Department of Laboratory Medicine, The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China.
Department of Respiratory and Critical Care Medicine, The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China.
BMJ Open. 2019 Aug 1;9(8):e027287. doi: 10.1136/bmjopen-2018-027287.
Serum and fluid laboratory markers are valuable for exploring the aetiologies of pleural effusion (PE) because of their relative non-invasiveness, low cost, objective result and short turnaround time. The diagnostic accuracy of these potential markers needs to be rigorously evaluated before their widespread application in clinical practice. Here, we plan to perform a Study Investigating Markers in PLeural Effusion (SIMPLE).
This is a prospective and double-blind clinical trial which is being performed at the Affiliated Hospital of Inner Mongolia Medical University, China. Adult patients admitted for the evaluation of aetiology of PE from September 2018 to July 2021 will be enrolled after informed consent. Pleural fluid and serum specimens will be collected and stored at -80°C for the laboratory analysis. The final diagnosis will be concurred with further imaging, microbiology, cytology and biopsy if needed. The results of investigated laboratory markers will be unknown to the clinicians who will make diagnosis and the clinical diagnoses will be unknown to the laboratory technicians who will determine markers. The diagnostic accuracy of investigated markers will be assessed using receiver operating characteristics (ROC) curve analysis, multivariable logistic regression model, decision curve analysis (DCA), net reclassification index (NRI) and integrated discriminatory index (IDI).
The study is approved by the Ethic Committee of the Affiliated Hospital of Inner Mongolia Medical University (NO: 2018011). The results of SIMPLE will be submitted to international scientific peer-reviewed journals or conferences in laboratory medicine or respiratory medicine, thoracic diseases.
Chinese Clinical Trial Registry (ChiCTR1800017449); Pre-results.
血清和体液实验室标志物在探索胸腔积液(PE)病因方面具有重要价值,因为它们相对无创、成本低、结果客观、周转时间短。在这些潜在标志物广泛应用于临床实践之前,需要严格评估其诊断准确性。在这里,我们计划进行一项研究胸腔积液标志物的研究(SIMPLE)。
这是一项在中国内蒙古医科大学附属医院进行的前瞻性、双盲临床试验。2018 年 9 月至 2021 年 7 月,经知情同意后,将招募因胸腔积液病因评估而入院的成年患者。采集胸腔积液和血清标本,储存在-80°C 用于实验室分析。最终诊断将与进一步的影像学、微生物学、细胞学和活检相结合,如果需要的话。调查实验室标志物的结果将不为做出诊断的临床医生所知,而将确定标志物的实验室技术人员也将不了解临床诊断。使用受试者工作特征(ROC)曲线分析、多变量逻辑回归模型、决策曲线分析(DCA)、净重新分类指数(NRI)和综合判别指数(IDI)评估调查标志物的诊断准确性。
该研究得到了内蒙古医科大学附属医院伦理委员会的批准(编号:2018011)。SIMPLE 的结果将提交给实验室医学或呼吸医学、胸部疾病领域的国际科学同行评议期刊或会议。
中国临床试验注册中心(ChiCTR1800017449);预结果。