维生素C不影响败血症患者的血小板计数:维生素C减轻器官功能障碍的随机试验的事后分析。

IF 2.7 Q4 Medicine
Critical care explorations Pub Date : 2025-09-05 eCollection Date: 2025-09-01 DOI:10.1097/CCE.0000000000001310
Mattia M Müller, Ruxandra Pinto, François Lamontagne, Neill K J Adhikari, Lorenzo Del Sorbo
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引用次数: 0

摘要

目的:维生素C与血小板计数和聚集行为的改变有关。鉴于最近的研究结果表明维生素C与感染性休克患者的不良结局之间存在关联,我们的目的是研究维生素C是否通过对血小板的影响影响感染性休克患者的死亡率。设计:维生素C减轻器官功能障碍(LOVIT)随机试验的事后分析(clinicaltrials.gov NCT03680274)。环境:多中心国际学习。患者:纳入ICU住院时间超过24小时、确诊或疑似感染、血管加压药物需求和血小板计数数据可用性的患者。干预:每6小时服用维生素C (50mg /kg体重),持续4天,或服用安慰剂。测量和主要结果:在参加LOVIT试验的863名患者中,859名患者在任何时候都有可用的血小板计数数据。虽然血小板计数的纵向轨迹与28天死亡率显著相关(风险比0.97 / 10 × 109/L增加,95% CI, 0.96-0.98),但维生素C对死亡率的影响与基线或随时间推移的血小板计数之间没有相互作用。结论:这些结果不支持维生素C通过影响血小板计数增加死亡风险的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vitamin C Does Not Affect Platelet Counts in Patients With Sepsis: A Post hoc Analysis of the Lessening Organ Dysfunction With Vitamin C Randomized Trial.

Vitamin C Does Not Affect Platelet Counts in Patients With Sepsis: A Post hoc Analysis of the Lessening Organ Dysfunction With Vitamin C Randomized Trial.

Objective: Vitamin C has been linked to alterations in platelet count and aggregation behavior. Given recent findings suggesting an association between vitamin C and adverse outcomes in patients with septic shock, we aimed to investigate whether vitamin C influences mortality in septic patients through its impact on platelets.

Design: Post hoc analysis of the Lessening Organ Dysfunction With Vitamin C (LOVIT) randomized trial (clinicaltrials.gov NCT03680274).

Setting: Multicenter international study.

Patients: Patients were included with an ICU stay of more than 24 hours, confirmed or suspected infection, vasopressor requirement, and availability of platelet count data.

Intervention: Vitamin C (50 mg/kg body weight) every 6 hours for 4 days, or placebo.

Measurements and main results: Of the 863 patients enrolled in the LOVIT trial, 859 had available platelet count data at any time. Although the longitudinal trajectory of platelet count was significantly associated with 28-day mortality (hazard ratio 0.97 per 10 × 109/L increase, 95% CI, 0.96-0.98), there was no interaction between the effect of vitamin C on mortality and either platelet count at baseline or over time.

Conclusions: These results do not support the hypothesis that vitamin C administration increases mortality risk by affecting platelet count.

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