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      The Efficacy and Safety of Arbekacin and Vancomycin for the Treatment in Skin and Soft Tissue MRSA Infection: Preliminary Study

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      https://www.riss.kr/link?id=A103897655

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      다국어 초록 (Multilingual Abstract)

      Background: Methicillin-resistant Staphylococcus aureus (MRSA) has become a one of the most important causes of nosocomial infections, and use of vancomycin for the treatment of MRSA infection has increased. Unfortunately, vancomycin-resistant enteroc...

      Background: Methicillin-resistant Staphylococcus aureus (MRSA) has become a one of the most important causes of nosocomial infections, and use of vancomycin for the treatment of MRSA infection has increased. Unfortunately, vancomycin-resistant enterococcus have been reported, as well as vancomycin-resistant S. aureus . Arbekacin is an antibacterial agent and belongs to the aminoglycoside family of antibiotics. It was introduced to treat MRSA infection. We studied the clinical and bacteriological efficacy and safety of arbekacin compared to vancomycin in the treatment of infections caused by MRSA.
      Materials and Methods: This was a retrospective case-control study of patients who were admitted to tertiary Hospital from January 1st, 2009 to December 31st, 2010, and received the antibiotics arbekacin or vancomycin. All the skin and soft tissue MRSA infected patients who received arbekacin or vancomycin were enrolled during the study period. The bacteriological efficacy response (BER) was classified with improved and failure. The improved BER was defined as no growth of MRSA, where failure was defined as growth of MRSA, culture at the end of therapy or during treatment. Clinical efficacy response (CER) was classified as improved and failure. Improved CER was defined as resolution or reduction of the majority of signs and symptoms related to the original infection. Failure was defined as no resolution and no reduction of majority of the signs and symptoms, or worsening of one or more signs and symptoms, or new symptoms or signs associated with the original infection or a new infection Results: Totally, 122 patients (63/99 in arbekacin, 59/168 in vancomycin group) with skin and soft tissue infection who recieved arbekacin or vancomcyin at least 4 days were enrolled and analysed. The bacteriological efficacy response [improved, arbekacin vs vancomycin; 73.0% (46/63), 95% confidence interval (CI) 60.3 to 83.4% vs 83.1% (49/59), 95% CI 71.0 to 91.6%] and clinical efficacy response [improved, arbekacin vs vancomycin; 67.2% (41/61), 95% CI 52.0 to 76.7 % vs 78.0% (46/59), 95%CI 65.3 to 87.7%] were similar between the two groups (P=0.264, 0.265). The complication rate was significantly higher in the vancomycin group [29/59(49.2%), 95% CI 35.9 to 62.5%] than arbekacin [10/63(15.9%), 95% CI 8.4 to 29.0%] (P <0.001).
      Conclusions: Arbekacin could be considered as an alternative antibiotics for vancomycin in skin and soft tissue infection with MRSA. However, further prospective randomized trials are needed to confirm this finding.

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      참고문헌 (Reference)

      1 김태형, "메티실린 내성 포도구균(MRSA) 감염에 대한 Arbekacin의임상적 효과 및 안전성" 대한내과학회 65 (65): 239-244, 2003

      2 Walsh TR, "prevalence and mechanisms ofvancomycin resistance in Staphylococcus aureus" 56 : 657-675, 2002

      3 Sievert DM, "Vancomycin-resistant Staphylococcus aureus in the United States, 2002-2006" 46 : 668-674, 2008

      4 Hwang JH, "Theusefulness of arbekacin compared to vancomycin" 31 : 1663-1666, 2012

      5 이종한, "Staphylococcus 균종과 그람음성 간균에 대한 Arbekacin의 시험관내 항균력" 대한진단검사의학회 27 (27): 292-297, 2007

      6 Lodise TP, "Relationship between initial vancomycin concentration-time profile and nephrotoxicity among hospitalizedpatients" 49 : 507-514, 2009

      7 Manjunath G, "Prediction equationsto estimate glomerular filtration rate: an update" 10 : 785-792, 2001

      8 Sato R, "Pharmacokinetic-pharmacodynamic relationship of arbekacinfor treatment of patients infected with methicillin-resistantStaphylococcus aureus" 50 : 3763-3769, 2006

      9 Nichols RL, "Optimal treatment of complicated skin andskin structure infections" 44 (44): 19-23, 1999

      10 정경태, "Nationwide Surveillance Study of Vancomycin-Intermediate Staphylococcus aureus Strains in Korean Hospitals from 2001 to 2006" 한국미생물·생명공학회 20 (20): 637-642, 2010

      1 김태형, "메티실린 내성 포도구균(MRSA) 감염에 대한 Arbekacin의임상적 효과 및 안전성" 대한내과학회 65 (65): 239-244, 2003

      2 Walsh TR, "prevalence and mechanisms ofvancomycin resistance in Staphylococcus aureus" 56 : 657-675, 2002

      3 Sievert DM, "Vancomycin-resistant Staphylococcus aureus in the United States, 2002-2006" 46 : 668-674, 2008

      4 Hwang JH, "Theusefulness of arbekacin compared to vancomycin" 31 : 1663-1666, 2012

      5 이종한, "Staphylococcus 균종과 그람음성 간균에 대한 Arbekacin의 시험관내 항균력" 대한진단검사의학회 27 (27): 292-297, 2007

      6 Lodise TP, "Relationship between initial vancomycin concentration-time profile and nephrotoxicity among hospitalizedpatients" 49 : 507-514, 2009

      7 Manjunath G, "Prediction equationsto estimate glomerular filtration rate: an update" 10 : 785-792, 2001

      8 Sato R, "Pharmacokinetic-pharmacodynamic relationship of arbekacinfor treatment of patients infected with methicillin-resistantStaphylococcus aureus" 50 : 3763-3769, 2006

      9 Nichols RL, "Optimal treatment of complicated skin andskin structure infections" 44 (44): 19-23, 1999

      10 정경태, "Nationwide Surveillance Study of Vancomycin-Intermediate Staphylococcus aureus Strains in Korean Hospitals from 2001 to 2006" 한국미생물·생명공학회 20 (20): 637-642, 2010

      11 Hiramatsu K, "Methicillin-resistant Staphylococcus aureus clinicalstrain with reduced vancomycin susceptibility" 40 : 135-136, 1997

      12 Wang G, "Increased vancomycinMICs for Staphylococcus aureus clinical isolatesfrom a university hospital during a 5-year period" 44 : 3883-3886, 2006

      13 이경원, "Increase of Ceftazidime- and Fluoroquinolone-Resistant Klebsiella pneumoniae and Imipenem-Resistant Acinetobacter spp. in Korea: Analysis of KONSAR Study Data from 2005 and 2007" 연세대학교의과대학 51 (51): 901-911, 2010

      14 Holmberg SD, "Health and economicimpacts of antimicrobial resistance" 9 : 1065-1078, 1987

      15 Kirby JT, "Geographic variations in garenoxacin (BMS284756) activitytested against pathogens associated with skin and softtissue infections: report from the SENTRY AntimicrobialSurveillance Program (2000)" 43 : 303-309, 2000

      16 Ryu JS, "Efficacy of teicoplaninin gram-positive bacterial infection" 24 : 183-189, 1992

      17 Suzuki K, "Efficacy and safety of arbekacin for staphylococcal infection in the NICU" 45 : 301-306, 2003

      18 Lee DG, "Efficacies of vancomycin, arbekacin, andgentamicin alone or in combination against methicillinresistantStaphylococcus aureus in an in vitro infectiveendocarditis model" 47 : 3768-3773, 2003

      19 Moet GJ, "Contemporary causes of skin and soft tissue infections inNorth America, Latin America, and Europe: report from theSENTRY Antimicrobial Surveillance Program (1998-2004)" 57 : 7-13, 2007

      20 Watanabe T, "Comparativestudies of the bactericidal, morphological and post-antibioticeffects of arbekacin and vancomycin against methicillinresistantStaphylococcus aureus" 39 : 471-476, 1997

      21 Wilson SE, "Clinical trial results with linezolid, an oxazolidinone,in the treatment of soft tissue and postoperativegram-positive infections" 2 : 25-35, 2001

      22 Nichols RL, "Clinical presentations of softtissueinfections and surgical site infections" 33 (33): 84-93, 2001

      23 Liu C, "Clinical practice guidelines bythe infectious diseases society of america for the treatmentof methicillin-resistant Staphylococcus aureus infectionsin adults and children: executive summary" 52 : 285-292, 2011

      24 Kobayashi Y, "Arbekacin" 5 : 227-230, 1995

      25 Wie SH, "Antimicrobialactivities of arbekacin against clinical isolates of Staphylococcusaureus and coagulase-negative Staphylococcusspecies" 33 : 254-260, 2001

      26 Hamilton-Miller JM, "Activity of the semi-synthetickanamycin B derivative, arbekacin against methicillinresistantStaphylococcus aureus" 35 : 865-868, 1995

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2010-02-25 학술지명변경 한글명 : 감염과화학요법 -> Infection and Chemotherapy
      외국어명 : Infection and Chemotherapy -> 미등록
      KCI등재후보
      2010-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2009-08-25 학술지명변경 외국어명 : 미등록 -> Infection and Chemotherapy KCI등재후보
      2008-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2008-01-01 평가 등재후보 탈락 (등재후보1차)
      2006-01-01 평가 등재후보 1차 FAIL (등재후보2차) KCI등재후보
      2005-05-27 학술지등록 한글명 : 감염과화학요법
      외국어명 : 미등록
      KCI등재후보
      2005-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2004-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.24 0.24 0.24
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.2 0.2 0.46 0.29
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