Srinivas Pavithra, Hunt Lauren N, Pouch Stephanie M, Thomas Keelie, Goff Debra A, Pancholi Preeti, Balada-Llasat Joan-Miquel, Bauer Karri A
Department of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, OH.
Department of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, OH.
Diagn Microbiol Infect Dis. 2018 Jun;91(2):194-198. doi: 10.1016/j.diagmicrobio.2018.01.028. Epub 2018 Feb 4.
Polymyxins are one of the last-line antibiotics for multidrug-resistant Acinetobacter baumannii. Reports have demonstrated the emergence of colistin heteroresistance in A. baumannii, which can complicate assessment of minimum inhibitory concentrations and promote resistance to colistin. We aimed to determine the presence of colistin heteroresistance in A. baumannii isolates and correlate the results with clinical and microbiological outcomes via a retrospective study of 24 adult patients: 12 blood and 12 invasive respiratory cultures positive for colistin-susceptible A. baumannii between 1 January 2013 and 31 July 2015. Heteroresistance testing was performed by plating a 100-μL bacterial cell suspension on Mueller-Hinton agar plates containing 0, 1, 2, and 4 μg/mL colistin, and assessing for growth at 24 and 48 h. Colistin heteroresistance was exhibited in 83% of isolates. Median age was 56 [43-65] years, 10 (42%) patients resided at a facility prior to admission, 5 (21%) had a chronic tracheostomy, 18 (75%) were in the intensive care unit at the time of culture collection, and median infection-related length of stay was 12 [7-15] days. Clinical and microbiological cures were achieved in 75% of patients. Overall infection-related mortality was 21%. Our study demonstrated a high rate of colistin heteroresistance in clinical isolates of colistin-susceptible A. baumannii, although this was not associated with suboptimal clinical outcomes due to the use of aggressive colistin dosing and combination therapy. Further studies are needed to establish the association between in vitro colistin heteroresistance and clinical and microbiological outcomes.
多粘菌素是治疗多重耐药鲍曼不动杆菌的最后一线抗生素之一。报告显示鲍曼不动杆菌中出现了对黏菌素的异质性耐药,这可能会使最低抑菌浓度的评估变得复杂,并促进对黏菌素的耐药性。我们旨在通过对24例成年患者进行回顾性研究,确定鲍曼不动杆菌分离株中黏菌素异质性耐药的存在情况,并将结果与临床和微生物学结果相关联:2013年1月1日至2015年7月31日期间,12份血液培养和12份侵袭性呼吸道培养中黏菌素敏感的鲍曼不动杆菌呈阳性。通过将100μL细菌细胞悬液接种在含有0、1、2和4μg/mL黏菌素的穆勒-欣顿琼脂平板上,并在24小时和48小时评估生长情况来进行异质性耐药检测。83%的分离株表现出黏菌素异质性耐药。中位年龄为56[43-65]岁,10例(42%)患者在入院前居住在医疗机构,5例(21%)有慢性气管造口术,18例(75%)在采集培养物时在重症监护病房,中位感染相关住院时间为12[7-15]天。75%的患者实现了临床和微生物学治愈。总体感染相关死亡率为21%。我们的研究表明,黏菌素敏感的鲍曼不动杆菌临床分离株中黏菌素异质性耐药率很高,尽管由于使用了积极的黏菌素给药和联合治疗,这与欠佳的临床结果无关。需要进一步研究来确定体外黏菌素异质性耐药与临床和微生物学结果之间的关联。