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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">422</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2020-15-2-92-107</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>INFECTION PROBLEMS IN ONCOHEMATOLOGY</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ПРОБЛЕМЫ ИНФЕКЦИЙ В ОНКОГЕМАТОЛОГИИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Current treatment options for infections caused by carbapenem-resistant Enterobacteriaceae in patients with hematological malignancies</article-title><trans-title-group xml:lang="ru"><trans-title>Современные возможности терапии инфекций, вызванных карбапенеморезистентными энтеробактериями, у больных с опухолями системы крови</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5973-5763</contrib-id><name-alternatives><name xml:lang="en"><surname>Klyasova</surname><given-names>G. A.</given-names></name><name xml:lang="ru"><surname>Клясова</surname><given-names>Г. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>4 Novyy Zykovskiy Proezd, Moscow 125167</italic></p></bio><bio xml:lang="ru"><p><bold>Галина Александровна Клясова </bold></p><p><italic>125167 Москва, Новый Зыковский проезд, 4 </italic></p></bio><email>klyasova.g@blood.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">National Research Center for Hematology, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр гематологии» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2020-07-16" publication-format="electronic"><day>16</day><month>07</month><year>2020</year></pub-date><volume>15</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>92</fpage><lpage>107</lpage><history><date date-type="received" iso-8601-date="2020-07-15"><day>15</day><month>07</month><year>2020</year></date><date date-type="accepted" iso-8601-date="2020-07-15"><day>15</day><month>07</month><year>2020</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/422">https://oncohematology.abvpress.ru/ongm/article/view/422</self-uri><abstract xml:lang="en"><p>Infections are a common complication in patients with hematological malignancies, especially during neutropenia. Recently, an increase in multidrug-resistant gram-negative pathogens has been observed in the etiology of infectious complications, including carbapenem-resistant Enterobacteriaceae. However, therapeutic options for treatment of these infections are limited. The review represents treatment options for infections caused by carbapenem-resistant Enterobacteriaceae, including the use of reserve drugs such as polymyxin, carbapenems, tigecycline, as well as a new antibiotic – ceftazidime-avibactam, which contains a new β-lactamase inhibitor with unique properties.</p></abstract><trans-abstract xml:lang="ru"><p>Инфекции являются частыми осложнениями у больных с опухолями системы крови, особенно в период нейтропении. В последнее время в этиологии инфекционных осложнений наблюдается увеличение количества полирезистентных грамотрицательных возбудителей, включая карбапенеморезистентные энтеробактерии, возможность терапии которых ограничена. В обзоре представлены варианты лечения инфекций, вызванных карбапенеморезистентными энтеробактериями, включающие как применение противомикробных препаратов резерва, таких как полимиксин, карбапенемы, тигециклин, так и нового антибиотика цефтазидима-авибактама, в состав которого входит новый ингибитор β-лактамаз с уникальными свойствами.</p></trans-abstract><kwd-group xml:lang="en"><kwd>carbapenem-resistant Enterobacteriaceae</kwd><kwd>haematological malignancy</kwd><kwd>carbapenemase</kwd><kwd>febrile neutropenia</kwd><kwd>ceftazidime-avibactam</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>карбапенеморезистентные энтеробактерии</kwd><kwd>опухоль системы крови</kwd><kwd>карбапенемазы</kwd><kwd>фебрильная нейтропения</kwd><kwd>цефтазидим-авибактам</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Klyasova G.A. Antimicrobial therapy. In: Program treatment of blood system diseases: collection of diagnostic algorithms and protocols for the treatment of blood system disorders. Ed.: V.G. Savchenko. Moscow: Praktika, 2012. Pp. 827–54. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Клясова Г.А. Антимикробная терапия. В кн.: Программное лечение заболеваний системы крови: сборник алгоритмов диагностики и протоколов лечения заболеваний системы крови. Под ред. В.Г. Савченко. М.: Практика, 2012. С. 827–54.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Klyasova G.A., Speranskaya L.L., Mironova A.V. et al. The pathogens causing sepsis in immunocompromised patients: structure and problems of antibiotic resistance. Results of multicenter cooperative study. Gematologiya i transfuziologiya = Hematology and Transfusiology 2007;52(1):11–8. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Клясова Г.А., Сперанская Л.Л., Миронова А.В. и др. Возбудители сепсиса у иммунокомпрометированных больных: структура и проблемы антибиотикорезистентности (результаты многоцентрового исследования). Гематология и трансфузиология 2007;52(1):11–8.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><mixed-citation>Puerta-Alcalde P., Cardozo C., Marco F. et al. Changing epidemiology of bloodstream infection in a 25-years hematopoietic stem cell transplant program: current challenges and pitfalls on empiric antibiotic treatment impacting outcomes. Bone Marrow Transplant 2020;55(3):603–12. DOI: 10.1038/s41409-019-0701-3.</mixed-citation></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Klyasova G.A., Okhmat V.A. Antimicrobial therapy. In: Diagnostic algorithms and protocols for the treatment of blood system disorders. Ed.: V.G. Savchenko. Moscow: Praktika 2018. T. 2. Pp. 1067–1114. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Клясова Г.А., Охмат В.А. Антимикробная терапия. В кн.: Алгоритмы диагностики и протоколы лечения заболеваний системы крови. Под ред. В.Г. Савченко. М.: Практика 2018. Том 2. C. 1067–1114.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><mixed-citation>De Angelis G., Fiori B., Menchinelli G. et al. Incidence and antimicrobial resistance trends in bloodstream infections caused by ESKAPE and Escherichia coli at a large teaching hospital in Rome, a 9-year analysis (2007-2015). Eur J Clin Microbiol Infect Dis 2018;37(9):1627–36. DOI: 10.1007/s10096-018-3292-9.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Pouch S.M., Satlin M.J. Carbapenemresistant Enterobacteriaceae in special populations: solid organ transplant recipients, stem cell transplant recipients, and patients with hematologic malignancies. Virulence 2017;8(4):391–402. DOI: 10.1080/21505594.2016.1213472.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Girmenia C., Rossolini G.M., Piciocchi A. et al. Infections by carbapenem-resistant Klebsiella pneumoniae in SCT recipients: a nationwide retrospective survey from Italy. Bone Marrow Transplant 2015;50(2):282–8. DOI: 10.1038/bmt.2014.231.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Trecarichi E.M., Pagano L., Martino B. et al. Bloodstream infections caused by Klebsiella pneumoniae in oncohematological patients: clinical impact of carbapenem resistance in a multicentre prospective survey. Am J Hematol 2016;91(11):1076–81. DOI: 10.1002/ajh.24489.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Klyasova G., Korobova A., Khrulnova S. et al. Trends in antimicrobial resistance in gram-negative pathogens among haematological patients: results of multicenter study. Abstract Book 2020 European Congress of Clinical Microbiology and Infectious Diseases 2020;4:4253.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Averbuch D., Tridello G., Hoek J. et al. Antimicrobial resistance in gram-negative rods causing bacteremia in hematopoietic stem cell transplant recipients: Intercontinental prospective study of the Infectious Diseases Working Party of the European Bone Marrow Transplantation Group. Clin Infect Dis 2017;13;65(11):1819–28. DOI: 10.1093/cid/cix646.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Ambler R.P. The structure of betalactamases. Philos Trans R Soc Lond B Biol Sci 1980;289(1036):321–31.</mixed-citation></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Sukhorukova M.V., Edelstein M.V., Ivanchik N.V. et al. Antimicrobial resistance of nosocomial Enterobacterales isolates in Russia: results of multicenter epidemiological study “MARATHON 2015–2016”. Klinicheskaya mikrobiologiya i antimikrobnaya khimioterapiya = Clinical Microbiology and Antimicrobial Chemotherapy 2019;21(2):147–59. (In Russ.). DOI: 10.36488/cmac.2019.2.147-159.</mixed-citation><mixed-citation xml:lang="ru">Сухорукова М.В., Эйдельштейн М.В., Иванчик Н.В. и др. Антибиотикорезистентность нозокомиальных штаммов Enterobacterales в стационарах России: результаты многоцентрового эпидемиологического исследования «МАРАФОН 2015–2016». Клиническая микробиология и антимикробная химиотерапия 2019;21(2):147–59. DOI: 10.36488/cmac.2019.2.147-159.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><mixed-citation>Tzouvelekis L., Markogiannakis A., Psichogiou M. et al. Carbapenemases in Klebsiella pneumoniae and other Enterobacteriaceae: anevolving crisis of global dimensions. Clin Microbiol Rev 2012;25:682–707. DOI: 10.1128/CMR.05035-11.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Rodríguez-Bano J., Cisneros J.M., Cobos-Triguerosd N. et al. Diagnosis and antimicrobial treatment of invasive infections due to multidrug-resistant Enterobacteriaceae. Guidelines of the Spanish Society of Infectious Diseases and Clinical Microbiology. Enferm Infecc Microbiol Clin 2015;33(5):337.e1–21. DOI: 10.1016/j.eimc.2014.11.009.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>De Maio Carrilho C.M.D., Marques de Oliveira L., Gaudereto J. et al. A prospective study of treatment of carbapenem-resistant Enterobacteriaceae infections and risk factors associated with outcome. BMC Infect Dis 2016;16:629. DOI: 10.1186/s12879-016-1979-z.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Tumbarello M., Trecarichi E.M., De Rosa F.G. et al. Infections caused by KPC-producing Klebsiella pneumoniae: differences in therapy and mortality in a multicentre study. J Antimicrob Chemother 2015;70(7):2133–43. DOI: 10.1093/jac/dkv086.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Gutiérrez-Gutiérrez B., Salamanca E., de Cueto M. et al. Effect of appropriate combination therapy on mortality of patients with bloodstream infections due to carbapenemase-producing Enterobacteriaceae (INCREMENT): a retrospective cohort study. Lancet Infect Dis 2017;7:726–34. DOI: 10.1016/S14733099(17)302281.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Akova M., Daikos G.L., Tzouvelekis L., Carmeli Y. Interventional strategies and current clinical experience with carbapenemase-producing gram-negative bacteria. Clin Microbiol Infect 2012;18(5):439–48. DOI: 10.1111/j.1469-0691.2012.03823.x.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Daikos G.L., Tsaousi S., Tzouvelekis L.S. et al. Carbapenemase-producing Klebsiella pneumoniae bloodstream infections: lowering mortality by antibiotic combination schemes and the role of carbapenems. Antimicrob Agents Chemother 2014;58(4):2322–8. DOI: 10.1128/AAC.02166-13.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Endimiani A., Perez F., Bajaksouzian S. et al. Evaluation of updated interpretative criteria for categorizing Klebsiella pneumoniae with reduced carbapenem susceptibility. J Clin Microbiol 2010;48(12):4417–25. DOI: 10.1128/JCM.02458-09.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Daikos G.L., Markogiannakis A. Carbapenemase-producing Klebsiella pneumoniae: (When) might we still consider treating with carbapenems? Clin Microbiol Infect 2011;17(8):1135–41. DOI: 10.1111/j.1469-0691.2011.03553.x.</mixed-citation></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Beloborodov V.B., Gruver K.P. Carbapenems in modern clinical practice. Russkiy meditsinskiy zhurnal = Russian Medical Journal 2012;18(17):1037–42. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Белобородов В.Б., Грувер К.П. Карбапенемы в современной клинической практике. Русский медицинский журнал 2012;18(17):1037–42.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><mixed-citation>Sheu C.C., Chang Y.T., Lin S.Y. et al. Infections caused by carbapenem-resistant Enterobacteriaceae: an update on therapeutic options. Front Microbiol 2019;30;10:80. DOI: 10.3389/fmicb.2019.00080.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Tsuji B.T., Pogue J.M., Zavascki A.P. et al. International consensus guidelines for the optimal use of the polymyxins: endorsed by the American College of Clinical Pharmacy (ACCP), European Society of Clinical Microbiology and Infectious Diseases (ESCMID), Infectious Diseases Society of America (IDSA), International Society for Anti-infective Pharmacology (ISAP), Society of Critical Care Medicine (SCCM), and Society of Infectious Diseases Pharmacists (SIDP). Pharmacotherapy 2019;39(1):10–39. DOI: 10.1002/phar.2209.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Bassetti M., Giacobbe D.R., Giamarellou H. et al. Management of KPC-producing Klebsiella pneumoniae infections. Clin Microbiol Infect 2018;24(2):133–44. DOI: 10.1016/j.cmi.2017.08.030.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Mashni O., Nazer L., Le J. Critical review of double-carbapenem therapy for the treatment of carbapenemaseproducing Klebsiella pneumoniae. Ann Pharmacother 2019;53(1):70–81. DOI: 10.1177/1060028018790573.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Roberts J.A., Abdul-Aziz M.H., Davis J.S. et al. Continuous versus intermittent β-lactam infusion in severe sepsis: a metaanalysis of individual patient data from randomized trials. Am J Respir Crit Care Med 2016;15;194(6):681–91. DOI: 10.1164/rccm.201601-0024OC.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Vardakas K.Z., Voulgaris G.L., Maliaros A. et al. Prolonged versus short-term intravenous infusion of antipseudomonal β-lactams for patients with sepsis: a systematic review and meta-analysis of randomized trials. Lancet Infect Dis 2018;18(1):108–20. DOI: 10.1016/S1473-3099(17)30615-1.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Bulik C.C., Nicolau D.P. Double-carbapenem therapy for carbapenemase-producing Klebsiella pneumoniae. Antimicrob Agents Chemother 2011;55(6):3002–4. DOI: 10.1128/AAC.01420-10.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>De Pascale G., Martucci G., Montini L. et al. Double carbapenem as a rescue strategy for the treatment of severe carbapenemase-producing Klebsiella pneumoniae infections: a two-center, matched case-control study. Crit Care 2017;21(1):173. DOI: 10.1186/s13054-017-1769-z.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Oliva A., Scorzolini L., Castaldi D. et al. Double-carbapenem regimen, alone or in combination with colistin, in the treatment of infections caused by carbapenemresistant Klebsiella pneumoniae (CR-Kp). J Infect 2017;74(1):103–6. DOI: 10.1016/j.jinf.2016.10.002.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Monaco M., Giani T., Raffone M. et al. Colistin resistance superimposed to endemic carbapenem-resistant Klebsiella pneumoniae: a rapidly evolving problem in Italy, November 2013 to April 2014. Euro Surveill 2014;23;19(42):20939. DOI: 10.2807/1560-7917.es2014.19.42.20939.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Falagas M.E., Bliziotis I.A., Tam V.H. Intraventricular or intrathecal use of polymyxins in patients with gramnegative meningitis: a systematic review of the available evidence. Int J Antimicrob Agents 2007;29(1):9–25. DOI: 10.1016/j.ijantimicag.2006.08.024.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Nation R.L., Garonzik S.M., Thamlikitkul V. et al. Dosing guidance for intravenous colistin in critically-ill patients. Clin Infect Dis 2017;1;64(5):565–71. DOI: 10.1093/cid/ciw839.</mixed-citation></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Eliseev E.V., Azizov I.S., Zubareva N.A. Review of the international consensus guidelines for the optimal use of the polymyxins. Klinicheskaya mikrobiologiya i antimikrobnaya khimioterapiya = Clinical Microbiology and Antimicrobial Chemotherapy 2019;21(4):282–309. (In Russ.). DOI: 10.36488/cmac.2019.4.282-309. [</mixed-citation><mixed-citation xml:lang="ru">Елисеев Е.В., Азизов И.С., Зубарева Н.А. Обзор международных согласительных рекомендаций по оптимальному использованию полимиксинов. Клиническая микробиология и антимикробная химиотерапия 2019;21(4):282–309. DOI: 10.36488/cmac.2019.4.282-309.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><mixed-citation>Falagas M.E., Giannopoulou K.P., Kokolakis G.N., Rafailidis P.I. Fosfomycin: use beyond urinary tract and gastrointestinal infections. Clin Infect Dis 2008;46:1069–77. DOI: 10.1086/527442.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Samonis G., Maraki S., Karageorgopoulos D.E. et al. Synergy of fosfomycin with carbapenems, colistin, netilmicin, and tigecycline against multidrug-resistant Klebsiella pneumoniae, Escherichia coli, and Pseudomonas aeruginosa clinical isolates. Eur J Clin Microbiol Infect Dis 2012;31:695–701. DOI: 10.1007/s10096-011-1360-5.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Parker S., Lipman J., Koulenti D. et al. What is the relevance of fosfomycin pharmacokinetics in the treatment of serious infections in critically ill patients? A systematic review. Int J Antimicrob Agents 2013;42:289–93. DOI: 10.1016/j.ijantimicag.2013.05.018.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Le J., McKee B., Srisupha-Olarn W., Burgess D.S. In vitro activity of carbapenems alone and in combination with amikacin against KPC-producing Klebsiella pneumoniae. J Clin Med Res 2011;3:106–10. DOI: 10.4021/jocmr551w.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Tanaseanu C., Milutinovic S., Calistru P.I. et al. Efficacy and safety of tigecycline versus levofloxacin for community-acquired pneumonia. BMC Pulm Med 2009;9;9:44. DOI: 10.1186/1471-2466-9-44.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Ramirez J., Dartois N., Gandjini H. et al. Randomized phase 2 trial to evaluate the clinical efficacy of two high-¬dosage tigecycline regimens versus imipenemcilastatin for treatment of hospitalacquired pneumonia. Antimicrob Agents Chemother 2013;57:1756–62. DOI: 10.1128/AAC.01232-12.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>De Pascale G., Montini L., Pennisi M. et al. High dose tigecycline in critically ill patients with severe infections due to multidrug-resistant bacteria. Crit Care 2014;5;18(3):R90. DOI: 10.1186/cc13858.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Moreno B.B., Simón I.F., García V.P. et al. Tigecycline therapy for infections due to carbapenemase-producing Klebsiella pneumoniae in critically ill patients. Scand J Infect Dis 2014;46(3):175–80. DOI: 10.3109/00365548.2013.861608.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Sbrana, F., Malacarne, P., Viaggi, B. et al. Carbapenem-sparing antibiotic regimens for infections caused by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae in intensive care unit. Clin Infect Dis 2013;56(5):697–700. DOI: 10.1093/cid/cis969.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Di Carlo P., Gulotta G., Casuccio A. et al. KPC-3 Klebsiella pneumoniae ST258 clone infection in postoperative abdominal surgery patients in an intensive care setting: analysis of a case series of 30 patients. BMC Anesthesiol 2013;3;13(1):13. DOI: 10.1186/1471-2253-13-13.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Geng T.T., Xu X., Huang M. High-dose tigecycline for the treatment of nosocomial carbapenem-resistant Klebsiella pneumoniae bloodstream infections: a retrospective cohort study. Medicine (Baltimore) 2018;97(8):e9961. DOI: 10.1097/MD.0000000000009961.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Ni W., Han Y., Liu J. et al. Tigecycline treatment for carbapenem-resistant Enterobacteriaceae infections: a systematic review and meta-analysis. Medicine (Baltimore) 2016;95(11):e3126. DOI: 10.1097/MD.0000000000003126.</mixed-citation></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">Kozlov R.S., Stetsyuk O.U., Andreeva I.V. Ceftazidime-avibactam: new rules for the game against multidrug-resistant gram-negative bacteria. Klinicheskaya mikrobiologiya i antimikrobnaya khimioterapiya = Clinical Microbiology and Antimicrobial Chemotherapy 2018;20(1):24–34. (In Russ.). DOI: 10.36488/cmac.2018.1.24-34.</mixed-citation><mixed-citation xml:lang="ru">Козлов Р.С., Стецюк О.У., Андреева И.В. Цефтазидим-авибактам: новые «правила игры» против полирезистентных грамотрицательных бактерий. Клиническая микробиология и антимикробная химиотерапия 2018;20(1):24–34. DOI: 10.36488/cmac.2018.1.24-34.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><mixed-citation>Karlowsky J.A., Kazmierczak K.M., Bouchillon S.K. et al. In vitro activity of ceftazidime-avibactam against clinical isolates of Enterobacteriaceae and Pseudomonas aeruginosa collected in Latin American countries: results from the INFORM Global Surveillance Program, 2012 to 2015. Antimicrob Agents Chemother 2019;27;63(4):e01814–8. DOI: 10.1128/AAC.01814-18.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>De Jonge B.L.M., Karlowsky J.A., Kazmierczak K.M. et al. In vitro susceptibility to ceftazidime-avibactam of carbapenem-nonsusceptible Enterobacteriaceae isolates collected during the INFORM global surveillance study (2012 to 2014). Antimicrob Agents Chemother 2016;22;60(5):3163–9. DOI: 10.1128/AAC.03042-15.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Castón J.J., Lacort-Peralta I., MartínDávila P. et al. Clinical efficacy of ceftazidime/avibactam versus other active agents for the treatment of bacteremia due to carbapenemase-producing Enterobacteriaceae in hematologic patients. Int J Infect Dis 2017;59:118–23. DOI: 10.1016/j.ijid.2017.03.021.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Tumbarello M., Trecarichi E.M., Corona A. et al. Efficacy of ceftazidime-avibactam salvage therapy in patients with infections caused by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae. Clin Infect Dis 2019;68(3):355–64. DOI: 10.1093/cid/ciy492.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Guimarãesa T., Nouérb S., Martinsc R. et al. Ceftazidime-avibactam as salvage therapy for infections caused by Enterobacteriales co-resistant to carbapenems and polymyxins. Antimicrob. Antimicrob Agents Chemother 2019;23;63(10):e00528–19. DOI: 10.1128/AAC.00528-19.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>van Duin D., Lok J.J., Earley M. et al. Colistin versus ceftazidime-avibactam in the treatment of infections due to carbapenem-resistant Enterobacteriaceae. Clin Infect Dis 2018;6;66(2):163–71. DOI: 10.1093/cid/cix783.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>De la Calle C., Rodríguez O., Morata L. et al. Clinical characteristics and prognosis of infections caused by OXA-48 carbapenemase-producing Enterobacteriaceae in patients treated with ceftazidimeavibactam. Int J Antimicrob Agents 2019;53(4):520–4. DOI: 10.1016/j.ijantimicag.2018.11.015.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Sousa A., Pérez-Rodríguez T., Soto A. et al. Effectiveness of ceftazidime/avibactam as salvage therapy for treatment of infections due to OXA-48 carbapenemase-producing Enterobacteriaceae. J Antimicrob Chemother 2018;73:3170–5. DOI: 10.1093/jac/dky295.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Wenzler E., Deraedt M.F., Harrington A.T., Danizger L.H. Synergistic activity of ceftazidime-avibactam and aztreonam against serine and metallo-β-lactamaseproducing gram-negative pathogens. Diagn Microbiol Infect Dis 2017;88(4):352–4. DOI: 10.1016/j.diagmicrobio.2017.05.009.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Shaw E., Rombauts A., Tubau F. et al. Clinical outcomes after combination treatment with ceftazidime/avibactam and aztreonam for NDM-1/OXA-48/CTX-M15-producing Klebsiella pneumoniae infection. J Antimicrob Chemother 2018;1;73(4):1104–6. DOI: 10.1093/jac/dkx496.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Falcone M., Daikos G.L., Tiseo G. et al. Efficacy of ceftazidime-avibactam plus aztreonam in patients with bloodstream infections caused by MBL-producing Enterobacterales. Clin Infect Dis 2020; 19;ciaa586. DOI: 10.1093/cid/ciaa586.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Micozzi A., Gentile G., Minotti C. et al. Carbapenem-resistant Klebsiella pneumoniae in high-risk haematological patients: factors favouring spread, risk factors and outcome of carbapenem-resistant Klebsiella pneumoniae bacteremias. BMC Infect Dis 2017;17(1):203. DOI: 10.1186/s12879-017-2297-9.</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Girmenia C., Bertaina A., Piciocchi A. et al. Incidence, risk Factors and outcome of pre-engraftment gram-negative bacteremia after allogeneic and autologous hematopoietic stem cell transplantation: An Italian prospective multicenter survey. Clin Infect Dis 2017;13;65(11):1884–96. DOI: 10.1093/cid/cix690.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Forcina A., Baldan R., Marasco V. et al. Control of infectious mortality due to carbapenemase-producing Klebsiella pneumoniae in hematopoietic stem cell transplantation. Bone Marrow Transplant 2017;52(1):114–9. DOI: 10.1038/bmt.2016.234.</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Viale P., Tumietto F., Giannella M. et al. Impact of a hospital-wide multifaceted programme for reducing carbapenemresistant Enterobacteriaceae infections in a large teaching hospital in northern Italy. Clin Microbiol Infect 2015;21:242–7. DOI: 10.1016/j.cmi.2014.10.020.</mixed-citation></ref></ref-list></back></article>
