Mjm. Bonten et al., THE SYSTEMIC INFLAMMATORY RESPONSE IN THE DEVELOPMENT OF VENTILATOR-ASSOCIATED PNEUMONIA, American journal of respiratory and critical care medicine, 156(4), 1997, pp. 1105-1113
Citations number
36
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
Ventilator-associated pneumonia (VAP) is the most frequent occurring i
nfection among mechanically ventilated patients. The clinical presenta
tion of VAP ranges from relatively benign to a severe illness with sep
tic shock. The influence of VAP on patient outcome has not been elucid
ated and its effects on the inflammatory response of the host are unkn
own. In a case-control study, the systemic inflammatory response was i
nvestigated in patients developing VAP as compared with control patien
ts matched on duration of mechanical ventilation and underlying diseas
es. Patients developing VAP (n = 42) were matched to a single control
(without VAP), who was matched on seven variables. VAP was diagnosed w
ith bronchoscopic techniques. The inflammatory response, reflected by
circulating levels of interleukin-6 (IL-6) and interleukin-8 (IL-8), w
as determined on the day of diagnosis (or day of matching for controls
), 4 and 2 d before diagnosis, and 2 d after diagnosis. The developmen
t of VAP was not associated with an increase in circulating levels of
IL-6 or IL-8. Among patients in which VAP was associated with a clinic
al presentation of severe sepsis or septic shock (n = 10), IL-6 and IL
-8 levels increased and were higher than in the corresponding controls
. Moreover, 60% of cases with severe sepsis or septic shock died as co
mpared with 20% of their matched controls (p = 0.06). Mortality rates
were similar in patients with uncomplicated VAP and their matched cont
rols (25% and 34%, respectively). High circulating levels of IL-6 and
IL-8 were associated with higher mortality rates. The clinical picture
of VAP can be subdivided into different types, ranging from uncomplic
ated to an infection associated with severe sepsis or septic shock, el
evated circulating levels of IL-6 and IL-8, and an increased mortality
rate.