Pm. Shah et al., EMPIRICAL MONOTHERAPY WITH MEROPENEM VERSUS IMIPENEM CILASTATIN FOR FEBRILE EPISODES IN NEUTROPENIC PATIENTS/, Infection, 24(6), 1996, pp. 480-484
In a nonblind, randomised, parallel-group shady, initial empirical mon
otherapy with meropenem 1 g intravenously every 8 h was compared to an
identical dosage of imipenem/cilastatin for the treatment of 66 Febri
le episodes in 61 adult neutropenic patients, 25/31 episodes treated w
ith meropenem and 24/30 imipenem/cilastatin-treated episodes were stil
l receiving unmodified therapy at 72 h (primary endpoint); this differ
ence was not statistically significant, By the end of the treatment co
urses, 18/31 meropenem-treated episodes had responded clinically (cure
d or improved) compared with 18/30 episodes treated with imipenem/cila
statin. Another ten episodes initially treated with meropenem and six
episodes treated with imipenem/cilastatin were cured after an addition
al antimicrobial agent had been administered (cured with modification)
, Satisfactory bacteriological responses (eradication plus presumed er
adication) at the end of unmodified therapy was 9/11 in the meropenem
group and 14/16 in the comparator group, Both regimes were well tolera
ted; however, there were more reports of nausea and/or vomiting in the
imipenem/cilastatin group C7/33 vs, 2/33 in the meropenem group). The
carbapenems meropenem and imipenem/cilastatin appear to be suitable a
gents for empirical monotherapy of febrile episodes in neutropenic pat
ients. Meropenem may be better tolerated than imipenem/cilastatin, all
owing optimal dosing in this patient population.