Literature DB >> 23263188

Clinical efficacy and safety of arbekacin sulfate in patients with MRSA sepsis or pneumonia: a multi-institutional study.

Tetsuya Matsumoto1, Hideaki Hanaki, Toshimi Kimura, Manabu Nemoto, Masaaki Higashihara, Hiroyuki Yokota, Shigeto Oda, Nobu Akiyama, Naoki Miyao, Minoru Yoshida, Tetsuo Yukioka, Kazui Soma, Kazuma Ohyashiki, Yukio Suzuki, Takao Arai, Keiichi Ikegami, Toshio Ichiwata, Yoshihito Otsuka, Masahiro Kobayashi, Kyoichi Totsuka, Keisuke Sunakawa.   

Abstract

Arbekacin (ABK) is an aminoglycoside and widely used in Japan for treatment of patients infected with methicillin-resistant Staphylococcus aureus (MRSA). Although, ABK has concentration-dependent antibacterial activity, the peak serum concentration (C (peak)) of ABK has not yet been fully investigated as an indicator of the efficacy of ABK. The present study was conducted in patients admitted to hospitals affiliated with the ABK Dose Finding Study Group, between October 2008 and June 2011, who had pneumonia or sepsis, the cause of which was identified or suspected to be MRSA. The initial target C (peak) was set at 15-20 μg/mL and therapeutic drug monitoring was conducted. Then the relationship between serum concentration and efficacy/safety of ABK was prospectively examined to obtain sufficient clinical efficacy. In total, 89 patients from 11 clinical sites in Japan were enrolled and 29 of these patients were subjected to efficacy analysis. The mean initial dose and C (peak) were 306.9 mg/day and 16.2 μg/mL, respectively. The efficacy rate was 95 % (19/20 patients) at 5-6 mg/kg or higher, 87.5 % (7/8) for sepsis and 90.5 % (19/21) for pneumonia, and the overall efficacy rate was 89.7 % (26/29). There was no increase in the incidence of adverse events. In conclusion, we recommend the initial dose of ABK at 5-6 mg/kg or higher and the dosage regimen should be adjusted to achieve C (peak) at 10-15 μg/mL or higher in the treatment of patients with pneumonia or sepsis caused by MRSA. This strategy would surely achieve low incidence of adverse events while obtaining high clinical efficacy.

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Year:  2012        PMID: 23263188     DOI: 10.1007/s10156-012-0519-z

Source DB:  PubMed          Journal:  J Infect Chemother        ISSN: 1341-321X            Impact factor:   2.211


  8 in total

1.  Clinical efficacy and safety of arbekacin for high-risk infections in patients with hematological malignancies.

Authors:  Katsuhiro Miura; Masaru Nakagawa; Hiromichi Takahashi; Yoshihito Uchino; Hitomi Kodaira; Noriyoshi Iriyama; Masashi Sakagami; Shimon Ohtake; Sumiko Kobayashi; Atsuko Hojo; Daisuke Kurita; Yujin Kobayashi; Machiko Kusuda; Yukio Hirabayashi; Yoshihiro Hatta; Masami Takei
Journal:  Int J Hematol       Date:  2015-12-29       Impact factor: 2.490

2.  Pharmacokinetic-Pharmacodynamic Target Attainment Analyses To Support Dose Selection for ME1100, an Arbekacin Inhalation Solution.

Authors:  Sujata M Bhavnani; Jeffrey P Hammel; Elizabeth A Lakota; M Courtney Safir; Brian D VanScoy; Yu Nagira; Christopher M Rubino; Nobuo Sato; Tomokazu Koresawa; Kenichiro Kondo; Paul G Ambrose
Journal:  Antimicrob Agents Chemother       Date:  2020-09-21       Impact factor: 5.191

3.  Arbekacin activity against contemporary clinical bacteria isolated from patients hospitalized with pneumonia.

Authors:  Helio S Sader; Paul R Rhomberg; David J Farrell; Ronald N Jones
Journal:  Antimicrob Agents Chemother       Date:  2015-03-23       Impact factor: 5.191

Review 4.  Arbekacin: another novel agent for treating infections due to methicillin-resistant Staphylococcus aureus and multidrug-resistant Gram-negative pathogens.

Authors:  Tetsuya Matsumoto
Journal:  Clin Pharmacol       Date:  2014-09-26

Review 5.  Clinical Usefulness of Arbekacin.

Authors:  Jae Hoon Lee; Chang-Seop Lee
Journal:  Infect Chemother       Date:  2016-03-31

6.  Clinical efficacy and safety in patients treated with teicoplanin with a target trough concentration of 20 μg/mL using a regimen of 12 mg/kg for five doses within the initial 3 days.

Authors:  Takashi Ueda; Yoshio Takesue; Kazuhiko Nakajima; Kaoru Ichiki; Kaori Ishikawa; Yoshiko Takai; Kumiko Yamada; Toshie Tsuchida; Naruhito Otani; Yoshiko Takahashi; Mika Ishihara; Shingo Takubo; Hiroki Ikeuchi; Motoi Uchino; Takeshi Kimura
Journal:  BMC Pharmacol Toxicol       Date:  2020-07-08       Impact factor: 2.483

7.  Clinical Efficacy and Safety of Arbekacin against Pneumonia in Febrile Neutropenia: A Retrospective Study in Patients with Hematologic Malignancies.

Authors:  Takashi Ohashi; Yukiyoshi Fujita; Hiroyuki Irisawa; Hidemasa Nakaminami; Takahiro Arai; Masumi Takahashi; Emi Momiyama; Naoya Murata; Kayoko Murayama; Taeko Saito
Journal:  Infect Chemother       Date:  2022-03

8.  Validation of Vancomycin Area under the Concentration-Time Curve Estimation by the Bayesian Approach Using One-Point Samples for Predicting Clinical Outcomes in Patients with Methicillin-Resistant Staphylococcus aureus Infections.

Authors:  Takashi Ueda; Yoshio Takesue; Kazuhiko Nakajima; Kaoru Ichiki; Kaori Ishikawa; Kumiko Yamada; Toshie Tsuchida; Naruhito Otani; Yoshiko Takahashi; Mika Ishihara; Shingo Takubo; Hiroki Ikeuchi; Motoi Uchino; Toshimi Kimura; Kazuaki Matsumoto; Kazutaka Oda; Takeshi Kimura
Journal:  Antibiotics (Basel)       Date:  2022-01-13
  8 in total

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