National Register Studies in Thoracic Surgery
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 20,000
- 试验地点
- 2
- 主要终点
- All-cause mortality
研究概览
简要总结
The overall project aim is to study risk and outcomes following thoracic surgery by cross-linking high-quality national Swedish health-data registers for population-based investigations of individual level clinically relevant patient data.
详细描述
The purpose of this research project is to study risks and outcomes in patients who underwent thoracic surgery, primarily for lung cancer. We aim to establish a fundament for the conduct of nationwide population-based studies by linking patient-level data from the Swedish quality register for thoracic surgery (ThoR) and other national health-data registers maintained by the government agencies Statistics Sweden and the National Board of Health and Welfare. Cross-linking patient-level data is possible through the Personal Identity Number assigned to every individual who has resided in Sweden on a permanent basis. The Swedish Personal Identity Number is the unique identifier in all national registers.
Specifically, we aim:
- To analyze the association between socioeconomic factors and prognosis in patients undergoing pulmonary resection for lung cancer.
- To investigate the implementation of minimally invasive surgery for lung cancer in Sweden.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 110 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •All adult patients who underwent thoracic surgery in Sweden during the study period
排除标准
- 未提供
结局指标
主要结局
All-cause mortality
时间窗: 15 years
Death from any cause
次要结局
- Postoperative complications(30 days)
研究者
Ulrik Sartipy, MD, PhD
MD, PhD
Karolinska University Hospital