Potential of cell-free hemoglobin and haptoglobin as prognostic markers in patients with ARDS and treatment with veno-venous ECMO.

IF 3.8 2区 医学 Q1 CRITICAL CARE MEDICINE Journal of Intensive Care Pub Date : 2023-04-20 DOI:10.1186/s40560-023-00664-5
Victoria Bünger, Oliver Hunsicker, Alexander Krannich, Felix Balzer, Claudia D Spies, Wolfgang M Kuebler, Steffen Weber-Carstens, Mario Menk, Jan A Graw
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Abstract

Background: Hemolysis is associated with increased mortality in patients with sepsis, ARDS, or therapy with extracorporeal membrane oxygenation (ECMO). To quantify a critical threshold of hemolysis in patients with ARDS and treatment with veno-venous ECMO, we aimed to identify cutoff values for cell-free hemoglobin (CFH) and haptoglobin (Hp) plasma concentrations associated with a significant increase in ICU mortality.

Methods: Patients with ARDS admitted to a tertiary ARDS referral center between 01/2007 and 12/2018 and treatment with veno-venous ECMO were included. Cutoff values for mean CFH (mCFH) and mean Hp (mHp) plasma concentrations dividing the cohort into groups with significantly different ICU mortalities were calculated and patient characteristics were compared. A multiple logistic regression model with stepwise backward variable selection was included. In addition, cutoff values for vulnerable relative timespans for the respective CFH and Hp concentrations were calculated.

Results: A quantitative cutoff value of 11 mg/dl for mCFH separated the cohort (n = 442) regarding ICU mortality (mCFH ≤ 11 mg/dl: 38%, [95%-CI: 32.22-43.93] (n = 277) vs. mCFH > 11 mg/dl: 70%, [61.99-76.47] (n = 165), p < 0.001). Analogously, a mHp cutoff value ≤ 0.39 g/l was associated with a significant increase in ICU mortality (mHp ≤ 0.39 g/l: 68.7%, [60.91-75.61] (n = 163) vs. mHp > 0.39 g/l: 38.7%, [33.01-44.72] (n = 279), p < 0.001). The independent association of ICU mortality with CFH and Hp cutoff values was confirmed by logistic regression adjusting for confounders (CFH Grouping: OR 3.77, [2.51-5.72], p < 0.001; Hp Grouping: OR 0.29, [0.19-0.43], p < 0.001). A significant increase in ICU mortality was observed when CFH plasma concentration exceeded the limit of 11 mg/dl on 13.3% of therapy days (≤ 13.3% of days with CFH > 11 mg/dl: 33%; [26.81-40.54] (n = 192) vs. > 13.3% of days with CFH > 11 mg/dl: 62%; [56.05-68.36] (n = 250), p < 0.001). Analogously, a mortality increase was detected when Hp plasma concentration remained ≤ 0.39 g/l for > 18.2% of therapy days (≤ 18.2% days with Hp ≤ 0.39 g/l: 27%; [19.80-35.14] (n = 138) vs. > 18.2% days with Hp ≤ 0.39 g/l: 60%; [54.43-65.70] (n = 304), p < 0.001).

Conclusions: Moderate hemolysis with mCFH-levels as low as 11 mg/dl impacts mortality in patients with ARDS and therapy with veno-venous ECMO. Furthermore, a cumulative dose effect should be considered indicated by the relative therapy days with CFH-concentrations > 11 mg/dl. In addition, also Hp plasma concentrations need consideration when the injurious effect of elevated CFH is evaluated.

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无细胞血红蛋白和触珠蛋白作为急性呼吸窘迫综合征(ARDS)患者预后指标和静脉-静脉ECMO治疗的潜力。
背景:溶血与败血症、急性呼吸窘迫综合征(ARDS)或体外膜氧合(ECMO)治疗患者死亡率增加有关。为了量化急性呼吸窘迫综合征患者和静脉-静脉ECMO治疗中溶血的临界阈值,我们旨在确定与ICU死亡率显著增加相关的无细胞血红蛋白(CFH)和触球蛋白(Hp)血浆浓度的临界值。方法:纳入2007年1月至2018年12月在三级ARDS转诊中心接受静脉-静脉ECMO治疗的ARDS患者。计算平均CFH (mCFH)和平均Hp (mHp)血浆浓度的截止值,将队列划分为ICU死亡率有显著差异的组,并比较患者特征。采用逐步后向变量选择的多元logistic回归模型。此外,计算了各自CFH和Hp浓度的脆弱相对时间跨度的截止值。结果:mCFH的定量临界值为11 mg/dl,分离了ICU死亡率的队列(n = 442) (mCFH≤11 mg/dl: 38%, [95% ci: 32.22-43.93] (n = 277)与mCFH > 11 mg/dl: 70%, [61.99-76.47] (n = 165), p 0.39 g/l: 38.7%, [33.01-44.72] (n = 279), p 11 mg/dl: 33%;(26.81 - -40.54) (n = 192)和> 13.3%的天CFH > 11 mg / dl: 62%;(56.05 - -68.36) (n = 250), p治疗天的18.2%(≤18.2%天与惠普≤0.39 g / l: 27%;(19.80 - -35.14) (n = 138)和> 18.2%天与惠普≤0.39 g / l: 60%;[54.43-65.70] (n = 304), p结论:mcfh水平低至11 mg/dl的中度溶血会影响ARDS患者的死亡率和静脉-静脉ECMO治疗。此外,cfh浓度> 11 mg/dl的相对治疗天数应考虑累积剂量效应。此外,在评估CFH升高的有害影响时,也需要考虑Hp血浆浓度。
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来源期刊
Journal of Intensive Care
Journal of Intensive Care Medicine-Critical Care and Intensive Care Medicine
CiteScore
11.90
自引率
1.40%
发文量
51
审稿时长
15 weeks
期刊介绍: "Journal of Intensive Care" is an open access journal dedicated to the comprehensive coverage of intensive care medicine, providing a platform for the latest research and clinical insights in this critical field. The journal covers a wide range of topics, including intensive and critical care, trauma and surgical intensive care, pediatric intensive care, acute and emergency medicine, perioperative medicine, resuscitation, infection control, and organ dysfunction. Recognizing the importance of cultural diversity in healthcare practices, "Journal of Intensive Care" also encourages submissions that explore and discuss the cultural aspects of intensive care, aiming to promote a more inclusive and culturally sensitive approach to patient care. By fostering a global exchange of knowledge and expertise, the journal contributes to the continuous improvement of intensive care practices worldwide.
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