Emergence of extensively drug-resistant Acinetobacter baumannii complex over 10 years: Nationwide data from the Taiwan Surveillance of Antimicrobial Resistance (TSAR) program
© Kuo et al.; licensee BioMed Central Ltd. 2012
Received: 11 June 2012
Accepted: 23 August 2012
Published: 28 August 2012
Acinetobacter baumannii complex (ABC) has emerged as an important pathogen causing a variety of infections. Longitudinal multicenter surveillance data on ABC from different sources in Taiwan have not been published. Using data from the Taiwan Surveillance of Antimicrobial Resistance (TSAR) conducted biennially, we investigated the secular change in resistance of 1640 ABC from 2002 to 2010 (TSAR period III to VII) to different antimicrobial agents and identified factors associated with imipenem-resistant and extensively drug-resistant ABC (IRABC and XDRABC).
Isolates were collected by TSAR from the same 26 hospitals located in all 4 regions of Taiwan. Minimum inhibitory concentrations (MIC) were determined by reference broth microdilution method. Isolates nonsusceptible to all tested aminoglycosides, fluoroquinolones, β-lactam, β-lactam/β-lactam inhibitors, and carbapenems were defined as extensively drug-resistant (XDR). Multivariate logistic regression analysis was performed to assess the relationship between predictor variables among patients with resistant ABC and patients with non-resistant ABC.
The prevalence of IRABC increased from 3.4% in 2002 to 58.7% in 2010 (P < 0.001; odds ratio [OR], 2.138; 95% confidence interval [CI], 1.947 to 2.347) and that of XDRABC increased from 1.3% in 2002 to 41.0% in 2010 (P < 0.001; OR, 1.970; 95% CI, 1.773-2.189). The rates of non-susceptibility to other antimicrobial agents remained high (>55%) over the years with some fluctuations before and after TSAR V (2006) on some agents. Multivariate analysis revealed that recovery from elderly patients, origins other than blood, from ICU settings, or geographic regions are independent factors associated with IRABC and XDRABC. Although the prevalence of XDRABC increased in all four regions of Taiwan over the years, central Taiwan had higher prevalence of XDRABC starting in 2008. Susceptibility to polymyxin remained high (99.8%).
This longitudinal multicenter surveillance program revealed significant increase and nationwide emergence of IRABC and XDRABC in Taiwan over the years. This study also identified factors associated with IRABC and XDRABC to help guide empirical therapy and at-risk groups requiring more intense interventional infection control measures with focused surveillance efforts.
KeywordsExtensively drug-resistant Acinetobacter baumannii complex Antimicrobial resistance
Acinetobacter spp., especially Acinetobacter baumannii complex (ABC), has emerged as an important pathogen causing a variety of infections including urinary tract infection, skin and soft tissue infections, and pneumonia and bloodstream infections with high morbidity and mortality . The ability to chronically colonize patients and cause outbreaks which are usually hard to eradicate poses significant challenge to infection control and increases healthcare expenditure . In addition to its intrinsic resistance to many commonly used antibiotics, this troublesome pathogen can gain additional mechanism rapidly in response to new broad-spectrum antibiotics [3, 4]. Due to treatment failure, drug-resistant strains have been associated with higher mortality and prolonged hospital stay compared with susceptible ones [5, 6].
Carbapenems such as imipenem and meropenem are the last resort of drugs for the treatment of multidrug-resistant pathogens including ABC. However, the incidence of carbapenem resistance in ABC increased steadily in the 2000s [4, 7]. In Europe, the MYSTIC program in 2006 revealed a considerable increase in carbapenem resistance rates to 42.5% . Worldwide, the SENTRY program documented an overall increase in imipenem nonsusceptibility from 34.5% in 2006 to 59.8% in 2009 . Imipenem-resistance in Taiwan ranged from 22% in 2000 to 25% in 2005 . Ampicillin/sulbactam, tigecycline, and colistin are possible options for imipenem-resistant ABC but decreasing susceptibility to these agents has also been reported . Surveillance is therefore important in providing useful information for physicians in choosing empirical antibiotics. It also helps to address specific resistant issues within a region to help identify targeted intervention measures [11, 12].
Although there have been reports of the high prevalence of drug-resistant ABC in Taiwan [13, 14], longitudinal nationwide surveillance data on isolates from different sources in Taiwan have not been published. The Taiwan Surveillance of Antimicrobial Resistance (TSAR) is a nationwide program at the National Health Research Institutes  and has been conducted biennially since 1998 . Using data from TSAR, we aimed at detailing the secular change of resistance to various antimicrobial agents in ABC from different sources over 10 years and identify factors associated with imipenem-resistant and extensively drug-resistant ABC (IRABC and XDRABC).
Study period and isolate collection process
The study period spanned from 2002 to 2010 (corresponding to TSAR period III to VII). Bacterial isolates were collected biennially from July to September by the TSAR program from the same 26 hospitals except TSAR V (2006), in which one hospital did not participate. These hospitals comprised 11 medical centers and 15 regional hospitals, and are located in all 4 regions of Taiwan including 7, 8, 8, and 3 in the north, central, south and east region, respectively. The majority of the Taiwan’s population lives in the western part (north, central and south regions) while the eastern part is the least populated region. The collection protocol was similar for all 5 rounds of TSAR as described previously [16, 17]. Briefly, each hospital first collected 50 outpatient isolates, 30 adult ICU and 100 non-ICU inpatient isolates, and 20 pediatric isolates. After completion of the above collection, an additional 20 (for TSAR III to V) to 50 (for TSAR VI and VII) isolates from blood and sterile body sites were collected. The isolates were collected sequentially without specifying species. All isolates were stored at −80°C for subsequent testing. The bacterial isolates were recovered from clinical samples taken as part of standard care. The study was approved by the Research Ethics Committee of National Health Research Institutes (EC960205).
Bacterial isolates and information
For Acinetobacter spp., isolates were subcultured to blood agar and McConkey agar plates at our laboratory for purity check and to confirm species identification. Either Vitek I (prior to 2008) or Vitek II (2008 and 2010) GN card was used (bioMérieux, Marcy l'Etoile, France). In addition, conventional biochemical tests including oxidase, Triple Sugar Iron, 42°C, malonate, and hemolysis on sheep blood agar were used to aid in confirmation of the A. baumannii complex . The hospital also provided information on specimen source and patient age. For analysis, samples from upper respiratory tract were designated as respiratory origin. Samples from pus/discharge included those from abscesses or wounds.
Minimum inhibitory concentrations (MIC) of different agents were determined by reference broth microdilution test following the guidelines of Clinical and Laboratory Standards Institute (CLSI) using custom designed Sensititre panels (Trek Diagnostics, West Essex, England)  Amikacin, ampicillin/sulbactam, ceftazidime, cefepime, ciprofloxacin, gentamicin, levofloxacin, imipenem, and piperacillin/tazobactam were tested on all isolates from each study year. Polymyxin B and tigecycline were tested on imipenem-resistant isolates in 2002 and 2004 and on all isolates from 2008–2010. Trimethoprim-sulfamethoxazole was tested on all isolates from 2002, 2004 and 2010. Control strains included Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 25922 and ATCC 35218. Results were interpreted using the CLSI breakpoints except for colistin and tigecycline, for which the EUCAST breakpoints (for Enterobacteriaceae) were used (http://www.eucast.org/clinical_breakpoints). Isolates nonsusceptible to all the tested aminoglycosides, fluoroquinolones, β-lactam, β-lactam/β-lactam inhibitors, and carbapenems were defined as extensively drug-resistant (XDR) [20, 21].This is a modification of the ECDC definition for XDR, which is defined as non-susceptibility to at least one agent in all but two or fewer antimicrobial categories .
Data and statistical analysis
For analysis of susceptibility rates in different year and patient groups, we used the Whonet software . Univariate analysis was done using Student’s t test/Mann–Whitney U test, or Fisher’s exact tests as appropriate. Multivariate logistic regression analysis was performed to assess the relationship between predictor variables among patients with resistant ABC and patients with non-resistant ABC. The variables included those identified in the univariate analysis as possibly being associated with resistance rate (P < 0.05). For comparison of resistance between regions and specimen types, these variables were entered in the multivariate analysis in a dummy form (resistance rate in northern Taiwan or that of blood samples as the reference group, respectively). For the trend test calculation, a continuous variable (TSAR period III to VII corresponding to 3 to 7, respectively) was used . All analyses were performed with the Statistical Package for the Social Sciences version 18.0 (SPSS, Chicago, IL, USA). A P < 0.05 was considered to be statistically significant.
Source breakdown of Acinetobacter baumannii complex from the Taiwan Surveillance of Antimicrobial Resistance (TSAR) by year
TSAR III (2002)
TSAR IV (2004)
TSAR V (2006)
TSAR VI (2008)
TSAR VII (2010)
TSAR III-VII Combined
Medical centers (11)
Regional hospitals (15)
Changes in non-susceptibility to different antimicrobial agents over the years
Secular trend of antimicrobial non-susceptibility in Acinetobacter baumannii complex from the 2002 to 2010 Taiwan Surveillance of Antimicrobial Resistance (TSAR) program
Resistance rate (%) by year
2002 to 2006b
2006 to 2010
The rates of non-susceptibility to other antimicrobial agents remained high (>55%) over the years although fluctuations were observed before and after TSAR V (2006) on some agents (Table 2 & Figure 1); non-susceptibility to amikacin, cefepime, ceftazidime, levofloxacin, and piperacillin/tazobactam increased significantly before 2006 (TSAR V), then stayed at a plateau and even declined thereafter (Table 2). In contrast, the rates of non-susceptibility to ampicillin/sulbactam (range 56.1% - 64.1%) fluctuated over 10 years without significant change (P = 0.775; OR, 1.010; 95% CI, 0.942 to 1.084), while that of gentamicin decreased slightly since 2004 (P = 0.034; OR, 0.883; 95% CI, 0.787 to 0.991). The overall rate of susceptibility to tigecycline (MIC < = 2 mg/L) and polymyxin B was 97.7% and 99.8%, respectively in 1,160 tested isolates and 98.1% and 100%, respectively in IRABC.
Factors associated with emergence of imipenem-resistant A. baumannii complex (IRABC)
Factors associated with imipenem-resistant Acinetobacter baumannii complex (IRABC) in Taiwan
Mean age ± SDc
65.0 ± 20.2
70.0 ± 18.8
Age 65 and olderc
Emergence of extensively drug-resistant A. baumannii complex (XDRABC)
Factors associated with emergence of XDRABC
Factors associated with extensively drug-resistant Acinetobacter baumannii complex (XDRABC) in Taiwan
Mean age ± SDc
65.4 ± 20.2
70.6 ± 18.1
Age 65 and olderc
This nationwide longitudinal study of 1,640 ABC over 10 years revealed the continuous increase of non-susceptibility to imipenem and emergence of XDRABC. For most other antibiotics, resistance rate increased from 2002 to 2006 but ceased to increase or even decreased thereafter. The prevalence of IRABC and XDRABC was independently affected by age of patients, specimen types, healthcare settings, and geographic regions.
Resistance to imipenem, which is often accompanied with resistance to multiple other agents, has increased in all parts of the world, ranging from 14.1% in Europe to 39.4% in Latin America in 2004–2006 , and from 34.5% in 2006 to 59.8% in 2009 overall worldwide . Our study revealed the rapid increase in the prevalence of imipenem-resistance over 10 years in Taiwan, from 3.4% in 2002 to 58.7% in 2010. The imipenem-nonsusceptible rate of 62.6% in isolates from Asia-Pacific in 2009 reported by the SENTRY study was comparable to our result .
Although XDRABC in Taiwan has been observed in other pilot studies [10, 14], this is the first study addressing the emergence of XDRABC in Taiwan over a long period. However, the variety of definition regarding XDR precluded the comparison of our data with previous ones. The definition of XDR in our study was in accordance to that of Tan et al.  and approached the consensus of European Centre for Disease Prevention and Control  except that not all isolates were tested for trimethoprim-sulfamethoxazole. However, almost all of XDRABC tested showed resistance to it.
Prolonged hospitalization, ICU stay, invasive medical procedures, and prior broad-spectrum antibiotic use, especially carbapenem, third-generation cephalosporins, and fluoroquinolones, have been shown to be risk factors for acquisition of IRABC [4, 7, 25]. These factors, as well as clonal dissemination [26, 27], likely all contributed to the increased prevalence of IRABC and XDRABC in Taiwan over the years. A recent study found carbapenem use in Taiwan hospitals increased by 86% between 2003 and 2008, which was significantly associated with increased healthcare associated IRABC infections . The same study also found that the largest increase in carbapenem use occurred in the central region, the area we found the highest prevalence of IRABC and XDRABC. Strain variability and differences in oxacillinase distribution [26, 27] may also account for regional differences and the changes in resistance after 2006, and remain to be investigated.
Based on the independent associated factors we identified, the prevalence of imipenem-resistance and XDRABC varied greatly. To our knowledge, variations in resistance profiles among ABC from different sample origins have rarely been addressed before. Whether the lower resistance of isolates from blood compared to other sample origins resulted from different clonality and/or impaired virulence in the cost of resistance  remained to be elucidated. Varied prevalence among different areas and healthcare settings (ICU) in Asia has been observed . The insignificant difference between medical centers and regional hospitals may have resulted from frequent transportation of patients and high density of hospitals in Taiwan. The advanced age may imply the underlying conditions of the patients. Higher prevalence of IRABC and XDRABC in ICU and regional variations within Taiwan likely reflect differences in patient populations and antibiotic use [28, 30].
The rate of resistance to polymyxin B in our study was only 0.2%, which is similar to that found in isolates from the Asia-Western Pacific region between 2006 and 2009 . In contrast, one study in Korea reported a resistance rate of 18.1% . As for tigecycline, 0.2% of IRABC isolates had MIC > 2 mg/L in Asia region  whereas our study found it to be 1.9% in Taiwan. Susceptibility to polymyxin remained high even for the XDRABC isolates in our study. However, in a pilot study by Jean et al., , the authors reported higher rate of resistance to colistin and tigecycline in Taiwan. The source of isolates differed in the two studies. Ours were from different patient groups of both teaching and regional hospitals while theirs were from ICUs of ten major teaching hospitals. The underlying conditions, disease severity, and amount of colistin and tigecycline used would be different. However, both studies revealed that compared to other antibiotics, tigecycline and polymyxin B (or its less toxic derivatives, colistin) remained an in vitro effective antimicrobial agent for the treatment of IRABC or XDRABC in Taiwan.
This longitudinal multicenter surveillance program revealed significant increase and nationwide emergence of IRABC and XDRABC in Taiwan despite that non-susceptibility to other antibiotics remained stable or declined over the past 6 years. This study also identified factors associated with their resistance to help guide empirical therapy and at-risk groups requiring more intense interventional infection control measures with focused surveillance efforts.
Imipenem-Resistant Acinetobacter baumannii Complex
Extensively Drug-Resistant Acinetobacter baumannii Complex.
We thank the following 26 hospitals for participating in the Taiwan Surveillance of Antimicrobial Resistance (TSAR): Buddhist Tzu Chi General Hospital, Cathay General Hospital, Changhua Christian Hospital, Cheng-Ching Hospital, Chung Shan Medical University Hospital, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Far Eastern Memorial Hospital, Hua-Lien Hospital, Jen-Ai Hospital, Kaohsiung Armed Forces General Hospital, Kaohsiung Chang Gung Memorial Hospital of the C. G. M. F, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung Veterans General Hospital, Kuang Tien General Hospital, Lo-Hsu Foundation, Inc., - Lotung Poh-Ai Hospital, Mennonite Christian Hospital, Min-Sheng Healthcare, National Cheng Kung University Hospital, Saint Mary's Hospital Luodong, Show Chwan Memorial Hospital, Tungs' Taichung MetroHarbor Hospital, Taichung Veterans General Hospital, Tainan Sin-Lau Hospital - the Presbyterian Church in Taiwan, Taipei City Hospital Heping Fuyou Branch, Taipei City Hospital Zhongxiao Branch, Tri-Service General Hospital.
We express our gratitude to Kuang-Hung Chen and Mei-Chun Chiang (Institute of Public Health, School of Medicine, National Yang-Ming University) for their help in the statistics. This project was supported by an intramural grant from the National Health Research Institutes.
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