Association Between Serum Anion Gap and Mortality in Critically Ill Patients with COPD in ICU: Data from the MIMIC IV Database

被引:14
作者
Chen, Xiaojing [1 ,2 ,3 ]
Yang, Qilin [4 ]
Gao, Li [1 ,2 ,3 ]
Chen, Weinan [1 ]
Gao, Xiaoyu [1 ,2 ,3 ]
Li, Yameng [1 ,2 ,3 ]
Ao, Liying [5 ]
Sun, Dejun [1 ,2 ,3 ,6 ]
机构
[1] Inner Mongolia Peoples Hosp, Dept Resp & Crit Care Med, Hohhot 010017, Peoples R China
[2] Inner Mongolia Peoples Hosp, NHC Key Lab Diag & Treatment COPD, Hohhot 010017, Peoples R China
[3] Inner Mongolia Peoples Hosp, Inner Mongolia Key Lab Resp Dis, Hohhot 010017, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 2, Dept Crit Care, Guangzhou, Peoples R China
[5] Inner Mongolia Peoples Hosp, Dept Otolaryngol, Hohhot 010017, Peoples R China
[6] Inner Mongolia Peoples Hosp, Dept Resp & Crit Care Med, 26 Zhaowuda Rd, Hohhot 010017, Peoples R China
基金
中国国家自然科学基金;
关键词
AG; COPD; mortality; MIMIC IV; ALL-CAUSE MORTALITY;
D O I
10.2147/COPD.S433619
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Serum anion gap (AG) has been proven to be associated with prognosis in critically ill patients. However, few studies have investigated the association between AG and all-cause mortality in critically ill patients with chronic obstructive pulmonary disease (COPD). Objective: We hypothesized that the initial AG level would predict the mortality risk in critically ill patients with COPD. Methods: This retrospective cohort study was based on the Medical Information Mart for Intensive Care (MIMIC) IV database. We extracted demographics, vital signs, laboratory tests, comorbidity, and scoring systems from the first 24 hours after patient ICU admission. Multivariable logistic regression analysis models were used to explore the association between serum AG levels and mortality. Interaction and stratified analyses were conducted including age, gender and comorbidity. Results: A total of 5531 critically ill patients with COPD were enrolled, composed of 53.6% male and 46.4% female with a median age of 73 years. The all-cause mortality of these patients during ICU hospitalization was 13.7%. The risk of all-cause mortality increased as the AG level increased in the univariate logistic regression analysis (OR=1.13, 95% CI: 1.11-1.15, p<0.01). After adjusting for all the covariates in multivariate logistic regression analysis, the odds ratio was 1.06 (95% CI: 1.04-1.09, p<0.01). Compared with the lowest AG group Q1 (<= 11mmol/L), the adjusted OR value for AG and mortality in Q2 (12-13mmol/L) was 0.89 (95% CI: 0.63-1.25, p=0.502), Q3 (14-15mmol/L) was 0.95 (95% CI: 0.68-1.34, p=0.788), and Q4 (>= 16mmol/L) was 1.49 (95% CI: 1.10-2.02, p=0.009) respectively. In addition, the results of the subgroup and stratified analyses were robust. Conclusion: AG is positively related to all-cause mortality in critically ill patients with COPD.
引用
收藏
页码:579 / 587
页数:9
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