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Comparison of colistin-carbapenem, colistin-sulbactam, and colistin plus other antibacterial agents for the treatment of extremely drug-resistant Acinetobacter baumannii bloodstream infections

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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


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