Effectiveness of Early Prone Positioning on Clinical Outcomes in Non-intubated Acute Respiratory Distress Syndrome (ARDS) Patients: A Quasi-experimental Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Change in arterial oxygenation (PaO₂ in mmHg)
研究概览
简要总结
This study aimed to evaluate the effectiveness of early prone positioning in improving clinical outcomes among non-intubated patients with Acute Respiratory Distress Syndrome (ARDS). Prone positioning, which involves placing patients on their stomachs, has been shown to improve outcomes in patients on mechanical ventilation. However, limited evidence exists for its use in non-intubated patients. The researchers conducted a quasi-experimental study at Jenin Governmental Hospital in Palestine, involving two groups: one received early prone positioning in addition to standard care, and the other received standard care alone. Key clinical outcomes included respiratory rate, oxygen saturation, need for intubation, length of Intensive Care Unit (ICU) stay, and mortality. This study adds to the growing evidence supporting non-invasive interventions for managing ARDS and may help inform future clinical guidelines in low-resource settings.
详细描述
Acute Respiratory Distress Syndrome (ARDS) is a life-threatening condition characterized by rapid-onset respiratory failure, low blood oxygen levels (hypoxemia), and bilateral pulmonary infiltrates. While prone positioning has become an established part of care for intubated patients with moderate to severe ARDS, its role in non-intubated, spontaneously breathing patients remains underexplored, particularly in resource-limited settings.
This quasi-experimental study assessed the clinical effectiveness of early implementation of prone positioning in non-intubated ARDS patients in the Intensive Care Unit (ICU) of Jenin Governmental Hospital, Palestine. The study was conducted from January to April 2024. A total of 100 adult patients who met the Berlin definition of ARDS and did not require immediate intubation were enrolled and divided into two groups of 50: the intervention group received early prone positioning alongside standard medical care, while the control group received only standard care without prone positioning.
The primary clinical endpoints included changes in oxygen saturation (SpO₂), respiratory rate, need for mechanical ventilation, and length of ICU stay. Additional variables such as arterial blood gas (ABG) parameters, hemodynamic stability, and patient tolerance to prone positioning were monitored throughout the ICU admission. Patients were followed until ICU discharge or in-hospital mortality.
The early prone positioning protocol was implemented within 24 hours of ARDS diagnosis. Patients were assisted to maintain the prone position for multiple daily sessions, each lasting 2-4 hours, depending on tolerance and clinical stability. Standardized nursing assessments and physician evaluations were performed to monitor safety and efficacy.
Data were analyzed using appropriate statistical methods to compare outcomes between groups. Ethical approval was obtained from the Arab American University Institutional Review Board (IRB reference: R-2024/B/84/N). The study provides insight into the feasibility, safety, and potential clinical benefit of prone positioning as a low-cost, non-invasive intervention for managing ARDS in non-intubated patients, with implications for ICU protocols in low- and middle-income countries (LMICs).
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
盲法说明
None. Due to the physical nature of the intervention (prone positioning), blinding was not feasible.
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
- •Awake patients diagnosed with Acute Respiratory Distress Syndrome (ARDS) according to established criteria.
- •Eligible for prone positioning combined with non-invasive respiratory support.
- •Willing and able to provide informed consent.
- •Aged 18 years or older.
- •Hemodynamically stable.
- •Conscious, normal mental status, able to follow instructions, and capable of self-positioning.
排除标准
- •Severe hemodynamic instability or other contraindications to prone positioning.
- •Inability to provide consent or participate actively.
- •Significant comorbidities that could confound outcomes.
- •Impaired consciousness or inability to change position.
- •Normal oxygen saturation without supplemental oxygen.
- •Respiratory fatigue or patients receiving end-of-life care
研究组 & 干预措施
Early Prone Positioning Protocol
Participants in this arm received early prone positioning as part of the study protocol. Patients were assisted into a prone position for 4 hours, with measurements taken at baseline, 2 hours, and 4 hours. The intervention was initiated soon after the Acute Respiratory Distress Syndrome (ARDS) diagnosis, according to clinical stability and eligibility. The procedure was supervised by trained Intensive Care Unit (ICU) nurses, with continuous monitoring for tolerance, oxygenation status, and safety.
干预措施: Early Prone Positioning Protocol (Procedure)
Standard Care
Participants in this arm received standard Intensive Care Unit (ICU) care without early implementation of prone positioning. Any use of prone positioning occurred at the discretion of the treating medical team and was not based on a standardized protocol. All other supportive treatments followed routine ICU protocols.
干预措施: Standard ICU Care (Other)
结局指标
主要结局
Change in arterial oxygenation (PaO₂ in mmHg)
时间窗: Baseline, 2 hours, and 4 hours after intervention
This outcome assesses the effect of early prone positioning on arterial oxygenation in non-intubated Acute Respiratory Distress Syndrome (ARDS) patients. The partial pressure of arterial oxygen (PaO₂) will be measured via arterial blood gas (ABG) analysis and compared between the intervention and control groups.
次要结局
- Change in peripheral oxygen saturation (SpO₂ in %)(Baseline, 2 hours, and 4 hours after intervention)
- Change in respiratory rate (breaths/minute)(Baseline, 2 hours, and 4 hours after intervention)
- Change in serum bicarbonate (HCO₃ in mmol/L)(Baseline, 2 hours, and 4 hours after intervention)
- Change in arterial carbon dioxide pressure (PaCO₂ in mmHg)(Baseline, 2 hours, and 4 hours after intervention)
- Change in blood pH(Baseline, 2 hours, and 4 hours after intervention)
- Incidence of complications(Baseline, 2 hours, and 4 hours after intervention)
研究者
Loai Muawiah Zabin
Assistant Professor, Faculty of Nursing
Arab American University (Palestine)