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首页> 外文期刊>BMC Infectious Diseases >Sputum signatures for invasive pulmonary aspergillosis in patients with underlying respiratory diseases (SPARED): study protocol for a prospective diagnostic trial
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Sputum signatures for invasive pulmonary aspergillosis in patients with underlying respiratory diseases (SPARED): study protocol for a prospective diagnostic trial

机译:潜在呼吸系统疾病(SPARED)患者的侵袭性肺曲霉病的痰标本:前瞻性诊断试验的研究方案

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Invasive pulmonary aspergillosis (IPA) has been increasingly reported in patients with underlying respiratory diseases (URD). Early diagnosis of IPA is crucial for mortality reduction and improved prognosis, yet remains difficult. Existing diagnostic tools for IPA largely rely on the detection of biomarkers based on serum or bronchoalveolar lavage fluid (BALF), both of which have their limitations. The use of sputum sample is non-invasive, and Aspergillus detection is feasible; however, the usefulness of sputum biomarkers for the diagnosis of IPA, especially in patients with URD, has not been systematically studied. This is a prospective diagnostic trial. At least 118 participants will be recruited from respiratory wards and intensive care units. IPA is defined according to the EORTC/MSG criteria modified for patients with URD. Induced sputum and blood will be collected, and BALF will be obtained by bronchoscopy. Sputum biomarkers, including galactomannan, Aspergillus DNA, triacetylfusarinine and bis(methylthio)gliotoxin will be determined, and the presence of a JF5 antigen will be examined with a lateral fluid device. The sensitivity, specificity, negative predictive value, positive predictive value and diagnostic odds ratio will be computed for different biomarkers and compared using the McNemar χ2 test. Receiver operating characteristic analyses will be performed, and the cut-off values will be established. Participants will receive follow-up evaluations at 3?months and 6?months after recruitment. The difference in hospital stay and survival will be analysed, and the relationships between the levels of biomarkers and hospital stay and survival will be analysed via regression models. We have developed and verified the feasibility of Aspergillus-related biomarker assays for sputum. The study findings will contribute to a novel look at the diagnostic performance of sputum biomarkers in IPA and provide important insight into the improvement of the early diagnosis of IPA, particularly in patients with URD. This study has been registered with the Chinese Clinical Trial Registry ( ChiCTR-DPD-16009070 ) on 24th of August 2016.
机译:患有基础呼吸系统疾病(URD)的患者中侵袭性肺曲霉病(IPA)的报道越来越多。 IPA的早期诊断对于降低死亡率和改善预后至关重要,但仍然很困难。现有的IPA诊断工具主要依靠基于血清或支气管肺泡灌洗液(BALF)的生物标志物的检测,这两种方法都有其局限性。痰标本的使用是非侵入性的,曲霉菌检测是可行的。然而,尚未系统研究痰液生物标志物在诊断IPA中的有用性,尤其是在URD患者中。这是一项前瞻性诊断试验。将从呼吸病房和重症监护室招募至少118名参与者。 IPA是根据为URD患者修改的EORTC / MSG标准定义的。将收集诱导的痰液和血液,并通过支气管镜检查获得BALF。将确定痰液生物标志物,包括半乳甘露聚糖,曲霉DNA,三乙酰夫萨林碱和双(甲硫基)胶质毒素,并用侧向流体装置检查JF5抗原的存在。将针对不同的生物标记物计算灵敏度,特异性,阴性预测值,阳性预测值和诊断比值比,并使用McNemarχ2检验进行比较。将执行接收机工作特性分析,并确定截止值。参加者将在招募后的3个月和6个月接受随访评估。将分析住院时间和生存率的差异,并通过回归模型分析生物标志物水平与住院时间和生存率之间的关系。我们已经开发并验证了与曲霉相关的生物标志物测定痰液的可行性。该研究结果将有助于对IPA中痰液生物标志物的诊断性能进行新颖的观察,并为改善IPA的早期诊断(尤其是对URD患者)提供重要的见识。该研究已于2016年8月24日在中国临床试验注册中心(ChiCTR-DPD-16009070)注册。

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