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https://hdl.handle.net/11499/7857
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DC Field | Value | Language |
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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 |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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