Dore Michael, Duffy Ryan, Caputo Laura, Huang Lily, Sidoti Salvatore, Cantrell Sarah, Glasgo Blair, Kerbow Christa
Durham Veteran's Affairs Medical Center, Durham, North Carolina, USA.
Duke University School of Medicine, Durham, North Carolina, USA.
J Hosp Med. 2025 Aug;20(8):866-873. doi: 10.1002/jhm.70041. Epub 2025 Apr 4.
Gram-negative bacteremia (GNB) is associated with significant morbidity and mortality. Transition to oral therapy has traditionally utilized fluoroquinolones or trimethoprim-sulfamethoxazole rather than beta-lactams due to concerns about pharmacokinetics and bioavailability despite a dearth of clinical data. The purpose of this meta-analysis is to evaluate the clinical efficacy of transition to oral beta-lactam therapy in uncomplicated GNB.
We performed a meta-analysis of published articles in MEDLINE, Embase, and Web of Science databases from inception to September 2024. Inclusion criteria included any study with adults (age >18 years of age) with uncomplicated GNB from any source. Primary outcomes included 30-day all-cause mortality and 30-day antibiotic failure rate.
Eight retrospective cohort studies were reviewed comprising 7500 patients. Twice as many patients were in the fluoroquinolones/trimethoprim-sulfamethoxazole group compared with the beta-lactams group (4998 vs. 2482). Patients in each group had similar average age (70 vs. 71), percent male (54% vs. 56%), percent urinary source (78% vs. 80%), duration of IV antibiotics (4.2 vs. 4.5), Pitt bacteremia score (1.1 vs. 1.4) and Charleston comorbid index (2 vs. 2). There was no statistically significant difference in the 30-day all-cause mortality rate between the fluoroquinolones/trimethoprim-sulfamethoxazole and the beta-lactams group: 2.06% versus 1.89% with a weighted relative risk ratio of 1.24 (95% confidence interval [CI]: 0.86-1.77) or the 30-day antibiotic failure rate: 2.08% vs. 3.42%, weighted relative risk ratio of 1.29 (95% CI: 0.97-1.71).
There is no statistically significant difference in 30-day mortality or antibiotic failure rates between BL and FQ/TMP-SMX as transition to oral therapy in treating uncomplicated GNB.
革兰氏阴性菌血症(GNB)与显著的发病率和死亡率相关。传统上,由于对药代动力学和生物利用度的担忧,尽管缺乏临床数据,但向口服治疗的过渡一直使用氟喹诺酮类药物或甲氧苄啶-磺胺甲恶唑,而非β-内酰胺类药物。本荟萃分析的目的是评估在非复杂性GNB中过渡到口服β-内酰胺类治疗的临床疗效。
我们对MEDLINE、Embase和Web of Science数据库中从创建到2024年9月发表的文章进行了荟萃分析。纳入标准包括任何针对来自任何来源的非复杂性GNB成年患者(年龄>18岁)的研究。主要结局包括30天全因死亡率和30天抗生素失败率。
回顾了八项回顾性队列研究,共7500例患者。与β-内酰胺类药物组相比,氟喹诺酮类药物/甲氧苄啶-磺胺甲恶唑组的患者数量是其两倍(4998例对2482例)。每组患者的平均年龄相似(70岁对71岁),男性百分比相似(54%对56%),尿液来源百分比相似(78%对80%),静脉用抗生素持续时间相似(4.2天对4.5天),皮特菌血症评分相似(1.1对1.4)以及查尔斯顿合并症指数相似(2对2)。氟喹诺酮类药物/甲氧苄啶-磺胺甲恶唑组与β-内酰胺类药物组之间的30天全因死亡率无统计学显著差异:分别为2.06%和1.89%,加权相对风险比为1.24(95%置信区间[CI]:0.86 - 1.77);30天抗生素失败率也无统计学显著差异:分别为2.08%和3.42%,加权相对风险比为1.29(95% CI:0.97 - 1.71)。
在治疗非复杂性GNB时,作为向口服治疗的过渡,β-内酰胺类药物(BL)与氟喹诺酮类药物/甲氧苄啶-磺胺甲恶唑(FQ/TMP-SMX)在30天死亡率或抗生素失败率方面无统计学显著差异。