去甲肾上腺素与 COVID-19 相关急性呼吸窘迫综合征重症患者压疮发生的关系:剂量反应分析

Ata Mahmoodpoor, Athanasios Chalkias, Morteza Izadi, Kievan Gohari-Moghadam, Farshid Rahimi-Bashar, Ayişe Karadağ, Masoum Khosh-Fetrat, Amir Vahedian-Azimi
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引用次数: 0

摘要

目的研究重症监护病房(ICU)中不同剂量去甲肾上腺素(NE)与 COVID-19 患者压力损伤(PIs)发生率之间的相关性:一项回顾性多中心研究针对 1078 名因急性呼吸窘迫综合征(ARDS)需要机械通气而入住重症监护病房的 COVID-19 患者。研究时间跨度为 2020 年 3 月至 2021 年 4 月,涉及伊朗五所大学附属医院。研究利用单变量和多变量二元逻辑回归分析以及线性和非线性剂量反应评估来评估 NE 剂量与 PI 发生概率之间的关系:多变量分析表明,24 小时内较高剂量的 NE(OR:1.832,95 % CI:1.218-2.754,P=0.004)和累积剂量(OR:1.408,95 % CI:1.204-1.975,P=0.048)与 PI 的发生有显著关系。此外,与低剂量或中等剂量的患者相比(>15 µg/min vs. ≤ 15 µg/min;OR:4.401,95 % CI:3.339-5.801,P=0.001),接受高剂量 NE 的患者发生 PIs 的风险增加了近四倍(无论 PIs 分期如何)。虽然线性剂量-反应分析未显示 NE 剂量(µg/min)与 PI 发生之间存在显著相关性(P>0.05),但非线性分析表明 NE 剂量≤ 9 µg/min 与 PI 发生风险降低有关:结论:将 NE 输注维持在 1-9 µg/min 的范围内似乎能最有效地降低 COVID-19 ICU 患者发生 PI 的可能性。较低的NE剂量(≤9 µg/min)与较低的PI发生风险相关,这表明在该患者群中,NE剂量以外的因素或使用其他血管加压剂可能对PI的形成起着至关重要的作用:临床实践的启示:临床医生不应提出特定的阈值,而应考虑开展进一步研究,以确定平衡微血管灌注和患者预后的最佳剂量。全面评估其他因素并有选择性地使用血管加压药至关重要。个体化治疗,包括定期监测和个性化治疗方案,对于这类患者获得最佳治疗效果至关重要。
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Association of norepinephrine with pressure ulcer development in critically ill patients with COVID-19-related acute respiratory distress syndrome: A dose-response analysis.

Objectives: To investigate the correlation between varying doses of norepinephrine (NE) and the incidence of pressure injuries (PIs) in COVID-19 patients in intensive care units (ICUs).

Design: A retrospective multicenter study was conducted on 1,078 COVID-19 patients admitted to ICUs with acute respiratory distress syndrome (ARDS) requiring mechanical ventilation. The research spanned from March 2020 to April 2021 across five university-affiliated hospitals in Iran. Univariate and multivariate binary logistic regression analyses, along with linear and non-linear dose-response assessments, were utilized to evaluate the relationship between NE dosages and the probability of PI development.

Findings: The multivariate analysis revealed a significant association between higher doses of NE administered over 24 h (OR: 1.832, 95 % CI: 1.218-2.754, P=0.004) and cumulative doses (OR: 1.408, 95 % CI: 1.204-1.975, P=0.048) with the occurrence of PIs. Moreover, patients receiving high NE doses had a nearly fourfold increased risk of developing PIs, regardless of PIs stage, compared to those on low or moderate doses (>15 µg/min vs. ≤ 15 µg/min; OR: 4.401, 95 % CI: 3.339-5.801, P=0.001). Although the linear dose-response analysis did not show a significant correlation between NE doses (µg/min) and PI development (P>0.05), the non-linear analysis indicated that NE doses ≤ 9 µg/min were associated with a reduced risk of PI development.

Conclusion: Maintaining NE infusion within the range of 1-9 µg/min appears to be most effective in reducing the likelihood of PIs in ICU patients with COVID-19. Lower NE doses (≤9 µg/min) were associated with a lower risk of PI development, suggesting that factors beyond NE dosage or the use of other vasopressors may play a crucial role in PI formation in this patient cohort.

Implications for clinical practice: Rather than suggesting a specific threshold, clinicians should consider further studies to determine the optimal dose that balances microvascular perfusion and patient outcomes. It is crucial to comprehensively evaluate additional factors and selectively use vasopressors. Individualized care, including regular monitoring and personalized treatment plans, is essential for achieving the best outcomes in this patient population.

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Potential issues related to subsyndromal delirium in the intensive care unit - Letter on Ma et al. The utilization of a prone position model based on big data is deemed essential - Response to Liang et al. The link between norepinephrine administration and pressure injury risk in patients with COVID-19-related ARDS - Letter on Mahmoodpoor et al. Oxygen saturation is a better index than arterial partial pressure of oxygen to predict pressure injuries in the intensive care unit - Letter on Han et al. Predicting non-response outcomes in prone-positioning for ARDS - Letter on Yan et al.
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