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      Different clinical characteristics and impact of carbapenem-resistance on outcomes between Acinetobacter baumannii and Pseudomonas aeruginosa bacteraemia: a prospective observational study

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          Abstract

          This study aimed to evaluate the differences in clinical characteristics and impact of carbapenem resistance (CR) on outcomes between Acinetobacter baumannii (Ab) and Pseudomonas aeruginosa (Pa) bacteraemia. We prospectively identified all patients with Ab and Pa bacteraemia in 10 hospitals over 1 year. Treatment failure was defined as all-cause 30-day mortality, persistent bacteraemia, or recurrent bacteraemia within 30 days. We included 304 Ab and 241 Pa bacteraemia cases. CR was detected in 216 patients (71%) with Ab bacteraemia and 55 patients (23%) with Pa bacteraemia. Treatment failure was significantly higher in CR-Ab than in CR-Pa (60.6% vs. 34.5%, P = 0.001). In Ab, severe sepsis or septic shock and high Pitt bacteraemia score were independent risk factors for treatment failure in the inappropriate empirical antibiotics group. In Pa, hospital-acquired infection and high Pitt bacteraemia score were independent risk factors for treatment failure in both groups. CR was an independent risk factor in Ab for treatment failure in both groups, but not in Pa bacteraemia. We demonstrated significant differences in clinical characteristics and impact of CR on clinical outcomes between Ab and Pa bacteraemia, suggesting that different treatment approaches may be needed.

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          A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation

          The objective of this study was to develop a prospectively applicable method for classifying comorbid conditions which might alter the risk of mortality for use in longitudinal studies. A weighted index that takes into account the number and the seriousness of comorbid disease was developed in a cohort of 559 medical patients. The 1-yr mortality rates for the different scores were: "0", 12% (181); "1-2", 26% (225); "3-4", 52% (71); and "greater than or equal to 5", 85% (82). The index was tested for its ability to predict risk of death from comorbid disease in the second cohort of 685 patients during a 10-yr follow-up. The percent of patients who died of comorbid disease for the different scores were: "0", 8% (588); "1", 25% (54); "2", 48% (25); "greater than or equal to 3", 59% (18). With each increased level of the comorbidity index, there were stepwise increases in the cumulative mortality attributable to comorbid disease (log rank chi 2 = 165; p less than 0.0001). In this longer follow-up, age was also a predictor of mortality (p less than 0.001). The new index performed similarly to a previous system devised by Kaplan and Feinstein. The method of classifying comorbidity provides a simple, readily applicable and valid method of estimating risk of death from comorbid disease for use in longitudinal studies. Further work in larger populations is still required to refine the approach because the number of patients with any given condition in this study was relatively small.
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            The Epidemiology of Carbapenem-Resistant Enterobacteriaceae: The Impact and Evolution of a Global Menace.

            Carbapenem-resistant Enterobacteriaceae (CRE) are a serious public health threat. Infections due to these organisms are associated with significant morbidity and mortality. Mechanisms of drug resistance in gram-negative bacteria (GNB) are numerous; β-lactamase genes carried on mobile genetic elements are a key mechanism for the rapid spread of antibiotic-resistant GNB worldwide. Transmissible carbapenem-resistance in Enterobacteriaceae has been recognized for the last 2 decades, but global dissemination of carbapenemase-producing Enterobacteriaceae (CPE) is a more recent problem that, once initiated, has been occurring at an alarming pace. In this article, we discuss the evolution of CRE, with a focus on the epidemiology of the CPE pandemic; review risk factors for colonization and infection with the most common transmissible CPE worldwide, Klebsiella pneumoniae carbapenemase-producing K. pneumoniae; and present strategies used to halt the striking spread of these deadly pathogens.
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              Treatment Options for Carbapenem-resistant Gram-negative Bacterial Infections

              Yohei Doi (2019)
              Abstract Antimicrobial resistance has become one of the greatest threats to public health, with rising resistance to carbapenems being a particular concern due to the lack of effective and safe alternative treatment options. Carbapenem-resistant gram-negative bacteria of clinical relevance include the Enterobacteriaceae, Pseudomonas aeruginosa, Acinetobacter baumannii, and more recently, Stenotrophomonas maltophilia. Colistin and tigecycline have been used as first-line agents for the treatment of infections caused by these pathogens; however, there are uncertainties regarding their efficacy even when used in combination with other agents. More recently, several new agents with activity against certain carbapenem-resistant pathogens have been approved for clinical use or are reaching late-stage clinical development. They include ceftazidime-avibactam, ceftolozane-tazobactam, meropenem-vaborbactam, imipenem-cilastatin-relebactam, plazomicin, eravacycline, and cefiderocol. In addition, fosfomycin has been redeveloped in a new intravenous formulation. Data regarding the clinical efficacy of these new agents specific to infections caused by carbapenem-resistant pathogens are slowly emerging and appear to generally favor newer agents over previous best available therapy. As more treatment options become widely available for carbapenem-resistant gram-negative infections, the role of antimicrobial stewardship will become crucial in ensuring appropriate and rationale use of these new agents.
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                Author and article information

                Contributors
                iammedkid@naver.com
                khsongmd@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                20 May 2022
                20 May 2022
                2022
                : 12
                : 8527
                Affiliations
                [1 ]GRID grid.412480.b, ISNI 0000 0004 0647 3378, Department of Internal Medicine, , Seoul National University Bundang Hospital, Seoul National University College of Medicine, ; Seongnam, Republic of Korea
                [2 ]GRID grid.413112.4, ISNI 0000 0004 0647 2826, Department of Internal Medicine, , Wonkwang University Hospital, ; Iksan, Republic of Korea
                [3 ]GRID grid.14005.30, ISNI 0000 0001 0356 9399, Department of Infectious Diseases, , Chonnam National University Medical School, ; Gwangju, Republic of Korea
                [4 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Department of Internal Medicine, , Seoul National University Hospital, Seoul National University College of Medicine, ; Seoul, Republic of Korea
                [5 ]GRID grid.411076.5, Department of Internal Medicine, , Ewha Womans University Hospital, ; Seoul, Republic of Korea
                [6 ]GRID grid.412588.2, ISNI 0000 0000 8611 7824, Department of Internal Medicine, , Pusan National University Hospital, ; Busan, Republic of Korea
                [7 ]GRID grid.488421.3, ISNI 0000000404154154, Department of Internal Medicine, , Hallym University Sacred Heart Hospital, ; Anyang, Republic of Korea
                [8 ]GRID grid.412479.d, Department of Internal Medicine, , Seoul Metropolitan Boramae Hospital, ; Seoul, Republic of Korea
                [9 ]GRID grid.411665.1, ISNI 0000 0004 0647 2279, Department of Internal Medicine, , Chungnam National University Hospital, ; Daejeon, Republic of Korea
                [10 ]GRID grid.411633.2, ISNI 0000 0004 0371 8173, Department of Internal Medicine, , Inje University Ilsan Paik Hospital, ; Goyang, Republic of Korea
                [11 ]GRID grid.412011.7, ISNI 0000 0004 1803 0072, Department of Internal Medicine, , Kangwon National University Hospital, ; Chuncheon, Republic of Korea
                [12 ]GRID grid.416355.0, ISNI 0000 0004 0475 0976, Present Address: Department of Internal Medicine, , Myongji Hospital, ; Goyang, Republic of Korea
                Article
                12482
                10.1038/s41598-022-12482-0
                9123196
                35595789
                cbc197f5-eb4b-4b92-8c5d-9f1898a354c3
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 31 December 2021
                : 5 May 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003725, National Research Foundation of Korea;
                Award ID: 2021R1F1A1063089
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100018688, Korea Disease Control and Prevention Agency;
                Award ID: 2017E280301
                Award Recipient :
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                © The Author(s) 2022

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                bacteria,pathogens
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                bacteria, pathogens

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