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创伤患者入院高血糖症及炎症反应的模式和影响:一项前瞻性临床研究。

Patterns and Effects of Admission Hyperglycemia and Inflammatory Response in Trauma Patients: A Prospective Clinical Study.

机构信息

Clinical Medicine, Weill Cornell Medical College, Doha, Qatar.

Trauma & Vascular Surgery, Clinical Research, Hamad General Hospital, Doha, Qatar.

出版信息

World J Surg. 2021 Sep;45(9):2670-2681. doi: 10.1007/s00268-021-06190-5. Epub 2021 Jun 11.

Abstract

BACKGROUND

The constellation of the initial hyperglycemia, proinflammatory cytokines and severity of injury among trauma patients is understudied. We aimed to evaluate the patterns and effects of on-admission hyperglycemia and inflammatory response in a level 1 trauma center. We hypothesized that higher initial readings of blood glucose and cytokines are associated with severe injuries and worse in-hospital outcomes in trauma patients.

METHODS

A prospective, observational study was conducted for adult trauma patients who were admitted and tested for on-admission blood glucose, hemoglobin A1c, interleukin (IL)-6, IL-18 and hs-CRP. Patients were categorized into four groups [non-diabetic normoglycemic, diabetic normoglycemic, diabetic hyperglycemic (DH) and stress-induced hyperglycemic (SIH)]. The inflammatory markers were measured on three time points (admission, 24 h and 48 h). Generalized estimating equations (GEE) were used to account for the correlation for the inflammatory markers. Pearson's correlation test and logistic regression analysis were also performed.

RESULTS

During the study period, 250 adult trauma patients were enrolled. Almost 13% of patients presented with hyperglycemia (50% had SIH and 50% had DH). Patients with SIH were younger, had significantly higher Injury Severity Score (ISS), higher IL-6 readings, prolonged hospital length of stay and higher mortality. The SIH group had lower Revised Trauma Score (p = 0.005), lower Trauma Injury Severity Score (p = 0.01) and lower GCS (p = 0.001). Patients with hyperglycemia had higher in-hospital mortality than the normoglycemia group (12.5% vs 3.7%; p = 0.02). A significant correlation was identified between the initial blood glucose level and serum lactate, IL-6, ISS and hospital length of stay. Overall rate of change in slope 88.54 (95% CI:-143.39-33.68) points was found more in hyperglycemia than normoglycemia group (p = 0.002) for IL-6 values, whereas there was no statistical significant change in slopes of age, gender and their interaction. The initial IL-6 levels correlated with ISS (r = 0.40, p = 0.001). On-admission hyperglycemia had an adjusted odds ratio 2.42 (95% CI: 1.076-5.447, p = 0.03) for severe injury (ISS > 12) after adjusting for age, shock index and blood transfusion.

CONCLUSIONS

In trauma patients, on-admission hyperglycemia correlates well with the initial serum IL-6 level and is associated with more severe injuries. Therefore, it could be a simple marker of injury severity and useful tool for patient triage and risk assessment.

TRIAL REGISTRATION

This study was registered at the ClinicalTrials.gov (Identifier: NCT02999386), retrospectively Registered on December 21, 2016. https://clinicaltrials.gov/ct2/show/NCT02999386 .

摘要

背景

创伤患者的初始高血糖、促炎细胞因子和损伤严重程度的星座研究不足。我们旨在评估 1 级创伤中心入院时高血糖和炎症反应的模式和影响。我们假设较高的初始血糖读数和细胞因子与严重损伤和创伤患者住院期间的不良结局有关。

方法

对入院时接受入院时血糖、糖化血红蛋白、白细胞介素 (IL)-6、IL-18 和高敏 C 反应蛋白检测的成年创伤患者进行前瞻性、观察性研究。患者分为四组[非糖尿病正常血糖、糖尿病正常血糖、糖尿病高血糖 (DH) 和应激性高血糖 (SIH)]。炎症标志物在三个时间点(入院时、24 小时和 48 小时)进行测量。使用广义估计方程 (GEE) 来解释炎症标志物的相关性。还进行了 Pearson 相关性检验和逻辑回归分析。

结果

在研究期间,纳入了 250 名成年创伤患者。近 13%的患者出现高血糖(50%为 SIH,50%为 DH)。SIH 组患者更年轻,损伤严重程度评分 (ISS) 更高,IL-6 读数更高,住院时间延长,死亡率更高。SIH 组的修订创伤评分(p=0.005)、创伤损伤严重程度评分(p=0.01)和格拉斯哥昏迷评分(p=0.001)均较低。高血糖组患者的住院死亡率高于正常血糖组(12.5%比 3.7%;p=0.02)。入院时血糖水平与血清乳酸、IL-6、ISS 和住院时间之间存在显著相关性。与正常血糖组相比,高血糖组 IL-6 值的总体斜率变化率为 88.54(95%CI:-143.39-33.68)点(p=0.002),而年龄、性别及其交互作用的斜率变化无统计学意义。初始 IL-6 水平与 ISS 相关(r=0.40,p=0.001)。入院时高血糖对严重损伤(ISS>12)的调整优势比为 2.42(95%CI:1.076-5.447,p=0.03),调整因素为年龄、休克指数和输血。

结论

在创伤患者中,入院时高血糖与初始血清 IL-6 水平密切相关,与更严重的损伤有关。因此,它可能是一种简单的损伤严重程度标志物,是患者分诊和风险评估的有用工具。

试验注册

本研究在 ClinicalTrials.gov(标识符:NCT02999386)注册,于 2016 年 12 月 21 日回溯注册。https://clinicaltrials.gov/ct2/show/NCT02999386

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdd8/8321976/28d43b664c90/268_2021_6190_Fig1_HTML.jpg

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