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Streamlining Safety Data Collection in Hospital-Acquired Bacterial Pneumonia and Ventilator-Associated Bacterial Pneumonia Trials: Recommendations of the Clinical Trials Transformation Initiative Antibacterial Drug Development Project Team

机译:简化医院获得性细菌性肺炎和呼吸机相关细菌性肺炎试验的安全数据收集:临床试验转化计划抗菌药物开发项目小组的建议

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Background. Resistant bacteria are one of the leading causes of hospital-acquired/ventilator-associated bacterial pneumonia (HABP/VABP). HABP/VABP trials are complex and difficult to conduct due to the large number of medical procedures, adverse events, and concomitant medications involved. Differences in the legislative frameworks between different regions of the world may also lead to excessive data collection. The Clinical Trials Transformation Initiative (CTTI) seeks to advance antibacterial drug development (ABDD) by streamlining clinical trials to improve efficiency and feasibility while maintaining ethical rigor, patient safety, information value, and scientific validity.
机译:背景。耐药细菌是医院获得性/呼吸机相关细菌性肺炎(HABP / VABP)的主要原因之一。由于大量的医疗程序,不良事件以及所涉及的药物治疗,HABP / VABP试验非常复杂且难以进行。世界不同地区之间立法框架的差异也可能导致过多的数据收集。临床试验转化计划(CTTI)寻求通过简化临床试验来提高抗菌药物开发(ABDD)的效率和可行性,同时保持道德上的严格性,患者安全性,信息价值和科学有效性。

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