早期目标肠内营养与减少机械通气重症成人院内死亡相关:一项回顾性队列研究

IF 3.6 3区 医学 Q1 RESPIRATORY SYSTEM BMJ Open Respiratory Research Pub Date : 2024-05-01 DOI:10.1136/bmjresp-2023-001962
Camilla S Powierza, Margaret M Doyle, Katherine Wasden, Taylor A Intihar, Amy S Korwin, Shyoko Honiden, Melissa P Knauert
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引用次数: 0

摘要

导言 成人重症患者尽早接受肠内营养(EN)被认为可以改善死亡率和发病率;专家指南建议成人重症患者尽早开始接受肠内营养。然而,关于肠内营养的理想时间表和剂量的研究仍然不足。研究目的 我们的目的是评估插管后 2 天内达到 70% 的推荐EN("早期目标EN")与机械通气的内科重症成人患者的临床预后之间的关系。我们假设早期目标EN与院内死亡的减少有关。方法 我们对 2013-2019 年期间入住内科重症监护病房的机械通气成人患者进行了一项回顾性队列研究。我们评估了患者在插管后直至拔管、死亡或 7 天内(以时间最短者为准)每天接受的推荐总 EN 的比例。在插管后 2 天内(即 "基线期")获得 70% 或更多推荐的每日 EN 总量的患者被视为达到了 "早期目标 EN";这些患者与未达到目标 EN 的患者("低 EN")进行了比较。主要结果是院内死亡;次要结果是成功拔管和出院时存活。结果 938 名患者符合资格标准,并在基线期存活。在插管后的 7 天内,64% 的患者达到了每日推荐热量的 70%;33% 的患者达到了早期EN目标。在未调整和调整模型中,早期目标EN与低EN相比,院内死亡发生率较低(未调整的亚分布HR(SHR)=0.63,P=0.0003;调整后的SHR=0.73,P=0.02)。早期目标EN还与较高的成功拔管率(SHR未调整=1.41,p<0.00001;SHR调整后=1.27,p=0.002)和出院存活率(SHR未调整=1.54,p<0.00001;SHR调整后=1.24,p=0.02)相关。结论 早期目标EN与院内死亡减少、拔管率提高和出院存活率提高等临床指标的显著改善相关。如有合理要求,可提供相关数据。
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Early goal enteral nutrition associated with decreased in-hospital death in mechanically ventilated critically ill adults: a retrospective cohort study
Introduction Early enteral nutrition (EN) in critically ill adult patients is thought to improve mortality and morbidity; expert guidelines recommend early initiation of EN in critically ill adults. However, the ideal schedule and dose of EN remain understudied. Study objective Our objective was to evaluate the relationship between achieving 70% of recommended EN within 2 days of intubation (‘early goal EN’) and clinical outcomes in mechanically ventilated medically critically ill adults. We hypothesised that early goal EN would be associated with reduced in-hospital death. Methods We conducted a retrospective cohort study of mechanically ventilated adult patients admitted to our medical intensive care unit during 2013–2019. We assessed the proportion of recommended total EN provided to the patient each day following intubation until extubation, death or 7 days whichever was shortest. Patients who received 70% or more of their recommended total daily EN within 2 days of intubation (ie, ‘baseline period’) were considered to have achieved ‘early goal EN’; these patients were compared with patients who did not (‘low EN’). The primary outcome was in-hospital death; secondary outcomes were successful extubation and discharge alive. Results 938 patients met eligibility criteria and survived the baseline period. During the 7-day postintubation period, 64% of all patients reached 70% of recommended daily calories; 33% of patients achieved early goal EN. In unadjusted and adjusted models, early goal EN versus low EN was associated with a lower incidence of in-hospital death (subdistribution HR (SHR) unadjusted=0.63, p=0.0003, SHR adjusted=0.73, p=0.02). Early goal EN was also associated with a higher incidence of successful extubation (SHR unadjusted=1.41, p<0.00001, SHR adjusted=1.27, p=0.002) and discharge alive (SHR unadjusted=1.54, p<0.00001, SHR adjusted=1.24, p=0.02). Conclusions Early goal EN was associated with significant improvement in clinical metrics of decreased in-hospital death, increased extubation and increased hospital discharge alive. Data are available on reasonable request.
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来源期刊
BMJ Open Respiratory Research
BMJ Open Respiratory Research RESPIRATORY SYSTEM-
CiteScore
6.60
自引率
2.40%
发文量
95
审稿时长
12 weeks
期刊介绍: BMJ Open Respiratory Research is a peer-reviewed, open access journal publishing respiratory and critical care medicine. It is the sister journal to Thorax and co-owned by the British Thoracic Society and BMJ. The journal focuses on robustness of methodology and scientific rigour with less emphasis on novelty or perceived impact. BMJ Open Respiratory Research operates a rapid review process, with continuous publication online, ensuring timely, up-to-date research is available worldwide. The journal publishes review articles and all research study types: Basic science including laboratory based experiments and animal models, Pilot studies or proof of concept, Observational studies, Study protocols, Registries, Clinical trials from phase I to multicentre randomised clinical trials, Systematic reviews and meta-analyses.
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