匈牙利塞格德嗜麦芽寡养单胞菌耐药性分型的10年单中心经验。

Márió Gajdács, Edit Urbán
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引用次数: 11

摘要

嗜麦芽窄养单胞菌是一种需氧、氧化酶阴性和过氧化氢酶阳性的芽孢杆菌。嗜麦芽葡萄球菌是公认的条件致病菌。由于侵入性医疗程序、器官移植和恶性疾病化疗的进步,这种病原体的相关性显著增加。嗜麦芽葡萄球菌感染的治疗具有挑战性,因为这些细菌对多种抗生素表现出内在耐药性,首选药物是磺胺甲恶唑/甲氧苄啶。我们的目的是评估来自不同临床样本的嗜麦芽链球菌的流行病学,以及这些样本在长期监测期间的耐药水平和耐药分型特征。本研究收集了2008年1月至2017年12月期间从血培养样本、呼吸样本和尿液样本中分离出的嗜麦芽葡萄球菌,共鉴定出嗜麦芽葡萄球菌817株(呼吸样本n = 579,占70.9%,血培养样本n = 175,占21.4%,尿液样本n = 63,占7.7%)。左氧氟沙星和粘菌素敏感性最高(92.2%;N = 753),其次是替加环素(90.5%,N = 739),一线药物磺胺甲恶唑/甲氧苄啶(87.4%,N = 714),而阿米卡星的表型耐药率最高(72.5%,N = 592)。磺胺甲恶唑/甲氧苄啶耐药的临床问题是一个复杂的问题,因为目前尚无治疗这些感染的指导方针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A 10-year single-center experience on Stenotrophomonas maltophilia resistotyping in Szeged, Hungary.

Stenotrophomonas maltophilia is an aerobic, oxidase-negative and catalase-positive bacillus. S. maltophilia is a recognized opportunistic pathogen. Due to the advancements in invasive medical procedures, organ transplantation and chemotherapy of malignant illnesses, the relevance of this pathogen increased significantly. The therapy of S. maltophilia infections is challenging, as these bacteria show intrinsic resistance to multiple classes of antibiotics, the first-choice drug is sulfamethoxazole/trimethoprim. Our aim was to assess the epidemiology of S. maltophilia from various clinical samples and the characterization of resistance-levels and resistotyping of these samples over a long surveillance period. The study included S. maltophilia bacterial isolates from blood culture samples, respiratory samples and urine samples and the data for the samples, received between January 2008 until December 2017, a total of 817 S. maltophilia isolates were identified (respiratory samples n = 579, 70.9%, blood culture samples n = 175, 21.4% and urine samples n = 63, 7.7%). Levofloxacin and colistin-susceptibility rates were the highest (92.2%; n = 753), followed by tigecycline (90.5%, n = 739), the first-line agent sulfamethoxazole/trimethoprim (87.4%, n = 714), while phenotypic resistance rate was highest for amikacin (72.5% of isolates were resistant, n = 592). The clinical problem of sulfamethoxazole/trimethoprim-resistance is a complex issue, because there is no guideline available for the therapy of these infections.

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