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In vitro pharmacodynamics of omadacycline against Escherichia coli and Acinetobacter baumannii.体外奥马环素对大肠杆菌和鲍曼不动杆菌的药效学研究。
J Antimicrob Chemother. 2021 Feb 11;76(3):667-670. doi: 10.1093/jac/dkaa508.
2
Activity of Omadacycline and Other Tetracyclines Against Contemporary Gram-Negative Pathogens from New York City Hospitals.奥马环素和其他四环素类药物对来自纽约市医院的当代革兰氏阴性病原体的活性。
Microb Drug Resist. 2021 Feb;27(2):190-195. doi: 10.1089/mdr.2019.0423. Epub 2020 Jun 22.
3
Tigecycline Versus Colistin in the Treatment of Carbapenem-resistant Complex Osteomyelitis.替加环素与黏菌素治疗耐碳青霉烯类复杂骨髓炎的疗效比较
J Bone Jt Infect. 2020 Feb 21;5(2):60-66. doi: 10.7150/jbji.42448. eCollection 2020.
4
Oral or intravenous antibiotics?口服抗生素还是静脉注射抗生素?
Aust Prescr. 2020 Apr;43(2):45-48. doi: 10.18773/austprescr.2020.008. Epub 2020 Apr 1.
5
Once-daily oral omadacycline versus twice-daily oral linezolid for acute bacterial skin and skin structure infections (OASIS-2): a phase 3, double-blind, multicentre, randomised, controlled, non-inferiority trial.每日口服奥马环素与每日口服利奈唑胺治疗急性细菌性皮肤和皮肤结构感染(OASIS-2):一项 3 期、双盲、多中心、随机、对照、非劣效性试验。
Lancet Infect Dis. 2019 Oct;19(10):1080-1090. doi: 10.1016/S1473-3099(19)30275-0. Epub 2019 Aug 29.
6
Pharmacodynamics of Omadacycline against Staphylococcus aureus in the Neutropenic Murine Thigh Infection Model.奥马环素对中性粒细胞减少症小鼠大腿感染模型中金黄色葡萄球菌的药效学研究。
Antimicrob Agents Chemother. 2019 Jun 24;63(7). doi: 10.1128/AAC.00624-19. Print 2019 Jul.
7
Infections Caused by Carbapenem-Resistant : An Update on Therapeutic Options.耐碳青霉烯类药物引起的感染:治疗选择的最新进展
Front Microbiol. 2019 Jan 30;10:80. doi: 10.3389/fmicb.2019.00080. eCollection 2019.
8
Omadacycline for Community-Acquired Bacterial Pneumonia.奥马环素治疗社区获得性细菌性肺炎。
N Engl J Med. 2019 Feb 7;380(6):517-527. doi: 10.1056/NEJMoa1800201.
9
Oral versus Intravenous Antibiotics for Bone and Joint Infection.口服与静脉用抗生素治疗骨与关节感染。
N Engl J Med. 2019 Jan 31;380(5):425-436. doi: 10.1056/NEJMoa1710926.
10
Partial Oral versus Intravenous Antibiotic Treatment of Endocarditis.部分口服与静脉抗生素治疗心内膜炎。
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口服奥马环素治疗耐革兰氏阴性病原体患者的真实世界多中心病例系列

Real-World, Multicenter Case Series of Patients Treated with Oral Omadacycline for Resistant Gram-Negative Pathogens.

作者信息

Morrisette Taylor, Alosaimy Sara, Lagnf Abdalhamid M, Frens Jeremy J, Webb Andrew J, Veve Michael P, Stevens Ryan, Bouchard Jeannette, Gore Tristan W, Ansari Iman, Rybak Michael J

机构信息

Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI, 48201, USA.

Department of Clinical Pharmacy and Outcomes Sciences, Medical University of South Carolina College of Pharmacy, 280 Calhoun Street, Charleston, SC, 29425, USA.

出版信息

Infect Dis Ther. 2022 Aug;11(4):1715-1723. doi: 10.1007/s40121-022-00645-5. Epub 2022 May 14.

DOI:10.1007/s40121-022-00645-5
PMID:35567718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9334473/
Abstract

INTRODUCTION

Antibiotic-resistant Gram-negative bacteria have been associated with substantial morbidity and mortality and have limited treatment options available. Omadacycline (OMC) is an aminomethylcycline antibiotic that has been shown to exhibit broad in vitro activity against antibiotic-resistant Gram-negative bacteria. Given the lack of real-world data, the primary objective of our report was to describe early experience with OMC for the treatment of resistant Gram-negative infections.

METHODS

This was a real-world, multicenter, observational cases series/pilot study conducted in the USA. Inclusion criteria included any adult patient aged ≥ 18 years who received OMC for ≥ 72 h either in the inpatient and/or outpatient setting. Clinical success was defined as a composite of 90-day survival from initiation of OMC, lack of alteration in treatment/addition of other antibiotic due to concerns of OMC failure, and lack of microbiologic recurrence within 30 days from the end of therapy.

RESULTS

Oral OMC was used in nine cases primarily for multidrug-resistant (MDR)/extensively drug-resistant (XDR) Gram-negative bacterial infections (55.6% XDR and/or carbapenem-resistant Acinetobacter baumannii [CRAB]). The majority of infections were of bone/joint (55.6%) origin, followed by intra-abdominal (33.3%) origin. Clinical success occurred in 66.7% of cases, with 80.0% success each in infections of bone/joint origin or those caused by CRAB. One patient experienced an adverse effect that was not treatment limiting while on therapy (gastrointestinal).

CONCLUSION

The use of oral OMC in MDR/XDR Gram-negative infections exhibited a relatively high success rate with minimal adverse effects. Real-world studies with larger case numbers are needed to confirm our initial findings.

摘要

引言

耐抗生素革兰氏阴性菌与大量发病和死亡相关,且可用的治疗选择有限。奥马环素(OMC)是一种氨基甲基环素类抗生素,已显示出对耐抗生素革兰氏阴性菌具有广泛的体外活性。鉴于缺乏真实世界数据,我们报告的主要目的是描述使用OMC治疗耐药革兰氏阴性菌感染的早期经验。

方法

这是一项在美国进行的真实世界、多中心、观察性病例系列/试点研究。纳入标准包括任何年龄≥18岁的成年患者,其在住院和/或门诊环境中接受OMC治疗≥72小时。临床成功定义为从开始使用OMC起90天存活、因担心OMC治疗失败而未改变治疗方案/未添加其他抗生素以及治疗结束后30天内无微生物复发的综合情况。

结果

9例患者使用了口服OMC,主要用于多重耐药(MDR)/广泛耐药(XDR)革兰氏阴性菌感染(55.6%为XDR和/或耐碳青霉烯鲍曼不动杆菌[CRAB])。大多数感染起源于骨/关节(55.6%),其次是腹腔内(33.3%)。66.7%的病例临床成功,骨/关节起源的感染或由CRAB引起的感染的成功率均为80.0%。1例患者在治疗期间出现了非治疗限制性的不良反应(胃肠道反应)。

结论

在MDR/XDR革兰氏阴性菌感染中使用口服OMC显示出相对较高的成功率且不良反应最小。需要更大病例数的真实世界研究来证实我们的初步发现。