OBJECTIVE. Afer twenty years of commercial availability of cefotaxime, the
objective of this study was to know the reasons and modes of use, administr
ation dosage as well as its effectiveness and tolerance in critically ill p
atients admittted to Intensive Care Units (ICU) in our country.
DESIGN. Open, prospective, observational, multicenter study.
SUBJECTS. All patients who had cefotaxime administered in monotherapy or in
combination with other antibiotics were included as cases in this study.
RESULTS. A total of 624 patients were included in 44 ICUs (average 14 cases
). Cefotaxime was indicated for therapy of 274 community-acquired infection
s (43.9%), 194 prophylaxis (31.1%), and 156 nosocomial infections (25.0%).
Both community-acquired pneumonia (149, 34.7%) and mechanical ventilation a
ssociated pneumonia (62, 14.4%) predominated, followed by trachebronchitis
(60, 13.9%) and central nervous system infections (42, 9.8%). Over half of
infections (222, 51.6%) presen ted as systemic inflammatory response syndro
me (SIRS), 133 (30.9%) as severe sepsis, and 75 (17.4%) as septic shock. In
374 (87.0%) out of the 430 cases of infection treatment, cefotaxime wan pr
escribed on an empirical basis and in 150 of them (40.1%) a further confirm
ation of the causative agent was obtained. In 120 (27.9%) cases, cefotaxime
was administered as monotherapy and in the remaining cases in association
with one or more antibiotics. The use of cefotaxime as prophylaxis was eval
uated as failure in 31 (16.0%) of the cases, whereas in treatment it was co
nsidered as failure in 98 (22.8%) of the 430 cases, 51 community-acquired i
nfections, 27 (27.3%) of ICU-acquired infections, and 20 (35.1%) nosocomial
infections acquired outside the ICU. In 127 (29.5%) of the 430 infection t
reatments the initial treatment was changed. The reasons for the change inc
luded clinical failure (36, 28.3%), recovery of an uncovered pathogen with
the antibiotic (40, 31.5%), emergence of multi-resistant pathogens (28, 22.
0%), to decrease the therapeautic spectrum (7, 5.5%), and other reasons (16
). Cefotoxime was also changed in 21 (6.0%) of the 194 cases in which it wa
s used as prophylaxis. In 32 (5.1%) patients 37 adverse effects were noted
which were associated with a possible or likely use of cefotaxime. Most not
ably, diarrhoea in 15 (2.4%) occasions and skin rash in 6 cases (1.0%).
CONCLUSIONS. Cefotaxime is still one of the therapies of choice for communi
ty-acquired and nosocomial infections as well as in different prophylactic
modes. It is mostly used on an empirical basis and associated with other an
tibiotics. Clinical and microbiological efficieny is high whereas adverse e
ffects related to its use have been scarce.