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