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1
Resistance Trends of Causing Urinary Tract Infections in Chongqing, 2011-2019.2011 - 2019年重庆地区引起尿路感染的病原菌耐药性趋势
Infect Drug Resist. 2021 Feb 9;14:475-481. doi: 10.2147/IDR.S295870. eCollection 2021.
2
Identifying the drivers of multidrug-resistant Klebsiella pneumoniae at a European level.在欧洲层面确定耐多药肺炎克雷伯菌的驱动因素。
PLoS Comput Biol. 2021 Jan 29;17(1):e1008446. doi: 10.1371/journal.pcbi.1008446. eCollection 2021 Jan.
3
Efficacy of β-lactam/β-lactamase inhibitors to treat extended-spectrum beta-lactamase-producing Enterobacterales bacteremia secondary to urinary tract infection in kidney transplant recipients (INCREMENT-SOT Project).β-内酰胺/β-内酰胺酶抑制剂治疗尿路感染继发产超广谱β-内酰胺酶肠杆菌科菌血症在肾移植受者中的疗效(INCREMENT-SOT 项目)。
Transpl Infect Dis. 2021 Jun;23(3):e13520. doi: 10.1111/tid.13520. Epub 2021 Jan 4.
4
Oral fosfomycin for the treatment of lower urinary tract infections among kidney transplant recipients-Results of a Spanish multicenter cohort.口服磷霉素治疗肾移植受者下尿路感染-一项西班牙多中心队列研究结果。
Am J Transplant. 2020 Feb;20(2):451-462. doi: 10.1111/ajt.15614. Epub 2019 Oct 28.
5
Current options for the treatment of infections due to extended-spectrum beta-lactamase-producing Enterobacteriaceae in different groups of patients.不同患者群体中治疗产超广谱β-内酰胺酶肠杆菌科感染的现有选择。
Clin Microbiol Infect. 2019 Aug;25(8):932-942. doi: 10.1016/j.cmi.2019.03.030. Epub 2019 Apr 12.
6
Updates on urinary tract infections in kidney transplantation.肾脏移植中尿路感染的最新研究进展。
J Nephrol. 2019 Oct;32(5):751-761. doi: 10.1007/s40620-019-00585-3. Epub 2019 Jan 28.
7
Current epidemiology, genetic evolution and clinical impact of extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae.产超广谱β-内酰胺酶大肠埃希菌和肺炎克雷伯菌的当前流行情况、遗传进化和临床影响。
Infect Genet Evol. 2018 Jul;61:185-188. doi: 10.1016/j.meegid.2018.04.005. Epub 2018 Apr 5.
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Treatment of Infections Caused by Extended-Spectrum-Beta-Lactamase-, AmpC-, and Carbapenemase-Producing Enterobacteriaceae.产超广谱β-内酰胺酶、AmpC 酶和碳青霉烯酶肠杆菌科细菌感染的治疗。
Clin Microbiol Rev. 2018 Feb 14;31(2). doi: 10.1128/CMR.00079-17. Print 2018 Apr.
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Discovery, research, and development of new antibiotics: the WHO priority list of antibiotic-resistant bacteria and tuberculosis.发现、研究和开发新抗生素:世界卫生组织抗微生物药物耐药性和结核病优先病原体清单。
Lancet Infect Dis. 2018 Mar;18(3):318-327. doi: 10.1016/S1473-3099(17)30753-3. Epub 2017 Dec 21.
10
Antimicrobial Resistance of Hypervirulent : Epidemiology, Hypervirulence-Associated Determinants, and Resistance Mechanisms.高毒力 耐药性:流行病学、高毒力相关决定因素和耐药机制。
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克服抗生素耐药性:产超广谱β-内酰胺酶(ESBL)肺炎克雷伯菌引起的尿路感染使用高剂量阿莫西林克拉维酸。

Breaking Antimicrobial Resistance: High-Dose Amoxicillin with Clavulanic Acid for Urinary Tract Infections Due to Extended-Spectrum Beta-Lactamase (ESBL)-Producing Klebsiella pneumoniae.

机构信息

Department of Immunology, Transplantology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.

Chair and Department of Medical Microbiology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Ann Transplant. 2023 May 16;28:e939258. doi: 10.12659/AOT.939258.

DOI:10.12659/AOT.939258
PMID:37190675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10199652/
Abstract

BACKGROUND Carbapenems are the primary treatment for urinary tract infections (UTIs) caused by extended-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae. However, the recurrence rate is high, and patients often require rehospitalization. We present the results of an observational study on patients with recurrent UTIs who were treated in an outpatient setting with maximal therapeutic oral doses of amoxicillin with clavulanic acid. MATERIAL AND METHODS All patients had pyuria and ESBL-producing K. pneumoniae in urine culture. The starting dosage was 2875 g of amoxicillin twice daily and 125 mg of clavulanic acid twice daily. We down-titrated the doses every 7-14 days and continued prophylactic therapy with amoxicillin/clavulanic acid at 250/125 mg for up to 3 months. We defined therapeutic failure as ESBL-positive K. pneumoniae in urine culture during therapy and recurrence as positive urine culture with the same strain within 1 month after the end of treatment. RESULTS We included 9 patients: 7 kidney graft recipients, 1 liver graft recipient, and 1 patient with chronic kidney disease. We observed no therapeutic failures and no recurrences in the study group during the study period. In 1 case, the patient experienced a subsequent UTI caused by ESBL-producing K. pneumoniae 4 months after completing the therapy. CONCLUSIONS In conclusion, it is possible to break the resistance of ESBL-producing K. pneumoniae strains with high doses of oral amoxicillin with clavulanic acid. Such treatment could be an alternative to carbapenems in select cases.

摘要

背景

产超广谱β-内酰胺酶(ESBL)的肺炎克雷伯菌引起的尿路感染(UTI)的主要治疗方法是使用碳青霉烯类药物。然而,复发率较高,患者往往需要再次住院治疗。我们报告了一项观察性研究结果,该研究纳入了在门诊接受最大治疗剂量阿莫西林克拉维酸口服治疗的复发性 UTI 患者。

材料和方法

所有患者的尿液培养均显示有脓尿和产 ESBL 的肺炎克雷伯菌。起始剂量为阿莫西林 2875 毫克,每日两次,克拉维酸 125 毫克,每日两次。每 7-14 天我们会减少剂量,并继续预防性使用阿莫西林/克拉维酸 250/125 毫克治疗,最长可达 3 个月。如果治疗期间尿液培养出 ESBL 阳性的肺炎克雷伯菌或治疗结束后 1 个月内再次出现相同菌株的阳性尿液培养,则定义为治疗失败和复发。

结果

我们共纳入 9 例患者:7 例肾移植受者,1 例肝移植受者,1 例慢性肾脏病患者。在研究期间,研究组未观察到治疗失败或复发。在 1 例患者中,在完成治疗后 4 个月,该患者出现了由产 ESBL 的肺炎克雷伯菌引起的后续 UTI。

结论

用高剂量阿莫西林克拉维酸口服治疗可以打破产 ESBL 的肺炎克雷伯菌菌株的耐药性。在某些情况下,这种治疗方法可能替代碳青霉烯类药物。