Webb Andrew J, Casal Gianna Lh, Newman Kelly A, Culshaw Justin R, Northam Kalynn A, Solomon Edmond J, Beargie Sarah M, Johnson Riley B, Lopez Natasha D, Hayes Bryan D, Roberts Russel J
Department of Pharmacy, Massachusetts General Hospital, Boston, USA.
Department of Pharmacy, Brigham and Women's Hospital, Boston, USA.
J Intensive Care Med. 2025 Mar;40(3):239-246. doi: 10.1177/08850666241270089. Epub 2024 Aug 7.
BackgroundPersistent vasopressor requirements are a common reason for delayed liberation from the intensive care unit (ICU) and adjunct oral agents are sometimes used to hasten time to vasopressor discontinuation. We sought to describe the use of droxidopa for vasopressor weaning in critically ill patients with prolonged hypotension.Materials and MethodsThis retrospective, single-arm, observational study included adult patients admitted to an ICU at two academic centers between 06/2016-07/2023 who received droxidopa for vasopressor weaning. Patients who received droxidopa prior to admission or for another indication were excluded. The primary outcome was time to vasopressor discontinuation, defined as when vasopressors were stopped and remained off for at least 24 h. Secondary outcomes included rates of tachycardia and hypotension post-initiation, norepinephrine equivalents pre- and post-initiation, concomitant oral agent use, and dosing. A subgroup analysis was conducted in patients receiving droxidopa via feeding tubes.ResultsA total of 30 patients met inclusion criteria. Median age was 62 years old, 12 (40%) were female, and 73% were in a cardiac/cardiac surgical ICU. Patients were on vasopressors for a median of 16 days prior to droxidopa initiation. Median (IQR) time to vasopressor discontinuation was 70 h (23-192) and norepinephrine equivalents decreased immediately after initiation (0.08 vs 0.02 mcg/kg/min, p < 0.001). MAP increased after droxidopa initiation (68.8 vs 66.5 mm Hg, p = 0.008) while heart rates were unchanged (86 vs 84 BPM, p = 0.37) after initiation. Patients who weaned from vasopressors within 72 h versus longer than 72 h after droxidopa initiation were more likely to be on lower norepinephrine equivalents prior to initiation (0.05 vs 0.12 mcg/kg/min, p = 0.013). Feeding tube administration did not impact time to vasopressor discontinuation (p = 0.93).ConclusionsDroxidopa may be considered an adjunct therapy for vasopressor weaning. Effects were similar when analyzing patients receiving droxidopa via feeding tube.
背景
持续需要血管升压药是重症监护病房(ICU)延迟脱机的常见原因,有时会使用辅助口服药物来加快血管升压药停用时间。我们试图描述多沙普明在长时间低血压的危重症患者中用于撤停血管升压药的情况。
材料和方法
这项回顾性、单臂观察性研究纳入了2016年6月至2023年7月期间在两个学术中心ICU住院、接受多沙普明进行血管升压药撤停的成年患者。入院前或因其他适应症接受多沙普明治疗的患者被排除。主要结局是血管升压药停用时间,定义为血管升压药停用且至少停用24小时。次要结局包括开始用药后心动过速和低血压的发生率、开始用药前后去甲肾上腺素等效剂量、口服药物的使用情况及剂量。对通过鼻饲管接受多沙普明治疗的患者进行亚组分析。
结果
共有30例患者符合纳入标准。中位年龄为62岁,12例(40%)为女性,73%在心脏/心脏外科ICU。患者在开始使用多沙普明前使用血管升压药的中位时间为16天。血管升压药停用的中位(IQR)时间为70小时(23 - 192),开始用药后去甲肾上腺素等效剂量立即降低(0.08对0.02 mcg/kg/min,p < 0.001)。开始使用多沙普明后平均动脉压(MAP)升高(68.8对66.5 mmHg,p = 0.008),而心率在开始用药后无变化(86对84次/分钟,p = 0.37)。在开始使用多沙普明后72小时内撤停血管升压药的患者与超过72小时撤停的患者相比,开始用药前的去甲肾上腺素等效剂量更低(0.05对0.12 mcg/kg/min,p = 0.013)。鼻饲管给药不影响血管升压药停用时间(p = 0.93)。
结论
多沙普明可被视为血管升压药撤停的辅助治疗。对通过鼻饲管接受多沙普明治疗的患者进行分析时,效果相似。