School of Medicine, Griffith University, Gold Coast, Queensland, Australia.
Centre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, University of Queensland, Woolloongabba, Queensland, Australia; Faculty of Medicine, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
Int J Antimicrob Agents. 2020 Mar;55(3):105839. doi: 10.1016/j.ijantimicag.2019.10.020. Epub 2019 Nov 5.
Combining aminoglycosides with β-lactam antibiotics for treating serious infections has not been associated with reduced mortality in previous meta-analyses. However, the multiple daily aminoglycoside dosing regimen principally used in most of the included studies is inconsistent with current practice.
To determine if a combination of an aminoglycoside administered as a single daily dose and a β-lactam antibiotic reduces all-cause mortality in patients compared with β-lactam antibiotic monotherapy.
A systematic review and meta-analysis of clinical studies was performed (Prospero registration number #68506). Studies were included if they compared β-lactam antibiotic monotherapy with combined β-lactam and single daily dose aminoglycoside therapy for treating serious infections. Studies investigating multiple daily dosing aminoglycoside regimens, infective endocarditis and febrile neutropaenia were excluded. Study quality was assessed using the PEDro and Newcastle-Ottawa scoring systems. The end points for outcome analyses were 30-day all-cause mortality, clinical cure and nephrotoxicity.
Four randomised controlled trials and five retrospective cohort studies were analysed. Compared with β-lactam antibiotic monotherapy, single daily aminoglycoside dosing in combination with β-lactam antibiotics was not associated with reduced mortality compared with β-lactam antibiotic monotherapy (n = 3686, OR 0.82, 95% CI 0.63-1.08, P = 0.10, I 42%). A subgroup analysis of cohort studies suggested reduced mortality with combination therapy (n = 3563, OR 0.79, 95% CI 0.64-0.99, P = 0.04, I 32%). No increased risk of nephrotoxicity was identified (n = 1110, OR 1.31, 95% CI 0.83-2.09, P = 0.40, I 0%).
The existing evidence suggests no added survival benefit from a single daily dosing regimen of an aminoglycoside when combined with β-lactam antibiotics.
在之前的荟萃分析中,联合使用氨基糖苷类药物和β-内酰胺类抗生素治疗严重感染并未降低死亡率。然而,大多数纳入研究中主要使用的多次每日氨基糖苷类药物给药方案与当前实践不一致。
确定与β-内酰胺类抗生素单药治疗相比,每日单次给予氨基糖苷类药物与β-内酰胺类抗生素联合治疗是否能降低患者的全因死亡率。
对临床研究进行了系统评价和荟萃分析(前瞻性登记号 #68506)。如果研究比较了β-内酰胺类抗生素单药治疗与联合β-内酰胺类药物和每日单次剂量氨基糖苷类药物治疗严重感染,将其纳入研究。排除了多次每日剂量氨基糖苷类药物方案、感染性心内膜炎和发热性中性粒细胞减少症的研究。使用 PEDro 和纽卡斯尔-渥太华评分系统评估研究质量。结局分析的终点为 30 天全因死亡率、临床治愈率和肾毒性。
分析了四项随机对照试验和五项回顾性队列研究。与β-内酰胺类抗生素单药治疗相比,每日单次氨基糖苷类药物联合β-内酰胺类抗生素治疗并未降低死亡率(n=3686,OR 0.82,95%CI 0.63-1.08,P=0.10,I 42%)。队列研究的亚组分析表明联合治疗降低了死亡率(n=3563,OR 0.79,95%CI 0.64-0.99,P=0.04,I 32%)。未发现肾毒性风险增加(n=1110,OR 1.31,95%CI 0.83-2.09,P=0.40,I 0%)。
现有证据表明,与β-内酰胺类抗生素联合使用时,每日单次给予氨基糖苷类药物方案并未带来生存获益的增加。