dc.contributor.author |
Batirel, A. |
|
dc.contributor.author |
Balkan, I.I. |
|
dc.contributor.author |
Karabay, O. |
|
dc.contributor.author |
Agalar, C. |
|
dc.contributor.author |
Akalin, S. |
|
dc.contributor.author |
Alici, O. |
|
dc.contributor.author |
Alp, E. |
|
dc.date.accessioned |
2019-08-16T12:32:56Z |
|
dc.date.available |
2019-08-16T12:32:56Z |
|
dc.date.issued |
2014 |
|
dc.identifier.issn |
0934-9723 |
|
dc.identifier.uri |
https://hdl.handle.net/11499/7857 |
|
dc.identifier.uri |
https://doi.org/10.1007/s10096-014-2070-6 |
|
dc.description.abstract |
The purpose of this investigation was to compare the efficacy of colistin-based therapies in extremely drug-resistant Acinetobacter spp. bloodstream infections (XDR-ABSI). A retrospective study was conducted in 27 tertiary-care centers from January 2009 to August 2012. The primary end-point was 14-day survival, and the secondary end-points were clinical and microbiological outcomes. Thirty-six and 214 patients [102 (47.7 %): colistin-carbapenem (CC), 69 (32.2 %): colistin-sulbactam (CS), and 43 (20.1 %: tigecycline): colistin with other agent (CO)] received colistin monotherapy and colistin-based combinations, respectively. Rates of complete response/cure and 14-day survival were relatively higher, and microbiological eradication was significantly higher in the combination group. Also, the in-hospital mortality rate was significantly lower in the combination group. No significant difference was found in the clinical (p=0.97) and microbiological (p=0.92) outcomes and 14-day survival rates (p=0.79) between the three combination groups. Neither the timing of initial effective treatment nor the presence of any concomitant infection was significant between the three groups (p>0.05) and also for 14-day survival (p>0.05). Higher Pitt bacteremia score (PBS), Acute Physiology and Chronic Health Evaluation II (APACHE II) score, Charlson comorbidity index (CCI), and prolonged hospital and intensive care unit (ICU) stay before XDR-ABSI were significant risk factors for 14-day mortality (p=0.02, p=0.0001, p=0.0001, p=0.02, and p=0.01, respectively). In the multivariable analysis, PBS, age, and duration of ICU stay were independent risk factors for 14-day mortality (p<0.0001, p<0.0001, and p=0.001, respectively). Colistin-based combination therapy resulted in significantly higher microbiological eradication rates, relatively higher cure and 14-day survival rates, and lower in-hospital mortality compared to colistin monotherapy. CC, CS, and CO combinations for XDR-ABSI did not reveal significant differences with respect to 14-day survival and clinical or microbiological outcome before and after propensity score matching (PSM). PBS, age, and length of ICU stay were independent risk factors for 14-day mortality. © 2014 Springer-Verlag. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Springer Verlag |
en_US |
dc.relation.ispartof |
European Journal of Clinical Microbiology and Infectious Diseases |
en_US |
dc.rights |
info:eu-repo/semantics/closedAccess |
en_US |
dc.subject |
amikacin |
en_US |
dc.subject |
aminoglycoside antibiotic agent |
en_US |
dc.subject |
carbapenem |
en_US |
dc.subject |
colistin |
en_US |
dc.subject |
doripenem |
en_US |
dc.subject |
gentamicin |
en_US |
dc.subject |
imipenem |
en_US |
dc.subject |
meropenem |
en_US |
dc.subject |
netilmicin |
en_US |
dc.subject |
piperacillin plus tazobactam |
en_US |
dc.subject |
rifampicin |
en_US |
dc.subject |
sulbactam |
en_US |
dc.subject |
sultamicillin |
en_US |
dc.subject |
tigecycline |
en_US |
dc.subject |
carbapenem derivative |
en_US |
dc.subject |
Acinetobacter baumannii |
en_US |
dc.subject |
adult |
en_US |
dc.subject |
APACHE |
en_US |
dc.subject |
article |
en_US |
dc.subject |
bloodstream infection |
en_US |
dc.subject |
Charlson Comorbidity Index |
en_US |
dc.subject |
concurrent infection |
en_US |
dc.subject |
drug dose reduction |
en_US |
dc.subject |
drug efficacy |
en_US |
dc.subject |
drug withdrawal |
en_US |
dc.subject |
eradication therapy |
en_US |
dc.subject |
female |
en_US |
dc.subject |
human |
en_US |
dc.subject |
intensive care unit |
en_US |
dc.subject |
length of stay |
en_US |
dc.subject |
loading drug dose |
en_US |
dc.subject |
major clinical study |
en_US |
dc.subject |
male |
en_US |
dc.subject |
monotherapy |
en_US |
dc.subject |
mortality |
en_US |
dc.subject |
nephrotoxicity |
en_US |
dc.subject |
neurotoxicity |
en_US |
dc.subject |
nonhuman |
en_US |
dc.subject |
Pitt bacteremia score |
en_US |
dc.subject |
priority journal |
en_US |
dc.subject |
propensity score |
en_US |
dc.subject |
risk factor |
en_US |
dc.subject |
scoring system |
en_US |
dc.subject |
survival rate |
en_US |
dc.subject |
treatment outcome |
en_US |
dc.subject |
treatment response |
en_US |
dc.subject |
Acinetobacter Infections |
en_US |
dc.subject |
aged |
en_US |
dc.subject |
bacteremia |
en_US |
dc.subject |
clinical trial |
en_US |
dc.subject |
comparative study |
en_US |
dc.subject |
drug combination |
en_US |
dc.subject |
drug effects |
en_US |
dc.subject |
isolation and purification |
en_US |
dc.subject |
microbial sensitivity test |
en_US |
dc.subject |
middle aged |
en_US |
dc.subject |
multicenter study |
en_US |
dc.subject |
multidrug resistance |
en_US |
dc.subject |
retrospective study |
en_US |
dc.subject |
Adult |
en_US |
dc.subject |
Aged |
en_US |
dc.subject |
Bacteremia |
en_US |
dc.subject |
Carbapenems |
en_US |
dc.subject |
Colistin |
en_US |
dc.subject |
Drug Resistance, Multiple, Bacterial |
en_US |
dc.subject |
Drug Therapy, Combination |
en_US |
dc.subject |
Female |
en_US |
dc.subject |
Humans |
en_US |
dc.subject |
Length of Stay |
en_US |
dc.subject |
Male |
en_US |
dc.subject |
Microbial Sensitivity Tests |
en_US |
dc.subject |
Middle Aged |
en_US |
dc.subject |
Retrospective Studies |
en_US |
dc.subject |
Risk Factors |
en_US |
dc.subject |
Sulbactam |
en_US |
dc.subject |
Treatment Outcome |
en_US |
dc.title |
Comparison of colistin-carbapenem, colistin-sulbactam, and colistin plus other antibacterial agents for the treatment of extremely drug-resistant Acinetobacter baumannii bloodstream infections |
en_US |
dc.type |
Article |
en_US |
dc.identifier.volume |
33 |
en_US |
dc.identifier.issue |
8 |
en_US |
dc.identifier.startpage |
1311 |
|
dc.identifier.startpage |
1311 |
en_US |
dc.identifier.endpage |
1322 |
en_US |
dc.identifier.doi |
10.1007/s10096-014-2070-6 |
|
dc.relation.publicationcategory |
Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı |
en_US |
dc.identifier.pmid |
24532009 |
en_US |
dc.identifier.scopus |
2-s2.0-84903819291 |
en_US |
dc.identifier.wos |
WOS:000338723600006 |
en_US |