Abbreviations: VAP, ventilator-associated pneumonia; ICU, intensive care unit; HAP, hospital acquired pneumonia; CPIS, chronic pulmonary infection score; MIC, minimum inhibitory concentration; ESBL, extended spectrum beta lactamase production; DDST, double disc synergy testing; MBL, metallo beta lactamase
IntroductionVentilator associated pneumonia (VAP) is defined as nosocomial pneumonia in patients on mechanical ventilator support (by endotracheal tube or tracheostomy) for >48h during their ICU stay, excluding any infection present or in incubation at the time of ICU admission.1 VAP is estimated to occur in 9-27% of all mechanically ventilated patients, with the highest risk being early in the course of hospitalization. 2,3 It is the second most common nosocomial infection in the intensive care unit (ICU) and the most common in mechanically ventilated patients. 4,5 The mortality with VAP is considerably high, varying from 24 to 50% and can reach as high as 76% in some specific settings.
6The etiologic agents widely differ according to the population of patients in an intensive care unit, duration of hospital stay, prior antimicrobial therapy and co-morbid conditions. Despite the advancements in antimicrobial regimes, VAP continues to be an important cause of morbidity and mortality. Inadequate antimicrobial therapy, such as inappropriate antimicrobial coverage, or delayed initiation of antimicrobials has been associated with higher hospital mortality in subjects with hospital acquired pneumonia (HAP) or VAP.
7Therefore the aim of this study was to analyse the microbiological and clinical profile of VAP in our hospital, risk factors and prevalence of multi-drug resistant organisms so as to implement effective prevention strategies.
Material and methodsThe study was conducted during the period of Jan 2014 to Dec 2014 in the ICUs of a large tertiary care hospital in North India. All mechanically ventilated patients developing pneumonia after >48 hrs of ventilation were included in the study. To diagnose VAP in the patients, Chronic Pulmonary Infection Score (CPIS) was used.8 Patients were screened for 1) New or persistent pulmonary infiltrates appeared on chest radiograph not otherwise explained. 2) fever 3) Leucocytosis 4) Oxygenation PaO 2 /Fio2 5) Purulent respiratory secretions. Early onset VAP was defined as pneumonia that occurred within 4days of intubation whereas late onset VAP defined as pneumonia after 4days of intubation. Only patients exhibiting bacteriologically documented pneumonia were studied; establishment of etiologic diagnosis required isolation of bacteria in significant quantity from samples of lower respiratory tract secretions (endotracheal secretions >105cfu/ ml, protected brush catheter >103 cfu/ml and bronchoalveolar lavages >104cfu/ml) or isolation of a definitive pathogen from a blood or pleural fluid culture.
9The microbiological samples were collected and processed according to standard protocols. 10 All the bacteria isolated were identified to the species level by standard biochemic...