Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China; International Research Center for Precision Medicine, Transformative Technology and Software Services, Changsha, Hunan, China.
Department of Pharmacy, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Int J Antimicrob Agents. 2024 Sep;64(3):107262. doi: 10.1016/j.ijantimicag.2024.107262. Epub 2024 Jun 28.
Polymyxin B, with its unique structure and mechanism of action, has emerged as a key therapeutic agent against Gram-negative bacteria. The study aims to explore potential factors to influence its effectiveness and safety.
A model-based meta-analysis of 96 articles was conducted, focusing on factors like dosage, bacterial species, and combined antibiotic therapy. The analysis evaluated mortality rates and incidence rate of renal dysfunction, also employing parametric survival models to assess 30-d survival rates.
In the study involving 96 articles and 9716 patients, polymyxin B's daily dose showed minimal effect on overall mortality, with high-dose group mortality at 33.57% (95% confidence intervals [CI]: 29.15-38.00) compared to the low-dose group at 35.44% (95% CI: 28.99-41.88), P = 0.64. Mortality significantly varied by bacterial species, with Pseudomonas aeruginosa infections at 58.50% (95% CI: 55.42-63.58). Monotherapy exhibited the highest mortality at 40.25% (95% CI: 34.75-45.76), P < 0.01. Renal dysfunction was more common in high-dose patients at 29.75% (95% CI: 28.52-30.98), with no significant difference across antibiotic regimens, P = 0.54. The 30-d overall survival rate for monotherapy therapy was 63.6% (95% CI: 59.3-67.5) and 70.2% (95% CI: 64.4-76.2) for association therapy with β-lactam drugs.
The dosage of polymyxin B does not significantly change death rates, but its effectiveness varies based on the bacterial infection. Certain bacteria like P. aeruginosa are associated with higher mortality. Combining polymyxin B with other antibiotics, especially β-lactam drugs, improves survival rates. Side effects depend on the dose, with lower doses being safer. These findings emphasize the importance of customizing treatment to balance effectiveness and safety.
多粘菌素 B 凭借其独特的结构和作用机制,已成为对抗革兰氏阴性菌的重要治疗药物。本研究旨在探讨可能影响其疗效和安全性的因素。
对 96 篇文章进行基于模型的荟萃分析,重点关注剂量、细菌种类和联合抗生素治疗等因素。该分析评估了死亡率和肾功能障碍发生率,并采用参数生存模型评估 30 天生存率。
在涉及 96 篇文章和 9716 名患者的研究中,多粘菌素 B 的日剂量对总死亡率的影响较小,高剂量组死亡率为 33.57%(95%置信区间[CI]:29.15-38.00),而低剂量组为 35.44%(95% CI:28.99-41.88),P=0.64。死亡率因细菌种类而异,铜绿假单胞菌感染的死亡率为 58.50%(95% CI:55.42-63.58)。单药治疗的死亡率最高,为 40.25%(95% CI:34.75-45.76),P<0.01。高剂量组肾功能障碍发生率为 29.75%(95% CI:28.52-30.98),不同抗生素方案之间无显著差异,P=0.54。单药治疗 30 天总生存率为 63.6%(95% CI:59.3-67.5),与β-内酰胺类药物联合治疗的 30 天总生存率为 70.2%(95% CI:64.4-76.2)。
多粘菌素 B 的剂量并不显著改变死亡率,但疗效因细菌感染而异。某些细菌,如铜绿假单胞菌,与更高的死亡率相关。多粘菌素 B 与其他抗生素联合使用,特别是β-内酰胺类药物,可提高生存率。副作用取决于剂量,低剂量更安全。这些发现强调了根据疗效和安全性调整治疗方案的重要性。