1 | Antimicrobials used in the empirical regimens should be chosen based on the local pattern of susceptibility. |
2 | Initiation of antimicrobial therapy should not be delayed in patients with high probability of VAP especially if the infection originates severe sepsis or septic shock. |
3 | In patients with no signs of severe sepsis or septic shock and no organisms present on Gram’s staining, antimicrobial therapy can be withheld pending culture results. |
4 | When a high rate of episodes is caused by extremely resistant GNB, empirical use of colistin and/or tygecycline may be justified. |
5 | The inclusion of a carbapenem (in extended infusion) in this empirical therapy seems reasonable especially for pathogens not covered by these antibiotics. |
6 | Addition of vancomycin or linezolid is recommended is Units with high prevalence of MRSA (>10% of episodes caused by MRSA). |
7 | The initial antibiotic treatment must be reassessed when the culture results are available. Depending on the clinical progress and the microbiological findings, clinicians should adjust therapy accordingly. |
8 | In episodes caused by very-difficult-to-treat GNB, it seems prudent to maintain combination therapy (if possible) until the clinical course appears clearly favorable. |
9 | Nebulized antibiotics should be considered in the directed therapy of patients who are nonresponsive to systemic antibiotics or in episodes caused by GNB strains with high CMI (intermediate). |
10 | Not all patients with MDR-VAP have to be treated for two weeks. Courses of treatment should be individualized. Procalcitonin may be of aid to stop antibiotics after eight days of adequate antimicrobial therapy. |