Center of Research & Disruption of Infectious Diseases, Department of Infectious Diseases, Copenhagen University Hospital-Amager and Hvidovre, Hvidovre, Denmark.
Department of Clinical Biochemistry, Copenhagen University Hospital-Amager and Hvidovre, Hvidovre, Denmark.
JAMA Netw Open. 2024 Jan 2;7(1):e2352314. doi: 10.1001/jamanetworkopen.2023.52314.
Gram-negative bacteremia is a global health concern, and optimizing the transition from intravenous (IV) to oral antibiotics is a critical step in improving patient treatment and resource utilization.
To assess the association of switching to oral antibiotics within 4 days after initial blood culture with 90-day all-cause mortality compared with prolonged IV antibiotic treatment for patients with uncomplicated gram-negative bacteremia.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study conducted using the target trial emulation framework included observational data from adults with uncomplicated gram-negative bacteremia in 4 hospitals in Copenhagen, Denmark, from January 1, 2018, through December 31, 2021. The duration of follow-up was 90 days. Eligibility criteria included a blood culture positive for growth of gram-negative bacteria, clinical stability within 4 days of initial blood culture, an available susceptibility report on day 4, and initiation of appropriate empirical IV antibiotic treatment within 24 hours of blood culture.
Switching to oral antibiotics within 4 days after initial blood culture compared with continuing IV antibiotic treatment for at least 5 days after initial blood culture.
The main outcome was 90-day all-cause mortality. Inverse probability of treatment weighting was applied to adjust for confounding. Intention-to-treat and per-protocol analyses were performed using pooled logistic regression to estimate absolute risk, risk difference (RD), and risk ratio (RR); 95% CIs were computed using bootstrapping.
A total of 914 individuals were included in the target trial emulation analysis (512 [56.0%] male; median age, 74.5 years [IQR, 63.3-83.2 years]); 433 (47.4%) transitioned early to oral antibiotic treatment, and 481 (52.6%) received prolonged IV treatment. Ninety-nine individuals (10.8%) died during follow-up. The proportion of individuals who died was higher in the group receiving prolonged IV treatment (69 [14.3%] vs 30 [6.9%]). In the intention-to-treat analysis, 90-day all-cause mortality risk was 9.1% (95% CI, 6.7%-11.6%) for the early-switch group and 11.7% (95% CI, 9.6%-13.8%) for the group receiving prolonged IV treatment; the RD was -2.5% (95% CI, -5.7% to 0.7%) and RR was 0.78 (95% CI, 0.60-1.10). In the per-protocol analysis, the RD was -0.1% (95% CI, -3.4% to 3.1%) and RR was 0.99 (95% CI, 0.70-1.40).
In this cohort study of uncomplicated gram-negative bacteremia, early transition to oral antibiotics within 4 days of initial blood culture was associated with 90-day all-cause mortality risk comparable to that of continuing IV antibiotic treatment and may be an effective alternative to prolonged IV treatment.
革兰氏阴性菌血症是一个全球性的健康问题,优化从静脉(IV)到口服抗生素的转换是改善患者治疗和资源利用的关键步骤。
评估与延长 IV 抗生素治疗相比,在初次血培养后 4 天内转为口服抗生素与单纯性革兰氏阴性菌血症患者 90 天全因死亡率的相关性。
设计、地点和参与者:本队列研究使用目标试验模拟框架进行,纳入了 2018 年 1 月 1 日至 2021 年 12 月 31 日期间丹麦哥本哈根 4 家医院中单纯性革兰氏阴性菌血症的成人的观察性数据。随访时间为 90 天。纳入标准包括血培养革兰氏阴性菌生长阳性、初次血培养后 4 天内临床稳定、第 4 天有可用的药敏报告以及初次血培养后 24 小时内开始适当的经验性 IV 抗生素治疗。
与至少在初次血培养后 5 天内继续 IV 抗生素治疗相比,在初次血培养后 4 天内转为口服抗生素。
主要结局为 90 天全因死亡率。应用逆概率治疗加权法来调整混杂因素。采用汇总逻辑回归进行意向治疗和方案分析,以估计绝对风险、风险差(RD)和风险比(RR);使用自举法计算 95%CI。
共纳入 914 名接受目标试验模拟分析的患者(512 名[56.0%]为男性;中位年龄为 74.5 岁[IQR,63.3-83.2 岁]);433 名(47.4%)早期转为口服抗生素治疗,481 名(52.6%)接受延长 IV 治疗。99 名(10.8%)患者在随访期间死亡。接受延长 IV 治疗的患者死亡率更高(69 [14.3%] vs 30 [6.9%])。意向治疗分析显示,早期转换组 90 天全因死亡率为 9.1%(95%CI,6.7%-11.6%),延长 IV 治疗组为 11.7%(95%CI,9.6%-13.8%);RD 为-2.5%(95%CI,-5.7%至 0.7%),RR 为 0.78(95%CI,0.60-1.10)。在方案分析中,RD 为-0.1%(95%CI,-3.4%至 3.1%),RR 为 0.99(95%CI,0.70-1.40)。
在这项关于单纯性革兰氏阴性菌血症的队列研究中,在初次血培养后 4 天内早期转为口服抗生素与 90 天全因死亡率风险相当,与延长 IV 抗生素治疗相比可能是一种有效的替代方法。