Difficult to treat resistance

  • 文章类型: Journal Article
    铜绿假单胞菌是最常见的医院病原菌之一,也是与抗菌素耐药性相关的主要新兴物种之一,已成为21世纪公共卫生的最大威胁之一。这种细菌具有多种毒力因子,这些毒力因子有助于急性和慢性感染的发病机理。本文旨在总结多重耐药性对铜绿假单胞菌毒力和适应性的影响。尽管通常认为抗性决定因素的获得与健身成本相关,多项研究支持耐药突变可能与毒力下降无关,和/或某些补偿性突变可能允许多药耐药菌株恢复其初始适应性.我们从微生物学的角度讨论了耐药谱和毒力之间的相互作用,以及结果的临床后果和经济影响。
    Pseudomonas aeruginosa is one of the most common nosocomial pathogens and part of the top emergent species associated with antimicrobial resistance that has become one of the greatest threat to public health in the twenty-first century. This bacterium is provided with a wide set of virulence factors that contribute to pathogenesis in acute and chronic infections. This review aims to summarize the impact of multidrug resistance on the virulence and fitness of P. aeruginosa. Although it is generally assumed that acquisition of resistant determinants is associated with a fitness cost, several studies support that resistance mutations may not be associated with a decrease in virulence and/or that certain compensatory mutations may allow multidrug resistance strains to recover their initial fitness. We discuss the interplay between resistance profiles and virulence from a microbiological perspective but also the clinical consequences in outcomes and the economic impact.
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  • 文章类型: Observational Study
    UNASSIGNED:新型的最后手段β-内酰胺抗生素现在可用于治疗由于产生新德里金属-β-内酰胺酶(NDM)的肠杆菌和具有难以治疗耐药性的非发酵菌引起的感染。然而,有关使用亚胺培南-西司他丁-释放巴坦(IMI-REL)的数据,头孢地洛(CFD)和头孢他啶-阿维巴坦加氨曲南(CAZ-AVI-ATM)在现实生活中很少见。这项研究旨在描述最后手段β-内酰胺抗生素的使用,微生物学和结果,在三级医院住院的患者中。
    UNASSIGNED:我们从2020/01/01到2022/08/31进行了单中心观察队列研究。我们筛查了尼姆大学医院收治的所有患者,这些患者在研究期间接受了≥1剂量的最后手段β-内酰胺抗生素,使用药房数据库。我们包括接受IMI-REL治疗的患者,CFD和CAZ-AVI-ATM。主要终点是无感染生存率。我们还计算了微生物和临床治愈率,反复感染,死亡和不良事件。
    UNASSIGNED:研究中纳入了27例患者,分析了30个疗程:CFD(N=24;80%),CAZ-AVI-ATM(N=3;10%)和IMI-REL(N=3;10%)。21名男性(70%)和9名女性(30%)使用抗生素,中位年龄为65岁[50-73.5],中位Charlson指数为1[0-2]。几乎所有患者碳青霉烯类耐药菌的危险因素均≥1,其中一半因重症COVID-19住院,大部分抗生素疗程(N=26;87%)与ICU入住相关.在研究人群中,在启动最后手段β-内酰胺治疗后第90天,无感染生存的概率为48.4%CI95%[33.2~70.5].临床失败率为30%,微生物失败率为33%,死亡率为23%。在5个抗生素疗程(17%)中记录了不良事件。在细节上,铜绿假单胞菌主要采用CFD和IMI-REL治疗,用CFD和CAZ-AVI-ATM,A.鲍曼不动杆菌与CFD,和NDM生产-K肺炎与CAZ-AVI-ATM和CFD。经过CFD治疗后,CAZ-AVI-ATM和IMI-REL,无感染生存率为48%CI95%[10.4-73.5],33.3%CI95%[6.7-100],66.7%可信区间95%[30-100],分别。
    UNASSIGNED:在现实生活中使用最后手段的β-内酰胺类抗微生物药物是一种安全有效的治疗选择,用于治疗与革兰氏阴性菌耐药相关的严重感染。
    Novel last resort beta-lactam antibiotics are now available for management of infections due to New-Delhi Metallo-Beta-Lactamase (NDM) producing Enterobacterales and non-fermenters with Difficult-to-Treat Resistance. However, data regarding the use of imipenem-cilastatin-relebactam (IMI-REL), cefiderocol (CFD) and ceftazidime-avibactam plus aztreonam (CAZ-AVI-ATM) are scarce in real-life settings. This study aimed to describe the use of last resort beta-lactam antibiotics, the microbiology and the outcome, in patients hospitalized in a tertiary hospital.
    We conducted a monocentric observational cohort study from 2020/01/01, to 2022/08/31. We screened all patients admitted to Nimes University Hospital who have received ≥ 1 dose of last resort beta-lactam antibiotics during the study period, using the Pharmacy database. We included patients treated with IMI-REL, CFD and CAZ-AVI-ATM. The primary endpoint was the infection-free survival rate. We also calculated rates of microbiological and clinical cure, recurrent infection, death and adverse events.
    Twenty-seven patients were included in the study and 30 treatment courses were analyzed: CFD (N=24; 80%), CAZ-AVI-ATM (N=3; 10%) and IMI-REL (N=3; 10%). Antibiotics were used in 21 males (70%) and 9 females (30%) with a median age at 65-year-old [50-73.5] and a median Charlson index at 1 [0-2]. Almost all the patients had ≥ 1 risk factor for carbapenem resistant bacteria, a half of them was hospitalized for severe COVID-19, and most of antibiotic courses (N=26; 87%) were associated with ICU admission. In the study population, the probability of infection-free survival at day-90 after last resort beta-lactam therapy initiation was 48.4% CI95% [33.2-70.5]. Clinical failure rate was at 30%, microbiological failure rate at 33% and mortality rate at 23%. Adverse events were documented in 5 antibiotic courses (17%). In details, P. aeruginosa were mainly treated with CFD and IMI-REL, S. maltophilia with CFD and CAZ-AVI-ATM, A. baumannii with CFD, and NDM producing-K. pneumoniae with CAZ-AVI-ATM and CFD. After a treatment course with CFD, CAZ-AVI-ATM and IMI-REL, the probability of infection-free survival was 48% CI95% [10.4-73.5], 33.3% CI95% [6.7-100], 66.7% CI95% [30-100], respectively.
    Use of last resort beta-lactam antimicrobials in real-life settings was a safe and efficient therapeutic option for severe infections related to Gram-negative bacteria with Difficult-to-Treat Resistance.
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  • 文章类型: Journal Article
    BACKGROUND: The management of non-fermentative gram-negative bloodstream infection (NFGN-BSI) offers numerous challenges. In this study the aim is to analyse a large cohort of patients with NFGN-BSI recruited in the northern Italy to describe epidemiology, etiological and susceptibility pattern, therapeutic management and outcome.
    METHODS: Multicentre retrospective cohort study of patients hospitalised at three large teaching hospitals in northern Italy in a fourth year period.
    RESULTS: 355 BSI episodes were analyzed, due to P. aeruginosa (72.7%), A. baumannii (16.6%), and Stenotrophomonas maltophilia (10.7%). Overall, 21.4% of isolates were defined as DTR, highest rate among A. baumannii (64.4%). All-cause 30-day mortality rate was 17.5%. Rates of XDR or DTR A. baumannii isolation were significantly higher in non-surviving patients. Independent risk factors for 30-day mortality were: age (HR 1.03, 95%CI 1.00-1.04, p = 0.003), septic shock (HR 2.84, 95%CI 1.67-4.82, p < 0.001) and BSI due to Acinetobacter baumannii (HR 2.23, 95%CI 1.27-3.94, p = 0.005).
    CONCLUSIONS: The overall prevalence of DTR was high in the NFGN BSI cohort analyzied, mainly among Acinetobacter baumannii episodes (64.4%). Acinetobacter baumannii is showed to be an independent predictor of mortality. These evidences marked the urgent need of new therapeutic options against this pathogen.
    BACKGROUND: 79/2017/O/OssN. Approved: March14th, 2017.
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