Department of Respiratory and Critical Care Medicine, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.
Department of Medical Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Front Endocrinol (Lausanne). 2023 Jan 9;13:1046736. doi: 10.3389/fendo.2022.1046736. eCollection 2022.
Hyperglycemia is one of the poor prognostic factors in critical ill sepsis patients with diabetes. We aimed to assess the interaction between admission glucose level and clinical endpoints in sepsis patients with diabetes admitted in the intensive care unit (ICU).
Data from the Medical Information Mart Intensive Care III database were used in this study. The study primary endpoint was 28-day mortality after ICU admission. Multivariate Cox regression models were used to explore the association between admission glucose level and the primary endpoint.
We included 3,500 sepsis patients with diabetes. Of participants with no hyperglycemia, mild hyperglycemia, and severe hyperglycemia, no differences were evident in hospital mortality, ICU mortality, or 28-day mortality (all 0.05). The multivariable Cox regression analysis demonstrated that severe hyperglycemia did not increase the risk of 28-day mortality (hazard ratio [HR]=1.06, 95% confidence interval [CI]: 0.86-1.31, =0.5880). Threshold effects analysis identified the inflection points for 28-day mortality as 110 mg/dl and 240 mg/dl. The HRs for 28-day mortality were 0.980 in the <110 mg/dl and 1.008 in the >240 mg/dl. A short-term survival advantage was observed in the 110-240 mg/dl group compared with that in the <110 mg/dl group; meanwhile, no adverse hazard was detected in the >240 mg/dl group. In the stratified analyses, the association effect between the three glucose groups (<110 mg/dl, 110-240 mg/dl, and ≥240 mg/dl) and 28-day mortality was consistent in terms of different sequential organ failure assessment (SOFA) scores and infection sites. The 28-day mortality of the 110-240 mg/dl group with a SOFA score of ≥10 was lower than that of the <110 mg/dl group (HR=0.61, 95% CI: 0.38-0.98).
Admission hyperglycemia was not a risk factor for short-term prognosis in critical ill sepsis patients with diabetes; a lower admission blood glucose level was associated with increased risk of poor prognosis. The potential benefit of higher admission glucose level on 28-day mortality in patients with a more severe condition remains a concern.
高血糖是合并糖尿病的危重症脓毒症患者预后不良的因素之一。本研究旨在评估入院时血糖水平与重症监护病房(ICU)内合并糖尿病的脓毒症患者临床终点之间的相互关系。
本研究使用了医疗信息集市重症监护 III 数据库的数据。研究的主要终点为 ICU 入住后 28 天死亡率。多变量 Cox 回归模型用于探讨入院时血糖水平与主要终点之间的关系。
我们纳入了 3500 例合并糖尿病的脓毒症患者。在无高血糖、轻度高血糖和重度高血糖的患者中,住院死亡率、ICU 死亡率或 28 天死亡率均无差异(均 P>0.05)。多变量 Cox 回归分析表明,重度高血糖并未增加 28 天死亡率的风险(危险比[HR]=1.06,95%置信区间[CI]:0.86-1.31,P=0.5880)。阈值效应分析确定 28 天死亡率的拐点为 110 mg/dl 和 240 mg/dl。28 天死亡率的 HR 在<110 mg/dl 组为 0.980,在>240 mg/dl 组为 1.008。与<110 mg/dl 组相比,110-240 mg/dl 组的短期生存优势更为明显,而>240 mg/dl 组未发现不良危险。在分层分析中,不同序贯器官衰竭评估(SOFA)评分和感染部位下,三组血糖水平(<110 mg/dl、110-240 mg/dl 和≥240 mg/dl)与 28 天死亡率之间的关联效应一致。SOFA 评分≥10 的 110-240 mg/dl 组的 28 天死亡率低于<110 mg/dl 组(HR=0.61,95%CI:0.38-0.98)。
入院时高血糖并不是合并糖尿病的危重症脓毒症患者短期预后的危险因素;入院时血糖水平较低与预后不良风险增加相关。在病情更严重的患者中,较高的入院血糖水平对 28 天死亡率的潜在获益仍值得关注。