OUTCOMES OF BACTEREMIA IN PATIENTS WITH CANCER AND NEUTROPENIA - OBSERVATIONS FROM 2 DECADES OF EPIDEMIOLOGIC AND CLINICAL-TRIALS

Citation
Ls. Elting et al., OUTCOMES OF BACTEREMIA IN PATIENTS WITH CANCER AND NEUTROPENIA - OBSERVATIONS FROM 2 DECADES OF EPIDEMIOLOGIC AND CLINICAL-TRIALS, Clinical infectious diseases, 25(2), 1997, pp. 247-259
Citations number
46
Categorie Soggetti
Microbiology,Immunology,"Infectious Diseases
ISSN journal
10584838
Volume
25
Issue
2
Year of publication
1997
Pages
247 - 259
Database
ISI
SICI code
1058-4838(1997)25:2<247:OOBIPW>2.0.ZU;2-V
Abstract
The prognostic significance of major organ and tissue infection was ex amined in 909 episodes of bacteremia that were selected from 10 consec utive, randomized clinical trials of antibiotic therapy for infection in patients with cancer and neutropenia. Extensive tissue infection si gnificantly compromised response to initial therapy (38% vs. 74%; P < .0001), ultimate outcome of infection (73% vs. 94%; P < .0001), median time to normalization of temperature (5.3 days vs. 2.5 days; P < .000 1), and survival (P < .0001). Other poor prognostic factors revealed b y logistic regression included shock (P < .0001) and bacteremia caused by Pseudomonas species (P = .03), Clostridium species (P = .006), or a pathogen resistant to antibiotics used for initial therapy (P < .000 1). Recovery of the granulocyte count predicted a superior response (P < .0001). Although the overall mortality rate was not significantly i ncreased when patients with bacteremia due to gram-negative organisms initially received monotherapy or when patients with bacteremia due to gram-positive organisms received delayed vancomycin therapy, these st rategies increased the duration of therapy by 25%. Patients with bacte remia due to alpha-hemolytic streptococcus died more often when vancom ycin was not included in the initial empirical regimen (P = .004). Bec ause of the prognostic significance of extensive tissue or major organ infection, this factor should be considered in decisions concerning m odification of therapy and use of colony-stimulating factors. The cost -effectiveness of initial monotherapy and delayed vancomycin therapy r emains to be demonstrated.