Retrospective Study to Evaluate the Tolerability and Safety of Acute Pain Service at Queen Mary Hospital Between 2009 to 2012
试验速览
- 阶段
- 不适用
- 入组人数
- 7,500
- 试验地点
- 1
- 主要终点
- Pain score
研究概览
简要总结
Acute pain service (APS) was introduced in 1990s at Queen Mary Hospital (QMH) as other countries. With accumulation of experience and clinical evidence, APS has been well established. A study conducted in 1997 suggested that monitoring, management protocol and nursing experience were mandatory to the safety for APS. Our recent study showed that pain relief of our post-operative patients using patient controlled analgesic with morphine was still not adequate. The results has driven us to continue the improvement of post-operative outcomes for our surgical patients. Tolerability and safety are always our concerns for patients using our APS. Therefore, the investigators aim to conduct this retrospective study in order to assess if the tolerability and safety of our present APS are adequate or not. The study results will help us to further improve our APS at QMH if necessary.
详细描述
Retrospective audit.
Acute pain service records at Division of Pain Management, Department of Anaesthesiology, Queen Mary Hospital will be identified, validated and analysed.
Data Collection
- Demographic data
- Type of operation
- Type of pain relief modality
- Pain score up to 72 hours postoperatively
- Types of operations and clinical variables
- Incidence of adverse events during APS care;
- Patients safety (ie respiratory depression)
Data Analysis For summarising analysis, mean or median with standard deviation or interquartile range will be reported. Parametric and non-parametric comparative tests will be used for analysis between/among patients with various characteristics. Kaplan Meier survival analysis and log-rank test will be used for duration of APS use.
研究设计
- 研究类型
- Observational
- 时间视角
- Retrospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Postoperative patients who were cared by the Acute Pain Service, Pain Management Team, Department of Anaesthesiology, Queen Mary Hospital between 2009 to 2012.
排除标准
- •Essential data were missing;
- •Patient participating in other research projects.
结局指标
主要结局
Pain score
时间窗: From postoperative 1 hour to postoperative 72 hour
次要结局
- Incidence of adverse events(From postoperative 1 hour to postoperative 72 hour)
研究者
Cheung Chi Wai
Clinical Associate Professor
The University of Hong Kong