Department of Anesthesiology, Intensive care and Emergency Medicine, National Pirogov Memorial Medical University, Vinnytsya, Ukraine.
Department of Microbiology, National Pirogov Memorial Medical University, Vinnytsya, Ukraine.
Acta Biomed. 2023 Apr 24;94(2):e2023084. doi: 10.23750/abm.v94i2.13910.
VAP remains the second leading cause of death among the patients with nosocomial infections and its incidence varies significantly from 5% to 60% reaching on average 10 %. It is of crucial importance to develop novel treatment approaches and optimize the existing ones. Thus, the aim of this pilot study was to study the laboratory-microbiological effect of inhaled aminoglycosides in a complex treatment of patients with ventilator-associatedpneumonia(VAP). Methods: To study the laboratory-microbiological effect of adjunctive inhaled aminoglycosides in the treatment of VAP, twenty enrolled patients were randomly subdivided into 2 groups (n=10). Amikacin was administered via a nebulizer starting from the first day of VAP manifestation. Inhalations were performed BID for 7 days via a nebulizer integrated into the breathing circuit. We assessed: cell membrane alterations in leukocytes, Annexin V/7-AAD staining for leukocytes, ROS detection assay for leukocytes.
Adjunctive administration of inhaled amikacin reduced the fluorescence intensity ratio more efficiently compared with the intravenous antimicrobial treatment with no aerosolized amikacin following both 48 h and 96 h of treatment. The amount of dead necrotic annexin V-negative, 7-AAD-positive leukocytes was significantly lower under the use of inhaled amikacin than at the beginning of treatment. Conclusions In this pilot study, we found that administration of aerosolized amikacin combined with the systemic antimicrobial therapy improves the clinical outcome of patients with VAP, effective early microbial decrease in the sputum, reduces reactive oxygen species generation in leukocytes and the degree of leukocyte apoptosis and necrosis, decreases VAP-mediated cell membrane alterations of circulating leukocytes.
呼吸机相关性肺炎(VAP)仍然是医院获得性感染患者的第二大死亡原因,其发病率差异很大,从 5%到 60%不等,平均为 10%。开发新的治疗方法和优化现有方法至关重要。因此,本研究旨在研究吸入氨基糖苷类药物在呼吸机相关性肺炎(VAP)患者综合治疗中的实验室微生物学效应。
为了研究辅助吸入氨基糖苷类药物在 VAP 治疗中的实验室微生物学效应,将 20 名入选患者随机分为 2 组(n=10)。从 VAP 表现的第一天开始,通过雾化器给予阿米卡星。通过集成到呼吸回路中的雾化器每天进行 2 次吸入,持续 7 天。我们评估了:白细胞细胞膜改变、白细胞 Annexin V/7-AAD 染色、白细胞 ROS 检测。
与未雾化阿米卡星的静脉抗菌治疗相比,辅助吸入阿米卡星在治疗后 48 小时和 96 小时更有效地降低了荧光强度比。在使用吸入阿米卡星的情况下,死亡的坏死 Annexin V 阴性、7-AAD 阳性白细胞的数量明显低于治疗开始时。
在这项初步研究中,我们发现联合使用雾化阿米卡星和全身抗菌治疗可改善 VAP 患者的临床结果,有效早期减少痰液中的微生物,减少白细胞中活性氧的产生和白细胞凋亡和坏死的程度,减少 VAP 介导的循环白细胞细胞膜改变。