跳至主要内容
临床试验/NCT00142766
NCT00142766已完成2 期

Sedation Management in Pediatric Patients Supported on Mechanical Ventilation

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)3 个研究点 分布在 1 个国家目标入组 245 人开始时间: 2004年2月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
245
试验地点
3
主要终点
Duration of Mechanical Ventilation

研究概览

简要总结

The purpose of this two-year project is to pilot test an intervention to change sedation management in pediatric patients supported on mechanical ventilation for acute respiratory failure in the pediatric intensive care unit (PICU). While ensuring patient comfort is an integral part of pediatric critical care, analgesic and sedative use in this patient population is associated with injury; specifically, comfort medications may depress spontaneous ventilation and prolong the duration of mechanical ventilation. Additionally, drug tolerance develops over time and may precipitate iatrogenic abstinence syndrome (chemical withdrawal) when the patient no longer requires sedation. Alternatively, suboptimal comfort management contributes to the patient not breathing synchronously with the ventilator and/or self-removal of breathing tubes.

Our group has developed and validated a nurse-implemented sedation algorithm (set of specific instructions) to guide titration of comfort medications that may optimize patient comfort and reduce the risk of under-medication, but this algorithm needs to be evaluated further. We hypothesize that pediatric patients managed per sedation protocol will experience fewer days of mechanical ventilation than patients receiving usual care. This research has the potential of revolutionizing sedation practices that are driven by and synchronized to patient needs.

详细描述

We propose a two-year project to pilot test and evaluate an intervention to change sedation management in pediatric patients supported on mechanical ventilation for acute respiratory failure in the PICU. Rather than seeking an elusive ideal drug, this unique nurse-led pilot study focuses on optimizing clinical decision making by: (a) multidisciplinary team education and consensus building; (b) multidisciplinary team identification of the patient's trajectory of illness and daily prescribing of a sedation goal; (c) a nurse-implemented sedation algorithm to guide titration of comfort medications; and(d)team feedback on clinical performance. This intervention models the most recent sedation clinical practice guideline published by the Society of Critical Care Medicine and addresses the only potentially manipulable factor influencing extubation failures rates in the Pediatric Intensive Care Unit.

The coordinating center, Children's Hospital Boston, developed, tested and currently uses the sedation algorithm as a standard of care. We will pilot the intervention in two separate previously selected PICUs that are matched on size and organization, academic affiliation and volume of patients supported on mechanical ventilation. One PICU will be randomized to receive early intervention while the other will first serve as a control, then will receive a delayed intervention.

The study design is a randomized controlled trial with delayed intervention in the control hospital. Because the intervention is an educational and organizational change directed at all PICU clinicians, the unit of randomization and analysis is the PICU. During the start-up phase, case report forms will be developed and a consensus meeting with all nurse and physician co-investigators will be conducted. The purpose of this consensus meeting will be to review the Children's Hospital Boston experience with the sedation algorithm and reach agreement on its application in the two PICUs. System nuances may impact protocol implementation and will require group discussion and multidisciplinary problem solving.

Study design includes baseline assessment of the organizational structure and comfort practices in both units. The PICU randomized to early intervention will then undergo training followed by implementation, a one-month respite, and post-data collection to evaluate the sustainability of the practice change. The PICU randomized to delayed intervention will start with pre-data collection, then undergo training followed by implementation. This design allows multiple comparisons; specifically, baseline to intervention/control, pre and post comparisons in both units, and sustainability in one unit.

Training will be multifaceted and will include all clinicians (physicians, nurses, clinical pharmacists and physicians-in-training) involved in the sedation management of intubated mechanically-ventilated patients. A multidisciplinary, cooperative approach is necessary to assure compliance and successful implementation of protocols. Training material will include discipline-specific lectures, informal discussions, video on sedation and opioid withdrawal scoring, bedside booklets, and physician order sheets. The research team will develop the supporting materials. Physician training will focus on sedation and opioid withdrawal scoring, identifying the patient's trajectory of illness, collaborating with nursing in prescribing the daily sedation goal, and completion of the standardized order template. Nursing content will likewise focus on sedation and opioid withdrawal scoring, trajectory analysis and collaboration, but also will include practical support on the daily "wake-up" test and titration of sedatives. Prior to the intervention phase, all physicians, physician-in-training, unit-based clinical pharmacist, charge nurses and full-time nursing staff will be required to document their understanding of the intervention by completion of a discipline-specific scenario-based self-assessment evaluation. Respiratory therapists will also require refresher instruction on extubation readiness testing and general information about sedation assessment and sedation algorithm.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Weeks 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Intubated and mechanically ventilated
  • •Pulmonary disease

排除标准

  • •Less than or equal to 2 weeks of age or 42 weeks corrected gestational age
  • •Greater than 18 years of age
  • •Intubated and mechanically ventilated for immediate post-operative care and stabilization
  • •Cyanotic heart disease with unrepaired or palliated right to left intracardiac shunt
  • •Critical airway (e.g. post laryngotracheal reconstruction)
  • •Ventilator dependent (including noninvasive) on PICU admission (chronic assisted ventilation)
  • •Neuromuscular respiratory failure
  • •Spinal cord injury above the lumbar region
  • •Managed by patient controlled analgesia (PCA)or epidural catheter
  • •Known allergy to any of the study medications (Morphine,Methadone, Midazolam, Lorazepam)
  • •Family/Medical team have decided not to provide full support(patient treatment considered futile)
  • •Previously enrolled into the current study or enrolled in any other sedation clinical trial concurrently or within the last 30 days

结局指标

主要结局

Duration of Mechanical Ventilation

时间窗: 28 days

次要结局

  • Time to Recovery of Lung Injury(28 days)
  • Duration of Weaning from Mechanical Ventilation(28 days)
  • Occurrence of Adverse Events(28 days)
  • Total Exposure to Comfort Medications(28 days)
  • Occurrence of Iatrogenic Abstinence Syndrome(28 days)
  • PICU costs(28 days)
  • Barriers to Successful Implementation of the Intervention(28 days)
  • PICU Length of Stay(28 days)

研究者

发起方
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
申办方类型
Nih
责任方
Principal Investigator
主要研究者

Martha Curley

Ellen and Robert Kapito Professor in Nursing Science

University of Pennsylvania

研究点 (3)

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