Ripa Marco, Galli Laura, Cinque Paola, Nozza Silvia, Spagnuolo Vincenzo, Tassan Din Chiara, Guffanti Monica, Lolatto Riccardo, Piromalli Girolamo, Carletti Silvia, Locatelli Massimo, Sanvito Francesca, Ponzoni Maurilio, Cantarelli Elisa, Tresoldi Cristina, Castagna Antonella
Unit of Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy
Vita-Salute San Raffaele University, Milan, Italy.
BMJ Open. 2025 Aug 12;15(8):e091113. doi: 10.1136/bmjopen-2024-091113.
INTRODUCTION: Infectious diseases are a major global health concern, responsible for significant morbidity and mortality. To advance the understanding and treatment of these diseases, biobanks and biorepositories play a crucial role in guaranteeing sample traceability through their entire life cycle (collection, acquisition and registration, processing, storage, distribution) and future analysis of clinical and biological data. METHODS AND ANALYSIS: The INfectious DIsease REgistry BIObank (INDI-REBIO) is an observational, prospective, monocentric, open-ended registry with ad hoc procedures and a systematic collection of uniform clinical, laboratory, imaging and therapeutic data of patients with suspected or microbiologically documented bacterial, viral, fungal and parasitic infectious diseases from the IRCCS San Raffaele Hospital (Milan, Italy). The study aims to collect both uniform data and biological samples such as blood and other relevant specimens. The registry aims to include significant patient numbers across various conditions (among others: bloodstream infections, endovascular infections as infective endocarditis, central nervous system infections, bone and joint infections, multidrug-resistant organisms (MDROs) colonisation, sexually transmitted infections, HIV infection, emerging and re-emerging infectious diseases), enabling comprehensive research on disease evolution, treatment outcomes and the identification of biomarkers. ETHICS AND DISSEMINATION: The study adheres to ethical principles outlined by the Helsinki Declaration and Good Clinical Practice guidelines. It has received ethical approval (Comitato Etico CET Lombardia 1, CET 138-2023) and is registered on clinicaltrials.gov (NCT06418048). Participants will provide informed consent and can withdraw at any time. The study results will be disseminated through major international conferences and submitted to peer-reviewed research journals. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov, NCT06418048.
引言:传染病是全球主要的健康问题,会导致大量发病和死亡。为了增进对这些疾病的理解和治疗,生物样本库和生物资源库在确保样本在其整个生命周期(采集、获取与登记、处理、储存、分发)中的可追溯性以及未来临床和生物学数据的分析方面发挥着关键作用。 方法与分析:传染病登记生物样本库(INDI - REBIO)是一项观察性、前瞻性、单中心、开放式登记研究,采用专门程序,系统收集来自意大利米兰圣拉斐尔科学研究所医院怀疑患有或微生物学确诊患有细菌、病毒、真菌和寄生虫传染病患者的统一临床、实验室、影像和治疗数据。该研究旨在收集统一数据以及血液等生物样本和其他相关标本。该登记研究旨在纳入各种病症的大量患者(包括但不限于:血流感染、感染性心内膜炎等血管内感染、中枢神经系统感染、骨和关节感染、多重耐药菌(MDROs)定植、性传播感染、HIV感染、新发和再发传染病),以便对疾病演变、治疗结果和生物标志物鉴定进行全面研究。 伦理与传播:该研究遵循《赫尔辛基宣言》和《良好临床实践指南》中概述的伦理原则。它已获得伦理批准(伦巴第地区伦理委员会CET 1,CET 138 - 2023),并在clinicaltrials.gov上注册(NCT06418048)。参与者将提供知情同意书,并且可以随时退出。研究结果将通过主要国际会议进行传播,并提交给同行评审的研究期刊。 试验注册号:ClinicalTrials.gov,NCT06418048。
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