Bristol Trials Centre, Bristol Medical School, University of Bristol, 1-5 Whiteladies Road, Clifton, BS8 1NU, Bristol, UK.
Bristol Centre for Antimicrobial Research & Evaluation (BCARE), Infection Sciences, Pathology, North Bristol NHS Trust, Bristol, UK.
J Antimicrob Chemother. 2022 Dec 23;78(1):196-204. doi: 10.1093/jac/dkac374.
To estimate the effect of treatment duration on in-hospital mortality in patients with Staphylococcus aureus blood stream infection and demonstrate the biases that can arise when immortal-time bias is ignored.
We compared three treatment strategies: short therapy (<10 days), intermediate (10-18 days) and long (>18 days).
Twenty-eight-day all-cause in-hospital mortality.
Using data from the BSI-FOO study, we implemented an approach proposed by Hernán to overcome confounding and immortal-time biases. The first stage is to clone all participants, so that each participant is assigned to each treatment strategy. Second, observations are censored when their data becomes inconsistent with their assigned strategy. Finally, inverse-probability weights are applied to adjust for potential selection. We compared our results to a naïve approach where immortal-time bias is ignored.
Of the 1903 participants in BSI-FOO, 587 were eligible and included in the analysis. After cloning, the weighted estimates of hazard ratio of mortality for short versus long therapy was 1.74 (95% CI 1.36, 2.24) and for intermediate versus long therapy was 1.09 (0.98, 1.22). In the naïve approach, the hazard ratios with reference to the long therapy group are 37.4 (95% CI 18.9 to 74.4) in the short therapy group and 4.1 (95% CI 1.9 to 8.9) in the intermediate therapy group.
Our findings suggest that duration of therapy >18 days is beneficial with respect to 28-day in-hospital mortality, however, there remains uncertainty around the efficacy of reducing duration of treatment to 10-18 days.
评估金黄色葡萄球菌血流感染患者的治疗持续时间对住院病死率的影响,并展示在忽略无固期限偏倚时可能出现的偏倚。
我们比较了三种治疗策略:短程治疗(<10 天)、中程(10-18 天)和长程(>18 天)。
28 天全因住院病死率。
利用 BSI-FOO 研究的数据,我们采用 Hernán 提出的方法来克服混杂和无固期限偏倚。第一阶段是克隆所有参与者,以使每个参与者被分配到每个治疗策略中。其次,当数据与其分配的策略不一致时,观察被截尾。最后,应用逆概率权重进行调整以校正潜在选择偏倚。我们将结果与忽略无固期限偏倚的简单方法进行了比较。
在 BSI-FOO 研究的 1903 名参与者中,有 587 名符合条件并纳入分析。在克隆后,与长程治疗相比,短程治疗死亡风险的加权估计风险比为 1.74(95%CI 1.36-2.24),中程治疗与长程治疗相比为 1.09(0.98-1.22)。在简单方法中,与长程治疗组相比,短程治疗组的风险比为 37.4(95%CI 18.9-74.4),中程治疗组为 4.1(95%CI 1.9-8.9)。
我们的研究结果表明,治疗持续时间>18 天有利于 28 天住院病死率,但对于将治疗持续时间缩短至 10-18 天的疗效仍存在不确定性。