Kv. Rolston, EXPANDING THE OPTIONS FOR RISK-BASED THERAPY IN FEBRILE NEUTROPENIA, Diagnostic microbiology and infectious disease, 31(2), 1998, pp. 411-416
Fever in neutropenic cancer patients is often due to the development o
f an infection. The standard management of febrile neutropenic patient
s involves the administration of empiric, hospital-based, parenteral a
ntibiotic therapy. Although this treatment strategy has evolved from e
xperience in high-risk patients with hematological malignancies, in wh
om bacterial infection can result in substantial morbidity and mortali
ty, it has been adopted for all patients with febrile neutropenia, lar
gely because of the inability of clinicians to reliably distinguish be
tween patients who are at high risk for developing such morbidity/mort
ality and those who are not. The development of risk-assessment models
has facilitated the recognition of high-, moderate-, and low-risk sub
groups among febrile neutropenic patients and allows the administratio
n of outpatient antibiotic therapy to the moderate- and low-risk group
s, with the same degree of efficacy and safety as hospital-based thera
py. Monotherapy with the carbapenems (imipenem/cilastatin and meropene
m), with their broad spectrum of activity and established efficacy in
high-risk patients, represents realistic options for risk-based treatm
ent oJ febrile neutropenic patients within and outside the hospital se
tting. (C) 1998 Elsevier Science Inc.