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Ceftazidimeavibactam use in children and adolescents 头孢他啶米巴坦在儿童和青少年中的应用
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.2.173-183
Оlga U. Stetsiouk, I. Andreeva, А. Lekmanov, Еlena V. Haykina
Abstract The increasing number of infections caused by multidrug-resistant gram-negative bacteria in children is a serious problem all over the world. Ceftazidim-avibactam is a promising antimicrobial drug recently approved in Russia for use in pediatric practice. This review provides information on the possible use of ceftazidime-avibactam in children with complicated intraabdominal infections (in combination with metronidazole); complicated urinary tract infections, including pyelonephritis; hospital-acquired pneumonia, including ventilator-associated pneumonia; infections caused by aerobic gram-negative microorganisms in patients with limited choice of antibacterial therapy. Based on the data on the in vitro activity of the drug, the results of clinical studies of pharmacokinetics, safety and efficacy of ceftazidimeavibactam for the treatment of infections in children the main clinical cases in which the use of ceftazidimeavibactam in pediatric practice is most justified and appropriate are identified.
摘要儿童多重耐药革兰氏阴性菌感染日益增多,是世界范围内普遍存在的严重问题。头孢他啶-阿维巴坦是一种很有前途的抗菌药物,最近在俄罗斯批准用于儿科实践。本综述提供了头孢他啶-阿维巴坦在并发腹腔内感染的儿童中可能使用的信息(与甲硝唑联合使用);复杂性尿路感染,包括肾盂肾炎;医院获得性肺炎,包括呼吸机相关肺炎;需氧革兰氏阴性微生物引起的感染在抗菌治疗选择有限的患者中。根据药物的体外活性数据,对头孢他啶meavibactam治疗儿童感染的药代动力学、安全性和有效性的临床研究结果,确定了头孢他啶meavibactam在儿科实践中使用最合理和最合适的主要临床病例。
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引用次数: 2
Genomic properties in Achromobacter spp. strains from cystic fibrosis patients in Russia 俄罗斯囊性纤维化患者无色杆菌菌株的基因组特性
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.3.220-225
Y. Bocharova, T.A. Saviniova, A. V. Chaplin, A. Lyamin, O. Kondratenko, S. Polikarpova, S. Zhilina, N. Fedorova, M. Korzhanova, N. A. Mayansky, I. Chebotar
Objective. To determine species, sequence-types, antimicrobial resistance and virulence genes in Achromobacter spp. isolates obtained from cystic fibrosis (CF) patients in Russia. Materials and Methods. Samples (sputum, nasopharyngeal swab) from 168 CF patients from 48 regions were studied. Whole-genome sequencing (WGS) was performed on MGISEQ-2000 platform. SPAdes software, Galaxy, ResFinder, Integrall, PubMLST were used for analysis of WGS data. Results. A total of 18 strains of Achromobacter spp. were isolated from 16 of 168 CF patients.Achromobacter xylosoxidans was the most prevalent and detected in 13⁄18 cases (72%). Studied Achromobacter spp. isolates belonged to 14 sequence types, including 8 new sequence types. An adaptive resistance gene carriage was a rare phenomenon (1⁄18 isolates). Conclusions. The Achromobacter spp. colonization rate of respiratory system in CF patients in Russia corresponds to the data reported in other countries. A. xylosoxidans isolates were the most prevalent (72%). Achromobacter spp. isolates from CF patients in Russia and show a high clonal diversity.
目标。目的:测定俄罗斯囊性纤维化(CF)患者分离的无色杆菌菌株的种类、序列类型、耐药性和毒力基因。材料与方法。研究了来自48个地区168例CF患者的痰、鼻咽拭子样本。全基因组测序(WGS)在MGISEQ-2000平台上进行。采用SPAdes、Galaxy、ResFinder、Integrall、PubMLST软件对WGS数据进行分析。结果168例CF患者中16例共分离到18株无色杆菌。其中以氧化木糖无色杆菌最常见,检出率为13 / 18(72%)。所分离的无色杆菌共有14种序列型,其中8种为新序列型。携带适应性耐药基因是一种罕见的现象(1 / 18株)。俄罗斯CF患者呼吸系统Achromobacter spp.定殖率与国外报道数据一致。以木糖氧化单胞菌最常见(72%)。从俄罗斯CF患者中分离的无色杆菌显示出较高的克隆多样性。
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引用次数: 0
In vitro activity of biapenem and other carbapenems against Russian clinical isolates of Pseudomonas aeruginosa, Acinetobacter spp., and Enterobacterales 双青霉烯和其他碳青霉烯类药物对俄罗斯临床分离株铜绿假单胞菌、不动杆菌和肠杆菌的体外活性研究
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.3.280-291
R. Kozlov, I. S. Azyzov, A. Dekhnich, N. Ivanchik, A. Kuzmenkov, Alexey А. Martinovich, A.V. Mikotina, M. Sukhorukova, I. V. Trushin, M. Edelstein
Objective. To evaluate in vitro activity of biapenem and other clinically available carbapenems against Russian clinical isolates of Enterobacterales, Pseudomonas aeruginosa и Acinetobacter spp., including isolates with acquired fermentative mechanisms of resistance to β-lactams. Materials and Methods. A total of 3139 Enterobacterales isolates, 793 P. aeruginosa isolates and 634 Acinetobacter spp. isolates from hospitalized patients in 63 hospitals from 35 Russian cities were included in the study during 2018-2019. Minimal inhibitory concentrations (MIC) for biapenem and other antimicrobials were determined in accordance with ISO 20776-1:2006. Carbapenemases genes were detected by commercially available real-time PCR kits AmpliSens® MDR KPC/OXA-48-FL and AmpliSens® MDR MBL-FL (Central Research Institute of Epidemiology, Russia). Data analysis and reporting was performed using AMRcloud online platform (www.amrcloud.net). Results. For all tested Escherichia coli isolates MIC50/90 were 0.06/0.125 mg/l for biapenem, 0.125⁄0.25 mg/l for imipenem, and 0.06/0.06 mg/l for meropenem. When MIC50/90 for ertapenem (0.015/0.125 mg/l for all isolates tested) were comparable to those of biapenem, a greater number of nosocomial E. coli isolates had MIC >4 mg/l for ertapenem (3.6%) than for biapenem (2.6%). MIC50/90 of Klebsiella pneumoniae for biapenem were 0.5⁄16 mg/l, for both imipenem and meropenem – 0.5⁄32 mg/l, for ertapenem – 2⁄32 mg/l. Resistance to oxyimino-β-lactams had no significant influence on activity of biapenem against Enterobacterales isolates. For 321 carbapenemase-producing K. pneumoniae isolates (ОХА-48 – 63.9%, NDM – 27.7%) biapenem has shown no advantages over imipenem and meropenem. МПК50/90 for nosocomial and community-acquired P. aeruginosa isolates were 8⁄64 mg/l and 0,5⁄16 mg/l for biapenem, 8⁄128 mg/l and 1⁄16 mg/l – for imipenem, 16⁄64 mg/l and 0,5⁄32 mg/l – for meropenem. All carbapenems, including biapenem, had very low in vitro activity against carbapenemaseproducing P. aeruginosa isolates. МПК50/90 of Acinetobacter spp. were 64⁄128 mg/l for biapenem, 64⁄128 mg/l – for imipenem, and 128⁄128 mg/l – for meropenem. Conclusions. According to the MIC distributions and MICs50/90 values independently of the presence of fermentative mechanisms of resistance to β-lactams, in vitro activity of biapenem against Russian clinical isolates of Enterobacterales, P. aeruginosa and Acinetobacter spp. was comparable to those of imipenem and meropenem.
目标。评估双青霉烯和其他临床可用的碳青霉烯类药物对俄罗斯肠杆菌、铜绿假单胞菌和不动杆菌临床分离株的体外活性,包括具有获得性发酵机制的对β-内酰胺耐药的分离株。材料与方法。2018-2019年,俄罗斯35个城市63家医院住院患者共分离出3139株肠杆菌、793株铜绿假单胞菌和634株不动杆菌。根据ISO 20776-1:2006测定了biapenem和其他抗菌剂的最低抑制浓度(MIC)。碳青霉烯酶基因检测采用市售实时PCR试剂盒AmpliSens®MDR KPC/OXA-48-FL和AmpliSens®MDR mll - fl(俄罗斯中央流行病学研究所)。结果:所有检测的大肠埃希菌分离株MIC50/90分别为:比阿培南0.06/0.125 mg/l、亚胺培南0.125 / 0.25 mg/l、美罗培南0.06/0.06 mg/l;当厄他培南的MIC50/90 (0.015/0.125 mg/l)与biapenem相当时,医院分离的大肠杆菌中厄他培南的MIC50/90(3.6%)比biapenem的MIC50/90多(2.6%)。双阿培南对肺炎克雷伯菌的MIC50/90为0.5⁄16 mg/l,亚胺培南和美罗培南对肺炎克雷伯菌的MIC50/90为0.5⁄32 mg/l,厄他培南对肺炎克雷伯菌的MIC50/90为2⁄32 mg/l。对氧亚胺-β-内酰胺类耐药对双青霉烯抗肠杆菌活性无显著影响。对于321株产碳青霉烯酶肺炎克雷伯菌(ОХА-48 - 63.9%, NDM - 27.7%),比亚胺培南和美罗培南没有优势。医院源性和社区获得性铜绿假单胞菌分离株的浓度分别为:比阿培南8⁄64 mg/l和0.5⁄16 mg/l,亚胺培南8⁄128 mg/l和1⁄16 mg/l,美罗培南16⁄64 mg/l和0.5⁄32 mg/l。所有碳青霉烯类,包括双青霉烯类,对产生碳青霉烯酶的铜绿假单胞菌的体外活性都很低。结论:根据MIC分布和独立于β-内酰胺耐药发酵机制存在的MICs50/90值,双阿培南对俄罗斯肠杆菌、铜绿假单胞菌和不动杆菌的体外活性与亚胺培南和美罗培南相当。
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引用次数: 2
Antimicrobial resistance and antimicrobial therapy modification during COVID19 pandemic in large tertiary hospital 大型三级医院2019冠状病毒病大流行期间抗菌药物耐药性及治疗方案修改
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.3.293-303
O. Romashov, O. Ni, A. Bykov, A. Kruglov, D. Protsenko, I. N. Tyurin
Objective. assessment of the evolution of the microbiological landscape of the hospital for the period of operation in 2020 into a pandemic of a new coronavirus infection in various departments, including intensive care units; change depending on the results of antibacterial therapy regimens. Materials and Methods. In a retrospective study, conducted from June to December 2020, in a multidisciplinary hospital working with COVID-19 infection, the resistance of isolated strains of microorganisms was analyzed in patients of different age groups. Resistance was assessed with test points in June and November 2020; depending on this, proposals were made to correct the internal (local) protocols of antimicrobial therapy. Results. The need for frequent and regular microbiological monitoring was confirmed. Further, we understood that the territories of the main and temporary hospital of the City Clinical Hospital No. 40 are heterogeneous and there are obvious differences both in structure and in the level of sensitivity. “In practice, these are two different hospitals”. Within the territories, the branches also differ from each other. When analyzing resistance in ICUs, it was revealed that within each hospital in each department, albeit similar in structure and profile of patients, there is a different level of resistance of strains. Conclusions. The structure of sensitivity generally corresponds to the world data, but for some pathogens it differs significantly. Microbiological monitoring should be carried out not only inside the hospital, but also inside the department. The increase in consumption of carbapenems and protected cephalosporins requires a reassessment of the practice of using AMP in any covid hospital, due to the impact on the epidemic situation both in the ICUs and in the hospital.
目标。2020年医院运营期间微生物景观演变为新型冠状病毒感染大流行在各科室包括重症监护室的演变评估;根据抗菌治疗方案的结果而变化。材料与方法。2020年6月至12月,在一家处理COVID-19感染的多学科医院进行了一项回顾性研究,分析了不同年龄组患者中分离出的微生物菌株的耐药性。在2020年6月和11月以试验点评估耐药性;在此基础上,提出了改进抗菌药物内部(局部)治疗方案的建议。此外,我们了解到40市临床医院主医院和临时医院的领土是异质的,在结构和敏感程度上都有明显的差异。“实际上,这是两家不同的医院”。在领土内,分支机构也彼此不同。在分析icu的耐药情况时,发现在各医院、各科室,虽然患者的结构和分布相似,但菌株的耐药水平不同。结论其敏感性结构总体上与世界数据一致,但对某些病原体的敏感性结构存在显著差异。微生物监测不仅要在医院内进行,而且要在科室内进行。碳青霉烯类和受保护的头孢菌素消费量的增加,需要重新评估在任何新冠医院使用AMP的做法,因为这对icu和医院的疫情都有影响。
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引用次数: 5
Bacteriophage therapy: back to the future 噬菌体疗法:回到未来
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.1.55-64
T. Perepanova, A. Kazachenko, P. L. Khazan, Yu A Malova
In connection with growing problem of antimicrobial resistance, the search for alternative treatments for infection is popular topic nowadays. This article represents an overview of published data on the therapeutic use of bacteriophages, specifically in urinary tract infections. The history of phage therapy of infectious diseases from the beginning of the 20th century to the present days is presented. The paper also discuss the mechanism of bacteriophages activity, differences between lytic and lysogenic phages, mechanisms of bacterial tolerance to phages and ways of its overcoming are. Authors present their own data on 30 years of clinical use of “bacteriophage cocktails” in the treatment and prevention of urological infection.
随着抗菌素耐药性问题的日益严重,寻找替代治疗感染的方法是当今流行的话题。这篇文章概述了已发表的关于噬菌体治疗用途的数据,特别是在尿路感染中。介绍了噬菌体治疗传染病的历史,从20世纪初到现在。本文还讨论了噬菌体的活性机制、溶解性噬菌体与溶原性噬菌体的区别、细菌对噬菌体的耐受机制及克服途径。作者介绍了30年来“噬菌体鸡尾酒”治疗和预防泌尿系统感染的临床应用数据。
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引用次数: 3
Safety profile assessment of drug products used for the pathogenetic treatment of COVID19 用于covid - 19病原治疗的药品的安全性评估
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.3.314-329
G. I. Syraeva, S. Mishinova, A. Kolbin, E.O. Eremenko
Objective. To review and summarize literature data in studies of safety of the drug products used for the pathogenetic treatment of COVID-19. Materials and Methods. As the first stage of monitoring the drug’s safety, which are used in the treatment of COVID-19 in Russia, a systematic review of studies of the drug’s safety profiles was carried out: mefloquine, hydroxychloroquine, azithromycin, lopinavir/ritonavir, favipiravir, tocilizumab, olokizumab, baricitinib in the international databases Medline, PubMed, ClinicalTrials.gov and Cochrane Library for the period 2019–2021. Results. The review included 51 articles that met the selection criteria. Based on the results of the review, it can be concluded that the safety profile (frequency, severity and severity) of most drugs repurposed for COVID-19 corresponds to those for the registered indications. At the same time, according to world experience, there is an increase in the number of reports of adverse drug reactions of hydroxychloroquine and azithromycin, which is provoked by the active use of these drugs for combination therapy. Conclusions. According to the literature, a high incidence of adverse events was noted in hydroxychloroquine, chloroquine and azithromycin. Subsequent analysis and comparison of the safety profiles of hydroxychloroquine, chloroquine and azithromycin with data from the national automated information system (AIS) database of Roszdravnadzor is a necessary component of effective and safe pharmacotherapy for COVID-19.
目标。回顾和总结新冠肺炎病原学治疗用药安全性研究的文献资料。材料与方法。作为监测该药物安全性的第一阶段,该药物在俄罗斯用于治疗COVID-19,系统回顾了该药物的安全性研究:甲氟喹、羟氯喹、阿奇霉素、洛匹那韦/利托那韦、favipiravir、tocilizumab、olokizumab、baricitinib在国际数据库Medline、PubMed、ClinicalTrials.gov和Cochrane Library中2019 - 2021年。该审查包括51篇符合选择标准的文章。根据审查结果,可以得出结论,大多数重新用于COVID-19的药物的安全性特征(频率、严重程度和严重程度)与注册适应症相对应。同时,根据国际经验,由于积极使用羟氯喹和阿奇霉素联合治疗,引起了羟氯喹和阿奇霉素药物不良反应的报道越来越多。结论:根据文献,羟氯喹、氯喹和阿奇霉素的不良事件发生率较高。随后将羟氯喹、氯喹和阿奇霉素的安全性与Roszdravnadzor国家自动信息系统(AIS)数据库的数据进行分析和比较,是有效和安全的药物治疗COVID-19的必要组成部分。
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引用次数: 0
The prevalence and antimicrobial susceptibility of circulating S. pneumoniae serotypes in adult population in Russia (epidemiological study «SPECTRUM») 俄罗斯成年人群中流行肺炎链球菌血清型的流行率和抗菌药物敏感性(流行病学研究«SPECTRUM»)
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.2.127-137
R. Kozlov, A. Muravyev, A. Chagaryan, N. Ivanchik, A. Kurkova, A. Kuzmenkov, I. V. Trushin, M. Sukhorukova
Objective. To estimate prevalence and antimicrobial susceptibility of circulated S. pneumoniae serotypes in adult population in different regions of the Russian Federation. Materials and Methods. A total of 500 isolates of S. pneumoniae obtained from patients with invasive pneumococcal disease (IPD), community-acquired pneumonia (CAP), sinusitis/acute otitis media (AOM) and healthy carriers from 29 centers were included in the study from 01 June 2019 to 15 January 2020. Re-identification, typing using real-time PCR with 27 primer pairs and antimicrobial susceptibility testing were performed in the central laboratory by standardized methods. Results. Among 50 isolates from patients with IPD, the following serotypes were detected: 3 (20.0%), 23F (10.0%), 6ABCD (8.0%), 19F (6.0%), 12ABF, 4, 7AF, 8, 9NL, 9VA, 15B (4.0% each), 1, 10A, 11AD, 14, 15AF, 18ABCF, 22AF, 33F/33A/37 (2.0% each). PCV-13 and PPV-23 covered 62.0% and 86.0% of those serotypes, respectively. Among 357 isolates from patients with CAP, the following serotypes were detected: 19F (12.3%), 6ABCD (11.5%), 3 (10.1%), 23F (5.9%), 14 (5.3%), 22AF (5.0%), 11AD (4.8%), 9NL (3.4%), 15AF (2.8%), 9VA (2.2%), 18ABCF (2.0%), 19A (1.7%), 12ABF (1.4%), 17F (0.8%), 16, 33F/33A/37, 7AF and 8 (0.6% each), 10A and 4 (0,3% each); serotypes were not specified due to the PCR typing protocol limitations for 106 (29.8%) isolates. PCV-13 and PPV-23 covered 51.9% and 68.7% of those serotypes, respectively. In patients with sinusitis/AOM (n = 48), serotypes were: 19F (18.8%), 6ABCD (16.7%), 23F (12.5%), 3 (12.5%), 18ABCF (6.3%), 11AD (4.2%), 14 (4.2%), 22AF (4.2%), 15AF, 4, 9VA (2.1% each). PCV-13 and PPV-23 covered 75.0% and 83.3% of those serotypes, respectively. In healthy nasopharyngeal carriers (n = 45), the following serotypes were detected: 19F (24.4%), 3 (17.8%), 6ABCD (17.8%), 11AD (13.3%), 23F (8.9%), 22AF (6.7%), 14 and 15AF (2.2% each). PCV-13 and PPV-23 covered 71.1% and 91.1% of those serotypes, respectively. Serotypes 14, 19F, and 19A were frequently resistant to three antibiotics – penicillin, erythromycin, and tetracycline. Resistance to respiratory quinolones was very low (0.7%) and detected among serotypes 14 and 9NL only. The majority of non-vaccine serotypes did not have substantial antimicrobial resistance problems. Conclusions. Despite the relatively low number of isolates in all but CAP group and limitations of PCR typing protocol, results of our study support the use of pneumococcal vaccines (PPV-23 and PCV-13) in Russian adult population, with some advantages of PPV-23 over PCV-13.
目标。目的评估俄罗斯联邦不同地区成年人群中流行肺炎链球菌血清型的流行率和抗菌药物敏感性。材料与方法。2019年6月1日至2020年1月15日,研究人员将来自29个中心的侵袭性肺炎球菌病(IPD)、社区获得性肺炎(CAP)、鼻窦炎/急性中耳炎(AOM)患者和健康携带者的500株肺炎链球菌纳入研究。结果50株IPD患者分离株中检出血清型分别为3(20.0%)、23F(10.0%)、6ABCD(8.0%)、19F(6.0%)、12ABF、4、7AF、8、9NL、9VA、15B(各4.0%)、1、10A、11AD、14、15AF、18ABCF、22AF、33F/33A/37(各2.0%)。PCV-13和PPV-23的血清型覆盖率分别为62.0%和86.0%。在357株CAP患者分离株中检出以下血清型:19F(12.3%)、6ABCD(11.5%)、3(10.1%)、23F(5.9%)、14(5.3%)、22AF(5.0%)、11AD(4.8%)、9NL(3.4%)、15AF(2.8%)、9VA(2.2%)、18ABCF(2.0%)、19A(1.7%)、12ABF(1.4%)、17F(0.8%)、16、33F/33A/37、7AF和8(各0.6%)、10A和4(各0.3%);106株(29.8%)分离株由于PCR分型方案的限制,未明确血清型。PCV-13和PPV-23的血清型覆盖率分别为51.9%和68.7%。鼻窦炎/AOM患者(48例)血清型分别为:19F(18.8%)、6ABCD(16.7%)、23F(12.5%)、3(12.5%)、18ABCF(6.3%)、11AD(4.2%)、14(4.2%)、22AF(4.2%)、15AF、4、9VA(各占2.1%)。PCV-13和PPV-23分别覆盖75.0%和83.3%的血清型。在健康鼻咽带菌者(n = 45)中,检出血清型分别为19F(24.4%)、3(17.8%)、6ABCD(17.8%)、11AD(13.3%)、23F(8.9%)、22AF(6.7%)、14和15AF(各2.2%)。PCV-13和PPV-23分别覆盖了71.1%和91.1%的血清型。血清型14、19F和19A常对青霉素、红霉素和四环素三种抗生素耐药。呼吸道喹诺酮类药物耐药率很低(0.7%),仅在14和9NL血清型中检测到。结论:尽管除CAP组外所有血清型的分离株数量相对较少,且PCR分型方案存在局限性,但我们的研究结果支持在俄罗斯成年人群中使用肺炎球菌疫苗(PPV-23和PCV-13), PPV-23比PCV-13具有一定的优势。
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引用次数: 5
New regimens and new medications in the treatment of tuberculosis: keeping step? 结核病治疗的新方案和新药物:保持同步?
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.1.27-42
D. Ruzanov, A. M. Skriagina, I. Buinevich, S. Goponiako, G. Balasaniantc, E. Khimova
Rapid tests detecting Mycobacterium tuberculosis and drug resistance which are universally implemented in medical practice has dramatically improved the diagnosis of rifampicin-resistant tuberculosis and shortened turnaround time thus enabling early etiotropic therapy. However, permanently increasing drug resistance of M. tuberculosis makes treatment less effective. Furthermore, long treatment courses are required due to low sterilizing activity of treatment regimens used for drug-resistant tuberculosis which leads to greater toxic effects, reduces patients’ adherence to treatment and consumes resources of medical care systems. Current phthisiology needs new effective medications and short treatment regimens, otherwise elimination of tuberculosis by 2050 is impossible. This review summarizes the information about treatment of drugresistant TB, including repurposed drugs, new medications and treatment regimens.
在医疗实践中普遍实施的检测结核分枝杆菌和耐药性的快速试验,极大地改善了对利福平耐药结核病的诊断,缩短了周转时间,从而实现了早期致病因治疗。然而,结核分枝杆菌耐药性的持续增加使得治疗效果降低。此外,由于用于耐药结核病的治疗方案的消毒活性低,导致更大的毒性作用,降低患者对治疗的依从性并消耗医疗保健系统的资源,因此需要长疗程的治疗。当前的生理学需要新的有效药物和短期治疗方案,否则到2050年消除结核病是不可能的。本文综述了耐药结核病的治疗信息,包括重新使用的药物、新的药物和治疗方案。
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引用次数: 1
Mucormycosis: modern diagnostics and treatment, existing problems and new trends in antifungal therapy 毛霉病:现代诊断和治疗,存在的问题和抗真菌治疗的新趋势
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.3.226-238
M. Popova, Y. Rogacheva
Over the last decade, the introduction of new antifungal drugs and diagnostic procedures has improved the prognosis of hematological patients with invasive fungal disease (IFD), primarily invasive aspergillosis. Despite effective antifungal prophylaxis against the most common IFD caused by Aspergillus spp., rates of IFD due to rare pathogens being resistant to most antifungal drugs, including mucormycosis have been increased. The main group of patients having a high risk of mucormycosis is deeply immunocompromised patients who received chemotherapy for acute leukemia, patients undergoing allogeneic bone marrow transplantation, or treated with corticosteroids for graft-versushost disease. Currently, the urgency of this complication is significantly higher due to COVID-19 pandemic and extensive use of corticosteroids for the treatment of COVID-19. Despite the fact that the criteria for the diagnosis of IFD EORTC/MSG 2008 and 2020 have been developed and implemented into practice in most countries, mucormycosis still remains a difficult-to-diagnose IFD, where the factor of rapid diagnosis is a main factor of treatment success. Medications available for the treatment of IFD include polyenes, triazoles, and echinocandins. For a long time, the drug of choice for the treatment of mucormycosis was liposomal amphotericin B. However, a new effective drug has been approved for the treatment of both mucormycosis and IFD, caused by multiple pathogens – isavuconazole. This review presents new data on the epidemiology of mucormycosis, diagnosis approaches and current international treatment guidelines.
在过去十年中,新的抗真菌药物和诊断方法的引入改善了血液病侵袭性真菌病(IFD)患者的预后,主要是侵袭性曲霉病。尽管对最常见的由曲霉引起的IFD进行了有效的抗真菌预防,但由于罕见病原体对大多数抗真菌药物(包括毛霉病)具有耐药性而导致的IFD发生率有所增加。毛霉病高风险的主要患者群体是因急性白血病接受化疗的免疫功能低下患者、接受同种异体骨髓移植的患者或因移植物抗宿主病接受皮质类固醇治疗的患者。目前,由于COVID-19大流行和广泛使用皮质类固醇治疗COVID-19,这一并发症的紧迫性大大提高。尽管大多数国家已经制定并实施了IFD诊断标准EORTC/MSG 2008和2020,但毛霉病仍然是一种难以诊断的IFD,其中快速诊断的因素是治疗成功的主要因素。可用于治疗IFD的药物包括多烯、三唑和棘白菌素。长期以来,治疗毛霉病的首选药物是两性霉素b脂质体。然而,一种新的有效药物已被批准用于治疗毛霉病和由多种病原体引起的IFD - isavuconazole。这篇综述介绍了毛霉病流行病学、诊断方法和当前国际治疗指南的新数据。
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引用次数: 2
COVID19 associated pulmonary aspergillosis covid - 19相关肺曲霉病
Q4 Medicine Pub Date : 2021-01-01 DOI: 10.36488/cmac.2021.3.239-246
N. Ovsyannikov, O. Bilevich
The novel coronavirus (COVID-19) pandemic announced by the World Health Organization in March 2020 assigned medical community to the new tasks that require immediate solutions. Recent studies have shown that invasive aspergillosis associated with COVID-19 often complicates a course of the disease and leads to death. This review aims to describe the diagnosis and therapy challenges due to COVID-19 associated invasive pulmonary aspergillosis.
世界卫生组织于2020年3月宣布的新型冠状病毒(COVID-19)大流行给医学界分配了需要立即解决的新任务。最近的研究表明,与COVID-19相关的侵袭性曲霉病往往使病程复杂化并导致死亡。本文综述了COVID-19相关的侵袭性肺曲霉病的诊断和治疗挑战。
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引用次数: 13
期刊
Klinicheskaia mikrobiologiia i antimikrobnaia khimioterapiia
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