Effects of Implementing Evidence-Based Clinical Nutrition Practice Guidelines in Surgical Intensive Care Units: A Cohort Study
概览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 200
- 主要终点
- Adherence of ICU Healthcare Professionals to Clinical Nutrition Practice Guidelines
概览
简要总结
The goal of this interventional clinical trial is to evaluate whether the implementation of an evidence-based, context-adapted clinical nutrition practice guideline can improve clinical nutrition management in surgical intensive care units (ICUs) in China. The guideline is selected based on the best available evidence from existing surgical and critical care nutrition guidelines, adapted to the Chinese healthcare context, and implemented using an i-PARIHS-guided translation strategy. The trial involves ICU healthcare professionals working in surgical ICUs of tertiary general hospitals, while assessing nutrition-related clinical outcomes among surgical critically ill patients.
The main questions it aims to answer are:
Does guideline implementation improve ICU healthcare professionals' adherence to recommended clinical nutrition practice guidelines?
Does the implementation of the clinical nutrition practice guideline improve the proportion of surgical critically ill patients who achieve recommended energy and protein intake targets during ICU stay?
Researchers will compare outcomes before and after guideline implementation to determine whether the i-PARIHS-guided guideline translation improves nutrition management processes, healthcare professional performance, and patient-related clinical outcomes.
Participants will:
Complete baseline and post-implementation assessments related to clinical nutrition knowledge, attitudes, and practices.
Participate in guideline-based education, training, and implementation activities guided by the i-PARIHS framework.
Apply the adapted clinical nutrition practice guideline during routine clinical care in surgical ICUs.
Be evaluated through on-site audits, questionnaires, and clinical data collection during the implementation process.
详细描述
This study is an interventional, multicenter implementation clinical trial designed to translate and apply an evidence-based clinical nutrition practice guideline in surgical intensive care units (ICUs) in China, guided by the i-PARIHS framework. The guideline is developed through a structured process that includes identification of best available evidence from existing surgical and critical care nutrition guidelines, contextual adaptation to the Chinese healthcare setting, guideline item localization, and expert consensus validation.
The implementation strategy is informed by the i-PARIHS framework, with particular emphasis on facilitation, local context assessment, and engagement of key stakeholders. A series of structured implementation activities, including education, training, on-site facilitation, audit and feedback, and continuous process optimization, are conducted to support guideline uptake in routine clinical practice. The implementation process follows a pre- and post-implementation design, allowing for comparison of outcomes before and after guideline translation.
The primary outcomes focus on (1) adherence of ICU healthcare professionals to recommended clinical nutrition practice guidelines and (2) the proportion of surgical critically ill patients achieving recommended energy and protein intake targets during ICU stay.
Secondary outcomes are assessed to comprehensively evaluate the impact of guideline implementation on nutrition delivery processes and patient-related clinical outcomes. These include:
Timing of enteral nutrition initiation after ICU admission
Frequency of enteral nutrition interruptions during ICU stay
Global Leadership Initiative on Malnutrition (GLIM) classification at ICU discharge
Cumulative daily energy and protein balance, including total caloric and protein surplus or deficit per day during ICU stay
Laboratory indicators at ICU discharge, including urea-to-creatinine ratio, serum albumin, globulin, interleukin-6 (IL-6), and C-reactive protein (CRP)
Length of ICU stay
Clinical outcomes during ICU hospitalization
All-cause 28-day mortality
Data are collected through a combination of on-site clinical audits, standardized questionnaires, electronic medical record extraction, and laboratory testing. Outcomes related to healthcare professionals are measured using structured adherence assessment tools and knowledge-attitude-practice evaluations, while patient-related outcomes are derived from routinely collected clinical and laboratory data.
The feasibility, appropriateness, and effectiveness of the guideline implementation are evaluated based on changes in outcome measures, process indicators, and participant satisfaction. The findings of this study are intended to inform scalable and context-sensitive strategies for optimizing clinical nutrition management in surgical ICUs within the Chinese healthcare system.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •For ICU healthcare professionals:
- •Employed at one of the participating study sites (tertiary general hospitals)
- •Holds a valid Registered Nurse license issued in the People's Republic of China
- •Currently working in frontline clinical nursing care in a surgical intensive care unit (ICU) during the study period
- •At least 1 year of clinical working experience
- •Able to understand the study objectives and procedures
- •Willing to participate and able to provide written informed consent
- •For surgical critically ill patients (outcome assessment population):
- •Aged 18 years or older
- •Admitted to a surgical ICU due to surgical-related conditions, including trauma, infection, malignancy, or postoperative complications
排除标准
- •For ICU healthcare professionals:
- •Currently pregnant, breastfeeding, or planning pregnancy during the study period
- •Temporarily assigned, rotating, externally dispatched, on long-term training, or on leave during the study period, making continuous participation impossible
- •Participation in other interventional studies that may interfere with the implementation of this study
- •Determined by the research team to have cognitive, communication, or other conditions that would make participation inappropriate
- •For surgical critically ill patients:
- •Diagnosed with brain death or awaiting organ donation
- •Pregnant or breastfeeding women
- •Concurrent participation in other nutrition-related clinical trials
研究组 & 干预措施
Guideline Implementation Group
Participants in this single-arm study will receive an evidence-based, context-adapted clinical nutrition practice guideline implemented in surgical intensive care units (ICUs) using an i-PARIHS-guided translation strategy. The implementation includes guideline localization, expert consensus validation, education and training, on-site facilitation, audit and feedback, and continuous process optimization. Outcomes will be assessed before and after guideline implementation to evaluate changes in healthcare professional adherence to clinical nutrition recommendations and nutrition-related clinical outcomes among surgical critically ill patients.
干预措施: Guideline Implementation (Behavioral)
结局指标
主要结局
Adherence of ICU Healthcare Professionals to Clinical Nutrition Practice Guidelines
时间窗: At baseline (prior to implementation) and at 6 months after implementation.
Adherence of ICU healthcare professionals to clinical nutrition practice guidelines, assessed using structured audit tools based on key guideline recommendations, including nutrition assessment, initiation and delivery of nutrition support, monitoring, and documentation practices.
次要结局
- Proportion of Surgical Critically Ill Patients Achieving Energy and Protein Intake Targets During ICU Stay(From ICU admission (Day 1) to ICU discharge)