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      Teicoplanin and vancomycin as treatment for glycopeptide-susceptible Enterococcus faecium bacteraemia: a propensity score-adjusted non-inferior comparative study

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          Abstract

          Objectives

          Limited evidence is available regarding alternative therapeutic agents to vancomycin in treating glycopeptide-susceptible Enterococcus faecium (GSEF) bacteraemia. This study assessed the effectiveness and safety of teicoplanin compared with vancomycin for treating GSEF bacteraemia.

          Patients and methods

          This was a retrospective, non-inferiority cohort study. Patients aged ≥18 years who developed GSEF bacteraemia and received either teicoplanin or vancomycin were included. The primary effectiveness outcome was the clinical success at the end of treatment, with a generalized linear model using the propensity score for selecting the agent as a covariate. We used an absolute difference of 20% in clinical success as the non-inferiority margin. Using multivariable logistic regression, the primary safety outcome was the incidence of acute kidney injury (AKI).

          Results

          In total, 164 patients (74 and 90 in the teicoplanin and vancomycin groups, respectively) were included. Overall, 64.9% (48/74) and 48.9% (44/90) of patients in the teicoplanin and vancomycin groups, respectively, achieved the primary effectiveness outcome. A generalized linear analysis showed an adjusted effectiveness difference of 9.9% (95% CI, −0.9% to 20.0%; P = 0.07), indicating non-inferiority of teicoplanin versus vancomycin. The incidence of AKI was 8.1% (6/74) and 24.4% (22/90) in the teicoplanin and vancomycin groups, respectively, with an adjusted OR of 0.242 (95% CI, 0.068 to 0.864; P = 0.029), indicating significantly lower AKI risk in the teicoplanin than in the vancomycin group.

          Conclusions

          Teicoplanin is a safe and useful alternative therapeutic agent for treating GSEF bacteraemia.

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          Most cited references46

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          KDIGO Clinical Practice Guidelines for Acute Kidney Injury

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            Revised equations for estimated GFR from serum creatinine in Japan.

            Estimation of glomerular filtration rate (GFR) is limited by differences in creatinine generation among ethnicities. Our previously reported GFR-estimating equations for Japanese had limitations because all participants had a GFR less than 90 mL/min/1.73 m2 and serum creatinine was assayed in different laboratories. Diagnostic test study using a prospective cross-sectional design. New equations were developed in 413 participants and validated in 350 participants. All samples were assayed in a central laboratory. Hospitalized Japanese patients in 80 medical centers. Patients had not participated in the previous study. Measured GFR (mGFR) computed from inulin clearance. Estimated GFR (eGFR) by using the modified isotope dilution mass spectrometry (IDMS)-traceable 4-variable Modification of Diet in Renal Disease (MDRD) Study equation using the previous Japanese Society of Nephrology Chronic Kidney Disease Initiative (JSN-CKDI) coefficient of 0.741 (equation 1), the previous JSN-CKDI equation (equation 2), and new equations derived in the development data set: modified MDRD Study using a new Japanese coefficient (equation 3), and a 3-variable Japanese equation (equation 4). Performance of equations was assessed by means of bias (eGFR - mGFR), accuracy (percentage of estimates within 15% or 30% of mGFR), root mean squared error, and correlation coefficient. In the development data set, the new Japanese coefficient was 0.808 (95% confidence interval, 0.728 to 0.829) for the IDMS-MDRD Study equation (equation 3), and the 3-variable Japanese equation (equation 4) was eGFR (mL/min/1.73 m2) = 194 x Serum creatinine(-1.094) x Age(-0.287) x 0.739 (if female). In the validation data set, bias was -1.3 +/- 19.4 versus -5.9 +/- 19.0 mL/min/1.73 m2 (P = 0.002), and accuracy within 30% of mGFR was 73% versus 72% (P = 0.6) for equation 3 versus equation 1 and -2.1 +/- 19.0 versus -7.9 +/- 18.7 mL/min/1.73 m(2) (P < 0.001) and 75% versus 73% (P = 0.06) for equation 4 versus equation 2 (P = 0.06), respectively. Most study participants had chronic kidney disease, and some may have had changing GFRs. The new Japanese coefficient for the modified IDMS-MDRD Study equation and the new Japanese equation are more accurate for the Japanese population than the previously reported equations.
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              CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting.

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                Author and article information

                Contributors
                Journal
                J Antimicrob Chemother
                J Antimicrob Chemother
                jac
                Journal of Antimicrobial Chemotherapy
                Oxford University Press (US )
                0305-7453
                1460-2091
                May 2023
                15 March 2023
                15 March 2023
                : 78
                : 5
                : 1231-1240
                Affiliations
                Department of Pharmacy, The University of Tokyo Hospital , Tokyo, Japan
                Department of Pharmacy, The University of Tokyo Hospital , Tokyo, Japan
                The Education Center for Clinical Pharmacy, Graduate School of Pharmaceutical Sciences, The University of Tokyo , Tokyo, Japan
                Department of Infectious Diseases, The University of Tokyo Hospital , Tokyo, Japan
                Department of Infection Control and Prevention, The University of Tokyo Hospital , Tokyo, Japan
                Department of Pharmacy, The University of Tokyo Hospital , Tokyo, Japan
                Department of Infectious Diseases, The University of Tokyo Hospital , Tokyo, Japan
                Department of Infection Control and Prevention, The University of Tokyo Hospital , Tokyo, Japan
                Department of Pharmacy, The University of Tokyo Hospital , Tokyo, Japan
                Author notes
                Corresponding author. E-mail: ryamaguchi-tky@ 123456g.ecc.u-tokyo.ac.jp
                Author information
                https://orcid.org/0000-0003-2012-0299
                https://orcid.org/0000-0002-4072-9096
                https://orcid.org/0000-0003-3073-6564
                Article
                dkad079
                10.1093/jac/dkad079
                10154127
                36918748
                3673bf76-4ffa-43f0-840a-ed6e315dba37
                © The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 25 November 2022
                : 28 February 2023
                Page count
                Pages: 10
                Funding
                Funded by: Japan Society for the Promotion of Science, doi 10.13039/501100001691;
                Award ID: JP22H04300
                Categories
                Original Research
                AcademicSubjects/MED00740
                AcademicSubjects/MED00290
                AcademicSubjects/MED00230

                Oncology & Radiotherapy
                Oncology & Radiotherapy

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