dc.contributor.author |
Samonis, G |
en |
dc.contributor.author |
Koutsounaki, E |
en |
dc.contributor.author |
Karageorgopoulos, DE |
en |
dc.contributor.author |
Mitsikostas, P |
en |
dc.contributor.author |
Kalpadaki, C |
en |
dc.contributor.author |
Bozionelou, V |
en |
dc.contributor.author |
Bompolaki, I |
en |
dc.contributor.author |
Sgouros, J |
en |
dc.contributor.author |
Taktikou, V |
en |
dc.contributor.author |
Falagas, ME |
en |
dc.date.accessioned |
2014-03-01T02:08:52Z |
|
dc.date.available |
2014-03-01T02:08:52Z |
|
dc.date.issued |
2012 |
en |
dc.identifier.issn |
09349723 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/29735 |
|
dc.subject.other |
amikacin |
en |
dc.subject.other |
antiinfective agent |
en |
dc.subject.other |
ceftazidime |
en |
dc.subject.other |
ofloxacin |
en |
dc.subject.other |
aged |
en |
dc.subject.other |
article |
en |
dc.subject.other |
chemically induced disorder |
en |
dc.subject.other |
drug combination |
en |
dc.subject.other |
female |
en |
dc.subject.other |
human |
en |
dc.subject.other |
kidney disease |
en |
dc.subject.other |
male |
en |
dc.subject.other |
methodology |
en |
dc.subject.other |
middle aged |
en |
dc.subject.other |
mortality |
en |
dc.subject.other |
neoplasm |
en |
dc.subject.other |
neutropenia |
en |
dc.subject.other |
prospective study |
en |
dc.subject.other |
pyrexia idiopathica |
en |
dc.subject.other |
survival |
en |
dc.subject.other |
treatment outcome |
en |
dc.subject.other |
Aged |
en |
dc.subject.other |
Amikacin |
en |
dc.subject.other |
Anti-Bacterial Agents |
en |
dc.subject.other |
Ceftazidime |
en |
dc.subject.other |
Drug Therapy, Combination |
en |
dc.subject.other |
Female |
en |
dc.subject.other |
Fever of Unknown Origin |
en |
dc.subject.other |
Humans |
en |
dc.subject.other |
Kidney Diseases |
en |
dc.subject.other |
Male |
en |
dc.subject.other |
Middle Aged |
en |
dc.subject.other |
Neoplasms |
en |
dc.subject.other |
Neutropenia |
en |
dc.subject.other |
Ofloxacin |
en |
dc.subject.other |
Prospective Studies |
en |
dc.subject.other |
Survival Analysis |
en |
dc.subject.other |
Treatment Outcome |
en |
dc.title |
Empirical therapy with ceftazidime combined with levofloxacin or once-daily amikacin for febrile neutropenia in patients with neoplasia: A prospective comparative study |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1007/s10096-011-1454-0 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1007/s10096-011-1454-0 |
en |
heal.publicationDate |
2012 |
en |
heal.abstract |
Combination antimicrobial therapy represents common practice in the treatment of febrile neutropenia aiming to broaden the antimicrobial spectrum against Gram-negative pathogens. We did a prospective, nonrandomized, comparative study to evaluate ceftazidime plus either levofloxacin or once-daily amikacin as empirical regimens for febrile neutropenia in patients with solid tumor or hematopoietic neoplasm in a region of high baseline resistance prevalence. We included 285 febrile neutropenic episodes in 235 individual patients. One hundred forty-eight cases received levofloxacin and 137 received amikacin, both in combination with ceftazidime. More cases in the levofloxacin than the amikacin group had underlying hematological malignancy; most other characteristics of the two groups were well balanced. Nephrotoxicity requiring treatment discontinuation occurred in one case in the amikacin group. No difference in clinical success (79.7% vs. 80.3%, p>0.99) or all-cause mortality (12.8% vs. 11.7%, p=0.86) was noted between the levofloxacin and the amikacin groups, even after adjustment for the independent predictor variables for each endpoint. Sepsis at presentation, presence of localizing symptoms/signs of infection, and isolation of a nonsusceptible Gram-negative pathogen independently predicted both clinical success and all-cause mortality. Additionally, underlying solid tumor independently predicted clinical success, while poor prognosis of the underlying neoplasia and skin/soft tissue infection independently predicted mortality. Ceftazidime plus levofloxacin had similar effectiveness to ceftazidime plus amikacin as empirical regimens for febrile neutropenia. Nephrotoxicity with once-daily amikacin was minimal. Inappropriate empirical therapy was associated with worse prognosis. © Springer-Verlag 2011. |
en |
heal.journalName |
European Journal of Clinical Microbiology and Infectious Diseases |
en |
dc.identifier.doi |
10.1007/s10096-011-1454-0 |
en |
dc.identifier.volume |
31 |
en |
dc.identifier.issue |
7 |
en |
dc.identifier.spage |
1389 |
en |
dc.identifier.epage |
1398 |
en |