J. Carratala et al., TREATMENT OF PENICILLIN-RESISTANT PNEUMOCOCCAL BACTEREMIA IN NEUTROPENIC PATIENTS WITH CANCER, Clinical infectious diseases, 24(2), 1997, pp. 148-152
We identified 17 cases of pneumococcal bacteremia among 340 neutropeni
c cancer patients with bacteremia. Pneumonia was more frequent in pati
ents with pneumococcal bacteremia than in those with bacteremia due to
other organisms: 12 (71%) of 17 patients with pneumococcal bacteremia
had pneumonia, whereas only 23 (7%) of 323 patients with nonpneumococ
cal bacteremia had pneumonia (P < .001). Eight (47%) of the 17 episode
s of pneumococcal bacteremia were caused by penicillin-resistant strai
ns (MICs ranged from 0.12 mu g/mL to 4 mu g/mL; these penicillin-resis
tant pneumococci showed varying degrees of diminished susceptibility t
o all beta-lactams studied, especially ceftazidime (MICs of this drug
ranged from 1 mu g/mL to 64 mu g/mL). Imipenem was the beta-lactam age
nt most active against these organisms (MICs ranged from 0.03 mu g/mL
to 0.25 mu g/mL). Patients with penicillin-resistant pneumococcal bact
eremia received inappropriate empirical antibiotic therapy more often
than did patients with bacteremia due to susceptible strains (i.e., 4
(50%) of 8 patients vs. 0 of 9, respectively; P < .05). Eight (47%) of
the 17 patients with pneumococcal bacteremia died. In areas where pen
icillin-resistant pneumococci are highly endemic, these findings shoul
d be considered in selecting empirical antibiotic therapy for neutrope
nic patients with cancer who are suspected of having pneumonia.