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2
Effectiveness of adjunctive clindamycin in β-lactam antibiotic-treated patients with invasive β-haemolytic streptococcal infections in US hospitals: a retrospective multicentre cohort study.辅助克林霉素治疗美国医院中β-内酰胺类抗生素治疗的侵袭性β-溶血性链球菌感染患者的疗效:一项回顾性多中心队列研究。
Lancet Infect Dis. 2021 May;21(5):697-710. doi: 10.1016/S1473-3099(20)30523-5. Epub 2020 Dec 14.
3
Outcomes of β-Hemolytic Streptococcal Necrotizing Skin and Soft-tissue Infections and the Impact of Clindamycin Resistance.β-溶血性链球菌坏死性皮肤和软组织感染的结局及克林霉素耐药的影响。
Clin Infect Dis. 2021 Dec 6;73(11):e4592-e4598. doi: 10.1093/cid/ciaa976.
4
Treatment of Necrotizing Soft Tissue Infections: Antibiotics.坏死性软组织感染的治疗:抗生素。
Adv Exp Med Biol. 2020;1294:87-103. doi: 10.1007/978-3-030-57616-5_7.
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Reduced Susceptibility of Streptococcus pyogenes to β-Lactam Antibiotics Associated with Mutations in the Gene Is Geographically Widespread.化脓性链球菌对与该基因中的突变相关的β-内酰胺抗生素敏感性降低在地理上广泛存在。
J Clin Microbiol. 2020 Mar 25;58(4). doi: 10.1128/JCM.01993-19.
6
Risk Factors and Predictors of Mortality in Streptococcal Necrotizing Soft-tissue Infections: A Multicenter Prospective Study.链球菌坏死性软组织感染的死亡风险因素和预测因素:一项多中心前瞻性研究。
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Correlation Between Immunoglobulin Dose Administered and Plasma Neutralization of Streptococcal Superantigens in Patients With Necrotizing Soft Tissue Infections.免疫球蛋白剂量与坏死性软组织感染患者链球菌超抗原血浆中和作用的相关性。
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Streptococcus pyogenes pbp2x Mutation Confers Reduced Susceptibility to β-Lactam Antibiotics.化脓性链球菌 pbp2x 突变导致对β-内酰胺类抗生素的敏感性降低。
Clin Infect Dis. 2020 Jun 24;71(1):201-204. doi: 10.1093/cid/ciz1000.
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Patient's characteristics and outcomes in necrotising soft-tissue infections: results from a Scandinavian, multicentre, prospective cohort study.患者在坏死性软组织感染的特点和结果:来自斯堪的纳维亚,多中心,前瞻性队列研究的结果。
Intensive Care Med. 2019 Sep;45(9):1241-1251. doi: 10.1007/s00134-019-05730-x. Epub 2019 Aug 22.
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Necrotizing skin and soft-tissue infections in the intensive care unit.重症监护病房中的皮肤和软组织坏死性感染。
Clin Microbiol Infect. 2020 Jan;26(1):8-17. doi: 10.1016/j.cmi.2019.06.031. Epub 2019 Jul 5.

利福平辅助治疗增加 A 组链球菌组织感染模型中的抗生素疗效。

Adjunctive Rifampicin Increases Antibiotic Efficacy in Group A Streptococcal Tissue Infection Models.

机构信息

Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.

Royal Devon and Exeter Hospital, Exeter, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2021 Oct 18;65(11):e0065821. doi: 10.1128/AAC.00658-21. Epub 2021 Sep 7.

DOI:10.1128/AAC.00658-21
PMID:34491807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8522778/
Abstract

Biofilm has recently been highlighted as a complicating feature of necrotizing soft tissue infections (NSTI) caused by Streptococcus pyogenes (i.e., group A Streptococcus [GAS]) contributing to a persistence of bacteria in tissue despite prolonged antibiotic therapy. Here, we assessed the standard treatment of benzylpenicillin and clindamycin with or without rifampin in a tissue-like setting. Antibiotic efficacy was evaluated by CFU determination in a human organotypic skin model infected for 24 or 48 h with GAS strains isolated from NSTI patients. Antibiotic effect was also evaluated by microcalorimetric metabolic assessment in infections of cellular monolayers providing continuous measurements over time. Adjunctive rifampin resulted in enhanced antibiotic efficacy of bacterial clearance in an organotypic skin tissue model, 97.5% versus 93.9% ( = 0.006). Through microcalorimetric measurements, adjunctive rifampin resulted in decreased metabolic activity and extended lag phase for all clinical GAS strains tested ( < 0.05). In addition, a case report is presented of adjunctive rifampin treatment in an NSTI case with persistent GAS tissue infection. The findings of this study demonstrate that adjunctive rifampin enhances clearance of GAS biofilm in an tissue infection model.

摘要

生物膜最近被强调为化脓性链球菌(即 A 组链球菌(GAS))引起的坏死性软组织感染(NSTI)的一个复杂特征,尽管长期使用抗生素治疗,但仍导致细菌在组织中持续存在。在这里,我们在类似组织的环境中评估了苯唑西林和克林霉素联合或不联合利福平的标准治疗。通过在感染 GAS 菌株 24 或 48 小时的人体器官型皮肤模型中进行 CFU 测定,评估抗生素的疗效,这些菌株是从 NSTI 患者中分离出来的。通过细胞单层感染的微量量热代谢评估,还评估了抗生素的作用,该评估提供了随时间的连续测量。辅助利福平导致在器官型皮肤组织模型中清除细菌的抗生素疗效增强,97.5%对 93.9%( = 0.006)。通过微量量热测量,辅助利福平导致所有测试的临床 GAS 菌株的代谢活性降低和迟滞期延长( < 0.05)。此外,还报告了在 GAS 组织感染持续存在的 NSTI 病例中辅助利福平治疗的病例报告。本研究的结果表明,辅助利福平可增强 GAS 生物膜在组织感染模型中的清除。