Dan He , Shuqun Hu , Ningjun Zhao , Xianliang Yan , Chenglei Su
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Sensitivity analysis and subgroup analysis were conducted.</div></div><div><h3>Results</h3><div>111 patients were enrolled. The unfavorable group (CPC 3–5, <em>n</em> = 69) had significantly higher serum concentrations of HA and Sdc-1 than the favorable group (CPC 1–2, <em>n</em> = 42) (HA:149.7 ng/ml vs. 824.8 ng/ml, <em>P</em> < 0.001; Sdc-1: 303.8 ng/L vs. 447.0 ng/L, <em>P</em> = 0.026)but not HS. Elevated serum HA concentrations was an independent risk factor for unfavorable 30-day neurological function (OR = 2.485, 95 % CI = 1.656–3.729). For the 30-day mortality, the nonsurvivor group (<em>n</em> = 53) had significantly higher serum concentrations of HA, HS and Sdc-1 (HA: 177.3 ng/ml vs. 1106.7 ng/ml, <em>P</em> <em><</em> 0.001; HS: 2403.7 ng/ml vs. 3383.3 ng/ml <em>P</em> = 0.030; Sdc-1: 352.1 ng/L vs. 487.8 ng/L, <em>P</em> = 0.005) than the survivor group (<em>n</em> = 58). However, only elevated serum HA and Sdc-1 concentrations are independent risk factors for 30-day mortality (HA: HR = 2.321, 95 % CI = 1.776–3.035; Sdc-1: HR = 1.702, 95 % CI = 1.038–2.792).</div></div><div><h3>Conclusions</h3><div>Elevated serum HA at 24 h after CA is an independent risk factor for 30-day unfavorable neurological function or mortality and elevated serum Sdc-1 concentrations is an independent risk factor for 30-day mortality. Our results suggested the potential value of serum glycocalyx shedding components as predictors for the outcomes in post-CA patients.</div></div>","PeriodicalId":15451,"journal":{"name":"Journal of critical care","volume":"87 ","pages":"Article 155026"},"PeriodicalIF":2.9000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Elevated glycocalyx shedding components as the early predictors of unfavorable outcomes in patients after cardiac arrest: A single-center observational study\",\"authors\":\"Dan He , Shuqun Hu , Ningjun Zhao , Xianliang Yan , Chenglei Su\",\"doi\":\"10.1016/j.jcrc.2025.155026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>To assess the association of serum glycocalyx shedding components (Heparan sulfate, HS; Hyaluronic acid, HA; Syndecan-1, Sdc-1) with outcomes after CA.</div></div><div><h3>Methods</h3><div>Patients who were comatose for >24 h after CA in the intensive care unit (ICU) of the Affiliated Hospital of Xuzhou Medical University from 9/2021 to 04/2023 were enrolled. Serum samples were collected 24 h after CA to measure the concentrations of glycocalyx shedding components. The outcomes were the 30-day Cerebral Performance Categories (CPC) scale and 30-day mortality. The association of glycocalyx shedding with outcomes was examined by regression analysis. The area under the curve was used to evaluate the value of glycocalyx shedding for predicting outcomes. Sensitivity analysis and subgroup analysis were conducted.</div></div><div><h3>Results</h3><div>111 patients were enrolled. The unfavorable group (CPC 3–5, <em>n</em> = 69) had significantly higher serum concentrations of HA and Sdc-1 than the favorable group (CPC 1–2, <em>n</em> = 42) (HA:149.7 ng/ml vs. 824.8 ng/ml, <em>P</em> < 0.001; Sdc-1: 303.8 ng/L vs. 447.0 ng/L, <em>P</em> = 0.026)but not HS. Elevated serum HA concentrations was an independent risk factor for unfavorable 30-day neurological function (OR = 2.485, 95 % CI = 1.656–3.729). For the 30-day mortality, the nonsurvivor group (<em>n</em> = 53) had significantly higher serum concentrations of HA, HS and Sdc-1 (HA: 177.3 ng/ml vs. 1106.7 ng/ml, <em>P</em> <em><</em> 0.001; HS: 2403.7 ng/ml vs. 3383.3 ng/ml <em>P</em> = 0.030; Sdc-1: 352.1 ng/L vs. 487.8 ng/L, <em>P</em> = 0.005) than the survivor group (<em>n</em> = 58). However, only elevated serum HA and Sdc-1 concentrations are independent risk factors for 30-day mortality (HA: HR = 2.321, 95 % CI = 1.776–3.035; Sdc-1: HR = 1.702, 95 % CI = 1.038–2.792).</div></div><div><h3>Conclusions</h3><div>Elevated serum HA at 24 h after CA is an independent risk factor for 30-day unfavorable neurological function or mortality and elevated serum Sdc-1 concentrations is an independent risk factor for 30-day mortality. 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引用次数: 0
摘要
目的:探讨血清糖萼脱落组分(硫酸乙酰肝素,HS;透明质酸;方法:选取徐州医科大学附属医院重症监护病房(ICU)于2021年9月至2023年4月间CA后昏迷时间为bb10 ~ 24h的患者。CA后24 h采集血清,测定糖萼脱落成分的浓度。结果为30天脑功能分类(CPC)量表和30天死亡率。通过回归分析检验糖萼脱落与预后的关系。曲线下面积用于评价糖萼脱落对预测预后的价值。进行敏感性分析和亚组分析。结果:纳入111例患者。不良组(CPC 3-5, n = 69)血清HA和Sdc-1浓度明显高于良好组(CPC 1-2, n = 42) (HA:149.7 ng/ml vs. 824.8 ng/ml, P)。结论:CA后24 h血清HA升高是30天神经功能不良或死亡率的独立危险因素,血清Sdc-1浓度升高是30天死亡率的独立危险因素。我们的研究结果表明,血清糖萼脱落成分作为预测ca后患者预后的潜在价值。
Elevated glycocalyx shedding components as the early predictors of unfavorable outcomes in patients after cardiac arrest: A single-center observational study
Objective
To assess the association of serum glycocalyx shedding components (Heparan sulfate, HS; Hyaluronic acid, HA; Syndecan-1, Sdc-1) with outcomes after CA.
Methods
Patients who were comatose for >24 h after CA in the intensive care unit (ICU) of the Affiliated Hospital of Xuzhou Medical University from 9/2021 to 04/2023 were enrolled. Serum samples were collected 24 h after CA to measure the concentrations of glycocalyx shedding components. The outcomes were the 30-day Cerebral Performance Categories (CPC) scale and 30-day mortality. The association of glycocalyx shedding with outcomes was examined by regression analysis. The area under the curve was used to evaluate the value of glycocalyx shedding for predicting outcomes. Sensitivity analysis and subgroup analysis were conducted.
Results
111 patients were enrolled. The unfavorable group (CPC 3–5, n = 69) had significantly higher serum concentrations of HA and Sdc-1 than the favorable group (CPC 1–2, n = 42) (HA:149.7 ng/ml vs. 824.8 ng/ml, P < 0.001; Sdc-1: 303.8 ng/L vs. 447.0 ng/L, P = 0.026)but not HS. Elevated serum HA concentrations was an independent risk factor for unfavorable 30-day neurological function (OR = 2.485, 95 % CI = 1.656–3.729). For the 30-day mortality, the nonsurvivor group (n = 53) had significantly higher serum concentrations of HA, HS and Sdc-1 (HA: 177.3 ng/ml vs. 1106.7 ng/ml, P< 0.001; HS: 2403.7 ng/ml vs. 3383.3 ng/ml P = 0.030; Sdc-1: 352.1 ng/L vs. 487.8 ng/L, P = 0.005) than the survivor group (n = 58). However, only elevated serum HA and Sdc-1 concentrations are independent risk factors for 30-day mortality (HA: HR = 2.321, 95 % CI = 1.776–3.035; Sdc-1: HR = 1.702, 95 % CI = 1.038–2.792).
Conclusions
Elevated serum HA at 24 h after CA is an independent risk factor for 30-day unfavorable neurological function or mortality and elevated serum Sdc-1 concentrations is an independent risk factor for 30-day mortality. Our results suggested the potential value of serum glycocalyx shedding components as predictors for the outcomes in post-CA patients.
期刊介绍:
The Journal of Critical Care, the official publication of the World Federation of Societies of Intensive and Critical Care Medicine (WFSICCM), is a leading international, peer-reviewed journal providing original research, review articles, tutorials, and invited articles for physicians and allied health professionals involved in treating the critically ill. The Journal aims to improve patient care by furthering understanding of health systems research and its integration into clinical practice.
The Journal will include articles which discuss:
All aspects of health services research in critical care
System based practice in anesthesiology, perioperative and critical care medicine
The interface between anesthesiology, critical care medicine and pain
Integrating intraoperative management in preparation for postoperative critical care management and recovery
Optimizing patient management, i.e., exploring the interface between evidence-based principles or clinical insight into management and care of complex patients
The team approach in the OR and ICU
System-based research
Medical ethics
Technology in medicine
Seminars discussing current, state of the art, and sometimes controversial topics in anesthesiology, critical care medicine, and professional education
Residency Education.