TREATMENT OF VENTILATOR-ASSOCIATED PNEUMONIA WITH PIPERACILLIN-TAZOBACTAM AMIKACIN VERSUS CEFTAZIDIME/AMIKACIN - A MULTICENTER, RANDOMIZED CONTROLLED TRIAL/
C. Brunbuisson et al., TREATMENT OF VENTILATOR-ASSOCIATED PNEUMONIA WITH PIPERACILLIN-TAZOBACTAM AMIKACIN VERSUS CEFTAZIDIME/AMIKACIN - A MULTICENTER, RANDOMIZED CONTROLLED TRIAL/, Clinical infectious diseases, 26(2), 1998, pp. 346-354
In a randomized trial conducted in 27 intensive care units, we compare
d the clinical efficacy and safety of piperacillin-tazobactam (TAZ; 4
g/0.5 g q.i.d.) and of ceftazidime (CAZ; 1 g q.i.d,), both combined wi
th amikacin (7.5 mg/kg b.i.d.), as therapy for ventilator-associated p
neumonia (VAP; acquired after greater than or equal to 48 hours of mec
hanical ventilation). VAP was diagnosed with use of protected samples
and quantitative cultures, and outcome was assessed blindly from treat
ment. Of 204 patients suspected of having VAP and randomized to a trea
tment arm of the study, 127 (64%) had bacteriologically confirmed infe
ctions, of which 37% were polymicrobial and 32% involved Pseudomonas a
eruginosa; 115 patients (51 TAZ and 64 CAZ recipients) remained evalua
ble as per protocol. Clinical/bacteriologic cure rates (TAZ vs, CAZ, 5
1% vs. 36%; 95% confidence interval of difference, -0.2% to 30.2%), an
d 28-day mortality rates (16% vs. 20%) were similar; however, fewer ba
cteriologic failures occurred with TAZ (33% vs. 51%; P=.05). We conclu
de that the two regimens were of equivalent clinical efficacy in thera
py for confirmed VAP.