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Comparison of the therapeutic effects of amikacin and Omadacycline tosylate on carbapenem-resistant pneumonia caused by Klebsiella pneumoniae

Published on Feb. 28, 2026Total Views: 55 times Total Downloads: 11 times Download Mobile

Author: ZHU Yangdan 1, 2 HU Xiaoyan 1

Affiliation: 1. Department of Respiratory and Critical Care Medicine, Hangzhou Ninth Hospital, Hangzhou 311225, China 2. Zhejiang University of Traditional Chinese Medicine, Hangzhou 310053, China

Keywords: Amikacin Omadacycline tosylate Carbapenem-resistant Klebsiella pneumoniae Pulmonary infection

DOI: 10.12173/j.issn.2097-4922.202503065

Reference: ZHU Yangdan, HU Xiaoyan. Comparison of the therapeutic effects of amikacin and Omadacycline tosylate on carbapenem-resistant pneumonia caused by Klebsiella pneumoniae[J]. Yaoxue QianYan Zazhi, 2026, 30(2): 256-262. DOI: 10.12173/j.issn.2097-4922.202503065.[Article in Chinese]

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Abstract

Objective  To compare the therapeutic effects of amikacin and Omadacycline tosylate on pneumonia caused by carbapenem-resistant community-acquired Klebsiella pneumoniae (CRKP).

Methods  The relevant data of patients with pulmonary infection caused by CRKP who were treated in the Department of Respiratory and Critical Care Medicine of Hangzhou Ninth Hospital from March 2022 to February 2024 were retrospectively analyzed. According to the treatment plans, they were divided into the amikacin group and the omadacycline tosylate group. The time of disappearance of clinical symptoms, changes in inflammatory factors and immune indicators (CD4+/CD8+ T ratio) and adverse reactions were compared between the two groups of patients.

Results  A total of 86 patients were enrolled, including 41 in the amikacin group and 45 in the omadacycline tosylate group. After treatment, the disappearance time of clinical symptoms such as cough with sputum, lung shadows, and lung rales and the time for body temperature to return to normal in the omadacycline tosylate group were shorter than those in the amikacin group (P﹤0.05). After treatment, the levels of serum white blood cells, neutrophils, C-reactive protein, interleukin-6, and procalcitonin in the omadacycline tosylate group were lower than those in the amikacin group (P﹤0.05). The CD4+/CD8+ T ratio in the omadacycline tosylate group was significantly higher than that in the amikacin group after treatment (P﹤0.05). During the treatment, there was no statistical difference in the incidence of adverse reactions between the two groups (P﹥0.05).

Conclusion  Compared with amikacin, the treatment of pulmonary infection caused by CRKP with Omadacycline tosylate can shorten the disappearance time of clinical symptoms, improve inflammatory response, enhance immune level, and has no significant adverse reactions, which has significant clinical application value.

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