Department of Internal Medicine Division of Pulmonary and Critical Care, University of Michigan, Ann Arbor, MI.
Department of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
Chest. 2020 Aug;158(2):571-578. doi: 10.1016/j.chest.2020.02.071. Epub 2020 Apr 9.
Little is known about the prevalence, predictors, and outcomes of late vasopressor administration which evolves after admission to the ICU.
What is the epidemiology of late vasopressor administration in the ICU?
We retrospectively studied a cohort of veterans admitted to the Veterans Administration ICUs for ≥ 4 days from 2014 to 2017. The timing of vasopressor administration was categorized as early (only within the initial 3 days), late (on day 4 or later and none on day 3), and continuous (within the initial 2 days through at least day 4). Regressions were performed to identify patient factors associated with late vasopressor administration and the timing of vasopressor administration with posthospitalization discharge mortality.
Among the 62,206 hospitalizations with at least 4 ICU days, late vasopressor administration occurred in 5.5% (3,429 of 62,206). Patients with more comorbidities (adjusted OR [aOR], 1.02 per van Walraven point; 95% CI, 1.02-1.03) and worse severity of illness on admission (aOR, 1.01 per percentage point risk of death; 95% CI, 1.01-1.02) were more likely to receive late vasopressor therapy. Nearly 50% of patients started a new antibiotic within 24 h of receiving late vasopressor therapy. One-year mortality after survival to discharge was higher for patients with continuous (adjusted hazard ratio [aHR], 1.48; 95% CI, 1.33-1.65) and late vasopressor administration (aHR, 1.26; 95% CI, 1.15-1.38) compared with only early vasopressor administration.
Late vasopressor administration was modestly associated with comorbidities and admission illness severity. One-year mortality was higher among those who received late vasopressor administration compared with only early vasopressor administration. Research to understand optimization of late vasopressor therapy administration may improve long-term mortality.
在入住 ICU 后发展的晚期血管加压素治疗的流行程度、预测因素和结果知之甚少。
ICU 中晚期血管加压素治疗的流行病学是什么?
我们回顾性研究了 2014 年至 2017 年期间在退伍军人事务部 ICU 住院时间≥4 天的退伍军人队列。血管加压素的给药时间分为早期(仅在前 3 天内)、晚期(第 4 天或以后且第 3 天无给药)和连续(前 2 天内至少至第 4 天)。进行回归分析以确定与晚期血管加压素治疗相关的患者因素,以及血管加压素治疗时机与住院后出院死亡率之间的关系。
在至少有 4 天 ICU 住院时间的 62206 例住院患者中,有 5.5%(3429/62206)接受了晚期血管加压素治疗。合并症较多的患者(校正比值比[OR],每增加 1 个 van Walraven 点为 1.02;95%CI,1.02-1.03)和入院时严重程度较差的患者(OR,每增加 1%死亡风险的百分点为 1.01;95%CI,1.01-1.02)更有可能接受晚期血管加压素治疗。近 50%的患者在接受晚期血管加压素治疗后 24 小时内开始使用新的抗生素。与仅早期血管加压素治疗相比,连续(校正危险比[aHR],1.48;95%CI,1.33-1.65)和晚期血管加压素治疗(aHR,1.26;95%CI,1.15-1.38)的患者出院后 1 年死亡率更高。
晚期血管加压素治疗与合并症和入院疾病严重程度有一定的相关性。与仅早期血管加压素治疗相比,接受晚期血管加压素治疗的患者 1 年死亡率更高。研究了解晚期血管加压素治疗管理的优化可能会改善长期死亡率。