İstanbul某三级医院静脉注射磷霉素治疗多重耐药感染的回顾性评价

Q4 Medicine
Sibel DOĞAN KAYA, Yeşim Uygun Kızmaz
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引用次数: 0

摘要

简介:磷霉素已开始再次作为一种可能的治疗选择,用于注射耐药细菌病原体的病例。其主要作用机制是抑制细胞壁合成的第一步;这种机制对革兰氏阳性和革兰氏阴性菌群都有效。然而,它对产生多药耐药的细菌的临床疗效在很大程度上是未知的。因此,我们的目的是评估在三级保健中心静脉注射磷霉素的临床和微生物效果。方法:回顾性分析2018年1月至2022年12月在该院就诊的18岁及以上因感染而静脉给予磷霉素治疗至少24小时的成人患者。结果:71例患者纳入我们的研究。患者男女比例为35/36,平均年龄为61.5±17.0(18-84)岁。平均治疗时间为10.6天(11.3-+11.4)。22名重症监护室患者(31%)和49名其他诊所患者(69%)纳入研究。菌血症18例(26%),肺炎15例(21%),伤口感染14例(19%),呼吸机相关性肺炎13例(18%),尿路感染5例(8%),腹部感染4例(6%),心内膜炎2例(3%)。其中,碳青霉烯敏感肺炎克雷伯菌18株(44%)、耐药肺炎克雷伯菌(17.5%)、MRSA 5株(12.5%)、耐药空气假单胞菌5株(12%)、大肠埃希菌4株(10%)、鲍曼不动杆菌1株(2.5%)、肠杆菌1株(2.5%)。看看潜在的疾病,我们的一个病人有糖尿病,另一个病人有慢性肾衰竭。平均降钙素原(PCT)和C反应蛋白(CRP)(临界值0.5 ng/mL)分别为2.53±1.2 ng/mL和89.7±21.9 mg/dl。计算患者在磷霉素IV治疗前后钠(Na)、钾(K)、谷丙转氨酶(AST)、谷丙转氨酶(ALT)、肌酐中位数,差异无统计学意义。联合应用磷霉素IV的临床为:美罗培南31例(44%)、粘菌素15例(26%)、替加环素18例(26%)、万古霉素3例(4%)、阿米卡星3例(4%)、达托霉素1例(1%)。结论:根据我们的研究结果,磷霉素是治疗多重耐药感染的一种安全有效的选择。因此,我们的结果与文献一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retrospective Evaluation of Intravenous Fosfomycin in Multi-drug Resistant Infections at A Tertiary Care Hospital in İstanbul
Introduction: Fosfomycin has started to be used again as a possible therapeutic alternative in cases injected with resistant bacterial pathogens. Its primary mechanism of action is inhibition of the first step of cell wall synthesis; This mechanism is effective against both Gram-positive and Gram- negative bacterial groups. However, its clinical efficacy against bacteria that develop multidrug resistance is largely unknown. Therefore, we aimed to evaluate the clinical and microbiological efficacy of intravenous Fosfomycin in a tertiary care center. Methods: The group of adult patients aged 18 years and over who applied to the hospital between January 2018 and December 2022 and were given intravenous fosfomycin therapy for at least 24 hours due to any infection were retrospectively analyzed. Results: 71 patients were included in our study. The female/male ratio of these patients was 35/36, and the mean age was 61.5±17.0 (18-84). The avarage time to treatment was 10.6 days (11.3-+11.4). 22 patients (31%) from Intensive Care Unit and 49 (69%) patients from other clinics were included in the study. 18 bacteremia (26%), 15 pneumonia (21%), 14 wound infections (19%), 13 ventilator-associated pneumonia (18%), 5 urinary tract infections (UTI) (8%), 4 abdominal infections (6%) and 2 endocarditis (3%). Detected causative microorganisms were 18 carbapenem susceptible Klebsiella pneumoniae (44%), pandrug resistan Klebsiella pneumoniae (17.5%), 5 MRSA (12.5%), 5 pandrug resistan Pseudomonas aerinosa (12%) ,4 Escherichia coli (10%), 1 Acinetobacterbaumanii (2.5%) and 1 Enterobacter spp. (2.5%). Looking at the underlying diseases, one of our patients had diabetes mellitus and another patient had chronic renal failure. Mean procalcitonin (PCT) and C reaktive protein (CRP) (cutoff value0.5 ng/mL) values were 2.53±1.2 ng/ml and 89.7±21.9 mg/dl, respectively. Median sodium (Na), potassium (K), AST, ALT, and creatinine values of the patients before and after fosfomycin IV treatment were calculated and there was no statistically significant difference. Clinics combined with fosfomycin IV were as follows: 31 meropenem (44%), 15 colistin (26%), 18 tigecycline (26%), 3 vancomycin (4%), 3 amikacin (4%) and 1 daptomycin (1%). Conclusions: According to the results of our study, it was seen that Fosfomycin is a safe and effective option in the treatment of multidrug-resistant infections. Accordingly, our results are compatible with the literature.
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