Feeding intolerance score in critically ill patients with enteral nutrition: A post hoc analysis of a prospective study

被引:7
|
作者
Lin, Jiajia [1 ]
Liu, Yang [1 ]
Ke, Lu [1 ,2 ]
Li, Gang [1 ]
Lv, Cheng [1 ]
Zhou, Jing [1 ]
Ye, Bo [1 ]
Li, Baiqiang [1 ]
Yang, Qi [1 ]
Tong, Zhihui [1 ]
Li, Weiqin [1 ,2 ]
Li, Jieshou [3 ]
机构
[1] Nanjing Univ, Dept Crit Care Med, Jinling Hosp, Med Sch, 305 East Thongshan Rd, Nanjing 210002, Peoples R China
[2] Nanjing Univ, Natl Inst Healthcare Data Sci, Nanjing, Peoples R China
[3] Nanjing Univ, Jinling Hosp, Dept Gen Surg, Med Sch, 305 East Zhongshan Rd, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
critical illness; enteral nutrition; feeding intolerance; gastrointestinal symptoms; mortality; RESIDUAL GASTRIC VOLUME; INTENSIVE-CARE; RISK-FACTORS; GASTROINTESTINAL SYMPTOMS; CLINICAL CONSEQUENCES; APACHE-II; PREVALENCE; DEFINITIONS; MANAGEMENT; OUTCOMES;
D O I
10.1002/ncp.10788
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background Feeding intolerance (FI) is common in critically ill patients fed with enteral nutrition. Although there is increasing evidence showing the association between FI and mortality, no reliable quantitative assessment was available in clinical practice. In this study, we proposed a FI scoring system based on gastrointestinal (GI) symptoms to assist the implementation of enteral nutrition and assessed its association with 28-day mortality. Methods This is a post hoc analysis based on data collected in a previous cross-sectional study. All adult patients who were enterally fed were included. Various definitions of FI were compared. The area under the receiver operating characteristic (AUROC) was used to assess the predictive performance for 28-day mortality. Pearson correlation coefficient and the variance inflation factor were applied to detect collinearity among variables. Multiple logistic regression analysis was used to determine the risk factors for 28-day mortality. Results Of the 1098 patients included, 200 (18.2%) were nonsurvivors. The incidence of GI symptoms was higher in nonsurvivors on the study day. The multiple logistic regression analysis showed that the proposed FI score was an independent risk factor for 28-day mortality (odds ratio [OR]: 1.37; 95% CI, 1.25-1.51; P < .001). Moreover, the FI score showed better predictive accuracy for 28-day mortality than the other definitions (AUROC: 0.633 [95% CI, 0.591-0.675] for the FI score vs 0.595 (95% CI, 0.557-0.633] for the best-performing FI definition [P = 0.001]). Conclusions FI score is independently associated with 28-day mortality in critically ill patients with acceptable predictive accuracy.
引用
收藏
页码:869 / 877
页数:9
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