Actively implementing an evidence-based feeding guideline for critically ill patients (NEED): a multicenter, cluster-randomized, controlled trial

Authors:Ke, Lu; Lin, Jiajia; Doig, Gordon S.; van Zanten, Arthur R. H.; Wang, Yang; Xing, Juan; Zhang, Zhongheng; Chen, Tao; Zhou, Lixin; Jiang, Dongpo; Shi, Qindong; Lin, Jiandong; Liu, Jun; Cheng, Aibin; Liang, Yafeng; Gao, Peiyang; Sun, Junli; Liu, Wenming; Yang, Zhenyu; Zhang, Rumin; Xing, Wei; Zhang, An; Zhou, Zhigang; Zhou, Tingfa; Liu, Yang; Tong, Fei; Wang, Qiuhui; Pan, Aijun; Huang, Xiaobo; Fan, Chuming; Lu, Weihua; Shi, Dongwu; Wang, Lei; Li, Wei; Gu, Liming; Xie, Yingguang; Sun, Rongqing
Source:Critical Care, 2022, 26(1): 46.
DOI:10.1186/s13054-022-03921-5

Summary

Background: Previous cluster-randomized controlled trials evaluating the impact of implementing evidence-based guidelines for nutrition therapy in critical illness do not consistently demonstrate patient benefits. A large-scale, sufficiently powered study is therefore warranted to ascertain the effects of guideline implementation on patient-centered outcomes. @@@ Methods: We conducted a multicenter, cluster-randomized, parallel-controlled trial in intensive care units (ICUs) across China. We developed an evidence-based feeding guideline. ICUs randomly allocated to the guideline group formed a local "intervention team", which actively implemented the guideline using standardized materials, a graphical feeding protocol, and live online education outreach meetings conducted by members of the study management committee. ICUs assigned to the control group remained unaware of the guideline content. All ICUs enrolled patients who were expected to stay in the ICU longer than seven days. The primary outcome was allcause mortality within 28 days of enrollment. @@@ Results: Forty-eight ICUs were randomized to the guideline group and 49 to the control group. From March 2018 to July 2019, the guideline ICUs enrolled 1399 patients, and the control ICUs enrolled 1373 patients. Implementation of the guideline resulted in significantly earlier EN initiation (1.20 vs. 1.55 mean days to initiation of EN; difference -0.40 [95% CI -0.71 to - 0.09]; P= 0.01) and delayed PN initiation (1.29 vs. 0.80 mean days to start of PN; difference 1.06 [95% CI 0.44 to 1.67]; P= 0.001). There was no significant difference in 28-day mortality (14.2% vs. 15.2%; difference - 1.6% [95% CI - 4.3% to 1.2%]; P=0.42) between groups. @@@ Conclusions: In this large-scale, multicenter trial, active implementation of an evidence-based feeding guideline reduced the time to commencement of EN and overall PN use but did not translate to a reduction in mortality from critical illness.

  • Institution
    青岛大学; 6; 汕头大学; 北京大学; 苏州大学; 中国医科大学; 南方医科大学; 西安交通大学; 电子科技大学; 广东省人民医院; 南昌大学; 山东大学; 中山大学; 哈尔滨医科大学; 郑州大学; 5; 浙江大学; 中国医学科学院; 南京大学; 河北医科大学; 广州医学院; 安徽医科大学; 佛山市第一人民医院; 内蒙古医学院; 中国人民解放军第四军医大学; 华中科技大学

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