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Antibiotics profile map of clinical A. baumannii strains isolated from health institutions in Turkey: a database search study and analysis of publications from 2011 to 2022
Bulletin of the National Research Centre volume 47, Article number: 15 (2023)
Abstract
Background
Acinetobacter baumannii is recognized as a major threat that causes healthcare-associated infections and causes a huge challenge to the health system worldwide. This research study was designed to detect the types and profiles of antibiotics tested against A. baumannii clinical strains in Turkey to evaluate their effectiveness and reevaluate their usage.
Main body of the abstract
The study depended on data search strategy using the online electronic database. We carried out a detailed analysis to all original research articles from 2011 to 2022 all conducted in Turkey. The study involved 91 articles and revealed about 40 antibiotics tested from 2006 to 2021 against A. baumannii with a different frequency. The more frequency antibiotics tested by health institutions in Turkey during this period included 15 antibiotics which are (Amikacin, Gentamicin, Imipenem, Meropenem, Cefoperazone–sulbactam, Ceftazidime, Cefepime, Ampicillin/sulbactam, Piperacillin, Piperacillin/tazobactam, Ciprofloxacin, Levofloxacin, Trimethoprim–Sulfamethoxazole, Colistin and Tigecycline). The frequency of resistance rate with percentage of (80–100%) shown by A. baumannii against these antibiotics was as follows (40.96%, 50.64%, 77.77%, 78.31%, 46.15%, 94.11%, 88.23%, 80.85%, 95.46%, 91.93%, 93.42%, 82.85%, 53.57%, 2.66%, 3.70%), respectively. From 2016 to 2021, an increase in resistance rates by A. baumannii against Colistin and Tigecycline was indicated noticeably. The 0% resistance rates during this period against Colistin were reported in a percentage of 16.6%, while the appearance of highly noticeable resistance (from 80 to 100 = 3.70%) against Tigecycline and the continuous elevation of resistance rates against this drug was worrisome.
Short conclusion
Stability in high resistance rates against some antibiotics for the last 10 years and the increase in resistance rates against effective antibiotics by A. baumannii should undergo for more studies and re-evaluation.
Introduction
Acinetobacter baumannii is a major threat that causing healthcare-associated infections. And because of the increasing rates of resistance and the high mortality caused by A. baumannii, as well as the lack of effective treatment options due to the very few available drugs that can control these bacteria, the world health organization has been designated this bacteria as a priority 1-critical that urgently requires a new antibiotic innovation to control them (Tacconelli et al. 2018). Serious nosocomial infections caused by A. baumannii include pulmonary, meningitis, bacteremia/sepsis, urinary tract, wound and soft tissue infections as well peritonitis, osteomyelitis, synovitis and conjunctivitis (Gedefie et al. 2021; Roy et al. 2022; Nguyen and Joshi 2021). The rate of these infections increases obviously in intensive care units (ICUs) particularly patients requiring special equipment such as mechanical ventilation, endotracheal incubators and catheters in addition to patients suffering of trauma or burn and patients who underwent a recent surgery (Falcone et al. 2021; Ababneh et al. 2022). Infections due to A. baumannii are correlated with a high rate of mortality through causing serious infections, septic shock, and deaths (Vrancianu et al. 2020; Lee et al. 2022), besides increased costs and duration of hospitalization and limited therapeutic choices especially in (ICUs) (Ibrahim et al. 2021; Mohd Sazlly Lim et al. 2019). Even with suitable treatment, the mortality rate of infections caused by these bacteria can increase highly after one month stay in hospital (Falcone et al. 2022). Although A. baumannii resistance rates are reported in a variable value from region to region, they have been developing steadily and are occurring more rapidly than the innovation of novel antibiotics. Various clinical studies comparing single therapy to combination therapies showed similar mortality rates with no significant statistical difference in clinical cure. Mortality of 30 days in combination and in the monotherapy group was 43.3% and 42.9%, respectively (Giamarellou and Karaiskos 2022). Significant increase in resistance shown by Acinetobacter species to nearly all present anti-microbial drugs makes treatment options very limited for patients with A. baumannii infection and put the health institutions around the world in great concern. Our study is designed to introduce a detailed profile of antibiotics tested against A. baumannii between 2006 and 2021 in different health associations of Turkey. The study may provide a review about the antibiotics used in the past and re-evaluate the antibiotics policies to be applied in the future.
Materials and methods
The online electronic database was searched for studies regarding A. baumannii isolated from clinical samples in health institutions of Turkey to detect the antibiotics profile of these isolates.
Search strategy
The studies were screened in PubMed, Google Scholar and Google search for articles published in English and Turkish between 2011 and 2022. During the screening process, the text words or search terms used in combinations were “Acinetobacter spp.,” “A. baumannii,” “antibiotic resistance,” “antibiotic susceptibility” and “Turkey.”
Criteria for studies
The research involved only studies that contained antibiotics profile of A. baumannii isolated from clinical samples. These studies were published in English and Turkish. Case reports, antibiotics profile of Acinetobacter spp. and antibiotics profile of A. baumannii isolated only from environmental samples are excluded from the study.
Article selection and data collection
The studies should have been conducted in Turkey, the data presented should have been published in the years 2011–2022, the language should be English or Turkish, and papers should be original research articles providing access to the full text. The contents of the articles including titles, abstracts, materials and methods, results and discussion were all examined and assessed for data extraction. We extracted the following information from the articles that was finally included: all numerical values given in the studies regarding the rates of susceptibility and resistance of all antibiotics tested through the antibiotic susceptibility test against the clinical strains of A. baumannii, Date and year of publication, Duration of study, Number of isolates, Types of samples or site of infection, Ward of isolation, Mortality rates, The institution where the study was conducted and which region in Turkey.
Results
Study characteristics of included publications
All the details of study characteristics are summarized in Table 1. The study included 91 articles carried out in Turkey. The institutions, where the studies conducted in, involved state hospitals and clinic centers which included 92 and about 67 teaching hospitals. All these health institutions were distributed in different regions of Turkey and covered 41 states of Turkey which are Adana, Adiyaman, Afyonkarahisar, Amasya, Ankara, Balikesir, Bolu, Bursa, Çanakkale, Diyarbakir, Düzce, Elaziğ, Erzurum, Gaziantep, Giresun, Isparta, İstanbul, İzmir, Kahramanmaraş, Karabük, Kayseri, Kirikkale, Kirşehir, Kocaeli, Konya, Manisa, Mardin, Mersin, Muğla, Niğde, Ordu, Rize, Sakarya, Samsun, Şanliurfa, Tekirdağ, Tokat, Trabzon, Van, Zonguldak and Kuzey Kıbrıs (Northern Cyprus). With exclusion articles that indicated different cities or institutions as a source of isolates, we found that frequency of studies was more in Ankara, Istanbul and Izmir with (13, 12, 8 articles), respectively. The studies were published between 2011 and 2022 with a frequency numbers of 3 articles in 2011, 4 in 2012, 13 in 2013, 17 in 2014, 6 in 2015, 11 in 2016, 6 in 2017, 3 in 2018, 8 in 2019, 10 in 2020, 6 in 2021 and 4 in 2022. The articles covered studies that were performed between 2006 and 2021. In 5 articles, all the years of study are included in Table 1 because of the absence of the average of resistance rates. The date of study in 3 articles was unclear, so we could not include the rates of resistance in these articles with other numbers in analysis of the results. The total of A. baumannii clinical isolates was 24,425 isolates. A. baumannii were collected from diverse clinical specimens that included bronchial lavage, tracheal aspirate, bronchial washing fluid/bronchial brushing, transbronchial biopsy, blood, wound, throat swab, urine, sputum, catheter tip, cerebrospinal fluid, thoracentesis material, pleural fluid, peritoneal fluid, aspiration fluid, ear, paracentesis fluid, skin/mucosa, exudates and discharge samples. Majority of samples were taken from hospitalized patients admitted to intensive care units.
Antibiotic resistance shown by A. baumannii clinical strains
Analysis of the 91 articles concentrated on the antibiotics tested through antibiotic susceptibility test conducted by the health institutions in Turkey from 2006 to 2021 for detecting resistance and susceptibility of A. baumannii against these antibiotics. Antibiotic susceptibility methods used in the articles included: 40 articles used automated system (30 used VITEK 2 system and 10 used Phoenix 100 system). Twenty-six articles used disk diffusion method. Thirteen articles used mixed methods (automated system and disk diffusion method). Six articles used broth microdilution method. One article used only the E-Test method, and five articles did not mention the method. The results of the antibiotic susceptibility test were interpreted based on the recommendation of the Clinical Laboratory Standards Institute (CLSI) in majority of articles 80.5%, while the European Committee on Antimicrobial Susceptibility Testing (EUCAST) recommendations used in 19.5%.
The antibiotics profiles extracted from the studies are detailed in Table 2. The data showed the following results.
Aminoglycosides
Amikacin, Gentamicin, Netilmicin and Tobramycin were the antibiotics of aminoglycoside group used in studies included in the research during the period from 2006 to 2021. Amikacin was used in 76 articles and Gentamycin in 70 articles, while Netilmicin and Tobramycin were used in 27 and 21 articles, respectively. Resistance rate percentages of A. baumannii against aminoglycosides were as follows.
Amikacin
2007–2012: 68.1, 86.7, 32, 40, 100, 100, 63, 70.01, 100, 64, 100, 59, 86, 100, 71.7, 62, 74, 60, 52, 73, 53, 60, 75.3, 78.9, 44, 97, 91.8, 88, 84.6, 81.8, 84.2, 65, 56, 46, 71.1, 62, 50.
2012–2016: 73, 67.1, 81, 67.5, 86.3, 85.2, 86.3, 68.1, 60.7, 35.2, 79.3, 55.7, 65.6, 100, 63, 70, 94.81, 82, 92, 89, 94.2, 91.8, 72.92, 40, 81, 53.5, 52.9, 100.
2016–2021: 53, 59.3, 79, 90.7, 55.7, 46.6, 68.2, 73.5, 12.5, 77.6, 100, 97.8, 93.3, 39.2, 87.5, 83.3, 95, 98.5, 53.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 40.97%, from 50–70 = 48.19%, < 50 = 10.84%.
Gentamicin
2007–2012: 80, 39, 100, 48, 34.16, 100, 100, 90, 67, 54, 89, 90, 74.7, 11, 10, 11, 22, 75.7, 86, 77.1, 19.3, 84, 85, 93.9, 96, 76.5, 66, 87.2, 83.4, 82.5, 59.5, 62.
2012–2016: 65, 68.6, 76.8, 87, 74.1, 75.76, 77.2, 82.1, 83.6, 72.1, 100, 69, 84.3, 86.62, 86, 69.7, 74, 92, 95.8, 100, 93.7, 47, 88, 60.5, 55.7, 100.
2016–2021: 25, 60.5, 63.5, 66.9, 50.4, 70.5, 73.5, 78.9, 100, 95.7, 86, 89, 92.9, 93.2, 87.5, 82.3, 83.3, 90.7, 74.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 50.65%, from 50–70 = 36.36%, < 50 = 12.99%.
Netilmicin
2007–2012: 54.2, 39, 0, 89, 0, 6, 26.6, 13.7, 55, 41.7, 52.1, 57.6, 53, 57.
2012–2016: 36, 85.2, 58.7, 19.5, 97.2, 27.8, 94.3, 21, 36.
2016–2019: 92, 43.3, 72.7, 79.4, 75.8.
2019–2021: no data found.
The total percentage of resistance rates frequency appears as follows:
From 80–100 = 17.85%, from 50–70 = 35.72%, < 50 = 46.43%
Tobramycin
2007–2012: 36.3, 40.56, 58, 36.5, 55, 21.1, 84, 54.2, 54, 46.3, 68.1, 22.9.
2012–2016: 100, 37.8, 25.4, 0, 78, 100.
2016–2021: 47.5, 60.8, 100, 67.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 18.18%, from 50–70 = 36.36%, < 50 = 45.46%.
Carbapenems
Doripenem, Ertapenem, Imipenem and Meropenem were the antibiotics of Carbapenem group used in studies included in the research during the period from 2006 to 2021. Imipenem was found in 72 articles and Meropenem in 74 articles, while Ertapenem was found in 2 articles and Doripenem in 1 article. Resistance rate percentages of A. baumannii against Carbapenems were as follows.
Imipenem
2007–2012: 91.7, 53.3, 86, 20, 100, 100, 95, 80.07, 100, 71, 92, 100, 91, 57, 72.1, 50, 77, 78, 80, 70.2, 86, 74.5, 91.9, 93, 91, 100, 54, 92.3, 94.4, 98.9, 91.5, 100, 87.5, 100, 61.5, 74.3, 81.5, 100.
2012–2016: 100, 100, 73.2, 100, 91.3, 80, 90.91, 89.1, 91.1, 94.9, 73.8, 100, 84, 94.3, 98.5, 96, 100, 98, 97.1, 94.2, 99.4, 100, 95, 100, 95.3, 100, 100.
2016–2021: 73.7, 96, 94.4, 72.7, 97.1, 60.9, 100, 97.8, 92.8, 96.7, 98.6, 85, 100, 83.3, 100, 88. The total percentage of resistance rates frequency appears as follows: From 80–100 = 77.78%, from 50–70 = 20.99%, < 50 = 1.23%.
Meropenem
2007–2012:0.53.3, 86, 20, 100, 100, 94, 78.29, 100, 72, 92, 100, 91, 75, 73, 45, 71, 75, 88, 77, 86.6, 76.3, 100, 93.5, 92.7, 94, 100, 73.5, 98, 94.4, 98.9, 92, 100, 83.3, 78.6, 100, 58.3, 58.3, 71.4, 81.5, 100.
2012–2016: 100, 100, 91.6, 82.3, 93.94, 90.3, 89.8, 94.9, 73.8, 100, 86.9, 100, 94.3, 98.5, 96, 100, 98, 97.7, 94.2, 100, 95, 100, 100, 100.
2016–2021: 81.5, 72.8, 96, 95.2, 96.1, 81.7, 72.7, 97.1, 92.9, 100, 97.8, 93.1, 96.9, 95.9, 97.5, 100, 83.3, 100, 88.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 78.32%, from 50–70 = 19.28%, < 50 = 2.40%.
Ertapenem
2007–2012: no data found.
2012–2017: 99.6, 97.8.
2017–2021: no data found.
Doripenem
2007–2012: 100.
2012–2021: no data found.
Cephalosporins
(First generation) Cephalothin and (second generation) Cefuroxime were mentioned in 1 article for each of them, and third-generation Cephalosporins were found as follows: Cefixime in one article, Cefoperazone–sulbactam in 34 article, Cefotaxime in 14 articles, Ceftazidime in 61 article, Ceftriaxone in 15 article and (fourth generation) Cefepime was mentioned in 46 articles. All these antibiotics of this group used in studies were included in the research during the period from 2006 to 2021. Resistance rate percentages of A. baumannii against Cephalosporins were as follows:
Cephalothin
Two articles: One is performed in 2008 and the other from 2015–2017, and the two articles referred to 100% as a resistance rate.
Cefuroxime
Only one study was found performed between 2008 and 2012 and indicated 97.3% as a resistance rate against this antibiotic.
Cefoperazone–sulbactam
2007–2012: 63.9, 65, 26.7, 57, 36.6, 0, 87, 89, 79, 100, 92, 73.5, 73.6, 94.2, 77, 88.8, 45.7, 88.4, 78, 90.3, 89, 100, 21, 0, 9.1, 16.7.
2012–2016: 100, 98.15, 79.3, 77.8, 93.94, 79, 69.5, 93.6, 100, 98.3, 96.2, 69, 91.
2016–2021: no data found.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 46.16%, from 50–70 = 33.33%, < 50 = 20.51%.
Ceftazidime
2007–2012: 100, 86.7, 94, 86.6, 100, 97, 80.78, 100, 94, 95, 93, 100, 76.2, 96.1, 84, 98.9, 100, 97.8, 97.9, 98.9, 94.5, 100, 89.4, 100, 92.3, 91.4, 96.3, 100.
2012–2016: 100, 100, 86.6, 89, 100, 93.4, 86.7, 96.97, 96.8, 94.9, 88.6, 78.7, 100, 94.3, 99, 98.51, 100, 98.3, 98.9, 99.4, 100, 95, 98.5, 100, 100.
2016–2021: 80.5, 71.2, 98, 96.7, 95.3, 81.6, 75, 97.1, 100, 94.2, 98.6, 95, 100, 83.3, 100.
The total percentage of resistance rates appears as follows: From 80–100 = 94.12%, from 50–70 = 5.88%, < 50 = 0%.
Ceftriaxone
2007–2012: 100, 97, 100, 100, 100, 23.9.
2012–2016: 100, 85.4, 100, 100, 100.
2016–2021: 72.8, 96.5, 100.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 85.72%, from 50–70 = 7.14%, < 50 = 7.14%
Cefotaxime
2007–2012: 3.55, 97, 96, 100, 85, 98, 100, 98, 97.8, 100, 100, 100, 100.
2012–2016: 84.1, 78, 56, 98.9, 92.7, 100.
2016–2021: no data found.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 89.48%, from 50–70 = 5.26%, < 50 = 5.26%.
Cefixime
Only one study was found performed between 2011 and 2012 and indicated 81.13% as a resistance rate against this antibiotic.
Cefepime
2007–2012: 92, 100, 100, 97, 100, 95, 100, 95, 86, 94.8, 97.2, 95.3, 78, 100, 97.6, 100, 100, 96.8, 89.5, 100, 67.8, 100, 61.5, 80, 100, 100.
2012–2016: 82.9, 98, 100, 91.1, 82.2, 96.97, 93.7, 94.7, 32.8, 100, 96, 97.03, 100, 98.3, 99, 100, 100, 93. 2016–2021: 74.6, 97.5, 95.6, 72.7, 95.7, 100, 95.1. The total percentage of resistance rates frequency appears as follows: From 80–100 = 88.24%, from 50–70 = 9.80%, < 50 = 1.96%.
Monobactams
Aztreonam was the antibiotics of this group and mentioned in 5 articles: 2007–2012: 100, 100, 91.7. 2012–2016: 62.9, 63, 99.8. 2016–2021: 100. The total percentage of resistance rates frequency appears as follows: From 80–100 = 71.43%, from 50–70 = 28.57%, < 50 = 0%.
Penicillins
Antibiotics of this group found in research were Amoxicillin/clavulanate and Ampicillin found in 5 articles, Ampicillin/sulbactam in 42 articles, Piperacillin in 20 articles, Piperacillin/tazobactam in 59 articles, Ticarcillin and Ticarcillin/clavulanate found in 2 and 6 articles, respectively.
Amoxicillin/clavulanate
2007–2012: 100, 96.8, 70.3, 15.2.
2012–2017: 100.
2017–2021: no data found.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 60%, from 50–70 = 20%, < 50 = 20%.
Ampicillin
2007–2012: 100, 100, 100, 61.8.
2012–2017: 99.5.
2017–2021: no data found.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 80%, from 50–70 = 20%, < 50 = 0%.
Ampicillin/sulbactam
2007–2012: 40, 100, 53.3, 100, 97, 97.35, 100, 100, 82, 72.5, 96.8, 95.7, 97.9, 90.6, 93.5, 87.5, 11.9.
2012–2016: 100, 76.8, 100, 91.4, 88.9, 91.7, 69.6, 13.1, 100, 96.1, 94.07, 94, 98.3, 98.6, 100, 99.4, 100, 74, 100, 100, 100.
2016–2021: 62.8, 86.1, 94.5, 72.7, 95.7, 87.5, 100, 66.6, 100.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 80.86%, from 50–70 = 12.76%, < 50 = 6.38%.
Piperacillin
2007–2012: 100, 100, 97, 90.03, 100, 99, 100, 69.2, 100, 100, 100, 100, 100.
2012–2016: 100, 84.1, 100, 97.4, 99.5, 100, 89.
2016–2021: 99.6, 96.2.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 95.46%, from 50–70 = 4.54%, < 50 = 0%.
Piperacillin/tazobactam
2007–2012:100, 93.3, 94, 80, 0, 97, 96, 84, 97, 81.1, 90, 97.2, 96, 96, 100, 91.7, 100, 98.1, 98.9, 96, 48.6, 99, 95.5, 100, 85.7.
2012–2016: 100, 100, 81.7, 78, 100, 93.2, 82.2, 96.97, 92.8, 97.5, 75.4, 100, 92.6, 95, 97.7, 92, 100, 98.6, 98.1, 94.2, 100, 100, 93, 100, 100.
2016–2021: 82, 74, 99, 97.6, 98.9, 83.5, 72.7, 97.1, 95.7, 100, 91.6, 98.6.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 91.94%, from 50–70 = 4.84%, < 50 = 3.22%.
Ticarcillin
2007–2012: 100, 100.
2012–2021: no data found.
Ticarcillin/clavulanate
2007–2012: 97.9, 100, 97.1, 98.5.
2012–2018: 99.3, 97.5
2018–2021: No data found.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 100%, from 50–70 = 0%, < 50 = 0%.
Quinolones/fluoroquinolones
Antibiotics of this group found in research were Ciprofloxacin found in 68 articles, Levofloxacin in 33 articles, Ofloxacin and moxifloxacin which are found in one article for each of them.
Ciprofloxacin
2007–2012: 100, 99, 53.3, 81, 94, 87.5, 92, 76, 100, 92, 86.8, 81.1, 86, 95, 98.2, 95.7, 85, 100, 98, 100, 96.2, 97.8, 97, 100, 100, 82.9, 99, 90.47, 92.3, 91.4, 96.3, 100.
2012–2016: 100, 100, 84.1, 98, 100, 93.2, 83, 97.3, 91.7, 96.2, 77, 100, 93.4, 95, 98.51, 94, 100, 97.7, 98.8, 100, 100, 100, 100, 100, 97.7, 100, 100.
2016–2021: 81, 73.7, 97, 95.6, 94.3, 80.5, 72.7, 97.1, 100, 95.7, 93.4, 96.6, 98.6, 95, 100, 100, 92.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 93.42%, from 50–70 = 6.58%, < 50 = 0%.
Levofloxacin
2007–2012: 60, 89, 69.7, 100, 73, 94, 95.5, 81.1, 90, 100, 90.3, 95.8, 71.4.
2012–2016: 90.9, 82.2, 95.3, 89.5, 86, 74.6, 100, 97.77, 100, 97.7, 97.5, 96.9, 82, 93, 100.
2016–2021: 93, 95.5, 97.1, 60.1, 100, 91.6, 91.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 82.85%, from 50–70 = 17.15%, < 50 = 0%.
Ofloxacin
Only one study was found performed between 2007 and 2008 and indicated 98% as a resistance rate against this antibiotic.
Moxifloxacin
Only one study was found performed between 2009 and 2010 and indicated 22.62% as a resistance rate against this antibiotic.
Sulfonamides
Trimethoprim–Sulfamethoxazole was the only antibiotic used from this group and was mentioned in 50 articles.
2007–2012: 93.3, 59, 69, 81.13, 100, 83, 64.9, 63.7, 91.9, 91, 91.7, 85.4, 73.6, 72, 67.5, 77.5, 73, 92.3, 85.7, 96.3, 71.3.
2012–2016: 100, 95, 50, 89, 77.8, 68.9, 81.2, 91.1, 72.1, 96, 100, 88.3, 80.6, 76.8, 53, 96, 73.3, 100, 79.3.
2016–2021: 61.9, 73.9, 68.9, 59, 81.8, 82.3, 100, 58.7, 75.6, 85.7, 93.2, 90, 83.8, 50, 93.8, 63.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 53.57%, from 50–70 = 46.43%, < 50 = 0%.
Tetracyclines
This group included Doxycycline, Minocycline and Tetracycline. Doxycycline and Minocycline are mentioned in 2 articles, while Tetracycline in 17 articles.
Doxycycline
Two articles were performed in 2015 and 2018 and referred to 100% and 91.2%, respectively, as a resistance rate.
Minocycline
Two articles were performed in 2015 and 2018 and referred to 100% and 76.5%, respectively, as a resistance rate.
Tetracycline
2007–2012: 100, 70, 70.46, 55, 78, 87.8, 66.3, 72.
2012–2016: 94, 19.5, 97.7, 77.2, 76.4, 100, 93.7, 86.4, 83.
2016–2021: no data found.
The total percentage of resistance rates frequency appears as follows: From 80–100 = 47.05%, from 50–70 = 47.05%, < 50 = 5.90%.
Polypeptides
Colistin was tested in 72 articles, while Polymyxin B in one article.
Polymyxin B
One article was conducted between 2009 and 2011, and the resistance rate was 0%.
Colistin
2007–2012: 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 14, 0, 0, 0, 0, 2.9, 6, 0, 0, 0, 0, 0.6, 0, 0, 0, 0,
2012–2016: 0, 0, 0, 1.4, 0.29, 0, 5.5, 0.8, 0, 5.1, 0, 0, 3.5, 0, 0, 0, 0, 100, 0, 0, 2.1, 0.3, 2.9, 0, 1.2, 0, 0, 0, 0, 100
2016–2021: 6.8, 28, 0.5, 2.5, 3, 1.8, 13.6, 17.6, 0, 12.5, 2.2, 12.8, 9.1, 1.4, 0, 10.5, 0, 9.2.
The total percentage of resistance rates frequency appears as follows: 0 = 58.66%, from 0–10 = 29.33%, from 10–20 = 8%, from 20–30 = 1.33%, from 30–90 = 0%, 100 = 2.66%.
Tigecycline
This antibiotic found to be tested in 54 articles.
2007–2012: 0, 0, 0, 29, 0, 0, 11, 0, 6.6, 0, 37.7, 25, 44.9, 12.5, 34.8, 81.3, 23, 1, 2, 5.7, 2.7, 0.
2012–2016: 0, 40.8, 6.9, 72.4, 18.2, 41.3, 5.1, 3.8, 64, 6.1, 88.9, 66.7, 10.37, 0, 26.6, 49.3, 0, 1.7, 45.8, 2, 9.3, 11.4.
2016–2021: 30, 11, 21.7, 22, 58.8, 73.9, 18.7, 5.9, 6.8, 10. The total percentage of resistance rates frequency appears as follows: 0 = 20.37%, from 0–10 = 27.77%, from 10–20 = 11.11%, from 20–40 = 14.81%, from 40–80 = 16.66%, from 80–100 = 3.70%.
Sulbactam
This antibiotic was mentioned in 5 articles.
2007–2012: 26.6, 8
2012–2016: 100, 100
2018–2021: 73.9
The total percentage of resistance rates frequency appears as follows: From 80–100 = 40%, from 50–70 = 20%, < 50 = 40%.
Others
Chloramphenicol
One article was conducted between 2006 and 2010 and referred to 100% as a resistance rate.
Fosfomycin
Two articles were conducted between 2008–2012 and 2012–2017 and referred to 48.6% and 100%, respectively, as a resistance rate.
Nitrofurans
Nitrofurantoin was the antibiotics of this group and mentioned in two articles conducted between 2012–2014 and 2015–2017 and referred to 99.1% and 97.8%, respectively, as a resistance rate.
Rifampicin
Two articles were conducted between 2009–2011 and 2009–2010 and referred to 35% and 47.62%, respectively, as a resistance rate.
Based on all previous results, we found that 15 antibiotics were tested continuously at high frequency over the study years.
Trends in antibiotic resistance that occurred most frequently over the years were represented by a graph in Fig. 1. The overall percentages of a resistance rate for these antibiotics used between 2007 and 2021 were also represented by a graph in Fig. 2.
Groups: 6 articles used the group of antibiotic to indicate the resistance rate.
Aminoglycosides
2012 (33), 2014–2015 (70.9).
b-lactams
2012 (100).
Carbapenems
2007–2010 (92), 2013–2014 (100), 2014–2015 (100), 2014–2015 (91.8), 2014–2018 (75).
Cephalosporins
2014–2015 (93.8), 2014–2018 (100).
Quinolones
2007–2010 (88), 2014–2015 (98), 2014–2018 (100).
Conclusions
Emerging of highly resistant A. baumannii to most available antimicrobial agents led to a high incidence of morbidity and fatality mostly for intensive care units patients (Vrancianu et al. 2020; Lee et al. 2022). A 9-year research conducted in a university hospital in Turkey revealed that 81.9% of pathogens detected in clinical specimens were Gram-negative bacteria and A. baumannii constituted 34.8% and was the most frequent bacteria in patients with pneumonia, catheter infections, sepsis, wound infections and meningitides. The same study found that A. baumannii was the most common bacteria in intensive care units with a rate of 34.8% (Yetkin et al. 2018). In our study, we found that A. baumannii was isolated from intensive care units patients in 72.5% of the articles. Our study also revealed that about 40 antibiotics were tested against A. baumannii from 2006 to 2021 with a different frequency and these antibiotics were Amikacin, Gentamicin, Netilmicin, Tobramycin, Doripenem, Ertapenem, Imipenem, Meropenem, Cephalothin, Cefuroxime, Cefixime, Cefoperazone–sulbactam, Cefotaxime, Ceftazidime, Ceftriaxone, Cefepime, Aztreonam, Amoxicillin/clavulanate, Ampicillin, Ampicillin/sulbactam, Piperacillin, Piperacillin/tazobactam, Ticarcillin, Ticarcillin/clavulanate, Ciprofloxacin, Levofloxacin, Ofloxacin, moxifloxacin, Trimethoprim–Sulfamethoxazole, Doxycycline, Minocycline, Tetracycline, Colistin, Polymyxin B, Tigecycline, Sulbactam, Chloramphenicol, Fosfomycin, Nitrofurantoin and Rifampicin. But the frequent antibiotics that constitute the clear map of antibiotics used by health institutions in Turkey against A. baumannii for the last 10 years were Amikacin, Gentamicin, Imipenem, Meropenem, Cefoperazone–sulbactam, Ceftazidime, Cefepime, Ampicillin/sulbactam, Piperacillin, Piperacillin/tazobactam, Ciprofloxacin, Levofloxacin, Trimethoprim–Sulfamethoxazole, Colistin and Tigecycline. These 15 antibiotics were tested continuously with a large frequency during the last years against A. baumannii. The results referred to the stability for years of the high resistance rates against some antibiotics and increase in the resistance rates against other antibiotics. We found, for example, that highly resistance rates of A. baumannii against Imipenem, Meropenem, Cefoperazone–sulbactam, Ceftazidime, Cefepime, Ampicillin/sulbactam, Ciprofloxacin were steadily stable for the last 10 years. This result goes with data surveillance report published by World Health Organization (WHO) which included the antimicrobial resistance surveillance in Europe 2020–2022. The report showed that resistance phenotype (%) by Acinetobacter spp. against Carbapenem (Imipenem/Meropenem) in Turkey from 2016–2020 was as follows: 2016 (91.6), 2017 (91.5%), 2018 (92.2%), 2019 (90.4%) and 2020 (93.1%) and for Fluoroquinolone (Ciprofloxacin/Levofloxacin) as follows: 2016 (92.1%), 2017 (92.6%), 2018 (94.4%) 2019 (90.7%) and 2020 (93.6%) (European Centre for Disease Prevention and Control World Health Organization. Regional Office for Europe. Antimicrobial resistance surveillance in Europe 2022–2020 data 2022). Similar findings for Imipenem, Meropenem, Ampicillin/sulbactam and Ciprofloxacin have been reported in a very recent article (Çiftçi et al. 2022). The analysis in our study showed clearly that the increase in resistance rate against Colistin and Tigecycline was in ascending pattern for the last 5 years especially for Colistin which is considered as the last option for treatment. This result is compatible with analysis study on Colistin resistance in A. baumannii species in Turkey. The study which included 44 articles found a partial decrease in Colistin sensitivity in some regions over the years and more decrease in others. The study reported İzmir, Samsun, Diyarbakır, Düzce and Ankara as cities with the lowest Colistin susceptibility with rates of 81.8%, 82.4%, 94%, 94.1% and 95.8%, respectively. The study concluded that resistance development against Colistin has increased over the years (Görgün et al. 2021). According to the recent report by World Health Organization, the number of isolates of Acinetobacter spp. reported by laboratories in Turkey was increased from 2.463 isolates in 2016 to 3.170 in 2020. The report also indicated that percentage of isolates was higher in males and in age group 65 and over in year 2020 (European Centre for Disease Prevention and Control World Health Organization. Regional Office for Europe. Antimicrobial resistance surveillance in Europe 2022–2020 data 2022).
The continuous increase in A. baumannii numbers in health institutions especially in intensive care units with the high mortality caused by this pathogen needs huge studies and to be more highlighted. So we introduced in this study a detailed analysis about the picture of antibiotics profile that is used and tested against A. baumannii by different health institutions from different cities of Turkey from 2006 to 2021. We believe that the detailed numbers in our study can give a clear map about the types of antibiotics used continuously and the susceptibility profile regarding these antibiotics for the last 10 years. All the information in this study can be used by all health associations of Turkey including state hospitals and clinics and academic teaching hospitals to re-evaluate all the antibiotics used against A. baumannii. Although treatment options still very limited for A. baumannii, the reevaluation can answer the question about the reasonability of using the antibiotics that gave stability in high resistant rates for five years or even more. A study included four university hospitals and one state hospital in Ankara and concluded that the reduced consumption of Carbapenems was associated with decreased Carbapenems-resistant by Acinetobacter spp. and Pseudomonas spp. (Altunsoy et al. 2011). According to our results, we believe that the evaluation can also clarify that the continuous using of effective antibiotics as Colistin and Tigecycline can lead to decrease in Colistin sensitivity in few years. Therefore, reconsideration of antibiotic policies by the health institutions as well as the wise application of antibiotics in the future against A. baumannii is highly recommended. Precise and detailed studies regarding antibiotics used by every health setting against A. baumannii must be reported annually because of the rapid development in resistance by this pathogen. Long studies without annual numbers and mixed studies from different clinics or from different cities are not recommended because these studies may not give the real numbers about resistance phenotype by A. baumannii against antibiotics. For example, during analyzing the articles we found that a multicenter study that depended on collection of A. baumannii strains from hospitals located at 12 different provinces of Turkey reported a lower resistant rates against some antibiotics (Beriş et al. 2016). Therefore, we suggest that sensitivity test for A. baumannii strains must perform by the same clinic and in the same region of isolation. Recent study found that positive blood cultures were linked with increased odds of 90-day mortality comparing to urine cultures in patients with Carbapenem-resistant Acinetobacter baumannii (CRAB) and Carbapenem-resistant Pseudomonas aeruginosa (CRPA) (Vivo et al. 2022). Related findings were noticed during analysis of articles in our study, since we found that A. baumannii strains isolated from specific specimens gave a high resistance rate against some antibiotics. For example, in two studies a high resistance rate by A. baumannii strains most isolated from blood samples against Colistin and Tigecycline was reported with percentage of 14% for Colistin and 40.8 for Tigecycline (Bozkurt-Guzel et al. 2014; Karagöz et al. 2014). On the contrary, a different study reported a low resistance rate with (14.5%) against Tetracycline by A. baumannii strains isolated from blood. Another article in our study referred to clear difference in resistance rate against Colistin by A. baumannii strains isolated from sputum which gave 0% resistance rate and A. baumannii strains isolated from deep tracheal aspirate which gave 10.5%.resistance rate (Şenol et al. 2022). All these results may highlight the value of further studies to be performed regarding the relationship between the susceptibility of A. baumannii against antibiotics and the type of specimen that A. baumannii isolated from. More information in that field would improve treatment of patients infected with this pathogen in a timely manner. Combination therapy should take more attention in future studies. The use of at a minimum two active agents if possible is recommend according to the guidelines for treatment of Carbapenem-resistant Acinetobacter baumannii released by Infectious Disease Society of America (IDSA). The (IDSA) described the therapy of Ampicillin-sulbactam (high dose when the causative agent is indicated as resistant) combined with either Tigecycline or Minocycline as preferred choice (Tamma et al. 2022). Taking in consideration all the above issues in addition to obligatory infection control actions providing sufficient area and developing systems in intensive care units can support the aims in combating A. baumannii in hospitals. Therefore, efforts by all medical institutions related to critical care must be more activated and effective procedures to fight these organisms that cause high mortality should become a priority.
This study can assist in giving a precise image about antibiotics profiles used within the last years. As well, we believe that findings in our research are corresponding to the nationwide antibiotic restriction program (NARP) which is released in Turkey in 2003 and proved its effectiveness in reducing the costs and antibiotic resistance which is the same goal that we seek through work in this study. Our results may promote the development of alternative antimicrobial regimens for treatment of A. baumannii and may improve antibiotics regimens to be applied in the future. Further surveillance and studies on the development and epidemiological characteristic of clinical A. baumannii strains are required.
Availability of data and materials
Not applicable.
References
Ababneh Q, Abulaila S, Jaradat Z (2022) Isolation of extensively drug resistant Acinetobacter baumannii from environmental surfaces inside intensive care units. Am J Infect Control 50(2):159–165. https://doi.org/10.1016/j.ajic.2021.09.001
Ak O, Haciseyitoglu D, Cag Y, Gencer S, Biteker F, Ozer S (2016) In vitro activities of colistin combined with imipenem, tigecycline or cefoperazone-sulbactam against multidrug-resistant Acinetobacter baumannii blood-stream isolates. Dis Mol Med 4(4):51. https://doi.org/10.5455/dmm.20160830024755
Albayrak H, Bayraktar MT, Yıldız ZF (2021) Antibiotic resistance profile of Acinetobacter species isolated from blood cultures of inpatients in Harran University Hospital. Harran Üniversitesi Tıp Fakültesi Dergisi (j Harran Univ Med Fac) 18(2):165–169. https://doi.org/10.35440/hutfd.889541
Alp E, Eren E, Elay G, Cevahir F, Esmaoğlu A, Rello J (2017) Efficacy of loading dose of colistin in Acinetobacter baumannii ventilator-associated pneumonia. Infez Med 25(4):311–319
Altun HU, Yagci S, Bulut C et al (2014) Antimicrobial susceptibilities of clinical Acinetobacter baumannii isolates with different genotypes. Jundishapur J Microbiol 7(12):e13347. https://doi.org/10.5812/jjm.13347
Altun Ş, Koçak Tufan Z, Altun B, Önde U, Kınıklı S, Demiröz AP (2016) Growing OXA-23 type strains among carbapenem-resistant Acinetobacter baumannii and tigecycline as an alternate combination therapy. Turk J Med Sci 46(6):1894–1899. https://doi.org/10.3906/sag-1508-20
Altunsoy A, Aypak C, Azap A, Ergönül Ö, Balık I (2011) The impact of a nationwide antibiotic restriction program on antibiotic usage and resistance against nosocomial pathogens in Turkey. Int J Med Sci 8(4):339–344. https://doi.org/10.7150/ijms.8.339
Arabaci C, Karabulut N (2020) Acinetobacter species and their antibiotic resistance profiles isolated from various clinical specimens between 2014 and 2018. Ann Med Res 27(2):476–483. https://doi.org/10.5455/annalsmedres.2019.12.911
Asgin N, Otlu B, Cakmakliogullari EK, Celik B (2019) High prevalence of TEM, VIM, and OXA-2 beta-lactamases and clonal diversity among Acinetobacter baumannii isolates in Turkey. J Infect Dev Ctries 13(9):794–801. https://doi.org/10.3855/jidc.11684
Aşik G, Özdemir M, Kurtoğlu MG et al (2014) Detection of the frequency of PER-1 type extended-spectrum β-lactamase-producing Acinetobacter baumannii clinical isolates in Turkey: a multicenter study. Turk J Med Sci 44(6):1041–1046. https://doi.org/10.3906/sag-1309-126
Atasoy AR, Ciftci IH, Petek M (2015) Modifying enzymes related aminoglycoside: analyses of resistant Acinetobacter isolates. Int J Clin Exp Med 8(2):2874–2880
Atik TK, Atik B, Kilinç O et al (2018) Epidemiological evaluation of an Acinetobacter baumannii outbreak observed at an intensive care unit. Saudi Med J 39(8):767–772. https://doi.org/10.15537/smj.2018.8.22431
Atik TK, Çetinkaya RA, Özyurt M et al (2019) Identification of oxa-gene in Acinetobacter baumannii isolates obtained from clinical specimens and the clonality between these isolates. Nobel Medicus 15(3):44–51
Aydın M, Ergönül Ö, Azap A et al (2018) Rapid emergence of colistin resistance and its impact on fatality among healthcare-associated infections. J Hosp Infect 98(3):260–263. https://doi.org/10.1016/j.jhin.2017.11.014
Aye GL, Emel SC, Buket CA, Levent OZ (2012) In vitro synergistic activity of carbapenems in combination with other antimicrobial agents against multidrug-resistant Acinetobacter baumannii. Afr J Microbiol Res 6(12):2985–2992
Ayhan M, Kalem AK, Hasanoglu I et al (2021) Intrathecal and intraventricular administration of antibiotics in gram-negative nosocomial meningitis in a research hospital in Turkey. Turk Neurosurg 31(3):348–354. https://doi.org/10.5137/1019-5149.JTN.29844-20.2
Barış A, Bulut ME, Öncül A, Bayraktar B (2017) Distribution of Clinical Isolates at Species Level and Their Antibiotic Susceptibilities in Intensive Care Units Patients. Türk Yoğun Bakım Derneği Dergisi 15(1):21–27. https://doi.org/10.4274/tybdd.55707
Bayram Y, Parlak M, Aypak C, Bayram I (2013) Three-year review of bacteriological profile and antibiogram of burn wound isolates in Van. Turkey Int J Med Sci 10(1):19–23. https://doi.org/10.7150/ijms.4723
Bayram Y, Gultepe B, Bektas A, Parlak M, Guducuoglu H (2015) Evaluation of antibiotic resistance in Acinetobacter baumannii strains isolated from various clinical samples. Klimik Dergisi 26(2):49–53. https://doi.org/10.5152/kd.2013.17
Bayramoglu G, Kaya S, Besli Y et al (2012) Molecular epidemiology and the clinical significance of Acinetobacter baumannii complex isolated from cerebrospinal fluid in neurosurgical intensive care unit patients. Infection 40(2):163–172. https://doi.org/10.1007/s15010-011-0215-4
Beriş FŞ, Budak EE, Gülek D et al (2016) Investigation of the frequency and distribution of beta-lactamase genes in the clinical isolates of Acinetobacter baumannii collected from different regions of Turkey: a multicenter study. Mikrobiyol Bul 50(4):511–521. https://doi.org/10.5578/mb.2917
Boral B, Unaldi Ö, Ergin A, Durmaz R, Eser ÖK (2019) Acinetobacter Study Group. A prospective multicenter study on the evaluation of antimicrobial resistance and molecular epidemiology of multidrug-resistant Acinetobacter baumannii infections in intensive care units with clinical and environmental features. Ann Clin Microbiol Antimicrob 18(1):19. https://doi.org/10.1186/s12941-019-0319-8
Bozkurt-Guzel C, Savage PB, Akcali A, Ozbek-Celik B (2014) Potential synergy activity of the novel Ceragenin, CSA-13, against Carbapenem-resistant Acinetobacter baumannii strains isolated from bacteremia patients. Biomed Res Int 2014:1–5. https://doi.org/10.1155/2014/710273
Büyük A, Yilmaz FF, Gül Yurtsever S, Hoşgör LM (2017) Antibiotic Resistance Profiles and Genotypes of Acinetobacter baumannii Isolates and In Vitro Interactions of Various Antibiotics in Combination with Tigecycline and Colistin. Turk J Pharm Sci 14(1):13–18. https://doi.org/10.4274/tjps.44127
Çağlan E, Nigiz Ş, Sancak B, Gür D (2019) Resistance and heteroresistance to colistin among clinical isolates of Acinetobacter baumannii. Acta Microbiol Immunol Hung 67(2):1–5. https://doi.org/10.1556/030.66.2019.021
Cakirlar FK, Gonullu N (2014) The susceptibility to colistin and tigecycline of carbapenem-resistant Acinetobacter baumannii isolates in Turkey. Int J Infect Dis 21:85. https://doi.org/10.1016/j.ijid.2014.03.605
Cetin ES, Tekeli A, Ozseven AG, Us E, Aridogan BC (2013) Determination of in vitro activities of polymyxin B and rifampin in combination with ampicillin/sulbactam or cefoperazone/sulbactam against multidrug-resistant Acinetobacter baumannii by the E-test and checkerboard methods. Jpn J Infect Dis 66(6):463–468. https://doi.org/10.7883/yoken.66.463
Çetinkol Y, Telli M, Altunçekiç Yıldırım A, Çalgın MK (2016) Evaluation of the efficacy of colistin/sulbactam combination on carbapenem-resistant Acinetobacter baumannii strains. Mikrobiyol Bul 50(3):460–465. https://doi.org/10.5578/mb.26289
Ceyhan-Guüvensen N, Keskin D, Sankur F (2017) Antibiotic resistance ratio of Acinetobacter baumannii against to ten antibiotics and multidrug resistance index. Fresenius Environ Bull 25:8316–8320
Cicek AC, Karagoz A, Koksal E et al (2013) A single clone Acinetobacter baumannii outbreak in a state hospital in Turkey. Jpn J Infect Dis 66(3):245–248. https://doi.org/10.7883/yoken.66.245
Cicek AC, Saral A, Iraz M et al (2014) OXA- and GES-type β-lactamases predominate in extensively drug-resistant Acinetobacter baumannii isolates from a Turkish University Hospital. Clin Microbiol Infect 20(5):410–415. https://doi.org/10.1111/1469-0691.12338
Çıçek AÇ, Düzgün AÖ, Saral A et al (2013) Detection of class 1 integron in Acinetobacter baumannii isolates collected from nine hospitals in Turkey. Asian Pac J Trop Biomed 3(9):743–747. https://doi.org/10.1016/S2221-1691(13)60149-5
Çiftci İH, Aşik G, Karakeçe E et al (2013) Distribution of blaOXA genes in Acinetobacter baumannii strains: a multicenter study. Mikrobiyol Bul 47(4):592–602. https://doi.org/10.5578/mb.6388
Çiftçi İH, Kılbaş İ, Kahraman Kılbaş EP (2022) The war against the resistance of Acinetobacter Baumannii: a meta-analysis of findings in Türkiye. Erciyes Med J 44(5):447–454. https://doi.org/10.14744/etd.2022.94770
Çil B, Kütük E, Kabak M, Yıldız T, Hocanlı İ (2022) Acinetobacteria baumannıı infection in the intensive care unit-risk factors and antibiotic resistance. New Trends Med Sci 3(1):55–60
Çolakoğlu Ş, Alişkan H, Göçmen J (2014) Kan Kültürlerinden İzole Edilen Acinetobacter baumannii ve Pseudomonas aeruginosa Suşlarının Antibiyotik Duyarlılık Profilleri (2012–2014). Türk Mikrobiyoloji Cemiyeti Dergisi 44(4):132–138. https://doi.org/10.5222/TMCD.2014.132
Dede B, Kadanalı A, Karagöz G, Çomoğlu Ş, Bektaşoğlu MF, Yücel FM (2013) Investigation of antibiotic resistance of Acinetobacter baumannii strains isolated from various clinical samples in intensive care unit. Bakırköy Tıp Dergisi Bakirkoy. https://doi.org/10.5350/BTDMJB201309105
Demir T, Buyukguclu T (2013) Evaluation of the in vitro activity of fosfomycin tromethamine against Gram-negative bacterial strains recovered from community- and hospital-acquired urinary tract infections in Turkey. Int J Infect Dis 17(11):e966–e970. https://doi.org/10.1016/j.ijid.2013.04.005
Deveci Ö, Dal T, Tekin R, Bozkurt F, Tekin A, Dayan S (2013) Carbapenem resistance in Acinetobacter baumannii: where is it heading? Infez Med 21(3):211–215
Direkel Ş, Uzunoğlu-Karagöz E, Keleş S, Yapar K (2015) Antibiotic resistance rates of Acinetobacter baumannii strains isolated from various clinical samples in Giresun Prof. Dr. Atilla ilhan Ozdemir State Hospital. Gazi Med J 26(3):92–96
Direkel Ş, Çopur Çiçek A, Karagöz A et al (2016) Antimicrobial susceptibility and molecular characterization of multidrug-resistant Acinetobacter baumannii isolated in an university hospital. Mikrobiyol Bul 50(4):522–534. https://doi.org/10.5578/mb.34158
Doğan A, Gezer Y (2021) Treatment combinations and prognosis in multiple resistant Acinetobacter baumannii and Carbapenem resistant Klebsiella pneumonıae/oxytoca isolates. J Immunol Clin Microbiol 6(3):121–128
Doğan M, Taşbent FE, Feyzioğlu B, Baykan M (2014) Investigation of colistin, tigecycline and other antibiotic resistance profiles of Acinetobacter species isolated from several clinical specimens. ANKEM Dergisi 28(4):138–143. https://doi.org/10.5222/ankem.2014.138
Durdu B, Kritsotakis EI, Lee ACK et al (2018) Temporal trends and patterns in antimicrobial-resistant Gram-negative bacteria implicated in intensive care unit-acquired infections: A cohort-based surveillance study in Istanbul, Turkey. J Glob Antimicrob Resist 14:190–196. https://doi.org/10.1016/j.jgar.2018.04.015
Ece G, Samlioglu P, Atalay S, Kose S (2014) Evaluation of the in vitro colistin susceptibility of Pseudomonas aeruginosa and Acinetobacter baumannii strains at a tertiary care centre in Western Turkey. Infez Med 22(1):36–40
Ece G, Erac B, Yurday Cetin H, Ece C, Baysak A (2015) Antimicrobial susceptibility and clonal relation between Acinetobacter baumannii Strains at a Tertiary Care Center in Turkey. Jundishapur J Microbiol 8(2):e15612. https://doi.org/10.5812/jjm.15612
Ertugrul G, Hayriye G, Mustafa Z (2013) Effectiveness of menthol and folium menthae piperitae against Acinetobacter baumannii. Afr J Microbiol Res 7(23):2870–2874. https://doi.org/10.5897/AJMR12.1166
Ertürk A, Çiçek AÇ, Gümüş A et al (2014) Molecular characterisation and control of Acinetobacter baumannii isolates resistant to multi-drugs emerging in inter-intensive care units. Ann Clin Microbiol Antimicrob 13:36. https://doi.org/10.1186/s12941-014-0036-2
European Centre for Disease Prevention and Control & World Health Organization. Regional Office for Europe. Antimicrobial resistance surveillance in Europe 2022–2020 data. (2022). World Health Organization. Regional Office for Europe. https://apps.who.int/iris/handle/10665/351141. License: CC BY-NC-SA 3.0 IGO
Falcone M, Tiseo G, Nicastro M et al (2021) Cefiderocol as rescue therapy for Acinetobacter baumannii and other Carbapenem-resistant Gram-negative Infections in intensive care unit patients. Clin Infect Dis 72(11):2021–2024. https://doi.org/10.1093/cid/ciaa1410
Falcone M, Tiseo G, Leonildi A et al (2022) Cefiderocol-compared to colistin-based regimens for the treatment of severe infections caused by carbapenem-resistant Acinetobacter baumannii. Antimicrob Agents Chemother 66(5):e0214221. https://doi.org/10.1128/aac.02142-21
Gedefie A, Demsis W, Ashagrie M et al (2021) Acinetobacter baumannii biofilm formation and its role in disease pathogenesis: a review. Infect Drug Resist 14:3711–3719. https://doi.org/10.2147/IDR.S332051
Giamarellou H, Karaiskos I (2022) Current and potential therapeutic options for infections caused by difficult-to-treat and pandrug resistant gram-negative bacteria in critically ill patients. Antibiotics (basel) 11(8):1009. https://doi.org/10.3390/antibiotics11081009
Gorgun S, Guzel M, Gunal O, Kılıc SS (2020) The efficiency of Colistin, Minocycline, Tigecycline, and Doxycycline against multidrug-resistant Acinetobacter strains. Ann Clin Anal Med. https://doi.org/10.4328/ACAM.20207
Görgün S, Usanmaz M, Odabaşı H (2021) A meta-analysis study on colistin resistance in Acinetobacter baumannii species in Turkey. World J Adv Res Rev 10(2):090–097
Gozalan A, Ünaldı Ö, Kıırca F et al (2020) Molecular characterisation of Carbapenem-resistant Acinetobacter baumannii bloodstream infections in intensive care units. Türk Hijyen Ve Deneysel Biyoloji Dergisi 77(1):15–24. https://doi.org/10.5505/TurkHijyen.2019.53323
Gozutok F, Mutlu Sariguzel F, Celik I, Berk E, Aydin B, Guzel D (2013) Investigation of antimicrobial resistance rates of Acinetobacter baumannii strains from nosocomial infections. ANKEM Dergisi 27(1):7–12. https://doi.org/10.5222/ankem.2013.007
Guckan R, Kilinc C, Demir AD, Capraz A, Yanik K (2017) Antimicrobial susceptibility of Acinetobacter baumannii complex isolated from different clinical samples in a tertiary care hospital. J Antibiotics Res. https://doi.org/10.15744/2574-5980.1.103
Güdül Havuz S (2022) Acinetobacter baumannii strains grown in endotracheal aspirate culture in Samsun Bafra State Hospital intensive care units and the effect of COVID-19 on Acinetobacter baumannii strains (2019–2020). Türk Hijyen Ve Deneysel Biyoloji Dergisi 79(2):229–242. https://doi.org/10.5505/TurkHijyen.2022.48753
Güler E, Hürdoğanoğlu U, Farhan Almasoodi LH, Çakır N, Süer K (2022) Distribution of microorganisms and antibiotic resistance rates isolated from blood cultures: 5-year evaluation in a University Hospital in Northern Cyprus. Konuralp Medical Journal 14(1):13–22
Gultekin E, Uyanik MH, Hanci H, Erdil Z, Gelen FN, Celebi S (2014) Antimicrobial susceptibility of nonfermentative gram negative bacteria isolated from blood cultures. ANKEM Dergisi 28(3):79–85. https://doi.org/10.5222/ankem.2014.079
Gür H, Hazırolan G (2019) Detection of distribution and antibiotic susceptibility profiles of nonfermentative gram negative bacteria isolated from blood cultures. ANKEM Dergisi 33(2):49–57. https://doi.org/10.5222/ankem.2019.1915
Gür Vural D, Durupinar B (2016) Araştırılması§ Karbapenem Dirençli Acinetobacter baumannii Klinik İzolatlarında Sınıf D Beta Laktamaz Varlığının Araştırılması. Türk Mikrobiyoloji Cemiyeti Dergisi 46(4):181–187. https://doi.org/10.5222/TMCD.2016.181
Güven T, Yilmaz G, Güner HR, Kaya Kalem A, Eser F, Taşyaran MA (2014) Increasing resistance of nosocomial Acinetobacter baumannii: are we going to be defeated? Turk J Med Sci 44(1):73–78. https://doi.org/10.3906/sag-1211-21
Guven Gokmen T, Akcimen B, Kayar B, Marzi M, Koksal F (2016) The outbreak of Acinetobacter baumannii producing OXA-23 and OXA-51 type carbapenemases in a state hospital. J Exp Clin Med 33(3):157–161. https://doi.org/10.5835/jecm.omu.33.03.006
Hosoglu S, Hascuhadar M, Yasar E, Uslu S, Aldudak B (2012) Control of an Acinetobacter [corrected] baumannii outbreak in a neonatal ICU without suspension of service: a devastating outbreak in Diyarbakir, Turkey [published correction appears in Infection. 2012 Feb;40(1):107]. Infection 40(1):11–18. https://doi.org/10.1007/s15010-011-0180-y
Ibrahim S, Al-Saryi N, Al-Kadmy IMS, Aziz SN (2021) Multidrug-resistant Acinetobacter baumannii as an emerging concern in hospitals. Mol Biol Rep 48(10):6987–6998. https://doi.org/10.1007/s11033-021-06690-6
Kalin G, Alp E, Akin A, Coskun R, Doganay M (2014) Comparison of colistin and colistin/sulbactam for the treatment of multidrug resistant Acinetobacter baumannii ventilator-associated pneumonia. Infection 42(1):37–42. https://doi.org/10.1007/s15010-013-0495-y
Karadag Gecgel S, Demir C (2017) Increased colistin resistance of Acinetobacter species in intensive care unit-acquired infections in a tertiary care hospital. Int Arabic J Antimicrob Agents. https://doi.org/10.3823/815
Karagöz A, Baran I, Aksu N, Acar S, Durmaz R (2014) Characterization and determination of antibiotic resistance profiles of a single clone Acinetobacter baumannii strains isolated from blood cultures. Mikrobiyol Bul 48(4):566–576. https://doi.org/10.5578/mb.8276
Keskin H, Tekeli A, Dolapci İ, Öcal D (2014) Klinik örneklerden izole edilen Acinetobacter baumannii suşlarında beta-laktamaz kaynaklı direncin moleküler karakterizasyonu [Molecular characterization of beta-lactamase-associated resistance in Acinetobacter baumannii strains isolated from clinical samples]. Mikrobiyol Bul 48(3):365–376
Konca C, Tekin M, Geyik M (2021) Susceptibility patterns of multidrug-resistant Acinetobacter baumannii. Indian J Pediatr 88(2):120–126. https://doi.org/10.1007/s12098-020-03346-4
Kostakoğlu U, Ertürk A, Yildiz İE et al (2020) Antibiotic resistance and integron gene cassettes in Acinetobacter baumannii isolates produced in lower respiratory tract samples taken from the intensive care unit. Kırıkkale Üniversitesi Tıp Fakültesi Dergisi 22(3):450–546. https://doi.org/10.24938/kutfd.789547
Lee CM, Kim CJ, Kim SE et al (2022) Risk factors for early mortality in patients with carbapenem-resistant Acinetobacter baumannii bacteraemia. J Glob Antimicrob Resist 31:45–51. https://doi.org/10.1016/j.jgar.2022.08.010
Metan G, Sariguzel F, Sumerkan B, Tv R, Dijkshoorn L (2013) Clonal diversity and high prevalence of OXA-58 among Acinetobacter baumannii isolates from blood cultures in a tertiary care centre in Turkey [published correction appears in Infect Genet Evol. 2013 Jun;16:447–8]. J Mol Epidemiol Evolut Genet Infect Dis 2013(14):92–97. https://doi.org/10.1016/j.meegid.2012.11.003
Metan G, Pala Ç, Kaynar L, Cevahir F, Alp E (2014) A nightmare for haematology clinics: extensively drug-resistant (XDR) Acinetobacter baumannnii. Infez Med 22(4):277–282
Mohd Sazlly Lim S, Zainal Abidin A, Liew SM, Roberts JA, Sime FB (2019) The global prevalence of multidrug-resistance among Acinetobacter baumannii causing hospital-acquired and ventilator-associated pneumonia and its associated mortality: a systematic review and meta-analysis. J Infect 79(6):593–600. https://doi.org/10.1016/j.jinf.2019.09.012
Nemli A, Demirdal T (2016) Impact of appropriate empirical antibiotic therapy on clinical outcome in patients with Acinetobacter baumannii bacteremia. Open Forum Infect Dis. https://doi.org/10.1093/ofid/ofw172.805
Nguyen M, Joshi SG (2021) Carbapenem resistance in Acinetobacter baumannii, and their importance in hospital-acquired infections: a scientific review. J Appl Microbiol 131(6):2715–2738. https://doi.org/10.1111/jam.15130
Özcan N, Dal T, Can Ş, Tekin A, Gül K (2015) OXA Carbapenemase genes in multidrug-resistant A. baumannii strains in Southeast of Turkey. SMU Med J 2(2):21–32
Ozdemir H, Kendirli T, Ergün H et al (2011) Nosocomial infections due to Acinetobacter baumannii in a pediatric intensive care unit in Turkey. Turk J Pediatr 53(3):255–260
Ozekinci T, Habip Z, Onder N, Koçoglu ME (2020) Antibiotic resistance of Acinetobacter baumannii strains isolated in 2015–2018 years. Van Med J 27(3):340–344. https://doi.org/10.5505/vtd.2020.73384
Özkul C, Hazırolan G (2020) Oxacillinase gene distribution, antibiotic resistance, and their correlation with biofilm formation in Acinetobacter baumannii bloodstream isolates. Microb Drug Resist 27(5):637–646. https://doi.org/10.1089/mdr.2020.0130
Ozyurt S, Kostakoglu U, Yildiz IE et al (2020) Investigation of the clonal associations in Acinetobacter Baumannii strains isolated from the respiratory samples of patients in a tertiary research hospital. Niger J Clin Pract 23(8):1155–1162. https://doi.org/10.4103/njcp.njcp_549_18
Roy S, Chowdhury G, Mukhopadhyay AK, Dutta S, Basu S (2022) Convergence of biofilm formation and antibiotic resistance in Acinetobacter baumannii infection. Front Med (lausanne) 9:793615. https://doi.org/10.3389/fmed.2022.793615
Ruh E, Gazi U, Güvenir M, Süer K, Çakır N (2016) Antibiotic resistance rates of Pseudomonas aeruginosa, Acinetobacter baumannii and Klebsiella pneumoniae isolated from a university-affiliated hospital in North Cyprus. Türk Hijyen Ve Deneysel Biyoloji Dergisi 73(4):333–344
Şafak B, Kilinç O, Tunç N (2016) Klinik Örneklerden İzole Edilen Acinetobacter baumannii Suşlarının Antibiyotik Duyarlılık Oranlarının İncelenmesi. Investigation of antibiotic susceptibility of Acinetobacter baumannii isolated from clinical specimens (2010–2016). Flora İnfeksiyon Hastalıkları Ve Klinik Mikrobiyoloji Dergisi 21(2):77–81
Şahin AR, Doğruer D, Nazik S et al (2019) Hastane Kökenli Patojenlerde Artan Antimikrobiyal Direnç Sorunu: Acinetobacter baumannii. Online Türk Sağlık Bilimleri Dergisi 4(2):156–169. https://doi.org/10.26453/otjhs.462304
Saral A, Cinemre S, Okumus F et al (2021) Investigation of class 1 integrons with antibiotic resistance genes in multidrug-resistant Acinetobacter baumannii strains and determination of plant extract effects on multidrug-resistant isolates. Farmacia 69(5):914–918. https://doi.org/10.31925/farmacia.2021.5.13
Sargin Altunok E, Koc MM (2014) Comparison of antibiotic resistance rates in Acinetobacter strains isolated from intensive care units by year. ANKEM Dergisi 28(1):1–7. https://doi.org/10.5222/ankem.2014.001
Sarı AN, Biçmen M, Gülay Z (2013) The first report on the outbreak of OXA-24/40-like carbapenemase-producing Acinetobacter baumannii in Turkey. Jpn J Infect Dis 66(5):439–442
Say Coskun US, Caliskan E, Copur Cicek A, Turumtay H, Sandalli C (2019) β-lactamase genes in carbapenem resistance Acinetobacter baumannii isolates from a Turkish university hospital. J Infect Dev Ctries 13(1):50–55. https://doi.org/10.3855/jidc.10556
Şenol FF, Bahçeci İ, Arslan N et al (2022) Comparison of respiratory tract pathogens and antibiotic susceptibility profiles of patients diagnosed with COVID-19 with pre-COVID-19. J Health Sci Med 5(2):510–516. https://doi.org/10.32322/jhsm.1010249
Şimşek M, Demir C (2020) Determination of colistin and tigecycline resistance profile of Acinetobacter baumannii strains from different clinical samples in a territory hospital in Turkey. J Health Sci Med Res 38(2):81–91. https://doi.org/10.31584/jhsmr.2020727
Tacconelli E, Carrara E, Savoldi A, Harbarth S, Mendelson M, Monnet DL et al (2018) WHO pathogens priority list working group. Discovery, research, and development of new antibiotics: the WHO priority list of antibiotic-resistant bacteria and tuberculosis. Lancet Infect Dis 18(3):318–327. https://doi.org/10.1016/S1473-3099(17)30753-3
Tamma PD, Aitken SL, Bonomo RA et al (2022) Infectious diseases society of america guidance on the treatment of AmpC β-lactamase-producing enterobacterales, carbapenem-resistant Acinetobacter baumannii, and Stenotrophomonas maltophilia infections. Clin Infect Dis 74(12):2089–2114. https://doi.org/10.1093/cid/ciab1013
Tasbakan MS, Pullukcu H, Sipahi OR, Tasbakan MI, Aydemir S, Bacakoglu F (2011) Is tigecyclin a good choice in the treatment of multidrug-resistant Acinetobacter baumannii pneumonia? J Chemother 23(6):345–349. https://doi.org/10.1179/joc.2011.23.6.3455
Tasdogan A (2020) Risk factors of mortality from Acinetobacter Baumannii infection in intensive care units. Eurasian J Med Investig 4(1):55–60. https://doi.org/10.14744/ejmi.2019.24282
Temocin F, Erdinc FS, Tulek N et al (2015) Synergistic effects of sulbactam in multi-drug-resistant Acinetobacter baumannii. Braz J Microbiol 46(4):1119–1124. https://doi.org/10.1590/S1517-838246420140101
Turkoglu M, Mirza E, Tunçcan ÖG et al (2011) Acinetobacter baumannii infection in patients with hematologic malignancies in intensive care unit: risk factors and impact on mortality. J Crit Care 26(5):460–467. https://doi.org/10.1016/j.jcrc.2011.04.007
Uğur M, Genç S (2019) Three year resistance profile of Acinetobacter baumannii and Pseudomonas aeruginosa strains isolated from intensive care units. Turk J Intensive Care 17(3):130–137. https://doi.org/10.4274/tybd.galenos.2018.94103
Uskudar-Guclu A, Altay-Kocak A, Akcil Ok M, Tutluoglu B, Basustaoglu AC (2021) Respiratory Study Group. Antibacterial resistance in lower respiratory tract bacterial pathogens: a multicenter analysis from Turkey. J Infect Dev Ctries 15(2):254–262. https://doi.org/10.3855/jidc.12599
Uzun B, Gungor S, Yurtsever SG, Afsar İ, Demirci M (2012) Evalution of resistance to various antibiotics in Pseudomonas aeruginosa and Acinetobacter baumannii strains isolated from blood cultures of intensive care patients. ANKEM Dergisi 26(2):55–60. https://doi.org/10.5222/ankem.2012.055
Uzunoglu E, Direkel S et al (2017) Co-existance of isaba1/blaoxa-51/23 is increasing in carbapenem rersistant Acinetobacter baumannii isolates in Turkey. Acta Med Mediterr 33(6):1001. https://doi.org/10.19193/0393-6384_2017_6_159
Vivo A, Fitzpatrick MA, Suda KJ et al (2022) Epidemiology and outcomes associated with carbapenem-resistant Acinetobacter baumannii and carbapenem-resistant Pseudomonas aeruginosa: a retrospective cohort study. BMC Infect Dis 22(1):491. https://doi.org/10.1186/s12879-022-07436-w
Vrancianu CO, Gheorghe I, Czobor IB, Chifiriuc MC (2020) Antibiotic resistance profiles, molecular mechanisms and innovative treatment strategies of Acinetobacter baumannii. Microorganisms 8(6):935. https://doi.org/10.3390/microorganisms8060935
Yavaş S, Yetkin MA, Kayaaslan B et al (2016) Investigating the in vitro synergistic activities of several antibiotic combinations against carbapenem-resistant Acinetobacter baumannii isolates. Turk J Med Sci 46(3):892–896. https://doi.org/10.3906/sag-1408-14
Yetkin F, Yakupogullari Y, Kuzucu C et al (2018) Pathogens of intensive care unit-acquired infections and their antimicrobial resistance: a 9-year analysis of data from a University Hospital. Jundishapur J Microbiol 11(10):e67716. https://doi.org/10.5812/jjm.67716
Yilmaz Ş, Hasdemir U, Aksu B, Altınkanat Gelmez G, Söyletir G (2020) Alterations in AdeS and AdeR regulatory proteins in 1-(1-naphthylmethyl)-piperazine responsive colistin resistance of Acinetobacter baumannii. J Chemother 32(6):286–293. https://doi.org/10.1080/1120009X.2020.1735118
Zeka AN, Poirel L, Sipahi OR et al (2014) GES-type and OXA-23 carbapenemase-producing Acinetobacter baumannii in Turkey. J Antimicrob Chemother 69(4):1145–1146. https://doi.org/10.1093/jac/dkt465
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Abed, A.B., Korcan, S.E. & Güngör, S. Antibiotics profile map of clinical A. baumannii strains isolated from health institutions in Turkey: a database search study and analysis of publications from 2011 to 2022. Bull Natl Res Cent 47, 15 (2023). https://doi.org/10.1186/s42269-023-00982-6
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DOI: https://doi.org/10.1186/s42269-023-00982-6