2 cohorts; 11.8 (5.7) days and 10.7 (4.8) days for the 15 d and 8 d cohorts respectively (p = 0.66). At 3 months, 88% of all patients had been evaluated. Out of 96 patients in the 15 d and 102 patients in the 8 d cohort, the mortality rate was almost identical: 17.4% and 17.2% respectively (p = 0.99).

Nine patients experienced an adverse event requiring treatment modification: 5 in the 15 d and 4 in the 8 d cohort. The cause of the event was cutaneous in 4 cases, digestive (C. difficile) in 3 cases and hepatic in 2 cases. 19 patients experienced septic shock (10 in the 15 d and 9 in the 8 d groups), 17 in the absence of new infectious event, and 2 in the presence of an undocumented infectious intercurrent event.

Eight patients experienced a relapse of the initial pulmonary infection with isolation of the same pathogen in pulmonary samples; 2 in the 15 d and 6 in the 8 d cohort (NS). One pneumococcus and 1 methicillin-resistant Staphylococcus aureus (MRSA) pathogen (initial presence of 1 MSSA pathogen) persisted in the 15 d cohort. One Haemophilus, 1 Serratia, 3 MSSA and 1 MRSA (initial presence of 1 MSSA) persisted in the 8 d cohort. For both durations, the median delay between treatment initiation and relapse diagnosis was 11.6 days (min = 7; max = 18).

Secondary nosocomial infections during the 21 days after randomization

A secondary infection was diagnosed in 19.3% of patients in the 15 d cohort and 35.3% of patients in the 8 d cohort (p<0.01) (Table 9). Comparisons between patients with and without secondary infections are depicted in table 10. Patients presented more pulmonary infections than extrapulmonary infections. 116 BAL were performed during the follow-up. 71 BAL done after initiation of the treatment were negative (26 for the 15 days and 45 for the 8 days arms, p = 0.01). There was no difference in the proportion of patients with a negative BAL, respectively 24 (22.0%) and 33 (28.7%) for the 15 and 8 days groups (p = 0.27). The isolated bacteria are reported in table 11. In patients in whom antibiotics were not started immediately, we also did not find any mortality difference at day 21. We compared the superinfection rate in patients receiving either a third generation cephalosporin or amoxicilline-clavulanic acid. Overall, there was no difference (respectively 28% and 26.4%). We analysed this superinfection rate according to the length of treatment and to the type of antibiotic (third generation cephalosporin or amoxicilline-clavulanic acid) and did not find any significant difference (15 days group respectively 20% and 18%; 8 days group respectively 37% and 33%).

Table 10. Comparisons between patients with and without secondary infections.

Taking into consideration the onset of a secondary infection as an added failure criterion, the percentages of cured patients (clinical success) were 64.2% in the 15 d cohort and 49.1% in the 8 d cohort (d = 15.1%). 95% two-sided CI for difference was [2.3% to 27.9%]. Taking into account the limit of equivalence (10%), equivalence between the 2 treatments was rejected.

Other secondary criteria

Sixty-four patients in the 15 d cohort (58.7%) and 66 (56.9%) in the 8 d cohort had been discharged alive from the ICU by day 21. The mean duration of hospitalization in ICU was 15.7 (5) days in the 15 d cohort and 15.9 (5.1) days in the 8 d cohort (p = 0.82). The length of stay in ICU after treatment initiation was 11.9 (4.4) days in the 15 d cohort and 11.3 (3.7) days in the 8 d cohort (p = 0.42). The mean duration of intubation in ICU was 13.4 (5.9) days in the 15 d cohort and 13.6 (5.3) days in the 8 d cohort (p = 0.81). The number of patients intubated at day 21 did not differ between the 2 groups (36 in the 15 d cohort and 40 in the 8 d cohort; p = 0.88).

The mean duration of antibiotic treatment (all molecules grouped together) during the 21 days of follow up was 15.4 (3.4) days for the 15 d and 11.3 (4.7) days for the 8 d cohort (p<0.01). The median durations of antibiotic treatment during the 21 days of follow up were 15 and 8 days respectively. The number of patients still on antibiotics on day 21 was significantly different between both groups; 20 patients in the 15 d cohort and 39 in the 8 d cohort (p = 0.01). Among these patients, 13 in the 15 d cohort and 18 in the 8 d cohort had left ICU (p = 0.41).


The results of this prospective, randomized study showed that 15 and 8 days of initially appropriate antibiotic treatment for EOVAP were equivalent according to the rate of complete clinical recovery. Additionally, 21 and 90-day mortality rates as well as durations of mechanical ventilation and of ICU stay were not different between both strategies. However, the rate of secondary infections was higher in the 8 d cohort than in the 15 d cohort, resulting in a lower rate of clinical cure in the 8 d strategy when including the occurrence of a secondary infection [11]. Despite this difference, the number of days of antibiotic treatment was lower in the 8 d cohort and around 50% of the secondary infections remained sensitive to the first-line treatment.

In the present study, VAP was defined as early when it occurred between 1 and 8 days after initiation of mechanical ventilation. Moreover, antibiotic choice was protocolized using quite limited-spectrum antibiotics and appropriate first-line antibiotics were a pre-requisite for patient inclusion in our study. Compared to our definition, early onset pneumonia has been commonly defined as occurring in the first 4 days. However, extended periods of 5 to 7 days have been used in the literature [9], [23], [24], [25], [31]. To note, 94% of our patients were included in the 6 days following initiation of mechanical ventilation. The bacteriology of EOVAP rarely consists of multiresistant pathogens. Microbiological data from BAL fluid of our patients confirmed this with a strong predominance of MSSA, streptococci, Haemophilus and enterobacteriacae species. Although the isolation of resistant bacteria has been reported in EOVAP [8], [9], [32], the percentage of resistant bacteria only accounted for 13% of those isolated in a recent study [7], and a strategy using limited-spectrum antibiotics allowed for appropriate treatment in 80% of cases of EOVAP [33], [34]. To note, polymicrobial samples were more common in our 15 d cohort. The reason for this is not clear, but the sensitivity of the bacteria to the initial treatment means that it probably had no real impact. As for all our patients, a polymicrobial incidence of around 50% was reported during VAP. Combes et al found that the epidemiology and outcomes of patients with monomicrobial and polymicrobial VAP did not differ significantly [35]. In our study, polymicrobial samples were not detrimental to recovery.

Until recently, recommendations for treatment duration of VAP were based only on the advice of experts [4], [18], [30] as there was no prospective, randomized study available when the present trial was initiated. Chastre et al. found no clear advantage in prolonging antibiotic treatment to 15 days compared with 8 days when treating late-onset VAP [11]. Our data strongly suggest that a 8-day treatment of EOVAP enables recovery in the same proportions as a 15-day regimen using the same clinical and microbiological cure criteria than those used in other studies [36], [37], [38]. Equivalence was obtained according to the criteria that we defined at first, in particular that the onset of a secondary pulmonary infection did not exclude the possibility that the primary infection had been cured. These data confirm recommendations for reducing treatment to 7–8 days for EOVAP [4], [12], [16], [39]. Moreover, the reception of negative microbiological samples [16], as well as the clinical response evaluated by composite scores [12], [40] may help to securely shorten the duration of antibiotic treatment of VAP. Recently, the implementation of an antibiotic protocol for VAP including these tools has indeed been associated with a reduction of antibiotic treatment duration from 10.1 (8) to 6.2 (3.3) days associated with a reduction in the duration of mechanical ventilation [31]. These objectives have now been extended to early- and late-onset pneumonia by learned societies [18], [19], [20] except if the etiologic agent was P. aeruginosa or an Acinetobacter species which carry a greater risk of relapse. Prolonged antibiotic therapy may also be justifiable in cases of pulmonary infections caused by MRSA due to the delayed response to treatment [41], and the increased risk of relapse [42]. Further research is required to determine if a 8-day treatment of resistant bacteria EOVAP is safe since these cases have been excluded from the present study.

In our study, the rate of secondary pulmonary and extrapulmonary infections was significantly higher in the 8 d cohort. The risk of acquiring a nosocomial infection is high during the first few days following admission to ICU [43], [44], and patients frequently develop several infections simultaneously or close together [44], [45]. An early but short treatment of VAP could therefore lead to a higher rate of infections rapidly unmasked after antibiotic stop or treated too shortly. Indeed, a majority of superinfections in the 8d cohort occurred in the few days following the end of antibiotic treatment. In the multicenter trial of 8 vs 15 days of antibiotic treatment for late onset VAP by Chastre et al [11], neither relapses nor superinfection rates were different between both strategies. Several reasons related to the type of infection and to their treatment may explain this difference. First, whereas in this latter study, over 80% of patients had received curative antibiotics in the 15 days prior to inclusion, this situation did not apply to any of our patients. Moreover, broad spectrum antibiotics were used in the Chastre et al [11] study according to the isolated bacteria. Finally, a combination of antibiotics including an aminoglycoside was used in more than 90% on day 1 and was still administered on day 8 in more than 30% of patients while in our study, we protocolized the use of narrow spectrum antibiotics and aminoglycosides were stopped on day 5.

We did not recommend using fluoroquinolones and proposed an aminoglycoside treatment with a limited duration, identical in the 2 cohorts. Nevertheless, the use of combination therapy is debatable considering the bacteria expected in EOVAP. Indeed, a recent trial suggested that monotherapy is associated with similar outcomes compared with combination therapy in patients who have suspected late VAP and who are at low risk for difficult-to-treat gram-negative bacteria, [46]. This strategy would probably be applicable to our patients, excepted in patients with septic shock.

Several limitations were apparent in our study. First, although it was planned, it has not been possible to accurately quantify the number of patients who were not included in the study, as well as the microbiologic characteristics of their VAP. Nevertheless, the non-inclusion of the most critically-ill patients cannot be the main reason. Indeed, patients with a deep source of infection (abscess or purulent pleurisy) as well as immunodeficient patients were excluded from the study. Moreover, mean SAPS II was 39, 70% of the study population had 2 organ failures and 18 patients presented with bacteriemia. Second, except for mortality rate, follow-up was limited to 21 days. However, only 31% of patients were still hospitalized on day 21, what limits the interest and validity of a longer follow-up. Third, although this study enrolled patients in 13 centers, 6 of them included 96% of patients. However, 5 patients were included in low inclusion rate centers in each arm. Moreover, randomisation was processed by center to avoid any center effect. Fourth, patients were treated with a combined therapy. While the aminoglycosides are not great pneumonia drugs, they clearly have some benefit resulting in a synergistic effect with beta-lactams and a larger antibiotic spectrum. As a consequence, aminoglycosides might have skewed the results toward equivalence.

In conclusion, our study enabled us to recommend reduced treatment duration of 8 days for early-onset VAP, while respecting the contra indications. The higher rate of secondary infections in the 8 days than in the 15 days treatment strategy highlights the importance of rigorous clinical monitoring and the possible interest of biological markers for securing this strategy.


We would like to thank also Dr S Boussat, Dr C Cornette and Dr D Talon for their involvement in writing the protocol, Alexia Cairey-Remonay and Franck Monnien for gathering the data, Marc Puyraveau for the statistical analysis, Mélanie Cole and Dave Baguley for translating the original French protocol and manuscript.

Study, collaborative investigation group: the following French centers and investigators: Capellier, Belle, Patry, Boussat, Navellou, Desmettre, Baguley (CHU, Besançon), Charpentier, Welfringer (Hôpital Central, Nancy), Annane (CHU, Garches), Blasco (CHU, Besançon), Papazian, Roch, Le Bel (Hôpital Ste Marguerite, Marseille)Léon, Cousson (Hôpital Robert Debré, Reims), Novara (Hôpital Européen Georges Pompidou, Paris), Diehl (Hôpital Européen Georges Pompidou, Paris) Bollaert, Bocquet (Hôpital Central, Nancy) Freysz, Milesi (Hôpital Général, Dijon), Meunier (Hôpital Lyon Sud, Pierre-Benite), Guery (Hôpital Chatiliez, Tourcoing) Aube (Hôpital Général, Dijon), Faller, Ruyer (CHG, Belfort), Sauder (Hospices Civils, Strasbourg), Poisson (Hôpital Dr Schaffner, Lens), Launoy, Freys (Hôpital Hautepierre, Strasbourg), Réal (Hôpital du Hasenrain, Mulhouse), Guiot (C.H.R. ND de Bon Secours, Metz), Laplatte (Hôpital Louis Pasteur, Colmar), Martin (Hôpital Nord, Marseille), Guerin (Hôpital de la Croix Rousse, Lyon), Robert (Hôpital Bel-Air, Thionville), Floriot (Hôpital Paul Morel, Vesoul), Meyer (Hôpital Européen Georges Pompidou, Paris), Nevière (Hôpital Calmette, Lille).

Author Contributions

Conceived and designed the experiments: GC HM SL MM LP. Performed the experiments: GC DA TD JC CC LP CF GB AR. Analyzed the data: HM MM SL GC. Contributed reagents/materials/analysis tools: HM MM SL. Wrote the paper: GC HM LP MM DA.


  1. 1. Fagon JY, Stephan F, Novara A (1995) Epidemiologie des pneumopathies acquises sous ventilation artificielle. In: Chastre J, Fagon JY, editors. Pneumopathies nosocomiales et ventilation artificielle. Paris: Masson. pp. 1–12.
  2. 2. Joshi N, Localio AR, Hamory BH (1992) A predictive risk index for nosocomial pneumonia in the intensive care unit. Am J Med 93: 135–142.
  3. 3. Bregeon F, Papazian L, Visconti A, Gregoire R, Thirion X, et al. (1997) Relationship of microbiologic diagnostic criteria to morbidity and mortality in patients with ventilator-associated pneumonia. JAMA 277: 655–662.
  4. 4. Chastre J, Fagon JY (2002) Ventilator-associated pneumonia. Am J Respir Crit Care Med 165: 867–903.
  5. 5. A'Court CD, Garrard CS (1995) Nosocomial pneumonia in the ICU: New perspectives on current controversies. In Vincent JL, editor. Yearbook of Intensive Care and Emergency Medicine. Berlin: Springer-Verlag. pp. 726–747.
  6. 6. Craven DE, Steger KA, Barat LM, Duncan RA (1992) Nosocomial pneumonia: Epidemiology and infection control. Intensive Care Med 18: S3–9.
  7. 7. Giard M, Lepape A, Allaouchiche B, Guerin C, Lehot JJ, et al. (2008) Early- and late-onset ventilator-associated pneumonia acquired in the intensive care unit: comparison of risk factors. J Crit Care 23: 27–33.
  8. 8. Verhamme KM, De Coster W, De Roo L, De Beenhouwer H, Nollet G, et al. (2007) Pathogens in early-onset and late-onset intensive care unit-acquired pneumonia. Infect Control Hosp Epidemiol 28: 389–97.
  9. 9. Gastmeier P, Sohr D, Geffers C, Rüden H, Vonberg RP, et al. (2009) Early- and late-onset pneumonia: is this still a useful classification? Antimicrob Agents Chemother 53: 2714–8.
  10. 10. Esperatti M, Ferrer M, Theessen A, Liapikou A, Valencia M, et al. (2010) Nosocomial Pneumonia in the Intensive Care Unit Acquired during Mechanical Ventilation or Not. Am J Respir Crit Care Med 182: 1533–1539.
  11. 11. Chastre J, Wolff M, Fagon JY, Chevret S, Thomas F, et al. (2003) Comparison of 8 vs 15 days of antibiotic therapy for ventilator-associated pneumonia in adults: A randomized trial. JAMA 290: 2588–2598.
  12. 12. Singh N, Rogers P, Atwood CW, Wagener MM, Yu VL (2000) Short-course empiric antibiotic therapy for patients with pulmonary infiltrates in the intensive care unit. A proposed solution for indiscriminate antibiotic prescription. Am J Respir Crit Care Med 162: 505–511.
  13. 13. Luyt CE, Chastre J, Fagon JY (2004) Value of the clinical pulmonary infection score for the identification and management of ventilator-associated pneumonia. Intensive Care Med 30: 844–852.
  14. 14. Charles PE, Kus E, Aho S, Prin S, Doise JM, et al. (2009) Serum procalcitonin for the early recognition of nosocomial infection in the critically ill patients: A preliminary report. BMC Infect Dis 9: 49.
  15. 15. Bouadma L, Luyt CE, Tubach F, Cracco C, Alvarez A, et al. (2010) Use of procalcitonin to reduce patients' exposure to antibiotics in intensive care units (PRORATA trial): a multicentre randomised controlled trial. Lancet 375: 463–74.
  16. 16. Dennesen PJ, van der Ven AJ, Kessels AG, Ramsay G, Bonten MJ (2001) Resolution of infectious parameters after antimicrobial therapy in patients with ventilator-associated pneumonia. Am J Respir Crit Care Med 163: 1371–1375.
  17. 17. Marrie TJ (1994) Community-acquired pneumonia. Clin Infect Dis 18: 501–513 quiz 514-505.
  18. 18. Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia (2005) Am J Respir Crit Care Med 171: 388–416.
  19. 19. Rotstein C, Evans G, Born A, Grossman R, Light RB, et al. (2008) Clinical practice guidelines for hospital-acquired pneumonia and ventilator-associated pneumonia in adults. Can J Infect Dis Med Microbiol 19: 19–53.
  20. 20. Masterton RG, Galloway A, French G, et al. (2008) Guidelines for themanagement of hospital-acquired pneumonia in the UK: report of the working party on hospital-acquired pneumonia of the British Society for Antimicrobial Chemotherapy. J Antimicrob Chemother 62: 5–34.
  21. 21. Capellier G (2003) Nosocomial pneumonia. When to stop antibiotherapy (paper presented at the annual meeting of the International Symposium on Intensive Care and Emergency Medicine, Bruxelles).
  22. 22. Capellier G (2004) Comparaison de deux durées de traitements au cours des pneumopathies nosocomiales précoces acquises sous ventilation mécanique: 8 jours versus 15 jours (paper presented at the annual meeting of the Société Française de Réanimation Médicale, Paris).
  23. 23. Giantsou E, Liratzopoulos N, Efraimidou E, Panopoulou M, Alepopoulou E, et al. (2005) Both early-onset and late-onset ventilator-associated pneumonia are caused mainly by potentially multiresistant bacteria. Intensive Care Med 31: 1488–94.
  24. 24. Heyland DK, Cook DJ, Griffith L, Keenan SP, Brun-Buisson C (1999) Canadian Critical Care Trials Group (1999) The attributable morbidity and mortality of ventilator-associated pneumonia in the critically ill patient. Am J Respir Crit Care Med 159: 1249–56.
  25. 25. Trouillet JL, Chastre J, Vuagnat A, Joly-Guillou ML, Combaux D, et al. (1998) Ventilator-associated pneumonia caused by potentially drug-resistant bacteria. Am J Respir Crit Care Med 157: 531–39.
  26. 26. Weinberg PF, Matthay MA, Webster RO, Roskos KV, Goldstein IM, et al. (1984) Biologically active products of complement and acute lung injury in patients with the sepsis syndrome. Am Rev Respir Dis 130: 791–796.
  27. 27. SFAR (1992) Antibioprophylaxie en milieu chirurgical chez l'adulte. Paris: Réanimation SFAR editor.230 p.
  28. 28. Dunnett CW, Gent M (1977) Significance testing to establish equivalence between treatments, with special reference to data in the form of 2×2 tables. Biometrics 33: 593–602.
  29. 29. Gart JJ (1971) The comparison of proportions: A review of significance tests, confidence interval and adjustments for stratification. Review of the International Statistical Institute 39: 148–169.
  30. 30. Koeman M, Bonten MJ (2003) When can empiric therapy for intensive care unit-acquired pneumonia be withheld or withdrawn? Semin Respir Infect 18: 122–8.
  31. 31. Nachtigall I, Tamarkin A, Tafelski S, Deja M, Halle E, et al. (2009) Impact of adherence to standard operating procedures for pneumonia on outcome of intensive care unit patients. Crit Care Med 37: 159–166.
  32. 32. Ferrer M, Liapikou A, Valencia M, Esperatti M, Theessen A, et al. (2010) Validation of the American Thoracic Society-Infectious Diseases Society of America guidelines for hospital-acquired pneumonia in the intensive care unit. Clin Infect Dis 50: 945–52.
  33. 33. Leone M, Garcin F, Bouvenot J, Boyadjev I, Visintini P, et al. (2007) Ventilator-associated pneumonia: breaking the vicious circle of antibiotic overuse. Crit Care Med 35: 379–85.
  34. 34. Lancaster JW, Lawrence KR, Fong JJ, Doron SI, Garpestad E, et al. (2008) Impact of an institution-specific hospital-acquired pneumonia protocol on the appropriateness of antibiotic therapy and patient outcomes. Pharmacotherapy 28: 852–862.
  35. 35. Combes A, Figliolini C, Trouillet JL, Kassis N, Wolff M, et al. (2002) Incidence and outcome of polymicrobial ventilator-associated pneumonia. Chest 121: 1618–1623.
  36. 36. Brun-Buisson C, Sollet JP, Schweich H, Briere S, Petit C (1998) Treatment of ventilator-associated pneumonia with piperacillin-tazobactam/amikacin versus ceftazidime/amikacin: a multicenter, randomized controlled trial. VAP Study Group. Clin Infect Dis 26: 346–54.
  37. 37. Alvarez-Lerma F, Insausti-ordenana J, Jorda-marcos R, Maravii-Poma E, Torres Marti A, et al. (2001) Efficacy and tolerability of piperacillin tazobactam versus ceftazidime in association with amikacin for treating nosocomial pneumonia in intensive care patients: a prospective randomized multicenter trial. Intensive Care Med 27: 493–502.
  38. 38. Fagon JY, Patrick H, Haas DW, Torres A, Gibert C, et al. (2000) Treatment of Gram-positive Nosocomial Pneumonia: Prospective Randomized Comparison of Quinupristin/Dalfopristin versus Vancomycin. Am J Respir Crit Care Med 161: 753–62.
  39. 39. Pugh RJ, Cooke RP, Dempsey G (2010) Short course antibiotic therapy for Gram-negative hospital-acquired pneumonia in the critically ill. J Hosp Infect 74: 337–43.
  40. 40. Luna CM, Blanzaco D, Niederman MS, Matarucco W, Baredes NC, et al. Resolution of ventilator-associated pneumonia: Prospective evaluation of the clinical pulmonary infection score as an early clinical predictor of outcome. Crit Care Med 31: 676–682.
  41. 41. Vidaur L, Planas K, Sierra R, Dimopoulos G, Ramirez A, et al. (2008) Ventilator-associated pneumonia: impact of organisms on clinical resolution and medical resources utilization. Chest 133: 625–32.
  42. 42. Combes A, Luyt CE, Fagon JY, Wolff M, Trouillet JL, et al. (2007) Early predictors for infection recurrence and death in patients with ventilator-associated pneumonia. Crit Care Med 35: 146–54.
  43. 43. Cook DJ, Mulrow CD, Haynes RB (1997) Systematic reviews: Synthesis of best evidence for clinical decisions. Ann Intern Med 126: 376–380.
  44. 44. Osmon S, Warren D, Seiler SM, Shannon W, Fraser VJ, et al. (2003) The Influence of Infection on Hospital Mortality for Patients Requiring >48 h of Intensive Care. Chest 124: 1021–1029.
  45. 45. Meduri GU, Mauldin GL, Wunderink RG, Leeper KV, Jones CB, et al. (1994) Causes of fever and pulmonary densities in patients with clinical manifestations of ventilator-associated pneumonia. Chest 106: 221–235.
  46. 46. Heyland DK, Dodek P, Muscedere J, Day A, Cook D (2008) Canadian critical care trials group (2008) Randomized trial of combination versus monotherapy for the empiric treatment of suspected ventilator-associated pneumonia. Crit Care Med 36: 737–44.