VENTILATOR ASSOCIATED PNEUMONIA
AbstractVentilator Associated Pneumonia (VAP) is defined as nosocomial pneumonia that occurred 48 hours after
the patient had a mechanical ventilation support either from endotracheal tube or tracheostomy tube. VAP
ussually charactherized by 3 component sign of systemic infection: fever, tachycardia and leukocytosis
followed by new infiltrate sign or a worsening scheme on the chest x ray and bacteriologic findings of the
causal of lung infection, but acctually we can diagnosed a VAP based on the findings of a number of
criteria: histopathologic examination of the lung tissue from an open biopsy, a fast cavity formation of a
lung infiltrate without any sign of tuberculosis or malignancy and a positive pleural fluid culture, in which
the species that found on the blood culture and airway were the same.
The insidens of VAP are high, according to the foreign literature approximately between 9 – 27 % from all
Intensive Care Unit population. This condition made VAP as the first causal of a nosocomial infection in
the Intensive Care Unit. The mortality rate of VAP is also high, Chastre and Fagon stated that the crude
mortality rate can reach of 76%. Early onset VAP which occurred on the first 4th day after admission in the
Intensive Care Unit ussually had a better prognosis because of caused by a still antibiotic sensitive
pathogens. The Late onset VAP which occurred after 5 days or more after hospitalization, has worse
prognosis because of caused by a multidrug resistance (MDR) pathogens. In order to define the pathogens
that caused VAP, some scientist made a classification of VAP patient based on the degree of disease, risk
factor and the onset, which is the group I with mild-moderate degree, common risk factor and the onset is
anytime during hospitalization or a severe degree with an early onset, ussually caused by a gram negative
bacteria. The group II, patient with a mild-moderate degree, specific risk factor that happened anytime
during hospitalization, ussually caused by all bacteria in the group I added with an anaerob bacteria. The
group III, patient with a severe degree, early onset with specific risk factor or a late onset, ussually caused by Pseudomonas aeruginosa, Acinetobacter sp and MRSA. Other approach is by classifying the bacteria
causing VAP in a primary endogen, secondary and eksogen type.
Prevention of VAP can be done by 2 different ways, first by a non pharmachologic way, routine and
standard things that ussually done in the ICU, but this action still could not enough in lowering the insidens
of VAP. Second, by a pharmachologic way, Selective Decontamination of the Digestive Tract (SSD) and
Oropharyngeal Decontamitation (OD). SSD is proven effective empirically in preventing VAP but the used
of antimicrobial can caused a higher risk on resistention. SDD is not recommended as a routine action in
preventing VAP so that OD with the used of antiseptic is preferred as another alternative.
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How to Cite
WIRYANA, Made. VENTILATOR ASSOCIATED PNEUMONIA. journal of internal medicine, [S.l.], nov. 2012. Available at: <https://ojs.unud.ac.id/index.php/jim/article/view/3843>. Date accessed: 28 feb. 2020.
Ventilator associated pneumonia, mechanical ventilation, critically ill patients