Oral Chlorhexidine effect on ICU mortality and ventilator-associated pneumonia

口服洗必太对 ICU 死亡率和呼吸机相关性肺炎的影响

• 批准号: 7313219
• 负责人: CATHERINE J BINKLEY
• 金额: $ 27.28万
• 依托单位: UNIVERSITY OF LOUISVILLE
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-07-10 至 2009-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7313219
• 关键词: Accounting; Address; Admission activity; Alcohols; Aspirate substance; Bacteria; Case Fatality Rates; Chlorhexidine; Clinical; Clinical Data; Clinical Trials; Condition; Control Groups; Controlled Clinical Trials; Critical Care; Critical Illness; Data Coordinating Center; Databases; Development; Diagnosis; Diagnostic; Double-Blind Method; Economics; Enrollment; Environmental air flow; General Population; Goals; Grant; Health Care Costs; Health Policy; Health Professional; Hearing; Hospitals; Hour; Human Resources; Incidence; Infection; Intensive Care Units; Intervention; Irrigation; K-Series Research Career Programs; Laboratories; Lead; Legal; Length; Length of Stay; Logistics; Lung; Manuals; Measures; Mechanical ventilation; Medical; Medical center; Methodology; Microscopy; Monitor; Morbidity - disease rate; Mouthwash; Multi-Drug Resistance; Multi-Institutional Clinical Trial; Neurologic; Nosocomial Infections; Nosocomial pneumonia; Operative Surgical Procedures; Oral; Oral cavity; Oropharyngeal; Outcome; Outcome Study; Patient Recruitments; Patients; Pharmaceutical Preparations; Phase III Clinical Trials; Physicians; Placebo Control; Placebos; Pneumonia; Population; Population Study; Preventive; Preventive Intervention; Procedures; Public Health; Randomized; Randomized Clinical Trials; Recruitment Activity; Regression Analysis; Research; Research Design; Research Institute; Research Personnel; Risk; Risk Factors; Sampling; Score; Solutions; Specimen; Sputum; Standardization; Stratification; Structure of parenchyma of lung; Swab; Testing; Time; Tooth structure; Toothbrushing; United States; United States National Institutes of Health; Upper arm; Ventilator; antimicrobial; antimicrobial drug; chlorhexidine gluconate; clinical research site; cost; cost effectiveness; day; design; disorder control; experience; human disease; mortality; oral care; pathogen; prevent; respiratory; toothbrush; treatment effect

DESCRIPTION (provided by applicant): Nosocomial pneumonia is the second most common hospital-acquired infection and most common intensive care unit infection. It is associated with significant morbidity and mortality. Aspiration of oropharyngeal contents is considered a major risk factor for pneumonia, especially in mechanically ventilated patients. Whether application of oral antimicrobial agents such as chlorhexidine reduces the risk of pneumonia in the general intensive care unit patient population remains controversial. The proposed Phase III clinical trial will be a five-year, four-center placebo-controlled randomized clinical trial with a chlorhexidine oral application as the intervention. The research will extend previous findings in a general ICU population study sample by using well-validated clinical and scoring criteria for major outcomes. The proposed trial will be powered to evaluate a composite primary outcome of ventilator-associated pneumonia (VAP) and/or mortality with 535 patients in the control group and 535 patients in the intervention group. A 2 year planning grant is requested to refine the study design and methodology, develop a Manual of Operating Procedures, refine patient recruitment approaches, organize potential study centers for standardization of approach and diagnostic criteria, and establish administrative and monitoring committees. Personnel from the four clinical sites and the data coordinating center will participate in these activities as part of the Clinical Trial Planning Committee. The Phase III clinical trial would be the first outcome study properly powered to evaluate the effect of chlorhexidine oral application on pneumonia and/or mortality, and associated morbidity outcomes in mechanically ventilated patients with various indications for ICU admission (including surgical, medical, and neurological). It may provide evidence for changing health care policy by showing that a simple, inexpensive oral care preventive intervention reduces the morbidity, mortality, and costs associated with nosocomial pneumonia.

描述（由申请人提供）：医院获得性肺炎是第二常见的医院获得性感染，也是最常见的重症监护病房感染。它与显著的发病率和死亡率相关。吸入口咽内容物被认为是肺炎的主要危险因素，特别是在机械通气患者中。在普通重症监护室患者人群中，口服抗菌药物（如洗必泰）是否能降低肺炎风险仍存在争议。拟议的III期临床试验将是一项为期五年的四中心安慰剂对照随机临床试验，以氯己定口服应用作为干预措施。该研究将通过使用经过充分验证的临床和主要结局评分标准，扩展先前在一般ICU人群研究样本中的发现。拟议的试验将有把握度评价呼吸机相关性肺炎（VAP）和/或死亡率的复合主要结局，对照组535例患者和干预组535例患者。申请2年规划补助金，以完善研究设计和方法，制定操作程序手册，完善患者招募方法，组织潜在的研究中心以实现方法和诊断标准的标准化，并建立行政和监测委员会。来自四个临床研究中心和数据协调中心的人员将作为临床试验计划委员会的一部分参与这些活动。III期临床试验将是第一项有适当把握度的结局研究，以评估氯己定口服应用对患有各种ICU适应症（包括外科、内科和神经科）的机械通气患者的肺炎和/或死亡率以及相关发病率结局的影响。它可以提供证据，改变卫生保健政策，显示一个简单的，廉价的口腔护理预防性干预措施，降低发病率，死亡率和成本与医院获得性肺炎。