Clinical outcomes of tigecycline alone or in combination with other antimicrobial agents for the treatment of patients with healthcare-associated multidrug-resistant Acinetobacter baumannii infections

被引:89
作者
Lee, Y. -T. [1 ,2 ,3 ]
Tsao, S. -M. [1 ,2 ,3 ]
Hsueh, P. -R.
机构
[1] Chung Shan Med Univ Hosp, Inst Med, Taichung, Taiwan
[2] Chung Shan Med Univ Hosp, Sch Med, Taichung, Taiwan
[3] Chung Shan Med Univ Hosp, Dept Internal Med, Div Infect Dis, Taichung, Taiwan
关键词
IN-VITRO; NOSOCOMIAL INFECTIONS; EFFICACY; SURVEILLANCE; SULBACTAM; EPIDEMIOLOGY; SAFETY; IMIPENEM/CILASTATIN; ANTIBIOTICS; MULTICENTER;
D O I
10.1007/s10096-013-1870-4
中图分类号
R51 [传染病];
学科分类号
100201 [内科学];
摘要
Tigecycline (TG) has been shown to be active in vitro against Acinetobacter baumannii, although data on the clinical efficacy of TG alone or in combination for the treatment of infections due to multidrug-resistant A. baumannii (MDRAB) remain limited. The purpose of this study was to investigate the clinical outcomes of patients with healthcare-associated infections (HAIs) caused by MDRAB who were treated with imipenem/cilastatin and sulbactam, and TG alone or in combination with other antibiotics. A total of 386 patients with HAIs caused by MDRAB were retrospectively analyzed and grouped into TG and non-TG groups, depending on whether they received TG treatment. Of the 266 patients in the TG group, 108 were treated with TG alone and 158 were treated with TG in combination with ceftazidime, ceftriaxone, piperacillin/tazobactam, or a carbapenem. All 120 patients in the non-TG group were treated with imipenem/cilastatin and sulbactam. The primary outcome measure was 30-day mortality after TG treatment and the secondary outcome was clinical outcome. There were no significant differences in survival rates between the two groups. However, the rate of unfavorable outcome was significantly lower (p < 0.05) among patients in the TG group than among patients in the non-TG group. The most significant predictor of unfavorable outcome was sepsis, whereas TG treatment and microbial eradication were the most significant predictors of favorable outcomes. Our study represents the largest study of patients with MDRAB infection treated with TG and expands our understanding of the role of TG therapy alone or in combination with other agents for the treatment of HAI caused by MDRAB.
引用
收藏
页码:1211 / 1220
页数:10
相关论文
共 52 条
[1]
[Anonymous], 2011, Performance standards for antimicrobial susceptibility testing: twenty-first informational supplement
[2]
[Anonymous], INDIAN J MED MICROBI, V30, P69
[3]
Tigecycline use in serious nosocomial infections: a drug use evaluation [J].
Bassetti, Matteo ;
Nicolini, Laura ;
Repetto, Ernestina ;
Righi, Elda ;
Del Bono, Valerio ;
Viscoli, Claudio .
BMC INFECTIOUS DISEASES, 2010, 10
[4]
Tigecycline [J].
Bhattacharya, M. ;
Parakh, A. ;
Narang, M. .
JOURNAL OF POSTGRADUATE MEDICINE, 2009, 55 (01) :65-68
[5]
AMERICAN-COLLEGE OF CHEST PHYSICIANS SOCIETY OF CRITICAL CARE MEDICINE CONSENSUS CONFERENCE - DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ ;
ABRAMS, JH ;
BERNARD, GR ;
BIONDI, JW ;
CALVIN, JE ;
DEMLING, R ;
FAHEY, PJ ;
FISHER, CJ ;
FRANKLIN, C ;
GORELICK, KJ ;
KELLEY, MA ;
MAKI, DG ;
MARSHALL, JC ;
MERRILL, WW ;
PRIBBLE, JP ;
RACKOW, EC ;
RODELL, TC ;
SHEAGREN, JN ;
SILVER, M ;
SPRUNG, CL ;
STRAUBE, RC ;
TOBIN, MJ ;
TRENHOLME, GM ;
WAGNER, DP ;
WEBB, CD ;
WHERRY, JC ;
WIEDEMANN, HP ;
WORTEL, CH .
CRITICAL CARE MEDICINE, 1992, 20 (06) :864-874
[6]
In vitro activity of tigecycline against 3989 Gram-negative and Gram-positive clinical isolates from the United States Tigecycline Evaluation and Surveillance Trial (TEST Program; 2004) [J].
Bouchillon, SK ;
Hoban, DJ ;
Johnson, BM ;
Johnson, JL ;
Hsiung, A ;
Dowzicky, MJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2005, 52 (03) :173-179
[7]
The rising problem of antimicrobial resistance in the intensive care unit [J].
Brusselaers, Nele ;
Vogelaers, Dirk ;
Blot, Stijn .
ANNALS OF INTENSIVE CARE, 2011, 1
[8]
Trends in the Susceptibility of Clinically Important Resistant Bacteria to Tigecycline: Results from the Tigecycline In Vitro Surveillance in Taiwan Study, 2006 to 2010 [J].
Chen, Yen-Hsu ;
Lu, Po-Liang ;
Huang, Cheng-Hua ;
Liao, Chun-Hsing ;
Lu, Chin-Te ;
Chuang, Yin-Ching ;
Tsao, Shih-Ming ;
Chen, Yao-Shen ;
Liu, Yung-Ching ;
Chen, Wei-Yu ;
Jang, Tsrang-Neng ;
Lin, Hsiu-Chen ;
Chen, Chih-Ming ;
Shi, Zhi-Yuan ;
Pan, Sung-Ching ;
Yang, Jia-Ling ;
Kung, Hsiang-Chi ;
Liu, Chun-Eng ;
Cheng, Yu-Jen ;
Liu, Jien-Wei ;
Sun, Wu ;
Wang, Lih-Shinn ;
Ko, Wen-Chien ;
Yu, Kwok-Woon ;
Chiang, Ping-Cherng ;
Lee, Ming-Hsun ;
Lee, Chun-Ming ;
Hsu, Gwo-Jong ;
Hsueh, Po-Ren .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (03) :1452-1457
[9]
Tetracycline antibiotics: Mode of action, applications, molecular biology, and epidemiology of bacterial resistance [J].
Chopra, I ;
Roberts, M .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2001, 65 (02) :232-+
[10]
[CLSI] Clinical and Laboratory Standards Institute, 2006, M2A9 CLSI