B. Meisenberg et al., PROPHYLACTIC ANTIBIOTICS ELIMINATE BACTEREMIA AND ALLOW SAFE OUTPATIENT MANAGEMENT FOLLOWING HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS STEM-CELL RESCUE, Supportive care in cancer, 4(5), 1996, pp. 364-369
Citations number
16
Categorie Soggetti
Oncology,Rehabilitation,"Medicine, General & Internal
This study examines the effectiveness of prophylactic ciprofloxacin an
d rifampin following high-dose chemotherapy and autologous stem cell r
escue (HDC/ASCR). Specific endpoints included the incidence of fever,
clinically documented infection, bacteremia, and readmission rates fro
m an outpatient bone marrow trans plant setting following infection or
fever. A group of 97 patients receiving 134 cycles of HDC/ASCR were s
tudied. Patients were given ciprofloxacin 750 mg p.o. twice daily and
rifampin 300 mg p.o. twice daily beginning on the day of stem cell rei
nfusion (24-48 h after completion of high-dose chemotherapy). Most pat
ients were either discharged to an outpatient setting following comple
tion of their chemotherapy or received all of their chemotherapy in an
outpatient setting. Febrile neutropenia was treated with empirical an
tibiotics in an outpatient setting unless it was complicated by hypote
nsion, renal failure, severe mucositis or other problems. The median d
uration of neutropenia (absolute neutrophil count below 500/mm(3)) was
7 days. Neutropenic fever occurred in 62% of patients but clinically
documented bacterial infection occurred in only 2 (1.5%) patients duri
ng their neutropenic period. No bacteremia was noted. Readmission to t
he hospital following fever or infection occurred in 26% of patients m
aintained in the outpatient setting. There were no deaths from a bacte
rial infection in this study although 1 patient (0.7%) died from asper
gillosis. Prophylactic ciprofloxacin and rifampin is a well-tolerated
and highly effective combination that effectively decreases the risk o
f both gram-positive and gram-negative bacterial infection following H
DC/ASCR. It facilitates outpatient management of myelosuppressed patie
nts receiving autologous stem cell rescue.