Carbapenems

碳青霉烯类
  • 文章类型: Systematic Review
    背景:在人类中检测耐碳青霉烯的铜绿假单胞菌(CR-PA)对于防止传播很重要。然而,检测CR-PA的最佳培养方法未知.本系统综述旨在确定哪种培养方法最敏感,以及哪种培养方法用于检测人体中的CR-PA。第二,为了建立考虑周转时间(TAT)的最可行的培养方法,第三,提供用于检测运输的采样点的概述。
    方法:我们系统地搜索了电子数据库Embase,MedlineOvid,科克伦,Scopus,CINAHL,和WebofScience,直到2023年1月27日。所有诊断准确性研究,比较两种或多种培养方法以检测CR-PA,以及最近关于CR-PA携带或感染人的暴发或监测报告,描述培养方法及其结果,有资格列入。我们使用QUADAS-2指南进行诊断准确性研究,使用STROBE或ORION指南进行爆发监测研究,以评估偏倚风险。
    结果:纳入了6项诊断准确性研究。发现富集肉汤增加CR-PA的检测。使用富集肉汤将TAT延长18-24小时,然而,与常规培养基相比,选择性培养基可以减少24小时的TAT。总的来说,纳入了124项疫情监测研究,其中17项研究采用监测样本,116项研究采用临床样本。在使用监测样本的疫情监测研究中,肛周,直肠拭子或粪便是最常见的取样部位/样本(13/17,76%).在是否使用以及使用哪种富集肉汤和选择性培养基方面观察到了各种各样的变化。
    结论:我们发现在将材料接种到选择性培养基上之前使用富集步骤以检测CR-PA的益处。需要更多的研究来确定最敏感的采样地点和培养方法。
    背景:本研究已在PROSPEROInternational前瞻性系统评价登记册中注册(注册号:CRD4202020207390,http://www。crd.约克。AC.uk/PROSPERO/display_record。asp?ID=CRD42020207390)。
    BACKGROUND: Detection of carbapenem-resistant Pseudomonas aeruginosa (CR-PA) in humans is important to prevent transmission. However, the most optimal culture method to detect CR-PA is unknown. This systematic review aims to determine which culture method is most sensitive and which culture methods are used to detect CR-PA in humans. Second, to establish the most feasible culture method taking into account the turnaround time (TAT), and third, to provide an overview of the sampling sites used to detect carriage.
    METHODS: We systematically searched the electronic databases Embase, Medline Ovid, Cochrane, Scopus, CINAHL, and Web of Science until January 27, 2023. All diagnostic accuracy studies comparing two or more culture methods to detect CR-PA and recent outbreak or surveillance reports on CR-PA carriage or infection in humans, which describe culture methods and their results, were eligible for inclusion. We used QUADAS-2 guideline for diagnostic accuracy studies and the STROBE or ORION guideline for outbreak-surveillance studies to assess the risk of bias.
    RESULTS: Six diagnostic accuracy studies were included. An enrichment broth was found to increase the detection of CR-PA. Using an enrichment broth extended the TAT by 18-24 h, yet selective media could reduce the TAT by 24 h compared to routine media. In total, 124 outbreak-surveillance studies were included, of which 17 studies with surveillance samples and 116 studies with clinical samples. In outbreak-surveillance studies with surveillance samples, perianal, rectal swabs or stools were the most common sampling site/specimen (13/17, 76%). A large variety was observed in whether and which kind of enrichment broth and selective media were used.
    CONCLUSIONS: We found a benefit of using an enrichment step prior to inoculation of the material onto selective media for the detection of CR-PA. More research is needed to determine the most sensitive sampling site and culture method.
    BACKGROUND: This study was registered in the PROSPERO International prospective register of systematic reviews (registration number: CRD42020207390, http://www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42020207390 ).
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  • 文章类型: Journal Article
    背景:本荟萃分析旨在比较头孢他啶-阿维巴坦联合治疗与单药治疗耐碳青霉烯革兰氏阴性菌(CR-GNB)的疗效。
    方法:PubMed的文献检索,Embase,Cochrane图书馆,和ClinicalTrials.gov进行到2023年9月1日。仅包括比较CZA联合治疗与单一治疗对CR-GNB感染的研究。
    结果:共纳入25项研究(23项回顾性观察性研究和2项前瞻性研究),涉及2676例患者。接受联合治疗的研究组和接受单药治疗的对照组30天死亡率无显著差异(风险比[RR]0.91;95%置信区间[CI]0.71-1.18)。此外,在住院死亡率方面,研究组和对照组之间没有观察到显著差异(RR1.00;95%CI0.79-1.27),14天死亡率(RR1.54;95%CI0.24-9.91),90天死亡率(RR1.18;95%CI0.62-2.22),临床治愈率(RR0.95;95%CI0.84-1.08)。然而,联合组的微生物根除率高于对照组(RR1.15;95%CI1.00-1.32).
    结论:与单药治疗相比,CZA联合治疗没有产生额外的临床益处。然而,联合治疗可能与良好的微生物学结局相关.
    BACKGROUND: This meta-analysis was conducted to compare the efficacy of ceftazidime-avibactam combination therapy with that of monotherapy in the treatment of carbapenem-resistant Gram-negative bacterial (CR-GNB).
    METHODS: A literature search of PubMed, Embase, the Cochrane Library, and ClinicalTrials.gov was conducted until September 1, 2023. Only studies that compared CZA combination therapy with monotherapy for CR-GNB infections were included.
    RESULTS: A total of 25 studies (23 retrospective observational studies and 2 prospective studies) involving 2676 patients were included. There was no significant difference in 30-day mortality between the study group receiving combination therapy and the control group receiving monotherapy (risk ratio [RR] 0.91; 95% confidence interval [CI] 0.71-1.18). In addition, no significant differences were observed between the study and the control group in terms of in-hospital mortality (RR 1.00; 95% CI 0.79-1.27), 14-day mortality (RR 1.54; 95% CI 0.24-9.91), 90-day mortality (RR 1.18; 95% CI 0.62-2.22), and clinical cure rate (RR 0.95; 95% CI 0.84-1.08). However, the combination group had a borderline higher microbiological eradication rate than the control group (RR 1.15; 95% CI 1.00-1.32).
    CONCLUSIONS: Compared to monotherapy, CZA combination therapy did not yield additional clinical benefits. However, combination therapy may be associated with favorable microbiological outcomes.
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  • 文章类型: Clinical Trial
    厄他培南诱导的神经毒性尚未得到很好的表征,并且可能被低估。我们对文献进行了系统回顾,并纳入了华盛顿大学医学院卫生系统的11例其他病例。总共125例患者病例被纳入数据分析。平均年龄是72岁,62%和42%的患者有肾功能障碍和先前存在的中枢神经系统(CNS)疾病,分别。只有15%的患者根据肾功能接受了不适当的高厄他培南给药。患者在中位数为4天后出现神经系统体征和症状(四分位距,3-9天)。最常见的临床特征是癫痫发作(70%),意识水平改变或谵妄(27%),和幻觉(17%)。在我们的卫生系统中,估计发病率为102个厄他培南课程中的1个。当患有肾功能障碍或易感中枢神经系统疾病的患者出现神经系统体征和症状时,应怀疑厄他培南神经毒性。特别是在开始使用抗生素后的几天内。这项研究强调了需要进行大型前瞻性研究来评估厄他培南神经毒性的真实发生率和结果。
    Ertapenem-induced neurotoxicity has not been well characterized and is potentially underreported. We conducted a systematic review of the literature and included 11 additional cases from the University of Washington Medicine health system. A total of 125 individual patient cases were included in the data analysis. The mean age was 72 years, and 62% and 42% of patients had renal dysfunction and preexisting central nervous system (CNS) conditions, respectively. Only 15% of patients received inappropriately high ertapenem dosing based on kidney function. Patients developed neurological signs and symptoms after a median of 4 days (interquartile range, 3-9 days). The most common clinical features were seizures (70%), altered level of consciousness or delirium (27%), and hallucinations (17%). An estimated incidence in our health system was 1 in 102 courses of ertapenem. Ertapenem neurotoxicity should be suspected when a patient with renal dysfunction or predisposing CNS conditions develops neurological signs and symptoms, especially within several days after initiating the antibiotic. This study underscores the need for a large prospective study to assess the true incidence and outcomes of ertapenem neurotoxicity.
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  • 文章类型: Systematic Review
    抗菌素耐药性(AMR)在全球范围内被认为是一项重大的健康挑战,但其程度在许多地区仍不清楚。至关重要的是优先考虑AMR患病率的基础评估,以促进实验室监测的实施。采用一种健康的观点,本研究概述了中东AMR的现状。
    为了综合中东AMR的当前知识状况,描绘不同部门的贡献(人类健康,动物健康,和环境),并辨别OneHealth干预措施在减轻AMR方面的有效性。
    通过PubMed进行了详尽的文献检索,ScienceDirect,谷歌学者。根据规定的资格标准筛选和评估潜在文章的资格。完成了数据合成,并对结果进行了专题报道和讨论。
    该研究包括23项研究,并在2019年至2023年之间发表。大多数研究揭示了治疗感染的重大挑战,重症监护病房的耐药性非常普遍,特别是针对超广谱β-内酰胺酶和耐碳青霉烯的革兰氏阴性菌。儿科人群中的粘菌素和亚胺培南耐药进一步强调了理解和解决该地区各种耐药机制的紧迫性。泌尿病原体的研究,菌血症,生物膜的形成凸显了AMR的多方面挑战。对关键抗生素耐药性的出现强调了定制治疗策略的紧迫性。
    考虑到人类的相互联系,动物,和环境健康,一种健康观点势在必行。多样化的挑战需要协调一致的努力,包括创新干预措施和公共卫生政策。通过未来的研究弥合现有差距对于在该地区打击AMR的循证和特定环境战略至关重要。
    UNASSIGNED: Antimicrobial resistance (AMR) is recognized globally as a significant health challenge, but its extent remains unclear in many regions. It is crucial to prioritize a foundational evaluation of AMR prevalence to facilitate the implementation of laboratory-based surveillance. Adopting a One Health perspective, this study outlines the present AMR status in the Middle East.
    UNASSIGNED: To synthesize the current state of knowledge on AMR in the Middle East, delineate the contributions of different sectors (human health, animal health, and environment), and discern the effectiveness of One Health interventions in mitigating AMR.
    UNASSIGNED: An exhaustive literature search was conducted via PubMed, ScienceDirect, and Google Scholar. Potential articles were screened and assessed for eligibility based on prescribed eligibility criteria. Data synthesis was done, and the results were reported and discussed thematically.
    UNASSIGNED: Twenty-three studies were included in the study and published between 2019 and 2023. Most studies reveal substantial challenges in treating infections, with a significant prevalence of resistance in critical care units, particularly against extended-spectrum beta-lactamases and carbapenem-resistant Gram-negative bacteria. Colistin and imipenem resistance in pediatric populations further emphasize the urgency of understanding and addressing diverse resistance mechanisms in the region. Studies on urinary pathogens, bacteremia, and biofilm formation highlight the multifaceted challenge of AMR. The emergence of resistance to key antibiotics emphasizes the urgency for tailored treatment strategies.
    UNASSIGNED: Given the interconnectedness of human, animal, and environmental health, a One Health perspective is imperative. The diverse challenge demands coordinated efforts, including innovative interventions and public health policies. Bridging existing gaps through future research is crucial for evidence-based and context-specific strategies in combating AMR in the region.
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  • 文章类型: Journal Article
    重症监护病房(ICU)是专门管理危重病人的专门环境,对耐药细菌特别敏感。其中,耐碳青霉烯类革兰氏阴性菌(CR-GNB)对ICU患者的生命构成重大威胁。碳青霉烯酶的产生是CR-GNB的关键耐药机制,随着抗性基因的转移,抗生素耐药性(AMR)的广泛出现。CR-GNB感染在ICU中普遍存在,强调迫切需要预防和控制措施,以降低与CR-GNB传播或感染相关的死亡率。本综述概述了ICU中围绕CR-GNB的关键方面。我们研究了细菌耐药性的机制,ICU中CR-GNB感染常见的耐药基因,以及针对碳青霉烯酶基因型的治疗选择。此外,我们强调了重要的预防措施,以阻止CR-GNB在ICU中的传播和传播,在回顾临床预测建模研究领域取得的进展的同时,这对实际应用具有极好的潜力。
    Intensive care units (ICUs) are specialized environments dedicated to the management of critically ill patients, who are particularly susceptible to drug-resistant bacteria. Among these, carbapenem-resistant Gram-negative bacteria (CR-GNB) pose a significant threat endangering the lives of ICU patients. Carbapenemase production is a key resistance mechanism in CR-GNB, with the transfer of resistance genes contributing to the extensive emergence of antimicrobial resistance (AMR). CR-GNB infections are widespread in ICUs, highlighting an urgent need for prevention and control measures to reduce mortality rates associated with CR-GNB transmission or infection. This review provides an overview of key aspects surrounding CR-GNB within ICUs. We examine the mechanisms of bacterial drug resistance, the resistance genes that frequently occur with CR-GNB infections in ICU, and the therapeutic options against carbapenemase genotypes. Additionally, we highlight crucial preventive measures to impede the transmission and spread of CR-GNB within ICUs, along with reviewing the advances made in the field of clinical predictive modeling research, which hold excellent potential for practical application.
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  • 文章类型: Journal Article
    产生碳青霉烯酶的革兰氏阴性菌(CP-GNB)感染威胁公众健康,死亡率高,发病率和治疗费用。尽管澳大利亚的频率仍然很低(2022年报告的CP-GNB感染总数为907),blaIMP-4在许多州都建立了低水平的地方性。在澳大利亚产生碳青霉烯酶的肠杆菌分离株中,单独的亚胺酶金属-β-内酰胺酶类型占所有碳青霉烯酶的一半以上,特别是阴沟肠杆菌。新德里金属-β-内酰胺酶占澳大利亚所有碳青霉烯酶的近25%,主要在大肠杆菌中被鉴定。OXA-48样碳青霉烯酶包括几乎所有碳青霉烯酶的10%,并且主要见于肺炎克雷伯菌和大肠杆菌中。尽管肺炎克雷伯菌碳青霉烯酶型碳青霉烯酶在澳大利亚很少见,一些地方爆发了。澳大利亚大多数耐碳青霉烯(CR)铜绿假单胞菌菌株不产生碳青霉烯酶。最后,OXA-23样碳青霉烯酶在澳大利亚的CR-鲍曼不动杆菌菌株中绝大多数为阳性。CR-GNB感染的治疗挑战医生。美国食品和药物管理局批准的10种新的抗生素对至少一些CR-GNB感染有效,只有三个被批准在澳大利亚使用。在这种情况下,在澳大利亚,对可用于治疗CR-GNB感染的新型抗菌药物的需求仍未满足。以及对新机制的迫切要求,将抗生素销售与其可用性“脱钩”。在这篇叙述性评论中,我们旨在概述澳大利亚碳青霉烯耐药的流行病学和临床意义,因为它与肠杆菌有关,铜绿假单胞菌和鲍曼不动杆菌。
    Carbapenemase-producing gram-negative bacteria (CP-GNB) infections threaten public health with high mortality, morbidity and treatment costs. Although frequencies remain low in Australia (total number of CP-GNB infections reported was 907 in 2022), blaIMP-4 has established low levels of endemicity in many states. Imipenemase metallo-β-lactamase types alone accounted for more than half of all carbapenemases in carbapenemase-producing Enterobacterales isolates in Australia, particularly in Enterobacter cloacae complex. New Delhi metallo-β-lactamase constitutes almost 25% of all carbapenemases in Australia and was identified predominantly in Escherichia coli. The OXA-48-like carbapenemases include almost 10% of all carbapenemases and are mainly seen in Klebsiella pneumoniae and E. coli. Although K. pneumoniae carbapenemase-type carbapenemases are rare in Australia, some local outbreaks have occurred. Most carbapenem-resistant (CR) Pseudomonas aeruginosa strains in Australia do not produce carbapenemases. Finally, OXA-23-like carbapenemases are overwhelmingly positive in CR-Acinetobacter baumannii strains in Australia. Treatment of CR-GNB infections challenges physicians. Of 10 new antibiotics active against at least some CR-GNB infections that are approved by the US Food and Drug Administration, just three are approved for use in Australia. In this context, there is still an unmet need for novel antibacterials that can be used for the treatment of CR-GNB infections in Australia, as well as a pressing requirement for new mechanisms to \'de-link\' antibiotic sales from their availability. In this narrative review, we aim to overview the epidemiology and clinical significance of carbapenem resistance in Australia as it pertains to Enterobacterales, P. aeruginosa and A. baumannii.
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  • 文章类型: Meta-Analysis
    尚未系统地研究实体器官移植(SOT)受者中耐碳青霉烯类革兰氏阴性菌(CRGNB)的负担。这里,我们发现了与CRGNB感染和SOT接受者定植相关的危险因素。
    这项研究包括在CRGNB感染的SOT患者中进行的观察性研究,报告了与死亡率相关的危险因素,感染或定植。相关记录将在PubMed中搜索,Embase和WebofScience,从数据库建设时间到2023年3月1日。
    共纳入23项研究,13,511名参与者,能够评估27个潜在风险因素。有CRGNB的SOT受者中1年死亡率的合并患病率为44.5%。长时间的机械通气,联合移植,再次手术和移植前CRGNB定植是SOT受者发生CRGNB感染的重要因素。肾脏替代疗法,LT后CRGNB定殖,LT前肝病和终末期肝病模型评分增加感染风险。重新移植,移植前使用碳青霉烯和输尿管支架的使用增加了CRGNB定植的风险。
    我们的研究表明,患有CRGNB感染的SOT接受者有更高的死亡风险。侵入性操作可能是导致CRGNB感染的主要因素。
    UNASSIGNED: The burden of carbapenem-resistant gram-negative bacteria (CRGNB) among solid organ transplant (SOT) recipients has not been systematically explored. Here, we discern the risk factors associated with CRGNB infection and colonization in SOT recipients.
    UNASSIGNED: This study included observational studies conducted among CRGNB-infected SOT patients, which reported risk factors associated with mortality, infection or colonization. Relevant records will be searched in PubMed, Embase and Web of Science for the period from the time of database construction to 1 March 2023.
    UNASSIGNED: A total of 23 studies with 13,511 participants were included, enabling the assessment of 27 potential risk factors. The pooled prevalence of 1-year mortality among SOT recipients with CRGNB was 44.5%. Prolonged mechanical ventilation, combined transplantation, reoperation and pre-transplantation CRGNB colonization are salient contributors to the occurrence of CRGNB infections in SOT recipients. Renal replacement therapy, post-LT CRGNB colonization, pre-LT liver disease and model for end-stage liver disease score increased the risk of infection. Re-transplantation, carbapenem use before transplantation and ureteral stent utilization increaesd risk of CRGNB colonization.
    UNASSIGNED: Our study demonstrated that SOT recipients with CRGNB infections had a higher mortality risk. Invasive procedure may be the main factor contribute to CRGNB infection.
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  • 文章类型: Journal Article
    背景:关于脓毒症患者长期使用β-内酰胺类抗生素与间歇性使用的两项最新研究并未得出一致的结论,进一步导致围绕延长β-内酰胺抗生素输注策略有效性的争议。我们进行了系统回顾和荟萃分析,以评估长期和间歇性β-内酰胺输注在成人脓毒症患者中的有效性和安全性。
    方法:我们系统地搜索了PubMed,EMBASE,和CochraneLibrary数据库,用于比较脓毒症患者长期和间歇性β-内酰胺输注的原始随机对照试验。随机效应模型用于评估死亡率,临床成功,微生物的成功,和不良事件。我们还进行了亚组分析,以探讨各种因素对死亡率的影响。使用相对风险(RR)和相应的95%置信区间(CI)来计算二分结果的总体效应大小。该荟萃分析在PROSPERO(CRD42023463905)中注册。
    结果:我们评估了15项研究,涉及2130名患者。在我们的综合评估中,我们发现全因死亡率显着降低(RR,0.83;95%CI0.72-0.97;P=0.02),临床成功率显着提高(RR,1.16;95%CI1.03-1.31;P=0.02)在长时间输注组与间歇输注组相比,而微生物成功没有产生统计学上显著的结果(RR,1.10;95%CI0.98-1.23;P=0.11)。两组间不良事件无显著差异(RR,0.91;95%CI0.64-1.29;P=0.60)。此外,从亚组分析中得出了显著的结论,包括样本量超过每组20个人的研究(RR,0.84;95CI0.72-0.98;P=0.03),2010年后进行的研究(RR,0.84;95CI0.72-0.98;P=0.03),涉及主要由革兰氏阴性菌引起的感染的病例(RR,0.81;95CI0.68-0.96;P=0.02),以及负荷剂量(RR,0.84;95%CI0.72-0.97;P=0.02)和青霉素的使用(RR,0.61;95%CI0.38-0.98;P=0.04)。
    结论:与间歇输注相比,长期输注β-内酰胺类抗生素可显著降低脓毒症患者的全因死亡率,并在不增加不良事件的情况下提高临床成功率.
    BACKGROUND: The two latest studies on prolonged versus intermittent use of β-lactam antibiotics in patients with sepsis did not reach consistent conclusions, further contributing to the controversy surrounding the effectiveness of the prolonged β-lactam antibiotics infusion strategy. We conducted a systemic review and meta-analysis to evaluate the efficacy and safety of prolonged and intermittent β-lactam infusion in adult patients with sepsis.
    METHODS: We systematically searched PubMed, EMBASE, and Cochrane Library databases for original randomized controlled trials comparing prolonged and intermittent β-lactam infusion in sepsis patients. A random-effects model was used to evaluate mortality, clinical success, microbiological success, and adverse events. We also conducted subgroup analyses to explore the impact of various factors on the mortality rates. Relative risk (RR) and corresponding 95% confidence intervals (CIs) were used to calculate the overall effect sizes for dichotomous outcomes. This meta-analysis was registered in PROSPERO (CRD42023463905).
    RESULTS: We assessed 15 studies involving 2130 patients. In our comprehensive assessment, we found a significant reduction in all-cause mortality (RR, 0.83; 95% CI 0.72-0.97; P = 0.02) and a notable improvement in clinical success (RR, 1.16; 95% CI 1.03-1.31; P = 0.02) in the prolonged infusion group compared to the intermittent infusion group, whereas microbiological success did not yield statistically significant results (RR, 1.10; 95% CI 0.98-1.23; P = 0.11). No significant differences in adverse events were observed between the two groups (RR, 0.91; 95% CI 0.64-1.29; P = 0.60). Additionally, remarkable conclusions were drawn from subgroup analyses including studies with sample sizes exceeding 20 individuals per group (RR, 0.84; 95%CI 0.72-0.98; P = 0.03), research conducted post-2010 (RR, 0.84; 95%CI 0.72-0.98; P = 0.03), cases involving infections predominantly caused by Gram-negative bacteria (RR, 0.81; 95%CI 0.68-0.96; P = 0.02), as well as the administration of a loading dose (RR, 0.84; 95% CI 0.72-0.97; P = 0.02) and the use of penicillin (RR, 0.61; 95% CI 0.38-0.98; P = 0.04).
    CONCLUSIONS: Compared to intermittent infusion, prolonged infusion of β-lactam antibiotics significantly decreases all-cause mortality among patients with sepsis and enhances clinical success without increasing adverse events.
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  • 文章类型: Meta-Analysis
    背景:耐碳青霉烯鲍曼不动杆菌(CRAB)感染的最佳治疗方法仍存在争议。
    目的:描述头孢地洛治疗CRAB感染的患者的结局,并比较头孢地洛与最佳可用疗法(BAT)的疗效。
    方法:我们搜索了MEDLINE,Cochrane图书馆和EMBASE筛选截至2023年9月发表的原始报告研究合格标准:RCT和观察性研究调查30天死亡率,临床失败,头孢地洛或BAT参与者治疗的患者的微生物学失败或ADRs发生率:因CRAB干预而感染的患者:头孢地洛单药或与其他潜在活性剂联合使用或BAT对BIAS风险的评估:我们使用Cochrane偏差风险工具进行RCT,和纽卡斯尔渥太华量表进行观察研究。
    我们通过随机效应模型进行了荟萃分析,汇集了风险比(RR)。
    结果:我们筛选了801份原始报告,和18项研究(2项随机对照试验,13项队列研究和3项病例系列)纳入分析,总共733名接受头孢地洛治疗的患者,和473接收BAT。在接受头孢地洛的患者中,30天死亡率为42%(95%CI38-47%),微生物失败率48%(95%CI31-65%),临床失败率43%(95%CI32-55%),不良反应发生率为3%(95%CI1-6%)。与接受联合治疗的患者相比,接受头孢地洛单药治疗的患者的死亡率较低(RR:0.64;95%CI:0.43-0.94,p=0.024)。我们发现,与BAT相比,头孢地洛治疗组的死亡率显着降低(RR:0.74;95%CI:0.57-0.95,p=0.02),ADR发生率降低(RR:0.28;95%CI:0.09-0.91,p=0.03)。在微生物学和临床失败率方面没有观察到差异。
    结论:我们的数据加强了头孢地洛在CRAB感染中的疗效和安全性。
    BACKGROUND: The best treatment for carbapenem-resistant Acinetobacter baumannii (CRAB) infections is still a matter of debate.
    OBJECTIVE: To describe the outcomes of patients treated with cefiderocol for CRAB infections, and to compare the efficacy of cefiderocol versus best available therapy (BAT).
    METHODS: We searched MEDLINE, the Cochrane Library and EMBASE to screen original reports published up to September 2023.
    METHODS: Randomized controlled trials (RCTs) and observational studies investigating 30-day mortality, clinical failure, microbiological failure or rate of adverse drug reactions of patients treated with cefiderocol or BAT.
    METHODS: Patients with infections due to CRAB.
    METHODS: Cefiderocol in monotherapy or in combination with other potentially active agents or BAT.
    UNASSIGNED: We used the Cochrane Risk of Bias Tool for RCTs, and the Newcastle Ottawa scale for observational studies.
    UNASSIGNED: We conducted a meta-analysis pooling risk ratios (RRs) through random effect models.
    RESULTS: We screened 801 original reports, and 18 studies (2 RCTs, 13 cohort studies and 3 case-series) were included in the analysis, for a total 733 patients treated with cefiderocol, and 473 receiving the BAT. Among patients receiving cefiderocol, the 30-day mortality rate was 42% (95% CI 38-47%), the rate of microbiological failure 48% (95% CI 31-65%), the clinical failure rate 43% (95% CI 32-55%), and the rate of ADRs was 3% (95% CI 1-6%). A lower mortality rate was observed among patients receiving cefiderocol monotherapy as compared to those treated with combination regimens (RR: 0.64; 95% CI: 0.43-0.94, p = 0.024). We found a significantly lower mortality rate (RR: 0.74; 95% CI: 0.57-0.95, p = 0.02) and a lower rate of ADRs (RR: 0.28; 95% CI: 0.09-0.91, p = 0.03) in the group treated with cefiderocol as compared to BAT. No difference was observed in microbiological and clinical failure rate.
    CONCLUSIONS: Our data strengthen the efficacy and safety profile of cefiderocol in CRAB infections.
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